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Benzenamine, 3-[[(3-bromo-2-methylimidazo[1,2-a]pyridin-8-yl)oxy]methyl]-2,4-dichloro -N-methyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

160641-96-3

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160641-96-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 160641-96-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,0,6,4 and 1 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 160641-96:
(8*1)+(7*6)+(6*0)+(5*6)+(4*4)+(3*1)+(2*9)+(1*6)=123
123 % 10 = 3
So 160641-96-3 is a valid CAS Registry Number.

160641-96-3Relevant academic research and scientific papers

Novel heteroaryl alkylamide derivatives useful as bradykinin receptor modulators

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Page 26-27, (2010/02/08)

This invention is directed towards novel alkylamide derivatives as bradykinin receptor antagonists useful for the treatment of bradykinin modulated disorders such as pain, inflammation, asthma and allergy. Furthermore, the present invention is directed to novel alkylamide derivatives as bradykinin receptor agonists useful for the treatment of bradykinin modulated disorders such as hypertension and the like.

NOVEL HETEROARYL ALKYLAMIDE DERIVATIVES USEFUL AS BRADYKININ RECEPTOR MODULATORS

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Page/Page column 57, (2010/02/07)

This invention is directed towards novel alkylamide derivatives as bradykinin receptor antagonists useful for the treatment of bradykinin modulated disorders such as pain, inflammation, asthma and allergy. Furthermore, the present invention is directed to novel alkylamide derivatives as bradykinin receptor agonists useful for the treatment of bradykinin modulated disorders such as hypertension and the like.

A novel class of orally active non-peptide bradykinin B2 receptor antagonists. 1. Construction of the basic framework

Abe, Yoshito,Kayakiri, Hiroshi,Satoh, Shigeki,Inoue, Takayuki,Sawada, Yuki,Imai, Keisuke,Inamura, Noriaki,Asano, Masayuki,Hatori, Chie,Katayama, Akira,Oku, Teruo,Tanaka, Hirokazu

, p. 564 - 578 (2007/10/03)

A novel class of potent, selective, and orally active non-peptide bradykinin (BK) B2 receptor antagonists were designed and synthesized starting from 8-benzyloxyimidazo[1,2-α]pyridine derivative 2. The unique screening lead (2) was discovered b

IMIDAZO [1,2-A] PYRIDINES AND THEIR PHARMACEUTICAL USE

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, (2008/06/13)

The invention relates to novel bradykinin antagonists of the formula: STR1 wherein R 1 is halogen,R 2 and R 3 are each hydrogen, lower alkyl, halo(lower)alkyl or acyl,R 4 is aryl having suitable substituent(s), or a heterocyclic group optionally having suitable substituent(s),Q is O or N--R 11, in which R 11 is hydrogen or acyl, andA is lower alkylene,and pharmaceutically acceptable salts thereof.

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