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Results: 1-7 |
Results: 7
THE DISCOVERY OF POTENT AND SELECTIVE DOPAMINE-D4 RECEPTOR ANTAGONISTS
Authors: FARACI WS ZORN SH SANNER MA FLIRI A
Citation: Ws. Faraci et al., THE DISCOVERY OF POTENT AND SELECTIVE DOPAMINE-D4 RECEPTOR ANTAGONISTS, Current opinion in chemical biology, 2(4), 1998, pp. 535-540
SYNTHESIS, SAR AND PHARMACOLOGY OF CP-293,019 - A POTENT, SELECTIVE DOPAMINE D-4 RECEPTOR ANTAGONIST
Authors: SANNER MA CHAPPIE TA DUNAISKIS AR FLIRI AF DESAI KA ZORN SH JACKSON ER JOHNSON CG MORRONE JM SEYMOUR PA MAJCHRZAK MJ FARACI WS COLLINS JL DUIGNAN DB DIPRETE CC LEE JS TROZZI A
Citation: Ma. Sanner et al., SYNTHESIS, SAR AND PHARMACOLOGY OF CP-293,019 - A POTENT, SELECTIVE DOPAMINE D-4 RECEPTOR ANTAGONIST, Bioorganic & medicinal chemistry letters, 8(7), 1998, pp. 725-730
SYNTHESIS AND ORAL EFFICACY OF A 4-(BUTYLETHYLAMINO)PYRROLO[2,3-D]PYRIMIDINE - A CENTRALLY ACTIVE CORTICOTROPIN-RELEASING FACTOR(1) RECEPTOR ANTAGONIST
Authors: CHEN YL MANSBACH RS WINTER SM BROOKS E COLLINS J CORMAN ML DUNAISKIS AR FARACI WS GALLASCHUN RJ SCHMIDT A SCHULZ DW
Citation: Yl. Chen et al., SYNTHESIS AND ORAL EFFICACY OF A 4-(BUTYLETHYLAMINO)PYRROLO[2,3-D]PYRIMIDINE - A CENTRALLY ACTIVE CORTICOTROPIN-RELEASING FACTOR(1) RECEPTOR ANTAGONIST, Journal of medicinal chemistry, 40(11), 1997, pp. 1749-1754
POSTTRANSLATIONAL AMINO-ACID EPIMERIZATION - ENZYME-CATALYZED ISOMERIZATION OF AMINO-ACID-RESIDUES IN PEPTIDE CHAINS
Authors: HECK SD FARACI WS KELBAUGH PR SACCOMANO NA THADEIO PF VOLKMANN RA
Citation: Sd. Heck et al., POSTTRANSLATIONAL AMINO-ACID EPIMERIZATION - ENZYME-CATALYZED ISOMERIZATION OF AMINO-ACID-RESIDUES IN PEPTIDE CHAINS, Proceedings of the National Academy of Sciences of the United Statesof America, 93(9), 1996, pp. 4036-4039
2-AMINO-4-METHYLPYRIDINE AS A POTENT INHIBITOR OF INDUCIBLE NO SYNTHASE ACTIVITY IN-VITRO AND IN-VIVO
Authors: FARACI WS NAGEL AA VERDRIES KA VINCENT LA XU H NICHOLS LE LABASI JM SALTER ED PETTIPHER ER
Citation: Ws. Faraci et al., 2-AMINO-4-METHYLPYRIDINE AS A POTENT INHIBITOR OF INDUCIBLE NO SYNTHASE ACTIVITY IN-VITRO AND IN-VIVO, British Journal of Pharmacology, 119(6), 1996, pp. 1101-1108
INHIBITION OF HUMAN-LEUKOCYTE ELASTASE (HLE) BY NOVEL BICYCLIC BETA-LACTAMS
Authors: FARACI WS BAKKER AV SPENCER RW WILLIAMS RA JASYS VJ KELLOGG MS VOLKMANN RA
Citation: Ws. Faraci et al., INHIBITION OF HUMAN-LEUKOCYTE ELASTASE (HLE) BY NOVEL BICYCLIC BETA-LACTAMS, Bioorganic & medicinal chemistry letters, 3(11), 1993, pp. 2271-2276
BERYLLIUM COMPETITIVELY INHIBITS BRAIN MYOINOSITOL MONOPHOSPHATASE, BUT UNLIKE LITHIUM DOES NOT ENHANCE AGONIST-INDUCED INOSITOL PHOSPHATE ACCUMULATION
Authors: FARACI WS ZORN SH BAKKER AV JACKSON E PRATT K
Citation: Ws. Faraci et al., BERYLLIUM COMPETITIVELY INHIBITS BRAIN MYOINOSITOL MONOPHOSPHATASE, BUT UNLIKE LITHIUM DOES NOT ENHANCE AGONIST-INDUCED INOSITOL PHOSPHATE ACCUMULATION, Biochemical journal, 291, 1993, pp. 369-374
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