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Bioorganic & Medicinal Chemistry Letters|March 21, 2007
Structure-activity relationships, and drug metabolism and pharmacokinetic properties for indazole piperazine and indazole piperidine inhibitors of ROCK-IIYangbo Feng, Michael D Cameron, Bozena Frackowiak, et al.Analytical Biochemistry|June 28, 2005
Time-resolved Forster resonance energy transfer assays for the binding of nucleotide and protein substrates to p38alpha protein kinaseWen Xiao Zhang, Ruixiu Wang, Douglas Wisniewski, et al.The Journal of Biological Chemistry|March 6, 2009
Structure-activity relationships and X-ray structures describing the selectivity of aminopyrazole inhibitors for c-Jun N-terminal kinase 3 (JNK3) over p38Ted Kamenecka, Jeff Habel, Derek Duckett, et al.Bioorganic & Medicinal Chemistry Letters|May 13, 2009
Synthesis and SAR of piperazine amides as novel c-jun N-terminal kinase (JNK) inhibitorsYouseung Shin, Weiming Chen, Jeff Habel, et al.Bioorganic & Medicinal Chemistry Letters|October 20, 2009
Benzothiazoles as Rho-associated kinase (ROCK-II) inhibitorsYan Yin, Li Lin, Claudia Ruiz, et al.Proceedings of the National Academy of Sciences of the United States of America|March 1, 2018
Identification of a highly neurotoxic α-synuclein species inducing mitochondrial damage and mitophagy in Parkinson's diseaseDiego Grassi, Shannon Howard, Minghai Zhou, et al.ACS Medicinal Chemistry Letters|June 6, 2014
Discovery of Potent and Selective Urea-Based ROCK Inhibitors and Their Effects on Intraocular Pressure in RatsYan Yin, Michael D Cameron, Li Lin, et al.Journal of Medicinal Chemistry|October 7, 2008
Discovery of substituted 4-(pyrazol-4-yl)-phenylbenzodioxane-2-carboxamides as potent and highly selective Rho kinase (ROCK-II) inhibitorsYangbo Feng, Yan Yin, Amiee Weiser, et al.Bioorganic & Medicinal Chemistry Letters|November 8, 2008
Chroman-3-amides as potent Rho kinase inhibitorsYen Ting Chen, Thomas D Bannister, Amiee Weiser, et al.Bioorganic & Medicinal Chemistry Letters|October 19, 2011
Discovery and optimization of indoles and 7-azaindoles as Rho kinase (ROCK) inhibitors (part-I)Sarwat Chowdhury, E Hampton Sessions, Jennifer R Pocas, et al.Pageof 3