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Results: 1-11 |
Results: 11

Authors: DELUCCA GV
Citation: Gv. Delucca, STEREOSPECIFIC, STEREOSELECTIVE REARRANGEMENT OF HEXAHYDRO-1,3-DIAZEPIN-2-ONES TO TETRAHYDROPYRIMIDIN-2-ONES AND IMIDAZOLIDIN-2-ONES, A USEFUL ROUTE FOR THE SYNTHESIS OF HIV PROTEASE INHIBITORS, Journal of organic chemistry, 63(14), 1998, pp. 4755-4766

Authors: DELUCCA GV KIM UT LIANG J CORDOVA B KLABE RM GARBER S BACHELER LT LAM GN WRIGHT MR LOGUE KA ERICKSONVIITANEN S KO SS TRAINOR GL
Citation: Gv. Delucca et al., NONSYMMETRIC P2 P2' CYCLIC UREA HIV PROTEASE INHIBITORS - STRUCTURE-ACTIVITY RELATIONSHIP, BIOAVAILABILITY, AND RESISTANCE PROFILE OF MONOINDAZOLE-SUBSTITUTED P2 ANALOGS/, Journal of medicinal chemistry, 41(13), 1998, pp. 2411-2423

Authors: HODGE CN LAM PYS EYERMANN CJ JADHAV PK RU Y FERNANDEZ CH DELUCCA GV CHANG CH KALTENBACH RF HOLLER ER WOERNER F DANEKER WF EMMETT G CALABRESE JC ALDRICH PE
Citation: Cn. Hodge et al., CALCULATED AND EXPERIMENTAL LOW-ENERGY CONFORMATIONS OF CYCLIC UREA HIV PROTEASE INHIBITORS, Journal of the American Chemical Society, 120(19), 1998, pp. 4570-4581

Authors: DELUCCA GV ERICKSONVIITANEN S LAM PYS
Citation: Gv. Delucca et al., CYCLIC HIV PROTEASE INHIBITORS CAPABLE OF DISPLACING THE ACTIVE-SITE STRUCTURAL WATER MOLECULE, Drug discovery today, 2(1), 1997, pp. 6-18

Authors: DELUCCA GV
Citation: Gv. Delucca, SYNTHESIS AND EVALUATION OF IMIDAZOLIDINONES AS NONPEPTIDE HIV-PROTEASE INHIBITORS, Bioorganic & medicinal chemistry letters, 7(5), 1997, pp. 495-500

Authors: DELUCCA GV
Citation: Gv. Delucca, SYNTHESIS AND EVALUATION OF DELTA-LACTAMS AS NONPEPTIDE HIV-PROTEASE INHIBITORS, Bioorganic & medicinal chemistry letters, 7(5), 1997, pp. 501-504

Authors: DELUCCA GV LIANG J ALDRICH PE CALABRESE J CORDOVA B KLABE RM RAYNER MM CHANG CH
Citation: Gv. Delucca et al., DESIGN, SYNTHESIS, AND EVALUATION OF TETRAHYDROPYRIMIDINONES AS AN EXAMPLE OF A GENERAL-APPROACH TO NONPEPTIDE HIV PROTEASE INHIBITORS, Journal of medicinal chemistry, 40(11), 1997, pp. 1707-1719

Authors: LAM PYS RU Y JADHAV PK ALDRICH PE DELUCCA GV EYERMANN CJ CHANG CH EMMETT G HOLLER ER DANEKER WF LI LZ CONFALONE PN MCHUGH RJ HAN Q LI RH MARKWALDER JA SEITZ SP SHARPE TR BACHELER LT RAYNER MM KLABE RM SHUM LY WINSLOW DL KORNHAUSER DM JACKSON DA ERICKSONVIITANEN S HODGE CN
Citation: Pys. Lam et al., CYCLIC HIV PROTEASE INHIBITORS - SYNTHESIS, CONFORMATIONAL-ANALYSIS, P2 P2' STRUCTURE-ACTIVITY RELATIONSHIP, AND MOLECULAR RECOGNITION OF CYCLIC UREAS/, Journal of medicinal chemistry, 39(18), 1996, pp. 3514-3525

Authors: NUGIEL DA JACOBS K WORLEY T PATEL M KALTENBACH RF MEYER DT JADHAV PK DELUCCA GV SMYSER TE KLABE RM BACHELER LT RAYNER MM SEITZ SP
Citation: Da. Nugiel et al., PREPARATION AND STRUCTURE-ACTIVITY RELATIONSHIP OF NOVEL P1 P1'-SUBSTITUTED CYCLIC UREA-BASED HUMAN-IMMUNODEFICIENCY-VIRUS TYPE-1 PROTEASE INHIBITORS/, Journal of medicinal chemistry, 39(11), 1996, pp. 2156-2169

Authors: RIPKA WC DELUCCA GV BACH AC POTTORF RS BLANEY JM
Citation: Wc. Ripka et al., PROTEIN BETA-TURN MIMETICS .1. DESIGN, SYNTHESIS, AND EVALUATION IN MODEL CYCLIC-PEPTIDES, Tetrahedron, 49(17), 1993, pp. 3593-3608

Authors: RIPKA WC DELUCCA GV BACH AC POTTORF RS BLANEY JM
Citation: Wc. Ripka et al., PROTEIN BETA-TURN MIMETICS .2. DESIGN, SYNTHESIS, AND EVALUATION IN THE CYCLIC PEPTIDE GRAMICIDIN-S, Tetrahedron, 49(17), 1993, pp. 3609-3628
Risultati: 1-11 |