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Results: 1-10 |
Results: 10
HIGHLY ENANTIOSELECTIVE CHIRAL BASE-MEDIATED [2,3]-WITTIG REARRANGEMENT
Authors: GIBSON SE HAM P JEFFERSON GR
Citation: Se. Gibson et al., HIGHLY ENANTIOSELECTIVE CHIRAL BASE-MEDIATED [2,3]-WITTIG REARRANGEMENT, Chemical communications, (1), 1998, pp. 123-124
THE SELECTIVE 5-HT1B RECEPTOR INVERSE AGONIST TETRAHYDROSPIRO[FURO[2,3-F]INDOLE-3,4'-PIPERIDINE] (SB-224289) POTENTLY BLOCKS TERMINAL 5-HT AUTORECEPTOR FUNCTION BOTH IN-VITRO AND IN-VIVO
Authors: GASTER LM BLANEY FE DAVIES S DUCKWORTH DM HAM P JENKINS S JENNINGS AJ JOINER GF KING FD MULHOLLAND KR WYMAN PA HAGAN JJ HATCHER J JONES BJ MIDDLEMISS DN PRICE GW RILEY G ROBERTS C ROUTLEDGE C SELKIRK J SLADE PD
Citation: Lm. Gaster et al., THE SELECTIVE 5-HT1B RECEPTOR INVERSE AGONIST TETRAHYDROSPIRO[FURO[2,3-F]INDOLE-3,4'-PIPERIDINE] (SB-224289) POTENTLY BLOCKS TERMINAL 5-HT AUTORECEPTOR FUNCTION BOTH IN-VITRO AND IN-VIVO, Journal of medicinal chemistry, 41(8), 1998, pp. 1218-1235
NOVEL AND SELECTIVE 5-HT2C 2B RECEPTOR ANTAGONISTS AS POTENTIAL ANXIOLYTIC AGENTS - SYNTHESIS, QUANTITATIVE STRUCTURE-ACTIVITY-RELATIONSHIPS, AND MOLECULAR MODELING OF SUBSTITUTED 1-(3-PYRIDYLCARBAMOYL)INDOLINES/
Authors: BROMIDGE SM DABBS S DAVIES DT DUCKWORTH DM FORBES IT HAM P JONES GE KING FD SAUNDERS DV STARR S THEWLIS KM WYMAN PA BLANEY FE NAYLOR CB BAILEY F BLACKBURN TP HOLLAND V KENNETT GA RILEY GJ WOOD MD
Citation: Sm. Bromidge et al., NOVEL AND SELECTIVE 5-HT2C 2B RECEPTOR ANTAGONISTS AS POTENTIAL ANXIOLYTIC AGENTS - SYNTHESIS, QUANTITATIVE STRUCTURE-ACTIVITY-RELATIONSHIPS, AND MOLECULAR MODELING OF SUBSTITUTED 1-(3-PYRIDYLCARBAMOYL)INDOLINES/, Journal of medicinal chemistry, 41(10), 1998, pp. 1598-1612
CHIRAL BASE-MEDIATED ASYMMETRIC FUNCTIONALIZATION OF TRICARBONYLCHROMIUM(0) COMPLEXES OF BENZYL SULFIDES
Authors: GIBSON SE HAM P JEFFERSON GR SMITH MH
Citation: Se. Gibson et al., CHIRAL BASE-MEDIATED ASYMMETRIC FUNCTIONALIZATION OF TRICARBONYLCHROMIUM(0) COMPLEXES OF BENZYL SULFIDES, Journal of the Chemical Society. Perkin transactions. I, (15), 1997, pp. 2161-2162
ETHYL-3-PYRIDYL)OXY]-5-PYRIDYL]CARBAMOYL]-INDOLINE (SB-242084) - THE FIRST SELECTIVE AND BRAIN PENETRANT 5-HT2C RECEPTOR ANTAGONIST
Authors: BROMIDGE SM DUCKWORTH M FORBES IT HAM P KING FD THEWLIS KM BLANEY FE NAYLOR CB BLACKBURN TP KENNETT GA WOOD MD CLARKE SE
Citation: Sm. Bromidge et al., ETHYL-3-PYRIDYL)OXY]-5-PYRIDYL]CARBAMOYL]-INDOLINE (SB-242084) - THE FIRST SELECTIVE AND BRAIN PENETRANT 5-HT2C RECEPTOR ANTAGONIST, Journal of medicinal chemistry, 40(22), 1997, pp. 3494-3496
SYNTHESIS, BIOLOGICAL-ACTIVITY, AND MOLECULAR MODELING STUDIES OF SELECTIVE 5-HT2C 2B RECEPTOR ANTAGONISTS/
Authors: FORBES IT DABBS S DUCKWORTH DM HAM P JONES GE KING FD SAUNDERS DV BLANEY FE NAYLOR CB BAXTER GS BLACKBURN TP KENNETT GA WOOD MD
Citation: It. Forbes et al., SYNTHESIS, BIOLOGICAL-ACTIVITY, AND MOLECULAR MODELING STUDIES OF SELECTIVE 5-HT2C 2B RECEPTOR ANTAGONISTS/, Journal of medicinal chemistry, 39(25), 1996, pp. 4966-4977
IN-VITRO AND IN-VIVO PROFILE OF SB-206553, A POTENT 5-HT2C 5-HT2B RECEPTOR ANTAGONIST WITH ANXIOLYTIC-LIKE PROPERTIES/
Authors: KENNETT GA WOOD MD BRIGHT F CILIA J PIPER DC GAGER T THOMAS D BAXTER GS FORBES IT HAM P BLACKBURN TP
Citation: Ga. Kennett et al., IN-VITRO AND IN-VIVO PROFILE OF SB-206553, A POTENT 5-HT2C 5-HT2B RECEPTOR ANTAGONIST WITH ANXIOLYTIC-LIKE PROPERTIES/, British Journal of Pharmacology, 117(3), 1996, pp. 427-434
LCARBAMOYL)-1,2,3,5-TETRAHYDROPYRROLO[2,3-F]INDOLE - A NOVEL 5-HT2C 5-HT2B RECEPTOR ANTAGONIST WITH IMPROVED AFFINITY, SELECTIVITY, AND ORAL ACTIVITY
Authors: FORBES IT HAM P BOOTH DH MARTIN RT THOMPSON M BAXTER GS BLACKBURN TP GLEN A KENNETT GA WOOD MD
Citation: It. Forbes et al., LCARBAMOYL)-1,2,3,5-TETRAHYDROPYRROLO[2,3-F]INDOLE - A NOVEL 5-HT2C 5-HT2B RECEPTOR ANTAGONIST WITH IMPROVED AFFINITY, SELECTIVITY, AND ORAL ACTIVITY, Journal of medicinal chemistry, 38(14), 1995, pp. 2524-2530
THE IDENTIFICATION OF A NOVEL RENIN INHIBITOR OF EQUIVALENT EFFICACY FOLLOWING ORAL OR INTRAVENOUS ADMINISTRATION
Authors: SMITH SA ALBARAZANJI KA BUCKINGHAM RE CASSIDY F COLDWELL MC FINNEY FJL HADLEY MS HAM P LAWRENCE SA NASH DJ TINGLEY EJR WATSON JM
Citation: Sa. Smith et al., THE IDENTIFICATION OF A NOVEL RENIN INHIBITOR OF EQUIVALENT EFFICACY FOLLOWING ORAL OR INTRAVENOUS ADMINISTRATION, Bioorganic & medicinal chemistry letters, 4(11), 1994, pp. 1291-1296
N-(1-METHYL-5-INDOLYL)-N'-(3-PYRIDYL)UREA HYDROCHLORIDE - THE 1ST SELECTIVE 5-HT(1C) RECEPTOR ANTAGONIST
Authors: FORBES IT KENNETT GA GADRE A HAM P HAYWARD CJ MARTIN RT THOMPSON M WOOD MD BAXTER GS GLEN A MURPHY OE STEWART BA BLACKBURN TP
Citation: It. Forbes et al., N-(1-METHYL-5-INDOLYL)-N'-(3-PYRIDYL)UREA HYDROCHLORIDE - THE 1ST SELECTIVE 5-HT(1C) RECEPTOR ANTAGONIST, Journal of medicinal chemistry, 36(8), 1993, pp. 1104-1107
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