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Development of Kinase Inhibitors via Metal-Catalyzed C?H Arylation of 8-Alkyl-thiazolo[5,4-f]-quinazolin-9-ones Designed by Fragment-Growing Studies.

ABSTRACT: Efficient metal catalyzed C?H arylation of 8-alkyl-thiazolo[5,4-f]-quinazolin-9-ones was explored for SAR studies. Application of this powerful chemical tool at the last stage of the synthesis of kinase inhibitors allowed the synthesis of arrays of molecules inspired by fragment-growing studies generated by molecular modeling calculations. Among the potentially active compounds designed through this strategy, FC162 (4c) exhibits nanomolar IC₅₀ values against some kinases, and is the best candidate for the development as a DYRK kinase inhibitor.

SUBMITTER: Couly F

PROVIDER: S-EPMC6225322 | biostudies-literature | 2018 Aug

REPOSITORIES: biostudies-literature

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Development of Kinase Inhibitors via Metal-Catalyzed C⁻H Arylation of 8-Alkyl-thiazolo[5,4-f]-quinazolin-9-ones Designed by Fragment-Growing Studies.

Couly Florence F Harari Marine M Dubouilh-Benard Carole C Bailly Laetitia L Petit Emilie E Diharce Julien J Bonnet Pascal P Meijer Laurent L Fruit Corinne C Besson Thierry T

Molecules (Basel, Switzerland) 20180829 9

Efficient metal catalyzed C⁻H arylation of 8-alkyl-thiazolo[5,4-f]-quinazolin-9-ones was explored for SAR studies. Application of this powerful chemical tool at the last stage of the synthesis of kinase inhibitors allowed the synthesis of arrays of molecules inspired by fragment-growing studies generated by molecular modeling calculations. Among the potentially active compounds designed through this strategy, FC162 (4c) exhibits nanomolar IC50 values against some ...[more]

PMID: 30158487

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