148356-47-2

Basic information

• Product Name: genistein 7-O-(tri-O-acetyl-β-L-quinovopyranoside)
• Synonyms: genistein 7-O-(tri-O-acetyl-β-L-quinovopyranoside)
• CAS NO: 148356-47-2
• Molecular Weight: 542.496
• Mol File: 148356-47-2.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: genistein 7-O-(tri-O-acetyl-β-L-quinovopyranoside)(CAS DataBase Reference)
• NIST Chemistry Reference: genistein 7-O-(tri-O-acetyl-β-L-quinovopyranoside)(148356-47-2)
• EPA Substance Registry System: genistein 7-O-(tri-O-acetyl-β-L-quinovopyranoside)(148356-47-2)

Safety Data

• Hazardous Substances Data: 148356-47-2(Hazardous Substances Data)

Upstream product

• 148356-61-0 1-(2-acetoxy-4,6-dihydroxyphenyl)-3,3-dimethoxy-2-(4-hydroxyphenyl)propan-1-one 
• 36807-84-8 tri-O-acetyl-α-L-quinovopyranosyl bromide 
• 446-72-0 5,7-Dihydroxy-3-(4-hydroxy-phenyl)-chromen-4-on 

Relevant articles and documents

Syntheses of Isoflavones and Isoflavone Glycosides, and Their Inhibitory Activity against Bovine Liver &β-Galactosidase

To clarify the relationship between the structure and inhibitory action toward β-D-galactosidase (EC 3.2.1.21) of isoflavones and isoflavone glycosides, a number of polyhydroxyisoflavones, and the α-L-rhamnosides and β-L-quinovosides of daidzein and genistein were synthesized.Among the polyhydroxyisoflavones, 2',3',4',7-tetrahydroxyisoflavone showed the strongest inhibitory activity (Ki = 26 * 10-6 M).Among the glycosides, all the L-rhamnosides were strong inhibitors, of which genistein 4',7-di-O-α-L-rhamnoside was the strongest (Ki = 4.44 * 10-6 M), while all the isoflavone β-L-quinovosides were considerably weak or possessed no inhibition.