60213-69-6

Basic information

• Product Name: oleanolic acid-3-O-β-D-glucopyranosyl (1→2)-α-L-arabinopyranoside
• Synonyms: Oleanolic acid-3-O-beta-D-glucopyranosyl (1→2)-alpha-L-arabinopyranoside;oleanolic acid-3-O-β-D-glucopyranosyl (1→2)-α-L-arabinopyranoside;Akebiasaponin PE;Fatsiaside C1;Glycoside E;2)-alpha-L-arabinopyranoside;Oleanolic acid 3-O-beta-D-glucopyranosyl (1→Oleanolic acid-3-O-β-D-glucopyranosyl (1→2)-α-L-arabinopyranoside(CAS：60213-69-6)
• CAS NO: 60213-69-6
• Molecular Formula: C₄₁H₆₆O₁₂
• Molecular Weight: 750.9555
• Product Categories: Triterpenoids;chemical reagent;pharmaceutical intermediate;phytochemical;reference standards from Chinese medicinal herbs (TCM).;standardized herbal extract
• Mol File: 60213-69-6.mol
• Article Data: 7

Chemical Properties

• Melting Point: 220-221℃
• Boiling Point: 849.6°C at 760 mmHg
• Flash Point: 250.7°C
• Appearance: /
• Density: 1.32±0.1 g/cm3 (20 ºC 760 Torr)
• Vapor Pressure: 1.4E-33mmHg at 25°C
• Refractive Index: 1.601
• CAS DataBase Reference: oleanolic acid-3-O-β-D-glucopyranosyl (1→2)-α-L-arabinopyranoside(CAS DataBase Reference)
• NIST Chemistry Reference: oleanolic acid-3-O-β-D-glucopyranosyl (1→2)-α-L-arabinopyranoside(60213-69-6)
• EPA Substance Registry System: oleanolic acid-3-O-β-D-glucopyranosyl (1→2)-α-L-arabinopyranoside(60213-69-6)

Safety Data

• Hazardous Substances Data: 60213-69-6(Hazardous Substances Data)

Usage

General Description

Oleanolic acid-3-O-β-D-glucopyranosyl (1→2)-α-L-arabinopyranoside, also known as oleanolic acid glycoside, is a natural triterpenoid compound found in various plant sources, including grapes, olives, and figs. It has been studied for its potential pharmacological properties, including anti-inflammatory, antioxidant, and anti-cancer effects. Oleanolic acid glycoside has been shown to inhibit the growth of certain types of cancer cells and to have protective effects on the liver. It may also have potential in the treatment of diabetes and cardiovascular diseases. Overall, oleanolic acid glycoside is a promising compound with a wide range of potential therapeutic applications.

InChI:InChI=1/C41H66O12/c1-36(2)14-16-41(35(48)49)17-15-39(6)21(22(41)18-36)8-9-26-38(5)12-11-27(37(3,4)25(38)10-13-40(26,39)7)52-34-32(28(44)23(43)20-50-34)53-33-31(47)30(46)29(45)24(19-42)51-33/h8,22-34,42-47H,9-20H2,1-7H3,(H,48,49)/t22-,23+,24-,25?,26-,27+,28+,29-,30+,31-,32-,33-,34+,38+,39-,40-,41+/m1/s1

Upstream product

• 85899-62-3 3-O-[β-D-glucopyranosyl (1->2)-α-L-arabinopyranosyl] oleanolic acid 28-O-[β-D-glucopyranosyl (1->6)-β-D-glucopyranosyl] ester 
• 1229037-84-6 C₄₈H₇₂O₁₂ 
• 120768-65-2 ciwujianoside A₁ 

Downstream Products

• 508-02-1 Oleanolic acid 

Relevant articles and documents

Facile synthesis of four natural triterpene saponins with important antitumor activity

The first synthesis of four natural triterpene saponins, which exhibit significant antitumor activities, was concisely achieved by adopting a stepwise glycosylation. The key intermediate 13 was afforded via Bu2SnO-mediated regioseletive benzoylation. Duri

Triterpenoid glycosides of Fatsia japonica. II. Isolation and structure of glycosides from the leaves

The previously known triterpenoid 3-O-α-L-arabinopyranosides of oleanolic and echinocystic acids and hederagenin, 3-O-β-D-glucopyranosyl-(1→2)-O-α-L-arabinopyranosides of oleanolic acid and hederagenin, in addition to 28-O-α-L-rhamnopyranosyl-(1→4)-O-β-D-glucopyranosyl-(1→6)-O-β-D-glucopyranosyl ethers of the 3-O-α-L-arabinopyranoside of hederagenin, and 3-O-β-D-glucopyranosyl-(1→2)-O-α-L-arabinopyranosides of oleanolic acid and hederagenin, respectively, are isolated from leaves of Fatsia japonica (Araliaceae). The structures of the glycosides are confirmed by chemical methods and 13C NMR spectroscopy.

Saponins from Leaves of Acanthopanax senticosus HARMS., Ciwujia. II. Structures of Ciwujianosides A1, A2, A3 A4 and D3

Further investigation of the chemical constituents of the leaves of Acanthopanax senticosus HARMS. resulted in the isolation of five new triterpenoid saponins, named ciwujianosides A1 (1), A2 (2), A3 (3), D3 (4) and A4 (5).The structures of these saponins were elucidated as follows: 1, 3-O-β-glucopyranosyl-(1->2)-α-arabinopyranosyloleanolic acid 28-O-α-rhamnopyranosyl-(1->4)-β-glucopyranosyl-(1->6)-β-glucopyranosyl ester; 2, 3-O-β-glucopyranosyl-(1->2)-α-arabinopyranosyl-30-norolean-12,20(29)-dien-28-oic acid 28-O-α-rhamnopyranosyl-(1->4)-β-glucopyranosyl-(1->6)-β-glucopyranosyl ester; 3, 3-O-α-rhamnopyranosyl-(1->2)-α-arabinopyranosylmesembryanthemoidigenic acid 28-O-α-rhamnopyranosyl-(1->4)-β-glucopyranosyl-(1->6)-β-glucopyranosyl ester; 4, 3-O-α-arabinopyranosylmesembryanthemoidigenic acid 28-O-α-rhamnopyranosyl-(1->4)-6-O-acetyl-β-glucopyranosyl-(1->6)-β-glucopyranosyl ester; 5, 3-O-β-glucopyranosyl-(1->2)-α-arabinopyranosylmesembryanthemoidigenic acid 28-O-α-rhamnopyranosyl-(1->4)-6-O-acetyl-β-glucopyranosyl-(1->6)-β-glucopyranosyl ester.Keywords: Acanthopanax senticosus; Araliaceae; saponin; Chinese folk medicine; ciwujianoside; oleanolic acid glycoside; noroleanolic acid glycoside; mesembryanthemoidigenic acid glycoside; ciwujia