Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Jeanne, Maruani"'
Autor:
R. Alonso, Jean pierre Martinolle, Sarran Lionel, Jeanne Maruani, Annie Cudennec, Claudine Planchenault, Bernard Ferrari, Olivier Finance, Gérard Le Fur, Philippe Soubrie, Tiziano Croci, Katalin Urban-Szabo, Jean Gougat, Fabio Guagnini, Martine Poncelet
Publikováno v:
Journal of Pharmacology and Experimental Therapeutics. 309:661-669
The biochemical and pharmacological properties of a novel non-peptide antagonist of the bradykinin (BK) B1 receptor, SSR240612 [(2 R )-2-[((3 R )-3-(1,3-benzodioxol-5-yl)-3-{[(6-methoxy-2-naphthyl)sulfonyl]amino}propanoyl)amino]-3-(4-{[2 R ,6 S )-2,6
Autor:
David Shire, J. C. Breliere, Daniel Caput, Francis Barth, Michel Heaulme, P. Ferrara, Gérard Le Fur, Murielle Rinaldi-Carmona, Christian Congy, Jeanne Maruani, Serge Martinez, Philippe Soubrie, Bernard Calandra, Gervais Neliat
Publikováno v:
FEBS Letters. 350:240-244
SR141716A is the first selective and orally active antagonist of the brain cannabinoid receptor. This compound displays nanomolar affinity for the central cannabinoid receptor but is not active on the peripheral cannabinoid receptor. In vitro, SR1417
Autor:
J. Souilhac, J.C. Brelière, R. Calassi, X. Emonds-Alt, Philippe Soubrie, G. Le Fur, Jeanne Maruani, Christiane Gueudet, M. Jung, M. Poncelet, M.C. Barnouin
Publikováno v:
Neuropharmacology. 33:167-179
SR 140333 (1-2-[3-(3,4-dichlorophenyl)-1-(3-isopropoxyphenylacetyl)piperidin-3-yl]ethyl-4-phenyl -1-azonia-bicyclo[2.2.2]octane, chloride), a potent non peptide ligand of the substance P (SP) NK1 receptor subtype with high affinity for NK1 receptors
Autor:
Gérard Le Fur, Michele Arnone, Philippe Soubrie, Christian Congy, Didier Oustric, Olivier Finance, Murielle Rinaldi-Carmona, Jeanne Maruani, Francis Barth, Martine Poncelet, Serge Martinez, Alain Pério
Publikováno v:
The Journal of pharmacology and experimental therapeutics. 310(3)
Based on binding, functional, and pharmacological data, this study introduces SR147778 [5-(4-bromophenyl)-1-(2,4-dichloro-phenyl)-4-ethyl- N -(1-piperidinyl)-1 H -pyrazole-3-carboxamide] as a highly potent, selective, and orally active antagonist for
Autor:
Jean, Gougat, Bernard, Ferrari, Lionel, Sarran, Claudine, Planchenault, Martine, Poncelet, Jeanne, Maruani, Richard, Alonso, Annie, Cudennec, Tiziano, Croci, Fabio, Guagnini, Katalin, Urban-Szabo, Jean-Pierre, Martinolle, Philippe, Soubrié, Olivier, Finance, Gérard, Le Fur
Publikováno v:
The Journal of pharmacology and experimental therapeutics. 309(2)
The biochemical and pharmacological properties of a novel non-peptide antagonist of the bradykinin (BK) B(1) receptor, SSR240612 [(2R)-2-[((3R)-3-(1,3-benzodioxol-5-yl)-3-[[(6-methoxy-2-naphthyl)sulfonyl]amino]propanoyl)amino]-3-(4-[[2R,6S)-2,6-dimet
Publikováno v:
Neuroscience letters. 343(3)
Administration of the cannabinoid CB1 receptor antagonist SR141716 (3–10 mg/kg i.p.) abolished neuropeptide Y-induced overeating and significantly reduced ethanol and sucrose intake in CB1 wild-type (+/+) mice. In CB1 receptor knockout (−/−) mi
Autor:
Michele Arnone, M. Poncelet, Philippe Soubrie, Jeanne Maruani, Marie-Hélène Thiébot, G Le Fur, Frederique Chaperon
Publikováno v:
Psychopharmacology. 132(1)
SR 141716, a selective central CB1 cannabinoid receptor antagonist, markedly and selectively reduces sucrose feeding and drinking as well as neuropeptide Y-induced sucrose drinking in rats. SR 141716 also decreases ethanol consumption in C57BL/6 mice
Publikováno v:
Behavioural Pharmacology. 7:65
Active cannabimimetic drugs are known to bind to two receptor subtypes: one, called CB1, is mainly localised in the central nervous system while the other (CB2) is expressed preferentially in the immune system. SR 141716A has been demonstrated to hav
Autor:
Murielle, Rinaldi-Carmona, Francis, Barth, Christian, Congy, Serge, Martinez, Didier, Oustric, Alain, Prio, Martine, Poncelet, Jeanne, Maruani, Michle, Arnone, Olivier, Finance, Philippe, Soubri, Grard, Le Fur
Publikováno v:
The Journal of Pharmacology and Experimental Therapeutics; September 2004, Vol. 310 Issue: 3 p905-14, 10p