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A series of urea-based Rho kinase (ROCK) inhibitors were designed and evaluated. The discovered compounds had excellent enzyme and cellular potency, high kinase selectivity, high aqueous solubility, good porcine corneal penetration, and appropriate DMPK profiles for topical applications as antiglaucoma therapeutics.
P. Lograsso. Translational Research Institute, Department of Molecular Therapeutics, 130 Scripps Way, #2A1, Jupiter, FL 33458, United States. lograsso@scripps.edu
11.14 Investigational drugs; pharmacological experiments (Part of: 11 Medical treatment)