53962-19-9

Basic information

• Product Name: b-D-Glucopyranosiduronic acid, (3b,16a,21b,22a)-16,21,22,28-tetrahydroxyolean-12-en-3-ylO-6-deoxy-a-L-mannopyranosyl-(1®2)-O-b-D-galactopyranosyl-(1®3)-O-[b-D-glucopyranosyl-(1®2)]- (9CI)
• Synonyms: Oleanane,b-D-glucopyranosiduronic acidderiv.; Deacyljegosaponin; Desacyljegosaponin; Jegosaponin, deacyl-
• CAS NO: 53962-19-9
• Molecular Formula: C54H88 O25
• Molecular Weight: 1137.28
• Mol File: 53962-19-9.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: b-D-Glucopyranosiduronic acid, (3b,16a,21b,22a)-16,21,22,28-tetrahydroxyolean-12-en-3-ylO-6-deoxy-a-L-mannopyranosyl-(1®2)-O-b-D-galactopyranosyl-(1®3)-O-[b-D-glucopyranosyl-(1®2)]- (9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: b-D-Glucopyranosiduronic acid, (3b,16a,21b,22a)-16,21,22,28-tetrahydroxyolean-12-en-3-ylO-6-deoxy-a-L-mannopyranosyl-(1®2)-O-b-D-galactopyranosyl-(1®3)-O-[b-D-glucopyranosyl-(1®2)]- (9CI)(53962-19-9)
• EPA Substance Registry System: b-D-Glucopyranosiduronic acid, (3b,16a,21b,22a)-16,21,22,28-tetrahydroxyolean-12-en-3-ylO-6-deoxy-a-L-mannopyranosyl-(1®2)-O-b-D-galactopyranosyl-(1®3)-O-[b-D-glucopyranosyl-(1®2)]- (9CI)(53962-19-9)

Safety Data

• Hazardous Substances Data: 53962-19-9(Hazardous Substances Data)

Upstream product

• 1160430-52-3 21,22-di-O-tigloyl barringtogenol 3-O-β-D-glucopyranosyl(1->2)[α-L-rhamnopyranosyl(1->2)-β-D-galactopyranosyl(1->3)]-β-D-glucopyranosiduronic acid 
• 2978-11-2 p-nitrobenzyl-N,N′-diisopropylisourea 

Downstream Products

• 3615-41-6 L-Rhamnose 
• 50-99-7 D-glucose 
• 59-23-4 D-Galactose 
• 6556-12-3 D-Glucuronic acid 
• 13844-01-4 barringtogenol C 
• 80681-52-3 C₂₆H₄₅NO₂₀ 

Relevant articles and documents

Medicinal flowers. XXXVI.1) Acylated oleanane-type triterpene saponins with inhibitory effects on melanogenesis from the flower buds of Chinese Camellia japonica

Four acylated oleanane-type triterpene oligoglycosides, sanchakasaponins E-H, were isolated from the flower buds of Camellia japonica cultivated in Yunnan province, China, together with four known triterpene oligoglycosides. The chemical structures of the new triterpene oligoglycosides were elucidated on the basis of chemical and physicochemical evidence. The inhibitory effects of the triterpene oligoglycoside constituents on melanogenesis in theophylline-stimulated B16 melanoma 4A5 cells were investigated.