U.S. patent application number 14/987937 was filed with the patent office on 2016-05-05 for tricyclic nucleosides and oligomeric compounds prepared therefrom.
The applicant listed for this patent is UNIVERSITAT BERN. Invention is credited to Branislav Dugovic, Christian Leumann, Jory Lietard.
Application Number | 20160122372 14/987937 |
Document ID | / |
Family ID | 47997409 |
Filed Date | 2016-05-05 |
United States Patent
Application |
20160122372 |
Kind Code |
A1 |
Leumann; Christian ; et
al. |
May 5, 2016 |
TRICYCLIC NUCLEOSIDES AND OLIGOMERIC COMPOUNDS PREPARED
THEREFROM
Abstract
The present invention provides novel tricyclic nucleosides and
oligomeric compounds prepared therefrom. Incorporation of one or
more of the tricyclic nucleosides into an oligomeric compound is
expected to enhance one or more properties of the oligomeric
compound. Such oligomeric compounds can also be included in double
stranded compositions. In certain embodiments, the oligomeric
compounds provided herein are expected to hybridize to a portion of
a target RNA resulting in loss of normal function of the target
RNA.
Inventors: |
Leumann; Christian; (Bern,
CH) ; Dugovic; Branislav; (Bern, CH) ;
Lietard; Jory; (Bern, CH) |
|
Applicant: |
Name |
City |
State |
Country |
Type |
UNIVERSITAT BERN |
Bern |
|
CH |
|
|
Family ID: |
47997409 |
Appl. No.: |
14/987937 |
Filed: |
January 5, 2016 |
Related U.S. Patent Documents
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Application
Number |
Filing Date |
Patent Number |
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14385050 |
Sep 12, 2014 |
9249178 |
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PCT/EP2013/055498 |
Mar 15, 2013 |
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14987937 |
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Current U.S.
Class: |
536/24.5 ;
549/220 |
Current CPC
Class: |
C12N 2310/11 20130101;
C07H 19/06 20130101; C07H 19/02 20130101; C12N 15/113 20130101;
C07H 19/04 20130101; C07H 21/00 20130101; C07H 19/16 20130101; C07F
9/65517 20130101; A61P 43/00 20180101 |
International
Class: |
C07F 9/655 20060101
C07F009/655; C12N 15/113 20060101 C12N015/113 |
Foreign Application Data
Date |
Code |
Application Number |
Mar 15, 2012 |
EP |
12159716.5 |
Claims
1. A tricyclic nucleoside described by general Formula I:
##STR00014## wherein: Bx is heterocyclic base moiety; one of
T.sup.1 and T.sup.2 is hydroxyl (--OH) or a protected hydroxyl and
the other of T.sup.1 and T.sup.2 is a phosphate or a reactive
phosphorus group; q.sup.1 and q.sup.2 are each, independently, H, F
or Cl, at least one of q.sup.3, q.sup.4 and q.sup.5 is,
independently, a group described by a general formula
--A.sup.1-X.sub.h-A.sup.2-Y.sub.n, wherein A.sup.1 is a
C.sub.k-alkyl, C.sub.k-alkenyl or C.sub.1-alkynyl, with k being an
integer selected from the range of 0 to 20, X.sub.h is
--C(.dbd.O)--, --C(.dbd.O)NR--, --O--, --O--, --S--, --NR--,
--C(.dbd.O)R, --C(.dbd.O)OR, C(.dbd.O)NR.sub.2--, --OR, --SR or
--NR.sub.2, with each R being selected independently from H,
methyl, ethyl, propyl, butyl, acetyl and 2-hydroxyethyl, and h is 0
or 1, A.sup.2 is a C.sub.i-alkyl, C.sub.i-alkenyl or
C.sub.i-alkynyl, with i being an integer selected from the range of
0 to 20, Y is a substituent group attached to any carbon atom on
A.sup.1 and/or A.sup.2, selected from --F, --Cl, --Br, .dbd.O,
--OR, --SR, --NR.sub.2, --NR.sub.3.sup.+, NHC(.dbd.NH)NH.sub.2,
--CN, --NC, --NCO, --NCS, --SCN, --COR, --CO.sub.2R, CONR.sub.2,
--R, with each R being selected independently from H, methyl,
ethyl, propyl, butyl, acetyl and 2-hydroxyethyl, and n is 0, 1, 2,
3, 4, 5 or 6, wherein k+i equals at least 1, the other ones of
q.sup.3, q.sup.4 and q.sup.5 are, independently, H, F or Cl, one of
z.sup.1 and z.sup.2 is H, --OH, F, Cl, OCH.sub.3, OCF.sub.3,
OCH.sub.2CH.sub.3, OCH.sub.2CF.sub.3, OCH.sub.2-CH.dbd.CH.sub.2,
O(CH.sub.2).sub.2-OCH.sub.3,
O(CH.sub.2).sub.2-O(CH.sub.2).sub.2-N(CH.sub.3).sub.2OCH.sub.2C(.dbd.O)
--N(H)CH.sub.3,
OCH.sub.2C(.dbd.O)--N(H)--(CH.sub.2).sub.2-N(CH.sub.3).sub.2 or
OCH.sub.2-N(H)--C(.dbd.NH)NH.sub.2.
2. The tricyclic nucleoside of claim 1, wherein Bx is uracil,
thymine, cytosine, 5-methyl-cytosine, adenine or guanine.
3. The tricyclic nucleoside of any one of the preceding claims,
wherein T.sup.1 is hydroxyl or protected hyroxyl, and wherein
T.sup.2 is a reactive phosphorus group selected from an
H-phosphonate or a phosphoramidite.
4. The tricyclic nucleoside of any one of the preceding claims,
wherein T.sup.4 is 4,4'-dimethoxytrityl and T.sup.2 is
diisopropylcyanoethoxy phosphoramidite or a controlled pore glass
surface.
5. The tricyclic nucleoside of any one of the preceding claims,
wherein q.sup.3 is described by the general formula
--A.sup.1X.sub.h-A.sup.2-Y.sub.n, and q.sup.4 and q.sup.5,
independently of each other, are H, F or Cl.
6. The tricyclic nucleoside of any one of the preceding claims,
wherein k is an interger from 3 to 16, h is 0, i is 0 and n is 1,
2, or 3.
7. The tricyclic nucleoside of any one of the preceding claims 1 to
5, wherein k is 1, h is 1 and X is --O--, COO--, CONH-- or CONR--,
i is an integer from 3 to 16 and n is 1, 2, or 3.
8. The tricyclic nucleoside of any one of the preceding claims 6 to
7, wherein n is 1 and Y is selected from NH.sub.2, NHR, NR.sub.2,
NR.sub.3.sup.+ and NHC(.dbd.NH)NH.sub.2, with R having the meaning
defined above.
9. The nucleoside of claim 8, wherein Y is in the
.omega.-position.
10. The tricyclic nucleoside of any one of the preceding claims,
wherein the sum of i+k is an integer from 3 to 16, particularly
from 3 to 12, more particularly from 5 to 10.
11. The tricyclic nucleoside of any one of preceding claims,
wherein A.sup.1 is CH.sub.2, h is 1 and X.sub.h is --C(.dbd.O)O--,
C(.dbd.O)NH--, and A.sup.2 is a C2 to C16 alkyl, Y.sub.n is
NH.sub.2 and n is 0 or 1.
12. The tricyclic nucleoside of claim 1, wherein A.sup.1 is
CH.sub.2.
13. The tricyclic nucleoside of claim 1, wherein k is 0.
14. A tricyclic nucleoside selected from the group of ##STR00015##
wherein Bx is selected from uracil, thymine, cytosine,
5-methylcytosine, adenine and guanine.
15. An oligomeric compound comprising at least one tricyclic
nucleoside according to any one of claims 1 to 0, wherein said
oligomeric compound comprises from 8 to 40 monomeric subunits.
16. The oligomeric compound of claim 15, wherein each Bx is,
independently, uracil, thymine, cytosine, 5-methylcytosine, adenine
or guanine.
17. The oligomeric compound of any one of claims 15 to 16, wherein
each internucleoside linking group is, independently, a
phosphodiester internucleoside linking group or a phosphorothioate
internucleoside linking group.
18. The oligomeric compound of any one of claims 15 to 17,
comprising a first region having at least two contiguous tricyclic
nucleosides having Formula II.
19. The oligomeric compound of claim 18 comprising a second region
having at least two contiguous monomeric subunits wherein each
monomeric subunit in the second region is a modified nucleoside
different from the tricyclic nucleosides of Formula II of said
first region.
20. The oligomeric compound of claim 19 further comprising a third
region located between said first and second regions wherein each
monomer subunit in the third region is independently, a nucleoside
or a modified nucleoside that is different from each tricyclic
nucleoside of Formula II of the first region and each monomer
subunit of the second region.
21. The oligomeric compound of any one of claims 15 to 20
comprising a gaped oligomeric compound having an internal region of
from 6 to 14 contiguous monomer subunits flanked on each side by an
external region of from 1 to 5 contiguous monomer subunits wherein
each monomer subunit in each external region is a tricyclic
nucleoside of Formula II and each monomer subunit in the internal
region is, independently, a nucleoside or a modified
nucleoside.
22. The oligomeric compound of any one of claims 15 to 21,
comprising one or several nucleotide blocks selected from
##STR00016## wherein T.sup.3 and T.sup.4 have the meanings outlined
above. Use of a trycyclic nucleoside according to any of claims 1
to 0 in the method for solid-phase synthesis of an oligonucleotide.
Description
FIELD OF THE INVENTION
[0001] The present invention relates to tricyclic alkyl-substituted
nucleosides described by the general Formula I and oligomeric
compounds prepared therefrom.
BACKGROUND OF THE INVENTION
[0002] Antisense technology is an effective means for reducing the
expression of specific gene products and can therefore be useful in
therapeutic, diagnostic, and research applications. Generally, the
principle behind antisense technology is that an antisense compound
(a sequence of oligonucleotides or analogues thereof) hybridizes to
a target nucleic acid and modulates gene expression activities or
function, such as transcription and/or translation. Regardless of
the specific mechanism, its sequence-specificity makes antisense
compounds attractive as tools for target validation and gene
functionalization, as well as therapeutics to selectively modulate
the expression of gens involved in the pathogenesis of
diseases.
[0003] Chemically modified nucleosides are routinely incorporated
into antisense compounds to enhance its properties, such as
nuclease resistance, pharmacokinetics or affinity for a target RNA.
Chemical modifications have improved the potency and efficacy of
antisense compounds, improving their potential for oral delivery or
subcutaneous administration, or decreasing their potential for side
effects. Chemical modifications increasing potency of antisense
compounds allow administration of lower doses, which reduces the
potential for toxicity. Modifications increasing the resistance to
degradation result in slower clearance from the body, allowing for
less frequent dosing. The synthesis of tricyclic nucleosides
(Steffens et al., Helvetica Chimca Acta, 1997, 80, 2426-2439) and
their incorporation into oligomeric compounds has been reported in
the literature (Steffens et al., J. Am. Chem. Soc., 1997, 119,
115-11549; Steffens et al., J. Am. Chem. Soc., 1999, 121,
3249-3255; Renneberg et al., J. Am. Chem. Soc., 2002, 124,
5993-6002; Scheidegger et al., Chem. Eur. J., 2006, 12, 8014-8023).
Fully modified tricyclic oligonucleotides were shown to be more
stable against nucleolytic degradation in fetal calf serum compared
to unmodified oligodeoxynucleotides and to produce biological
antisense effects in cellular assays, such as splice restoration of
mutant .beta.-globin (Renneberg et al., Nucleic Acids Res. 2002,
30, 2751-2757); or exon skipping in cyclophilin A (Ittig et al.,
Nucleic Acids Research, 2004, 32, 346-353).
BRIEF SUMMARY OF THE INVENTION
[0004] Provided herein are tricyclic nucleosides having Formula I
and oligomeric compounds prepared therefrom. More particularly,
tricyclic nucleosides having Formula I are useful for incorporation
at one or more positions of an oligomeric compound. In certain
embodiments, the oligomeric compounds, provided herein are
characterized by one or more enhanced properties such as nuclease
stability, cell permeability, bioavialability or toxicity. In
certain embodiments, the oligomeric compounds as provided herein
hybridize to a portion of a target RNA resulting in loss of normal
function of the target RNA. The oligomeric compounds provided
herein are also useful as primers and probes in diagnostic
applications. In certain embodiments, oligomers comprising
tricyclic nucleosides provided herein show significantly
improved--compared to unmodified DNA or RNA oligomers-cellar uptake
independent of transfecting reagents such as liposomes. In certain
embodiments, oligomers comprising tricyclic nucleosides provided
herein show significantly increased--compared to unmodified DNA or
RNA oligomers--thermal stability (duplex melting point).
[0005] The variables are defined individually in further detail
herein. It is to be understood that the tricyclic nucleosides
having Formula I and the oligomeric compounds provided herein
include all combinations of the embodiments disclosed and variables
defined herein. According to a first aspect of the invention, a
tricyclic nucleoside is provided that is described by the general
Formula I:
##STR00001##
wherein:
[0006] Bx is a heterocyclic base moiety;
[0007] one of T.sup.1 and T.sup.2 is hydroxyl (--OH) or a protected
hydroxyl and the other of T.sup.1 and T.sup.2 is a phosphate or a
reactive phosphorus group, with T.sup.1 optionally being a solid
support for oligonucleotide synthesis;
[0008] q.sup.1 and q.sup.2 are each, indepedently, H, F or Cl,
[0009] at least one of q.sup.3,q.sup.4 and q.sup.5 is,
independently, a group described by a general
formula--A.sup.1-X.sub.h-A.sup.2-Y.sub.n, wherein [0010] A.sup.1 is
C.sub.k-alkyl, C.sub.k-alkenyl or C.sub.k-alkynyl, with k being an
integer selected from the range of 0 to 20, [0011] X.sub.h is
--C(.dbd.O)--, --C(.dbd.O)NR--, --O--, --S--, --NR--, --C(.dbd.O)R,
--C(.dbd.O)OR, --C(.dbd.O)NR.sub.2, with each R being selected
independently from H, methyl, ethyl, propyl, butyl, acetyl and
2-hydroxyethyl, and h is 0 or 1, [0012] A.sup.2 is a C.sub.i-alkyl,
C.sub.i-alkenyl or C.sub.i-alkynyl, with i being an integer
selected from the range of 0 to 20, [0013] Y is a substituent group
attached to any carbon atom on A.sup.1 and/or A.sup.2, selected
from --F, --Cl, --Br, .dbd.O, --OR, --SR, --NR.sub.2,
--NR.sub.3.sup.+, NHC(.dbd.NH)NH.sub.2, --CN, --NC, --NCO, --NCS,
--SCN, --COR, --CO.sub.2R, CONR.sub.2, --R, with each R being
selected independently from H, methyl, ethyl, propyl, butyl, acetyl
and 2-hydroxyethyl, and n is 0, 1, 2, 3, 4, 5 or 6, [0014] wherein
k+i equals at least 1, [0015] and wherein any --OR, --SR,
--NR.sub.2, --CO.sub.2R, CONR.sub.2 for which R is H may optionally
be protected by a protecting group used in solid phase
oligonucleotide chemistry,
[0016] the other ones of q.sup.3, q.sup.4 are, independently, H, F
or Cl,
[0017] one of z.sup.1 and z.sup.2 is H and the other of z.sup.1 and
z.sup.2 is H, --OH, F, Cl, OCH.sub.3, OCF.sub.3, OCH.sub.2CH.sub.3,
OCH.sub.2CF.sub.3, OCH.sub.2-CH.dbd.CH.sub.2,
O(CH.sub.2).sub.2-OCH.sub.3,
O(CH.sub.2).sub.2-O(CH.sub.2).sub.2-N(CH.sub.3).sub.2,
OCH.sub.2C(.dbd.O) --N(H)CH.sub.3,
OCH.sub.2C(.dbd.O)--N(H)--(CH.sub.2).sub.2-N(CH.sub.3).sub.2 or
OCH.sub.2-N(H)--C(.dbd.NH)NH.sub.2.
[0018] One of ordinary skill in the art of chemistry understands
that--concerning the selection of oxygen (.dbd.O) as a substituent
group --the oxygen atom is attached via a double bond to any carbon
atom on A.sup.1 and A.sup.2. A C.sub.k-alkyl, C.sub.k-alkenyl or
C.sub.k-alkynyl in the context of the present specification refers
to an alkyl, alkenyl or alkynyl moiety, respectively, having k
carbon atoms in a linear chain. The index i of A.sup.2 is applied
similarly. It is understood that embodiments for which k is 0,
A.sup.1 is not present, and for embodiments for which i is 0,
A.sup.2 is not present. If n substituent groups are present, these
can be present both on A.sup.1 and A.sup.2.
[0019] In some embodiments, Bx is a pyrimidine, substituted
pyrimidine, purine or substituted purine. In some embodiments, Bx
is selected from uracil, thymine, cytosine, 5-methylcytosine,
adenine and guanine. In some embodiments, Bx is an aromatic
heterocyclic moiety capable of forming base pairs when incorporated
into DNA or RNA oligomers in lieu of the bases uracil, thymine,
cytosine, 5-methylcytosine, adenine and guanine.
[0020] In some embodiments, T.sup.1 is hydroxyl or protected
hydroxyl, and T.sup.2 is reactive phosphorus group selected from an
H-phosphonate or a phosphoramidite. In some embodiments, T.sup.1 is
a triphosphate group and T.sup.2 is OH. In some embodiments,
T.sup.1 is 4,4'-dimethoxytrityl and T.sup.2 is
diisopropylcyanoethoxy phosphoramidite. In some embodiments,
T.sup.1 is a controlled pore glass surface. According to certain
embodiments of this embodiment, T.sup.1 is a long chain alkylamine
controlled pore glass surface or similar solid phase support used
in oligonucleotide solid phase synthesis, to which a
3'-O-succinylated nucleoside is linked via an amide function.
[0021] In some embodiments, one of z.sup.1 and z.sup.2 is F,
OCH.sub.3 or O(CH.sub.2).sub.2-OCH.sub.3. In some embodiments, one
of z.sup.1 and z.sup.2 is F. In some embodiments, one of z.sup.1
and z.sup.2 is F and the other one is H. In some embodiments,
z.sup.1 and z.sup.2 are each H. In some embodiments, z.sup.1 and
z.sup.2 are each F. In some embodiments, z.sup.1 and z.sup.2 are
each H.
[0022] In some embodiments, q.sup.1 and q.sup.2 are H. In some
embodiments, one of q.sup.1 and q.sup.2 is F and the other one is
H.
[0023] In certain embodiments, the tricyclic nucleoside carried in
position q.sup.3, q.sup.4 one substituent having 3 to about 18
carbon atoms, optionally with a cationic group on the chain. Such
substituents are useful for incorporation into oligonucleotides
that, as a function of the alkyl substituent chain length and
substitution and the number of such modified nucleotides, provide
improved transport of the oligonucleotide in the body, and improved
cellular uptake. Without wishing to be bound by theory, the
inventors hypothesize that the observed behavior of such modified
oligonucleotides may at least partially be explained by
self-aggregation of the oligonucleotides by hydrophobic
interaction.
[0024] Embodiments A): In some embodiments, the substituent is a
C.sub.3 to C.sub.16 alkyl moiety, i.e. k is 3, 4, 5, 6, 7, 8, 9,
10, 11, 12, 13, 14, 15 or 16, h is 0, i is 0 and n is 1, 2, or 3.
In a subgroup thereof, a C.sub.3 to C.sub.16 alkyl moiety is in
position q.sup.3; q.sup.4 and q.sup.5 are H, and optionally, one of
q.sup.1 and q.sup.2 is H and the other one is F or Cl, or both of
q.sup.1 and q.sup.2 are H. In another subgroup thereof, a C.sub.3
to C.sub.16 alkyl moiety having 1-6 substituents is in position
q.sup.4 or q.sup.5, the other one of q.sup.4 and q.sup.3, are H,
and optionally, one of q.sup.1 and q.sup.2 is H and the other one
is F or Cl, or both of q.sup.1 and q.sup.2 are H.
[0025] Embodiments B): In some embodiments, the substituent is an
acetic acid C.sub.3 to C.sub.16 amide or ester, i.e. k is 1, h is 1
and X is COO--, CONH-- or CONR--, i is 3, 4, 5, 6, 7, 8, 9, 10, 11,
12, 13, 14, 15 or 16 and n is 1, 2, or 3. In a subgroup thereof, an
acetic acid C.sub.3 to C.sub.16 amide or ester is in position
q.sup.3; q.sup.4 and q.sup.5 are H, and optionally, one of q.sup.1
and q.sup.2 is H and the other one is F or Cl, or both of q.sup.3
and q.sup.2 are H. In another subgroup thereof, an acetic acid
C.sub.3 to C.sub.16 amide or ester is in position q.sup.4 or
q.sup.5, the other one of q.sup.4 and q.sup.5, and q.sup.3, are H,
and optionally, one of q.sup.1 and q.sup.2 is H and the other one
is F or Cl, or both of q.sup.1 and q.sup.2 are H.
[0026] Embodiments C): In some embodiments, the substituents is an
C.sub.3 to C.sub.16 alkoxy moiety, i.e. k is 0, h is 1 and X is
--O--, i is 3, 4, 5, 6 7, 8,9, 10, 11, 12, 13, 14, 15 or 16 and n
is 1, 2, or 3. In a subgroup thereof, a C.sub.3 to C.sub.16 alkoxy
moiety is in position q.sup.3; q.sup.4 and q.sup.5 are H, and
optionally, one of q.sup.1 and q.sup.2 is H and the other one is F
or Cl, or both of q.sup.1 and q.sup.2 are H. In another subgroup
therof, a C.sub.3 to C.sub.16 alkoxy moiety is in position q.sup.4
or q.sup.5, the other one of q.sup.4 and q.sup.5, and q.sup.3, are
H, and optionally, one of q.sup.1 and q.sup.2 is H and the other
one if F or Cl, or both of q.sup.1 and q.sup.2 are H.
[0027] Embodiments D): In some embodiments, q.sup.3 is the group
described by the general formula--A.sup.1-X.sub.h-A.sup.2-Y.sub.n,
k and i independently are 0, 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12,
13, 14 or 15 and the sum of k and i is at least 3 and no more than
17, h is 1 and X is selected from COO--, CONH--, CONR--, --O--, and
CO, and n is 0, 1, 2, or 3. In a subgroup thereof, q.sup.4 and
q.sup.5 are H, and optionally, one of q.sup.1 and q.sup.2 is H and
the other one is F or Cl, or both of q.sup.1 and q.sup.2 are H.
[0028] Embodiments E): In some embodiments, either of q.sup.4 or
q.sup.5 is the group described by the general
formula--A.sup.1-X.sub.h-A.sup.2-Y.sub.n, k and i independently are
0, 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14 or 15 and the sum
of k and i is at least 3 and no more than 17, h is 1 and X is
selected from COO--, CONH, CONR--, --O--, and CO, and n is 0, 1, 2,
or 3. In a subgroup thereof, the other one of q.sup.4 and q.sup.5,
and q.sup.3, are H, and optionally, one of q.sup.1 and q.sup.2 is H
and the other one is F or Cl, or both of q.sup.1 and q.sup.2 are
H.
[0029] Further defining the embodiments of group A, B, C, D and E,
a subgroup of any one of these embodiments is characterized by n
being 1 and the substituent Y being a cationic substituent selected
from NH.sub.2, NHR, NR.sub.2, NR.sub.3.sup.+and
NHC(.dbd.NH)NH.sub.2 (guanidyl), with R having the meaning outlined
above. In some of these embodiments, the cationic substituent is
positioned on the .omega.-position (terminal C) of the alkyl chain
being farthest away from the nucleoside ring (A.sup.1 in
embodiments of group A, A.sup.2 in embodiments of group B, C, D and
E).
[0030] Embodiments F): In some embodiments, the tricyclic
nucleoside carries one substituent that is defined by the following
parameters: k is 0, h is 1, X.sub.h is --O--, --C(.dbd.O)O-- or
--C(.dbd.O)NH-- and A.sup.2-Y is (CH.sub.2).sub.mCH.sub.3,
(CH.sub.2).sub.mCH.sub.2OH, (CH.sub.2).sub.mCH.sub.2NH.sub.2, or
(CH.sub.2).sub.mCH.sub.2NHC(.dbd.NH)NH.sub.2, with m being 1, 2, 3,
4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15 or 16. In a subgroup
therof, the substituent as defined in the previous sentence is in
position q.sup.3; in another subgroup, the substituent as defined
in the previous sentence is in position q.sup.4 or q.sup.5. All
other positions of q.sup.3, and q.sup.4 and q.sup.5 are H.
Optionally, one of q.sup.1 and q.sup.2 is H and the other one is F
or Cl, or both of q.sup.1 and q.sup.2 are H.
[0031] Embodiments having a single substituent q.sup.3: In some
embodiments, q.sup.1, q.sup.2, q.sup.4 and q.sup.5 are H and
q.sup.3 is a group described by the general
formula--A.sup.1-.sub.h-A.sup.2-Y.sub.n. Specific examples are
given as groups G, H, I and J.
[0032] Embodiments G): In some embodiments, q.sup.3 is [0033]
--(CH.sub.2).sub.mCH.sub.3, --(CH.sub.2).sub.mCH.sub.2OH,
(CH.sub.2).sub.mCH.sub.2NH.sub.2,
(CH.sub.2).sub.mCH.sub.2NHC(.dbd.NH)NH.sub.2, or [0034]
--CO(CH.sub.2).sub.mCH.sub.3, CO--(CH.sub.2).sub.mCH.sub.2OH,
CO(CH.sub.2).sub.mCH.sub.2NH.sub.2, or
CO(CH.sub.2).sub.mCH.sub.2NHC(.dbd.NH)NH.sub.2, [0035]
--COO(CH.sub.2).sub.mCH.sub.3, COO(CH.sub.2).sub.mCH.sub.2OH,
COO(CH.sub.2).sub.mCH.sub.2NH.sub.2, or
COO(CH.sub.2).sub.mCH.sub.2NHC(.dbd.NH)NH.sub.2, or [0036]
--CONH(CH.sub.2).sub.mCH.sub.3, CONH(CH.sub.2).sub.mCH.sub.2OH,
CONH(CH.sub.2).sub.mCH.sub.2NH.sub.2, or
CONH(CH.sub.2).sub.mCH.sub.2NHC(.dbd.NH)NH.sub.2, with m being 1,
2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15 or 16. In a subgroup
therof, m is 3, 4, 5, 6, 7 or 8.
[0037] The length of the alkyl chain allows careful adjustment of
delivery, bioavialability or permeability features of an
oligonucleotide compound into which a nucleoside having this
particular modification of q.sup.3 is incorporated.
[0038] Embodiments H): In some embodiments, q.sup.3 is a group
described by the general formula--A.sup.1-A.sub.h-A.sup.2-Y.sub.n,
wherein [0039] k of A.sup.1 is 0, h is 1, X.sub.h is --O--, A.sup.2
is C.sub.5-alkyl and n of Y.sub.nis 0, thus, q.sup.3 is
--O--(CH.sub.2).sub.4CH.sub.3, or [0040] k is 0, h is 1, X.sub.h is
--C(.dbd.O)O--, A.sup.2 is C.sub.6-alkyl and n is 0, thus, q.sup.3
is --C(.dbd.O)O--(CH.sub.2).sub.5CH.sub.3, or [0041] A.sup.1 is
C.sub.2-alkyl, h is 1, X.sub.h is --C(.dbd.O)O--, A.sup.2 is
C.sub.6-alkyl and n is 0, thus q.sup.3 is
--(CH.sub.2).sub.2-C(.dbd.O)O--(CH.sub.2).sub.5CH.sub.3, or [0042]
k is 0, h is 1, X.sub.h is --C(.dbd.O)--, A.sup.2 is C.sub.4-alkyl
and n is 0, thus, q.sup.3 is --C(.dbd.O)--(CH.sub.2).sub.3CH.sub.3,
or [0043] k is 0, h is 0, A.sup.2 is C.sub.8-alkyl, n is 1, and
Y.sub.n is --OH, wherein the substituent group --OH is attached to
the .omega.-carbon atom of he C.sub.8-alkyl of A.sup.2, thus,
q.sup.3 is --(CH.sub.2).sub.7CH.sub.2OH, or [0044] A.sup.1 is
--CH.sub.2--, h is 1, X.sub.h is --CO.sub.2H, wherein i and n are
each 0, thus, q.sup.3 is --CH.sub.2-COOH, or [0045] A.sup.1 is
CH.sub.2, h is 1, X.sub.h is --C(.dbd.O)O--, A.sup.2 is
C.sub.2-alkyl and n is 0, thus, q.sup.3 is
--CH.sub.2-C(.dbd.O)O--CH.sub.2CH.sub.3, or [0046] A.sup.1 is
CH.sub.2, h is 1, X.sub.h is --CONH.sub.2, i and n are each 0,
thus, q.sup.3 is --CH.sub.2-CONH.sub.2, or [0047] A.sup.1 is
CH.sub.2, h is 1, X.sub.h is --C(.dbd.O)O--, A.sup.2 is
C.sub.16-alkyl and n is 0, thus, q.sup.3 is
CH.sub.2-C(.dbd.O)O--(CH.sub.2).sub.15CH.sub.3, or [0048] A.sup.1
is CH.sub.2, h is 1, X.sub.h is --C(.dbd.O)O--, A.sup.2 is
C.sub.3-alkyl, n is 1 and Y.sub.n is --NH.sub.2, wherein the
substituent group --NH.sub.2 is attached to the .omega.-carbon atom
of the C.sub.3-alkyl of A.sup.2, thus, q.sup.3 is
CH.sub.2-C(.dbd.O)O--(CH.sub.2).sub.3NH.sub.2, or [0049] A.sup.1 is
CH.sub.2, h is 1, X.sub.h is--C(.dbd.O)NH--, A.sup.2 is
C.sub.3-alkyl of A.sup.2, thus, q.sup.3 is
CH.sub.2-C(.dbd.O)NH--(CH.sub.2).sub.3NH.sub.2, or [0050] A.sup.1
is CH.sub.2, h is 1, X.sub.h is --C(.dbd.O)NH--, A.sup.2 is
C.sub.3-alkyl, n is 1 and Y.sub.n is --OH, wherein the substituent
group --OH is attached to the .omega.carbon atom of the
C.sub.3-alkyl of A.sup.2, thus, q.sup.3 is
CH.sub.2C(.dbd.O)NH--(CH.sub.2).sub.3OH.
[0051] Embodiment 1): In some embodiments, q.sup.3 is a group
described by the general formula formula--A.sup.1-X.sub.h-
A.sup.2-Y.sub.n, wherein A.sup.1 is CH.sub.2, h is 1, X.sub.h is
--C(.dbd.O)OR, C(.dbd.O)NR.sub.2, --C(.dbd.O)O--or --C(.dbd.O)NR--,
with each R being selected independently from H, methyl, ethyl,
propyl,butyl, acetyl and 2-hydroxyethyl in particular from H,
methyl, ethyl, propyl and butyl. In a subgroup thereof, z.sup.1,
z.sup.2, q.sup.1, q.sup.2, q.sup.4 and q.sup.5 are H. In a further
subgroup thereof, q.sup.3 is one of --CH.sub.2COOH,
--CH.sub.2C(.dbd.O)OCH.sub.2CH.sub.3, --CH.sub.3,
--CH.sub.2CONH.sub.2, CH.sub.2C).dbd.O)O(CH.sub.2).sub.3NH.sub.2,
--CH.sub.2COO(CH.sub.2).sub.12-16CH.sub.3,
--CH.sub.2COO(CH.sub.2).sub.12-16NH.sub.2, or
--CH.sub.2C(.dbd.O))--(CH.sub.2).sub.3NH(Fmoc).
[0052] Embodiments J): In some embodiments, q.sup.3 is one of
--CH.sub.2COOH, --CH.sub.2C(.dbd.O)OCH.sub.2CH.sub.3,
CH.sub.2CONH.sub.2, --CH.sub.2C(.dbd.O)O(CH.sub.2).sub.3NH.sub.2,
--CH.sub.2COO(CH.sub.2).sub.12-16CH.sub.3, or
--CH.sub.2COO(CH.sub.2).sub.12-16NH.sub.2, or
--CH.sub.2C(.dbd.O)O--(CH.sub.2).sub.3NH(Fmoc).
[0053] In a further subgroup thereof, the tricyclic nucleoside is
selected from the group of
##STR00002##
wherein Bx is selected from uracil, thymine, cytosine,
5-methylcytosine, adenine and guanine.
[0054] Also provide herein are nucleoside precursor compounds as
exemplified by compound 8 of Example 1, compound 13 of Example 2 or
compound 17 of Example 3, in particular:
##STR00003##
wherein Bx is selected from uracil, thymine, cytosine,
5-methylcytosine, adenine and guanine.
[0055] Embodiments K): In some embodiments, k is 0, h is 1, X.sub.h
is --CR.sub.2--, --C(.dbd.O)--, --C(.dbd.O)O--, --C(.dbd.O)NR--,
--O--, --S--, --NR--, with each R being selected independently from
H, methyl, ethyl, propyl and butyl, A.sup.2 is a C.sub.i-alkyl,
C.sub.i-alkenyl or C.sub.i-alkynyl, with i being selected from any
integer in the range of 1 to 20, Y is a substituent group attached
to any carbon atom on A.sup.2, selected from --F, --Cl, --Br, --OR,
--SR, --NR.sub.2, --CN, --NC, --NCO, --NCS, --SCN, --COR,
--CO.sub.2R, CONR.sub.2, with each R being selected independently
from H, methyl, ethyl, propyl, and butyl, and n is 0, 1, 2, 3, 4, 5
or 6.
[0056] Embodiments L): In some embodiments, k is 0, h is 1, X.sub.h
is --CR.sub.2--, --C(.dbd.O)--, --C(O.dbd.O)O--, --C(.dbd.O)NR--,
--O--, --S--, --NR--, with each R being selected independently from
H, methyl, ethyl, propyl, and butyl, A.sup.2 is a C.sub.i-alkyl,
C.sub.i-alkenyl or C.sub.i-alkynyl, with i being selected from any
integer in the range of 1 to 20, Y is a substituent group attached
to any carbon atom on A.sup.2, selected from --F, --Cl, --BR, --OR,
--SR, --NR.sub.2, --CN, --NC, --NCO, --NCS, --SCN, --COR,
--CO.sub.2R, with each R being selected independently from H,
methyl, ethyl, propyl, and butyl, and n is 0, 1, 2, 3, 4, 5 or 6,
wherein if z.sup.1, z.sup.2, q.sup.1, q.sup.2, q.sup.4 and q.sup.5
are H, q.sup.3 is one of --CH.sub.2COOH,
--CH.sub.2C(.dbd.O)OCH.sub.2CH.sub.3, --CH.sub.2CONH.sub.2.
--CH.sub.2C(.dbd.O)O(CH.sub.2).sub.3NH.sub.2,
--CH.sub.2COO(CH.sub.2).sub.12NH.sub.2, or
--CH.sub.2C(.dbd.O)O--(CH.sub.2).sub.3NH(Fmoc), in particular one
of --CH.sub.2C(.dbd.O)OCH.sub.2CH.sub.3,
--CH.sub.2C(.dbd.O)O(CH.sub.2).sub.3NH.sub.2.
--CH.sub.2COO(CH.sub.2).sub.15CH.sub.3 or
--CH.sub.2C(.dbd.O)O--(CH.sub.2).sub.3NH(Fmoc).
[0057] Embodiments M): In some embodiments, A.sup.1 is CH.sub.2, h
is 1, X.sub.h is --CR.sub.2--, --C(.dbd.O)--, --C(.dbd.O)O--,
C(.dbd.O)NR--, --O--, --S--, --NR--, with each R being selected
independently from H, methyl, ethyl, propyl and butyl, A.sup.2 is a
C.sub.i-alkyl, C.sub.i-alkenyl or C.sub.i-alkynl, with i being
selected from any integer in the range of 1 to 20, Y is a
substituent group attached to any carbon atom on A.sup.2, selected
from --F, --Cl, --Br, --OR, --SR, --NR.sub.2, --CN, --NC, --NCO,
--NCS, --SCN, --COR, --CO.sub.2R, CONR.sub.2, with each R being
selected independently from H, methyl, ethyl, propyl, and butyl,
and n is 0, 1, 2, 3, 4, 5 or 6.
[0058] Embodiments N): In some embodiments, A.sup.1 is CH.sub.2, h
is 1, X.sub.h is --CR.sub.2--, --C(.dbd.O)--, --C(.dbd.O)O--,
--C(.dbd.O)NR--, --O--, --S--, --NR--, with each R being selected
independently from H, methyl, ethyl, propyl, and butyl, A.sup.2 is
a C.sub.i-alkyl, C.sub.i-alkenyl or C.sub.i-alkynyl, with i
selected from any integer in the range of 1 to 20, Y is a
substituent group attached to any carbon atom on A.sup.2, selected
from --F, --Cl, --Br, --OR, --SR, --NR.sub.2, --CN, --NC, --NCO,
--NCS, --SCN, --COR, --CO.sub.2R, CONR.sub.2, with each R being
selected independently from H, methyl, ethyl, propyl, and butyl,
and n is 0, 1, 2, 3, 4, 5 or 6, wherein if z.sup.1, z.sup.2,
q.sup.1, q.sup.2, q.sup.4 and q.sup.5 is one of --CH.sub.2COOH,
--CH.sub.2C(.dbd.O)OCH.sub.2CH.sub.3, --CH.sub.2CONH.sub.2,
--CH.sub.2C(.dbd.O)O(CH.sub.2).sub.3NH.sub.2,
--CH.sub.2COO(CH.sub.2).sub.12-16CH.sub.3,
--CH.sub.2COO(CH.sub.2).sub.12-16NH.sub.2, or
--CH.sub.2C(.dbd.O))--(CH.sub.2).sub.3NH(Fmoc), in particular one
of --CH.sub.2C(.dbd.O)OCH.sub.2CH.sub.3,
--CH.sub.2C(.dbd.O)O(CH.sub.2).sub.3NH.sub.2,
--CH.sub.2COO(CH.sub.2).sub.15CH.sub.3 or
--CH.sub.2C(.dbd.O)O--(CH.sub.2).sub.3NH(Fmoc).
[0059] Embodiments O): In some embodiments, one of q.sup.3, q.sup.4
and q.sup.5 is selected from CH.sub.2COOH, CH.sub.2CONH.sub.2,
CH.sub.2COO(CH.sub.2).sub.3-6CH.sub.3,
--CH.sub.2COO(CH.sub.2).sub.3-7NH.sub.2,
--CH.sub.2COO(CH.sub.2).sub.3-7NHC(.dbd.NH)NH.sub.2,
CONH(CH.sub.2).sub.3-6CH.sub.3, CONH(CH.sub.2 ).sub.3-7OH,
CONH(CH.sub.2).sub.3-7CH.sub.2NH.sub.2, or
CONH(CH.sub.2).sub.3-7CH.sub.2NHC(.dbd.NH)NH.sub.2.
[0060] In some embodiments, at least one of q.sub.1, q.sub.2,
q.sub.3, q.sub.4 and q.sub.5 is F, and one of q.sub.3, q.sub.4 and
q.sub.5 is the group described by the general formula
formula--A.sup.1-X.sub.h-A.sup.2-Y.sub.n.
[0061] In some embodiments, q.sup.3 and z.sup.1 is F, and one of
q.sup.4 and q.sup.5 is the group described by the general formula
formula--A.sup.1-X.sub.h-A.sup.2-Y.sub.n.
[0062] In some embodiments, q.sup.3 is selected from the group
described by the general formula --A.sup.1-X.sub.h-A.sup.2-Y.sub.n
and one of z.sup.1, z.sup.2, q.sup.1, q.sup.2, q.sup.4 and q.sup.5
is F.
[0063] In some embodiments, q.sup.3 is the group described by the
general formula --A.sup.1-X.sub.h-A.sup.2-Y.sub.n, A.sup.1 is
CH.sub.2, h is 1, X.sub.h is --C(.dbd.O)OH, C(.dbd.O)ONH.sub.2--,
--C(.dbd.O)-- or C(.dbd.O)NR--, with each R being selected
independently from H, methyl, ethyl, propyl, butyl, acetyl and
2-hydroxyethyl, in particular from H, methyl, ethyl, propyl, butyl,
and one of z.sup.1, z.sup.2, q.sup.1, q.sup.2, q.sup.4 and q.sup.5
is F.
[0064] In some embodiments, two of q.sup.3, q.sup.4 and q.sup.5 are
a group described by the general formula formula
--A.sup.1-X.sub.h-A.sup.2-Y.sub.n.
[0065] In some embodiments, q.sup.3 is a group described by the
general formula formula --A.sup.1-X.sub.h-A.sup.2-Y.sub.n, wherein
A.sup.1 is CH.sub.2,h is 1, X.sub.h is --C(.dbd.O)OH,
C(.dbd.O)NH--, --C(.dbd.O)O--or --C(.dbd.O)NR--, with each R being
selected independently from H, methyl, ethyl, propyl, butyl, acetyl
and 2-hydroxyethyl, in particular from H, methyl, ethyl, propyl and
butyl, and one of q.sup.4 or q.sup.5 is a group described by the
general formula formula --A.sup.1-X.sub.h-A.sup.2-Y.sub.n as
defined above, while the other one is H.
[0066] According to a second aspect of the invention, an oligomeric
compound is provided comprising at least one tricyclic nucleoside
having Formula II:
##STR00004##
wherein independently for each tricyclic nucleoside of Formula II:
[0067] Bx is a heterocyclic base moiety; [0068] one of T.sup.3 and
T.sup.4 is an internucleoside linking group attaching the tricyclic
nucleoside of Formula II to the oligomeric compound and the other
of T.sup.3 and T.sup.4 is hydroxyl, a protected hydroxyl, a 5' or
3' terminal group or an internucleoside linking group attaching the
tricyclic nucleoside to the oligomeric compound; [0069] q.sup.1 and
q.sup.2 are each, independently, H, F or Cl, [0070] at least one of
q.sup.3, q.sup.4 and q.sup.5 is, independently, a group described
by a general formula --A.sup.1-X.sub.h-A.sup.2-Y.sub.n, wherein
[0071] A.sup.1 is a C.sub.k-alkyl, C.sub.k-alkenyl or
C.sub.k-alkynyl, with k being an integer selected from the range of
0 to 20, [0072] X.sub.k is --C(.dbd.O)--, --C(.dbd.O)O--,
--C(.dbd.O)NR--, --O--, --S--, --NR--, --C(.dbd.O)R, --C(.dbd.O)OR,
--C(.dbd.O)NR.sub.2, --OR, --SR or --NR.sub.2, with each R being
selected independently from H, methyl, ethyl, propyl, butyl, acetyl
and 2-hydroxyethyl, and h is 0 or 1, [0073] A.sup.2 is
C.sub.i-alkyl, C.sub.i-alkenyl or C.sub.i-alkynyl, with i being an
integer selected from the range of 0 to 20, [0074] Y is a
substituent group attached to any carbon atom on a.sup.1 and/or
A.sup.2, selected from --F, --Cl, --Br, --O, --OR, --SR,
--NR.sub.2, --NR.sub.3.sup.+, NHC(.dbd.NH)NH.sub.2, --CN, --NC,
--NCO, --NCS, --SCN, --COR, --CO.sub.2R, CONR.sub.2, --R, with each
R being selected independently from H, methyl, ethyl, propyl,
butyl, acetyl and 2-hydroxethyl, and n is 0, 1, 2, 3, 4, 5 or 6,
[0075] wherein k+i equals at least 1, [0076] the other ones of
q.sup.3, q.sup.4 and q.sup.5 are, independently, H, F or Cl, [0077]
one of z.sup.1 and z.sup.2 is H and the other of z.sup.1 and
z.sup.2 is H, --OH, F, Cl, OCH.sub.3, OCF.sub.3, OCH.sub.2CH.sub.3,
OCH.sub.2CF.sub.3, OCH.sub.2-CH.dbd.CH.sub.2,
O(CH.sub.2).sub.2-OCH.sub.3, O(CH.sub.2).sub.2-N(CH.sub.3).sub.2,
OCH.sub.2C(.dbd.O)--N(H)CH.sub.3,
OCH.sub.2C(.dbd.O)--N(H)--(CH.sub.2).sub.2-N(CH.sub.3).sub.2 or
OCH.sub.2-NH(H)--C(.dbd.NH)NH.sub.2, [0078] and wherein said
oligomeric compound comprises from 8 to 40 monomeric subunits.
[0079] In some embodiments of this aspect of the invention, Bx is a
pyrimidine, substituted pyrimidine, purine or substituted purine.
In some embodiments, Bx is selected from uracil, thymine, cytosine,
5-methylcytosine, adenine and guanine. In some embodiments, Bx is
an aromatic heterocyclic moiety capable of forming base pairs when
incorporated into DNA or RNA oligomers in lieu of the bases uracil,
thymine, cytosin, 5-methylcytosine, adenine and guanine.
[0080] In some embodiments, one of z.sup.1 and z.sup.2 is F,
OCH.sub.3 or O(CH.sub.2).sub.2-OCH.sub.3 for each tricyclic
nucleoside of Formula II. In some embodiments, one of z.sup.1 and
z.sup.2 is F for each tricyclic nucleoside of Formula II. In some
embodiments, z.sup.1 and z.sup.2 are each F for each tricyclic
nucleoside of Formula II. In some embodiments, one of z.sup.1 and
z.sup.2 is F and the other one is H for each tricyclic nucleoside
of Formula II. In some embodiments, z.sup.1 and z.sup.2 are each H
for each tricyclic nucleoside of Formula II.
[0081] In some embodiments, q.sup.1 and q.sup.2 are each H for each
tricyclic nucleoside of Formula II. In some embodiments, one of
q.sup.1 and q.sup.2 is F and the other is H for each tricyclic
nucleoside of Formula II. In some embodiments, q.sup.1 and q.sup.2
are each F for each tricyclic nucleoside of Formula II.
[0082] In some embodiments of this aspect of the invention, each
internucleoside linking group is, independently, a phosphodiester
internucleoside linking group or a phosphorothioate internucleoside
linking group. In some embodiments, essentially each
internucleoside linking group is a phosphorothioate internucleoside
linking group.
[0083] In some embodiments, the oligomeric compound of the
invention comprises a first region having at least two contiguous
tricyclic nucleosides having Formula II. In some embodiments, the
oligomeric compound of the invention comprises a first region
having at least two contiguous tricyclic nucleosides having Formula
II and a second region having at least two contiguous monomeric
subunits wherein each monomeric subunit in the second region is a
modified nucleoside different from the tricyclic nucleosides of
Formula II of said first region. According to another alternative
of this embodiment, the oligomeric compound comprises a third
region located between said first and second regions wherein each
monomer subunit in the third region is independently, a nucleoside
or a modified nucleoside that is different from each tricyclic
nucleoside of Formula II of the first region and each monomer
subunit of the second region.
[0084] In some embodiments, the oligomeric compound of the
invention comprises a gapped oligomeric compound having an internal
region of from 6 to 14 contiguous monomer subunits flanked on each
side by an external region of from 1 to 5 contiguous monomer
subunits wherein each monomer subunit in each external region is a
tricyclic nucleoside of Formula II and each monomer subunit in the
internal region is, independently, a nucleoside or modified
nucleoside. In some embodiments, said internal region comprises
from about 8 to about 14 contiguous
.beta.-D-2'-deoxyribonucleosides. In some embodiments, said
internal region comprises from about 9 to about 12 contiguous
.beta.-D-2'-deoxyribonucleosides.
[0085] In some embodiments, each tricyclic nucleoside of Formula II
comprised in the oligomeric compound of the invention is selected
from the embodiment group A above. In some embodiments, each
tricyclic nucleoside of Formula II comprised in the oligomeric
compound of the invention is selected from the embodiment group B
above. In some embodiments, each tricyclic nucleoside of Formula II
comprised in the oligomeric compound of the invention is selected
from the embodiment group C above. In some embodiments, each
tricyclic nucleoside of Formula II comprised in the oligomeric
compound of the invention is selected from the embodiment group D
above. In some embodiments, each tricyclic nucleoside of Formula II
comprised in the oligomeric compound of the invention is selected
from the embodiment group E above. In some embodiments, each
tricyclic nucleoside of Formula II comprised in the oligomeric
compound of the invention is selected from the embodiment group f
above. In some embodiments, each tricyclic nucleoside of Formula II
comprised in the oligomeric compound of the invention is selected
from the embodiment group G above. In some embodiments, each
tricyclic nucleoside of Formula II comprised in the oligomeric
compound of the invention is selected from the embodiment group H
above. In some embodiments, each tricyclic nucleoside of Formula II
comprised in the oligomeric compound of the invention is selected
from the embodiment group I above. In some embodiments, each
tricyclic nucleoside of Formula II comprised in the oligomeric
compound of the invention is selected from the embodiment group J
above. In some embodiments, each tricyclic nucleoside of Formula II
comprised in the oligomeric compound of the invention is selected
from the embodiment group K above. In some embodiments, each
tricyclic nucleoside of Formula II comprised in the oligomeric
compound of the invention is selected from the embodiment group L
above. In some embodiments, each tricyclic nucleoside of Formula II
comprised in the oligomeric compound of the invention is selected
from the embodiment group M above. In some embodiments, each
tricyclic nucleoside of Formula II comprised in the oligomeric
compound of the invention is selected from the embodiment group N
above.
[0086] In some embodiments, q.sup.3 and C.sub.1-C.sub.20alkyl,
substituted C.sub.1-C.sub.20alkyl, C.sub.1-C.sub.20alkenyl,
substituted C.sub.1-C.sub.20alkenyl, C.sub.1-C.sub.20alkynyl,
substituted C.sub.1-C.sub.20alkynyl, C.sub.1-C.sub.20alkoxy,
substituted C.sub.1-C.sub.20alkoxy, amino, substituted amino, thiol
or substituted thiol for each tricyclic nucleoside of Formula II.
In some embodiments, one of q.sup.4 and q.sup.5 is H and the other
of q.sup.4 and q.sup.5 is C.sub.1-C.sub.20alkyl, substituted
C.sub.1-C.sub.20alkyl, C.sub.1-C.sub.20alkenyl, substituted
C.sub.1-C.sub.20alkenyl, C.sub.1-C.sub.20alkynyl, substituted
C.sub.1-C.sub.20alkynyl, C.sub.1-C.sub.20alkoxy, substituted
C.sub.1-C.sub.20alkoxy, amino, substituted amino, thiol or
substituted thiol for each tricyclic nucleoside of Formula II.
[0087] In some embodiments, q.sup.3 is C.sub.1-C.sub.6alkyl,
substituted C.sub.1-C.sub.6alkenyl, substituted
C.sub.1-C.sub.6alkenyl, C.sub.1-C.sub.6alkynyl, substituted
C.sub.1-C.sub.6alkoxy, substituted C.sub.1-C.sub.6alkoxy, amino,
substituted amino, thiol or substituted thiol for each tricyclic
nucleoside of Formula II. In some embodiments, one of q.sup.4 and
q.sup.5 is H and the other of q.sup.4 and q.sup.5 is
C.sub.1-C.sub.6alkyl, C.sub.1-C.sub.6alkenyl, substituted
C.sub.1-C.sub.6alkenyl, C.sub.1-C.sub.6alkynyl, substituted
C.sub.1-C.sub.6alkynyl, C.sub.1-C.sub.6alkoxy, substituted
C.sub.1-C.sub.6alkoxy, amino, substituted amino, thiol or
substituted thiol for each tricyclic nucleoside of Formula II.
[0088] In some embodiments, the oligomeric compound of the
invention comprises one or several nucleotide blocks selected from
the group consisting of
##STR00005##
[0089] In some embodiments, at least two of q.sup.3, q.sup.4 and
q.sup.5 are a group described by the general formula formula
--A.sup.1-X.sub.h-A.sup.2-Y.sub.n for each tricyclic nucleoside of
Formula II.
[0090] According to yet another aspect of the invention, a method
for solid-phase synthesis of an oligonucleotide is provided,
comprising the use of the invention, a nucleoside according to the
first aspect of the invention. According to this aspect of the
invention, a nucleoside according to the first aspect of the
invention, any reactive OH, NH.sub.2 or other reactive group being
protected by a protective group as laid out elsewhere herein, is
used e.g. as a phosphoamidite activated building block and
incorporated into the nascent oligomeric chain. The methods and
reagents useful for such purpose are known to the skilled person
and are exemplified by the examples provided herein.
[0091] In certain embodiments, gapped oligomeric compounds are
provided comprising an internal region of from 6 to 14 contiguous
monomer subunits flanked on each side by an external region of from
1 to 5 contiguous monomer subunits wherein each monomer subunit in
each external region is a tricyclic nucleoside of Formula II and
each monomer subunit in the internal region is, independently, a
nucleoside or modified nucleoside. In certain embodiments, the
internal region comprises from about 8 to about 14 contiguous
.beta.-D-2'-deoxyribonucleosides. In certain embodiments, the
internal region comprises from about 9 to about 12 contiguous
.beta.-D-2'-deoxyribonucleosides.
[0092] In certain embodiments, methods of inhibiting gene
expression are provided comprising contacting a cell with an
oligomeric compound comprising a 5' modified nucleoside as provided
herein or a double stranded composition comprising at least one
oligomeric compound comprising a 5'0 modified nucleoside as
provided herein wherein said oligomeric compound comprises from
about 8 to about 40 monomeric subunits and is complementary to a
target RNA. In certain embodiments, the cell is in an animal. In
certain embodiments, the cell is in a human. In certain
embodiments, the target RNA is selected from mRNA, pre-mRNA and
micro RNA. In certain embodiments, the target RNA is mRNA. In
certain embodiments, the target RNA is human mRNA. In certain
embodiments, the target RNA is cleaved thereby inhibiting its
function. In certain embodiments, the methods further comprise
detecting the levels of target RNA.
[0093] In certain embodiments, in vitro methods of inhibiting gene
expression are provided comprising contacting one or more cells or
a tissue with an oligomeric compound or double stranded composition
as provided herein.
[0094] In certain embodiments, oligomeric compounds or a double
stranded composition as provided herein are used for use in an in
vivo method of inhibiting gene expression said method comprising
contacting one or more cells, a tissue or an animal with one of the
oligomeric compounds or a double stranded composition as provided
herein.
[0095] In certain embodiments, oligomeric compounds and double
stranded compositions as provided herein are used in medical
therapy.
[0096] In certain embodiments, for each tricyclic nucleoside of
Formula II, the placement of the substituent group generally
defined as --A.sup.1-X.sub.h-A.sup.2-Y.sub.n at one of the
substituent positions q.sup.3, q.sup.4, q.sup.5 enhances
biodistribution, cellular uptake or delivery of oligomers. In
certain embodiments, for each tricyclic nucleoside of Formula II,
the placement of the substituent group F at one of the substituent
positions q.sup.1,q.sup.2,q.sup.3,q.sup.4,q.sup.5,z.sup.1 or
z.sup.2 enhances one or more properties of the oligomeric compound
such as for example, and without limitation, stability, nuclease
resistance, binding affinity, specificity, absorption, cellular
distribution, cellular uptake, charge, pharmacodynamics and
pharmacokinetics. In certain embodiments, for each tricyclic
nucleoside of Formula II, it is expected that the placement of F at
one of the substituent positions
q.sup.1,q.sup.2,q.sup.3,q.sup.4,q.sup.5,z.sup.1 or z.sup.2 will
enhance the binding affinity.
DETAILED DESCRIPTION OF THE INVENTION
[0097] Provided herein are novel tricyclic nucleosides having
Formula I and oligomeric compounds prepared therefrom. The
tricyclic nucleosides having Formula I are useful for enhancing one
or more properties of the oligomeric compounds they are
incorporated into such as but not limited to nuclease resistance,
cell entry, intracellular delivery, transport in the body,
particularly in the blood, case of pharmaceutical formulation and
drug metabolism. In certain embodiments, the oligomeric compounds
provided herein hybridize to a portion of a target RNA resulting in
loss of normal function of the target RNA. In certain embodiments,
tricyclic nucleosides having Formula I are provided that can be
incorporated into antisense oligomeric compounds to reduce target
RNA, such as messenger RNA, in vitro and in vivo. In one aspect the
reduction or loss of function of target RNA is useful for
inhibition of gene expression via numerous pathways. Such pathways
include for example the steric blocking of transcription and/or
translation of mRNA and cleavage of mRNA via single or double
stranded oligomeric compounds. The oligomeric compounds provided
herein are also expected to be useful as primers and probes in
diagnostic applications.
[0098] In certain embodiments, double stranded compositions are
provided wherein each double stranded composition comprises: [0099]
a first oligomeric compound and a second oligomeric compound
wherein the first oligomeric compound is complementary to the
second oligomeric compound and the second oligomeric compound is
complementary to a nucleic acid target; [0100] at least one of the
first and second oligomeric compounds comprises at least one
tricyclic nucleoside of Formula II; and [0101] wherein said
compositions optionally comprise one or more terminal groups.
[0102] As used herein the term "alkyl," refers to a saturated
straight or branched hydrocarbon radical containing up to 24,
particularly up to 20, carbon atoms. Examples of alkyl groups
include without limitation, methyl, ethyl, propyl, butyl,
isopropyl, n-hexyl, octyl, decyl, dodecyl and the like. Alkyl
groups typically include from 1 to about 20 carbon atoms, more
typically from 1 to about 12 carbon atoms (C.sub.1-C.sub.12alkyl)
with from 1 to about 6 carbon atoms being more preferred. The term
"lower alkyl" as used herein includes from 1 to about 6 carbon
atoms.
[0103] As used herein the term "alkenyl,"0 refers to a straight or
branched hydrocarbon chain radical containing up to 24,
particularly up to 20, carbon atoms and having at least one
carbon-carbon double bond. Examples of alkyl groups include without
limitation, ethenyl, propenyl, butenyl, 1-methyl-2-buten-1-yl,
dienes suc as 1,3-butadiene and the like. Alkenyl groups typically
include from 2 to about 20 carbon atoms, more typically from 2 to
about 12 carbon atoms with from 2 to about 6 carbon atoms being
more preferred.
[0104] As used herein the term "alkenyl," refers to a straight or
branched hydrocarbon radical containing up to 24, particularly up
to 20, carbon atoms and having at least one carbon-carbon triple
bond.
[0105] Examples of alkynyl groups include, without limitation,
ethynyl, 1-propynl, 1-butynyl, and the like. Alkynyl groups
typically include from 2 to about 20 carbon atoms, more typically
from 2 to about 12 carbon atoms with from 2 to about 6 carbon atoms
being more preferred.
[0106] As used herein the term "alkoxy," refers to a radical formed
between an alkyl group and an oxygen atom wherein the oxygen atom
is used to attach the alkoxy group to a parent molecule. Examples
of alkoxy groups include without limitation, methoxy, ethoxy,
propoxy, isopropoxy, n-butoxy, sec-butoxy, tert-butoxy, n-pentoxy,
neopentoxy, n-hexoxy and the like. Alkoxy groups as used herein may
optionally include further substituent groups.
[0107] As used herein the term "aminoalkyl" refers to an amino
substituted C.sub.1-C.sub.12alkyl radical. The alkyl portion of the
radical forms a covalent bond with a parent molecule. the amino
group can be located at any position and the aminoalkyl group can
be substituted with a further substituent group at the alkyl and/or
amino portions.
[0108] As used herein the term "protecting group," refers to a
labile chemical moiety, which is known in the art to protect
reactive groups including without limitation, hydroxyl, amino and
thiol groups, against undesired reactions during synthetic
procedures. Protecting groups are typically used selectively to
protect sites during reactions at other reactive sites and can then
be removed to leave the unprotected group as is or available for
further reactions. Protecting groups as known in the are are
described generally in Greene's Protective Groups in Organic
Synthesis, 4th edition, John Wiley & Sons, New York, 2007.
[0109] Groups can be selectively incorporated into oligomeric
compounds as provided herein as precursors. For example an amino
group can be placed into a compound as provided herein as an azido
group that can be chemically converted to the amino group at a
desired point in th synthesis. Generally, groups are protected or
present as precursors that will be inert to reactions that modify
other areas of the parent molecule for conversion into their final
groups at an appropriate time. Further representative protecting or
precursor groups are discussed in Agrawal et al., Protocols for
Oligonucleotide Conjugates, Humana Press; New Jersey, 1994, 26,
1-72.
[0110] Examples of hydroxyl protecting groups include without
limitation, acetyl, t-butyl, t-butoxymethyl, methoxymethyl,
tetrahydropyranyl, 1-ethoxyethyl, 1-(2-chloroethoxy)ethyl,
p-chlorophenyl, 2,4-dinitrophenyl, benzyl, 2,6-dichlorobenzyl,
diphenylmethyl, p-nitrobenzyl, bis(2-acetoxyethoxy)methyl (ACE),
2-trimethylsilylethyl, trimethylsilyl, triethylsilyl,
t-butyldimethylsilyl, t-butyldiphenylsilyl, triphenylsilyl,
[(triisopropylsilyl)oxy]methyl (TOM), benzoylformate, chloracetyl,
trichloracetyl, trifluoroacetyl, pivaloyl, p-phenylbenzoyl,
9-fluorenylmethyl carbonate, mesylate, tosylate, triphenylmethyl
(trityl), monomethoxytrityl, dimethoxytrityl (DMT),
trimethoxytrityl, 1(2-fluorophenyl)-4-methoxypiperidin-4-yl (FPMP),
9-phenylxanthine-9-yl (Pixyl) and 9-(p-methoxyphenyl)xanthine-9-yl
(MOX). Wherein more commonly used hydroxyl protecting groups
include without limitation, benzyl, 2,6-dichlorobenzyl,
t-butyl-diphenylsilyl, benzoyl, mesylate, tosylate, dimethoxytrityl
(DMT), 9-phenylxanthine-9-yl (Pixyl) and
9-(p-methoxyphenyl)xanthine-9-yl (MOX).
[0111] Examples of amino protecting groups include without
limitation, carbamate-protecting groups, such as
2-trimethylsilylethoxycarbonyl (Teoc),
1-methyl-1-(4-biphenylyl)ethoxycarbonyl (Bpoc), t-butoxycarbonyl
(BOC), allyloxycarbonyl (Alloc), 9-fluorenylmethyloxycarbonyl
(Fmoc), and benzyloxycarbonyl (Cbz); amide-protecting groups, such
as formyl, acetyl, trihaloacetyl, benzoyl, and nitrophenylacetyl;
sulfonamide-protecting groups, such as 2-nitrobenzenesulfonyl; and
imine- and cyclic imide-protecting groups, such as phthalimido and
dithiasuccinoyl. Examples of thiol protecting groups include
without limitation, triphenylmethyl (trityl), benzyl (Bn), and the
like.
[0112] The compounds described herein contain one or more
asymmetric centers and thus give rise to enantiomers,
diastereomers, and other stereoisomeric forms that may be defined,
in terms of absolute sterochemistry, as (R) or (S). Included herein
are all such possible isomers, as well as their racemic and
optically pure forms. The configuration of any carbon-carbon double
bond appearing herein is selected for convenience only and is not
intended to limit a particular configuration unless the text so
states.
[0113] In some embodiments, an alkyl, alkenyl or alkynyl group as
used herein may optionally include one or more further substituent
groups. The terms "substituent" and "substituent group" are meant
to include groups that are typically added to other groups or
parent compounds to enhance desired properties or provide other
desired effects. Substituent groups can be protected or unprotected
and can be added to one available site or to many available sites
in a parent compound. Substituent groups may also be further
substituted with other substituent groups and may be attached
directly or via a linking group such as an alkyl or hydrocarbyl
group to a parent compound.
[0114] Substituent groups amenable herein include without
limitation, halogen, oxygen, hydroxyl, alkyl, alkenyl, alkynyl,
acyl (--C(O)R.sub.aa), carboxyl (--C(O)O--R.sub.aa), aliphatic
groups, alicyclic groups, alkoxy, substituted oxy (--O--R.sub.aa),
aryl, aralkyl, heterocyclic radical, heteroaryl, heteroarylalkyl,
amino (--N(R.sub.bb)(R.sub.cc)), imino(.dbd.NR.sub.bb), amido
(--C(O)N(R.sub.bb)(R.sub.cc) or --N(R.sub.bb)C(O)R.sub.aa), azido
(--N.sub.3), nitro (--NO.sub.2), cyano (--CN), isocyano (--NC),
cyanato (--OCN), isocyanato (--NCO), thiocyanato (--SCN);
isothiocyanato (--NCS); carbamido (--OC(O)N(R.sub.bb)(R.sub.cc) or
--N(R.sub.bb)C(O)R.sub.aa), ureido
(--N(R.sub.bb)(C(O)N(R.sub.bb)(R.sub.cc)), thioureido
(--N(R.sub.bb)C(S)N(R.sub.bb)(R.sub.cc)), guanidinyl
(--N(R.sub.bb)C(.dbd.NR.sub.bb) --N(R.sub.bb)(R.sub.cc)), amidinyl
(--C(.dbd.NR.sub.bb)N(R.sub.bb)(R.sub.cc) or
--N(R.sub.bb)C(.dbd.NR.sub.bb)(R.sub.aa)), thiol (--SR.sub.bb),
sulfinyl (--S(O)R.sub.bb), sulfonyl (--S(O).sub.2R.sub.bb) and
sulfonamidyl (--S(O).sub.2N(R.sub.bb)(R.sub.cc) or
--N(R.sub.bb)S(O).sub.2R.sub.bb). Wherein each R.sub.aa, R.sub.bb
and R.sub.cc is, independently, H, an optionally linked chemical
functional group or a further substituent group with a preferred
list including without limitation, H, alkyl, alkenyl, alkynyl,
aliphatic, alkoxy, acyl, aryl, aralkyl, heteroaryl, alicyclic,
heterocyclic and heteroarylalkyl. Selected substituents within the
compounds described herein are present to a recursive degree.
[0115] In this context, "recursive substituent" means that a
substituent may recite another instance of itself. Because of the
recursive nature of such substituents, theoretically, a large
number may be present in any given claim. One of ordinary skill in
the art of medicinal chemistry and organic chemistry understands
that the total number of such substituents is reasonably limited by
the desired properties of the compound intended. Such properties
include, by way of example and not limitation, physical properties
such as molecular weight, solubility or logP, application
properties such as activity against the intended target and
practical properties such as ease of synthesis.
[0116] Recursive substituents are an intended aspect of the
invention. One of ordinary skill in the art of medicinal and
organic chemistry understands the versatility of such substituents.
To the degree that recursive substituents are present in a claim of
the invention, the total number will be determined as set forth
above.
[0117] In some embodiments, an alkyl, alkenyl or alkynyl group as
used herein contains one, two or three further substituent groups
selected independently from the group of --F, --Cl, --Br, .dbd.O,
NH.sub.2, SH, OH, OR, SR, NHR, --NR.sub.2, --CN, --NC, --NCO,
--NCS, --SCN, --COR, --CO.sub.2R, CONR.sub.2, --R with R being
selected from methyl, ethyl, propyl, butyl, acetyl and
2-hydroxyethyl.
[0118] In some embodiments, an alkyl, alkenyl or alkynyl group as
used herein contains no further substituent groups but consists
only of carbon and hydrogen atoms.
[0119] As used herein, the term "nucleobase" refers to unmodified
or naturally occurring nucleobases which include, but are not
limited to, the purine bases adenine (A) and guanin (G), and the
pyrimidine bases thymine (T), cytosine (C) and uracil (U). As used
herein, the term "heterocyclic base moiety" refers to unmodified or
naturally occurring nucleobases as well and modified or
non-naturally occurring nucleobases and synthetic mimetics thereof
(such as for example phenoxazines). In certain embodiments, a
heterocyclic base moiety is any heterocyclic system that contains
one or more atoms or groups of atoms capable of hydrogen bonding to
a heterocyclic base of a nucleic acid.
[0120] In certain embodiments, heterocyclic base moieties include
without limitation modified nucleobases such as 5-methylcytosine
(5-me-C), 5-hydroxymethyl cytosine, xanthine, hyposanthine,
2-amino-adenine, 6-methyl and other alkyl derivatives of adenine
and guanine, 2-propyl and other alkyl derivatives of adenine and
guanine, 2-thiouracil, 2-thiothymine and 2-thiocytosine,
5-halouracil and cytosine, 5-propynyl (--C.dbd.C--CH.sub.3) uracil
and cytosine and other alkynyl derivatives of pyrimidine bases,
6-azo uracil, cytosine and thymine, 5-uracil (pseudouracil),
4-thiouracil, 8-halo, 8-amino, 8-thiol, 8-thioalkyl, 8-hydroxyl and
other 8-substituted adenines and guanines, 5-halo particularly
5-bromo, 5-trifluoromethyl and other 5-substituted uracils and
cytosines, 7-methylguanine and 7-methyladenine, 2-F-adenine,
2-amino-adenine, 8-azaguanine and 8-azaadenine, 7-deazaguanine and
7-deazaadenine, 3-deazaguanine and 3-deazaadenine, universal bases,
hydrophobic bases, promiscuous bases, size-expanded bases, and
fluorinated bases as defined herein.
[0121] In certain embodiments, heterocyclic base moieties include
without limitation tricyclic pryimidines such as
1,3-diazaphenoxazine-2-one, 1,3-diazaphenothiazine-2-one and
9-(2-aminoethoxy)-1,3-diazaphenoxazine-2-one (G-clamp).
Heterocyclic base moieties also include those in which the purine
or pyrimidine base is replaced with other heterocycles, for example
7-deaza-adenine, 7-deazaguanosine, 2-aminopyridine and 2-pyridone.
Further heterocyclic base moieties include without limitation those
known to the art skilled (see for example: U.S. Pat. No. 3,687,808;
Swayze et al., The Medicinal Chemistry of Oligonucleotides in
Antisense a Drug Technology, Chapter 6, pages 143-182, Crooke, S.
T., ed., 2008); The Concise Encyclopedia Of Polymer Science And
Engineering, Kroschwitz, J. I., Ed., John Wiley & Sons, 1990,
858-859; Englisch et al., Angewandte Chemie, International Edition,
1991, 30, 613; Sanghvi, Y. S., Chapter 15, Antisense Research and
Applications, Crooke, S. T. and Lebleu, B., Eds., CRC Press, 1993,
273-302.
[0122] As used herein the term "sugar moiety" refers to naturally
occurring sugars having a furanose ring, synthetic or non-naturally
occurring sugars having a modified furanose ring and sugar
surrogates wherein the furanose ring has been replaced with a
cyclic ring system such as for example a morpholino or hexitol ring
system or a non-cyclic sugar surrogate such as that used in peptide
nucleic acids. Illustrative examples of sugar moieties useful in
the preparation of oligomeric compounds include without limitation,
.beta.-D-ribose, .beta.-D-2'-deoxyribose, substituted sugars (such
as 2',5' and bis substituted sugars), 4'-S-sugars (such as
4'-S-ribose, 4'-S-2'-deoxyribose and 4'--S--2'-substituted ribose),
tricyclic modified sugars (such as for example when the ribose ring
has been replaced with a morpholino, a hexitol ring system or an
open non-cyclic system). As used herein, the term "nucleoside"
refers to a nucleobase-sugar combination. The two most common
classes of such nucleobases are purines and pyrimidines.
[0123] As used herein, the term nucleotide refers to a nucleoside
further comprising a modified or unmodified phosphate
internucleoside linking group or a non-phosphate internucleoside
linking group. For nucleotides that include a pentofuranosyl sugar,
the internucleoside linking group can be linked to either the 2',3'
or 5' hydroxyl moiety of the sugar. The phosphate internucleoside
linking groups are routinely used to convalently link adjacent
nucleosides to one another to form a linear polymeric compound.
[0124] The term "nucleotide mimetic" as used herein is meant to
include monomers that incorporate into oligomeric compounds with
sugar and linkage surrogate groups, such as for example peptide
nucleic acids (PNA) or morpholinos (linked by
--N(H)--C(.dbd.O)--O--). In general, the heterocyclic base at each
position is maintained for hybridization to a nucleic acid target
but the sugar and linkage is replaced with surrogate groups that
are expected to function similar to native groups but have one or
more enhanced properties.
[0125] As used herein the term "nucleoside mimetic" is intended to
include those structures used to replace the sugar and the base at
one or more positions of an oligomeric compound. Examples of
nucleoside mimetics include without limitation nucleosides wherein
the heteroxyclic base moiety is replaced with a phenoxazine moiety
(for example the 9-(2-aminoethoxy)-1,3-diazaphenoxazine-2-one
group, also referred to as a G-clamp which forms four hydrogen
bonds when hybridized with a guanosine base) and further
replacement of the sugar moiety with a group such as for example a
morpholino, a cyclohexenyl or a bicyclo[3.1.0]hexyl.
[0126] As used herein the term "modified nucleoside" is meant to
include all manner of modifies nucleosides that can be incorporated
into an oligomeric compound using oligomer synthesis. The term is
intended to include modifications made to a nucleoside such as
modified stereochemical configurations, one or more substitutions,
and deletion of groups as opposed to the use of surrogate groups
which are described elsewhere herein. The term includes nucleosides
having a furanose sugar (or 4'-S analog) portion and can include a
heterocyclic base or can be an abasic nucleoside. One group of
representative modified nucleosides includes without limitation,
substituted nucleosides (such as 2',5', and/or 4' substituted
nucleosides) 4'-S-modified nucleosides, (such as
4'-S-ribonucleosides, 4'-S-2'-deoxyribonucleosides and
4'-S-2'-substituted ribonucleosides), bicyclic modified nucleosides
(such as for example, bicyclic nucleosides wherein the sugar moiety
has a 2'-O--CHR.sub.a-4' bridging group, wherein R.sub.a is H,
alkyl or substituted alkyl) and base modified nucleosides. The
sugar can be modified with more than one of these modifications
listed such as for example a bicyclic modified nucleoside further
including a 5'-substitution or a 5' or 4' substituted nucleoside
further including a 2' substituent. The term modified nucleoside
also includes combinations of these modifications suc as base and
sugar modified nucleosides. These modifications are meant to be
illustrative and not exhaustive as other modifications are known in
the art and are also envisioned as possible modifications for the
modified nucleosides describer herein. As used herein the term
"monomer subunit" is meant to include all manner of monomer units
that are amenable to oligomer synthesis with one preferred list
including monomer subunits such as .beta.-D-ribonucleosides,
.beta.-D-2'-deoxyribnucleosides, modified nucleosides, including
substituted nucleosides (such as 2',5' and bis substituted
nucleosides), 4'-S-modifies nucleosides, (such as
4'-S-ribonucleosides, 4'-S-2'-deoxyribonucleosides and
4'-S-2'-substituted ribonucleosides), bicyclic modified nucleosides
(such as bicyclic nucleosides wherein the sugar moiety has a
2'--O--CHR.sub.a4' bridging group, wherein R.sub.a is H, alkyl or
substituted alkyl), other modified nucleosides, nucleoside
mimetics, nucleosides having sugar surrogates and the tricyclic
nucleosides as provided herein. Many other monocyclic, bicyclic and
tricyclic ring systems are known in the art and are suitable s
sugar surrogates that can be used to modify nucleosides for
incorporation into oligomeric compounds as provided herein (see for
example review article: Leumann, Christian J. Bioorg. & Med.
Chem., 2002, 10, 841-854). Such ring systems can undergo various
additional substitutions to further enhance their activity.
[0127] As used herein the term "reactive phosphorus" is meant to
include groups that are covalently linked to a monomer subunit that
can be further attached to an oligomeric compound that are useful
for forming internucleoside linkages including for example
phosphodiester and posphoramidite, internucleoside linkaes. Such
reactive phosphorus groups are known in the art and contain
phosphorus atoms in P.sup.III or P.sup.v valence state including,
but not limited to, phosphoramidite, H-phosphonate, phosphate
triesters and phosphorus containing chiral auxiliaries. In certain
embodiments, reactive phosphorus groups are selected from
diisopropylcyanoethoxy phosphoramidite
(--O*---P[N[(CH(CH.sub.3).sub.2]2]O(CH.sub.2).sub.2CN) and
H-phosphonate (--O*--P(.dbd.O)(H)OH), wherein the O* is provided
from the Markush group for the monomer. A preferred synthetic solid
phase synthesis utilizes phosphoramidites (P.sup.III chemistry) as
reactive phosphites. The intermediate phosphite compounds are
subsequently oxidized to the phosphate or thiophosphate (P.sup.v
chemistry) using known methods to yield, phosphodiester or
phosphorothioate internucleoside linkages.
[0128] Additional reactive phosphates and phosphites are disclosed
in Tetrahedron Report Number 309 (Beaucage and Iyer, Tetrahedron,
1992, 48, 2223-2311).
[0129] As used herein, "ogligonucleotide" refers to a compound
comprising a plurality of linked nucleosides. In certain
embodiments, one or more of the plurality of nucleosides is
modified. In certain embodiments, an oligonucleotide comprises one
or more ribonucleosides (RNA) and/or deoxyribonucleosides
(DNA).
[0130] The term "oligonucleoside" refers to a sequence of
nucleosides that are joined by internucleoside linkages that do not
have phosphorus atoms. Internucleoside linkages of this type
include short chain alkyl, cycloalkyl, mixed heteroatom alkyl,
mixed heteroatom cycloalkyl, one or more short chain heteroatomic
and one or more short chain heterocyclic. These internucleoside
linkages include without limitation, siloxane, sulfide, sulfoxide,
sulfone, acetyl, formacetyl, thioformacetyl, methylene formacetyl,
thioformacetyl, alkeneyl, sulfamate, methyleneimino,
methylenchydrazino, sulfonate, sulfonamide, amide and others having
mixed N, O, S and CH.sub.2 component parts.
[0131] As used herein, the term "oligometric compound" refers to a
contiguous sequence of linked monomer subunits. Each linked monomer
subunit normally includes a heterocyclic base moiety but monomer
subunits also includes those without a heterocyclic base moiety
such as abasic monomer subunits. At least some and generally most
if not essentially all of the heterocyclic bases in an oligomeric
compound are capable of hybridizing to a nucleic acid molecule,
normally a preselected RNA target. The term "oligomeric compound"
therefore includes oligonucleotides, oligonucleotide analogs and
oligonucleosides. It also includes polymers having one or a
plurality of nucleoside mimetics and or nucleosides having sugar
surrogate groups.
[0132] In certain embodiments, oligomeric compounds comprise a
plurality of monomer subunits independently selected from naturally
occurring nucleosides, non-naturally occurring nucleosides,
modified nucleosides, nucleoside mimetic, and nucleosides having
sugar surrogate groups. In certain embodiments, oligomeric
compounds are single stranded. In certain embodiments, oligomeric
compounds are double stranded comprising a double-stranded duplex.
In certain embodiments, oligomeric compounds comprise one or more
conjugate groups and/or terminal groups.
[0133] As used herein the term "internucleoside linkage" or
"internuecleoside linking group" is meant to include all manner of
internucleoside linking groups known in the art including but not
limited to, phosphorus containing internucleoside linking groups
such as phosphodiester and phosphorothioate, and non-phosphorus
containing internucleoside linking groups such as formacetyl and
methyleneimino. Internucleoside linkages also includes neutral
non-ionic internucleoside linkages such as
amide-3(3'---CH.sub.2C(.dbd.O)--N(H)-5'),
amide-4(3'-CH.sub.2-N(H)--C(.dbd.O)-5') and methylphosphonate
wherein a phosphorus atom is not always present.
[0134] In certain embodiments, oligomeric compounds as provided
herein can be prepared having one or more internucleoside linkages
containing modified e.g. non-naturally occurring internucleoside
linkages. The two main classes of internucleoside linkages are
defined by the presence or absence of a phosphorus atom. Modified
internucleoside linkages having a phosphorus atom include without
limitation, phosphorothioates, chiral phosphorothioates,
phosphorodithioates, phosphotriesters, aminoalkylphosphotriesters,
methyl and other alkyl phosphonates including 3'-alkylene
phosphonates, 5'-alkylene phosphonates and chiral phosphonates,
phosphinates, phosphoramidates including 3'-amino phosphoramidate
and aminoalkylphosphoramidates, thionophosphoramidates,
thionoalkylphosphonates, thionoalkylphosphotriesters,
selenophosphates and boranophosphates having normal 3'-5' linkages,
2'-5' linked analogs of these, and those having inverted polarity
wherein one or more internucleotide linkages is a 3' to 3',5' to 5'
or 2' to 2' linkage.
[0135] Oligonucleotides having inverted polarity can comprise a
single 3' to 3' linkage at the 3'-most internucleotide linkage i.e.
a single inverted nucleoside residue which may be absic (the
nucleobase is missing or has a hydroxyl group in place thereof).
Various salts, mixed salts and free acid forms are also
included.
[0136] In certain embodiments, oligomeric compounds as provided
herein can be prepared having one or more non-phosphorus containing
internucleoside linkages. Such oligomeric compounds include without
limitation, those that are formed by short chain alkyl or
cycloalkyl internucleoside linkages, mixed heteroatom and alky or
cycloalkyl internucleoside linkages, or one or more short chain
heteroatomic or heterocyclic internucleoside linkages. These
include those having siloxane backbones; sulfide, sulfoxide and
sulfone backbones; formacetyl and thioformacetyl backbones;
methylene formacetyl and thioformacetyl backbones; riboacetyl
backbones; alkene containing backbones; sulfamate backbones;
methyleneimino and methylenehydrazino backbones; sulfonate and
sulfonamide backbones; amide backbones; and others having mixed N,
O, S and Ch.sub.2 component parts.
[0137] Representative U.S. patents that teach the preparation of
the above oligonucleosides include without limitation, U.S. Pat.
Nos. 5,034,506; 5,166,315; 5,185,444; 5,214,134; 5,216,141;
5,234,033; 5,264,562; 5,264,564; 5,405,938; 5,434,257; 5,466,677;
5,470,967; 5,489,677; 5,541,307; 5,561,225; 5,596,086; 5,602,240;
5,608,046; 5,610,289; 5,618,704; 5,623,070; 5,663,312; 5,633,360;
5,677,437; 5,677,439; 5,646,269 and 5,792,608, certain of which are
commonly owned with this application, and each of which is herein
incorporated by reference.
[0138] In certain embodiments, the oligomeric compounds as provided
herein can be modified by covalent attachment of one or more
conjugate groups. In general, conjugate groups modify one or more
properties of the oligomeric compounds they are attached to. Such
oligonucleotide properties include without limitation,
pharmacodynamics, pharmacokinetics, binding, absorption, cellular
distribution, cellular uptake, charge and clearance. Conjugate
groups are routinely used in the chemical arts and are linked
directly or via an optional linking moiety or linking group to a
parent compound such as an oligomeric compound. A preferred list of
conjugate groups includes without limitation, intercalators,
reporter molecules, polyamines, polyamides, polyethylene glycols,
thioethers, polyethers, cholesterols, thiocholesterols, cholic acid
moieties, folate, lipids, phospholipids, biotin, phenazine,
phenanthridine, anthraquinone, adamantane, acridine, fluoresceins,
rhodamines, coumarins and dyes.
[0139] In certain embodiments, the oligomeric compounds as provided
herein can be modified by covalent attachment of one or more
terminal groups to the 5' or 3'-terminal groups. A terminal group
can also be attached at any other position at one of the terminal
ends of the oligomeric compound. As used herein the terms
"5'-terminal group", "3'- terminal group", "terminal group" and
combinations thereof are meant to include useful groups known to
the art skilled that can be placed on one or both of the terminal
ends, including but not limited to the 5' and 3'-ends of an
oligomeric compound respectively, for various purposes such as
enabling the tracking of the oligomeric compound (a fluorescent
label or other reporter group), improving the pharmacokinectics or
pharmacodynamics of the oligomeric compound (such as for example:
uptake and/or delivery) or enhancing one or more other desirable
properties of the oligomeric compound (a group for improving
nuclease stability or binding affinity). In certain embodiments, 5'
and 3'-terminal groups include without limitation, modified or
unmodified nucleosides, two or more linked nucleosides that are
independently, modified or unmodified; conjugate groups; capping
groups; phosphate moieties; and protecting groups.
[0140] As used herein the term "phosphate moiety" refers to a
terminal phosphate group that includes phosphates as well as
modified phosphates. The phosphate moiety can be located at either
terminus but is preferred at the 5'-terminal nucleoside. In one
aspect, the terminal phosphate is unmodified having the formula
--O-13 P(.dbd.O)(OH)OH. In another aspect, the terminal phosphate
is modified such that one or more of the O and OH groups are
replaced with H, O, S, N(R) or alkyl where R is H, an amino
protecting group or unsubstituted or substituted alkyl. In certain
embodiments, the 5'0 and or 3' terminal group can comprise from 1
to 3 phosphate moieties that are each, independently, unmodified
(di or tri-phosphates) or modified.
[0141] As used herein, the term "phosphorus moiety" refers to a
group having the formula:
##STR00006##
wherein:
[0142] R.sub.x and R.sub.y are each, independently, hydroxyl,
protected hydroxyl group, thiol, protected thiol group,
C.sub.1-C.sub.6 alkyl, substituted C.sub.1-C.sub.6 alkyl,
C.sub.1-C.sub.6 alkoxy, substituted C.sub.1-C.sub.6 alkoxy,
protected amino or substituted amino; and
[0143] R.sub.z is O or S.
[0144] As a monomer such as a phosphoramidite or H-phoramidite or
H-phosphonate the protected phosphorus moiety is preferred to
maintain stability during oligomer synthesis. After incorporation
into an oligomeric compound the phosphorus moiety can include
deprotected groups.
[0145] Phosphorus moieties included herein can be attached to a
monomer, which can be used in the preparation of oligomeric
compounds, wherein the monomer may be attached using O, S, NR.sub.d
or CR.sub.eR.sub.f, wherein R.sub.d includes without limitation H,
C.sub.1-C.sub.6 alkyl, substituted C.sub.1-C.sub.6 alkyl,
C.sub.1-C.sub.6 alkoxy, substituted C.sub.1-C.sub.6 alkoxy,
C.sub.2-C.sub.6 alkenyl, substituted C.sub.2-C.sub.6 alkenyl,
C.sub.2-C.sub.6 alkynyl, substituted C.sub.2-C.sub.6 alkynyl or
substituted acyl, and R.sub.e and R.sub.f each, independently,
include without limitation H, halogen, C.sub.1- C.sub.6 alkyl,
substituted C.sub.1-C.sub.6 alkoxy or substituted C.sub.1-C.sub.6
alkoxy. Such linked phosphorus moieties include without limitation,
phosphates, modified phosphates, thiophosphates, modified
thiophosphates, phosphonates, modified phosphonates,
phosphoramidates and modified phosphoramidates.
[0146] The relative ability of a chemically-modified oligomeric
compound to bind to complementary nucleic acid strands, as compared
to natural oligonucleotides, is measured by obtaining the melting
temperature of a hybridization complex of said chemically-modified
oligomeric compound with its complementary unmodified target
nucleic acid. The melting temperature (T.sub.m), a characteristic
physical property of double helixes, denotes the temperature in
degrees centigrade at which 50% helical versus coiled
(unhybridized) forms are present. T.sub.m (also commonly referred
to as binding affinity) is measured by using the UV spectrum to
determine the formation and breakdown (melting) of hybridization.
Base stacking, which occurs during hybridization, is accompanied by
a reduction in UV absorption (hypochromicity). Consequently a
reduction in UV absorption indicates a higher T.sub.m.
[0147] It is known in the art that the relative duplex stability of
an antisense compound:RNA target duplex can be modulated through
incorporation of chemically-modified nucleosides into the antisense
compound. Sugar-modified nucleosides have provided the most
efficient means of modulating the T.sub.m of an antisense compound
with its target RNA. Sugar-modified nucleosides that increase the
population of or lock the sugar in the C3'-endo (Northern, RNA-like
sugar pucker) configuration have predominantly provided a per
modification T.sub.m increase for antisense compounds toward a
complementary RNA target. Sugar-modified nucleosides that increase
the population of or lock the sugar in the C2'-endo (Southern,
DNA-like sugar pucker) configuration predominantly provide a per
modification Tm decrease for antisense compounds toward a
complementary RNA target. The sugar pucker of a given
sugar-modified nucleoside is not the only factor that dictates the
ability of the nucleoside to increase or decrease an antisense
compound's T.sub.m toward complementary RNA. For example, the
sugar-modified nucleoside tricyclo DNA is predominantly in the
C2'-endo conformation, however it imparts a 1.9 to 3.degree. C. per
modification increase in T.sub.m toward a complementary RNA.
Another example of a sugar-modified high-affinity nucleoside that
does not adopt the C3'-endo conformation is .alpha.-L-LNA
(described in more detail herein).
[0148] As used herein, "T.sub.m" (melting temperature) is the
temperature at which the two strands of a duplex nucleic acid
separate. The T.sub.m is often used as a measure of duplex
stability of an antisense compound toward a complementary RNA
molecule.
[0149] As used herein, "complementarity" in reference to
nucleobases refers to a nucleobase that is capable of base pairing
with another nucleobase. For example, in DNA, adenine (A) is
complementary to thymine (T). For example, in RNA, adenine (A) is
complementary to uraacil (U). In certain embodiments, complementary
nucleobase refers to a nucleobase of an antisense compound that is
capable of base pairing with a nucleobase of its target nucleic
acid. For example, if a nucleobase at a certain position of an
antisense compound is capable of hydrogen bonding with a nucleobase
at a certain position of a target nucleic acid, then the position
of hydrogen bonding between the oligonucleotide and the target
nucleic acid is considered to be complementary at that nucleobase
pair. Nucleobases or more broadly, heterocyclic base moieties,
comprising certain modifications may maintain the ability to pair
with a counterpart nucleobase and thus, are still capable of
complementarity.
[0150] As used herein, "non-complementary" in reference to
nucleobases refers to a pair of nucleobase that do not form
hydrogen bonds with one another or otherwise support
hybridization.
[0151] As used herein, "complementary" in reference to linked
nucleosides, oligonucleotides, oligomeric compounds, or nucleic
acids, refers to the capacity of an oligomeric compound to
hybridize to another oligomeric compound or nucleic acid through
nucleobase or more broadly, heterocyclic base, complementarity. In
certain embodiments, an antisense compound and its target are
complementary to each other when a sufficient number of
corresponding positions in each molecule are occupied by
nucleobases that can bond with each other to allow stable
association between the antisense compound and the target. One
skilled in the art recognizes that the inclusion of mismatches is
possible without eliminating the ability of the oligomeric
compounds to remain in association. Therefore, described herein are
antisense compounds that may comprise up to about 20% nucleotides
that are mismatched (i.e., are not nucleobase complementary to the
corresponding nucleotides of the target). Preferably the antisense
compounds contain no more that about 15%, more preferably not more
than about 10%, most preferably not more than 5% or no mismatches.
The remaining nucleotides are nucleobase complementary or otherwise
do not disrupt hybridization (e.g., universal bases). One of
ordinary skill in the art would recognize the compounds provided
herein are at least 80%, at least 85%, at least 90%, at least 95%,
at least 96%, at least 97%, at least 98%, at least 99% or 100%
complementary to a target nucleic acid.
[0152] It is understood in the art that the sequence of an
oligomeric compound need not be 100% complementary to that of its
target nucleic acid to be specifically hybridizable. Moreover, an
oligomeric compound may hybridize over one or more segments such
that intervening or adjacent segments are not involved in the
hybridization event (e.g., a loop structure or hairpin structure).
In certain embodiments, oligomeric compounds can comprise at least
about 70%, at least about 80%, at least about 90%, at least about
95%, or at least about 99% sequence complementarity to a target
region within the target nucleic acid sequence to which they are
targeted. For example, an oligomeric compound in which 18 of 20
nucleobases of the oligomeric compound are complementary to a
target region, and would therefore specifically hybridize, would
represent 90 percent complementarity. In this example, the
remaining noncomplementary nucleobases may be clustered or
interspersed with complementary nucleobases and need not be
contiguous to each other or to complementary nucleobases. As such,
an oligomeric compound which is 18 nucleobases in length having 4
(four) noncomplementary nucleobases which are flanked by two
regions of complete complementarity with the target nucleic acid
would have 77.8% overall complementarity with the target nucleic
acid and would thus fall within this scope. Percent complementarity
of an oligomeric compound with a region of a target nucleic acid
can be determined routinely using BLAST programs (basic local
alignment search tools) and PowerBLAST programs known in the art
(Altschul et al., J. Mol. Biol., 1990, 215, 403-410; Zhang and
Madden, Genome Res., 1997, 7, 649-656).
[0153] As used herein, "hybridization" refers to the pairing of
complementary oligomeric compounds (e.g., an antisense compound and
its target nucleic acid). While not limited to a particular
mechanism, the most common mechanism of pairing involves hydrogen
bonding, which may be Watson-Crick, Hoogsteen or reversed Hoogsteen
hydrogen bonding, between complementary nucleoside or nucleotide
bases (nucleobases). For example, the natural base adenine is
nucleobase complementary to the natural nucleobases thymidine and
uracil which pair through the formation of hydrogen bonds. The
natural base guanine is nucleobase complementary to the natural
bases cytosine and 5-methyl cytosine. Hybridization can occur under
varying circumstances.
[0154] As used herein, "target nucleic acid" refers to any nucleic
acid molecule the expression, amount, or activity of which is
capable of being modulated by an antisense compound. In certain
embodiments, the target nucleic acid is DNA or RNA. In certain
embodiments, the target RNA is mRNA, pre-mRNA, non-coding RNA,
pri-microRNA, pre-microRNA, mature microRNA, promoter-directed RNA,
or natural antisense transcripts. For example, the target nucleic
acid can be a cellular gene (or mRNA transcribed from the gene)
whose expression is associated with a particular disorder or
disease state, or a nucleic acid molecule from an infectious agent.
In certain embodiments, target nucleic acid is a viral or bacterial
nucleic acid.
[0155] Further included herein are oligomeric compounds such as
antisense oligomeric compounds, antisense oligonucleotides,
ribozymes, external guide sequence (EGS) oligonucleotides,
alternate splicers, primers, probes, and other oligomeric compounds
which hybridize to at least a portion of the target nucleic acid.
As such, these oligomeric compounds may be introduced in the form
of single-stranded, double-stranded, circular or hairpin oligomeric
compounds and may contain structural elements such as internal or
terminal bulges or loops. Once introduced to a system, the
oligomeric compounds provided herein may elicit the action of one
or more enzymes or structural proteins to effect modification of
the target nucleic acid. Alternatively, the oligomeric compound may
inhibit the activity the target nucleic acid through an
occupancy-based method, thus interfering with the activity of the
target nucleic acid.
[0156] One non-limiting example of such an enzyme is RNAse H, a
cellular endonuclease which cleaves the RNA strand of an RNA:DNA
duplex. It is known in the art that single-stranded oligomeric
compounds which are "DNA-like" elicit RNAse H. Activation of RNase
H, therefore, results in cleavage of the RNA target, thereby
greatly enhancing the efficiency of oligonucleotide-mediated
inhibition of gene expression. Similar roles have been postulated
for other ribonucleases such as those in the rNase III and
ribonuclease L family of enzymes.
[0157] While one form of oligomeric compound is a single-stranded
antisense oligonucleotide, in many species the introduction of
double-stranded structures, such as double-stranded RNA (dsRNA)
molecules, has been shown to induce potent and specific
antisense-mediated reduction of the function of a gene or its
associated gene products. This phenomenon occurs in both plants and
animals and is believed to have an evolutionary connection to viral
defense and transposon silencing.
[0158] As used herein, the term "pharmaceutically acceptable salts"
refers to salts that retain the desired activity of the compound
and do not impart undesired toxicological effects thereto. The term
"pharmaceutically acceptable salt" includes a salt prepared from
pharmaceutically acceptable non-toxic acids or bases, including
inorganic or organic acids and bases.
[0159] Pharmaceutically acceptable salts of the oligomeric
compounds described herein may be prepared by methods well-known in
the art. For a review of pharmaceutically acceptable salts, see
Stahl and Wermuth, Handbook of Pharmaceutical Salts: Properties,
Selection and Use (Wiley-VCH, Weinheim, Germany, 200). Sodium salts
of antisense oligonucleotides are useful and are well accepted for
therapeutic administration to humans. Accordingly, in certain
embodiments the oligomeric compounds described herein are in the
form of a sodium salt.
[0160] In certain embodiments, oligomeric compounds provided herein
comprise from about 8 to about 80 monomer subunits in length. One
having ordinary skill in the art will appreciate that this embodies
oligomeric compounds of 8, 0, 10, 11, 12, 13, 14, 15, 16, 17, 18,
19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, 30, 31, 32, 33, 34, 35,
36, 37, 38, 39, 40, 41, 42, 43, 44, 45, 46, 47, 48, 49, 50, 51, 52,
53, 54, 55, 56, 57, 58, 59, 60, 61, 62, 63, 64, 65, 66, 67, 68, 69,
70, 71, 72, 73, 74, 75, 76, 77, 78, 79, or 80 monomer subunits in
length, or any range therewithin.
[0161] Oligomeric compounds are routinely prepared using solid
support methods as opposed to solution phase methods. Commercially
available equipment commonly used for the preparation of oligomeric
compounds that utilize the solid support method is sold by several
vendors including, for example, Applied Biosystems (Foster City,
Calif.). Any other means for such synthesis known in the art may
additionally or alternatively be employed. Suitable solid phase
techniques, including automated synthesis techniques, are described
in Oligonucleotides and Analogues, a Practical Approach, F.
Eckstein, Ed., Oxford University Press, New York, 1991.
[0162] The synthesis of RNA and related analogs relative to the
synthesis of DNA and related analogs has been increasing as efforts
in RNA interference and micro RNA increase. The primary RNA
synthesis strategies that are presently being used commercially
include 5'-O-DMT-2'-O-t-butyldimethylsilyl (TBDMS),
5'-O-DMT-2'-O-[1(2-fluorophenyl)-4-methoxypiperidin-4-yl] (FPMP),
2'--O-[(triisopropylsilyl)oxy]methyl
(2'--O--CH.sub.2-O--Si(iPr).sub.3 (TOM) and the 5'-O-silyl
ether-2'-ACE (5'-O-bis(trimethylsiloxy)cyclododecyloxysilyl ether
(DOD)-2'-O-bis(2-2'-acetoxyethoxy)methyl (ACE). A current list of
some of the major companies currently offering RNA products include
Pierce Nucleic Acid Technologies, Dharmacon Research Inc., Ameri
Biotechnologies Inc., and Integrated DNA Technologies, Inc. One
company, Princeton Separation, is marketing an RNA synthesis
activator advertised to reduce coupling times especially with TOM
and TBDMS chemistries. The primary groups being used for commercial
RNA synthesis are: TBDMS: 5'-O-DMT-2'-O-t-butyldimethylsilyl; TOM:
2'-O-[(triisopropylsilyl)oxy]methyl; DOD/ACE:
(5'-O-bis(trimethylsiloxy)cyclododecyloxysilyl
ether-2'-O-bis(2-acetoxyethoxy)methyl; and FPMP:
5'-O-DMT-2'-O-[1(2-fluorophenyl)-4-ethoxypieridin-4-yl]. In certain
embodiments, each of the aforementioned RNA synthesis strategies
can be used herein. In certain embodiments, the aforementioned RNA
synthesis strategies can be performed together in a hybrid fashion
e.g. using a 5'-protecting group from one strategy with a
2'-O-protecting from another strategy.
[0163] In some embodiments, "suitable target segments" may be
employed in a screen for additional oligomeric compounds that
modulate the expression of a selected protein. "Modulators" are
those oligomeric compounds that decrease or increase the expression
of a nucleic acid molecule encoding a protein and which comprise at
least an 8-nucleobase portion which is complementary to a suitable
target segment. The screening method comprises the steps of
contacting a suitable target segment of a nucleic acid molecule
encoding a protein with one or more candidate modulators, and
selecting for one or more candidate modulators which decrease or
increase the expression of a nucleic acid molecule encoding a
protein. Once it is shown that the candidate modulator or
modulators are capable of modulating (e.g. either decreasing or
increasing) the expression of a nucleic acid molecule encoding a
peptide, the modulator may then be employed herein in further
investigative studies of the function of the peptide, or for use as
a research, diagnostic, or therapeutic agent. In the case of
oligomeric compounds targets to microRNA, candidate modulators may
be evaluated by the extent to which they increase the expression of
a microRNA target RNA or protein (as interference with the activity
of a microRNA will result in the increased expression of one or
more targets of the microRNA).
[0164] As used herein, "expression" refers to the process by which
a gene ultimately results in a protein. Expression includes, but is
not limited to, transcription, splicing, post-transcriptional
modification, and translation.
[0165] Suitable target segments may also be combined with their
respective complementary oligomeric compounds provided herein to
form stabilized double-stranded (duplexed) oligonucleotides. such
double stranded oligonucleotide moieties have been shown in the art
to modulate target expression and regulate translation as well as
RNA processing via an antiscense mechanism. Moreover, the
double-stranded moieties may be subject to chemical modifications
(Fire et al., Nature, 1998, 391, 806-811; Timmons and Fire, Nature,
1998, 395, 854; Timmons et al., Gene, 2001, 263, 103-112; Tabara et
al., Science, 1998, 282, 430-431; Montgomery et al., Proc. Natl.
Acad. Sci. USA, 1998, 95, 15002-15507; Tuschl et al., Genes Dev.,
1999, 13, 3191-3197; Elbashir et al., Nature, 2001, 411, 494-498;
Elbashir et al., Genes Dev., 2001, 15, 188-200). For example, such
double-stranded moieties have been shown to inhibit the target by
the classical hybridization of antisense strand of the duplex to
the target, thereby triggering enzymatic degradation of the target
(Tijsterman et al., Science, 2002, 295, 694-697).
[0166] The oligomeric compounds provided herein can also be applied
in the areas of drug discovery and target validation. In certain
embodiments, provided herein is the use of the oligomeric compounds
and targets identified herein in drug discovery efforts to
elucidate relationships that exist between proteins and a disease
state, phenotye, or condition. These methods include detecting or
modulating a target peptide comprising contacting a sample, tissue,
cell, or organism with one or more oligomeric compounds provided
herein, measuring the nucleic acid or protein level of the target
and/or a related phenotypic or chemical endpoint at some time after
treatment, and optionally comparing the measured value to a
non-treated sample or sample treated with a further oligomeric
compound as provided herein. These methods can also be performed in
parallel or in combination with other experiments to determine the
function of unknown genes for the process of target validation or
to determine the validity of a particular gene product as a target
for treatment or prevention of a particular disease, condition, or
phenotype. In certain embodiments, oligomeric compounds are
provided for use in therapy. In certain embodiments, the therapy is
reducing target messenger RNA.
[0167] As used herein, the term "dose" refers to a specified
quantity of a pharmaceutical agent provided in a single
administration. In certain embodiments, a dose may be administered
in two or more boluses, tablets, or injections. for example, in
certain embodiments, where subcutaneous administration is desired,
the desired dose requires a volume not easily accommodated by a
single injection. In such embodiments, two or more injections may
be used to achieve the desired dose. In certain embodiments, a dose
may be administered in two or more injections to minimize injection
site reaction in an individual.
[0168] In certain embodiments, chemically-modified oligomeric
compounds are provided herein that may have a higher affinity for
target RNAs than does non-modified DNA. In certain such
embodiments, higher affinity in turn provides increased potency
allowing for the administration of lower doses of such compounds,
reduced potential for toxicity, improvement in therapeutic index
and decreased overall cost of therapy.
[0169] Effect of nucleoside modifications on rNAi activity is
evaluated according to existing literature (Elbashir et al.,
Nature, 2001, 411, 494-498; Nishikura et al., Cell, 2001, 107,
415-416; and Bass et al., Cell, 2000, 101, 235-238).
[0170] In certain embodiments, oligomeric compounds provided herein
can be utilized for diagnostics, therapeutics, prophylaxis and as
research reagents and kits. Furthermore, antisense
oligonucleotides, which are able to inhibit gene expression with
exquisite specificity, are often used by these of ordinary skill to
elucidate the function of particular genes or to distinguish
between functions of various members of a biological pathway. In
certain embodiments, oligomeric compounds provided herein can be
utilized either alone or in combination with other oligomeric
compounds or other therapeutics as tools in differential and/or
combinatorial analyses to elucidate expression patterns of a
portion or the entire complement of gens expressed within cells and
tissues. Oligomeric compounds can also be effectively used as
primers and probes under conditions favoring gene amplification or
detection, respectively. These primers and probes are useful in
methods requiring the specific detection of nucleic acid molecules
encoding proteins and in the amplification of the nucleic acid
molecules for detection or for use in further studies.
Hybridization of oligomeric compounds as provided herein,
particularly the primers and probes, with a nucleic acid can be
detected by means known in the art. such means may include
conjugation of an enzyme to the oligonucleotide, radiolabelling of
the oligonucleotide or any other suitable detection means. Kits
using such detection means for detecting the level of selected
proteins in a sample may also be prepared.
[0171] As one nonlimiting example, expression patterns within cells
or tissues treated with one or more of the oligomeric compounds
provided herein are compared to control cells or tissues not
treated with oligomeric compounds and the patterns produced are
analyzed for differential levels of gene expression as they
pertain, for example, to disease association, signaling pathway,
cellular localization, expression level, size, structure or
function of the genes examined. These analyses can be performed on
stimulated or unstimulated cells and in the presence or absence of
other compounds and or oligomeric compounds which affect expression
patterns.
[0172] Examples of methods of gene expression analysis known in the
art include DNA arrays or microarrays (Brazma and Vilo, FEBS Lett.,
2000, 480, 17-24; Celis, et al., FEBS Lett., 2000, 480, 2-16), SAGE
(serial analysis of gene expression)(Madden, et al., Drug Discov.
Today, 2000, 5, 415-425), READS (restriction enzyme amplification
of digested cDNAs) (Prashar and Weissman, Methods Enzymol., 1999,
303, 258-72), TOGA (total gene expression analysis) (Sutcliffe, et
al., Proc. Natl. Acad. Sci. USA, 2000, 97, 1976-81), protein arrays
and proteomics (Celis, et al., FEBS Lett., 2000, 480, 2-16;
Jungblut, et al., Electrophoresis, 1999, 20, 2100-10), expressed
sequence tag (EST) sequencing (Celis, et al., FEBS Lett., 2000,
480, 2-16; Larsson, et al., J. Biotechnol., 2000, 80, 143-57),
subtractive RNA fingerprinting (SuRF) (Fuchs, et al., Anal.
Biochem., 2000, 286, 91-98; Larson, et al., Cytometry, 2000, 41,
203-208), subtractive cloning, differential display (DD) (Jurecic
and Belmont, Curr. Opin. Microbiol., 2000, 3, 316-21), comparative
genomic hybridization (Carulli, et al., J. Cell Biochem. Suppl.,
1998, 31, 286-96), FISH (fluorescent in situ hybridization)
techniques (Going and Gusterson, Eur. J. Cancer, 1999, 35,
1895-904) and mass spectrometry methods (To, Comb. Chem. High
Throughput Screen, 2000, 3, 235-41).
[0173] Those skilled in the art, having possession of the present
disclosure will be able to prepare oligomeric compounds, comprising
a contiguous sequence of linked monomer subunits, of essentially
any viable length to practice the methods disclosed herein. Such
oligomeric compounds will include at least one and preferably a
plurality of the tricyclic nucleosides provided herein and may also
include other monomer subunits including but not limited to
nucleosides, modified nucleosides, nucleosides comprising sugar
surrogate groups and nucleoside mimetics.
[0174] While in certain embodiments, oligomeric compounds provide
herein can be utilized as described, the following examples serve
only to illustrate and are not intended to be limiting. Wherever
alternatives for single separable features such as, for example,
any of the alternatives given for q.sup.1,q.sup.4,T.sup.1, or
T.sup.2, or A.sup.1,A.sup.2,X, h, Y or n, are laid out herein as
"embodiments", it is to be understood that such alternatives may be
combined freely to form discrete embodiments of the invention
disclosed herein.
Examples (General Methods)
[0175] .sup.1H and .sup.13C NMR spectra were recorded on a 300 MHz
and 75 MHz Bruker spectrometer, respectively.
[0176] Synthesis of Nucleoside Phosphoramidites
[0177] The preparation of nucleoside phosphoramidites is performed
following procedures that are illustrated herein and in the art
such as but not limited to U.S. Pat. No. 6,426,220 and
WO02/36743.
[0178] Synthesis of Oligomeric Compounds
[0179] The oligomeric compounds used in accordance with this
invention may be conveniently and routinely made through solid
phase synthesis. Oligomeric compounds: Unsubstituted and
substituted phosphodiester (P.dbd.O) oligomeric compounds can be
synthesized on an automated DNA synthesizer (for example Applied
Biosystems model 394) using standard phosphoramidite chemistry with
oxidation by iodine. In certain embodiments, phosphorothioate
internucleoside linkages (P.dbd.S) are synthesized similar to
phosphodiester internucleoside linkages with the following
exceptions: thiation is effected by utilizing a 10% w/v solution of
3,H-1,2-benzodithiole-3-one 1,1-dioxide in acetonitrile for the
oxidation of the phosphite linkages. The thiation reaction step
time is increased to 180 sec and preceded by the normal capping
step. After cleavage from the CPG column and deblocking in
concentrated ammonium hydroxide at 55.degree. C. (12-16 hr), the
oligomeric compounds are recovered by precipitating with greater
than 3 volumes of ethanol from a 1 M NH.sub.4OAc solution.
Phosphinate internucleoside linkages can be prepared as described
in U.S. Pat. No. 5,508,270. Alkyl phosphonate internucleoside
linkages can be prepared as described in U.S. Pat. No. 4,469,863.
3'-Deoxy-3'-methylene phosphonate internucleoside linkages can be
prepared as described in U.S. Pat. Nos. 5,610,289 or 5,625,050.
Phosphoramidite internucleoside linkages can be prepared as
described in U.S. Pat. No. 5,625,775 or U.S. Pat. No. 5,366,878.
Alkylphosphonothioate internucleoside linkages can be prepared as
described in published PCT applications PCT/US94/00902 and
PCT/US93/06976 (published as WO 94/17093 and WO 94/02499,
respectively). 3'-Deoxy-3'-amino phosphoramidate internucleoside
linkages can be prepared as described in U.S. Pat. No. 5,476,925.
Phosphoriester internucleoside linkages can be prepared as
described in U.S. Pat. No. 5,023,243. Borano phosphate
internucleoside linkages can be prepared as described in U.S. Pat.
Nos. 5,130,302 and 5,177,198. Oligomeric compounds having one or
more non-phosphorus containing internucleoside linkages including
without limitation methylenmethylimino linked oligonucleosides,
also identified as MMI linked oligonucleosides,
methylenedimethylhydrazo linked oligonucleosides, also identified
as MDH linked oligonucleosides, methylenecarbonylamino linked
oligonucleosides, also identified as amide-3 linked
oligonucleosides, and methyleneaminocarbonyl linked
oligonucleosides, also identified as amide-4 linked
oligonucleosides, as well as mixed backbone oligomeric compounds
having, for instance, alternating MMI and P.dbd.O or P.dbd.S
linkages can be prepared as described in U.S. Pat. Nos. 5,378,825,
5,386,023, 5,489,677, 5,602,240 and 5,610,289. Formacetal and
thioformacetal internucleoside linkages can be prepared as
described in U.S. Pat. Nos. 5,264,562 and 5,264,564. Ethylene oxide
internucleoside linkages can be prepared as described in U.S. Pat.
No. 5,223,618.
[0180] Isolation and Purification of Oligomeric Compounds
[0181] After cleavage from the controlled pore glass solid support
or other support medium and deblocking in concentrated ammonium
hydroxide at 55.degree. C. for 12-16 hours, the oligomeric
compounds, including without limitation oligonucleotides and
oligonucleosides, are recovered by precipitation out of 1 M
NH.sub.4OAc with .ltoreq.3 volumes of ethanol. synthesized
oligomeric compounds are analyzed by electrospray mass spectrometry
(molecular weight determination) and by capillary gel
electrophoresis. The relative amounts of phosphorothioate and
phosphodiester linkages obtained in the synthesis is determined by
the ration of correct molecular weight relative to the -16 amu
product (+/-32 +/-48). For some studies oligomeric compounds are
purified by HPLC, as described by Chiang et al., J Biol. Chem.
1991, 266, 18162-18171. Results obtained with HPLC-purified
material are generally similar to those obtained with non-HPLC
purified material.
Example 1
Preparation of Compound 10
##STR00007## ##STR00008##
[0183] Compound 1 was prepared according to published procedures by
Steffens et al., Helvetica Chimica Acta, 1997, 80, 2426-2439 and
was obtained as an anomeric mixture (.alpha.:.beta.=4:1).
Alkylation with ethyl iodoacetate yielded compound 2 as a mixture
of 4 isomers, that was subsequently converted into the silylenol
ether by treatment with LiHDMS and TBDMS-Cl at -78.degree. C. At
this stage the anomeric mixture was separated by column
chromatography. The .alpha.-anomer of 3 was treated with Et.sub.2Zn
to give 4 in about 40% yield, together with about 30% of the
corresponding epimeric cyclopropane. Compound 4 was then converted
into glycal 5 by treatment with TMS-triflate. NIS mediated
nucleosidation of 5 with perilylated thymine yielded
sterospecifically the iodonucleoside 6 that was subsequently
deiondinated to the tricyclic nucleoside 7 by radical reduction
with Bu.sub.3SnH. Removal of the silyl protecting groups with HF in
pyridine afforded compound 8 that was subsequently tritylated and
phosphitylated to give the desired phosphoramidite 10. All the
structures were confirmed by spectral analysis.
Example 2
[0184] Preparation of Compound 15
##STR00009##
[0185] Compound 7 was prepared as illustrated in Example 1. Basic
hydrolysis of 7 with KOH afforded acid 11 that was converted into
compound 12 by treatment with Fmoc protected aminopropanol and the
condensing agent EDC. Removal of the silyl protecting groups
followed by tritylation and phosphitylation yielded the desired
phosphoramidite 15. All the structures were confirmed by spectral
analysis.
Example 3
[0186] Preparation of Compound 19
[0187] Compound 11 was prepared as illustrated in Example 2 and was
esterified to compound 16 with hexadecanol and EDC as condensing
agent. Desilylation with HF followed by tritylation with DMT-Cl and
phosphitylation lead to the desired phosphoramidite 19. All the
structures were confirmed by spectral analysis.
##STR00010##
Example 4
[0188] Preparation of Compound 21
[0189] Compound 11 was prepared as illustrated in Example 2 and was
converted to compound 20 with the singly protected
1,3-diaminopropane and EDC as condensing agent. Desilylation with
HF afforded compound 21. All the structures were confirmed by
spectral analysis.
##STR00011##
Example 5
[0190] Preparation of Oligomeric Compounds
[0191] Following synthetic procedures well known in the art, some
of which are illustrated herein, oligomeric compounds are prepared
having at least one tricyclic nucleosides, using one or more of the
phosphoramidite compounds illustrated in the Examples such as DMT
phosphoramidites (see Compound 10, Compound 15 or Compound 19).
Example 6
[0192] Preparation of Oligomeric Compounds for Tm Study
[0193] Following standard automated DNA synthesis protocols
oligomeric compounds were prepared comprising one or more tricyclic
nucleosides for Tm studies. After cleavage from the solid support,
the oligomeric compounds were purified by ion exchange HPLC and
analyzed by LCMS using standard procedures. The Tm of the modifies
10 mer oligomeric compounds were compared to an unmodified 10 mer
DNA oligonucleotide when duplexed to either DNA or RNA. Tm's were
determined using a Cary 100 Bio spectrophotometer with the Cary Win
UV thermal program was used to measure absorbance vs. temperature.
For the T.sub.m experiments, the oligomeric compounds were prepared
at a concentration of 1.2 .mu.M in a buffer of 150 mM NaCl, 10 mM
phosphate, 0.1 mM EDTA at pH 7. The concentration determined at
85.degree. C. was 1.2 .mu.M after mixing of equal volumes of
selected oligomeric compound and complementary RNA or DNA. The
oligomeric compounds were hybridized with a complementary RNA or
DNA by heating the duplex to 90.degree. C. for 5 minutes and then
cooling to room temperature. T.sub.m measurements were taken using
a spectrophotometer while the duplex solution was heated in a
cuvette at a rate of 0.5.degree. C./min starting at 15.degree. C.
until the temperature was 85.degree. C. T.sub.m values were
determined using Vant Hoff calculations (A.sub.260 vs temperature
curve) using non self-complementary sequences where the minimum
absorbance related to the duplex and the maximum absorbance related
to the non-duplex single strand are manually integrated into the
program.
TABLE-US-00001 .DELTA.Tm/mod .DELTA.Tm/mod SEQ (.degree. C.)
(.degree. C.) ID NO. Sequence (5' to 3') vs DNA vs RNA A01
AACTGTCACG 0 0 A02 AACTGT.sub.bCACG -0.9 +0.4 A03 AACTGT.sub.dCACG
+0.5 +2.1 A04 AACT.sub.bGTCACG +0.1 +2.4 A05 AACT.sub.dGTCACG +0.4
+2.4 A06 AACT.sub.bGT.sub.bCACG -0.7 +0.5 A07
AACT.sub.cGT.sub.cCACG -1.0 +1.3 A08 AACT.sub.dGT.sub.dCACG -0.6
+1.2 A09 AACT.sub.eGT.sub.eCACG -13.0 10.2 A10
AACT.sub.fGT.sub.fCACG -2.0 +1.3 A11
A.sub.aA.sub.aC.sub.aT.sub.aG.sub.aT.sub.aC.sub.aA.sub.aC.sub.aG.sub.a
+1.3 +2.1 A12
A.sub.aA.sub.aC.sub.aT.sub.aG.sub.aT.sub.dC.sub.aA.sub.aC.sub.aG.sub.a
-2.8 -0.6 A13
A.sub.aA.sub.aC.sub.aT.sub.dG.sub.aT.sub.aC.sub.aA.sub.aC.sub.aG.sub.a
-3.8 -2.6 A14
A.sub.aA.sub.aC.sub.aT.sub.bG.sub.aT.sub.bC.sub.aA.sub.aC.sub.aG.sub.a
+1.1 +2.0 A15
A.sub.aA.sub.aC.sub.aT.sub.cG.sub.aT.sub.cC.sub.aA.sub.aC.sub.aG.sub.a
+1.1 +2.0 A16
A.sub.aA.sub.aC.sub.aT.sub.dG.sub.aT.sub.dC.sub.aA.sub.aC.sub.aG.sub.a
+1.1 +2.3
The Tms of the unmodified oligomeric compound A01 are 47.9.degree.
C. and 48.degree. C. duplexed with DNA or RNA respectively. Each
internucleoside linking group is phosphodiester. Each nucleoside
not followed by a subscript is a .beta.-D-20'-deoxyribonucleoside
and each nucleoside followed by a subscript "a" to subscript "f"
are as defined below.
##STR00012##
Example 7
[0194] Preparation of Oligomeric Compounds for Uptake Studies Into
HeLa Cells
[0195] Hela cells were grown at 37.degree. C. in Dulbecco'Modified
Eagle's Medium (DMEM, Invitrogen) supplemented with 10% (v/v) Fetal
Calf Serum (Amimed), 100 units/ml penicillin (Invitrogen) and 100
.mu.g/ml streptomycin (Invitrogen). For transfection experiments,
1.times.10.sup.5 cells were seeded in duplicate in six-well plates,
half of them containing cover slips, 24 h before transfection.
Then, the medium was replaced by a solution of oligonucleotide (10
.mu.M final concentration) having the sequence
5'-T-t-T-t-T-t-T-t-T-t-FAM-3' where T is deoxythymidine and t is
either tc.sup.eeT(sunscript b of example 6), tc.sup.hdT (subscript
e of example 6) or tcT (subscript a of example 6) and FAM is
6-carboxyfluorescein, in DMEM +/+ (FCS, P/S).
[0196] The transfection medium was removed after 48 h at 37.degree.
C. and cells were washed with 2.times.1 ml PBS and resuspended in 1
ml fresh DMEM +/+, Fixation of the cells on the cover slips was
carried out using a solution of paraformaldehyde (1 ml, 3.7% in
PBS) for 10 min followed by washing with PBS (2.times.1 ml),
permeabilization of the cell membrane with Triton x-100 (0.2%,
Promega) for 10 min and washing with PB (2.times.1 ml). The cover
slips were treated with a few drops of polyvinylalcohol (Mowiol)
and nuclear stain 40,60-diamidino-2-phenylindole (DAPI). Cells were
analyzed by fluorescence microscopy (Leica DMI6000 B, Leica
Microsystems; software: Leica Application Suite) 48 h post
transfection.
##STR00013##
The microscopy pictures show strong fluorescein fluorescence in the
cytosol of cells treated with oligonucleotides containing
tc.sup.hdT (subscript e of example 6), while no fluorescence is
observed when oligonucleotides containing tc.sup.eeT (sunscript b
of example 6) or tcT (subscript a of example 6) were used.
Example 8
[0197] Preparation of Oligomeric Compounds for Uptake Studies Into
HEK293T Cells
[0198] HEK293T cells were grown at 37.degree. C. in Dulbecco's
Modified Eagle's Medium (DMEM, Invitrogen) supplemented with 10%
(v/v) Fetal Calf Serum (Amimed), 100 units/ml penicillin
(Invitrogen) and 100 .mu.g/ml streptomycin (Invitrogen). For
transfection experiments, 2.times.10.sup.5 cells were seeded in
duplicate in six-well plates, half of them containing cover slips,
24 h before transfection. Then, the medium was replaced by a
solution of oligonucleotide (10 .mu.M final concentration) having
the sequence 5'-T-t-T-t-T-t-T-t-T-t-FAM-3' where T is
deoxythymidine and t is either unmodified deoxythymidine,
tc.sup.eeT (sunscript b of example 6), tc.sup.hdT (subscript e of
example 6) or tcT (subscript a of example 6) and FAM is
6-carboxyfluorescein, in DMEM +/+ (FCS, P/S). The transfection
medium was removed after 48 h at 37.degree. C. and cells were
washed with 2.times.1 ml PBS and resuspended in 1 ml fresh DMEM
+/+. Fixation of the cells on the cover slips was carried out using
a solution of paraformaldehyde (1 ml, 3.7% in PBS) for 10 min
followed by washing with PBS (2.times.1 ml), permeabilization of
the cell membrane with Triton x-100 (0.2%, Promega) for 10 min and
washing with PBS (2.times.1 ml). The cover slips were treated with
a few drops of polyvinylalcohol (Mowiol) and nuclear stain
40,60-diamidino-2-phenylindole (DAPI). Cells were analyzed by
fluorescence microscopy (Leica DMI6000 B, Leica Microsystems:
software: Leica Application Suite) 48 h post transfection.
[0199] The microscopy pictures show strong fluorescein fluorescence
in the cytosol of cells treated with oligonucleotides containing
tc.sup.hdT (subscript e of example 5), while no fluorescence is
observed when oligonucleotides containing tc.sup.eeT (subscript b
of example 5) or tcT (subscript a of example 5) were used.
Sequence CWU 1
1
20110DNAArtificial SequenceSequence for biophysical analysis
1aactgtcacg 10210DNAArtificial SequenceSynthetic oligomer with
modified nucleoside according to Example 6 2aactgncacg
10310DNAArtificial SequenceSynthetic oligomer with modified
nucleoside according to Example 6 3aactgncacg 10410DNAArtificial
SequenceSynthetic oligomer with modified nucleoside according to
Example 6 4aacngtcacg 10510DNAArtificial SequenceSynthetic oligomer
with modified nucleoside according to Example 6 5aacngtcacg
10610DNAArtificial SequenceSynthetic oligomer with modified
nucleosides according to Example 6 6aacngncacg 10710DNAArtificial
SequenceSynthetic oligomer with modified nucleosides according to
Example 6 7aacngncacg 10810DNAArtificial SequenceSynthetic oligomer
with modified nucleosides according to Example 6 8aacngncacg
10910DNAArtificial SequenceSynthetic oligomer with modified
nucleosides according to Example 6 9aacngncacg 101010DNAArtificial
SequenceSynthetic oligomer with modified nucleosides according to
Example 6 10aacngncacg 101110DNAArtificial SequenceSynthetic
oligomer for biophysical analysis 11nnnnnnnnnn 101210DNAArtificial
SequenceSynthetic oligomer for biophysical analysis 12nnnnnnnnnn
101310DNAArtificial SequenceSynthetic oligomer for biophysical
analysis 13nnnnnnnnnn 101410DNAArtificial SequenceSynthetic
oligomer for biophysical analysis 14nnnnnnnnnn 101510DNAArtificial
SequenceSynthetic oligomer for biophysical analysis 15nnnnnnnnnn
101610DNAArtificial SequenceSynthetic oligomer for biophysical
analysis 16nnnnnnnnnn 101710DNAArtificial SequenceSynthetic
oligomer for biophysical analysis 17tntntntntn 101810DNAArtificial
SequenceSynthetic oligomer for biophysical analysis 18tntntntntn
101910DNAArtificial SequenceSynthetic oligomer for biophysical
analysis 19tntntntntn 102010DNAArtificial SequenceSynthetic
oligomer for biophysical analysis 20tttttttttt 10
* * * * *