Authors:
DOMAGALA JM
BADER JP
GOGLIOTTI RD
SANCHEZ JP
STIER MA
SONG YT
PRASAD JVNV
TUMMINO PJ
SCHOLTEN J
HARVEY P
HOLLER T
GRACHECK S
HUPE D
RICE WG
SCHULTZ R
Citation: Jm. Domagala et al., A NEW CLASS OF ANTI-HIV-1 AGENTS TARGETED TOWARD THE NUCLEOCAPSID PROTEIN NCP7 - THE 2,2'-DITHIOBISBENZAMIDES, Bioorganic & medicinal chemistry, 5(3), 1997, pp. 569-579
Authors:
HAGEN SE
PRASAD JVNV
BOYER FE
DOMAGALA JM
ELLSWORTH EL
GAJDA C
HAMILTON HW
MARKOSKI LJ
STEINBAUGH BA
TAIT BD
LUNNEY EA
TUMMINO PJ
FERGUSON D
HUPE D
NOUHAN C
GRACHECK SJ
SAUNDERS JM
VANDERROEST S
Citation: Se. Hagen et al., SYNTHESIS OF 5,6-DIHYDRO-4-HYDROXY-2-PYRONES AS HIV-1 PROTEASE INHIBITORS - THE PROFOUND EFFECT OF POLARITY ON ANTIVIRAL ACTIVITY, Journal of medicinal chemistry, 40(23), 1997, pp. 3707-3711
Authors:
RENAU TE
GAGE JW
DEVER JA
ROLAND GE
JOANNIDES ET
SHAPIRO MA
SANCHEZ JP
GRACHECK SJ
DOMAGALA JM
JACOBS MR
REYNOLDS RC
Citation: Te. Renau et al., STRUCTURE-ACTIVITY-RELATIONSHIPS OF QUINOLONE AGENTS AGAINST MYCOBACTERIA - EFFECT OF STRUCTURAL MODIFICATIONS AT THE 8-POSITION, Antimicrobial agents and chemotherapy, 40(10), 1996, pp. 2363-2368
Authors:
RENAU TE
SANCHEZ JP
GAGE JW
DEVER JA
SHAPIRO MA
GRACHECK SJ
DOMAGALA JM
Citation: Te. Renau et al., STRUCTURE-ACTIVITY-RELATIONSHIPS OF THE QUINOLONE ANTIBACTERIALS AGAINST MYCOBACTERIA - EFFECT OF STRUCTURAL-CHANGES AT N-1 AND C-7, Journal of medicinal chemistry, 39(3), 1996, pp. 729-735
Citation: Te. Renau et al., THE SYNTHESIS OF 3-BROMO-2,4,5-TRIFLUOROBENZOIC ACID AND ITS CONVERSION TO 8-BROMOQUINOLONECARBOXYLIC ACIDS, Journal of heterocyclic chemistry, 33(4), 1996, pp. 1407-1411
Authors:
PRASAD JVNV
TUMMINO PJ
FERGUSON D
SAUNDERS J
VANDERROEST S
MCQUADE TJ
HELDSINGER A
REYNER EL
STEWART BH
GUTTENDORF RJ
PARA KS
LUNNEY EA
GRACHECK SJ
DOMAGALA JM
Citation: Jvnv. Prasad et al., NONPEPTIDIC HIV PROTEASE INHIBITORS - 4-HYDROXY-PYRAN-2-ONE INHIBITORS WITH FUNCTIONAL TETHERS TO P-1 PHENYL RING TO REACH S-3 POCKET OF THE ENZYME, Biochemical and biophysical research communications, 221(3), 1996, pp. 815-820
Authors:
PRASAD JVN
PARA KS
TUMMINO PJ
FERGUSON D
MCQUADE TJ
LUNNEY EA
RAPUNDALO ST
BATLEY BL
HINGORANI G
DOMAGALA JM
GRACHECK SJ
BHAT TN
LIU BS
BALDWIN ET
ERICKSON JW
SAWYER TK
Citation: Jvn. Prasad et al., NONPEPTIDIC POTENT HIV-1 PROTEASE INHIBITORS - -HYDROXY-6-PHENYL-2-OXO-2H-PYRAN-3-YL)THIOMETHANES THAT SPAN P-1-P-2' SUBSITES IN A UNIQUE MODE OF ACTIVE-SITE BINDING, Journal of medicinal chemistry, 38(6), 1995, pp. 898-905
Authors:
SANCHEZ JP
GOGLIOTTI RD
DOMAGALA JM
GRACHECK SJ
HUBAND MD
SESNIE JA
COHEN MA
SHAPIRO MA
Citation: Jp. Sanchez et al., THE SYNTHESIS, STRUCTURE-ACTIVITY, AND STRUCTURE-SIDE EFFECT RELATIONSHIPS OF A SERIES OF 8-ALKOXYQUINOLONE AND 5-AMINO-8-ALKOXYQUINOLONE ANTIBACTERIAL AGENTS, Journal of medicinal chemistry, 38(22), 1995, pp. 4478-4487
Authors:
RENAU TE
SANCHEZ JP
SHAPIRO MA
DEVER JA
GRACHECK SJ
DOMAGALA JM
Citation: Te. Renau et al., EFFECT OF LIPOPHILICITY AT N-1 ON ACTIVITY OF FLUOROQUINOLONES AGAINST MYCOBACTERIA, Journal of medicinal chemistry, 38(15), 1995, pp. 2974-2977
Authors:
PRASAD JVNV
LUNNEY EA
FERGUSON D
TUMMINO PJ
RUBIN JR
REYNER EL
STEWART BH
GUTTENDORF RJ
DOMAGALA JM
SUVOROV LI
GULNIK SV
TOPOL IA
BHAT TN
ERICKSON JW
Citation: Jvnv. Prasad et al., HIV PROTEASE INHIBITORS POSSESSING A NOVEL, HIGH-AFFINITY, AND ACHIRAL P-1' P-2' LIGAND WITH A UNIQUE PATTERN OF IN-VITRO RESISTANCE - IMPORTANCE OF A CONFORMATIONALLY-RESTRICTED TEMPLATE IN THE DESIGN OF ENZYME-INHIBITORS/, Journal of the American Chemical Society, 117(45), 1995, pp. 11070-11074
Citation: Jm. Domagala, STRUCTURE-ACTIVITY AND STRUCTURE-SIDE-EFFECT RELATIONSHIPS FOR THE QUINOLONE ANTIBACTERIALS (VOL 33, PG 685, 1994), Journal of antimicrobial chemotherapy, 34(5), 1994, pp. 851-851
Citation: Jm. Domagala, STRUCTURE-ACTIVITY AND STRUCTURE-SIDE-EFFECT RELATIONSHIPS FOR THE QUINOLONE ANTIBACTERIALS, Journal of antimicrobial chemotherapy, 33(4), 1994, pp. 685-706
Authors:
HAGEN SE
DOMAGALA JM
GRACHECK SJ
SESNIE JA
STIER MA
SUTO MJ
Citation: Se. Hagen et al., SYNTHESIS AND ANTIBACTERIAL ACTIVITY OF NEW QUINOLONES CONTAINING A 7-[3-(1-AMINO-1-METHYLETHYL)-1-PYRROLIDINYL] MOIETY - GRAM-POSITIVE AGENTS WITH EXCELLENT ORAL ACTIVITY AND LOW SIDE-EFFECT POTENTIAL, Journal of medicinal chemistry, 37(6), 1994, pp. 733-738
Authors:
LUNNEY EA
HAGEN SE
DOMAGALA JM
HUMBLET C
KOSINSKI J
TAIT BD
WARMUS JS
WILSON M
FERGUSON D
HUPE D
TUMMINO PJ
BALDWIN ET
BHAT TN
LIU BS
ERICKSON JW
Citation: Ea. Lunney et al., A NOVEL NONPEPTIDE HIV-1 PROTEASE INHIBITOR - ELUCIDATION OF THE BINDING MODE AND ITS APPLICATION IN THE DESIGN OF RELATED ANALOGS, Journal of medicinal chemistry, 37(17), 1994, pp. 2664-2677
Authors:
PRASAD JVNV
PARA KS
LUNNEY EA
ORTWINE DF
DUNBAR JB
FERGUSON D
TUMMINO PJ
HUPE D
TAIT BD
DOMAGALA JM
HUMBLET C
BHAT TN
LIU BS
GUERIN DMA
BALDWIN ET
ERICKSON JW
SAWYER TK
Citation: Jvnv. Prasad et al., NOVEL SERIES OF ACHIRAL, LOW-MOLECULAR-WEIGHT, AND POTENT HIV-1 PROTEASE INHIBITORS, Journal of the American Chemical Society, 116(15), 1994, pp. 6989-6990
Authors:
HUBAND MD
COHEN MA
MESERVEY MA
ROLAND GE
YODER SL
DAZER ME
DOMAGALA JM
Citation: Md. Huband et al., IN-VITRO ANTIBACTERIAL ACTIVITIES OF PD 138312 AND PD 140248, NEW FLUORONAPHTHYRIDINES WITH OUTSTANDING GRAM-POSITIVE POTENCY, Antimicrobial agents and chemotherapy, 37(12), 1993, pp. 2563-2570
Citation: Ra. Bucsh et al., SYNTHESIS AND ANTIMICROBIAL EVALUATION OF A SERIES OF 7-[3-AMINO (OR AMINOMETHYL)-4-ARYL (OR CYCLOPROPYL)-1-PYRROLIDINYL]-4-QUINOLONE- AND -1,8-NAPHTHYRIDONE-3-CARBOXYLIC ACIDS, Journal of medicinal chemistry, 36(26), 1993, pp. 4139-4151