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Results: 1-9 |
Results: 9
DEVELOPMENT OF A SENSITIVE AND QUANTITATIVE ANALYTICAL METHOD FOR 1H-4-SUBSTITUTED IMIDAZOLE HISTAMINE H-3-RECEPTOR ANTAGONISTS UTILIZING HIGH-PERFORMANCE LIQUID-CHROMATOGRAPHY AND DABSYL DERIVATIZATION
Authors: HANDLEY MK HIRTH WW PHILLIPS JG ALI SM KHAN A FADNIS L TEDFORD CE
Citation: Mk. Handley et al., DEVELOPMENT OF A SENSITIVE AND QUANTITATIVE ANALYTICAL METHOD FOR 1H-4-SUBSTITUTED IMIDAZOLE HISTAMINE H-3-RECEPTOR ANTAGONISTS UTILIZING HIGH-PERFORMANCE LIQUID-CHROMATOGRAPHY AND DABSYL DERIVATIZATION, Journal of chromatography B. Biomedical sciences and applications, 716(1-2), 1998, pp. 239-249
NEW ACETYLENE BASED HISTAMINE H-2-RECEPTOR ANTAGONISTS DERIVED FROM THE MARINE NATURAL PRODUCT VERONGAMINE
Authors: ALI SM TEDFORD CE GREGORY R YATES SL PHILLIPS JG
Citation: Sm. Ali et al., NEW ACETYLENE BASED HISTAMINE H-2-RECEPTOR ANTAGONISTS DERIVED FROM THE MARINE NATURAL PRODUCT VERONGAMINE, Bioorganic & medicinal chemistry letters, 8(10), 1998, pp. 1133-1138
RECENT ADVANCES IN THE DEVELOPMENT OF HISTAMINE H-3 RECEPTOR LIGANDS
Authors: TEDFORD CE YATES SL GREGORY R PAWLOWSKI GP KHAN MA ALI SM FADNIS L PHILLIPS JG
Citation: Ce. Tedford et al., RECENT ADVANCES IN THE DEVELOPMENT OF HISTAMINE H-3 RECEPTOR LIGANDS, Naunyn-Schmiedeberg's archives of pharmacology, 358(1), 1998, pp. 117-117
RECENT ADVANCES IN THE DEVELOPMENT OF HISTAMINE H-3 RECEPTOR LIGANDS
Authors: TEDFORD CE YATES SL GREGORY R PAWLOWSKI GP KHAN MA ALI SM FADNIS L PHILLIPS JG
Citation: Ce. Tedford et al., RECENT ADVANCES IN THE DEVELOPMENT OF HISTAMINE H-3 RECEPTOR LIGANDS, Naunyn-Schmiedeberg's archives of pharmacology, 358(1), 1998, pp. 98-98
HIGH ANTAGONIST POTENCY OF GT-2227 AND GT-2331, NEW HISTAMINE H-3 RECEPTOR ANTAGONISTS, IN 2 FUNCTIONAL MODELS
Authors: TEDFORD CE HOFFMANN M SEYEDI N MARUYAMA R LEVI R YATES SL ALI SM PHILLIPS JG
Citation: Ce. Tedford et al., HIGH ANTAGONIST POTENCY OF GT-2227 AND GT-2331, NEW HISTAMINE H-3 RECEPTOR ANTAGONISTS, IN 2 FUNCTIONAL MODELS, European journal of pharmacology, 351(3), 1998, pp. 307-311
DIASTEREOSELECTIVE SYNTHESIS OF ENYLMETHYL-1H-IMIDAZOL-4-YL)CYCLOPROPANECARBOXYLIC ACIDS - KEY INTERMEDIATES FOR THE PREPARATION OF POTENT AND CHIRAL HISTAMINE H-3 RECEPTOR AGENTS
Authors: KHAN MA YATES SL TEDFORD CE KIRSCHBAUM K PHILLIPS JG
Citation: Ma. Khan et al., DIASTEREOSELECTIVE SYNTHESIS OF ENYLMETHYL-1H-IMIDAZOL-4-YL)CYCLOPROPANECARBOXYLIC ACIDS - KEY INTERMEDIATES FOR THE PREPARATION OF POTENT AND CHIRAL HISTAMINE H-3 RECEPTOR AGENTS, Bioorganic & medicinal chemistry letters, 7(23), 1997, pp. 3017-3022
PHARMACOLOGICAL CHARACTERIZATION OF GT-2016, A NON-THIOUREA-CONTAINING HISTAMINE H3 RECEPTOR ANTAGONIST - IN-VITRO AND IN-VIVO STUDIES
Authors: TEDFORD CE YATES SL PAWLOWSKI GP NALWALK JW HOUGH LB KHAN MA PHILLIPS JG DURANT GJ FREDERICKSON RCA
Citation: Ce. Tedford et al., PHARMACOLOGICAL CHARACTERIZATION OF GT-2016, A NON-THIOUREA-CONTAINING HISTAMINE H3 RECEPTOR ANTAGONIST - IN-VITRO AND IN-VIVO STUDIES, The Journal of pharmacology and experimental therapeutics, 275(2), 1995, pp. 598-604
STUDIES ON THE GLUCURONIDATION OF DOPAMINE-D-1 RECEPTOR ANTAGONISTS, SCH-39166 AND SCH-23390, BY HUMAN LIVER-MICROSOMES
Authors: TEPHLY TR COFFMAN B STYCZYNSKI P RIOS G CHARKOWSKI DM VANROLLINS M MCQUADE RD TEDFORD CE
Citation: Tr. Tephly et al., STUDIES ON THE GLUCURONIDATION OF DOPAMINE-D-1 RECEPTOR ANTAGONISTS, SCH-39166 AND SCH-23390, BY HUMAN LIVER-MICROSOMES, Drug metabolism and disposition, 22(5), 1994, pp. 713-718
DETERMINATION OF PLASMA AND BRAIN CONCENTRATIONS OF SCH-39166 AND THEIR CORRELATION TO CONDITIONED AVOIDANCE-BEHAVIOR IN RATS
Authors: TEDFORD CE COFFIN VL RUPERTO V COHEN M MCQUADE RD JOHNSON R KIM HK LIN CC
Citation: Ce. Tedford et al., DETERMINATION OF PLASMA AND BRAIN CONCENTRATIONS OF SCH-39166 AND THEIR CORRELATION TO CONDITIONED AVOIDANCE-BEHAVIOR IN RATS, Psychopharmacology, 113(2), 1993, pp. 199-204
Risultati: 1-9 |