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Results: 1-8 |
Results: 8
SYNTHESIS OF N-GLYOXYLYL PEPTIDES AND THEIR IN-VITRO EVALUATION AS HIV-1 PROTEASE INHIBITORS
Authors: QASMI D DEROSNY E RENE L BADET B VERGELY I BOGGETTO N REBOUDRAVAUX M
Citation: D. Qasmi et al., SYNTHESIS OF N-GLYOXYLYL PEPTIDES AND THEIR IN-VITRO EVALUATION AS HIV-1 PROTEASE INHIBITORS, Bioorganic & medicinal chemistry, 5(4), 1997, pp. 707-714
SYNTHESIS AND INHIBITION OF HUMAN-LEUKOCYTE ELASTASE BY FUNCTIONALIZED N-ARYL AZETIDIN-2-ONES - EFFECT OF DIFFERENT SUBSTITUENTS ON THE AROMATIC RING
Authors: JOYEAU R FELK A GUILAUME S WAKSELMAN M VERGELY I DOUCET C BOGGETTO N REBOUDRAVAUX M
Citation: R. Joyeau et al., SYNTHESIS AND INHIBITION OF HUMAN-LEUKOCYTE ELASTASE BY FUNCTIONALIZED N-ARYL AZETIDIN-2-ONES - EFFECT OF DIFFERENT SUBSTITUENTS ON THE AROMATIC RING, Journal of Pharmacy and Pharmacology, 48(12), 1996, pp. 1218-1230
ESTERS AND AMIDES OF (CHLOROMETHYL)1-2-OXO-2H-1-BENZOPYRAN-3-CARBOXYLIC ACID AS INHIBITORS OF ALPHA-CHYMOTRYPSIN - SIGNIFICANCE OF THE AROMATIC NATURE OF THE NOVEL ESTER-TYPE COUMARIN FOR STRONG INHIBITORY ACTIVITY
Authors: POCHET L DOUCET C SCHYNTS M THIERRY N BOGGETTO N PIROTTE B JIANG KY MASEREEL B DETULLIO P DELARGE J REBOUDRAVAUX M
Citation: L. Pochet et al., ESTERS AND AMIDES OF (CHLOROMETHYL)1-2-OXO-2H-1-BENZOPYRAN-3-CARBOXYLIC ACID AS INHIBITORS OF ALPHA-CHYMOTRYPSIN - SIGNIFICANCE OF THE AROMATIC NATURE OF THE NOVEL ESTER-TYPE COUMARIN FOR STRONG INHIBITORY ACTIVITY, Journal of medicinal chemistry, 39(13), 1996, pp. 2579-2585
INHIBITION OF HUMAN-LEUKOCYTE ELASTASE BY FUNCTIONALIZED N-ARYL AZETIDIN-2-ONES - SUBSTITUENT EFFECTS AT C-3 AND BENZYLIC POSITIONS
Authors: VERGELY I BOGGETTO N OKOCHI V GOLPAYEGANI S REBOUDRAVAUX M KOBAITER R JOYEAU R WAKSELMAN M
Citation: I. Vergely et al., INHIBITION OF HUMAN-LEUKOCYTE ELASTASE BY FUNCTIONALIZED N-ARYL AZETIDIN-2-ONES - SUBSTITUENT EFFECTS AT C-3 AND BENZYLIC POSITIONS, European journal of medicinal chemistry, 30(3), 1995, pp. 199-208
PROGRESS TOWARDS NEW CONFORMATIONALLY CONSTRAINED HIV-1 PROTEASE INHIBITORS
Authors: BENATALAH Z TRIGUI N SICSIC S TONNAIRE T DEROSNY E BOGGETTO N REBOUD M
Citation: Z. Benatalah et al., PROGRESS TOWARDS NEW CONFORMATIONALLY CONSTRAINED HIV-1 PROTEASE INHIBITORS, European journal of medicinal chemistry, 30(11), 1995, pp. 891-900
CYCLIC-PEPTIDES AS SELECTIVE SUBSTRATES AND SUICIDE SUBSTRATE PRECURSORS OF TRYPSIN-LIKE PROTEINASES
Authors: BOGGETTO N VILAIN AC MONTAGNE JJ REBOUDRAVAUX M MAZALEYRAT JP XIE J WAKSELMAN M
Citation: N. Boggetto et al., CYCLIC-PEPTIDES AS SELECTIVE SUBSTRATES AND SUICIDE SUBSTRATE PRECURSORS OF TRYPSIN-LIKE PROTEINASES, Bulletin de la Societe chimique de France, 131(2), 1994, pp. 152-166
EVALUATION OF THE INHIBITORY ACTIVITY ON SERINE AND ASPARTIC PROTEASES OF 4-AMINO-4H-1,2,4-TRIAZOLE AND 5-AMINOTHIAZOLE DERIVATIVES STRUCTURALLY RELATED TO BETA-LACTAM ANTIBIOTICS
Authors: VILAIN AC PIROTTE B VERGELY I BOGGETTO N MASEREEL B SCHYNTS M DELARGE J REBOUDRAVAUX M
Citation: Ac. Vilain et al., EVALUATION OF THE INHIBITORY ACTIVITY ON SERINE AND ASPARTIC PROTEASES OF 4-AMINO-4H-1,2,4-TRIAZOLE AND 5-AMINOTHIAZOLE DERIVATIVES STRUCTURALLY RELATED TO BETA-LACTAM ANTIBIOTICS, Journal of Pharmacy and Pharmacology, 45(5), 1993, pp. 466-472
NEW MECHANISM-BASED INACTIVATORS OF TRYPSIN-LIKE PROTEINASES - SELECTIVE INACTIVATION OF UROKINASE BY FUNCTIONALIZED CYCLOPEPTIDES INCORPORATING A SULFONIOMETHYL-SUBSTITUTED M-AMINOBENZOIC ACID RESIDUE
Authors: WAKSELMAN M XIE J MAZALEYRAT JP BOGGETTO N VILAIN AC MONTAGNE JJ REBOUDRAVAUX M
Citation: M. Wakselman et al., NEW MECHANISM-BASED INACTIVATORS OF TRYPSIN-LIKE PROTEINASES - SELECTIVE INACTIVATION OF UROKINASE BY FUNCTIONALIZED CYCLOPEPTIDES INCORPORATING A SULFONIOMETHYL-SUBSTITUTED M-AMINOBENZOIC ACID RESIDUE, Journal of medicinal chemistry, 36(11), 1993, pp. 1539-1547
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