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Journal of Medicinal Chemistry|June 17, 2009
Betulinic acid derivatives as human immunodeficiency virus type 2 (HIV-2) inhibitorsZhao Dang, Weihong Lai, Keduo Qian, et al.Journal of Medicinal Chemistry|June 17, 2009
One scaffold, three binding modes: novel and selective pteridine reductase 1 inhibitors derived from fragment hits discovered by virtual screeningChidochangu P Mpamhanga, Daniel Spinks, Lindsay B Tulloch, et al.Journal of Medicinal Chemistry|May 1, 2009
Antimalarial peroxide dyads from natural artemisinin and hydroxyalkylated 1,2,4-trioxanesAxel G Griesbeck, Jörg Neudörfl, Achim Hörauf, et al.Journal of Medicinal Chemistry|May 1, 2009
Evaluation of homology modeling of G-protein-coupled receptors in light of the A(2A) adenosine receptor crystallographic structureAndrei A Ivanov, Dov Barak, Kenneth A JacobsonJournal of Medicinal Chemistry|May 1, 2009
Synthesis and biological characterization of B-ring amino analogues of potent benzothiadiazine hepatitis C virus polymerase inhibitorsJohn T Randolph, Charles A Flentge, Peggy P Huang, et al.Journal of Medicinal Chemistry|May 6, 2009
Molecular and conformational determinants of pituitary adenylate cyclase-activating polypeptide (PACAP) for activation of the PAC1 receptorSteve Bourgault, David Vaudry, Isabelle Ségalas-Milazzo, et al.Journal of Medicinal Chemistry|December 30, 2008
A series of halogenated heterodimeric inhibitors of prostate specific membrane antigen (PSMA) as radiolabeled probes for targeting prostate cancerK P Maresca, S M Hillier, F J Femia, et al.Journal of Medicinal Chemistry|January 1, 2009
Carbonic anhydrase inhibitors. Comparison of chlorthalidone and indapamide X-ray crystal structures in adducts with isozyme II: when three water molecules and the keto-enol tautomerism make the differenceClaudia Temperini, Alessandro Cecchi, Andrea Scozzafava, et al.Journal of Medicinal Chemistry|October 9, 2008
Efficient solid-phase synthesis of FK228 analogues as potent antitumoral agentsSalvatore Di Maro, Rey-Chen Pong, Jer-Tsong Hsieh, et al.Journal of Medicinal Chemistry|October 10, 2008
Synthesis and evaluation of structurally constrained quinazolinone derivatives as potent and selective histamine H3 receptor inverse agonistsTsuyoshi Nagase, Takashi Mizutani, Etsuko Sekino, et al.Pageof 3,141