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Results: 1-14 |
Results: 14
A NOVEL AND T-CELL SPECIFIC DUAL INHIBITOR OF NF-KAPPA-B AND AP-1 SUPPRESSES ALLOREACTIVITY IN MICE THROUGH ITS ANTIPROLIFERATIVE EFFECT MEDIATED BY INHIBITION OF IL-2 PRODUCTION
Authors: MORIKAWA M SHERWOOD SW SHORTHOUSE R SUTO MJ MANNING AM MORRIS RE
Citation: M. Morikawa et al., A NOVEL AND T-CELL SPECIFIC DUAL INHIBITOR OF NF-KAPPA-B AND AP-1 SUPPRESSES ALLOREACTIVITY IN MICE THROUGH ITS ANTIPROLIFERATIVE EFFECT MEDIATED BY INHIBITION OF IL-2 PRODUCTION, The FASEB journal, 12(5), 1998, pp. 5376-5376
SOLUTION-PHASE PARALLEL SYNTHESIS USING ION-EXCHANGE RESINS
Authors: SUTO MJ GAYOFUNG LM PALANKI MSS SULLIVAN R
Citation: Mj. Suto et al., SOLUTION-PHASE PARALLEL SYNTHESIS USING ION-EXCHANGE RESINS, Tetrahedron, 54(16), 1998, pp. 4141-4150
A GENERAL AND REGIOSPECIFIC SYNTHESIS OF 5,8-DISUBSTITUTED ALPHA-TETRALONES
Authors: ROSEN MD DOUBLEDAY MD SUTO MJ
Citation: Md. Rosen et al., A GENERAL AND REGIOSPECIFIC SYNTHESIS OF 5,8-DISUBSTITUTED ALPHA-TETRALONES, Synthetic communications, 28(18), 1998, pp. 3491-3502
5-N-(3',5'-BIS(TRIFLUOROMETHYL)PHRNYL)-CARBOXAMIDE - A POTENT INHIBITOR OF NF-KAPPA-B-MEDIATED AND AP-1-MEDIATED GENE-EXPRESSION IDENTIFIEDUSING SOLUTION-PHASE COMBINATORIAL CHEMISTRY
Authors: SULLIVAN RW BIGAM CG ERDMAN PE PALANKI MSS ANDERSON DW GOLDMAN ME RANSONE LJ SUTO MJ
Citation: Rw. Sullivan et al., 5-N-(3',5'-BIS(TRIFLUOROMETHYL)PHRNYL)-CARBOXAMIDE - A POTENT INHIBITOR OF NF-KAPPA-B-MEDIATED AND AP-1-MEDIATED GENE-EXPRESSION IDENTIFIEDUSING SOLUTION-PHASE COMBINATORIAL CHEMISTRY, Journal of medicinal chemistry, 41(4), 1998, pp. 413-419
A NOVEL INHIBITOR OF NUCLEAR FACTOR-KAPPA-B AND ACTIVATOR PROTEIN-1, TRANSCRIPTION FACTORS IN T-CELLS SUPPRESSES HOST-VERSUS-GRAFT ALLOREACTIVITY IN-VIVO
Authors: MORIKAWA M SHORTHOUSE RA SUTO MJ GOLDMAN ME MORRIS RE
Citation: M. Morikawa et al., A NOVEL INHIBITOR OF NUCLEAR FACTOR-KAPPA-B AND ACTIVATOR PROTEIN-1, TRANSCRIPTION FACTORS IN T-CELLS SUPPRESSES HOST-VERSUS-GRAFT ALLOREACTIVITY IN-VIVO, Transplantation proceedings, 29(1-2), 1997, pp. 1269-1270
ION-EXCHANGE RESINS FOR SOLUTION-PHASE PARALLEL SYNTHESIS OF CHEMICALLIBRARIES
Authors: GAYO LM SUTO MJ
Citation: Lm. Gayo et Mj. Suto, ION-EXCHANGE RESINS FOR SOLUTION-PHASE PARALLEL SYNTHESIS OF CHEMICALLIBRARIES, Tetrahedron letters, 38(4), 1997, pp. 513-516
TRACELESS LINKER - OXIDATIVE ACTIVATION AND DISPLACEMENT OF A SULFUR-BASED LINKER
Authors: GAYO LM SUTO MJ
Citation: Lm. Gayo et Mj. Suto, TRACELESS LINKER - OXIDATIVE ACTIVATION AND DISPLACEMENT OF A SULFUR-BASED LINKER, Tetrahedron letters, 38(2), 1997, pp. 211-214
PEPTIDE INHIBITORS OF I-KAPPA-B PROTEASE - MODIFICATION OF THE C-TERMINI OF Z-LLF-CHO
Authors: SUTO MJ SULLIVAN RW RANSONE LJ
Citation: Mj. Suto et al., PEPTIDE INHIBITORS OF I-KAPPA-B PROTEASE - MODIFICATION OF THE C-TERMINI OF Z-LLF-CHO, Bioorganic & medicinal chemistry letters, 6(24), 1996, pp. 2925-2930
SP100030 IS A NOVEL T-CELL-SPECIFIC TRANSCRIPTION FACTOR INHIBITOR THAT POSSESSES IMMUNOSUPPRESSIVE ACTIVITY IN-VIVO
Authors: GOLDMAN ME RANSONE LJ ANDERSON DE GAARDE WA SUTO MJ SULLIVAN RW SHORTHOUSE R MORIKAWA M MORRIS RE
Citation: Me. Goldman et al., SP100030 IS A NOVEL T-CELL-SPECIFIC TRANSCRIPTION FACTOR INHIBITOR THAT POSSESSES IMMUNOSUPPRESSIVE ACTIVITY IN-VIVO, Transplantation proceedings, 28(6), 1996, pp. 3106-3109
USE OF PENTAFLUOROPHENYL ESTERS FOR ONE-POT PROTECTION ACTIVATION OF AMINO AND THIOL CARBOXYLIC-ACIDS
Authors: GAYO LM SUTO MJ
Citation: Lm. Gayo et Mj. Suto, USE OF PENTAFLUOROPHENYL ESTERS FOR ONE-POT PROTECTION ACTIVATION OF AMINO AND THIOL CARBOXYLIC-ACIDS, Tetrahedron letters, 37(28), 1996, pp. 4915-4918
SYNTHESIS OF BOXAZOMYCIN B AND RELATED ANALOGS
Authors: SUTO MJ TURNER WR
Citation: Mj. Suto et Wr. Turner, SYNTHESIS OF BOXAZOMYCIN B AND RELATED ANALOGS, Tetrahedron letters, 36(40), 1995, pp. 7213-7216
AN EFFICIENT METHOD FOR THE SYNTHESIS OF (R)-3-(1-AMINO-1-METHYLETHYL)PYRROLIDINES FOR THE ANTIINFECTIVE AGENT, PD-138312
Authors: FEDIJ V LENOIR EA SUTO MJ ZELLER JR WEMPLE J
Citation: V. Fedij et al., AN EFFICIENT METHOD FOR THE SYNTHESIS OF (R)-3-(1-AMINO-1-METHYLETHYL)PYRROLIDINES FOR THE ANTIINFECTIVE AGENT, PD-138312, Tetrahedron : asymmetry, 5(7), 1994, pp. 1131-1134
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
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
STEREOSELECTIVE MICHAEL ADDITIONS OF NITROMETHANE YIELDING 3R(1S N-SUBSTITUTED AMINOETHYL)PYRROLIDINES
Authors: PLUMMER JS EMERY LA STIER MA SUTO MJ
Citation: Js. Plummer et al., STEREOSELECTIVE MICHAEL ADDITIONS OF NITROMETHANE YIELDING 3R(1S N-SUBSTITUTED AMINOETHYL)PYRROLIDINES, Tetrahedron letters, 34(47), 1993, pp. 7529-7532
Risultati: 1-14 |