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Results: 1-7 |
Results: 7
SERINE DERIVED NK1 ANTAGONISTS 1 - THE EFFECT OF MODIFICATIONS TO THESERINE SUBSTITUENTS
Authors: ELLIOTT JM CASCIERI MA CHICCHI G DAVIES S KELLEHER FJ KURTZ M LADDUWAHETTY T LEWIS RT MACLEOD AM MERCHANT KJ SADOWSKI S STEVENSON GI
Citation: Jm. Elliott et al., SERINE DERIVED NK1 ANTAGONISTS 1 - THE EFFECT OF MODIFICATIONS TO THESERINE SUBSTITUENTS, Bioorganic & medicinal chemistry letters, 8(14), 1998, pp. 1845-1850
STEREOSELECTIVITY IN THE BIRCH REDUCTION OF 2-FUROIC ACID-DERIVATIVES
Authors: DONOHOE TJ HELLIWELL M STEVENSON CA LADDUWAHETTY T
Citation: Tj. Donohoe et al., STEREOSELECTIVITY IN THE BIRCH REDUCTION OF 2-FUROIC ACID-DERIVATIVES, Tetrahedron letters, 39(19), 1998, pp. 3071-3074
4,4-DISUBSTITUTED PIPERIDINE HIGH-AFFINITY NK1 ANTAGONISTS - STRUCTURE-ACTIVITY-RELATIONSHIPS AND IN-VIVO ACTIVITY
Authors: STEVENSON GI HUSCROFT I MACLEOD AM SWAIN CJ CASCIERI MA CHICCHI GG GRAHAM MI HARRISON T KELLEHER FJ KURTZ M LADDUWAHETTY T MERCHANT KJ METZGER JM MACINTYRE DE SADOWSKI S SOHAL B OWENS AP
Citation: Gi. Stevenson et al., 4,4-DISUBSTITUTED PIPERIDINE HIGH-AFFINITY NK1 ANTAGONISTS - STRUCTURE-ACTIVITY-RELATIONSHIPS AND IN-VIVO ACTIVITY, Journal of medicinal chemistry, 41(23), 1998, pp. 4623-4635
3-BENZYLOXY-2-PHENYLPIPERIDINE NK1 ANTAGONISTS - THE INFLUENCE OF ALPHA-METHYL SUBSTITUTION
Authors: SWAIN CJ WILLIAMS BJ BAKER R CASCIERI MA CHICCHI G FORREST M HERBERT R KEOWN L LADDUWAHETTY T LUELL S MACINTYRE DE METZGER J MORTON S OWENS AP SADOWSKI S WATT AP
Citation: Cj. Swain et al., 3-BENZYLOXY-2-PHENYLPIPERIDINE NK1 ANTAGONISTS - THE INFLUENCE OF ALPHA-METHYL SUBSTITUTION, Bioorganic & medicinal chemistry letters, 7(23), 1997, pp. 2959-2962
TACHYKININ NK1 RECEPTOR ANTAGONISTS ACT CENTRALLY TO INHIBIT EMESIS INDUCED BY THE CHEMOTHERAPEUTIC AGENT CISPLATIN IN FERRETS
Authors: TATTERSALL FD RYCROFT W FRANCIS B PEARCE D MERCHANT K MACLEOD AM LADDUWAHETTY T KEOWN L SWAIN C BAKER R CASCIERI M BER E METZGER J MACINTYRE DE HILL RG HARGREAVES RJ
Citation: Fd. Tattersall et al., TACHYKININ NK1 RECEPTOR ANTAGONISTS ACT CENTRALLY TO INHIBIT EMESIS INDUCED BY THE CHEMOTHERAPEUTIC AGENT CISPLATIN IN FERRETS, Neuropharmacology, 35(8), 1996, pp. 1121-1129
N-HETEROARYL-2-PHENYL-3-(BENZYLOXY)PIPERIDINES - A NOVEL CLASS OF POTENT ORALLY-ACTIVE HUMAN NK1 ANTAGONISTS
Authors: LADDUWAHETTY T BAKER R CASCIERI MA CHAMBERS MS HAWORTH K KEOWN LE MACINTYRE DE METZGER JM OWEN S RYCROFT W SADOWSKI S SEWARD EM SHEPHEARD SL SWAIN CJ TATTERSALL FD WATT AP WILLIAMSON DW HARGREAVES RJ
Citation: T. Ladduwahetty et al., N-HETEROARYL-2-PHENYL-3-(BENZYLOXY)PIPERIDINES - A NOVEL CLASS OF POTENT ORALLY-ACTIVE HUMAN NK1 ANTAGONISTS, Journal of medicinal chemistry, 39(15), 1996, pp. 2907-2914
MORPHOLINE-BASED SUBSTANCE-P ANTAGONISTS - ASSESSMENT OF THE 3-POINT BINDING MODEL
Authors: LADDUWAHETTY T KEOWN L CASCIERI MA SADOWSKI S
Citation: T. Ladduwahetty et al., MORPHOLINE-BASED SUBSTANCE-P ANTAGONISTS - ASSESSMENT OF THE 3-POINT BINDING MODEL, Bioorganic & medicinal chemistry letters, 4(16), 1994, pp. 1917-1920
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