Discovery of 5-pyrrolopyridinyl-2-thiophenecarboxamides as potent AKT kinase inhibitors

A pyrrolopyridinyl thiophene carboxamide 7 was discovered as a tractable starting point for a lead optimization effort in an AKT kinase inhibition program. SAR studies aided by a co-crystal structure of 7 in AKT2 led to the identification of AKT inhibitors with subnanomolar potency. Representative c...

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Veröffentlicht in:Bioorganic & medicinal chemistry letters 2009-04, Vol.19 (8), p.2244-2248
Hauptverfasser: Seefeld, Mark A., Rouse, Meagan B., McNulty, Kenneth C., Sun, Lihui, Wang, Jizhou, Yamashita, Dennis S., Luengo, Juan I., Zhang, ShuYun, Minthorn, Elisabeth A., Concha, Nestor O., Heerding, Dirk A.
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Sprache:eng
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Zusammenfassung:A pyrrolopyridinyl thiophene carboxamide 7 was discovered as a tractable starting point for a lead optimization effort in an AKT kinase inhibition program. SAR studies aided by a co-crystal structure of 7 in AKT2 led to the identification of AKT inhibitors with subnanomolar potency. Representative compounds showed antiproliferative activity as well as inhibition of phosphorylation of the downstream target GSK3β. A pyrrolopyridinyl thiophene carboxamide 7 was discovered as a tractable starting point for a lead optimization effort in an AKT kinase inhibition program. SAR studies aided by a co-crystal structure of 7 in AKT2 led to the identification of AKT inhibitors with subnanomolar potency. Representative compounds showed antiproliferative activity as well as inhibition of phosphorylation of the downstream target GSK3β.
ISSN:0960-894X
1464-3405
DOI:10.1016/j.bmcl.2009.02.094