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
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.