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Journal of Medicinal Chemistry|August 21, 2007
Structure-based optimization of protein tyrosine phosphatase 1B inhibitors: from the active site to the second phosphotyrosine binding siteDouglas P Wilson, Zhao-Kui Wan, Wei-Xin Xu, et al.Journal of Medicinal Chemistry|August 21, 2007
Prediction of protein-protein interaction inhibitors by chemoinformatics and machine learning methodsAlexander Neugebauer, Rolf W Hartmann, Christian D KleinJournal of Medicinal Chemistry|August 28, 2007
Use of density functional calculations to predict the regioselectivity of drugs and molecules metabolized by aldehyde oxidaseRhonda A Torres, Kenneth R Korzekwa, Daniel R McMasters, et al.Journal of Medicinal Chemistry|July 20, 2007
Design, synthesis, and in vivo SAR of a novel series of pyrazolines as potent selective androgen receptor modulatorsXuqing Zhang, Xiaojie Li, George F Allan, et al.Journal of Medicinal Chemistry|July 20, 2007
Synthesis, flow cytometric evaluation, and identification of highly potent dipyridamole analogues as equilibrative nucleoside transporter 1 inhibitorsWenwei Lin, John K BuolamwiniJournal of Medicinal Chemistry|July 31, 2007
Design, synthesis, and biological activity of 5,10-dihydro-dibenzo[b,e][1,4]diazepin-11-one-based potent and selective Chk-1 inhibitorsLe Wang, Gerard M Sullivan, Laura A Hexamer, et al.Journal of Medicinal Chemistry|July 31, 2007
Discovery of 1,4-dihydroxy-2-naphthoate [corrected] prenyltransferase inhibitors: new drug leads for multidrug-resistant gram-positive pathogensMichio Kurosu, Prabagaran Narayanasamy, Kallolmay Biswas, et al.Journal of Medicinal Chemistry|December 1, 1991
Molecular mechanics simulations on covalent complexes of mitomycin C and its analogues with left-handed DNA duplexesS N Rao, B S Iyengar, T P Wunz, et al.Journal of Medicinal Chemistry|August 2, 2007
Design of noncompetitive interleukin-8 inhibitors acting on CXCR1 and CXCR2Alessio Moriconi, Maria Candida Cesta, Maria Neve Cervellera, et al.Journal of Medicinal Chemistry|August 2, 2007
Novel N7- and N1-substituted cGMP derivatives are potent activators of cyclic nucleotide-gated channelsTimothy Strassmaier, Jeffrey W KarpenPageof 3,134