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Bioorganic & Medicinal Chemistry Letters|September 25, 2002
Succinimide hydroxamic acids as potent inhibitors of histone deacetylase (HDAC)Michael L Curtin, Robert B Garland, H Robin Heyman, et al.The Journal of Pharmacology and Experimental Therapeutics|January 22, 1998
The role of platelet-activating factor (PAF) and the efficacy of ABT-491, a highly potent and selective PAF antagonist, in experimental allergic rhinitisD H Albert, P E Malo, P Tapang, et al.Disease Models & Mechanisms|December 5, 2023
Physiological stress improves stem cell modeling of dystrophic cardiomyopathyDominic E Fullenkamp, Alexander B Willis, Jodi L Curtin, et al.Bioorganic & Medicinal Chemistry Letters|November 7, 2002
Trifluoromethyl ketones as inhibitors of histone deacetylaseRobin R Frey, Carol K Wada, Robert B Garland, et al.Journal of Medicinal Chemistry|June 19, 2008
7-Aminopyrazolo[1,5-a]pyrimidines as potent multitargeted receptor tyrosine kinase inhibitorsRobin R Frey, Michael L Curtin, Daniel H Albert, et al.Biochemical and Biophysical Research Communications|November 16, 2004
Differential protein acetylation induced by novel histone deacetylase inhibitorsK B Glaser, J Li, L J Pease, et al.Bioorganic & Medicinal Chemistry Letters|January 5, 1999
The design, synthesis, and structure-activity relationships of a series of macrocyclic MMP inhibitorsD H Steinman, M L Curtin, R B Garland, et al.Bioorganic & Medicinal Chemistry Letters|November 1, 2003
Heterocyclic ketones as inhibitors of histone deacetylaseAnil Vasudevan, Zhiqin Ji, Robin R Frey, et al.Journal of Enzyme Inhibition|October 28, 1999
Evaluation of the inhibition of other metalloproteinases by matrix metalloproteinase inhibitorsP A Marcotte, I N Elmore, Z Guan, et al.Bioorganic & Medicinal Chemistry Letters|September 11, 2004
Isoindolinone ureas: a novel class of KDR kinase inhibitorsMichael L Curtin, Robin R Frey, H Robin Heyman, et al.Pageof 18