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Results: 1-9 |
Results: 9
4H-1,2,4-PYRIDOTHIADIAZINE 1,1-DIOXIDES AND 2,3-DIHYDRO-4H-1,2,4-PYRIDOTHIADIAZINE 1,1-DIOXIDES CHEMICALLY RELATED TO DIAZOXIDE AND CYCLOTHIAZIDE AS POWERFUL POSITIVE ALLOSTERIC MODULATORS OF (R AMINO-3-(3-HYDROXY-5-METHYLISOXAZOL-4-YL)PROPIONIC ACID RECEPTORS - DESIGN, SYNTHESIS, PHARMACOLOGY, AND STRUCTURE-ACTIVITY-RELATIONSHIPS/
Authors: PIROTTE B PODONA T DIOUF O DETULLIO P LEBRUN P DUPONT L SOMERS F DELARGE J MORAIN P LESTAGE P LEPAGNOL J SPEDDING M
Citation: B. Pirotte et al., 4H-1,2,4-PYRIDOTHIADIAZINE 1,1-DIOXIDES AND 2,3-DIHYDRO-4H-1,2,4-PYRIDOTHIADIAZINE 1,1-DIOXIDES CHEMICALLY RELATED TO DIAZOXIDE AND CYCLOTHIAZIDE AS POWERFUL POSITIVE ALLOSTERIC MODULATORS OF (R AMINO-3-(3-HYDROXY-5-METHYLISOXAZOL-4-YL)PROPIONIC ACID RECEPTORS - DESIGN, SYNTHESIS, PHARMACOLOGY, AND STRUCTURE-ACTIVITY-RELATIONSHIPS/, Journal of medicinal chemistry, 41(16), 1998, pp. 2946-2959
ENANTIOSELECTIVE SYNTHESIS OF A PYRROLO-BENZOTHIADIAZINE DERIVATIVE S-18986, A NEW AMPA RECEPTOR-POSITIVE MODULATOR
Authors: DESOS P SERKIZ B MORAIN P LEPAGNOL J CORDI A
Citation: P. Desos et al., ENANTIOSELECTIVE SYNTHESIS OF A PYRROLO-BENZOTHIADIAZINE DERIVATIVE S-18986, A NEW AMPA RECEPTOR-POSITIVE MODULATOR, Bioorganic & medicinal chemistry letters, 6(24), 1996, pp. 3003-3008
STRUCTURE-ACTIVITY-RELATIONSHIPS IN A SERIES OF 2(1H)-QUINOLONES BEARING DIFFERENT ACIDIC FUNCTION IN THE 3-POSITION - 6,7-DICHLORO-2(1H)-OXOQUINOLINE-3-PHOSPHONIC ACID, A NEW POTENT AND SELECTIVE AMPA KAINATEANTAGONIST WITH NEUROPROTECTIVE PROPERTIES/
Authors: DESOS P LEPAGNOL JM MORAIN P LESTAGE P CORDI AA
Citation: P. Desos et al., STRUCTURE-ACTIVITY-RELATIONSHIPS IN A SERIES OF 2(1H)-QUINOLONES BEARING DIFFERENT ACIDIC FUNCTION IN THE 3-POSITION - 6,7-DICHLORO-2(1H)-OXOQUINOLINE-3-PHOSPHONIC ACID, A NEW POTENT AND SELECTIVE AMPA KAINATEANTAGONIST WITH NEUROPROTECTIVE PROPERTIES/, Journal of medicinal chemistry, 39(1), 1996, pp. 197-206
INTERACTION OF S-21007 WITH 5-HT3 RECEPTORS - IN-VITRO AND IN-VIVO CHARACTERIZATION
Authors: DELAGRANGE P EMERIT MB MERAHI N ABRAHAM C MORAIN P RAULT S RENARD P PFEIFFER B GUARDIOLALAMAITRE B HAMON M
Citation: P. Delagrange et al., INTERACTION OF S-21007 WITH 5-HT3 RECEPTORS - IN-VITRO AND IN-VIVO CHARACTERIZATION, European journal of pharmacology, 316(2-3), 1996, pp. 195-203
S-17625, A SELECTIVE AND COMPETITIVE NON-NMDA ANTAGONIST - CEREBRAL ANTIISCHEMIC EFFECTS IN RODENTS
Authors: MORAIN P LESTAGE P ROGER A BOBICHON C DESOS P CORDI A LEPAGNOL J
Citation: P. Morain et al., S-17625, A SELECTIVE AND COMPETITIVE NON-NMDA ANTAGONIST - CEREBRAL ANTIISCHEMIC EFFECTS IN RODENTS, British Journal of Pharmacology, 114, 1995, pp. 330-330
BIGUANIDE DERIVATIVES - AGONIST PHARMACOLOGY AT 5-HYDROXYTRYPTAMINE TYPE-3 RECEPTORS IN-VITRO
Authors: MORAIN P ABRAHAM C PORTEVIN B DENANTEUIL G
Citation: P. Morain et al., BIGUANIDE DERIVATIVES - AGONIST PHARMACOLOGY AT 5-HYDROXYTRYPTAMINE TYPE-3 RECEPTORS IN-VITRO, Molecular pharmacology, 46(4), 1994, pp. 732-742
THE ANTAGONIST PROPERTIES OF S-11978 ON 5HT3 RECEPTORS IN N1E-115 NEUROBLASTOMA-CELLS
Authors: MORAIN P ABRAHAM C LACOSTE JM MALEN C LAUBIE M GIESENCROUSE E
Citation: P. Morain et al., THE ANTAGONIST PROPERTIES OF S-11978 ON 5HT3 RECEPTORS IN N1E-115 NEUROBLASTOMA-CELLS, Fundamental and clinical pharmacology, 7(5), 1993, pp. 205-208
CHARACTERISTICS OF 5-HT3 BINDING-SITES IN N1E-115 NEUROBLASTOMA-CELLSUSING 3H-BRL 43694
Authors: ABRAHAM C MORAIN P
Citation: C. Abraham et P. Morain, CHARACTERISTICS OF 5-HT3 BINDING-SITES IN N1E-115 NEUROBLASTOMA-CELLSUSING 3H-BRL 43694, Journal of neurochemistry, 61, 1993, pp. 190000090-190000090
THE ANTAGONIST PROPERTIES OF S 11978 ON 5-HT3 RECEPTORS IN N1E-115 NEUROBLASTOMA-CELLS
Authors: MORAIN P ABRAHAM C LACOSTE JM MALEN C LAUBIE M GIESENCROUSE E
Citation: P. Morain et al., THE ANTAGONIST PROPERTIES OF S 11978 ON 5-HT3 RECEPTORS IN N1E-115 NEUROBLASTOMA-CELLS, Journal of neurochemistry, 61, 1993, pp. 190000091-190000091
Risultati: 1-9 |