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CAS

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126240-14-0

Cholestan-6-one,3,14,20,22-tetrahydroxy-, (3b,5a,22R)- (9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

126240-14-0

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  • Cholestan-6-one,3,14,20,22-tetrahydroxy-, (3b,5a,22R)- (9CI)

    Cas No: 126240-14-0

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126240-14-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 126240-14-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,6,2,4 and 0 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 126240-14:
(8*1)+(7*2)+(6*6)+(5*2)+(4*4)+(3*0)+(2*1)+(1*4)=90
90 % 10 = 0
So 126240-14-0 is a valid CAS Registry Number.

126240-14-0SDS

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 Tenuifoliol

1.2 Other means of identification

Product number -
Other names (3S,5S,8R,9S,10R,13R,14R,17S)-17-((1R,2R)-1,2-Dihydroxy-1,5-dimethyl-hexyl)-3,14-dihydroxy-10,13-dimethyl-hexadecahydro-cyclopenta[a]phenanthren-6-one

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:126240-14-0 SDS

126240-14-0Downstream Products

126240-14-0Relevant articles and documents

Steroidal glycosides from the bulbs of Fritillaria meleagris and their cytotoxic activities

Matsuo, Yukiko,Shinoda, Daisuke,Nakamaru, Aina,Mimaki, Yoshihiro

, p. 670 - 682 (2013)

Steroidal glycosides (1-18), including 10 new compounds (1-10), were isolated from the bulbs of Fritillaria meleagris (Liliaceae). The structures of the new compounds were determined by two-dimensional (2D) NMR analysis, and by hydrolytic cleavage followed by spectroscopic and chromatographic analysis. The isolated compounds and their aglycones were evaluated for cytotoxic activity against HL-60 human promyelocytic leukemia cells and A549 human lung adenocarcinoma cells. Morphological observation and flow cytometry analysis showed that 5β-spirostanol glycoside (2) and a cholestane derivative (17a) induced apoptotic cell death in HL-60 cells through different mechanisms of action. Furthermore, the (22R)-spirosolanol glycoside (11) selectively induced apoptosis in A549 cells without affecting the caspase-3 activity level.

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