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Results: 1-8 |
Results: 8
NEW AZA-DIPEPTIDE ANALOGS AS POTENT AND ORALLY ABSORBED HIV-1 PROTEASE INHIBITORS - CANDIDATES FOR CLINICAL DEVELOPMENT
Authors: BOLD G FASSLER A CAPRARO HG COZENS R KLIMKAIT T LAZDINS J MESTAN J PONCIONI B ROSEL J STOVER D TINTELNOTBLOMLEY M ACEMOGLU F BECK W BOSS E ESCHBACH M HURLIMANN T MASSO E ROUSSEL S UCCISTOLL K WYSS D LANG R
Citation: G. Bold et al., NEW AZA-DIPEPTIDE ANALOGS AS POTENT AND ORALLY ABSORBED HIV-1 PROTEASE INHIBITORS - CANDIDATES FOR CLINICAL DEVELOPMENT, Journal of medicinal chemistry, 41(18), 1998, pp. 3387-3401
SEMICOCHLIODINOL-A AND SEMICOCHLIODINOL-B - INHIBITORS OF HIV-1 PROTEASE AND EGF-R PROTEIN-TYROSINE KINASE RELATED TO ASTERRIQUINONES PRODUCED BY THE FUNGUS CHRYSOSPORIUM-MERDARIUM
Authors: FREDENHAGEN A PETERSEN F TINTELNOTBLOMLEY M ROSEL J METT H HUG P
Citation: A. Fredenhagen et al., SEMICOCHLIODINOL-A AND SEMICOCHLIODINOL-B - INHIBITORS OF HIV-1 PROTEASE AND EGF-R PROTEIN-TYROSINE KINASE RELATED TO ASTERRIQUINONES PRODUCED BY THE FUNGUS CHRYSOSPORIUM-MERDARIUM, Journal of antibiotics, 50(5), 1997, pp. 395-401
STEREOSELECTIVE SYNTHESIS OF (4S,5R,6S)-4-(5,6-EPOXY-6-PHENYL)-GAMMA-LACTONE
Authors: SOLLADIECAVALLO A ROCHE D BOLD G ACEMOGLU F TINTELNOTBLOMLEY M FISCHER J DECIAN A
Citation: A. Solladiecavallo et al., STEREOSELECTIVE SYNTHESIS OF (4S,5R,6S)-4-(5,6-EPOXY-6-PHENYL)-GAMMA-LACTONE, Tetrahedron : asymmetry, 7(6), 1996, pp. 1797-1810
PROFILE OF CGP-61755 - A NOVEL AND POTENT HIV-1 PROTEASE INHIBITOR THAT SHOWS ENHANCED ANTI-HIV ACTIVITY WHEN COMBINED WITH OTHER ANTIRETROVIRAL AGENTS IN-VITRO
Authors: LAZDINS JK BOLD G CAPRARO HG COZENS R FASSLER A FLESCH G KLIMKAIT T LANG M MESTAN J PONCIONI B ROSEL J STOVER D TINTELNOTBLOMLEY M WALKER MR WOODSCOOK K
Citation: Jk. Lazdins et al., PROFILE OF CGP-61755 - A NOVEL AND POTENT HIV-1 PROTEASE INHIBITOR THAT SHOWS ENHANCED ANTI-HIV ACTIVITY WHEN COMBINED WITH OTHER ANTIRETROVIRAL AGENTS IN-VITRO, Schweizerische medizinische Wochenschrift, 126(43), 1996, pp. 1849-1851
AZA-PEPTIDE ANALOGS AS POTENT HUMAN-IMMUNODEFICIENCY-VIRUS TYPE-1 PROTEASE INHIBITORS WITH ORAL BIOAVAILABILITY
Authors: FASSLER A BOLD G CAPRARO HG COZENS R MESTAN J PONCIONI B ROSEL J TINTELNOTBLOMLEY M LANG M
Citation: A. Fassler et al., AZA-PEPTIDE ANALOGS AS POTENT HUMAN-IMMUNODEFICIENCY-VIRUS TYPE-1 PROTEASE INHIBITORS WITH ORAL BIOAVAILABILITY, Journal of medicinal chemistry, 39(16), 1996, pp. 3203-3216
COMPARATIVE-ANALYSIS OF THE X-RAY STRUCTURES OF HIV-1 AND HIV-2 PROTEASES IN COMPLEX WITH CGP-53820, A NOVEL PSEUDOSYMMETRIC INHIBITOR (VOL3, PG 381, 1995)
Authors: PRIESTLE JP FASSLER A ROSEL J TINTELNOTBLOMLEY M STROP P GRUTTER MG
Citation: Jp. Priestle et al., COMPARATIVE-ANALYSIS OF THE X-RAY STRUCTURES OF HIV-1 AND HIV-2 PROTEASES IN COMPLEX WITH CGP-53820, A NOVEL PSEUDOSYMMETRIC INHIBITOR (VOL3, PG 381, 1995), Structure, 3(6), 1995, pp. 629-629
COMPARATIVE-ANALYSIS OF THE X-RAY STRUCTURES OF HIV-1 AND HIV-2 PROTEASES IN COMPLEX WITH CGP-53820, A NOVEL PSEUDOSYMMETRIC INHIBITOR
Authors: PRIESTLE JP FASSLER A ROSEL J TINTELNOTBLOMLEY M STROP P GRUTTER MG
Citation: Jp. Priestle et al., COMPARATIVE-ANALYSIS OF THE X-RAY STRUCTURES OF HIV-1 AND HIV-2 PROTEASES IN COMPLEX WITH CGP-53820, A NOVEL PSEUDOSYMMETRIC INHIBITOR, Structure, 3(4), 1995, pp. 381-389
NOVEL PSEUDOSYMMETRIC INHIBITORS OF HIV-1 PROTEASE
Authors: FASSLER A ROSEL J GRUTTER M TINTELNOTBLOMLEY M ALTERI E BOLD G LANG M
Citation: A. Fassler et al., NOVEL PSEUDOSYMMETRIC INHIBITORS OF HIV-1 PROTEASE, Bioorganic & medicinal chemistry letters, 3(12), 1993, pp. 2837-2842
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