U.S. patent application number 13/934960 was filed with the patent office on 2013-11-07 for benzoquinoline inhibitors of vesicular monoamine transporter 2.
The applicant listed for this patent is AUSPEX PHARMACEUTICALS, INC.. Invention is credited to Thomas G. Gant, Manouchehr Shahbaz.
Application Number | 20130296360 13/934960 |
Document ID | / |
Family ID | 42107127 |
Filed Date | 2013-11-07 |
United States Patent
Application |
20130296360 |
Kind Code |
A1 |
Gant; Thomas G. ; et
al. |
November 7, 2013 |
BENZOQUINOLINE INHIBITORS OF VESICULAR MONOAMINE TRANSPORTER 2
Abstract
The present invention relates to new benzoquinoline inhibitors
of vesicular monoamine transporter 2 (VMAT2), pharmaceutical
compositions thereof, and methods of use thereof. ##STR00001##
Inventors: |
Gant; Thomas G.; (Carlsbad,
CA) ; Shahbaz; Manouchehr; (Escondido, CA) |
|
Applicant: |
Name |
City |
State |
Country |
Type |
AUSPEX PHARMACEUTICALS, INC. |
LA JOLLA |
CA |
US |
|
|
Family ID: |
42107127 |
Appl. No.: |
13/934960 |
Filed: |
July 3, 2013 |
Related U.S. Patent Documents
|
|
|
|
|
|
Application
Number |
Filing Date |
Patent Number |
|
|
12562621 |
Sep 18, 2009 |
8524733 |
|
|
13934960 |
|
|
|
|
61097896 |
Sep 18, 2008 |
|
|
|
Current U.S.
Class: |
514/294 ;
546/95 |
Current CPC
Class: |
C07B 59/002 20130101;
A61K 31/4745 20130101; C07B 2200/05 20130101; A61K 45/06 20130101;
C07D 455/06 20130101; A61P 25/14 20180101; A61P 1/16 20180101; A61P
25/18 20180101; A61P 25/16 20180101; A61P 25/00 20180101; A61P
43/00 20180101; A61P 21/00 20180101 |
Class at
Publication: |
514/294 ;
546/95 |
International
Class: |
C07D 455/06 20060101
C07D455/06 |
Foreign Application Data
Date |
Code |
Application Number |
Sep 18, 2009 |
US |
PCT/US2009/057480 |
Claims
1. A compound of structural Formula I ##STR00042## or a salt
thereof, wherein: R.sub.1-R.sub.27 are independently selected from
the group consisting of hydrogen and deuterium; and at least one of
R.sub.1-R.sub.27 is deuterium.
2. The compound as recited in claim 1 wherein at least one of
R.sub.1-R.sub.27 independently has deuterium enrichment of no less
than about 10%.
3. The compound as recited in claim 1 wherein at least one of
R.sub.1-R.sub.27 independently has deuterium enrichment of no less
than about 50%.
4. The compound as recited in claim 1 wherein at least one of
R.sub.1-R.sub.27 independently has deuterium enrichment of no less
than about 90%.
5. The compound as recited in claim 1 wherein at least one of
R.sub.1-R.sub.27 independently has deuterium enrichment of no less
than about 98%.
6. The compound as recited in claim 1 wherein said compound has a
structural formula selected from the group consisting of
##STR00043## ##STR00044## ##STR00045## ##STR00046## ##STR00047##
##STR00048## ##STR00049## ##STR00050## ##STR00051## ##STR00052##
##STR00053## ##STR00054## ##STR00055## ##STR00056## ##STR00057##
##STR00058## ##STR00059## ##STR00060## ##STR00061## ##STR00062##
##STR00063## ##STR00064## ##STR00065## ##STR00066##
##STR00067##
7. The compound as recited in claim 1 wherein said compound has a
structural formula selected from the group consisting of
##STR00068## ##STR00069## ##STR00070##
8. The compound as recited in claim 7 wherein each position
represented as D has deuterium enrichment of no less than about
10%.
9. The compound as recited in claim 7 wherein each position
represented as D has deuterium enrichment of no less than about
50%.
10. The compound as recited in claim 7 wherein each position
represented as D has deuterium enrichment of no less than about
90%.
11. The compound as recited in claim 7 wherein each position
represented as D has deuterium enrichment of no less than about
98%.
12. The compound as recited in claim 7 wherein said compound has
the structural formula: ##STR00071##
13. The compound as recited in claim 7 wherein said compound has
the structural formula: ##STR00072##
14. A pharmaceutical composition comprising a compound as recited
in claim 1 together with a pharmaceutically acceptable carrier.
15. A compound having the structural formula: ##STR00073## or a
salt thereof.
16. The compound as recited in claim 15 wherein each position
represented as D has deuterium enrichment of no less than about
10%.
17. The compound as recited in claim 15 wherein each position
represented as D has deuterium enrichment of no less than about
50%.
Description
[0001] This application is a division of U.S. patent application
Ser. No. 12/562,621, filed Sep. 18, 2009, which claims the benefit
of priority of U.S. provisional application No. 61/097,896, filed
Sep. 18, 2008, the disclosures of which are hereby incorporated by
reference as if written herein in their entireties.
[0002] Disclosed herein are new benzoquinoline compounds,
pharmaceutical compositions made thereof, and methods to inhibit
vesicular monoamine transporter 2 (VMAT2) activity in a subject are
also provided for, for the treatment of chronic hyperkinetic
movement disorders.
[0003] Tetrabenazine (Nitoman, Xenazine, Ro 1-9569),
1,3,4,6,7,11b-Hexahydro-9,10-dimethoxy-3-(2-methylpropyl)-2H-benzo[a]quin-
oline, is a vesicular monoamine transporter 2 (VMAT2) inhibitor.
Tetrabenazine is commonly prescribed for the treatment of
Huntington's disease (Savani et al., Neurology 2007, 68(10), 797;
and Kenney et al., Expert Review of Neurotherapeutics 2006, 6(1),
7-17).
##STR00002##
[0004] In vivo, tetrabenazine is rapidly and extensively
metabolized to its reduced form,
3-isobutyl-9,10-dimethoxy-1,3,4,6,7,11b-hexahydro-2H-pyrido[2,1-a]isoquin-
olin-2-ol, which then binds specifically to VMAT2 (Zhang et al.,
AAPS Journal, 2006, 8(4), E682-692). Additional metabolic pathways
involve O-demethylation of the methoxy groups, as well as
hydroxylation of the isobutyl group (Schwartz et al., Biochem.
Pharmacol., 1966, 15, 645-655). Adverse effects associated with the
administration of tetrabenazine include neuroleptic malignant
syndrome, drowsiness, fatigue, nervousness, anxiety, insomnia,
agitation, confusion, orthostatic hypotension, nausea, dizziness,
depression, and Parkinsonism.
Deuterium Kinetic Isotope Effect
[0005] In order to eliminate foreign substances such as therapeutic
agents, the animal body expresses various enzymes, such as the
cytochrome P.sub.450 enzymes (CYPs), esterases, proteases,
reductases, dehydrogenases, and monoamine oxidases, to react with
and convert these foreign substances to more polar intermediates or
metabolites for renal excretion. Such metabolic reactions
frequently involve the oxidation of a carbon-hydrogen (C--H) bond
to either a carbon-oxygen (C--O) or a carbon-carbon (C--C)
.pi.-bond. The resultant metabolites may be stable or unstable
under physiological conditions, and can have substantially
different pharmacokinetic, pharmacodynamic, and acute and long-term
toxicity profiles relative to the parent compounds. For most drugs,
such oxidations are generally rapid and ultimately lead to
administration of multiple or high daily doses.
[0006] The relationship between the activation energy and the rate
of reaction may be quantified by the Arrhenius equation,
k=Ae.sup.-Eact/RT. The Arrhenius equation states that, at a given
temperature, the rate of a chemical reaction depends exponentially
on the activation energy (E.sub.act).
[0007] The transition state in a reaction is a short lived state
along the reaction pathway during which the original bonds have
stretched to their limit. By definition, the activation energy
E.sub.act for a reaction is the energy required to reach the
transition state of that reaction. Once the transition state is
reached, the molecules can either revert to the original reactants,
or form new bonds giving rise to reaction products. A catalyst
facilitates a reaction process by lowering the activation energy
leading to a transition state. Enzymes are examples of biological
catalysts.
[0008] Carbon-hydrogen bond strength is directly proportional to
the absolute value of the ground-state vibrational energy of the
bond. This vibrational energy depends on the mass of the atoms that
form the bond, and increases as the mass of one or both of the
atoms making the bond increases. Since deuterium (D) has twice the
mass of protium (.sup.1H), a C-D bond is stronger than the
corresponding C--.sup.1H bond. If a C--.sup.1H bond is broken
during a rate-determining step in a chemical reaction (i.e. the
step with the highest transition state energy), then substituting a
deuterium for that protium will cause a decrease in the reaction
rate. This phenomenon is known as the Deuterium Kinetic Isotope
Effect (DKIE). The magnitude of the DKIE can be expressed as the
ratio between the rates of a given reaction in which a C--.sup.1H
bond is broken, and the same reaction where deuterium is
substituted for protium. The DKIE can range from about 1 (no
isotope effect) to very large numbers, such as 50 or more.
Substitution of tritium for hydrogen results in yet a stronger bond
than deuterium and gives numerically larger isotope effects
[0009] Deuterium (.sup.2H or D) is a stable and non-radioactive
isotope of hydrogen which has approximately twice the mass of
protium (.sup.1H), the most common isotope of hydrogen. Deuterium
oxide (D.sub.2O or "heavy water") looks and tastes like H.sub.2O,
but has different physical properties.
[0010] When pure D.sub.2O is given to rodents, it is readily
absorbed. The quantity of deuterium required to induce toxicity is
extremely high. When about 0-15% of the body water has been
replaced by D.sub.2O, animals are healthy but are unable to gain
weight as fast as the control (untreated) group. When about 15-20%
of the body water has been replaced with D.sub.2O, the animals
become excitable. When about 20-25% of the body water has been
replaced with D.sub.2O, the animals become so excitable that they
go into frequent convulsions when stimulated. Skin lesions, ulcers
on the paws and muzzles, and necrosis of the tails appear. The
animals also become very aggressive. When about 30% of the body
water has been replaced with D.sub.2O, the animals refuse to eat
and become comatose. Their body weight drops sharply and their
metabolic rates drop far below normal, with death occurring at
about 30 to about 35% replacement with D.sub.2O. The effects are
reversible unless more than thirty percent of the previous body
weight has been lost due to D.sub.2O. Studies have also shown that
the use of D.sub.2O can delay the growth of cancer cells and
enhance the cytotoxicity of certain antineoplastic agents.
[0011] Deuteration of pharmaceuticals to improve pharmacokinetics
(PK), pharmacodynamics (PD), and toxicity profiles has been
demonstrated previously with some classes of drugs. For example,
the DKIE was used to decrease the hepatotoxicity of halothane,
presumably by limiting the production of reactive species such as
trifluoroacetyl chloride. However, this method may not be
applicable to all drug classes. For example, deuterium
incorporation can lead to metabolic switching. Metabolic switching
occurs when xenogens, sequestered by Phase I enzymes, bind
transiently and re-bind in a variety of conformations prior to the
chemical reaction (e.g., oxidation). Metabolic switching is enabled
by the relatively vast size of binding pockets in many Phase I
enzymes and the promiscuous nature of many metabolic reactions.
Metabolic switching can lead to different proportions of known
metabolites as well as altogether new metabolites. This new
metabolic profile may impart more or less toxicity. Such pitfalls
are non-obvious and are not predictable a priori for any drug
class.
[0012] Tetrabenazine is a VMAT2 inhibitor. The carbon-hydrogen
bonds of tetrabenazine contain a naturally occurring distribution
of hydrogen isotopes, namely .sup.1H or protium (about 99.9844%),
.sup.2H or deuterium (about 0.0156%), and .sup.3H or tritium (in
the range between about 0.5 and 67 tritium atoms per 10.sup.18
protium atoms). Increased levels of deuterium incorporation may
produce a detectable Deuterium Kinetic Isotope Effect (DKIE) that
could affect the pharmacokinetic, pharmacologic and/or toxicologic
profiles of tetrabenazine in comparison with tetrabenazine having
naturally occurring levels of deuterium.
[0013] Based on discoveries made in our laboratory, as well as
considering the literature, tetrabenazine is metabolized in humans
at the isobutyl and methoxy groups. The current approach has the
potential to prevent metabolism at these sites. Other sites on the
molecule may also undergo transformations leading to metabolites
with as-yet-unknown pharmacology/toxicology. Limiting the
production of these metabolites has the potential to decrease the
danger of the administration of such drugs and may even allow
increased dosage and/or increased efficacy. All of these
transformations can occur through polymorphically-expressed
enzymes, exacerbating interpatient variability. Further, some
disorders are best treated when the subject is medicated around the
clock or for an extended period of time. For all of the foregoing
reasons, a medicine with a longer half-life may result in greater
efficacy and cost savings. Various deuteration patterns can be used
to (a) reduce or eliminate unwanted metabolites, (b) increase the
half-life of the parent drug, (c) decrease the number of doses
needed to achieve a desired effect, (d) decrease the amount of a
dose needed to achieve a desired effect, (e) increase the formation
of active metabolites, if any are formed, (f) decrease the
production of deleterious metabolites in specific tissues, and/or
(g) create a more effective drug and/or a safer drug for
polypharmacy, whether the polypharmacy be intentional or not. The
deuteration approach has the strong potential to slow the
metabolism of tetrabenazine and attenuate interpatient
variability.
[0014] Novel compounds and pharmaceutical compositions, certain of
which have been found to inhibit VMAT2 have been discovered,
together with methods of synthesizing and using the compounds,
including methods for the treatment of VMAT2-mediated disorders in
a patient by administering the compounds as disclosed herein.
[0015] In certain embodiments of the present invention, compounds
have structural Formula I:
##STR00003##
or a salt, solvate, or prodrug thereof, wherein:
[0016] R.sub.1-R.sub.27 are independently selected from the group
consisting of hydrogen and deuterium; and
[0017] at least one of R.sub.1-R.sub.27 is deuterium.
[0018] In certain embodiments, Formula I can include a single
enantiomer, a mixture of the (+)-enantiomer and the (-)-enantiomer,
a mixture of about 90% or more by weight of the (-)-enantiomer and
about 10% or less by weight of the (+)-enantiomer, a mixture of
about 90% or more by weight of the (+)-enantiomer and about 10% or
less by weight of the (-)-enantiomer, an individual diastereomer,
or a mixture of diastereomers thereof.
[0019] Certain compounds disclosed herein may possess useful VMAT2
inhibiting activity, and may be used in the treatment or
prophylaxis of a disorder in which VMAT2 plays an active role.
Thus, certain embodiments also provide pharmaceutical compositions
comprising one or more compounds disclosed herein together with a
pharmaceutically acceptable carrier, as well as methods of making
and using the compounds and compositions. Certain embodiments
provide methods for inhibiting VMAT2. Other embodiments provide
methods for treating a VMAT2-mediated disorder in a patient in need
of such treatment, comprising administering to said patient a
therapeutically effective amount of a compound or composition
according to the present invention. Also provided is the use of
certain compounds disclosed herein for use in the manufacture of a
medicament for the prevention or treatment of a disorder
ameliorated by the inhibition of VMAT2.
[0020] The compounds as disclosed herein may also contain less
prevalent isotopes for other elements, including, but not limited
to, .sup.13C or .sup.14C for carbon, .sup.33S, .sup.34S, or
.sup.36S for sulfur, .sup.15N for nitrogen, and .sup.17O or
.sup.18O for oxygen.
[0021] In certain embodiments, the compound disclosed herein may
expose a patient to a maximum of about 0.000005% D.sub.2O or about
0.00001% DHO, assuming that all of the C-D bonds in the compound as
disclosed herein are metabolized and released as D.sub.2O or DHO.
In certain embodiments, the levels of D.sub.2O shown to cause
toxicity in animals is much greater than even the maximum limit of
exposure caused by administration of the deuterium enriched
compound as disclosed herein. Thus, in certain embodiments, the
deuterium-enriched compound disclosed herein should not cause any
additional toxicity due to the formation of D.sub.2O or DHO upon
drug metabolism.
[0022] In certain embodiments, the deuterated compounds disclosed
herein maintain the beneficial aspects of the corresponding
non-isotopically enriched molecules while substantially increasing
the maximum tolerated dose, decreasing toxicity, increasing the
half-life (T.sub.1/2), lowering the maximum plasma concentration
(C.sub.max) of the minimum efficacious dose (MED), lowering the
efficacious dose and thus decreasing the non-mechanism-related
toxicity, and/or lowering the probability of drug-drug
interactions.
[0023] All publications and references cited herein are expressly
incorporated herein by reference in their entirety. However, with
respect to any similar or identical terms found in both the
incorporated publications or references and those explicitly put
forth or defined in this document, then those terms definitions or
meanings explicitly put forth in this document shall control in all
respects.
[0024] As used herein, the terms below have the meanings
indicated.
[0025] The singular forms "a," "an," and "the" may refer to plural
articles unless specifically stated otherwise.
[0026] The term "about," as used herein, is intended to qualify the
numerical values which it modifies, denoting such a value as
variable within a margin of error. When no particular margin of
error, such as a standard deviation to a mean value given in a
chart or table of data, is recited, the term "about" should be
understood to mean that range which would encompass the recited
value and the range which would be included by rounding up or down
to that figure as well, taking into account significant
figures.
[0027] When ranges of values are disclosed, and the notation "from
n.sub.1 . . . to n.sub.2" or "n.sub.1-n.sub.2" is used, where
n.sub.1 and n.sub.2 are the numbers, then unless otherwise
specified, this notation is intended to include the numbers
themselves and the range between them. This range may be integral
or continuous between and including the end values.
[0028] The term "deuterium enrichment" refers to the percentage of
incorporation of deuterium at a given position in a molecule in the
place of hydrogen. For example, deuterium enrichment of 1% at a
given position means that 1% of molecules in a given sample contain
deuterium at the specified position. Because the naturally
occurring distribution of deuterium is about 0.0156%, deuterium
enrichment at any position in a compound synthesized using
non-enriched starting materials is about 0.0156%. The deuterium
enrichment can be determined using conventional analytical methods
known to one of ordinary skill in the art, including mass
spectrometry and nuclear magnetic resonance spectroscopy.
[0029] The term "is/are deuterium," when used to describe a given
position in a molecule such as R.sub.1-R.sub.27 or the symbol "D",
when used to represent a given position in a drawing of a molecular
structure, means that the specified position is enriched with
deuterium above the naturally occurring distribution of deuterium.
In one embodiment deuterium enrichment is no less than about 1%, in
another no less than about 5%, in another no less than about 10%,
in another no less than about 20%, in another no less than about
50%, in another no less than about 70%, in another no less than
about 80%, in another no less than about 90%, or in another no less
than about 98% of deuterium at the specified position.
[0030] The term "isotopic enrichment" refers to the percentage of
incorporation of a less prevalent isotope of an element at a given
position in a molecule in the place of the more prevalent isotope
of the element.
[0031] The term "non-isotopically enriched" refers to a molecule in
which the percentages of the various isotopes are substantially the
same as the naturally occurring percentages.
[0032] Asymmetric centers exist in the compounds disclosed herein.
These centers are designated by the symbols "R" or "S," depending
on the configuration of substituents around the chiral carbon atom.
It should be understood that the invention encompasses all
stereochemical isomeric forms, including diastereomeric,
enantiomeric, and epimeric forms, as well as D-isomers and
L-isomers, and mixtures thereof. Individual stereoisomers of
compounds can be prepared synthetically from commercially available
starting materials which contain chiral centers or by preparation
of mixtures of enantiomeric products followed by separation such as
conversion to a mixture of diastereomers followed by separation or
recrystallization, chromatographic techniques, direct separation of
enantiomers on chiral chromatographic columns, or any other
appropriate method known in the art. Starting compounds of
particular stereochemistry are either commercially available or can
be made and resolved by techniques known in the art. Additionally,
the compounds disclosed herein may exist as geometric isomers. The
present invention includes all cis, trans, syn, anti, entgegen (E),
and zusammen (Z) isomers as well as the appropriate mixtures
thereof. Additionally, compounds may exist as tautomers; all
tautomeric isomers are provided by this invention. Additionally,
the compounds disclosed herein can exist in unsolvated as well as
solvated forms with pharmaceutically acceptable solvents such as
water, ethanol, and the like. In general, the solvated forms are
considered equivalent to the unsolvated forms.
[0033] The term "bond" refers to a covalent linkage between two
atoms, or two moieties when the atoms joined by the bond are
considered to be part of larger substructure. A bond may be single,
double, or triple unless otherwise specified. A dashed line between
two atoms in a drawing of a molecule indicates that an additional
bond may be present or absent at that position.
[0034] The term "disorder" as used herein is intended to be
generally synonymous, and is used interchangeably with, the terms
"disease", "syndrome", and "condition" (as in medical condition),
in that all reflect an abnormal condition of the human or animal
body or of one of its parts that impairs normal functioning, is
typically manifested by distinguishing signs and symptoms.
[0035] The terms "treat," "treating," and "treatment" are meant to
include alleviating or abrogating a disorder or one or more of the
symptoms associated with a disorder; or alleviating or eradicating
the cause(s) of the disorder itself. As used herein, reference to
"treatment" of a disorder is intended to include prevention. The
terms "prevent," "preventing," and "prevention" refer to a method
of delaying or precluding the onset of a disorder; and/or its
attendant symptoms, barring a subject from acquiring a disorder or
reducing a subject's risk of acquiring a disorder.
[0036] The term "therapeutically effective amount" refers to the
amount of a compound that, when administered, is sufficient to
prevent development of, or alleviate to some extent, one or more of
the symptoms of the disorder being treated. The term
"therapeutically effective amount" also refers to the amount of a
compound that is sufficient to elicit the biological or medical
response of a cell, tissue, system, animal, or human that is being
sought by a researcher, veterinarian, medical doctor, or
clinician.
[0037] The term "subject" refers to an animal, including, but not
limited to, a primate (e.g., human, monkey, chimpanzee, gorilla,
and the like), rodents (e.g., rats, mice, gerbils, hamsters,
ferrets, and the like), lagomorphs, swine (e.g., pig, miniature
pig), equine, canine, feline, and the like. The terms "subject" and
"patient" are used interchangeably herein in reference, for
example, to a mammalian subject, such as a human patient.
[0038] The term "combination therapy" means the administration of
two or more therapeutic agents to treat a therapeutic disorder
described in the present disclosure. Such administration
encompasses co-administration of these therapeutic agents in a
substantially simultaneous manner, such as in a single capsule
having a fixed ratio of active ingredients or in multiple, separate
capsules for each active ingredient. In addition, such
administration also encompasses use of each type of therapeutic
agent in a sequential manner. In either case, the treatment regimen
will provide beneficial effects of the drug combination in treating
the disorders described herein.
[0039] The term "chronic hyperkinetic movement disorders" refers to
disorders characterized by non-purposeful, repetitive, disordered
motor acts, variously termed "compulsive", "rhythmical", or
"stereotyped." In humans, chronic hyperkinetic movement disorders
can be psychogenic (e.g., tics), idiopathic (as in, e.g.,
Tourette's syndrome and Parkinson's Disease, genetic (as in, e.g.,
the chorea characteristic of Huntington's Disease), infectious (as
in, e.g., Sydenham's Chorea), or, as in tardive dyskinesia,
drug-induced. Unless otherwise stated, "chronic hyperkinetic
movement disorders" refers to and includes all psychogenic,
idiopathic, genetic, and drug-induced movement disorders.
[0040] The term "stereotyped" refers to a repeated behavior that
appears repetitively with slight variation or, less commonly, as a
complex series of movements.
[0041] The term "VMAT2" refers to vesicular monoamine transporter
2, an integral membrane protein that acts to transport
monoamines--particularly neurotransmitters such as dopamine,
norepinephrine, serotonin, and histamine--from cellular cytosol
into synaptic vesicles.
[0042] The term "VMAT2-mediated disorder," refers to a disorder
that is characterized by abnormal VMAT2 activity. A VMAT2-mediated
disorder may be completely or partially mediated by modulating
VMAT2. In particular, a VMAT2-mediated disorder is one in which
inhibition of VMAT2 results in some effect on the underlying
disorder e.g., administration of a VMAT2 inhibitor results in some
improvement in at least some of the patients being treated.
[0043] The term "VMAT2 inhibitor", "inhibit VMAT2", or "inhibition
of VMAT2" refers to the ability of a compound disclosed herein to
alter the function of VMAT2. A VMAT2 inhibitor may block or reduce
the activity of VMAT2 by forming a reversible or irreversible
covalent bond between the inhibitor and VMAT2 or through formation
of a noncovalently bound complex. Such inhibition may be manifest
only in particular cell types or may be contingent on a particular
biological event. The term "VMAT2 inhibitor", "inhibit VMAT2", or
"inhibition of VMAT2" also refers to altering the function of VMAT2
by decreasing the probability that a complex forms between a VMAT2
and a natural substrate
[0044] The term "therapeutically acceptable" refers to those
compounds (or salts, prodrugs, tautomers, zwitterionic forms, etc.)
which are suitable for use in contact with the tissues of patients
without excessive toxicity, irritation, allergic response,
immunogenecity, are commensurate with a reasonable benefit/risk
ratio, and are effective for their intended use.
[0045] The term "pharmaceutically acceptable carrier,"
"pharmaceutically acceptable excipient," "physiologically
acceptable carrier," or "physiologically acceptable excipient"
refers to a pharmaceutically-acceptable material, composition, or
vehicle, such as a liquid or solid filler, diluent, excipient,
solvent, or encapsulating material. Each component must be
"pharmaceutically acceptable" in the sense of being compatible with
the other ingredients of a pharmaceutical formulation. It must also
be suitable for use in contact with the tissue or organ of humans
and animals without excessive toxicity, irritation, allergic
response, immunogenecity, or other problems or complications,
commensurate with a reasonable benefit/risk ratio. See, Remington:
The Science and Practice of Pharmacy, 21st Edition; Lippincott
Williams & Wilkins: Philadelphia, Pa., 2005; Handbook of
Pharmaceutical Excipients, 5th Edition; Rowe et al., Eds., The
Pharmaceutical Press and the American Pharmaceutical Association:
2005; and Handbook of Pharmaceutical Additives, 3rd Edition; Ash
and Ash Eds., Gower Publishing Company: 2007; Pharmaceutical
Preformulation and Formulation, Gibson Ed., CRC Press LLC: Boca
Raton, Fla., 2004).
[0046] The terms "active ingredient," "active compound," and
"active substance" refer to a compound, which is administered,
alone or in combination with one or more pharmaceutically
acceptable excipients or carriers, to a subject for treating,
preventing, or ameliorating one or more symptoms of a disorder.
[0047] The terms "drug," "therapeutic agent," and "chemotherapeutic
agent" refer to a compound, or a pharmaceutical composition
thereof, which is administered to a subject for treating,
preventing, or ameliorating one or more symptoms of a disorder.
[0048] The term "release controlling excipient" refers to an
excipient whose primary function is to modify the duration or place
of release of the active substance from a dosage form as compared
with a conventional immediate release dosage form.
[0049] The term "nonrelease controlling excipient" refers to an
excipient whose primary function do not include modifying the
duration or place of release of the active substance from a dosage
form as compared with a conventional immediate release dosage
form.
[0050] The term "prodrug" refers to a compound functional
derivative of the compound as disclosed herein and is readily
convertible into the parent compound in vivo. Prodrugs are often
useful because, in some situations, they may be easier to
administer than the parent compound. They may, for instance, be
bioavailable by oral administration whereas the parent compound is
not. The prodrug may also have enhanced solubility in
pharmaceutical compositions over the parent compound. A prodrug may
be converted into the parent drug by various mechanisms, including
enzymatic processes and metabolic hydrolysis. See Harper, Progress
in Drug Research 1962, 4, 221-294; Morozowich et al. in "Design of
Biopharmaceutical Properties through Prodrugs and Analogs," Roche
Ed., APHA Acad. Pharm. Sci. 1977; "Bioreversible Carriers in Drug
in Drug Design, Theory and Application," Roche Ed., APHA Acad.
Pharm. Sci. 1987; "Design of Prodrugs," Bundgaard, Elsevier, 1985;
Wang et al., Curr. Pharm. Design 1999, 5, 265-287; Pauletti et al.,
Adv. Drug. Delivery Rev. 1997, 27, 235-256; Mizen et al., Pharm.
Biotech. 1998, 11, 345-365; Gaignault et al., Pract. Med. Chem.
1996, 671-696; Asgharnejad in "Transport Processes in
Pharmaceutical Systems," Amidon et al., Ed., Marcell Dekker,
185-218, 2000; Balant et al., Eur. J. Drug Metab. Pharmacokinet.
1990, 15, 143-53; Balimane and Sinko, Adv. Drug Delivery Rev. 1999,
39, 183-209; Browne, Clin. Neuropharmacol. 1997, 20, 1-12;
Bundgaard, Arch. Pharm. Chem. 1979, 86, 1-39; Bundgaard, Controlled
Drug Delivery 1987, 17, 179-96; Bundgaard, Adv. Drug Delivery Rev.
1992, 8, 1-38; Fleisher et al., Adv. Drug Delivery Rev. 1996, 19,
115-130; Fleisher et al., Methods Enzymol. 1985, 112, 360-381;
Farquhar et al., J. Pharm. Sci. 1983, 72, 324-325; Freeman et al.,
J. Chem. Soc., Chem. Commun. 1991, 875-877; Friis and Bundgaard,
Eur. J. Pharm. Sci. 1996, 4, 49-59; Gangwar et al., Des. Biopharm.
Prop. Prodrugs Analogs, 1977, 409-421; Nathwani and Wood, Drugs
1993, 45, 866-94; Sinhababu and Thakker, Adv. Drug Delivery Rev.
1996, 19, 241-273; Stella et al., Drugs 1985, 29, 455-73; Tan et
al., Adv. Drug Delivery Rev. 1999, 39, 117-151; Taylor, Adv. Drug
Delivery Rev. 1996, 19, 131-148; Valentino and Borchardt, Drug
Discovery Today 1997, 2, 148-155; Wiebe and Knaus, Adv. Drug
Delivery Rev. 1999, 39, 63-80; Waller et al., Br. J. Clin. Pharmac.
1989, 28, 497-507.
[0051] The compounds disclosed herein can exist as therapeutically
acceptable salts. The term "therapeutically acceptable salt," as
used herein, represents salts or zwitterionic forms of the
compounds disclosed herein which are therapeutically acceptable as
defined herein. The salts can be prepared during the final
isolation and purification of the compounds or separately by
reacting the appropriate compound with a suitable acid or base.
Therapeutically acceptable salts include acid and basic addition
salts. For a more complete discussion of the preparation and
selection of salts, refer to "Handbook of Pharmaceutical Salts,
Properties, and Use," Stah and Wermuth, Ed., (Wiley-VCH and VHCA,
Zurich, 2002) and Berge et al., J. Pharm. Sci. 1977, 66, 1-19.
[0052] Suitable acids for use in the preparation of
pharmaceutically acceptable salts include, but are not limited to,
acetic acid, 2,2-dichloroacetic acid, acylated amino acids, adipic
acid, alginic acid, ascorbic acid, L-aspartic acid, benzenesulfonic
acid, benzoic acid, 4-acetamidobenzoic acid, boric acid,
(+)-camphoric acid, camphorsulfonic acid,
(+)-(1S)-camphor-10-sulfonic acid, capric acid, caproic acid,
caprylic acid, cinnamic acid, citric acid, cyclamic acid,
cyclohexanesulfamic acid, dodecylsulfuric acid,
ethane-1,2-disulfonic acid, ethanesulfonic acid,
2-hydroxy-ethanesulfonic acid, formic acid, fumaric acid,
galactaric acid, gentisic acid, glucoheptonic acid, D-gluconic
acid, D-glucuronic acid, L-glutamic acid, .alpha.-oxo-glutaric
acid, glycolic acid, hippuric acid, hydrobromic acid, hydrochloric
acid, hydroiodic acid, (+)-L-lactic acid, (.+-.)-DL-lactic acid,
lactobionic acid, lauric acid, maleic acid, (-)-L-malic acid,
malonic acid, (.+-.)-DL-mandelic acid, methanesulfonic acid,
naphthalene-2-sulfonic acid, naphthalene-1,5-disulfonic acid,
1-hydroxy-2-naphthoic acid, nicotinic acid, nitric acid, oleic
acid, orotic acid, oxalic acid, palmitic acid, pamoic acid,
perchloric acid, phosphoric acid, L-pyroglutamic acid, saccharic
acid, salicylic acid, 4-amino-salicylic acid, sebacic acid, stearic
acid, succinic acid, sulfuric acid, tannic acid, (+)-L-tartaric
acid, thiocyanic acid, p-toluenesulfonic acid, undecylenic acid,
and valeric acid.
[0053] Suitable bases for use in the preparation of
pharmaceutically acceptable salts, including, but not limited to,
inorganic bases, such as magnesium hydroxide, calcium hydroxide,
potassium hydroxide, zinc hydroxide, or sodium hydroxide; and
organic bases, such as primary, secondary, tertiary, and
quaternary, aliphatic and aromatic amines, including L-arginine,
benethamine, benzathine, choline, deanol, diethanolamine,
diethylamine, dimethylamine, dipropylamine, diisopropylamine,
2-(diethylamino)-ethanol, ethanolamine, ethylamine,
ethylenediamine, isopropylamine, N-methyl-glucamine, hydrabamine,
1H-imidazole, L-lysine, morpholine, 4-(2-hydroxyethyl)-morpholine,
methylamine, piperidine, piperazine, propylamine, pyrrolidine,
1-(2-hydroxyethyl)-pyrrolidine, pyridine, quinuclidine, quinoline,
isoquinoline, secondary amines, triethanolamine, trimethylamine,
triethylamine, N-methyl-D-glucamine,
2-amino-2-(hydroxymethyl)-1,3-propanediol, and tromethamine.
[0054] While it may be possible for the compounds of the subject
invention to be administered as the raw chemical, it is also
possible to present them as a pharmaceutical composition.
Accordingly, provided herein are pharmaceutical compositions which
comprise one or more of certain compounds disclosed herein, or one
or more pharmaceutically acceptable salts, prodrugs, or solvates
thereof, together with one or more pharmaceutically acceptable
carriers thereof and optionally one or more other therapeutic
ingredients. Proper formulation is dependent upon the route of
administration chosen. Any of the well-known techniques, carriers,
and excipients may be used as suitable and as understood in the
art; e.g., in Remington's Pharmaceutical Sciences. The
pharmaceutical compositions disclosed herein may be manufactured in
any manner known in the art, e.g., by means of conventional mixing,
dissolving, granulating, dragee-making, levigating, emulsifying,
encapsulating, entrapping or compression processes. The
pharmaceutical compositions may also be formulated as a modified
release dosage form, including delayed-, extended-, prolonged-,
sustained-, pulsatile-, controlled-, accelerated- and fast-,
targeted-, programmed-release, and gastric retention dosage forms.
These dosage forms can be prepared according to conventional
methods and techniques known to those skilled in the art (see,
Remington: The Science and Practice of Pharmacy, supra;
Modified-Release Drug Deliver Technology, Rathbone et al., Eds.,
Drugs and the Pharmaceutical Science, Marcel Dekker, Inc., New
York, N.Y., 2002; Vol. 126).
[0055] The compositions include those suitable for oral, parenteral
(including subcutaneous, intradermal, intramuscular, intravenous,
intraarticular, and intramedullary), intraperitoneal, transmucosal,
transdermal, rectal and topical (including dermal, buccal,
sublingual and intraocular) administration although the most
suitable route may depend upon for example the condition and
disorder of the recipient. The compositions may conveniently be
presented in unit dosage form and may be prepared by any of the
methods well known in the art of pharmacy. Typically, these methods
include the step of bringing into association a compound of the
subject invention or a pharmaceutically salt, prodrug, or solvate
thereof ("active ingredient") with the carrier which constitutes
one or more accessory ingredients. In general, the compositions are
prepared by uniformly and intimately bringing into association the
active ingredient with liquid carriers or finely divided solid
carriers or both and then, if necessary, shaping the product into
the desired formulation.
[0056] Formulations of the compounds disclosed herein suitable for
oral administration may be presented as discrete units such as
capsules, cachets or tablets each containing a predetermined amount
of the active ingredient; as a powder or granules; as a solution or
a suspension in an aqueous liquid or a non-aqueous liquid; or as an
oil-in-water liquid emulsion or a water-in-oil liquid emulsion. The
active ingredient may also be presented as a bolus, electuary or
paste.
[0057] Pharmaceutical preparations which can be used orally include
tablets, push-fit capsules made of gelatin, as well as soft, sealed
capsules made of gelatin and a plasticizer, such as glycerol or
sorbitol. Tablets may be made by compression or molding, optionally
with one or more accessory ingredients. Compressed tablets may be
prepared by compressing in a suitable machine the active ingredient
in a free-flowing form such as a powder or granules, optionally
mixed with binders, inert diluents, or lubricating, surface active
or dispersing agents. Molded tablets may be made by molding in a
suitable machine a mixture of the powdered compound moistened with
an inert liquid diluent. The tablets may optionally be coated or
scored and may be formulated so as to provide slow or controlled
release of the active ingredient therein. All formulations for oral
administration should be in dosages suitable for such
administration. The push-fit capsules can contain the active
ingredients in admixture with filler such as lactose, binders such
as starches, and/or lubricants such as talc or magnesium stearate
and, optionally, stabilizers. In soft capsules, the active
compounds may be dissolved or suspended in suitable liquids, such
as fatty oils, liquid paraffin, or liquid polyethylene glycols. In
addition, stabilizers may be added. Dragee cores are provided with
suitable coatings. For this purpose, concentrated sugar solutions
may be used, which may optionally contain gum arabic, talc,
polyvinyl pyrrolidone, carbopol gel, polyethylene glycol, and/or
titanium dioxide, lacquer solutions, and suitable organic solvents
or solvent mixtures. Dyestuffs or pigments may be added to the
tablets or dragee coatings for identification or to characterize
different combinations of active compound doses.
[0058] The compounds may be formulated for parenteral
administration by injection, e.g., by bolus injection or continuous
infusion. Formulations for injection may be presented in unit
dosage form, e.g., in ampoules or in multi-dose containers, with an
added preservative. The compositions may take such forms as
suspensions, solutions or emulsions in oily or aqueous vehicles,
and may contain formulatory agents such as suspending, stabilizing
and/or dispersing agents. The formulations may be presented in
unit-dose or multi-dose containers, for example sealed ampoules and
vials, and may be stored in powder form or in a freeze-dried
(lyophilized) condition requiring only the addition of the sterile
liquid carrier, for example, saline or sterile pyrogen-free water,
immediately prior to use. Extemporaneous injection solutions and
suspensions may be prepared from sterile powders, granules and
tablets of the kind previously described.
[0059] Formulations for parenteral administration include aqueous
and non-aqueous (oily) sterile injection solutions of the active
compounds which may contain antioxidants, buffers, bacteriostats
and solutes which render the formulation isotonic with the blood of
the intended recipient; and aqueous and non-aqueous sterile
suspensions which may include suspending agents and thickening
agents. Suitable lipophilic solvents or vehicles include fatty oils
such as sesame oil, or synthetic fatty acid esters, such as ethyl
oleate or triglycerides, or liposomes. Aqueous injection
suspensions may contain substances which increase the viscosity of
the suspension, such as sodium carboxymethyl cellulose, sorbitol,
or dextran. Optionally, the suspension may also contain suitable
stabilizers or agents which increase the solubility of the
compounds to allow for the preparation of highly concentrated
solutions.
[0060] In addition to the formulations described previously, the
compounds may also be formulated as a depot preparation. Such long
acting formulations may be administered by implantation (for
example subcutaneously or intramuscularly) or by intramuscular
injection. Thus, for example, the compounds may be formulated with
suitable polymeric or hydrophobic materials (for example as an
emulsion in an acceptable oil) or ion exchange resins, or as
sparingly soluble derivatives, for example, as a sparingly soluble
salt.
[0061] For buccal or sublingual administration, the compositions
may take the form of tablets, lozenges, pastilles, or gels
formulated in conventional manner. Such compositions may comprise
the active ingredient in a flavored basis such as sucrose and
acacia or tragacanth.
[0062] The compounds may also be formulated in rectal compositions
such as suppositories or retention enemas, e.g., containing
conventional suppository bases such as cocoa butter, polyethylene
glycol, or other glycerides.
[0063] Certain compounds disclosed herein may be administered
topically, that is by non-systemic administration. This includes
the application of a compound disclosed herein externally to the
epidermis or the buccal cavity and the instillation of such a
compound into the ear, eye and nose, such that the compound does
not significantly enter the blood stream. In contrast, systemic
administration refers to oral, intravenous, intraperitoneal and
intramuscular administration.
[0064] Formulations suitable for topical administration include
liquid or semi-liquid preparations suitable for penetration through
the skin to the site of inflammation such as gels, liniments,
lotions, creams, ointments or pastes, and drops suitable for
administration to the eye, ear or nose.
[0065] For administration by inhalation, compounds may be delivered
from an insufflator, nebulizer pressurized packs or other
convenient means of delivering an aerosol spray. Pressurized packs
may comprise a suitable propellant such as dichlorodifluoromethane,
trichlorofluoromethane, dichlorotetrafluoroethane, carbon dioxide
or other suitable gas. In the case of a pressurized aerosol, the
dosage unit may be determined by providing a valve to deliver a
metered amount. Alternatively, for administration by inhalation or
insufflation, the compounds according to the invention may take the
form of a dry powder composition, for example a powder mix of the
compound and a suitable powder base such as lactose or starch. The
powder composition may be presented in unit dosage form, in for
example, capsules, cartridges, gelatin or blister packs from which
the powder may be administered with the aid of an inhalator or
insufflator.
[0066] Preferred unit dosage formulations are those containing an
effective dose, as herein below recited, or an appropriate fraction
thereof, of the active ingredient.
[0067] Compounds may be administered orally or via injection at a
dose of from 0.1 to 500 mg/kg per day. The dose range for adult
humans is generally from 5 mg to 2 g/day. Tablets or other forms of
presentation provided in discrete units may conveniently contain an
amount of one or more compounds which is effective at such dosage
or as a multiple of the same, for instance, units containing 5 mg
to 500 mg, usually around 10 mg to 200 mg.
[0068] The amount of active ingredient that may be combined with
the carrier materials to produce a single dosage form will vary
depending upon the host treated and the particular mode of
administration.
[0069] The compounds can be administered in various modes, e.g.
orally, topically, or by injection. The precise amount of compound
administered to a patient will be the responsibility of the
attendant physician. The specific dose level for any particular
patient will depend upon a variety of factors including the
activity of the specific compound employed, the age, body weight,
general health, sex, diets, time of administration, route of
administration, rate of excretion, drug combination, the precise
disorder being treated, and the severity of the disorder being
treated. Also, the route of administration may vary depending on
the disorder and its severity.
[0070] In the case wherein the patient's condition does not
improve, upon the doctor's discretion the administration of the
compounds may be administered chronically, that is, for an extended
period of time, including throughout the duration of the patient's
life in order to ameliorate or otherwise control or limit the
symptoms of the patient's disorder.
[0071] In the case wherein the patient's status does improve, upon
the doctor's discretion the administration of the compounds may be
given continuously or temporarily suspended for a certain length of
time (i.e., a "drug holiday").
[0072] Once improvement of the patient's conditions has occurred, a
maintenance dose is administered if necessary. Subsequently, the
dosage or the frequency of administration, or both, can be reduced,
as a function of the symptoms, to a level at which the improved
disorder is retained. Patients can, however, require intermittent
treatment on a long-term basis upon any recurrence of symptoms.
[0073] Disclosed herein are methods of treating a VMAT2-mediated
disorder comprising administering to a subject having or suspected
of having such a disorder, a therapeutically effective amount of a
compound as disclosed herein or a pharmaceutically acceptable salt,
solvate, or prodrug thereof.
[0074] VMAT2-mediated disorders, include, but are not limited to,
chronic hyperkinetic movment disorders, and/or any disorder which
can lessened, alleviated, or prevented by administering a VMAT2
inhibitor. In certain embodiments, the chronic hyperkinetic
movement disorder is Huntington's disease.
[0075] In certain embodiments, a method of treating a
VMAT2-mediated disorder comprises administering to the subject a
therapeutically effective amount of a compound as disclosed herein,
or a pharmaceutically acceptable salt, solvate, or prodrug thereof,
so as to affect: (1) decreased inter-individual variation in plasma
levels of the compound or a metabolite thereof; (2) increased
average plasma levels of the compound or decreased average plasma
levels of at least one metabolite of the compound per dosage unit;
(3) decreased inhibition of, and/or metabolism by at least one
cytochrome P.sub.450 or monoamine oxidase isoform in the subject;
(4) decreased metabolism via at least one polymorphically-expressed
cytochrome P.sub.450 isoform in the subject; (5) at least one
statistically-significantly improved disorder-control and/or
disorder-eradication endpoint; (6) an improved clinical effect
during the treatment of the disorder, (7) prevention of recurrence,
or delay of decline or appearance, of abnormal alimentary or
hepatic parameters as the primary clinical benefit, or (8)
reduction or elimination of deleterious changes in any diagnostic
hepatobiliary function endpoints, as compared to the corresponding
non-isotopically enriched compound.
[0076] In certain embodiments, inter-individual variation in plasma
levels of the compounds as disclosed herein, or metabolites
thereof, is decreased; average plasma levels of the compound as
disclosed herein are increased; average plasma levels of a
metabolite of the compound as disclosed herein are decreased;
inhibition of a cytochrome P.sub.450 or monoamine oxidase isoform
by a compound as disclosed herein is decreased; or metabolism of
the compound as disclosed herein by at least one
polymorphically-expressed cytochrome P.sub.450 isoform is
decreased; by greater than about 5%, greater than about 10%,
greater than about 20%, greater than about 30%, greater than about
40%, or by greater than about 50% as compared to the corresponding
non-isotopically enriched compound.
[0077] Plasma levels of the compound as disclosed herein, or
metabolites thereof, may be measured using the methods described by
Li et al. Rapid Communications in Mass Spectrometry 2005, 19,
1943-1950; Jindal, et al., Journal of Chromatography, Biomedical
Applications 1989, 493(2), 392-7; Schwartz, et al., Biochemical
Pharmacology 1966, 15(5), 645-55; Mehvar, et al., Drug Metabolism
and Disposition 1987, 15(2), 250-5; Roberts et al., Journal of
Chromatography, Biomedical Applications 1981, 226(1), 175-82; and
any references cited therein or any modifications made thereof.
[0078] Examples of cytochrome P.sub.450 isoforms in a mammalian
subject include, but are not limited to, CYP1A1, CYP1A2, CYP1B1,
CYP2A6, CYP2A13, CYP2B6, CYP2C8, CYP2C9, CYP2C18, CYP2C19, CYP2D6,
CYP2E1, CYP2G1, CYP2J2, CYP2R1, CYP2S1, CYP3A4, CYP3A5, CYP3A5P1,
CYP3A5P2, CYP3A7, CYP4A11, CYP4B1, CYP4F2, CYP4F3, CYP4F8, CYP4F11,
CYP4F12, CYP4X1, CYP4Z1, CYP5A1, CYP7A1, CYP7B1, CYP8A1, CYP8B1,
CYP11A1, CYP11B1, CYP11B2, CYP17, CYP19, CYP21, CYP24, CYP26A1,
CYP26B1, CYP27A1, CYP27B1, CYP39, CYP46, and CYP51.
[0079] Examples of monoamine oxidase isoforms in a mammalian
subject include, but are not limited to, MAO.sub.A, and
MAO.sub.B.
[0080] The inhibition of the cytochrome P.sub.450 isoform is
measured by the method of Ko et al. (British Journal of Clinical
Pharmacology, 2000, 49, 343-351). The inhibition of the MAO.sub.A
isoform is measured by the method of Weyler et al. (J. Biol Chem.
1985, 260, 13199-13207). The inhibition of the MAO.sub.B isoform is
measured by the method of Uebelhack et al. (Pharmacopsychiatry,
1998, 31, 187-192).
[0081] Examples of polymorphically-expressed cytochrome P.sub.450
isoforms in a mammalian subject include, but are not limited to,
CYP2C8, CYP2C9, CYP2C19, and CYP2D6.
[0082] The metabolic activities of liver microsomes, cytochrome
P.sub.450 isoforms, and monoamine oxidase isoforms are measured by
the methods described herein.
[0083] Examples of improved disorder-control and/or
disorder-eradication endpoints, or improved clinical effects
include, but are not limited to, change from baseline in the chorea
score of the Unified Huntington's Disease Rating Scale (UHDRS).
[0084] Examples of diagnostic hepatobiliary function endpoints
include, but are not limited to, alanine aminotransferase ("ALT"),
serum glutamic-pyruvic transaminase ("SGPT"), aspartate
aminotransferase ("AST" or "SGOT"), ALT/AST ratios, serum aldolase,
alkaline phosphatase ("ALP"), ammonia levels, bilirubin,
gamma-glutamyl transpeptidase ("GGTP," ".gamma.-GTP," or "GGT"),
leucine aminopeptidase ("LAP"), liver biopsy, liver
ultrasonography, liver nuclear scan, 5'-nucleotidase, and blood
protein. Hepatobiliary endpoints are compared to the stated normal
levels as given in "Diagnostic and Laboratory Test Reference",
4.sup.th edition, Mosby, 1999. These assays are run by accredited
laboratories according to standard protocol.
[0085] Besides being useful for human treatment, certain compounds
and formulations disclosed herein may also be useful for veterinary
treatment of companion animals, exotic animals and farm animals,
including mammals, rodents, and the like. More preferred animals
include horses, dogs, and cats.
Combination Therapy
[0086] The compounds disclosed herein may also be combined or used
in combination with other agents useful in the treatment of
VMAT2-mediated disorders. Or, by way of example only, the
therapeutic effectiveness of one of the compounds described herein
may be enhanced by administration of an adjuvant (i.e., by itself
the adjuvant may only have minimal therapeutic benefit, but in
combination with another therapeutic agent, the overall therapeutic
benefit to the patient is enhanced).
[0087] Such other agents, adjuvants, or drugs, may be administered,
by a route and in an amount commonly used therefor, simultaneously
or sequentially with a compound as disclosed herein. When a
compound as disclosed herein is used contemporaneously with one or
more other drugs, a pharmaceutical composition containing such
other drugs in addition to the compound disclosed herein may be
utilized, but is not required.
[0088] In certain embodiments, the compounds disclosed herein can
be combined with one or more anti-psychotics, including, but not
limited to, chlorpromazine, levomepromazine, promazine,
acepromazine, triflupromazine, cyamemazine, chlorproethazine,
dixyrazine, fluphenazine, perphenazine, prochlorperazine,
thiopropazate, trifluoperazine, acetophenazine, thioproperazine,
butaperazine, perazine, periciazine, thioridazine, mesoridazine,
pipotiazine, haloperidol, trifluperidol, melperone, moperone,
pipamperone, bromperidol, benperidol, droperidol, fluanisone,
oxypertine, molindone, sertindole, ziprasidone, flupentixol,
clopenthixol, chlorprothixene, thiothixene, zuclopenthixol,
fluspirilene, pimozide, penfluridol, loxapine, clozapine,
olanzapine, quetiapine, tetrabenazine, sulpiride, sultopride,
tiapride, remoxipride, amisulpride, veralipride, levosulpiride,
lithium, prothipendyl, risperidone, clotiapine, mosapramine,
zotepine, pripiprazole, and paliperidone.
[0089] In certain embodiments, the compounds disclosed herein can
be combined with one or more benzodiazepines ("minor
tranquilizers"), including, but not limited to alprazolam,
adinazolam, bromazepam, camazepam, clobazam, clonazepam,
clotiazepam, cloxazolam, diazepam, ethyl loflazepate, estizolam,
fludiazepam, flunitrazepam, halazepam, ketazolam, lorazepam,
medazepam, dazolam, nitrazepam, nordazepam, oxazepam, potassium
clorazepate, pinazepam, prazepam, tofisopam, triazolam, temazepam,
and chlordiazepoxide.
[0090] In certain embodiments, the compounds disclosed herein can
be combined with olanzapine or pimozide.
[0091] The compounds disclosed herein can also be administered in
combination with other classes of compounds, including, but not
limited to, anti-retroviral agents; CYP3A inhibitors; CYP3A
inducers; protease inhibitors; adrenergic agonists;
anti-cholinergics; mast cell stabilizers; xanthines; leukotriene
antagonists; glucocorticoids treatments; local or general
anesthetics; non-steroidal anti-inflammatory agents (NSAIDs), such
as naproxen; antibacterial agents, such as amoxicillin; cholesteryl
ester transfer protein (CETP) inhibitors, such as anacetrapib;
anti-fungal agents, such as isoconazole; sepsis treatments, such as
drotrecogin-.alpha.; steroidals, such as hydrocortisone; local or
general anesthetics, such as ketamine; norepinephrine reuptake
inhibitors (NRIs) such as atomoxetine; dopamine reuptake inhibitors
(DARIs), such as methylphenidate; serotonin-norepinephrine reuptake
inhibitors (SNRIs), such as milnacipran; sedatives, such as
diazepham; norepinephrine-dopamine reuptake inhibitor (NDRIs), such
as bupropion; serotonin-norepinephrine-dopamine-reuptake-inhibitors
(SNDRIs), such as venlafaxine; monoamine oxidase inhibitors, such
as selegiline; hypothalamic phospholipids; endothelin converting
enzyme (ECE) inhibitors, such as phosphoramidon; opioids, such as
tramadol; thromboxane receptor antagonists, such as ifetroban;
potassium channel openers; thrombin inhibitors, such as hirudin;
hypothalamic phospholipids; growth factor inhibitors, such as
modulators of PDGF activity; platelet activating factor (PAF)
antagonists; anti-platelet agents, such as GPIIb/IIIa blockers
(e.g., abdximab, eptifibatide, and tirofiban), P2Y(AC) antagonists
(e.g., clopidogrel, ticlopidine and CS-747), and aspirin;
anticoagulants, such as warfarin; low molecular weight heparins,
such as enoxaparin; Factor VIIa Inhibitors and Factor Xa
Inhibitors; renin inhibitors; neutral endopeptidase (NEP)
inhibitors; vasopepsidase inhibitors (dual NEP-ACE inhibitors),
such as omapatrilat and gemopatrilat; HMG CoA reductase inhibitors,
such as pravastatin, lovastatin, atorvastatin, simvastatin, NK-104
(a.k.a. itavastatin, nisvastatin, or nisbastatin), and ZD-4522
(also known as rosuvastatin, or atavastatin or visastatin);
squalene synthetase inhibitors; fibrates; bile acid sequestrants,
such as questran; niacin; anti-atherosclerotic agents, such as ACAT
inhibitors; MTP Inhibitors; calcium channel blockers, such as
amlodipine besylate; potassium channel activators; alpha-muscarinic
agents; beta-muscarinic agents, such as carvedilol and metoprolol;
antiarrhythmic agents; diuretics, such as chlorothlazide,
hydrochlorothiazide, flumethiazide, hydroflumethiazide,
bendroflumethiazide, methylchlorothiazide, trichloromethiazide,
polythiazide, benzothlazide, ethacrynic acid, tricrynafen,
chlorthalidone, furosenilde, musolimine, bumetanide, triamterene,
amiloride, and spironolactone; thrombolytic agents, such as tissue
plasminogen activator (tPA), recombinant tPA, streptokinase,
urokinase, prourokinase, and anisoylated plasminogen streptokinase
activator complex (APSAC); anti-diabetic agents, such as biguanides
(e.g. metformin), glucosidase inhibitors (e.g., acarbose),
insulins, meglitinides (e.g., repaglinide), sulfonylureas (e.g.,
glimepiride, glyburide, and glipizide), thiozolidinediones (e.g.
troglitazone, rosiglitazone and pioglitazone), and PPAR-gamma
agonists; mineralocorticoid receptor antagonists, such as
spironolactone and eplerenone; growth hormone secretagogues; aP2
inhibitors; phosphodiesterase inhibitors, such as PDE III
inhibitors (e.g., cilostazol) and PDE V inhibitors (e.g.,
sildenafil, tadalafil, vardenafil); protein tyrosine kinase
inhibitors; antiinflammatories; antiproliferatives, such as
methotrexate, FK506 (tacrolimus, Prograf), mycophenolate mofetil;
chemotherapeutic agents; immunosuppressants; anticancer agents and
cytotoxic agents (e.g., alkylating agents, such as nitrogen
mustards, alkyl sulfonates, nitrosoureas, ethylenimines, and
triazenes); antimetabolites, such as folate antagonists, purine
analogues, and pyrridine analogues; antibiotics, such as
anthracyclines, bleomycins, mitomycin, dactinomycin, and
plicamycin; enzymes, such as L-asparaginase; farnesyl-protein
transferase inhibitors; hormonal agents, such as glucocorticoids
(e.g., cortisone), estrogens/antiestrogens,
androgens/antiandrogens, progestins, and luteinizing
hormone-releasing hormone anatagonists, and octreotide acetate;
microtubule-disruptor agents, such as ecteinascidins;
microtubule-stablizing agents, such as pacitaxel, docetaxel, and
epothilones A-F; plant-derived products, such as vinca alkaloids,
epipodophyllotoxins, and taxanes; and topoisomerase inhibitors;
prenyl-protein transferase inhibitors; and cyclosporins; steroids,
such as prednisone and dexamethasone; cytotoxic drugs, such as
azathiprine and cyclophosphamide; TNF-alpha inhibitors, such as
tenidap; anti-TNF antibodies or soluble TNF receptor, such as
etanercept, rapamycin, and leflunimide; and cyclooxygenase-2
(COX-2) inhibitors, such as celecoxib and rofecoxib; and
miscellaneous agents such as, hydroxyurea, procarbazine, mitotane,
hexamethylmelamine, gold compounds, platinum coordination
complexes, such as cisplatin, satraplatin, and carboplatin.
[0092] Thus, in another aspect, certain embodiments provide methods
for treating VMAT2-mediated disorders in a subject in need of such
treatment comprising administering to said subject an amount of a
compound disclosed herein effective to reduce or prevent said
disorder in the subject, in combination with at least one
additional agent for the treatment of said disorder. In a related
aspect, certain embodiments provide therapeutic compositions
comprising at least one compound disclosed herein in combination
with one or more additional agents for the treatment of
VMAT2-mediated disorders.
General Synthetic Methods for Preparing Compounds
[0093] Isotopic hydrogen can be introduced into a compound as
disclosed herein by synthetic techniques that employ deuterated
reagents, whereby incorporation rates are pre-determined; and/or by
exchange techniques, wherein incorporation rates are determined by
equilibrium conditions, and may be highly variable depending on the
reaction conditions. Synthetic techniques, where tritium or
deuterium is directly and specifically inserted by tritiated or
deuterated reagents of known isotopic content, may yield high
tritium or deuterium abundance, but can be limited by the chemistry
required. Exchange techniques, on the other hand, may yield lower
tritium or deuterium incorporation, often with the isotope being
distributed over many sites on the molecule.
[0094] The compounds as disclosed herein can be prepared by methods
known to one of skill in the art and routine modifications thereof,
and/or following procedures similar to those described in the
Example section herein and routine modifications thereof, and/or
procedures found in DaSilva et al., Appl. Radiat. Isot., 1993,
44(4), 673-676; Popp et al., J. Pharm. Sci., 1978, 67(6), 871-873;
Ivanov et al., Heterocycles 2001, 55(8), 1569-1572; U.S. Pat. No.
2,830,993; U.S. Pat. No. 3,045,021; WO 2007/130365; WO 2008/058261,
which are hereby incorporated in their entirety, and references
cited therein and routine modifications thereof. Compounds as
disclosed herein can also be prepared as shown in any of the
following schemes and routine modifications thereof.
[0095] The following schemes can be used to practice the present
invention. Any position shown as hydrogen may be optionally
substituted with deuterium.
##STR00004##
[0096] Compound 1 is reacted with compound 2 in an appropriate
solvent, such as nitromethane, in the presence of an appropriate
acid, such as ammonium acetate, at an elevated temperature to give
compound 3. Compound 3 is reacted with compound 4 in the presence
of an appropriate base, such as potassium carbonate, in an
appropriate solvent, such as N,N-dimethylformamide, at an elevated
temperature to afford compound 5. Compound 5 is reacted with an
appropriate reducing reagent, such as lithium aluminum hydride, in
an appropriate solvent, such as tetrahyrdofuran, at an elevated
temperature to give compound 6. Compound 6 is reacted with compound
7 in the presence of an appropriate acid, such as trifluoroacetic
acid, in an appropriate solvent, such as acetic acid, at an
elevated temperature to give compound 8. Compound 9 is reacted with
compound 10 and compound 11, in an appropriate solvent, such as
methanol, at an elevated temperature to afford compound 12.
Compound 12 is reacted with compound 13 in an appropriate solvent,
such as ethyl acetate, to give compound 14. Compound 14 is reacted
with compound 8 in an appropriate solvent, such as ethanol, at an
elevated temperature to give compound 15 of Formula I.
[0097] Deuterium can be incorporated to different positions
synthetically, according to the synthetic procedures as shown in
Scheme I, by using appropriate deuterated intermediates. For
example, to introduce deuterium at one or more positions of
R.sub.1-R.sub.6, compound 4 with the corresponding deuterium
substitutions can be used. To introduce deuterium at one or more
positions of R.sub.7-R.sub.9, compound 1 with the corresponding
deuterium substitutions can be used. To introduce deuterium at one
or more positions of R.sub.10 and R.sub.12, lithium aluminum
deuteride can be used. To introduce deuterium at R.sub.11, compound
2 with the corresponding deuterium substitution can be used. To
introduce deuterium at one or more positions of R.sub.13-R.sub.14,
compound 10 with the corresponding deuterium substitutions can be
used. To introduce deuterium at R.sub.15, compound 7 with the
corresponding deuterium substitution can be used. To introduce
deuterium at one or more positions of R.sub.16-R.sub.27, compound 9
with the corresponding deuterium substitutions can be used.
##STR00005##
[0098] Compound 8 is reacted with compound 16 in an appropriate
solvent, such as water, in the presence of an appropriate base,
such as sodium hydroxide, to yield a compound 15 of Formula I.
[0099] Deuterium can be incorporated to different positions
synthetically, according to the synthetic procedures as shown in
Scheme II, by using appropriate deuterated intermediates. For
example, to introduce deuterium at one or more positions of
R.sub.1-R.sub.12 and R.sub.15, compound 8 with the corresponding
deuterium substitutions can be used. To introduce deuterium at one
or more positions of R.sub.13-R.sub.14 and R.sub.16-R.sub.17, and
R.sub.19-R.sub.27, compound 16 with the corresponding deuterium
substitutions can be used. To introduce deuterium at R.sub.18,
deuterium oxide can be used.
[0100] Deuterium can also be incorporated to various positions,
selectively or non-selectively through a proton-deuterium exchange
method known in the art.
[0101] The invention is further illustrated by the following
examples. All IUPAC names were generated using CambridgeSoft's
ChemDraw 10.0.
EXAMPLE 1
3-Isobutyl-9,10-bis(methylamino)-3,4,6,7-tetrahydro-1H-pyrido[2,1-a]isoqui-
nolin-2(11bH)-one (tetrabenazine)
##STR00006##
[0102] Step 1
##STR00007##
[0103] 6,7-Dimethoxy-3,4-dihydroisoquinoline
[0104] Acetic acid/trifluoroacetic acid (100 mL) was added to a
solution of 2-(3,4-dimethoxyphenyl)ethanamine (20 g, 110.38 mmol,
1.00 equiv) and hexamethylenetetramine (31 g, 221.11 mmol, 2.00
equiv). The resulting solution was heated at reflux for about 5
hours in an oil bath. After adding water (100 mL), the solution was
extracted with dichloromethane (3.times.200 mL), and the organic
layers were combined and dried over anhydrous sodium sulfate.
Solids were removed by filtration, and the resulting filtrate was
concentrated in vacuo to give the title product as a yellow oil (20
g, yield=95%). LC-MS: m/z=192 (MH).sup.+.
Step 2
##STR00008##
[0105] 3-((Dimethylamino)methyl)-5-methyl-hexan-2-one
[0106] Paraformaldehyde (5.5 g, 183.33 mmol, 1.60 equiv) and
dimethylamine hydrochloride (10 g, 122.70 mmol, 1.00 equiv) were
added to a solution of 5-methylhexan-2-one (50 g, 437.83 mmol, 3.00
equiv) and methanol (30 mL). The resulting solution was heated at
reflux for about 16 hours, and then the pH was adjusted to about 8
with sodium hydroxide (10%). Standard extractive workup with ether
(3.times.100 mL) gave the title product as a yellow oil (12 g,
yield=57%).
Step 3
##STR00009##
[0107] (2-Acetyl-4-methyl-pentyl)-trimethyl-ammonium iodide
[0108] Iodomethane (20 g, 140.94 mmol, 2.00 equiv) was added
dropwise to a solution of
3-((dimethylamino)methyl)-5-methylhexan-2-one (12 g, 70.05 mmol,
1.00 equiv) and ethyl acetate (50 mL). The solution was stirred at
ambient temperature for about 16 hours., and the resulting
preciptant was collected by filtration to afford the title product
(15 g, yield=68%).
Step 4
##STR00010##
[0109]
3-Isobutyl-9,10-dimethoxy-3,4,6,7-tetrahydro-1H-pyrido[2,1-a]isoqui-
nolin-2(11bH)-one
[0110] (2-Acetyl-4-methyl-pentyl)-trimethyl-ammonium iodide (800
mg, 2.55 mmol, 1.00 equiv) was added to a solution of
6,7-dimethoxy-3,4-dihydroisoquinoline (100 mg, 2.62 mmol, 1.00
equiv) and ethanol (10 mL). The resulting solution was heated at
reflux for about 5 hours, and then water (20 mL) was added.
Following standard extractive workup with dichloromethane
(3.times.50 mL), the crude residue was purified by silica gel
column chromatography (ethyl acetate/petroleum ether (1:4)) to
afford the title compound as a white solid (300 mg, yield=36%).
.sup.1H NMR (300 MHz, CDCl.sub.3), .delta. 6.63 (s, 1H), 6.55 (s,
1H), 3.89 (s, 3H), 3.83 (s, 3H), 3.55 (s, 1H), 3.22-3.28 (m, 1H),
2.94-3.14 (m, 4H), 2.31-2.65 (m, 4H), 1.73-1.81 (t, 1H, J=11.4),
1.33-1.39 (m, 1H), 0.996-1.067 (t, 1H, J=10.5), 0.79-0.85 (m, 6H)
LC-MS: m/z=318 (MH).sup.+.
EXAMPLE 2
3-Isobutyl-9,10-d.sub.6-dimethoxy-3,4,6,7-tetrahydro-1H-pyrido[2,1-a]isoqu-
inolin-2(11bH)-one (d.sub.6-tetrabenazine)
##STR00011##
[0111] Step 1
##STR00012##
[0112] 4-(2-Nitrovinyl)benzene-1,2-diol
[0113] Ammonium acetate (5.6 g, 72.73 mmol, 1.00 equiv) was added
to a solution of 3,4-dihydroxybenzaldehyde (10 g, 72.41 mmol, 1.00
equiv) and nitromethane (50 mL). The resulting mixture was heated
at reflux for about 16 hours, and then concentrated in vacuo. The
resulting residue was then purified by silica gel column
chromotagraphy (ethyl acetate/petroleum ether (1:5)) to give the
title compound as a yellow oil (8 g, yield=61%).
Step 2
##STR00013##
[0114] d.sub.6-(E)-1,2-Dimethoxy-4-(2-nitrovinyl)benzene
[0115] d.sub.3-Iodomethane (4.3 g, 31 mmol, 1.10 equiv) was added
dropwise to a solution of (E)-4-(2-nitrovinyl)benzene-1,2-diol (5
g, 28 mmol, 1.00 equiv), dimethylformamide (50 mL), and potassium
carbonate (20 g, 140 mmol, 5.00 equiv). The resulting suspension
was stirred at about 50.degree. C. for about 16 hours. The
suspension was filtered, the filter cake was washed with ethyl
acetate, and the washes were combined with the filtrate. The
resulting mixture was then extracted with ethyl acetate
(200.times.3 mL) and washed with brine. The mixture was dried over
anhydrous sodium sulfate and concentrated in vacuo to give the
title product as a yellow oil (5 g, yield=77%).
Step 3
##STR00014##
[0116] 2-(3,4-d.sub.6-Dimethoxyphenyl)ethanamine
[0117] At about 0.degree. C., a solution of
d.sub.6-(E)-1,2-dimethoxy-4-(2-nitrovinyl)benzene (8 g, 44.17 mmol,
1.00 equiv) and tetrahydrofuran (20 mL) was added dropwise to a
solution of lithium aluminum hydride (1.6 g, 42.11 mmol, 1.00
equiv) and tetrahydrofuran (30 mL). The resulting solution was
heated at reflux for about 16 hours, and then water (10 mL) was
added. After removing solids by filtation, the filtrate was dried
over anhydrous magnesium sulfate and concentrated in vacuo to give
the title product as a yellow solid (6 g, yield=93%). LC-MS:
m/z=188 (MH).sup.+.
Step 4
##STR00015##
[0118] 6,7-d.sub.6-Dimethoxy-3,4-dihydroisoquinoline
[0119] The procedure of Example 1, Step 1 was followed, but
substituting 2-(3,4-d.sub.6-dimethoxyphenyl)ethanamine for
2-(3,4-dimethoxyphenyl)ethanamine. The title product was isolated
as a yellow oil (20 g, yield=95%).
Step 5
##STR00016##
[0120]
3-Isobutyl-9,10-d.sub.6-dimethoxy-3,4,6,7-tetrahydro-1H-pyrido[2,1--
a]isoquinolin-2(11bH)-one
[0121] The procedure of Example 1, Step 4 was followed but
substituting 6,7-d.sub.6-dimethoxy-3,4-dihydroisoquinoline for
6,7-dimethoxy-3,4-dihydroisoquinoline. The title product was
isolated as a white solid (300 mg, yield=35%). .sup.1H NMR (300
MHz, CDCl.sub.3), .delta. 6.63 (s, 1H), 6.55 (s, 1H), 3.55 (s, 1H),
3.22-3.28 (m, 1H), 2.94-3.14 (m, 4H), 2.31-2.65 (m, 4H), 1.73-1.81
(t, 1H, J=11.4), 1.33-1.39 (m, 1H), 0.99-1.06 (t, 1H, =10.5),
0.79-0.85 (m, 6H) LC-MS: m/z=326 (MH).sup.+.
[0122] The following compounds can generally be made using the
methods described above. It is expected that these compounds when
made will have activity similar to those described in the examples
above.
##STR00017## ##STR00018## ##STR00019## ##STR00020## ##STR00021##
##STR00022## ##STR00023## ##STR00024## ##STR00025## ##STR00026##
##STR00027## ##STR00028## ##STR00029## ##STR00030## ##STR00031##
##STR00032## ##STR00033## ##STR00034## ##STR00035## ##STR00036##
##STR00037## ##STR00038## ##STR00039## ##STR00040##
##STR00041##
[0123] Changes in the metabolic properties of the compounds
disclosed herein as compared to their non-isotopically enriched
analogs can be shown using the following assays. Compounds listed
above which have not yet been made and/or tested are predicted to
have changed metabolic properties as shown by one or more of these
assays as well.
Biological Activity Assays
In Vitro Liver Microsomal Stability Assay
[0124] Liver microsomal stability assays are conducted at 1 mg per
mL liver microsome protein with an NADPH-generating system in 2%
sodium bicarbonate (2.2 mM NADPH, 25.6 mM glucose 6-phosphate, 6
units per mL glucose 6-phosphate dehydrogenase and 3.3 mM magnesium
chloride). Test compounds are prepared as solutions in 20%
acetonitrile-water and added to the assay mixture (final assay
concentration 5 microgram per mL) and incubated at 37.degree. C.
Final concentration of acetonitrile in the assay should be <1%.
Aliquots (50 .mu.L) are taken out at times 0, 15, 30, 45, and 60
minutes, and diluted with ice cold acetonitrile (200 .mu.L) to stop
the reactions. Samples are centrifuged at 12,000 RPM for 10 minutes
to precipitate proteins. Supernatants are transferred to
microcentrifuge tubes and stored for LC/MS/MS analysis of the
degradation half-life of the test compounds. It has thus been found
that certain deuterium-enriched compounds disclosed herein that
have been tested in this assay showed an increased degradation
half-life as compared to the non-isotopically enriched drug. In
certain embodiments, the increase in degradation half-life is at
least 5%.
In Vitro Metabolism Using Human Cytochrome P.sub.450 Enzymes
[0125] The cytochrome P.sub.450 enzymes are expressed from the
corresponding human cDNA using a baculovirus expression system (BD
Biosciences, San Jose, Calif.). A 0.25 milliliter reaction mixture
containing 0.8 milligrams per milliliter protein, 1.3 millimolar
NADP.sup.+, 3.3 millimolar glucose-6-phosphate, 0.4 U/mL
glucose-6-phosphate dehydrogenase, 3.3 millimolar magnesium
chloride and 0.2 millimolar of a compound of Formula I, the
corresponding non-isotopically enriched compound or standard or
control in 100 millimolar potassium phosphate (pH 7.4) is incubated
at 37.degree. C. for 20 minutes. After incubation, the reaction is
stopped by the addition of an appropriate solvent (e.g.,
acetonitrile, 20% trichloroacetic acid, 94% acetonitrile/6% glacial
acetic acid, 70% perchloric acid, 94% acetonitrile/6% glacial
acetic acid) and centrifuged (10,000 g) for 3 minutes. The
supernatant is analyzed by HPLC/MS/MS.
TABLE-US-00001 Cytochrome P.sub.450 Standard CYP1A2 Phenacetin
CYP2A6 Coumarin CYP2B6 [.sup.13C]-(S)-mephenytoin CYP2C8 Paclitaxel
CYP2C9 Diclofenac CYP2C19 [.sup.13C]-(S)-mephenytoin CYP2D6
(+/-)-Bufuralol CYP2E1 Chlorzoxazone CYP3A4 Testosterone CYP4A [
.sup.13C]-Lauric acid
Monoamine Oxidase A Inhibition and Oxidative Turnover
[0126] The procedure is carried out using the methods described by
Weyler et al., Journal of Biological Chemistry 1985, 260,
13199-13207, which is hereby incorporated by reference in its
entirety. Monoamine oxidase A activity is measured
spectrophotometrically by monitoring the increase in absorbance at
314 nm on oxidation of kynuramine with formation of
4-hydroxyquinoline. The measurements are carried out, at 30.degree.
C., in 50 mM sodium phosphate buffer, pH 7.2, containing 0.2%
Triton X-100 (monoamine oxidase assay buffer), plus 1 mM
kynuramine, and the desired amount of enzyme in 1 mL total
volume.
Monooamine Oxidase B Inhibition and Oxidative Turnover
[0127] The procedure is carried out as described in Uebelhack et
al., Pharmacopsychiatry 1998, 31(5), 187-192, which is hereby
incorporated by reference in its entirety.
Determination of Tetrabenazine and an Active Metabolite by HPLC
[0128] The procedure is carried out as described in Roberts et al.,
Journal of Chromatography, Biomedical Applications 1981, 226(1),
175-82, which is hereby incorporated by reference in its
entirety.
Pharmacokinetic Assays of Tetrabenazine and its Major Metabolite in
Man and Rat
[0129] The procedure is carried out as described in Mehvar, et al.,
Drug Metabolism and Disposition 1987, 15(2), 250-5, which is hereby
incorporated by reference in its entirety.
Detecting Tetrabenazine Metabolites in Animals and Man
[0130] The procedure is carried out as described in Schwartz, et
al., Biochemical Pharmacology 1966, 15(5), 645-55, which is hereby
incorporated by reference in its entirety.
Mass Spectrometric Determination of Tetrabenazine
[0131] The procedure is carried out as described in Jindal, et al.,
Journal of Chromatography, Biomedical Applications 1989, 493(2),
392-7, which is hereby incorporated by reference in its
entirety.
In Vitro Radioligand Binding Assay
[0132] The procedure is carried out as described in Scherman et
al., Journal of Neurochemistry 1988, 50(4), 1131-36, which is
hereby incorporated by reference in its entirety.
In Vitro Radioligand Binding Assay
[0133] The procedure is carried out as described in Kilbourn et
al., Synapse 2002, 43(3), 188-194, which is hereby incorporated by
reference in its entirety.
In Vitro Radioligand Binding Assay
[0134] The procedure is carried out as described in Kilbourn et
al., European Journal of Pharmacology 1997, 331(2-3), 161-68, which
is hereby incorporated by reference in its entirety.
.sup.3H-Histamine Transport Assay
[0135] The procedure is carried out as described in Erickson et
al., Journal of Molecular Neuroscience 1995, 6(4), 277-87, which is
hereby incorporated by reference in its entirety.
[0136] From the foregoing description, one skilled in the art can
ascertain the essential characteristics of this invention, and
without departing from the spirit and scope thereof, can make
various changes and modifications of the invention to adapt it to
various usages and conditions.
* * * * *