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1-{2-[3-benzyl-6-(4-phenyl-[1,2,3]triazol-1-yl)-quinolin-2-yloxy]-5-fluoro-phenyl}-ethanone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1173290-10-2

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1173290-10-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1173290-10-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,7,3,2,9 and 0 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1173290-10:
(9*1)+(8*1)+(7*7)+(6*3)+(5*2)+(4*9)+(3*0)+(2*1)+(1*0)=132
132 % 10 = 2
So 1173290-10-2 is a valid CAS Registry Number.

1173290-10-2Relevant academic research and scientific papers

QUINOLINE, NAPHTHALENE AND CONFORMATIONALLY CONSTRAINED QUINOLINE OR NAPHTHALENE DERIVATES AS ANTI-MYCOBACTERIAL AGENTS

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Page/Page column 27, (2009/08/16)

The invention relates to a compound of general formula I, II, III, IV V VI, VII, VIII, IX, X or a tautomer and the stereochemically isomeric forms thereof or pharmaceutically acceptable salts thereof, a N-oxide form thereof or a pro-drug thereof. The compound is usable as a medicament for the treatment of mycobacterial disease

Design, synthesis and biological evaluation of novel triazole, urea and thiourea derivatives of quinoline against Mycobacterium tuberculosis

Upadhayaya, Ram Shankar,Kulkarni, Girish M.,Vasireddy, Nageswara Rao,Vandavasi, Jaya Kishore,Dixit, Shailesh S.,Sharma, Vivek,Chattopadhyaya, Jyoti

experimental part, p. 4681 - 4692 (2009/12/04)

A new series of 20 quinoline derivatives possessing triazolo, ureido and thioureido substituents have been synthesized and their antimycobacterial properties have been evaluated. Compounds 10, 22 and 24 inhibited Mycobacterium tuberculosis H37Rv up to 96%, 98% and 94% respectively, at a fixed concentration of 6.25 μg/mL. Minimum inhibitory concentration of 3.125 μg/mL was obtained for compound 10 and 24, while for compound 22 it was 6.25 μg/mL. Molecular docking calculations suggest critical hydrogen bonding and electrostatic interactions between polar functional groups (such as quinoline-nitrogen, urea-carbonyl and hydroxyl) of anti-mycobacterial (anti-TB) compounds and amino acids (Arg186 and Glu61) of ATP-synthase of M. tuberculosis, could be the probable reason for observed anti-mycobacterial action.

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