883097-33-4Relevant academic research and scientific papers
Highly selective and potent thiophenes as PI3K inhibitors with oral antitumor activity
Liu, Kevin K.-C.,Zhu, Jinjiang,Smith, Graham L.,Yin, Min-Jean,Bailey, Simon,Chen, Jeffrey H.,Hu, Qiyue,Huang, Qinhua,Li, Chunze,Li, Qing J.,Marx, Matthew A.,Paderes, Genevieve,Richardson, Paul F.,Sach, Neal W.,Walls, Marlena,Wells, Peter A.,Zou, Aihua
, p. 809 - 813 (2011/12/16)
Highly selective PI3K inhibitors with subnanomolar PI3Kα potency and greater than 7000-fold selectivity against mTOR kinase were discovered through structure-based drug design (SBDD). These tetra-substituted thiophenes were also demonstrated to have good
THIOPHENES AND THEIR USE AS PHOSPHATIDYLINOSITOL 3-KINASE (PI3K) INHIBITORS
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Page/Page column 44, (2009/09/05)
This invention provides thiophene compounds of formula (I) : wherein R1, R2, R3, R4, n, p, and m are as described in the specification. The compounds are inhibitors of PI3K and are thus useful for treating proliferative, inflammatory, or cardiovascular disorders.
