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Journal of Medicinal Chemistry|February 1, 1990
Functionalized congener approach for the design of novel muscarinic agents. Synthesis and pharmacological evaluation of N-methyl-N-[4-(1-pyrrolidinyl)-2-butynyl] amidesB J Bradbury, J Baumgold, K A JacobsonJournal of Medicinal Chemistry|February 1, 1990
Potential antitumor agents. 59. Structure-activity relationships for 2-phenylbenzimidazole-4-carboxamides, a new class of "minimal" DNA-intercalating agents which may not act via topoisomerase IIW A Denny, G W Rewcastle, B C BaguleyJournal of Medicinal Chemistry|February 1, 1990
Studies on Ca2+ channel antagonists. A 2-diazo-3,3,3-trifluoropropionamide derivative related to verapamil as a potential photoaffinity probeL J Theodore, W L Nelson, B Dave, et al.Journal of Medicinal Chemistry|April 19, 2011
Development of amidine-based sphingosine kinase 1 nanomolar inhibitors and reduction of sphingosine 1-phosphate in human leukemia cellsAndrew J Kennedy, Thomas P Mathews, Yugesh Kharel, et al.Journal of Medicinal Chemistry|April 19, 2011
Development of the fluorescent biosensor hCalmodulin (hCaM)L39C-monobromobimane(mBBr)/V91C-mBBr, a novel tool for discovering new calmodulin inhibitors and detecting calciumMartin Gonzalez-Andrade, Jose Rivera-Chavez, Alejandro Sosa-Peinado, et al.Journal of Medicinal Chemistry|April 29, 2011
Nobilamides A-H, long-acting transient receptor potential vanilloid-1 (TRPV1) antagonists from mollusk-associated bacteriaZhenjian Lin, Christopher A Reilly, Rowena Antemano, et al.Journal of Medicinal Chemistry|April 30, 2011
Adenosine-derived inhibitors of 78 kDa glucose regulated protein (Grp78) ATPase: insights into isoform selectivityAlba T Macias, Douglas S Williamson, Nicola Allen, et al.Journal of Medicinal Chemistry|July 1, 2011
Rational design of potent, small, synthetic allosteric inhibitors of thrombinPreetpal Singh Sidhu, Aiye Liang, Akul Y Mehta, et al.Journal of Medicinal Chemistry|July 26, 2011
A prodrug approach for improving antituberculosis activity of potent Mycobacterium tuberculosis type II dehydroquinase inhibitorsLorena Tizón, José M Otero, Verónica F V Prazeres, et al.Journal of Medicinal Chemistry|July 8, 2011
Synthesis and in vitro biological evaluation of carbonyl group-containing analogues for σ1 receptorsWei Wang, Jinquan Cui, Xiaoxia Lu, et al.Pageof 3,137