7,8-dichloro-1-oxo-β-carbolines as a versatile scaffold for the development of potent and selective kinase inhibitors with unusual binding modes.

Development of both potent and selective kinase inhibitors is a challenging task in modern drug discovery. The innate promiscuity of kinase inhibitors largely results from ATP-mimetic binding to the kinase hinge region. We present a novel class of substituted 7,8-dichloro-1-oxo-β-carbolines based on...

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Bibliographic Details
Main Authors: Huber, K, Brault, L, Fedorov, O, Gasser, C, Filippakopoulos, P, Bullock, A, Fabbro, D, Trappe, J, Schwaller, J, Knapp, S, Bracher, F
Format: Journal article
Language:English
Published: 2012