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63788-62-5

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63788-62-5 Usage

General Description

2-Acetylamino-4-methyl-thiazole-5-carboxylic acid is a chemical compound with pharmaceutical potential due to its ability to inhibit the production of bacterial biofilms, making it a promising candidate for the development of new antibiotics. It is also known for its anti-cancer properties and has been studied for its potential use in cancer treatment. Additionally, this compound has shown potential as an anti-inflammatory agent, making it a versatile and valuable chemical in the field of medicine and drug development.

Check Digit Verification of cas no

The CAS Registry Mumber 63788-62-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,7,8 and 8 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 63788-62:
(7*6)+(6*3)+(5*7)+(4*8)+(3*8)+(2*6)+(1*2)=165
165 % 10 = 5
So 63788-62-5 is a valid CAS Registry Number.

63788-62-5SDS

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 2-Acetylamino-4-methylthiazole-5-carboxylic acid

1.2 Other means of identification

Product number -
Other names 2-acetamido-4-methyl-1,3-thiazole-5-carboxylic acid

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:63788-62-5 SDS

63788-62-5Relevant articles and documents

Discovery of N-{5-[3-(3-hydroxypiperidin-1-yl)-1,2,4-oxadiazol-5-yl]-4- methyl-1,3-thiazol-2-yl}acetamide (TASP0415914) as an orally potent phosphoinositide 3-kinase γ inhibitor for the treatment of inflammatory diseases

Oka, Yusuke,Yabuuchi, Tetsuya,Oi, Takahiro,Kuroda, Shoichi,Fujii, Yasuyuki,Ohtake, Hidenori,Inoue, Tomoyuki,Wakahara, Shunichi,Kimura, Kayo,Fujita, Kiyoko,Endo, Mayumi,Taguchi, Kyoko,Sekiguchi, Yoshinori

, p. 7578 - 7583 (2014/01/06)

Class I phosphoinositide 3-kinases (PI3Ks), particularly PI3Kγ, have become attractive drug targets for inflammatory and autoimmune disorders such as rheumatoid arthritis. Herein, we describe the synthesis and the structure-activity relationships (SAR) of a series of 2-amino-5-oxadiazolyl thiazoles, culminating in the identification of 8j (TASP0415914), an orally potent inhibitor of phosphoinositide 3-kinase γ (PI3Kγ). TASP0415914 demonstrated good potency in a cell-based assay and, furthermore, exhibited in vivo efficacy in a collagen induced arthritis (CIA) model in mice after oral administration.

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