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Results: 1-6 |
Results: 6
INHIBITION OF STROMELYSIN-1 (MMP-3) BY P-1'-BIPHENYLYLETHYL CARBOXYALKYL DIPEPTIDES
Authors: ESSER CK BUGIANESI RL CALDWELL CG CHAPMAN KT DURETTE PL GIROTRA NN KOPKA IE LANZA TJ LEVORSE DA MACCROSS M OWENS KA PONPIPOM MM SIMEONE JP HARRISON RK NIEDZWIECKI L BECKER JW MARCY AI AXEL MG CHRISTEN AJ MCDONNELL J MOORE VL OLSZEWSKI JM SAPHOS C VISCO DM SHEN F COLLETTI A KRIETER PA HAGMANN WK
Citation: Ck. Esser et al., INHIBITION OF STROMELYSIN-1 (MMP-3) BY P-1'-BIPHENYLYLETHYL CARBOXYALKYL DIPEPTIDES, Journal of medicinal chemistry, 40(6), 1997, pp. 1026-1040
COMPARISON OF THE STRUCTURE OF HUMAN RECOMBINANT SHORT-FORM STROMELYSIN BY MULTIDIMENSIONAL HETERONUCLEAR NMR AND X-RAY CRYSTALLOGRAPHY
Authors: GOOLEY PR OCONNELL JF MARCY AI CUCA GC AXEL MG CALDWELL CG HAGMANN WK BECKER JW
Citation: Pr. Gooley et al., COMPARISON OF THE STRUCTURE OF HUMAN RECOMBINANT SHORT-FORM STROMELYSIN BY MULTIDIMENSIONAL HETERONUCLEAR NMR AND X-RAY CRYSTALLOGRAPHY, Journal of biomolecular NMR, 7(1), 1996, pp. 8-28
NONPEPTIDAL P-2 LIGANDS FOR HIV PROTEASE INHIBITORS - STRUCTURE-BASEDDESIGN, SYNTHESIS, AND BIOLOGICAL EVALUATION
Authors: GHOSH AK KINCAID JF WALTERS DE CHEN Y CHAUDHURI NC THOMPSON WJ CULBERSON C FITZGERALD PMD LEE HY MCKEE SP MUNSON PM DUONG TT DARKE PL ZUGAY JA SCHLEIF WA AXEL MG LIN J HUFF JR
Citation: Ak. Ghosh et al., NONPEPTIDAL P-2 LIGANDS FOR HIV PROTEASE INHIBITORS - STRUCTURE-BASEDDESIGN, SYNTHESIS, AND BIOLOGICAL EVALUATION, Journal of medicinal chemistry, 39(17), 1996, pp. 3278-3290
STROMELYSIN-1 - 3-DIMENSIONAL STRUCTURE OF THE INHIBITED CATALYTIC DOMAIN AND OF THE C-TRUNCATED PROENZYME
Authors: BECKER JW MARCY AI ROKOSZ LL AXEL MG BURBAUM JJ FITZGERALD PMD CAMERON PM ESSER CK HAGMANN WK HERMES JD SPRINGER JP
Citation: Jw. Becker et al., STROMELYSIN-1 - 3-DIMENSIONAL STRUCTURE OF THE INHIBITED CATALYTIC DOMAIN AND OF THE C-TRUNCATED PROENZYME, Protein science, 4(10), 1995, pp. 1966-1976
L-735,524 - THE DESIGN OF A POTENT AND ORALLY BIOAVAILABLE HIV PROTEASE INHIBITOR
Authors: DORSEY BD LEVIN RB MCDANIEL SL VACCA JP GUARE JP DARKE PL ZUGAY JA EMINI EA SCHLEIF WA QUINTERO JC LIN JH CHEN IW HOLLOWAY MK FITZGERALD PMD AXEL MG OSTOVIC D ANDERSON PS HUFF JR
Citation: Bd. Dorsey et al., L-735,524 - THE DESIGN OF A POTENT AND ORALLY BIOAVAILABLE HIV PROTEASE INHIBITOR, Journal of medicinal chemistry, 37(21), 1994, pp. 3443-3451
STRUCTURE-BASED DESIGN OF HIV-1 PROTEASE INHIBITORS - REPLACEMENT OF 2 AMIDES AND A 10-PI-AROMATIC SYSTEM BY A FUSED BIS-TETRAHYDROFURAN
Authors: GHOSH AK THOMPSON WJ FITZGERALD PMD CULBERSON JC AXEL MG MCKEE SP HUFF JR ANDERSON PS
Citation: Ak. Ghosh et al., STRUCTURE-BASED DESIGN OF HIV-1 PROTEASE INHIBITORS - REPLACEMENT OF 2 AMIDES AND A 10-PI-AROMATIC SYSTEM BY A FUSED BIS-TETRAHYDROFURAN, Journal of medicinal chemistry, 37(16), 1994, pp. 2506-2508
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