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(25R)-Spirost-5-ene-2α,3β-diol is a naturally occurring spirostane steroid compound found in plants, known for its various biological activities and potential therapeutic applications in the pharmaceutical and cosmetic industries.

511-97-7

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511-97-7 Usage

Uses

Used in Pharmaceutical Industry:
(25R)-Spirost-5-ene-2α,3β-diol is used as a pharmaceutical agent for its potential anti-inflammatory, anti-cancer, and anti-diabetic properties. It is valued for its antioxidant and immunomodulatory effects, which contribute to its therapeutic potential.
Used in Cosmetic Industry:
(25R)-Spirost-5-ene-2α,3β-diol is used as an ingredient in cosmetic products due to its beneficial properties for skin health and its potential to improve the appearance and condition of the skin.
Used in Traditional Medicine:
(25R)-Spirost-5-ene-2α,3β-diol is used in traditional medicine for its potential therapeutic effects on various ailments, leveraging its natural biological activities for health and wellness.

Check Digit Verification of cas no

The CAS Registry Mumber 511-97-7 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,1 and 1 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 511-97:
(5*5)+(4*1)+(3*1)+(2*9)+(1*7)=57
57 % 10 = 7
So 511-97-7 is a valid CAS Registry Number.
InChI:InChI=1/C27H42O4/c1-15-7-10-27(30-14-15)16(2)24-23(31-27)12-20-18-6-5-17-11-21(28)22(29)13-26(17,4)19(18)8-9-25(20,24)3/h5,15-16,18-24,28-29H,6-14H2,1-4H3/t15-,16+,18-,19+,20+,21-,22-,23+,24+,25+,26+,27-/m1/s1

511-97-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name Yuccagenin

1.2 Other means of identification

Product number -
Other names Spirost-5-ene-2,3-diol, (2α,3β,25R)-

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:511-97-7 SDS

511-97-7Upstream product

511-97-7Downstream Products

511-97-7Relevant academic research and scientific papers

Karataviosides G-K, five new bisdesmosidic steroidal glycosides from the bulbs of Allium karataviense

Kuroda, Minpei,Ori, Kazutomo,Takayama, Hiroshi,Sakagami, Hiroshi,Mimaki, Yoshihiro

, p. 96 - 104 (2015/01/16)

We have analyzed the steroidal glycosides in Allium karataviense bulbs, and isolated five new bisdesmosidic steroidal glycosides: karataviosides G-K (1-5). The structures were elucidated by extensive spectroscopic analysis, including 2D NMR and enzymatic and hydrolytic cleavage. Karatavioside G (1) is an entirely novel furostanol glycoside, which has an O-β-d-glucopyranosyl-(1 → 6)-β-d-glucopyranosyl-(1 → 6)-β-d-glucopyranosyl unit at C-26 of the aglycone. Although a variety of cholestanol glycosides have been isolated, mainly from Liliaceae and Agavaceae, karataviosides J and K (4 and 5) are also notable because they are the most polar cholestanol bisdesmosides discovered, in which a lycotetraose is attached to C-3 of the aglycone, and a glucose or O-glucosyl-(1 → 3)-glucose is attached at C-16. The isolated glycosides were also evaluated for their cytotoxic activities against cultured tumor cell lines.

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