4339-72-4

Usage

Uses

Used in Pharmaceutical Industry:
Oleanolic acid 3-acetate is used as a pharmaceutical ingredient for its hepatoprotective, anti-inflammatory, antioxidant, antitumor, and antiviral properties. These bioactive properties make it a valuable compound for the development of drugs targeting various health conditions.
Used in Traditional Medicine:
Oleanolic acid 3-acetate is used as a traditional medicine ingredient for its therapeutic effects. Its natural occurrence in plants and its wide range of health benefits make it a popular choice in various traditional medicine practices.
Used in Cosmetic Industry:
Oleanolic acid 3-acetate is used as an active ingredient in cosmetic products for its antioxidant and anti-inflammatory properties. These properties contribute to the protection and improvement of skin health, making it a sought-after component in skincare formulations.
Used in Nutraceutical Industry:
Oleanolic acid 3-acetate is used as a nutraceutical ingredient for its potential health benefits. Its antioxidant and anti-inflammatory properties, along with its hepatoprotective and antiviral activities, make it a valuable addition to dietary supplements and functional foods.

InChI:InChI=1/C32H50O4/c1-20(33)36-25-12-13-29(6)23(28(25,4)5)11-14-31(8)24(29)10-9-21-22-19-27(2,3)15-17-32(22,26(34)35)18-16-30(21,31)7/h9,22-25H,10-19H2,1-8H3,(H,34,35)/t22?,23?,24?,25-,29+,30-,31-,32+/m1/s1

Upstream product

• 67-56-1 methanol 
• 94795-68-3 (4aS,6aS,6bR,10S,12aR,12bR)-10-Acetoxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,6b,7,8,8a,9,10,11,12,12a,12b,13,14b-octadecahydro-2H-picene-4a-carboxylic acid (2R,3S,4S,5R,6R)-3,4,5-trihydroxy-6-methyl-tetrahydro-pyran-2-yl ester 
• 94795-66-1 (4aS,6aS,6bR,10S,12aR,12bR)-10-Acetoxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,6b,7,8,8a,9,10,11,12,12a,12b,13,14b-octadecahydro-2H-picene-4a-carboxylic acid (2S,3R,4S,5R)-3,4,5-trihydroxy-tetrahydro-pyran-2-yl ester 
• 94795-66-1 (4aS,6aS,6bR,10S,12aR,12bR)-10-Acetoxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,6b,7,8,8a,9,10,11,12,12a,12b,13,14b-octadecahydro-2H-picene-4a-carboxylic acid (2S,3R,4S,5S)-3,4,5-trihydroxy-tetrahydro-pyran-2-yl ester 
• 14162-53-9 β-D-glucopyranosyl oleanolate 
• 3495-07-6 (4aS,6aS,6bR,10S,12aR,12bR)-10-Acetoxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,6b,7,8,8a,9,10,11,12,12a,12b,13,14b-octadecahydro-2H-picene-4a-carboxylic acid (2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-hydroxymethyl-tetrahydro-pyran-2-yl ester 

Downstream Products

• 1721-57-9 Oleanolsaeuremethylester-acetat 
• 25493-69-0 (4aS,6aS,6bR,10S,12aR)-methyl 10-acetoxy-2,2,6a,6b,9,9,12a-heptamethyl-1,2,3,4,4a,5,6,6a,6b,7,8,8a,9,10,11,12,12a,12b,13,14b-icosahydropicene-4a-carboxylate 
• 35959-11-6 3β-acetoxy-13-hydroxy-12-oxo-oleanan-28-oic acid-lactone 
• 35738-25-1 11α,12α-epoxy-oleanan-28->13-olide-3β-yl acetate 
• 62498-83-3 (3β,12α) 3-acetyl-12-hydroxy-18β-olean-28-oic acid 28,13-lactone 
• 19897-41-7 3β-hydroxy-11α,12α-epoxy-olean-28,13β-olide 
• 14605-17-5 3β-acetoxy-11-oxo-18α-oleanen-(12)-oic acid-(28) 
• 14605-17-5 3β-acetoxy-11-oxo-olean-12-en-28-oic acid 
• 508-02-1 Oleanolic acid 
• 1137149-64-4 3-O-acetyloleanolic acid 2,3,4,6-tetra-O-benzoyl-β-D-galactopyranosyl ester 
• 1372616-20-0 C₅₆H₆₇NO₈ 
• 218600-44-3 bardoxolone 
• 65023-19-0 methyl 3β-hydroxy-12-oxoolean-9(11)-en-28-oate 
• 65023-20-3 methyl 3β-acetoxy-12-oxoolean-9(11)-en-28-oate 

Relevant academic research and scientific papers

SELECTIVE CLEAVAGE OF ESTER TYPE GLYCOSIDE-LINKAGES AND ITS APPLICATION TO STRUCTURE DETERMINATION OF NATURAL OLIGOGLYCOSIDES

On treatment with anhydrous LiI, 2,6-lutidine and anhydrous methanol, an ester type glycosyl linkage of acidic tri- and di-terpenes was selectively cleaved without decomposition of a reducing terminal of the resulting sugar moiety to give an anomeric mixture of methyl glycosides along with an aglycone or a pro-aglycone in quantitative yield.In this reaction, no hydrolysis of any other glycoside linkages took place.