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Results: 1-23 |
Results: 23
EFFECTS OF THE NOVEL HIGH-AFFINITY 5-HT1B 1D-RECEPTOR LIGAND FROVATRIPTAN IN HUMAN ISOLATED BASILAR AND CORONARY-ARTERIES/
Authors: PARSONS AA RAVAL P SMITH S TILFORD N KING FD KAUMANN AJ HUNTER J
Citation: Aa. Parsons et al., EFFECTS OF THE NOVEL HIGH-AFFINITY 5-HT1B 1D-RECEPTOR LIGAND FROVATRIPTAN IN HUMAN ISOLATED BASILAR AND CORONARY-ARTERIES/, Journal of cardiovascular pharmacology, 32(2), 1998, pp. 220-224
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
MATH METHODS IN TRANSISTOR MODELING - CONDITION NUMBERS FOR PARAMETEREXTRACTION
Authors: KING FD WINSON P SNIDER AD DUNLEAVY L LEVINSON DP
Citation: Fd. King et al., MATH METHODS IN TRANSISTOR MODELING - CONDITION NUMBERS FOR PARAMETEREXTRACTION, IEEE transactions on microwave theory and techniques, 46(9), 1998, pp. 1313-1314
SEROTONIN 5-HT3 AND 5-HT4 RECEPTOR ANTAGONISTS
Authors: GASTER LM KING FD
Citation: Lm. Gaster et Fd. King, SEROTONIN 5-HT3 AND 5-HT4 RECEPTOR ANTAGONISTS, Medicinal research reviews, 17(2), 1997, pp. 163-214
COMPARISON OF THE CARDIOVASCULAR EFFECTS OF THE NOVEL 5-HT1B 1D RECEPTOR AGONIST, SB-209509 (VML251), AND SUMATRIPTAN IN DOGS/
Authors: PARSONS AA PARKER SG RAVAL P CAMPBELL CA LEWIS VA GRIFFITHS R HUNTER AJ HAMILTON TC KING FD
Citation: Aa. Parsons et al., COMPARISON OF THE CARDIOVASCULAR EFFECTS OF THE NOVEL 5-HT1B 1D RECEPTOR AGONIST, SB-209509 (VML251), AND SUMATRIPTAN IN DOGS/, Journal of cardiovascular pharmacology, 30(1), 1997, pp. 136-141
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
COMPARISON OF THE CARDIOVASCULAR EFFECTS OF SB-209509 (VML-251) AND SUMATRIPTAN IN DOGS
Authors: PARSONS AA PARKER SG RAVAL P CAMPBELL CA HUNTER AJ HAMILTON TC KING FD
Citation: Aa. Parsons et al., COMPARISON OF THE CARDIOVASCULAR EFFECTS OF SB-209509 (VML-251) AND SUMATRIPTAN IN DOGS, British Journal of Pharmacology, 119, 1996, pp. 109-109
SB-209509 (VML-251), A POTENT CONSTRICTOR OF RABBIT BASILAR ARTERY WITH HIGH-AFFINITY AND SELECTIVITY FOR HUMAN 5-HT1D RECEPTORS
Authors: BROWN AM PARSONS AA RAVAL P PORTER R TILFORD NS GAGER TL PRICE GW WOOD MD KAUMANN AJ YOUNG RA RANA K WARRINGTON BH KING FD
Citation: Am. Brown et al., SB-209509 (VML-251), A POTENT CONSTRICTOR OF RABBIT BASILAR ARTERY WITH HIGH-AFFINITY AND SELECTIVITY FOR HUMAN 5-HT1D RECEPTORS, British Journal of Pharmacology, 119, 1996, pp. 110-110
A COMPARISON OF THE AGONIST PROFILE OF SB-209509 (VML-251) AND SUMATRIPTAN IN HUMAN ISOLATED BASILAR AND CORONARY-ARTERIES
Authors: RAVAL P TILFORD NS SMITH SJ PORTER R KING FD KAUMANN AJ HUNER AJ PARSONS AA
Citation: P. Raval et al., A COMPARISON OF THE AGONIST PROFILE OF SB-209509 (VML-251) AND SUMATRIPTAN IN HUMAN ISOLATED BASILAR AND CORONARY-ARTERIES, British Journal of Pharmacology, 119, 1996, pp. 111-111
THE SYNTHESIS, AND DOPAMINE D-2 AND SEROTONIN 5-HT3 RECEPTOR AFFINITYOF 3-AZA ANALOGS (PYRIDYL) OF 4-AMINO-5-CHLORO-2-METHOXYBENZAMIDES
Authors: COLDWELL MC GADRE A JERMAN J KING FD NASH D
Citation: Mc. Coldwell et al., THE SYNTHESIS, AND DOPAMINE D-2 AND SEROTONIN 5-HT3 RECEPTOR AFFINITYOF 3-AZA ANALOGS (PYRIDYL) OF 4-AMINO-5-CHLORO-2-METHOXYBENZAMIDES, Bioorganic & medicinal chemistry letters, 5(1), 1995, pp. 39-42
SYNTHESIS OF (ENDO) 3,9-DISUBSTITUTED DIAZABICYCLO[3.3.1]NONAN-7-AMINES
Authors: GREGORY JA JENNINGS AJ JOINER GF KING FD RAHMAN SK
Citation: Ja. Gregory et al., SYNTHESIS OF (ENDO) 3,9-DISUBSTITUTED DIAZABICYCLO[3.3.1]NONAN-7-AMINES, Tetrahedron letters, 36(1), 1995, pp. 155-158
IHYDRO-2H-[1,3]OXAZINO[3,2-A]INDOLE-10-CARBOXAMIDE HYDROCHLORIDE - THE FIRST POTENT AND SELECTIVE 5-HT4 RECEPTOR ANTAGONIST AMIDE WITH ORALACTIVITY
Authors: GASTER LM JOINER GF KING FD WYMAN PA SUTTON JM BINGHAM S ELLIS ES SANGER GJ WARDLE KA
Citation: Lm. Gaster et al., IHYDRO-2H-[1,3]OXAZINO[3,2-A]INDOLE-10-CARBOXAMIDE HYDROCHLORIDE - THE FIRST POTENT AND SELECTIVE 5-HT4 RECEPTOR ANTAGONIST AMIDE WITH ORALACTIVITY, Journal of medicinal chemistry, 38(24), 1995, pp. 4760-4763
SYNTHESIS AND 5-HT3 RECEPTOR ANTAGONIST POTENCY OF NOVEL (ENDO) 3,9-DIAZABICYCLO[3.3.1]NONAN-7-AMINO DERIVATIVES
Authors: BERMUDEZ J GASTER L GREGORY J JERMAN J JOINER GF KING FD RAHMAN SK
Citation: J. Bermudez et al., SYNTHESIS AND 5-HT3 RECEPTOR ANTAGONIST POTENCY OF NOVEL (ENDO) 3,9-DIAZABICYCLO[3.3.1]NONAN-7-AMINO DERIVATIVES, Bioorganic & medicinal chemistry letters, 4(20), 1994, pp. 2373-2376
BLOCKADE OF HUMAN ATRIAL 5-HT4 RECEPTORS BY SB-207710, A SELECTIVE AND HIGH-AFFINITY 5-HT4 RECEPTOR ANTAGONIST
Authors: KAUMANN AJ GASTER LM KING FD BROWN AM
Citation: Aj. Kaumann et al., BLOCKADE OF HUMAN ATRIAL 5-HT4 RECEPTORS BY SB-207710, A SELECTIVE AND HIGH-AFFINITY 5-HT4 RECEPTOR ANTAGONIST, Naunyn-Schmiedeberg's archives of pharmacology, 349(5), 1994, pp. 546-548
(1-BUTYL-4-PIPERIDINYL)METHYL 8-AMINO-7-CHLORO-1,4-BENZODIOXANE-5-CARBOXYLATE HYDROCHLORIDE - A HIGHLY POTENT AND SELECTIVE 5-HT4 RECEPTOR ANTAGONIST DERIVED FROM METOCLOPRAMIDE
Authors: GASTER LM JENNINGS AJ JOINER GF KING FD MULHOLLAND KR RAHMAN SK STARR S WYMAN PA WARDLE KA ELLIS ES SANGER GJ
Citation: Lm. Gaster et al., (1-BUTYL-4-PIPERIDINYL)METHYL 8-AMINO-7-CHLORO-1,4-BENZODIOXANE-5-CARBOXYLATE HYDROCHLORIDE - A HIGHLY POTENT AND SELECTIVE 5-HT4 RECEPTOR ANTAGONIST DERIVED FROM METOCLOPRAMIDE, Journal of medicinal chemistry, 36(25), 1993, pp. 4121-4123
)3-AMINO-6-CARBOXAMIDO-1,2,3,4-TETRAHYDROCARBAZOLE - A CONFORMATIONALLY RESTRICTED ANALOG OF 5-CARBOXAMIDOTRYPTAMINE WITH SELECTIVITY FOR THE SEROTONIN 5-HT1D RECEPTOR (VOL 36, PG 1919, 1993)
Authors: KING FD BROWN AM GASTER LM KAUMANN AJ MEDHURST AD PARKER SG PARSONS AA PATCH TL RAVAL P
Citation: Fd. King et al., )3-AMINO-6-CARBOXAMIDO-1,2,3,4-TETRAHYDROCARBAZOLE - A CONFORMATIONALLY RESTRICTED ANALOG OF 5-CARBOXAMIDOTRYPTAMINE WITH SELECTIVITY FOR THE SEROTONIN 5-HT1D RECEPTOR (VOL 36, PG 1919, 1993), Journal of medicinal chemistry, 36(21), 1993, pp. 3218-3218
(+ -) 3-AMINO-6-CARBOXAMIDO-1,2,3,4-TETRAHYDROCARBAZOLE - A CONFORMATIONALLY RESTRICTED ANALOG OF 5-CARBOXAMIDOTRYPTAMINE WITH SELECTIVITY FOR THE SEROTONIN 5-HT1D RECEPTOR/
Authors: KING FD BROWN AM GASTER LM KAUMANN AJ MEDHURST AD PARKER SG PARSONS AA PATCH TL RAVAL P
Citation: Fd. King et al., (+ -) 3-AMINO-6-CARBOXAMIDO-1,2,3,4-TETRAHYDROCARBAZOLE - A CONFORMATIONALLY RESTRICTED ANALOG OF 5-CARBOXAMIDOTRYPTAMINE WITH SELECTIVITY FOR THE SEROTONIN 5-HT1D RECEPTOR/, Journal of medicinal chemistry, 36(13), 1993, pp. 1918-1919
ENHANCED THERMAL-STABILITY OF SINTERED (ND,DY)(FE,CO)B MAGNETS BY THEADDITION OF TA OR TI
Authors: CHIN TS LIN CH HUANG YH YAU JM HEH SJ KING FD
Citation: Ts. Chin et al., ENHANCED THERMAL-STABILITY OF SINTERED (ND,DY)(FE,CO)B MAGNETS BY THEADDITION OF TA OR TI, IEEE transactions on magnetics, 29(6), 1993, pp. 2788-2790
[I-125] SB-207710, A POTENT, SELECTIVE RADIOLIGAND FOR 5-HT(4) RECEPTORS
Authors: BROWN AM YOUNG TJ PATCH TL CHEUNG CW KAUMANN AJ GASTER L KING FD
Citation: Am. Brown et al., [I-125] SB-207710, A POTENT, SELECTIVE RADIOLIGAND FOR 5-HT(4) RECEPTORS, British Journal of Pharmacology, 110, 1993, pp. 160000010-160000010
SB-204070 - A HIGHLY POTENT AND SELECTIVE 5-HT4 RECEPTOR ANTAGONIST
Authors: WARDLE KA ELLIS ES GASTER LM KING FD SANGER GJ
Citation: Ka. Wardle et al., SB-204070 - A HIGHLY POTENT AND SELECTIVE 5-HT4 RECEPTOR ANTAGONIST, British Journal of Pharmacology, 110, 1993, pp. 160000015-160000015
Risultati: 1-23 |