1581276-63-2

Basic information

• Product Name: (3beta,4alpha,16beta,21beta,22alpha)-Olean-12-ene-3,16,21,22,23,28-hexol 21-[(2E)-2-methyl-2-butenoate]
• Synonyms: (3beta,4alpha,16beta,21beta,22alpha)-Olean-12-ene-3,16,21,22,23,28-hexol 21-[(2E)-2-methyl-2-butenoate];O-Tigloylgymnemagenin, 21-;21-O-Tigloylgymnemagenin
• CAS NO: 1581276-63-2
• Molecular Formula: C35H56O7
• Molecular Weight: 588.81494
• Mol File: 1581276-63-2.mol
• Article Data: 2

Chemical Properties

• Appearance: /
• CAS DataBase Reference: (3beta,4alpha,16beta,21beta,22alpha)-Olean-12-ene-3,16,21,22,23,28-hexol 21-[(2E)-2-methyl-2-butenoate](CAS DataBase Reference)
• NIST Chemistry Reference: (3beta,4alpha,16beta,21beta,22alpha)-Olean-12-ene-3,16,21,22,23,28-hexol 21-[(2E)-2-methyl-2-butenoate](1581276-63-2)
• EPA Substance Registry System: (3beta,4alpha,16beta,21beta,22alpha)-Olean-12-ene-3,16,21,22,23,28-hexol 21-[(2E)-2-methyl-2-butenoate](1581276-63-2)

Safety Data

• Hazardous Substances Data: 1581276-63-2(Hazardous Substances Data)

Usage

General Description

The chemical "(3beta,4alpha,16beta,21beta,22alpha)-Olean-12-ene-3,16,21,22,23,28-hexol 21-[(2E)-2-methyl-2-butenoate]" is a complex compound with a molecular structure containing olean-12-ene-3,16,21,22,23,28-hexol and 2-methyl-2-butenoate. It is a triterpene alcohol ester, primarily found in certain plant species, and exhibits various biological activities, including anti-inflammatory, anti-cancer, and anti-diabetic properties. The compound has potential applications in pharmaceutical and medicinal industries for the development of new therapeutics and treatments for a range of health conditions.

Downstream Products

• 13844-01-4 barringtogenol C 
• 20853-07-0 protoaescigenin 

Relevant articles and documents

New saponins from the seeds of Aesculus chinensis

Eight new acylated polyhydroxyoleanene triterpenoidal saponins, aesculiosides A-H (1-8), along with four known ones, have been isolated from the seeds of Aesculus chinensis. On the basis of extensive NMR studies, the structures of the new compounds were determined to be 21-O- tigloylprotoaescigenin 3-O-[β-D-glucopyranosyl-(1→2)][β-D-glucopyranosyl- (1→4)]-β-D-glucuronopyranosyl acid (1), 21-O-angeloylprotoaescigenin 3-O- [β-D-glucopyranosyl-(1←2)[[β-D-glucopyranosyl-(1→)]-β-D- glucuronopyranosyl acid (2), 21,22-O-ditigloylprotoaescigenin 3-O-[β-D- glucopyranosyl-(1→2)][[β-D-glucopyranosyl-(1→4)]-β-D-glucuronopyranosyl acid (3), 21-O-tigloyl-22-O-angeloylprotoaescigenin 3-O-[β-D-glucopyranosyl- (1→2)] [β-D-glucopyranosyl-(1→4)-β-D-glucuronopyranosyl acid (4), 21,22- O-ditigloylprotoaescigenin 3-O-[β-D-glucopyranosyl-(1→2)][β-Δ- glucopyranosyl(1→4)]-methyl β-D-glucuronopyranosate (5), 21-O-tigloyl-22-O- angeloylprotoaescigenin 3-O-[β-D-glucopyranosyl-(1→2)-l]β-D- glucopyranosyl-(1→4)]-methyl β-D-glucuronopyranosate (6), 21-O-tigloyl-28- O-acetylprotoaescigenin 3-O-[β-D-glucopyranosyl-(1→2)][[β-D- glucopyranosyl-(1→4)]-methyl β-D-glucuronopyranosate (7) and 21-O-angeloyl- 28-O-acetylprotoaescigenin 3-O-[β-D-glucopyranosyl-(1→2)][β-D- glucopyranosyl-(1→4)]-methyl β-D-glucuronopyranosate (8).