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Results: 1-7 |
Results: 7
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-ACTIVITY-RELATIONSHIPS IN A SERIES OF ORALLY-ACTIVE GAMMA-HYDROXY BUTENOLIDE ENDOTHELIN ANTAGONISTS
Authors: PATT WC EDMUNDS JJ REPINE JT BERRYMAN KA REISDORPH BR LEE C PLUMMER MS SHAHRIPOUR A HALEEN SJ KEISER JA FLYNN MA WELCH KM REYNOLDS EE RUBIN R TOBIAS B HALLAK H DOHERTY AM
Citation: Wc. Patt et al., STRUCTURE-ACTIVITY-RELATIONSHIPS IN A SERIES OF ORALLY-ACTIVE GAMMA-HYDROXY BUTENOLIDE ENDOTHELIN ANTAGONISTS, Journal of medicinal chemistry, 40(7), 1997, pp. 1063-1074
DESIGN, SYNTHESIS, AND COCRYSTAL STRUCTURE OF A NONPEPTIDE SRC SH2 DOMAIN LIGAND
Authors: PLUMMER MS HOLLAND DR SHAHRIPOUR A LUNNEY EA FERGUS JH MARKS JS MCCONNELL P MUELLER WT SAWYER TK
Citation: Ms. Plummer et al., DESIGN, SYNTHESIS, AND COCRYSTAL STRUCTURE OF A NONPEPTIDE SRC SH2 DOMAIN LIGAND, Journal of medicinal chemistry, 40(23), 1997, pp. 3719-3725
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
DISCOVERY OF A NOVEL SERIES OF ORALLY-ACTIVE NONPEPTIDE ENDOTHELIN-A (ET(A)) RECEPTOR-SELECTIVE ANTAGONISTS
Authors: DOHERTY AM PATT WC EDMUNDS JJ BERRYMAN KA REISDORPH BR PLUMMER MS SHAHRIPOUR A LEE C CHENG XM WALKER DM HALEEN SJ KEISER JA FLYNN MA WELCH KM HALLAK H TAYLOR DG REYNOLDS EE
Citation: Am. Doherty et al., DISCOVERY OF A NOVEL SERIES OF ORALLY-ACTIVE NONPEPTIDE ENDOTHELIN-A (ET(A)) RECEPTOR-SELECTIVE ANTAGONISTS, Journal of medicinal chemistry, 38(8), 1995, pp. 1259-1263
DESIGN AND SYNTHESIS OF RENIN INHIBITORS - INCORPORATION OF TRANSITION-STATE ISOSTERE SIDE-CHAINS THAT SPAN FROM THE S1 TO THE S3 BINDING POCKETS AND EXAMINATION OF P3-MODIFIED RENIN INHIBITORS
Authors: PLUMMER MS SHAHRIPOUR A KALTENBRONN JS LUNNEY EA STEINBAUGH BA HAMBY JM HAMILTON HW SAWYER TK HUMBLET C DOHERTY AM TAYLOR MD HINGORANI G BATLEY BL RAPUNDALO ST
Citation: Ms. Plummer et al., DESIGN AND SYNTHESIS OF RENIN INHIBITORS - INCORPORATION OF TRANSITION-STATE ISOSTERE SIDE-CHAINS THAT SPAN FROM THE S1 TO THE S3 BINDING POCKETS AND EXAMINATION OF P3-MODIFIED RENIN INHIBITORS, Journal of medicinal chemistry, 38(15), 1995, pp. 2893-2905
Risultati: 1-7 |