104513-86-2

Basic information

• Product Name: Bayogenin 3-O-β-D-glucopyranoside
• Synonyms: Bayogenin 3-O-β-D-glucopyranoside;(2beta,3beta,4alpha)-3-(beta-D-Glucopyranosyloxy)-2,23-dihydroxy-olean-12-en-28-oic acid;Bayogenin 3-O-beta-D-glucopyranoside
• CAS NO: 104513-86-2
• Molecular Formula: C₃₆H₅₈O₁₀
• Molecular Weight: 650.83972
• Mol File: 104513-86-2.mol
• Article Data: 7

Chemical Properties

• Appearance: /
• CAS DataBase Reference: Bayogenin 3-O-β-D-glucopyranoside(CAS DataBase Reference)
• NIST Chemistry Reference: Bayogenin 3-O-β-D-glucopyranoside(104513-86-2)
• EPA Substance Registry System: Bayogenin 3-O-β-D-glucopyranoside(104513-86-2)

Safety Data

• Hazardous Substances Data: 104513-86-2(Hazardous Substances Data)

Usage

General Description

Bayogenin 3-O-β-D-glucopyranoside is a chemical compound belonging to the class of steroidal saponins, which are natural products with diverse biological activities. It consists of a steroid core structure attached to a sugar molecule, specifically a glucose unit. Bayogenin 3-O-β-D-glucopyranoside has been found in several plants, including traditional herbal medicines used in various cultures. It is known for its potential pharmacological properties, such as anti-inflammatory, anti-cancer, and antifungal effects. Additionally, it has been investigated for its potential role in the treatment of diabetes and cardiovascular diseases. Bayogenin 3-O-β-D-glucopyranoside is of interest to researchers for its potential therapeutic applications and as a natural product with medicinal benefits.

Upstream product

• 162901-83-9 3-O-β-D-glucopyranosyl bayogenin-28-O-β-D-glucopyranosyl ester 
• 1191300-09-0 β-D-xylopyranosyl-(1->4)-α-L-rhamnopyranosyl-(1->2)-[α-L-arabinopyranosyl-(1->3)]-α-L-arabinopyranosyl 3-O-β-D-glucopyranosyl-2β,3β,23-trihydroxyolean-12-en-28-oate 
• 1191300-10-3 β-D-xylopyranosyl-(1->4)-α-L-rhamnopyranosyl-(1->2)-[β-D-apio-D-furanosyl-(1->3)]-α-L-arabinopyranosyl 3-O-β-D-glucopyranosyl-2β,3β,23-trihydroxyolean-12-en-28-oate 
• 1191300-11-4 β-D-xylopyranosyl-(1->4)-[α-L-rhamnopyranosyl-(1->3)]-α-L-rhamnopyranosyl-(1->2)-[α-L-arabinopyranosyl-(1->3)]-α-L-arabinopyranosyl 3-O-β-D-glucopyranosyl-2β,3β,23-trihydroxyolean-12-en-28-oate 
• 1191300-14-7 β-D-xylopyranosyl-(1->4)-α-L-rhamnopyranosyl-(1->2)-{[β-D-apio-D-furanosyl-(1->3)]-4-O-(9-oxo-16-β-[(D-xylopyranosyl)oxy]hexadecanoyl)}-α-L-arabinopyranosyl 3-O-β-D-glucopyranosyl-2β,3β,23-trihydroxyolean-12-en-28-oate 

Downstream Products

• 465-00-9 bayogenin 

Relevant articles and documents

Five new triterpene saponins from Pulsatilla patens var. multifida

Five new oleanane-type glycosides (1-5), along with two known triterpene saponins, were isolated from the roots of Pulsatilla patens var. multifida (Ranunculaceae). The structures of the new triterpene saponins were elucidated as 3-O-β-D-glucopyranosyl(1→2)-β-D-galactopyranosyl hederagenin 28-O-β-D-glucopyran, osyl ester (1), hederagenin 3-O-[β-D- glucopyranosyl(1→2)][β-D-glucopyranosyl(1→6)]-β-D-galactopyranoside (2), 3-O-β-D-glucopyranosyl bayogenin 28-O-α-L-rhamnopyranosyl(1→4)-β-D- glucopyranosyl(1→6)-β-D glucopyranosyl ester (3), 3-O-β-D- glucopyranosyl(1→2)-β-D-galactopyranosyl oleanolic acid 28-O-α-L- rhamnopyranosyl(1→4)-β-D-glucopyranosyl(1→6):β-D-glucopyranosyl ester (4), and 3-O-[β-D-glucopyranosyl(1→2)][β-D-glucopyranosyl(1→6)]-β-D- galactopyranosyl hederagenin 28-O-α-L-rhamnopyranosyl(1→4)-β-n- glucopyranosyl(1→6)'β-D-glucopyranosyl ester (5). Structure elucidation was accomplished by 1D and 2D NMR (HMQC, HMBC, and ROESY) methods, FABMS, and hydrolysis.

Oleanane saponins from Bellis sylvestris Cyr. and evaluation of their phytotoxicity on Aegilops geniculata Roth

Six oleanane saponins were isolated for the first time from leaves of Bellis sylvestris Cyr., the southern daisy. Their structures were established by the extensive use of 2D-NMR experiments, including COSY, TOCSY, NOESY, HSQC, HMBC, CIGAR, H2BC, and HSQC-TOCSY, along with Q-TOF HRMS2 analysis. All of the compounds are constituted by bayogenin as aglycone, and characterized by the presence of an oligosaccharide moiety, consisting of two to four sugar unities esterified at the C-28 carboxyl carbon. One of the isolated compounds is a bisdesmoside containing an additional sugar moiety at the C-3 carbon. The phytotoxic activity assayed against Aegilops geniculata Roth., a coexisting test species, has been evaluated revealing that all the compounds, at the highest concentrations, showed strong phytotoxicity against the leaf development.

Phenolic and triterpenoid glycosides from Aster batangensis

A new phenolic glycoside, asterbatanoside A [p-hydroxyacetophenone-4-O-β-D-xylopyranosyl-(1 → 6)-β-D-glucopyranoside], and two new triterpenoid saponins, asterbatanoside B [2α,3β,23-trihydroxyolean-12-en-28-oic acid-28-O-β-D-glucopyranosyl-(1 → 6)-β-D-glucopyranoside] and asterbatanoside C [3-O-β-D-glucopyranosyl-2β,3β,23-trihydroxyolean-12-en-28- oicacid-28-O-β-D-glucopyranoside] were isolated from the roots of Aster batangensis. Their structures were determined by spectroscopic methods and chemical evidence. The total synthesis of asterbatanoside A is also reported. Copyright