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Abstract #46317 Published in IGR 13-2

Asymmetric synthesis of potent chroman-based Rho kinase (ROCK-II) inhibitors

Chen YT; Vojkovsky T; Fang X; Pocas JR; Grant W; Handy AMW; Schroter T; LoGrasso P; Bannister TD; Feng Y
MedChemComm 2011; 2: 73-75


Rho kinase (ROCK) is currently investigated as a target for various diseases such as glaucoma and spinal cord injury. Herein, we report the asymmetric synthesis of chroman 1, a highly potent ROCK inhibitor, and its analogs. The inhibitory properties of these compounds for ROCK-II and a selected set of highly homologous kinases are also discussed.

T. D. Bannister. Translational Research Institute, Scripps Florida, 130 Scripps Way #2A1, Jupiter FL 33458, United States. Email: tbannist@scripps.edu


Classification:

11.14 Investigational drugs; pharmacological experiments (Part of: 11 Medical treatment)



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