U.S. patent application number 16/120403 was filed with the patent office on 2019-12-26 for bergenin lipoic acid ester with antioxidant activity and a method of preparing the same.
This patent application is currently assigned to SHAANXI UNIVERSITY OF SCIENCE AND TECHNOLOGY. The applicant listed for this patent is Minyi JIA, Xingke JU, Han LI, Jie LI, Chengyuan LIANG, Songsong RUAN, Bin TIAN, Danni TIAN, Lei TIAN, Xuechuan WANG, Qianqian ZHAO. Invention is credited to Minyi JIA, Xingke JU, Han LI, Jie LI, Chengyuan LIANG, Songsong RUAN, Bin TIAN, Danni TIAN, Lei TIAN, Xuechuan WANG, Qianqian ZHAO.
Application Number | 20190389876 16/120403 |
Document ID | / |
Family ID | 64422257 |
Filed Date | 2019-12-26 |
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United States Patent
Application |
20190389876 |
Kind Code |
A1 |
TIAN; Bin ; et al. |
December 26, 2019 |
BERGENIN LIPOIC ACID ESTER WITH ANTIOXIDANT ACTIVITY AND A METHOD
OF PREPARING THE SAME
Abstract
A compound having the formula (I): ##STR00001## is disclosed. A
method of preparing the compound of formula (I) is also
disclosed.
Inventors: |
TIAN; Bin; (Xi'an, CN)
; JU; Xingke; (Xi'an, CN) ; TIAN; Lei;
(Xi'an, CN) ; LI; Jie; (Xi'an, CN) ; RUAN;
Songsong; (Xi'an, CN) ; JIA; Minyi; (Xi'an,
CN) ; TIAN; Danni; (Xi'an, CN) ; LI; Han;
(Xi'an, CN) ; ZHAO; Qianqian; (Xi'an, CN) ;
WANG; Xuechuan; (Xi'an, CN) ; LIANG; Chengyuan;
(Xi'an, CN) |
|
Applicant: |
Name |
City |
State |
Country |
Type |
TIAN; Bin
JU; Xingke
TIAN; Lei
LI; Jie
RUAN; Songsong
JIA; Minyi
TIAN; Danni
LI; Han
ZHAO; Qianqian
WANG; Xuechuan
LIANG; Chengyuan |
Xi'an
Xi'an
Xi'an
Xi'an
Xi'an
Xi'an
Xi'an
Xi'an
Xi'an
Xi'an
Xi'an |
|
CN
CN
CN
CN
CN
CN
CN
CN
CN
CN
CN |
|
|
Assignee: |
SHAANXI UNIVERSITY OF SCIENCE AND
TECHNOLOGY
Xi'an
CN
|
Family ID: |
64422257 |
Appl. No.: |
16/120403 |
Filed: |
September 3, 2018 |
Current U.S.
Class: |
1/1 |
Current CPC
Class: |
C07D 493/04 20130101;
A61P 17/18 20180101 |
International
Class: |
C07D 493/04 20060101
C07D493/04 |
Foreign Application Data
Date |
Code |
Application Number |
Jun 22, 2018 |
CN |
201810649372.5 |
Claims
1. (canceled)
2. A method of preparing a compound of the following formula (I):
##STR00004## comprising: reacting a compound of formula (II) with a
compound of formula (III) to obtain the compound of formula (I):
##STR00005## wherein the reaction of the compound of formula (II)
with the compound of formula (III) comprises the following steps:
placing the compound of formula (II) and the compound of formula
(III), in a molar ratio of 1:1 to 1:1.5, in a reactor; adding an
organic solvent and a catalyst to obtain a reaction mixture under
nitrogen atmosphere; and heating the reaction mixture at
50-60.degree. C. for 10-12 hours under sonication, wherein the
organic solvent is acetonitrile or tetrahydrofuran, and wherein the
catalyst is N,N'-dicyclohexylcarbodiimide,
1-ethyl-3-(3-dimethylaminopropyl)carbodiimide, or sulfuric
acid.
3. (canceled)
4. (canceled)
5. The method of claim 2, wherein the organic solvent is
acetonitrile.
6. The method of claim 2, wherein the molar ratio of the compound
of formula (II) and the compound of formula (III) is 1:1.2.
7. (canceled)
8. The method of claim 2, wherein the catalyst is
1-ethyl-3-(3-dimethylaminopropyl)carbodiimide.
9. The method of claim 2, wherein the reaction mixture is heated at
60.degree. C.
10. The method of claim 2, wherein the reaction mixture is heated
for 12 hours.
Description
[0001] The present invention claims priority to Chinese Patent
Application No. CN 201810649372.5, filed on Jun. 22, 2018, which is
incorporated by reference for all purposes as if fully set forth
herein.
FIELD OF THE INVENTION
[0002] The present invention relates to food chemistry field, in
particular, to a bergenin lipoic acid ester with antioxidant
activity and a method of preparing the same.
BACKGROUND OF THE INVENTION
[0003] Bergenin (compound of formula II) is a dihydroisocoumarin
derivative and is the main bioactive component of Saxifragaceae. In
1880, Garrean extracted the bergenin from the plant of the genus
Huer, but did not complete its structural determination until 1958.
Numerous studies have confirmed that bergenin has a variety of
biological activities, including anti-cancer, anti-hepatotoxicity,
anti-oxidation, anti-arrhythmia, anti-HIV and neuroprotective
properties. In addition, studies have shown that bergenin has an
anti-oxidative repair effect on tissue damage caused by 2,4-DNPH
and alcoholism, and at the same time has a certain effect on
eliminating the side effects of oxidants in blood and metabolism.
Takahashi et al. (Takahashi H, Kosaka M, Watanabe Y, et al.
Synthesis and neuroprotective activity of bergenin derivatives with
antioxidant activity. Bioorganic & Medicinal Chemistry, 2003,
11(8): 1781-1788.) The bergenin was obtained from Davidia
involucrata. It was found that bergenin has a good scavenging
effect on DPPH free radicals and superoxide anions, and the
antioxidant effect is remarkable. By modifying the sugar bond of
bergenin by binding with various fatty acids, its antioxidant
activity can be enhanced, indicating that the structural
modification of bergenin provides the possibility of obtaining
novel antioxidants.
[0004] Lipoic acid (LA) (compound of formula III), also known as
.alpha.-lipoic acid (ALA), is a natural disulfide compound that was
first isolated from pig liver by Reed in 1951. It is one of B
vitamins. As a natural antioxidant, lipoic acid is a water-soluble
and fat-soluble amphiphilic molecule. Both oxidized and reduced
forms have strong antioxidant effects in both water and lipid
environments. In addition, lipoic acid can exert anti-tumor effects
by inhibiting tumor angiogenesis, enhancing immunity, increasing
tumor sensitivity to chemotherapeutic drugs, and reversing tumor
resistance, so lipoic acid has high medical value and anti-aging
potential.
[0005] In the present invention, 11-hydroxyl group of bergenin is
dehydrated and condensed with lipoic acid carboxyl group to form an
ester bond, thereby obtaining a bergenin lipoic acid ester.
Preliminary antioxidant experiments show that the compound has
excellent antioxidant activity and has high medical research and
application value in the field of antioxidant health products.
SUMMARY OF THE INVENTION
[0006] In one embodiment, the present invention provides a bergenin
lipoic acid ester, which can be used as an excellent anti-oxidation
and preparation of scavenging free radical products in the fields
of food, health care products and medicine. The structural formula
of the compound of the present invention is as shown in Formula
(I):
##STR00002##
[0007] In another embodiment, present invention provides a method
of preparing the compound of formula (I). The method includes
reacting the compound of formula (II) with the compound of formula
(III) to obtain the compound of formula (I):
##STR00003##
[0008] In another embodiment, the reaction of the compound of
formula (II) with the compound of formula (III) includes the
following steps: placing the compound of formula (II) and the
compound of formula (III), in a molar ratio of 1:1 to 1:1.5, in a
reactor under nitrogen atmosphere; adding an organic solvent and a
catalyst to obtain a reaction mixture; and heating the reaction
mixture at 50-60.degree. C. for 10-12 hours under sonication.
[0009] In another embodiment, the organic solvent is acetonitrile
or tetrahydrofuran.
[0010] In another embodiment, the organic solvent is
acetonitrile.
[0011] In another embodiment, the molar ratio of the compound of
formula (II) and the compound of formula (III) is 1:1.2.
[0012] In another embodiment, the catalyst is
N,N'-dicyclohexylcarbodiimide (DCC),
1-ethyl-3-(3-dimethylaminopropyl)carbodiimide (EDC), or sulfuric
acid.
[0013] In another embodiment, the catalyst
1-ethyl-3-(3-dimethylaminopropyl)carbodiimide.
[0014] In another embodiment, the reaction mixture is heated at
60.degree. C.
[0015] In another embodiment, the reaction mixture is heated for 12
hours.
[0016] It is to be understood that both the foregoing general
description and the following detailed description are exemplary
and explanatory and are intended to provide further explanation of
the invention as claimed.
BRIEF DESCRIPTION OF THE DRAWINGS
[0017] The accompanying drawings, which are included to provide a
further understanding of the invention and are incorporated in and
constitute a part of this specification, illustrate embodiments of
the invention and together with the description serve to explain
the principles of the invention.
[0018] In the drawings:
[0019] FIG. 1 shows the scavenging activity of the compound of
formula (I) and control solutions at different concentrations.
DETAILED DESCRIPTION OF THE ILLUSTRATED EMBODIMENTS
[0020] Reference will now be made in detail to embodiments of the
present invention, example of which is illustrated in the
accompanying drawings. The following examples illustrate the
present invention, but the present invention is not limited to the
following examples.
Example 1
[0021] Preparation of Bergenin Lipoic Acid Ester (Compound of
Formula I)
[0022] In a 100 mL three-necked flask, 100 mg (0.31 mmoL) of
bergenin and 77 mg (0.37 mmoL) of lipoic acid were dissolved in 40
mL of acetonitrile in a molar ratio of 1:1.2 under nitrogen
atmosphere. A catalytic amount of EDC was slowly added under
magnetic stirring, the temperature was raised to 60.degree. C., and
the reaction was carried out for 12 hours. The reaction was traced
to completion by thin layer chromatography, and the heating was
stopped. The reaction mixture system was transferred to a
separatory funnel, and the lower phase was collected and
concentrated to obtain crude bergenin lipoic acid ester. The crude
bergenin lipoic acid ester was added to a pear-shaped separatory
funnel, and water and chloroform were added. The lower organic
layer was collected, dried over anhydrous sodium sulfate, and
concentrated under reduced pressure to obtain bergenin lipoic acid
ester, 88 mg, a yield of 54.2%.
[0023] .sup.1H-NMR (300 MHz, DMSO-d.sup.6) .delta. (ppm): 9.45-9.38
(2H, d), 6.87 (1H, s), 5.37 (1H, d), 5.05 (1H, m), 4.41-4.32 (3H,
m), 4.12-4.05 (3H, m), 3.63-3.56 (4H, m), 2.51 (2H, m), 2.28-2.24
(3H, m), 1.67-1.50 (6H, m), 1.12 (2H, m); .sup.13C-NMR (75 MHz,
DMSO-d.sup.6) .delta. (ppm): 167.7, 160.3, 143.1, 140.3, 139.0,
119.6, 111.5, 103.1, 75.5, 73.4, 70.0, 68.4, 55.3, 53.9, 50.3,
32.8, 28.7, 27.0, 23.6, 22.1; MS (ESI) for (M+H)+: 571.6.
Example 2
[0024] Preparation of Bergenin Lipoic Acid Ester
[0025] In a 100 mL three-necked flask, 150 mg (0.45 mmoL) of
bergenin and 111 mg (0.54 mmoL) of lipoic acid were dissolved in 40
mL of acetonitrile in a molar ratio of 1:1.2 under nitrogen
atmosphere. A catalytic amount of DCC was slowly added under
magnetic stirring, the temperature was raised to 60.degree. C., and
the reaction was carried out for 12 hours. The reaction was traced
to completion by thin layer chromatography, and the heating was
stopped. The reaction mixture system was transferred to a
separatory funnel, and the lower phase was collected and
concentrated to obtain crude bergenin lipoic acid ester. The crude
bergenin lipoic acid ester was added to a pear-shaped separatory
funnel, and water and chloroform were added. The lower organic
layer was collected, dried over anhydrous sodium sulfate, and
concentrated under reduced pressure to obtain bergenin lipoic acid
ester, 119 mg, a yield of 52.3%.
Example 3
[0026] Preparation of Bergenin Lipoic Acid Ester
[0027] In a 100 mL three-necked flask, 100 mg (0.31 mmoL) of
bergenin and 77 mg (0.37 mmoL) of lipoic acid were dissolved in 40
mL of acetonitrile in a molar ratio of 1:1.2 under nitrogen
atmosphere. A catalytic amount of concentrated sulfuric acid was
slowly added under magnetic stirring, the temperature was raised to
60.degree. C., and the reaction was carried out for 12 hours. The
reaction was traced to completion by thin layer chromatography, and
the heating was stopped. The reaction mixture system was
transferred to a separatory funnel, and the lower phase was
collected and concentrated to obtain crude bergenin lipoic acid
ester. The crude bergenin lipoic acid ester was added to a
pear-shaped separatory funnel, and water and chloroform were added.
The lower organic layer was collected, dried over anhydrous sodium
sulfate, and concentrated under reduced pressure to obtain bergenin
lipoic acid ester, 77 mg, a yield of 48.4%.
Example 4
[0028] Preparation of Bergenin Lipoic Acid Ester
[0029] In a 100 mL three-necked flask, 150 mg (0.45 mmoL) of
bergenin and 111 mg (0.54 mmoL) of lipoic acid were dissolved in 40
mL of tetrahydrofuran in a molar ratio of 1:1.2 under nitrogen
atmosphere. A catalytic amount of EDC was slowly added under
magnetic stirring, the temperature was raised to 60.degree. C., and
the reaction was carried out for 12 hours. The reaction was traced
to completion by thin layer chromatography, and the heating was
stopped. The reaction mixture system was transferred to a
separatory funnel, and the lower phase was collected and
concentrated to obtain crude bergenin lipoic acid ester. The crude
bergenin lipoic acid ester was added to a pear-shaped separatory
funnel, and water and chloroform were added. The lower organic
layer was collected, dried over anhydrous sodium sulfate, and
concentrated under reduced pressure to obtain bergenin lipoic acid
ester, 113 mg, a yield of 48.9%.
Example 5
[0030] Preparation of Bergenin Lipoic Acid Ester
[0031] In a 100 mL three-necked flask, 100 mg (0.31 mmoL) of
bergenin and 77 mg (0.37 mmoL) of lipoic acid were dissolved in 40
mL of tetrahydrofuran in a molar ratio of 1:1.2 under nitrogen
atmosphere. A catalytic amount of DCC was slowly added under
magnetic stirring, the temperature was raised to 60.degree. C., and
the reaction was carried out for 12 hours. The reaction was traced
to completion by thin layer chromatography, and the heating was
stopped. The reaction mixture system was transferred to a
separatory funnel, and the lower phase was collected and
concentrated to obtain crude bergenin lipoic acid ester. The crude
bergenin lipoic acid ester was added to a pear-shaped separatory
funnel, and water and chloroform were added. The lower organic
layer was collected, dried over anhydrous sodium sulfate, and
concentrated under reduced pressure to obtain bergenin lipoic acid
ester, 77 mg, a yield of 48.2%.
Example 6
[0032] Preparation of Bergenin Lipoic Acid Ester
[0033] In a 100 mL three-necked flask, 150 mg (0.45 mmoL) of
bergenin and 111 mg (0.54 mmoL) of lipoic acid were dissolved in 40
mL of tetrahydrofuran in a molar ratio of 1:1.2 under nitrogen
atmosphere. A catalytic amount of concentrated sulfuric acid was
slowly added under magnetic stirring, the temperature was raised to
60.degree. C., and the reaction was carried out for 12 hours. The
reaction was traced to completion by thin layer chromatography, and
the heating was stopped. The reaction mixture system was
transferred to a separatory funnel, and the lower phase was
collected and concentrated to obtain crude bergenin lipoic acid
ester. The crude bergenin lipoic acid ester was added to a
pear-shaped separatory funnel, and water and chloroform were added.
The lower organic layer was collected, dried over anhydrous sodium
sulfate, and concentrated under reduced pressure to obtain bergenin
lipoic acid ester, 108 mg, a yield of 46.7%.
Example 7
[0034] The antioxidant activity of bergenin lipoic acid ester
measured by a DPPH radical scavenging activity assay
[0035] 2,2-Diphenyl-1-picryl hydrazyl (DPPH) is an organic compound
composed of a stable organic radical. In the DPPH molecule, due to
the presence of multiple electron-withdrawing --NO.sub.2 and large
.pi. bonds of the benzene ring, nitrogen free radical is
stabilized. Its methanol solution is purple and has a maximum
absorption peak at 517 nm. After the addition of an antioxidant,
DPPH captures an electron to be paired with the free electron, and
the purple fades and turns into a yellow substance. The absorption
at 517 nm disappears, and the degree of fading is quantitatively
related to the number of electrons it captures. Based on this
principle, a spectrophotometer is used to detect the change of the
absorbance of the DPPH radical in the sample solution, and the
ability of the sample to provide hydrogen atoms and scavenge free
radicals can be measured.
[0036] Preparation of DPPH solution: measuring exact amount of
2,2-diphenyl-1-picryl hydrazyl (DPPH) and dissolving in methanol to
prepare a 0.2 mmol/L DPPH solution, stored at 0.degree. C. in
dark.
[0037] Preparation of test solutions: Vc (vitamin C, positive
control), bergenin lipoic acid ester (sample), bergenin (control),
lipoic acid (control), and mixture of bergenin and lipoic acid
(reference). The test solutions were serially diluted with
acetonitrile, and four groups of controls were separately dissolved
in a test tube with a certain amount of methanol to prepare the
same concentration gradient as the sample. The corresponding 4 sets
of control solutions were obtained (gradient settings are shown in
Table 1).
TABLE-US-00001 TABLE 1 Dilution gradient of the test solution
Number Test solution Concentration gradient/ ppm A Vitamin C 7.02,
140.4, 702, 2808, 7020, 17550 B Bergenin lipoic acid ester 7.02,
140.4, 702, 2808, 7020, 17550 C Bergenin 7.02, 140.4, 702, 2808,
7020, 17550 D Lipoic acid 7.02, 140.4, 702, 2808, 7020, 17550 E
Bergenin and lipoic acid 7.02, 140.4, 702, 2808, 7020, 17550
mixture (1:1)
[0038] Specific Steps:
[0039] Absorbance measurement: Take 2 mL of sample solution (Table
1, number B), add 2 mL of DPPH solution with concentration of
2*10.sup.-4 moL/L, mix and react in the dark at room temperature
for 30 min, adjust to zero with methanol, and measure at 517 nm.
The absorbance Ai was simultaneously measured for the absorbance Aj
of 2 mL of methanol mixed with 2 mL of the sample solution and the
absorbance Ao of 2 mL of DPPH solution mixed with 2 mL of
acetonitrile (The experimental results are shown in Table 2).
TABLE-US-00002 TABLE 2 Absorbance test results of each test
solution Concentration/ppm Sample Absorbance 7.02 140.4 702 2808
7020 17550 B Ai 0.993 0.621 0.461 0.257 0.230 0.223 Aj 0.194 0.189
0.200 0.201 0.204 0.205 Ao 1.103 C Ai 1.176 1.128 0.996 0.723 0.313
0.249 Aj 0.195 0.196 0.194 0.195 0.197 0.209 Ao 1.162 D Ai 1.023
0.994 0.826 0.622 0.373 0.292 Aj 0.192 0.199 0.196 0.210 0.195
0.199 Ao 1.044 E Ai 1.074 0.925 0.560 0.244 0.244 0.233 Aj 0.190
0.191 0.193 0.195 0.208 0.216 Ao 1.086
clearance rate (%)=[1-(Ai-Aj)/Ao]*100% Clearance calculation:
TABLE-US-00003 TABLE 3 DPPH clearance rate experiment results
Clearance rate/% ( n = 3) Concentration/ppm Vc B C D E 0.00 0.00
0.00 0.00 0.00 0.00 7.02 82.01 27.56 15.57 20.40 18.60 140.4 95.17
60.83 19.79 28.64 32.41 702 95.70 76.34 30.98 39.66 66.21 2808
99.90 94.92 54.56 60.54 90.49 7020 99.90 97.64 90.01 82.95
91.67
[0040] According to the experimental results of FIG. 1, bergenin
lipoic acid ester (B) showed a significant scavenging effect on
DPPH in a concentration-dependent manner. Its DPPH clearance rate
ranges from 27.56% (7.02 ppm) to 97.64% (7020 ppm), with a single
bergenin (C), lipoic acid (D), and a mixture of bergenin and lipoic
acid (1:1). The scavenging effect of B on DPPH is better than E,
and is close to the scavenging ability of Vc when the concentration
reaches above 2808 ppm. The above experimental results show that
bergenin lipoic acid ester has excellent antioxidant activity and a
good application prospect.
* * * * *