J 2011

Discovery of pyrazolo[1,5-a]pyrimidine-based CHK1 inhibitors: A template-based approach-Part 1.

DWYER, Michael; Kamil PARUCH; Marc LABROLI; Carmen ALVAREZ; Kerry KEERTIKAR et. al.

Basic information

Original name

Discovery of pyrazolo[1,5-a]pyrimidine-based CHK1 inhibitors: A template-based approach-Part 1.

Name in Czech

Discovery of pyrazolo[1,5-a]pyrimidine-based CHK1 inhibitors: A template-based approach-Part 1.

Authors

DWYER, Michael (840 United States of America); Kamil PARUCH (203 Czech Republic, guarantor, belonging to the institution); Marc LABROLI (840 United States of America); Carmen ALVAREZ (840 United States of America); Kerry KEERTIKAR (840 United States of America); Cory POKER (840 United States of America); Randall ROSSMAN (840 United States of America); Thierry FISCHMANN (840 United States of America); Jose DUCA (840 United States of America); Vincent MADISON (840 United States of America); David PARRY (840 United States of America); Nicole DAVIS (840 United States of America); Wolfgang SEGHEZZI (840 United States of America); Derek WISWELL (840 United States of America) and Timothy GUZI (840 United States of America)

Edition

Bioorganic & Medicinal Chemistry Letters, Elsevier, 2011, 0960-894X

Other information

Language

English

Type of outcome

Article in a journal

Field of Study

10401 Organic chemistry

Country of publisher

United States of America

Confidentiality degree

is not subject to a state or trade secret

Impact factor

Impact factor: 2.554

RIV identification code

RIV/00216224:14310/11:00051795

Organization unit

Faculty of Science

UT WoS

000285544400096

Keywords in English

Kinase CHK1 Pyrazolo[1 5-a]pyrimidine Template

Tags

Changed: 5/3/2012 11:19, Ing. Zdeňka Rašková

Abstract

In the original language

The synthesis and hit-to-lead SAR development of a pyrazolo[1,5-a]pyrimidine hit 4 is described leading to a series of potent, selective CHK1 inhibitors such as compound 17r. In the Letter, the further utility of the pyrazolo[1,5-a]pyrimidine template for the development of potent, selective kinase inhibitors is detailed.