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(25R)-5β-Spirostane-2β,3β-diol is a naturally occurring steroidal compound belonging to the spirostane family, characterized by its unique carbon skeleton structure. This specific compound features a 5β-spirostane core, with hydroxyl groups at the 2β and 3β positions. It is commonly found in various plant species, particularly in the roots and tubers, and has been studied for its potential biological activities, such as anti-inflammatory, immunosuppressive, and cytotoxic effects. The compound's structure and properties make it a subject of interest in the field of natural product chemistry and drug discovery, as it may serve as a lead compound for the development of new therapeutic agents.

469-97-6

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469-97-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 469-97-6 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 4,6 and 9 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 469-97:
(5*4)+(4*6)+(3*9)+(2*9)+(1*7)=96
96 % 10 = 6
So 469-97-6 is a valid CAS Registry Number.

469-97-6SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (25R)-5β-spirost-2β,3β-diol

1.2 Other means of identification

Product number -
Other names samogenin

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:469-97-6 SDS

469-97-6Relevant academic research and scientific papers

Steroidal glycosides from Agave utahensis and their cytotoxic activity

Yokosuka, Akihito,Jitsuno, Maki,Yui, Satoru,Yamazaki, Masatoshi,Mimaki, Yoshihiro

experimental part, p. 1399 - 1404 (2010/03/05)

Eight new spirostanol saponins (1-8) and three new furostanol saponins (9-11) were isolated from the whole plants of Agave utahensis. The structures of 1-11 were determined by analysis of extensive spectroscopic data. The saponins were evaluated for their

THE STEROIDAL GLYCOSIDES FROM THE CAUDEX OF YUCCA GLORIOSA

Nakano, Kimiko,Yamasaki, Tokushi,Imamura, Yukiko,Murakami, Kotaro,Takaishi, Yoshihisa,Tomimatsu, Toshiaki

, p. 1215 - 1218 (2007/10/02)

Five steroidal glycosides were isolated from the fresh caudex of Yucca gloriosa together with YG-1 and Ps-1 previously obtained from flowers and the structures of these glycosides were established to be smilagenin 3-O-β-D-glycopyranosyl-(1->2)-β-D-glucopyranoside (Ys-I), 3-O-β-D-glucopyranosyl-(1->2)-β-D-galactopyranoside (YS-II), 3-O-β-D-glucopyranosyl-(1->2)-3)>-β-D-glucopyranoside (YS-III), 3-O-β-D-glucopyranosyl-(1->2)-3)>-β-D-galactopyranoside (YS-IV) and samogenin 3-O-β-D-glucopyranosyl-(1->2)-β-D-galactopyranoside (YS-V), respectively.Key Word Index - Yucca gloriosa; Agavaceae; steroidal saponins; smilagenin glycosides; samogenin glycoside.

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