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Journal of Medicinal Chemistry|January 5, 1996
Biarylcarboxylic acids and -amides: inhibition of phosphodiesterase type IV versus [3H]rolipram binding activity and their relationship to emetic behavior in the ferretA J Duplantier, M S Biggers, R J Chambers, et al.Journal of Medicinal Chemistry|January 5, 1996
Binding of arylpiperazines, (aryloxy)propanolamines, and tetrahydropyridylindoles to the 5-HT1A receptor: contribution of the molecular lipophilicity potential to three-dimensional quantitative structure-affinity relationship modelsP Gaillard, P A Carrupt, B Testa, et al.Journal of Medicinal Chemistry|January 5, 1996
Structure-antigastrin activity relationships of new spiroglumide amido acid derivativesF Makovec, W Peris, S Frigerio, et al.Journal of Medicinal Chemistry|January 5, 1996
Substituted xanthines, pteridinediones, and related compounds as potential antiinflammatory agents. Synthesis and biological evaluation of inhibitors of tumor necrosis factor alphaH B Cottam, H Shih, L R Tehrani, et al.Journal of Medicinal Chemistry|January 5, 1996
Development of highly potent inhibitors of Ras farnesyltransferase possessing cellular and in vivo activityK Leftheris, T Kline, G D Vite, et al.Journal of Medicinal Chemistry|January 5, 1996
Diarylspiro[2.4]heptenes as orally active, highly selective cyclooxygenase-2 inhibitors: synthesis and structure-activity relationshipsH C Huang, J J Li, D J Garland, et al.Journal of Medicinal Chemistry|January 5, 1996
Tyrosine kinase inhibitors. 8. An unusually steep structure-activity relationship for analogues of 4-(3-bromoanilino)-6,7-dimethoxyquinazoline (PD 153035), a potent inhibitor of the epidermal growth factor receptorA J Bridges, H Zhou, D R Cody, et al.Journal of Medicinal Chemistry|January 5, 1996
Conformationally constrained analogues of diacylglycerol. 11. Ultrapotent protein kinase C ligands based on a chiral 5-disubstituted tetrahydro-2-furanone templateJ Lee, S Wang, G W Milne, et al.Journal of Medicinal Chemistry|January 5, 1996
Nonpeptide angiotensin II receptor antagonists: synthesis, biological activities, and structure-activity relationships of imidazole-5-carboxylic acids bearing alkyl, alkenyl, and hydroxyalkyl substituents at the 4-position and their related compoundsH Yanagisawa, Y Amemiya, T Kanazaki, et al.Journal of Medicinal Chemistry|January 5, 1996
Synthesis and antitumor evaluation of a highly potent cytotoxic DNA cross-linking polyamine analogue, 1,12-diaziridinyl-4,9-diazadodecaneY Li, J L Eiseman, D L Sentz, et al.Pageof 3,141