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Results: 1-12 |
Results: 12
ANTIBIOTIC SENSITIZATION USING BIPHENYL TETRAZOLES AS POTENT INHIBITORS OF BACTEROIDES-FRAGILIS METALLO-BETA-LACTAMASE
Authors: TONEY JH FITZGERALD PMD GROVERSHARMA N OLSON SH MAY WJ SUNDELOF JG VANDERWALL DE CLEARY KA GRANT SK WU JK KOZARICH JW POMPLIANO DL HAMMOND GG
Citation: Jh. Toney et al., ANTIBIOTIC SENSITIZATION USING BIPHENYL TETRAZOLES AS POTENT INHIBITORS OF BACTEROIDES-FRAGILIS METALLO-BETA-LACTAMASE, Chemistry & biology, 5(4), 1998, pp. 185-196
UNANTICIPATED INHIBITION OF THE METALLO-BETA-LACTAMASE FROM BACTEROIDES-FRAGILIS BY 4-MORPHOLINEETHANESULFONIC ACID (MES) - A CRYSTALLOGRAPHIC STUDY AT 1.85-ANGSTROM RESOLUTION
Authors: FITZGERALD PMD WU JK TONEY JH
Citation: Pmd. Fitzgerald et al., UNANTICIPATED INHIBITION OF THE METALLO-BETA-LACTAMASE FROM BACTEROIDES-FRAGILIS BY 4-MORPHOLINEETHANESULFONIC ACID (MES) - A CRYSTALLOGRAPHIC STUDY AT 1.85-ANGSTROM RESOLUTION, Biochemistry, 37(19), 1998, pp. 6791-6800
CIF APPLICATIONS .6. CIFLIB - AN APPLICATION-PROGRAM INTERFACE TO CIFDICTIONARIES AND DATA FILES
Authors: WESTBROOK JD HSIEH SH FITZGERALD PMD
Citation: Jd. Westbrook et al., CIF APPLICATIONS .6. CIFLIB - AN APPLICATION-PROGRAM INTERFACE TO CIFDICTIONARIES AND DATA FILES, Journal of applied crystallography, 30, 1997, pp. 79-83
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
A-PRIORI PREDICTION OF ACTIVITY FOR HIV-1 PROTEASE INHIBITORS EMPLOYING ENERGY MINIMIZATION IN THE ACTIVE-SITE (VOL 38, PG 308, 1995)
Authors: HOLLOWAY MK WAI JM HALGREN TA FITZGERALD PMD VACCA JP DORSEY BD LEVIN RB THOMPSON WJ CHEN LJ DESOLMS SJ GAFFIN N GHOSH AK GIULIANI EA GRAHAM SL GUARE JP HUNGATE RW LYLE TA SANDERS WM TUCKER TJ WIGGINS M WISCOUNT CM WOLTERSDORF OW YOUNG SD DARKE PL ZUGAY JA
Citation: Mk. Holloway et al., A-PRIORI PREDICTION OF ACTIVITY FOR HIV-1 PROTEASE INHIBITORS EMPLOYING ENERGY MINIMIZATION IN THE ACTIVE-SITE (VOL 38, PG 308, 1995), Journal of medicinal chemistry, 39(11), 1996, pp. 2280-2280
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
A-PRIORI PREDICTION OF ACTIVITY FOR HIV-1 PROTEASE INHIBITORS EMPLOYING ENERGY MINIMIZATION IN THE ACTIVE-SITE
Authors: HOLLOWAY MK WAI JM HALGREN TA FITZGERALD PMD VACCA JP DORSEY BD LEVIN RB THOMPSON WJ CHEN LJ DESOLMS SJ GAFFIN N GHOSH AK GIULIANI EA GRAHAM SL GUARE JP HUNGATE RW LYLE TA SANDERS WM TUCKER TJ WIGGINS M WISCOUNT CM WOLTERSDORF OW YOUNG SD DARKE PL ZUGAY JA
Citation: Mk. Holloway et al., A-PRIORI PREDICTION OF ACTIVITY FOR HIV-1 PROTEASE INHIBITORS EMPLOYING ENERGY MINIMIZATION IN THE ACTIVE-SITE, Journal of medicinal chemistry, 38(2), 1995, pp. 305-317
CONFORMATIONALLY CONSTRAINED HIV-1 PROTEASE INHIBITORS
Authors: VACCA JP FITZGERALD PMD HOLLOWAY MK HUNGATE RW STARBUCK KE CHEN LJ DARKE PL ANDERSON PS HUFF JR
Citation: Jp. Vacca et al., CONFORMATIONALLY CONSTRAINED HIV-1 PROTEASE INHIBITORS, Bioorganic & medicinal chemistry letters, 4(3), 1994, pp. 499-504
NOVEL CONFORMATIONALLY CONSTRAINED HIV-1 PROTEASE INHIBITORS - RATIONAL DESIGN, ENZYME-INHIBITION, AND X-RAY STRUCTURE OF AN ENZYME-INHIBITOR COMPLEX
Authors: KIM BM VACCA JP FITZGERALD PMD DARKE PL HOLLOWAY MK GUARE JP HANIFIN CM ARFORDBICKERSTAFF DJ ZUGAY JA WAI JM ANDERSON PS HUFF JR
Citation: Bm. Kim et al., NOVEL CONFORMATIONALLY CONSTRAINED HIV-1 PROTEASE INHIBITORS - RATIONAL DESIGN, ENZYME-INHIBITION, AND X-RAY STRUCTURE OF AN ENZYME-INHIBITOR COMPLEX, Bioorganic & medicinal chemistry letters, 4(18), 1994, pp. 2199-2204
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
HIV PROTEASE LIGAND COMPLEXES
Authors: FITZGERALD PMD
Citation: Pmd. Fitzgerald, HIV PROTEASE LIGAND COMPLEXES, Current opinion in structural biology, 3(6), 1993, pp. 868-874
Risultati: 1-12 |