Zobrazeno 1 - 10
of 36
pro vyhledávání: '"Robert Chicheportiche"'
Autor:
Marcel Rucheton, Caroline Palais, Priscille Bosc, Robert Chicheportiche, Arnaud Dupuy d'Angeac, Caroline Rosé, Hubert Graafland, Frédéric De Lamotte, Ilias Stefas, Anna-Karin Eriksson
Publikováno v:
Biochemical Journal
Biochemical Journal, Portland Press, 2006, 393 (1), pp.117-127. ⟨10.1042/BJ20050932⟩
Biochemical Journal, Portland Press, 2006, 393 (1), pp.117-127. ⟨10.1042/BJ20050932⟩
dangeac@univ-montp2.fr; International audience; Binding of beta 2GPI (beta2 glycoprotein I), a human plasma protein, to AnPLs (anionic phospholipids) plays a key role in the formation of antiphospholipid antibodies involved in autoimmune diseases lik
Publikováno v:
Journal of Heterocyclic Chemistry. 38:1113-1118
We report a study on the absorptive and emissive properties of 9-acridinones, 9-thioacridinones and 9-aminoacridines including six crown ether derivatives. The effect of solvents and of the addition of cations (Na+, K+, Ca2+ and Mg2+) on these proper
Publikováno v:
ChemInform. 33
We report a study on the absorptive and emissive properties of 9-acridinones, 9-thioacridinones and 9-aminoacridines including six crown ether derivatives. The effect of solvents and of the addition of cations (Na+, K+, Ca2+ and Mg2+) on these proper
Publikováno v:
Neuroscience Letters. 143:74-78
The olfactory bulb (OB) kindling is a model of limbic secondary generalized epilepsy. Ten days after the completion of OB kindling, we have studied the long term effects of both electrode insertion and kindling on the binding of [3H]diazepam to crude
Publikováno v:
Journal of Neurochemistry. 56:553-559
The phencyclidine (PCP) derivative, [3H]N-[1-(2-benzo[b]thiophenyl)cyclohexyl]piperidine ([3H]BTCP), was used to label in vivo the dopamine uptake complex in mouse brain. The striatum accumulated the highest level of total and specific binding. Drugs
Publikováno v:
Journal of Labelled Compounds and Radiopharmaceuticals. 28:1059-1064
After verification of the biological activity of 3-iodo-PCP by binding studies to the N-methyl D-aspartate gated channel, 3-[125I]iodo-PCP was prepared by reaction of sodium iodide with a triazene precursor. The radiochemical yield was optimized and
Autor:
Robert Chicheportiche, Jean Pierre Beaucourt, Michel Ponchant, Jean Marc Kamenka, Janique Guiramand
Publikováno v:
Journal of Neurochemistry
Journal of Neurochemistry, Wiley, 1992, 59 (2), pp.492-9. ⟨10.1111/j.1471-4159.1992.tb09397.x⟩
Journal of Neurochemistry, Wiley, 1992, 59 (2), pp.492-9. ⟨10.1111/j.1471-4159.1992.tb09397.x⟩
International audience; The binding properties of the 125I-labeled phencyclidine derivative N-[1-(3-[125I]iodophenyl)cyclohexyl]piperidine (3-[125I]iodo-PCP), a new ligand of the N-methyl-D-aspartate (NMDA)-gated ionic channel, were investigated. Ass
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a0c1a0994c09ba277d1265a603c1a843
https://hal.archives-ouvertes.fr/hal-00422127
https://hal.archives-ouvertes.fr/hal-00422127
Autor:
Jean Marc Kamenka, Robert Chicheportiche, M'Hamed Bellaidi, Isabelle Chaudieu, Houria Allaoua, Gérard Rondouin
Publikováno v:
Neuroscience letters. 131(2)
The regulation of the binding sites of [3H]TCP, a non-competitive ligand of the N-methyl-D-aspartate (NMDA) receptor, was studied on membranes prepared from different CNS regions of amygdaloid-kindled rats. The high-affinity binding sites (KdH = 4.2-
The Phencyclidine (PCP) derivatives [3H]BTCP and [3H]TCP were used to label in vivo the DA uptake complex and the NMDA receptor-associated PCP receptor, respectively, and to study the dual interaction of PCP-like drugs with these targets.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8884305f86b95912aab199b4c2227773
https://doi.org/10.1016/b978-0-08-041165-1.50086-7
https://doi.org/10.1016/b978-0-08-041165-1.50086-7
Publikováno v:
Neuroscience letters. 120(1)
Competitive N- methyl- d -aspartate (NMDA) receptor antagonists are known to protect neurones against hypoglycaemic damage. We tested N-[1-(2-thienyl)cyclohexyl]piperidine (TCP), a non-competitive NMDA antagonist, in a recovery model of hypoglycaemic