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Results: 1-11 |
Results: 11
STRUCTURE-BASED DESIGN OF NOVEL, DIPEPTIDE LIGANDS TARGETING THE PP60(SRC) SH2 DOMAIN
Authors: SHAHRIPOUR A PARA KS PLUMMER MS LUNNEY EA HOLLAND DR RUBIN JR HUMBLET C FERGUS JH MARKS JS SALTIEL AR SAWYER TK
Citation: A. Shahripour et al., STRUCTURE-BASED DESIGN OF NOVEL, DIPEPTIDE LIGANDS TARGETING THE PP60(SRC) SH2 DOMAIN, Bioorganic & medicinal chemistry letters, 7(9), 1997, pp. 1107-1112
THE ROLE OF 4-PHOSPHONODIFLUOROMETHYL-PHENYLALANINE AND 4-PHOSPHONO-PHENYLALANINE IN THE SELECTIVITY AND CELLULAR UPTAKE OF SH2 DOMAIN LIGANDS
Authors: STANKOVIC CJ SURENDRAN N LUNNEY EA PLUMMER MS PARA KS SHAHRIPOUR A FERGUS JH MARKS JS HERRERA R HUBBELL SE HUMBLET C SALTIEL AR STEWART BH SAWYER TK
Citation: Cj. Stankovic et al., THE ROLE OF 4-PHOSPHONODIFLUOROMETHYL-PHENYLALANINE AND 4-PHOSPHONO-PHENYLALANINE IN THE SELECTIVITY AND CELLULAR UPTAKE OF SH2 DOMAIN LIGANDS, Bioorganic & medicinal chemistry letters, 7(14), 1997, pp. 1909-1914
STRUCTURE-BASED DESIGN OF A NOVEL SERIES OF NONPEPTIDE LIGANDS THAT BIND TO THE PP60(SRC) SH2 DOMAIN
Authors: LUNNEY EA PARA KS RUBIN JR HUMBLET C FERGUS JH MARKS JS SAWYER TK
Citation: Ea. Lunney et al., STRUCTURE-BASED DESIGN OF A NOVEL SERIES OF NONPEPTIDE LIGANDS THAT BIND TO THE PP60(SRC) SH2 DOMAIN, Journal of the American Chemical Society, 119(51), 1997, pp. 12471-12476
NOVEL PHOSPHOTYROSINE MIMETICS IN THE DESIGN OF PEPTIDE LIGANDS FOR PP60(SRC) SH2 DOMAIN
Authors: SHAHRIPOUR A PLUMMER MS LUNNEY EA PARA KS STANKOVIC CJ RUBIN JR HUMBLET C FERGUS JH MARKS JS HERRERA R HUBBELL SE SALTIEL AR SAWYER TK
Citation: A. Shahripour et al., NOVEL PHOSPHOTYROSINE MIMETICS IN THE DESIGN OF PEPTIDE LIGANDS FOR PP60(SRC) SH2 DOMAIN, Bioorganic & medicinal chemistry letters, 6(11), 1996, pp. 1209-1214
A TOPLISS TREE ANALYSIS OF THE HIV-PROTEASE INHIBITORY ACTIVITY OF 6-PHENYL-4-HYDROXY-PYRAN-2-ONES
Authors: STEINBAUGH BA HAMILTON HW PRASAD JVNV PARA KS TUMMINO PJ FERGUSON D LUNNEY EA BLANKLEY CJ
Citation: Ba. Steinbaugh et al., A TOPLISS TREE ANALYSIS OF THE HIV-PROTEASE INHIBITORY ACTIVITY OF 6-PHENYL-4-HYDROXY-PYRAN-2-ONES, Bioorganic & medicinal chemistry letters, 6(10), 1996, pp. 1099-1104
NONPEPTIDIC HIV PROTEASE INHIBITORS - 3-(S-BENZYL SUBSTITUTED)-4-HYDROXY-6-(PHENYL SUBSTITUTED)-2H-PYRAN-2-ONE WITH AN INVERSE MODE OF BINDING
Authors: PRASAD JVNV PAVLOVSKY A PARA KS ELLSWORTH EL TUMMINO PJ NOUHAN C FERGUSON D
Citation: Jvnv. Prasad et al., NONPEPTIDIC HIV PROTEASE INHIBITORS - 3-(S-BENZYL SUBSTITUTED)-4-HYDROXY-6-(PHENYL SUBSTITUTED)-2H-PYRAN-2-ONE WITH AN INVERSE MODE OF BINDING, Bioorganic & medicinal chemistry letters, 6(10), 1996, pp. 1133-1138
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
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
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
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
A SIMPLE PROCEDURE FOR THE SYNTHESIS OF TED-SULFANYL)-4-HYDROXY-6-SUBSTITUTED-PYRAN-2-ONES
Authors: PARA KS ELLSWORTH EL PRASAD JVN
Citation: Ks. Para et al., A SIMPLE PROCEDURE FOR THE SYNTHESIS OF TED-SULFANYL)-4-HYDROXY-6-SUBSTITUTED-PYRAN-2-ONES, Journal of heterocyclic chemistry, 31(6), 1994, pp. 1619-1624
NOVEL SERIES OF ACHIRAL, LOW-MOLECULAR-WEIGHT, AND POTENT HIV-1 PROTEASE INHIBITORS
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
TITANIUM-MEDIATED CYCLIZATIONS OF BETA-KETO-ESTERS WITH ACETALS - A CONVENIENT ROUTE TO 2-CARBALKOXYCYCLOALKENONES
Authors: FUNK RL FITZGERALD JF OLMSTEAD TA PARA KS WOS JA
Citation: Rl. Funk et al., TITANIUM-MEDIATED CYCLIZATIONS OF BETA-KETO-ESTERS WITH ACETALS - A CONVENIENT ROUTE TO 2-CARBALKOXYCYCLOALKENONES, Journal of the American Chemical Society, 115(19), 1993, pp. 8849-8850
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