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Journal of Medicinal Chemistry|May 30, 2003
A novel somatostatin mimic with broad somatotropin release inhibitory factor receptor binding and superior therapeutic potentialIan Lewis, Wilfried Bauer, Rainer Albert, et al.Journal of Medicinal Chemistry|May 30, 2003
Three dimensional pharmacophore modeling of human CYP17 inhibitors. Potential agents for prostate cancer therapyOmoshile O Clement, Clive M Freeman, Rolf W Hartmann, et al.Journal of Medicinal Chemistry|May 30, 2003
Synthesis and biological activity of various derivatives of a novel class of potent, selective, and orally active prostaglandin D2 receptor antagonists. 1. Bicyclo[2.2.1]heptane derivativesSusumu Mitsumori, Tatsuo Tsuri, Tsunetoshi Honma, et al.Journal of Medicinal Chemistry|May 30, 2003
Synthesis and biological activity of various derivatives of a novel class of potent, selective, and orally active prostaglandin D2 receptor antagonists. 2. 6,6-Dimethylbicyclo[3.1.1]heptane derivativesSusumu Mitsumori, Tatsuo Tsuri, Tsunetoshi Honma, et al.Journal of Medicinal Chemistry|May 30, 2003
Discovery and structure-activity relationships of novel piperidine inhibitors of farnesyltransferaseShinji Nara, Rieko Tanaka, Jun Eishima, et al.Journal of Medicinal Chemistry|May 30, 2003
Analysis of 6-(2,2-Dichloroacetamido)chrysene interaction with the hypoxanthine phosphoribosyltransferase from Trypanosoma cruziFrancisco J Medrano, Mary A Wenck, Juan C Engel, et al.Journal of Medicinal Chemistry|August 21, 1992
3'-Azido-3',5'-dideoxythymidine-5'-methylphosphonic acid diphosphate: synthesis and HIV-1 reverse transcriptase inhibitionG A Freeman, J L Rideout, W H Miller, et al.Journal of Medicinal Chemistry|July 24, 1992
Structural requirements for neuropeptide Y18-36-evoked hypotension: a systematic studyR D Feinstein, J H Boublik, D Kirby, et al.Journal of Medicinal Chemistry|November 13, 1992
Opioid agonist and antagonist activities of morphindoles related to naltrindoleP S Portoghese, D L Larson, M Sultana, et al.Journal of Medicinal Chemistry|April 3, 1992
Optimization of the quinoline and substituted benzyl moieties of a series of phenyltetrazole leukotriene D4 receptor antagonistsJ S Sawyer, R F Baldwin, L E Rinkema, et al.Pageof 3,141