872576-64-2Relevant articles and documents
Synthesis and activity of quinolinyl-methylene-thiazolinones as potent and selective cyclin-dependent kinase 1 inhibitors
Chen, Shaoqing,Chen, Li,Le, Nam T.,Zhao, Chunlin,Sidduri, Achyutharao,Lou, Jian Ping,Michoud, Christophe,Portland, Louis,Jackson, Nicole,Liu, Jin-Jun,Konzelmann, Fred,Chi, Feng,Tovar, Christian,Xiang, Qing,Chen, Yingsi,Wen, Yang,Vassilev, Lyubomir T.
, p. 2134 - 2138 (2008/02/03)
A novel series of quinolinyl-methylene-thiazolinones has been identified as potent and selective cyclin-dependent kinase 1 (CDK1) inhibitors. Their synthesis and structure activity relationships (SAR) are described. Representative compounds from this class reversibly inhibit CDK1 activity in vitro, and block cell cycle progression in human tumor cell lines, suggesting a potential use as antitumor agents.
Thiazolinone 2-substituted quinolines
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Page/Page column 10, (2010/10/20)
Thiazolinone substituted quinoline derivatives where the quinoline ring is substituted at the 2 position which derivatives demonstrates CDK1 antiproliferative activity and are useful as anti-cancer agents.
Quinazoline thiazolinones
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Page/Page column 12, (2008/06/13)
Quinazoline thiazolinone derivatives which demonstrate CDK1 antiproliferative activity and are useful as anti-cancer agents.