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491850-53-4

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491850-53-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 491850-53-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,9,1,8,5 and 0 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 491850-53:
(8*4)+(7*9)+(6*1)+(5*8)+(4*5)+(3*0)+(2*5)+(1*3)=174
174 % 10 = 4
So 491850-53-4 is a valid CAS Registry Number.

491850-53-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-methyl-5-(trifluoromethyl)benzenesulfonyl chloride

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:491850-53-4 SDS

491850-53-4Upstream product

491850-53-4Relevant articles and documents

Targeting quinolone- and aminocoumarin-resistant bacteria with new gyramide analogs that inhibit DNA gyrase

Hurley, Katherine A.,Santos, Thiago M. A.,Fensterwald, Molly R.,Rajendran, Madhusudan,Moore, Jared T.,Balmond, Edward I.,Blahnik, Brice J.,Faulkner, Katherine C.,Foss, Marie H.,Heinrich, Victoria A.,Lammers, Matthew G.,Moore, Lucas C.,Reynolds, Gregory D.,Shearn-Nance, Galen P.,Stearns, Brian A.,Yao, Zi W.,Shaw, Jared T.,Weibel, Douglas B.

, p. 942 - 951 (2017)

Bacterial DNA gyrase is an essential type II topoisomerase that enables cells to overcome topological barriers encountered during replication, transcription, recombination, and repair. This enzyme is ubiquitous in bacteria and represents an important clinical target for antibacterial therapy. In this paper we report the characterization of three exciting new gyramide analogs - from a library of 183 derivatives - that are potent inhibitors of DNA gyrase and are active against clinical strains of Gram-negative bacteria (Escherichia coli, Shigella flexneri, and Salmonella enterica; 3 of 10 wild-type strains tested) and Gram-positive bacteria (Bacillus spp., Enterococcus spp., Staphylococcus spp., and Streptococcus spp.; all 9 of the wild-type strains tested). E. coli strains resistant to the DNA gyrase inhibitors ciprofloxacin and novobiocin display very little cross-resistance to these new gyramides. In vitro studies demonstrate that the new analogs are potent inhibitors of the DNA supercoiling activity of DNA gyrase (IC50s of 47-170 nM) but do not alter the enzyme's ATPase activity. Although mutations that confer bacterial cells resistant to these new gyramides map to the genes encoding the subunits of the DNA gyrase (gyrA and gyrB genes), overexpression of GyrA, GyrB, or GyrA and GyrB together does not suppress the inhibitory effect of the gyramides. These observations support the hypothesis that the gyramides inhibit DNA gyrase using a mechanism that is unique from other known inhibitors.

PYRAZOLO[1,5-A]PYRIDINES AND THEIR USE IN CANCER THERAPY

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Page/Page column 73-74, (2009/03/07)

Pyrazolo[1,5-a]pyridines are described, including methods for their preparation, and their use as agents or drugs for cancer therapy, both alone or in combination with radiation and/or other anticancer drugs.

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