1137149-71-3

Basic information

• Product Name: 3-O-(2,3,4,6-tetra-O-benzoyl-β-D-galactopyranosyl)oleanolic acid
• Synonyms: 3-O-(2,3,4,6-tetra-O-benzoyl-β-D-galactopyranosyl)oleanolic acid
• CAS NO: 1137149-71-3
• Molecular Weight: 1035.28
• Mol File: 1137149-71-3.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: 3-O-(2,3,4,6-tetra-O-benzoyl-β-D-galactopyranosyl)oleanolic acid(CAS DataBase Reference)
• NIST Chemistry Reference: 3-O-(2,3,4,6-tetra-O-benzoyl-β-D-galactopyranosyl)oleanolic acid(1137149-71-3)
• EPA Substance Registry System: 3-O-(2,3,4,6-tetra-O-benzoyl-β-D-galactopyranosyl)oleanolic acid(1137149-71-3)

Safety Data

• Hazardous Substances Data: 1137149-71-3(Hazardous Substances Data)

Upstream product

• 508-02-1 Oleanolic acid 
• 149707-75-5 2,3,4,6-tetra-O-benzoyl-1-O-trichloroacetimidoyl-α-D-galactopyranose 
• 257614-49-6 oleanolic acid trityl ester 
• 303114-51-4 oleanolic acid benzyl ester 
• 191276-09-2 2,3,4,6-tetra-O-benzoyl-α-D-galactopyranosyl trichloroacetimidate 

Relevant articles and documents

Synthesis and Evaluation of a Series of Oleanolic Acid Saponins as α-Glucosidase and α-Amylase Inhibitors

Sixteen naturally occurring oleanolic acid saponins and their derivatives were synthesized in an efficient and practical strategy, and their inhibitory activities against α-glucosidase and α-amylase were evaluated in vitro. Among all the compounds, 28-O-m

3 - monosaccharide acid oxygen glucoside oleanolic alkane type and wusu alkane triterpene saponin derivative and its preparation method and application

The invention discloses a 3-monouronic acid o-glycoside oleanane type and ursane type triterpenoid saponin derivative. The derivative has a structural formula as shown in the specification, wherein R4 is one of H atom, alkyl containing 1-10 carbons, alkyl

Facile synthesis of oleanolic acid monoglycosides and diglycosides

Oleanolic acid and its glycosides are important natural products, possessing various attractive biological activities such as antitumor, antivirus and anti-inflammatory properties. In the present work, fifteen oleanolic acid saponins bearing various sacch