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3415-45-0

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3415-45-0 Usage

General Description

Glycodeoxycholic acid is a bile acid that is formed from the conjugation of deoxycholic acid with glycine. It is an important component of bile and plays a crucial role in the digestion and absorption of fats and fat-soluble vitamins in the intestines. It helps emulsify dietary fats, making them more accessible for enzymatic digestion, and also facilitates the absorption of fatty acids, cholesterol, and fat-soluble vitamins in the small intestine. Additionally, glycodeoxycholic acid also has potential therapeutic applications in the treatment of certain liver and digestive disorders.

Check Digit Verification of cas no

The CAS Registry Mumber 3415-45-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,4,1 and 5 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 3415-45:
(6*3)+(5*4)+(4*1)+(3*5)+(2*4)+(1*5)=70
70 % 10 = 0
So 3415-45-0 is a valid CAS Registry Number.

3415-45-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name GLYCODEHYDROCHOLIC ACID

1.2 Other means of identification

Product number -
Other names GLYCINE DEHYDROCHOLATE

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:3415-45-0 SDS

3415-45-0Downstream Products

3415-45-0Relevant articles and documents

Synthesis, anticancer activities, antimicrobial activities and bioavailability of berberine-bile acid analogues

Li, Qingyong,He, Wuna,Zhang, Li,Zu, Yuangang,Zhu, Qiaochu,Deng, Xiaoqiu,Zhao, Tengfei,Gao, Wenqing,Zhang, Baoyou

scheme or table, p. 573 - 580 (2012/08/08)

Fifteen berberine-bile acid analogues were synthesized. Anticancer activities of these analogues compared with berberine (BBR) were evaluated in vitro; among the analogues, A4, B4, and B5 had higher cytotoxicity than that of BBR. Most of the analogues showed higher antimicrobial activity against Staphylococcus aureus ATCC 25923 and Staphylococcus albus ATCC 8799 than that of BBR, but Bacillus subtilis AS 1.398 and Escherichia coli ATCC 31343 were not sensitive to all of the analogues. A4 and B4 were stable in the serum stability assay. B4 showed promising oral bioavailability in mice.

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