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Results: 1-7 |
Results: 7
FRIZZLED PROTEINS CONSTITUTE A NOVEL FAMILY OF G-PROTEIN-COUPLED RECEPTORS, MOST CLOSELY-RELATED TO THE SECRETIN FAMILY
Authors: BARNES MR DUCKWORTH DM BEELEY LJ
Citation: Mr. Barnes et al., FRIZZLED PROTEINS CONSTITUTE A NOVEL FAMILY OF G-PROTEIN-COUPLED RECEPTORS, MOST CLOSELY-RELATED TO THE SECRETIN FAMILY, Trends in pharmacological sciences, 19(10), 1998, pp. 399-400
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
(4-METHYL-PIPERIDIN-1-YL)PROPYL]BENZENESULFONAMIDE - THE FIRST SELECTIVE 5-HT7 RECEPTOR ANTAGONIST
Authors: FORBES IT DABBS S DUCKWORTH DM JENNINGS AJ KING FD LOVELL PJ BROWN AM COLLIN L HAGAN JJ MIDDLEMISS DN RILEY GJ THOMAS DR UPTON N
Citation: It. Forbes et al., (4-METHYL-PIPERIDIN-1-YL)PROPYL]BENZENESULFONAMIDE - THE FIRST SELECTIVE 5-HT7 RECEPTOR ANTAGONIST, Journal of medicinal chemistry, 41(5), 1998, pp. 655-657
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
THE IMPACT OF GENOMICS ON DRUG DESIGN
Authors: BEELEY LJ DUCKWORTH DM
Citation: Lj. Beeley et Dm. Duckworth, THE IMPACT OF GENOMICS ON DRUG DESIGN, Drug discovery today, 1(11), 1996, pp. 474-480
CO-CYCLIZATIONS OF NITROGEN-CONTAINING ACETYLENES INDUCED BY A NICKELTRIPHENYLPHOSPHINE COMPLEX TO GIVE AMINOINDANE, ISOINDOLINE AND ISOINDOLINONE DERIVATIVES
Authors: DUCKWORTH DM LEEWONG S SLAWIN AMZ SMITH EH WILLIAMS DJ
Citation: Dm. Duckworth et al., CO-CYCLIZATIONS OF NITROGEN-CONTAINING ACETYLENES INDUCED BY A NICKELTRIPHENYLPHOSPHINE COMPLEX TO GIVE AMINOINDANE, ISOINDOLINE AND ISOINDOLINONE DERIVATIVES, Journal of the Chemical Society. Perkin transactions. I, (8), 1996, pp. 815-821
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
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