CN101284781A - 4-position acylated shikimic acid or low-carbon alcohol ester thereof, preparation and applications thereof - Google Patents
4-position acylated shikimic acid or low-carbon alcohol ester thereof, preparation and applications thereof Download PDFInfo
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Abstract
The invention designs and synthesizes 4-acylated shikimic acid or low carbon alcohol ester thereof. The shikimic acid is a natural product with biological activity, and has the effects of anti-thrombosis and reducing the injury of local cerebral ischemia. Because the polarity is high, the shikimic acid is not easy to be absorbed through oral administration, the synthesis of single acidated derivant, the improvement of the polarity, and the strengthening of the fatsoluble and the penetrating capacities of the blood brain barrier are of great significance; the 4-acylated shikimic acid or the low carbon alcohol ester thereof can be the compound with the unique biological activity, and can be developed into a novel medicine. Simultaneously, because the 4-acylated shikimic acid or the low carbon alcohol ester thereof perfectly keeps the three chiral centers of shikimic acid structurally, the 4-acylated shikimic acid or the low carbon alcohol ester thereof is starting material and intermediate which are synthesized through available chiral medicine. In addition, the 4-acylated shikimic acid or the low carbon alcohol ester thereof has intrinsic surface activity, which can be applied as a surface active agent in the medical field, the food field and the daily cosmetic field.
Description
Technical field
The invention belongs to the ester compound that forms on the specific hydroxyl in poly-hydroxy hexamethylene olefin(e) acid or its ester of low-carbon alcohol, is to belong to 4-position acylated shikimic acid or its ester of low-carbon alcohol derivative specifically.
Background technology
Shikimic acid is a kind of natural product with physiologically active that extracts from Chinese medicine Magnoliacea plant star anise, the effect [1] that antithrombotic is arranged and alleviate focal cerebral ischemia injury.But because it exists polarity big, oral difficult absorption can't be by shortcomings such as hemato encephalic barriers, has limited its application as medicine to a certain extent.In order to address this problem, people manage synthetic its derivative one after another, as SA-2 [2-5], iso propylidene shikimic acid [6-11] etc., are intended to improve its polarity, strengthen its fat-soluble and penetrativity hemato encephalic barrier.
Three chiral hydroxyl groups are arranged in the shikimic acid; one of them hydroxyl of an acidylate optionally; resulting single acylated derivatives, its profit partition characteristic will with shikimic acid itself, or its full acylated derivatives; or two acylated derivatives have significant difference; this is not only for research structure and active relation, and for effective high reactivity antithrombotic reagent can be provided thus, all is highly significant; with forming the compound that a class has unique physiologically active, develop into the new medicine of a class.Meanwhile, three chiral centres that 4-position acylated shikimic acid or its ester of low-carbon alcohol derivative are had because of intact maintenance shikimic acid itself structurally also have very important significance for the chiral drug or the synthetic of medicine intermediate of ad hoc structure.In addition, 4-position acylated shikimic acid or its ester of low-carbon alcohol itself have surfactivity, can be used as tensio-active agent anionic or non-ionic type and are applied to medicine, food or daily cosmetics field.
For this reason, the objective of the invention is to design synthetic 4-position acylated shikimic acid or its ester of low-carbon alcohol.
Reference:
[1] MA Yi (Ma Yi), Sun Jianning (Sun Jianning), Xu Qiuping (Xu Qiuping) .Inhibitory Effects of Shikimic Acid on PlateletAggragation and Blood Coagulation. (shikimic acid is to the restraining effect of platelet aggregation and blood coagulation), [J] Acta Pharmaceutica Sinica, 2000,35 (1): 1-3
[2] CHONG Zhao-zhong (planting million loyalties), XU Qiu-ping (Xu Qiuping), SUN Jian-ning (Sun Jianning) .Effects of triacetylshikimicacid on brain damage and blood rheology after focal cerebral ischemia in rats (SA-2 to focal cerebral ischemia after brain tissue impairment and hemorheological effect), Chin Pharm (Chinese pharmacy), 2000,35, (8): 520～523
[3] LI Xin-zhi (Li Xinzhi), CHONG Zhao-zhong (planting million loyalties), XU Qiu-ping (Xu Qiuping), et al.Inhibitory effect oftriacetylshikimic acid on plasma contents of vasoactive substances and brain myeloperoxidase activity duringfocal cerebral is chemical reperfusion in rats (SA-2 is to the restraining effect of blood plasma vaso-active substance amount in the Focal Ischemia-Reperfusion in Rats process and brains peroxidase activity) .Chin J Pharmacol Toxicol (Chinese J Pharmacol Toxicol) .2006,20 (1): 13～18
[4] HUANG Fengyang (Huang Fengyang), Xu Qiuping (Xu Qiuping), Sun Jianning (Sun Jianning), et al.Inhibitory effects oftriacetylshikimic acid on platelet aggregation (SA-2 is to the restraining effect of platelet aggregation) .ActaPharmaceutica Sinica (Acta Pharmaceutica Sinica), 1999,34 (5): 345～348
[5] CHONG Zhao-Zhong (planting million loyalties), SUN Jian-Ning (Sun Jianning), XU Qiu-Ping (Xu Qiuping) .Effects of triacetylshikimicacid on reperfusion induced brain damage and blood rheological changes of rats subjected to focal cerebralischemia (SA-2 to Focal Cerebral Ischemia Reperfusion after brain tissue impairment and hemorheological effect) Chin J PharmacolToxicol. (Chinese J Pharmacol Toxicol), 2001,15 (1): 1～5
[6] WANG Hong-tao (Wang Hongtao), JIN Hong-tao (Jin Hongtao), SUN Jian-ning (Sun Jianning), et al.Experimental studies onthe anti-thrombosis effect of 3,4-oxo-isopropylidene-shikimic acid. (experimental study of iso propylidene shikimic acid anti thrombotic action).Acta Pharmaceutica Sinica (Acta Pharmaceutica Sinica), 2002,37 (4): 245～248
[7] MA Yi (Ma Yi), Sun Jianning (Sun Jianning), Xu Qiuping (Xu Qiuping), et al.Effects of3,4-oxo-isopropylidene-shikimic acid on the PGI2 Release in Vascular Endothelial Cell (iso propylidene shikimic acid is to the influence of vascular endothelial cell delivery of prostacyclin) .Journal of Beijing University of TCM (Beijing University of Chinese Medicine's journal), 2003,26 (4): 25～27
[8] WANG Hong-Tan (Wang Hongtao), SUN Jian-Ning (Sun Jianning), XU Qiu-Ping (Xu Qiuping), et al.Effect of3,4-oxo-isopropylidene-shikimic acid on free radical metabolism in the brain issue of rats subjected tomiddle cerebral artery thrombosis (iso propylidene shikimic acid is to the influence of arteria cerebri media embolism rat cerebral tissue Radical Metabolism) .Chinese Pharmacological Bulletin (Chinese Pharmacological circular), 2002,18 (5): 569～571
[9] WANG Hong-Tan (Wang Hongtao), SUN Jian-Ning (Sun Jianning), XU Qiu-Ping (Xu Qiuping), et al.Effect of3,4-oxo-isopropylidene shikimic acid on brain edema and energy metabolism in rats subjected to middlecerebral artery thrombosis (iso propylidene shikimic acid is to the influence of arteria cerebri media embolism rat brain water content and energy metabolism).ChinJ Pharmacol Toxicol. (Chinese J Pharmacol Toxicol), 2002,16 (4): 270～272
[10] MA Yi (Ma Yi); SUN Jian-ning (Sun Jianning); XU Qiu-ping (Xu Qiuping); et al.Protective effect of3; 4-oxo-isopropylidene-shikimic acid on vascular endothelial cell injured by hydrogen peroxide (iso propylidene shikimic acid is to the provide protection of H2O2 vascular endothelial cell injury) .Acta Pharmaceutica Sinica (Chinese pharmacy); 2005,40 (13): 897～899
[11] ZHANG Gui-yan (Zhang Guiyan), MA Hong-fei (Ma Hongfei), LI Shu-zhi (Li Shuzhi), et al.Studies on determinationof 3,4-o-isopropylidene-shikimic acid by HPLC and its stability in Kangshunsu tablet (content and the stability study of the plain sheet of the anti-bolt of iso propylidene shikimic acid raw material and preparation thereof) .Chin Pharm (Acta Pharmaceutica Sinica), 1990,25 (1): 1020～1022
Summary of the invention
The present invention provides a class 4-position acylated shikimic acid or its ester of low-carbon alcohol derivative first, and its chemical formulation is as follows:
In the formula
| R= | H | Alkyl C 1～C 2 |
| R 1= | Straight-chain alkyl C 1～C 23, can be saturated or unsaturated. | Straight-chain alkyl C 15, C 19～C 23, can be saturated or unsaturated. |
The preparation method of 4-position acylated shikimic acid of the present invention or its ester of low-carbon alcohol is shown in following reaction formula:
In the formula
| R= | H | Alkyl C 1～C 2 |
| R 1= | Straight-chain alkyl C 1～C 23, can be saturated or unsaturated. | Straight-chain alkyl C 15, C 19～C 23, can be saturated or unsaturated. |
R
2=H, alkyl C
1～C
2, can be saturated or unsaturated.
This method is made up of the following step:
(1) with lipase is catalyzer; in specific reaction system; make the 4-hydroxyl of shikimic acid or shikimic acid first (second) ester and lipid acid or its ester of low-carbon alcohol (as fatty acid methyl ester; ethyl ester; vinyl acetate) esterification or alcoholysis reaction take place; generate the shikimic acid or shikimic acid first (second) ester of 4-position acidylate, obtain one by reactant shikimic acid or shikimic acid first (second) ester; lipid acid or its ester of low-carbon alcohol are (as fatty acid methyl ester; ethyl ester; vinyl acetate) and the shikimic acid of reaction product 4-position acidylate or shikimic acid first (second) ester and water or corresponding low-carbon alcohol (as methyl alcohol; ethanol) equilibrium mixture of Gou Chenging.
(2) this equilibrium mixture is carried out separation and Extraction, obtain the shikimic acid or shikimic acid first (second) ester of 4-position acidylate.
Used lipase can be Novozym435 in the preparation process, also can be the lipase kind of can this reaction of catalysis carrying out that can buy on steapsase or any other market.The reaction system that is adopted is made of solvent, reaction substrate and lipase.Solvent wherein can be acetone, tertiary amyl alcohol (2-methyl-2-butanols), hexane, toluene, ionic liquid, supercutical fluid, reactant itself and other any liquid that supplies this reaction of lipase catalysis therein to carry out.Be reflected at-30～200 ℃, preferably 35～65 ℃, 0.0001-0.5MPa preferably carries out under the condition of 0.001～0.005MPa.The step of reaction mixture being carried out separation and Extraction is the operating process that obtains pure substance from reaction mixture of extraction, crystallization, column chromatography, solvent recuperation and other any necessity.
The present invention estimates security, physiologically active and the surfactivity of 4-position acylated shikimic acid or its ester of low-carbon alcohol; find that such material is nontoxic, have anticoagulant physiologically active and certain surfactivity, be suitable as the functional surface promoting agent and be used for medical supplies, food or daily cosmetics.
Embodiment
In order to understand the present invention better, with embodiment it is described below, but does not place restrictions on content of the present invention.
Example 1, the shikimic acid enzymatic acylation is synthetic
Oleic acid (commercially available technical grade) the tertiary amyl alcohol solution that in a 500ml tool plug triangular flask, adds 1g shikimic acid and 200g 25%, put into the constant temperature air bath vibrator then and heat, make material reach 55 ℃, add Novozym 43510g then, allow system react 20hrs, obtain reaction mixture.This mixture finds to have the shikimic acid list acylate of a series of lipid acid such as oleic acid, linolic acid, Zoomeric acid, eicosanoic acid to generate through the HPLC-MS analyzing and testing.Corresponding molecular ion peak is respectively:
Single oleoyl shikimic acid: MS (m/z): 461 (M+Na
+), 437 (M
-1).
Single inferior oleoyl shikimic acid: MS (m/z): 459 (M+Na
+), 435 (M
-1).
Single palmitoleoyl shikimic acid: MS (m/z): 433 (M+Na
+), 409 (M
-1).
Single peanut acyl shikimic acid: MS (m/z): 467 (M+Na
+), 491 (M
-1).
Example 2, the enzymatic of lauroyl methyl shikimate is synthetic
The Laurate ethyl tertiary amyl alcohol solution that in a 500ml tool plug triangular flask, adds 1g methyl shikimate and 200g 25%, put into the constant temperature air bath vibrator then and heat, make material reach 55 ℃, add Novozym 43510g then, allow system react 20hrs, obtain reaction mixture.Detect with the TLC method, point sample on gel GF 254 plate, with chloroform-methanol-normal hexane-formic acid (5: 1: 1: 0.1) launch, can observe the appearance of reaction product, a new spot promptly appears near Rf=0.4-0.5, the Rf value of this spot and reactant methyl shikimate (Rf=0.35) and Laurate ethyl (Rf=0.8, iodine smoke the method colour developing) have notable difference.Note treating launching after the tertiary amyl alcohol volatilization, the evaporable tertiary amyl alcohol can not influence the Rf value again.Mixture mainly contains two kinds of materials through the HPLC-MS analyzing and testing in the reaction system: single lauroyl methyl shikimate and Laurate ethyl.The molecular ion peak of wherein single lauroyl methyl shikimate is:
MS(m/z)：393(M
++Na
+)，369(M
-1)。
Example 3, the enzymatic of palmityl shikimic acid is synthetic
The palmitinic acid tertiary amyl alcohol solution that in a 500ml tool plug triangular flask, adds 1g shikimic acid and 200g 25%, put into the constant temperature air bath vibrator then and heat, make material reach 55 ℃, add Novozym 435 10g then, allow system react 20hrs, obtain reaction mixture.Detect with the TLC method, point sample on gel GF 254 plate, with chloroform-methanol-normal hexane-formic acid (5: 1: 1: 0.1) launch, can observe the appearance of reaction product, a new spot promptly appears near Rf=0.4-0.5, the Rf of this spot has notable difference as for reactant shikimic acid (Rf=0.1) and palmitinic acid (Rf=0.8, iodine smoke the method colour developing).Note treating launching after the tertiary amyl alcohol volatilization, the evaporable tertiary amyl alcohol can not influence the Rf value again.
Example 4, the preparation of palmityl shikimic acid crude product
The liquid reaction mixture that 500ml is obtained in example 3 carefully pours in the pre-dry 500ml distilling flask, separates with enzyme, and enzyme is recyclable to be used again.The liquid that collection obtains is put vacuum distillation recovered solvent on the Rotary Evaporators.Residual solvent and moisture in the flask dry up with nitrogen, obtain the 35.72g solid, are the palmityl shikimic acid, the mixture of unreacted palmitinic acid and shikimic acid.
Example 5, the purifying of product and structural confirmation
Stay solid 35.72g in the distilling flask with what experiment obtained in 4, then solid is pulverized the back upper prop, separate with column chromatography silica gel (200～300 order).In φ 40 * 500mm tool plug core filtration chromatography post, go up sample, use 3 column volumes of hexane, 2 column volumes of ether (the sample solid almost disappears on this moment) then, 2 column volumes of chloroform-methanol-hexane (5: 1: 4), 2 column volumes of chloroform-methanol (5: 1), 1 column volume of methyl alcohol is as moving phase, wash-out successively, with the composition of TLC tracking monitor effluent liquid, obtain only to contain the effluent liquid of single reaction product component.If upper prop does not once reach purification effect, can go up column purification more once, φ 30 * 300mm tool plug core filtration chromatography post, 1 column volume of normal hexane, 2 column volumes of chloroform methanol (5: 1), 1 column volume of methyl alcohol carries out solvent recuperation to the effluent liquid that contains single anti-product component, obtains product 0.5328g, be faint yellow as if product, again-4 ℃ following 0.5ml-1ml methanol wash of using.Through structural confirmation, this product is a 4-palmityl shikimic acid.The physics and chemistry of its feature and structural analysis parameter are:
m.p.110-111℃
IR(KBr，cm
-1)：3353.53，2916.05，2849.45，1740.59，1695.36，1651.24.
1H?NMR(400MHz，DMSO)：δ(ppm)12.417(s，1H)，6.613(d，1H)，5.167(s，1H)，5.119(t，1H)，4.821(m，1H)，4.387(s，1H)，3.93(t，1H)，2.397(d，1H)，2.302(t，2H)，2.131(d，1H)，1.497(m，2H)，1.234(m，24H)，0.869(t，3H)
MS(m/z)：435.8(M
++Na
+)，411.7(M-1)。
Example 6, the acute toxicity test of 4-palmityl shikimic acid
Test used animal and be cleaning level ICR small white mouse, the male and female dual-purpose, in 4 ages in week, body weight 23-25g provides [credit number: SCXK (Soviet Union) 2007-0001] by Yangzhou University comparative medicine center.Experimental result is as follows:
Table 14-palmityl shikimic acid is to the influence of mouse body weight
Table 2 acute toxicity test result
By observing, the interior mouse activity of 1h all reduces after the administration, recovers normal activity behind the 4h gradually.Food-intake increases gradually in the test group 7d, and mouse appetite, spirit, hair color are all normal; Behind the 7d, take off neck and put to death, gross necropsy is not seen main organs pathology and intoxicating phenomenons such as the heart, liver, spleen, lung, kidney.Weigh every day in the observation period 7d, and the body weight of test group mouse constantly increases.Result of study shows, under the situation of the heavy dose of filling of 4-palmityl shikimic acid stomach, dead mouse do not occur, and the overt toxicity reaction is not arranged yet.Illustrate that its toxicity is very little, its maximum safe dose is more than 1.2g/kg.
Example 7, the 4-palmityl shikimic acid test of pesticide effectiveness: arteriovenous loop thrombus
Normal rat, male and female half and half are pressed table 1 random packet, the gastric infusion shikimic acid aqueous solution and the 4-palmityl shikimic acid aqueous solution (tween 10 hydrotropies, 0.05ml/10ml) and control group (isoconcentration tween 10 solution), successive administration 3d.1h abdominal injection 8% Chloral Hydrate 350mgkg after the last administration
-1Anesthesia, dorsal position is separated right carotid and left side external jugular vein with fixed.Put into No. 7 surgical thread (being about 8cm) of weighing in advance and be full of physiological saline in the polyethylene tube stage casing that 10cm is long, its two ends connect the intubate (being about 3cm) that is full of heparin, and an end inserts jugular vein, and the other end inserts arteria carotis communis.After opening bulldog clamp, organizer outer ring blood flow.Herba Clinopodii in behind the 15min, removal of thromboses is weighed rapidly, and this weight deducts silk thread weight and promptly gets wet weight of thrombus.
Thrombus inhibiting rate: (blank group wet weight of thrombus-administration group wet weight of thrombus)/blank group wet weight of thrombus
Statistical procedures: experimental data is represented with x ± s, judges the significance of difference with one-way analysis of variance.t
1T assay between expression shikimic acid and 4-palmityl shikimic acid and the blank group, t
2T assay between the blank group of expression and 4-palmityl shikimic acid and the shikimic acid.
Table 3 thrombus inhibiting rate
Variance analysis, P＜0.05; Compare with the blank group
*P＜0.01,
*P＜0.05
As shown in Table 3, the thrombus inhibiting rate of 4-palmityl shikimic acid group and shikimic acid group and the difference of control group have significance (P＜0.01), and 4-palmityl shikimic acid and shikimic acid all can suppress thrombosis, strengthen its anticoagulation function.4-palmityl shikimic acid thrombus inhibiting rate reaches 12.9%, is higher than the inhibiting rate (12.5%) of shikimic acid, but difference not significantly (P＞0.05) between 4-palmityl shikimic acid group and the shikimic acid group.
Claims (9)
1. a class 4-position acylated shikimic acid or its ester of low-carbon alcohol is characterized in that chemical formula is
In the formula
2. the preparation method of 4-position acylated shikimic acid as claimed in claim 1 or its ester of low-carbon alcohol; it is characterized in that with shikimic acid or shikimic acid first (second) ester be substrate; under the catalysis of lipase; in reaction system, make according to following reaction equation generation esterification with another substrate lipid acid or its ester of low-carbon alcohol (as fatty acid methyl ester, ethyl ester, vinyl acetate):
In the formula
R
2=H, alkyl C
1～C
2, can be saturated or unsaturated.
This method is made up of the following step:
(1) with lipase is catalyzer; in specific reaction system; make the 4-hydroxyl of shikimic acid or shikimic acid first (second) ester and lipid acid or its ester of low-carbon alcohol (as fatty acid methyl ester; ethyl ester; vinyl acetate) esterification or alcoholysis reaction take place; generate the shikimic acid or shikimic acid first (second) ester of 4-position acidylate, obtain one by reactant shikimic acid or shikimic acid first (second) ester; lipid acid or its ester of low-carbon alcohol are (as fatty acid methyl ester; ethyl ester; vinyl acetate) and the shikimic acid of reaction product 4-position acidylate or shikimic acid first (second) ester and water or corresponding low-carbon alcohol (as methyl alcohol; ethanol) equilibrium mixture of Gou Chenging.
(2) this equilibrium mixture is carried out separation and Extraction, obtain the shikimic acid or shikimic acid first (second) ester of 4-position acidylate.
3. the preparation method of 4-position acylated shikimic acid as claimed in claim 2 or its ester of low-carbon alcohol is characterized in that lipase, means Novozym435, any lipase kind of can this reaction of catalysis carrying out that can buy on steapsase and other market.
4. the synthetic method of 4-position acylated shikimic acid as claimed in claim 2 or its ester of low-carbon alcohol is characterized in that reaction system means the mixture that is made of together with lipase solvent, reactant.
5. the preparation method of 4-position acylated shikimic acid as claimed in claim 2 or its ester of low-carbon alcohol; it is characterized in that esterification or alcoholysis reaction mean that reaction system is under certain temperature, pressure; utilize lipase, the process of catalytic substrate generation chemical transformation formation reaction product.
6. the preparation method of 4-position acylated shikimic acid as claimed in claim 2 or its ester of low-carbon alcohol is characterized in that separation and Extraction is the operating process that obtains pure substance from reaction mixture of extraction, crystallization, column chromatography, solvent recuperation and other any necessity.
7. the preparation method of 4-position acylated shikimic acid as claimed in claim 4 or its ester of low-carbon alcohol is characterized in that solvent can be acetone, tertiary amyl alcohol (2-methyl-2-butanols), hexane, toluene, ionic liquid, supercutical fluid, reactant itself and other any liquid that supplies this reaction of lipase catalysis therein to carry out.
8. the preparation method of 4-position acylated shikimic acid as claimed in claim 5 or its ester of low-carbon alcohol is characterized in that esterification or alcoholysis reaction, at-30-200 ℃, carries out under the condition of 0.0001-0.5MPa.
9. 4-position acylated shikimic acid as claimed in claim 1 or its ester of low-carbon alcohol as the activeconstituents in the medical treatment product, medicinal intermediates or tensio-active agent in medicine, food, daily cosmetics Application for Field.
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|---|---|---|---|
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|---|---|---|---|
| CNA2008101238384A CN101284781A (en) | 2008-06-06 | 2008-06-06 | 4-position acylated shikimic acid or low-carbon alcohol ester thereof, preparation and applications thereof |
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ID=40057217
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Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN111041015A (en) * | 2019-12-31 | 2020-04-21 | 浙江工业大学 | Method for preparing (R) - (+) -N-acetyl-1-methyl-3-amphetamine at high temperature |
-
2008
- 2008-06-06 CN CNA2008101238384A patent/CN101284781A/en active Pending
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN111041015A (en) * | 2019-12-31 | 2020-04-21 | 浙江工业大学 | Method for preparing (R) - (+) -N-acetyl-1-methyl-3-amphetamine at high temperature |
| CN111041015B (en) * | 2019-12-31 | 2022-03-18 | 浙江工业大学 | Method for preparing (R) - (+) -N-acetyl-1-methyl-3-amphetamine at high temperature |
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