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N-{2'-[(tert-butylamino)sulfonyl]-1,1'-biphenyl-4-yl}-1-(7-isoquinolyl)-3-methyl-1H-pyrazole-5-carboxamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

218301-11-2

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218301-11-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 218301-11-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,8,3,0 and 1 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 218301-11:
(8*2)+(7*1)+(6*8)+(5*3)+(4*0)+(3*1)+(2*1)+(1*1)=92
92 % 10 = 2
So 218301-11-2 is a valid CAS Registry Number.

218301-11-2Relevant academic research and scientific papers

NOVEL GUANIDINE MIMICS AS FACTOR Xa INHIBITORS

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Page/Page column 39, (2010/02/13)

The present application describes nitrogen containing heteroaromatics and derivatives thereof of formula (I) or pharmaceutically acceptable salt forms thereof, wherein rings D-E represent guanidine mimics, which are useful as inhibitors of factor Xa.

Structure-based design of novel guanidine/benzamidine mimics: Potent and orally bioavailable factor Xa inhibitors as novel anticoagulants

Lam, Patrick Y. S.,Clark, Charles G.,Li, Renhua,Pinto, Donald J. P.,Orwat, Michael J.,Galemmo, Robert A.,Fevig, John M.,Teleha, Christopher A.,Alexander, Richard S.,Smallwood, Angela M.,Rossi, Karen A.,Wright, Matthew R.,Bai, Stephen A.,He, Kan,Luettgen, Joseph M.,Wong, Pancras C.,Knabb, Robert M.,Wexler, Ruth R.

, p. 4405 - 4418 (2007/10/03)

As part of an ongoing effort to prepare orally active factor Xa inhibitors using structure-based drug design techniques and molecular recognition principles, a systematic study has been performed on the pharmacokinetic profile resulting from replacing the

Guanidine mimics as factor Xa inhibitors

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Page column 90, (2010/02/04)

The present application describes nitrogen containing heteroaromatics and derivatives thereof of formula I: or pharmaceutically acceptable salt forms thereof, wherein rings D—E represent guanidine mimics, which are useful as inhibitors of factor Xa.

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