Synthesis and biological evaluation of 
7-substituted-1-(3-bromophenylamino)isoquinoline-4-carbonitriles as inhibitors 
of myosin light chain kinase and epidermal growth factor receptor

Rode, Harras B.; Sos, Martin L.; Grütter, Christian; Heynck, Stefanie; Simard, Jeffrey R.; Rauh, Daniel

doi:10.1016/j.bmc.2010.11.007

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Synthesis and biological evaluation of 7-substituted-1-(3-bromophenylamino)isoquinoline-4-carbonitriles as inhibitors of myosin light chain kinase and epidermal growth factor receptor

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Rode, Harras B.
Chemical Genomics Centre of the Max Planck Society, Otto-Hahn-Strasse 15, 44227 Dortmund, Germany;

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Sos, Martin L.
Funktionelle Krebsgenomforschung, Junior Research Groups, Max-Planck-Institut für neurologische Forschung, Managing Director: D. Yves von Cramon, Max Planck Institute for Metabolism Research, Managing Director: Jens Brüning, Max Planck Society;

Grütter, Christian
Chemical Genomics Centre of the Max Planck Society, Otto-Hahn-Strasse 15, 44227 Dortmund, Germany;

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Heynck, Stefanie
Funktionelle Krebsgenomforschung, Junior Research Groups, Max-Planck-Institut für neurologische Forschung, Managing Director: D. Yves von Cramon, Max Planck Institute for Metabolism Research, Managing Director: Jens Brüning, Max Planck Society;

Simard, Jeffrey R.
Chemical Genomics Centre of the Max Planck Society, Otto-Hahn-Strasse 15, 44227 Dortmund, Germany;

Rauh, Daniel
Chemical Genomics Centre of the Max Planck Society, Otto-Hahn-Strasse 15, 44227 Dortmund, Germany;

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Rode, H. B., Sos, M. L., Grütter, C., Heynck, S., Simard, J. R., & Rauh, D. (2011). Synthesis and biological evaluation of 7-substituted-1-(3-bromophenylamino)isoquinoline-4-carbonitriles as inhibitors of myosin light chain kinase and epidermal growth factor receptor. Bioorganic and Medicinal Chemistry, 19(1), 429-439. doi:10.1016/j.bmc.2010.11.007.

Cite as: https://hdl.handle.net/11858/00-001M-0000-0026-D981-E