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3-[(3-carboxypropanoyl)oxy]cholan-24-oic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

87826-99-1

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87826-99-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 87826-99-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,7,8,2 and 6 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 87826-99:
(7*8)+(6*7)+(5*8)+(4*2)+(3*6)+(2*9)+(1*9)=191
191 % 10 = 1
So 87826-99-1 is a valid CAS Registry Number.

87826-99-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-[3-(3-carboxypropanoyloxy)-10,13-dimethyl-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-17-yl]pentanoic acid

1.2 Other means of identification

Product number -
Other names -

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:87826-99-1 SDS

87826-99-1Downstream Products

87826-99-1Relevant academic research and scientific papers

Effect of a Lithocholic Acid Derivative on the Molecular Packing and Stability of Phospholipid Vesicles

Li, Zi-Chen,Li, Fu-Mian,Arase, Shinya,Takeoka, shinji,Tsuchide, Eishun

, p. 2199 - 2202 (1994)

A lithocholic acid derivative having high compatibility with phospholipid was synthesized and incorporated to the phospholipid bilayer membrane.A significant influennce of it on the molecular packing and the stability enhancement of the vesicle suspension were clarified by a fluorescence depolarization method and a turbidity measurement, respectively.

Synthesis and proteasome inhibition of lithocholic acid derivatives

Dang, Zhao,Lin, Andrew,Ho, Phong,Soroka, Dominique,Lee, Kuo-Hsiung,Huang, Li,Chen, Chin-Ho

supporting information; experimental part, p. 1926 - 1928 (2011/05/02)

A new class of proteasome inhibitors was synthesized using lithocholic acid as a scaffold. Modification at the C-3 position of lithocholic acid with a series of acid acyl groups yielded compounds with a range of potency on proteasome inhibition. Among the

Lithocholic acid analogues, new and potent α-2,3-sialyltransferase inhibitors

Chang, Kai-Hsuan,Lee, Lenselot,Chen, Jessica,Li, Wen-Shan

, p. 629 - 631 (2008/02/10)

A new type of noncompetitive α-2,3-sialyltransferase inhibitor has been synthesized; we report the discovery, preparation and inhibitory activity of sixteen lithocholic acid analogues. The Royal Society of Chemistry 2006.

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