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Benzenepropanoic acid, 3-cyano-a-[1-[[4-(4-pyridinyl)benzoyl]aMino]ethyl]-, Methyl ester, [R-(R*,R*)]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

193152-99-7

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193152-99-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 193152-99-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,3,1,5 and 2 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 193152-99:
(8*1)+(7*9)+(6*3)+(5*1)+(4*5)+(3*2)+(2*9)+(1*9)=147
147 % 10 = 7
So 193152-99-7 is a valid CAS Registry Number.

193152-99-7SDS

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 Methyl (2R,3R)-2-(3-cyanobenzyl)-3-{[4-(4-pyridinyl)benzoyl]amino }butanoate

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:193152-99-7 SDS

193152-99-7Relevant academic research and scientific papers

Otamixaban for treatment of elderly and renal impaired non-ST elevation myocardial infarction patients

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Page/Page column 8; 9, (2016/12/07)

The invention relates to the use of (2R,3R)-2-(3-carbamimidoyl-benzyl)-3-[4-(1-oxy-pyridin-4-yl)benzoylamino]-butyric acid methyl ester or a pharmaceutically acceptable salt thereof, for the preparation of a medicament for use in non-ST elevation myocardial infarction, said treatment comprising administering a therapeutically effective amount of (2R,3R)-2-(3-Carbamimidoyl-benzyl)-3-[4-(1-oxy-pyridin-4-yl)benzoylamino]-butyric acid methyl ester or a pharmaceutically acceptable salt thereof to a human patient, who is elderly and/or shows renal insufficiency and/or has a low body weight.

OTAMIXABAN FOR USE IN THE TREATMENT OF NON-ST ELEVATION ACUTE CORONARY SYNDROME IN PATIENTS PLANNED TO UNDERGO CORONARY ARTERY BYPASS GRAFTING

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, (2014/03/25)

The invention relates to otamixaban or a pharmaceutically acceptable salt thereof for use in the treatment of non-ST elevation acute coronary syndrome in patients planned to undergo coronary artery bypass grafting.

BENZOIC ACID SALT OF OTAMIXABAN

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, (2012/10/18)

The invention relates to a benzoic acid salt of methyl (2R,3R)-2-{3-[amino (imino) methyl]benzyl}-3-{[4-(1 -oxidopyridin-4-yl)benzoyl]amino}butanoate, and to a benzoic acid salt of methyl (2R,3R)-2-{3-[amino(imino)methyl]benzyl}-3-{[4-(1 -oxidopyridin-4- yl)benzoyl]amino}butanoate which is in a crystalline form or in at least partially crystalline form, as well as a process for the preparation of the same, methods of using such salt to treat subjects suffering from conditions which can be ameliorated by the administration of an inhibitor of Factor Xa.

Optimization of the beta-aminoester class of factor Xa inhibitors. Part 2: Identification of FXV673 as a potent and selective inhibitor with excellent In vivo anticoagulant activity.

Guertin, Kevin R,Gardner, Charles J,Klein, Scott I,Zulli, Allison L,Czekaj, Mark,Gong, Yong,Spada, Alfred P,Cheney, Daniel L,Maignan, Sebastian,Guilloteau, Jean-Pierre,Brown, Karen D,Colussi, Dennis J,Chu, Valeria,Heran, Christopher L,Morgan, Suzanne R,Bentley, Ross G,Dunwiddie, Christopher T,Leadley, Robert J,Pauls, Henry W

, p. 1671 - 1674 (2007/10/03)

Further optimization of the beta-aminoester class of factor Xa (fXa) inhibitors is described culminating in the identification of 9c (FXV673), a potent and selective factor Xa inhibitor with excellent in vivo anticoagulant activity. An X-ray structure of FXV673 bound to human fXa is also presented. Based on its selectivity, potent in vivo activity and favorable pre-clinical safety profile, FXV673 was selected for further development and is currently undergoing clinical trials.

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