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Results: 1-10 |
Results: 10
ANTI-HUMAN-IMMUNODEFICIENCY-VIRUS ACTIVITY, BIOAVAILABILITY AND DRUG-RESISTANCE PROFILE OF THE NOVEL PROTEINASE-INHIBITOR MDL-74,695
Authors: TAYLOR DL AHMED PS BRENNAN TM BRIDGES CG TYMS AS VANDORSSELAER V TARNUS C HORNSPERGER JM SCHIRLIN D
Citation: Dl. Taylor et al., ANTI-HUMAN-IMMUNODEFICIENCY-VIRUS ACTIVITY, BIOAVAILABILITY AND DRUG-RESISTANCE PROFILE OF THE NOVEL PROTEINASE-INHIBITOR MDL-74,695, Antiviral chemistry & chemotherapy, 8(3), 1997, pp. 205-214
SILICON-MEDIATED INACTIVATION OF DIAMINE OXIDASE
Authors: VANDORSSELAER V SCHIRLIN D MARCHAL P WEBER F DANZIN C
Citation: V. Vandorsselaer et al., SILICON-MEDIATED INACTIVATION OF DIAMINE OXIDASE, Bioorganic chemistry, 24(2), 1996, pp. 178-193
DIFLUOROMETHYLENEKETONE RETROAMIDE, A VERSATILE CONCEPT OF INACTIVATION OF PROTEOLYTIC-ENZYMES
Authors: SCHIRLIN D BALTZER S ALTENBURGER JM TARNUS C REMY JM
Citation: D. Schirlin et al., DIFLUOROMETHYLENEKETONE RETROAMIDE, A VERSATILE CONCEPT OF INACTIVATION OF PROTEOLYTIC-ENZYMES, Tetrahedron, 52(1), 1996, pp. 305-318
SILICON-MEDIATED INACTIVATION OF SEMICARBAZIDE-SENSITIVE AMINE OXIDASE
Authors: DANZIN C COLLARD JN MARCHAL P SCHIRLIN D
Citation: C. Danzin et al., SILICON-MEDIATED INACTIVATION OF SEMICARBAZIDE-SENSITIVE AMINE OXIDASE, Bioorganic & medicinal chemistry letters, 5(20), 1995, pp. 2363-2366
SYNTHESIS OF CRYSTALLINE ORTHOGONALLY N-PROTECTED (S)-2,3-DIAMINOPROPIONALDEHYDE OR (R)-2,3-DIAMINOPROPIONALDEHYDE FROM L-ASPARTIC OR D-ASPARTIC ACID
Authors: SCHIRLIN D ALTENBURGER JM
Citation: D. Schirlin et Jm. Altenburger, SYNTHESIS OF CRYSTALLINE ORTHOGONALLY N-PROTECTED (S)-2,3-DIAMINOPROPIONALDEHYDE OR (R)-2,3-DIAMINOPROPIONALDEHYDE FROM L-ASPARTIC OR D-ASPARTIC ACID, Synthesis, (11), 1995, pp. 1351-1352
BENEFICIAL REPLACEMENT OF THE P-1 PHENYLALANINE SIDE-CHAIN IN HIV-1 PROTEASE INHIBITORS OF THE DIFLUOROSTATONE TYPE
Authors: SCHIRLIN D VANDORSSELAER V TARNUS C TAYLOR DL TYMS AS BALTZER S WEBER F REMY JM BRENNAN T FARR R JANOWICK D
Citation: D. Schirlin et al., BENEFICIAL REPLACEMENT OF THE P-1 PHENYLALANINE SIDE-CHAIN IN HIV-1 PROTEASE INHIBITORS OF THE DIFLUOROSTATONE TYPE, Bioorganic & medicinal chemistry letters, 4(2), 1994, pp. 241-246
INCREASED ANTIVIRAL ACTIVITY OF HIV PROTEASE INHIBITORS OF THE DIFLUOROSTATONE TYPE BEARING (R)-VALINOL DERIVATIVES AS NOVEL C-TERMINI
Authors: VANDORSSELAER V SCHIRLIN D TARNUS C TAYLOR DL TYMS AS WEBER F BALTZER S REMY JM BRENNAN T JANOWICK D
Citation: V. Vandorsselaer et al., INCREASED ANTIVIRAL ACTIVITY OF HIV PROTEASE INHIBITORS OF THE DIFLUOROSTATONE TYPE BEARING (R)-VALINOL DERIVATIVES AS NOVEL C-TERMINI, Bioorganic & medicinal chemistry letters, 4(10), 1994, pp. 1213-1218
TRIMETHYLSILYLATED TRIFLUOROMETHYL KETONES, A NOVEL CLASS OF ACETYLCHOLINESTERASE INHIBITORS - BIOCHEMICAL AND PHARMACOLOGICAL PROFILE OF MDL-73,745
Authors: HORNSPERGER JM COLLARD JN HEYDT JG GIACOBINI E FUNES S DOW J SCHIRLIN D
Citation: Jm. Hornsperger et al., TRIMETHYLSILYLATED TRIFLUOROMETHYL KETONES, A NOVEL CLASS OF ACETYLCHOLINESTERASE INHIBITORS - BIOCHEMICAL AND PHARMACOLOGICAL PROFILE OF MDL-73,745, Biochemical Society transactions, 22(3), 1994, pp. 758-763
BIOCHEMICAL AND PHARMACOLOGICAL EVALUATION OF 2,4-DIFLUOROBENZYLDIMETHYLSILYLMETHANAMINE, A NEW HIGHLY SELECTIVE INHIBITOR OF MONOAMINE OXIDASE-B
Authors: DANZIN C ZREIKA M MARCHAL P PETTY M COLLARD JN SCHIRLIN D
Citation: C. Danzin et al., BIOCHEMICAL AND PHARMACOLOGICAL EVALUATION OF 2,4-DIFLUOROBENZYLDIMETHYLSILYLMETHANAMINE, A NEW HIGHLY SELECTIVE INHIBITOR OF MONOAMINE OXIDASE-B, Biochemical Society transactions, 22(3), 1994, pp. 768-773
DESIGN, SYNTHESIS, AND CONFORMATIONAL-ANALYSIS OF A NOVEL MACROCYCLICHIV-PROTEASE INHIBITOR
Authors: PODLOGAR BL FARR RA FRIEDRICH D TARNUS C HUBER EW CREGGE RJ SCHIRLIN D
Citation: Bl. Podlogar et al., DESIGN, SYNTHESIS, AND CONFORMATIONAL-ANALYSIS OF A NOVEL MACROCYCLICHIV-PROTEASE INHIBITOR, Journal of medicinal chemistry, 37(22), 1994, pp. 3684-3692
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