Zobrazeno 1 - 10
of 122
pro vyhledávání: '"F, Colpaert"'
Publikováno v:
Brain research. 1688
NLX-112 (a.k.a. F13640 or befiradol) possesses marked activity in a variety of animal models of pain and of neuropsychiatric disorders; it exhibits nanomolar affinity, exceptional selectivity and high agonist efficacy at 5-hydroxytryptamine1A (5-HT
Autor:
F. Colpaert
Publikováno v:
European Journal of Pain. 13
Publikováno v:
European Journal of Pain. 13
Autor:
A, Newman-Tancredi, M-B, Assié, J-C, Martel, C, Cosi, L Bruins, Slot, C, Palmier, I, Rauly-Lestienne, F, Colpaert, B, Vacher, D, Cussac
Publikováno v:
British journal of pharmacology. 151(2)
Combining 5-HT(1A) receptor activation with dopamine D(2)/D(3) receptor blockade should improve negative symptoms and cognitive deficits in schizophrenia. We describe the in vitro profile of F15063 (N-[(2,2-dimethyl-2,3-dihydro-benzofuran-7-yloxy)eth
Autor:
Jean-Paul Ribet, B. Bonnaud, Claude Belin, B. Vacher, F. Colpaert, Monique Tillard, Jean-Louis Maurel, R. Pena
Publikováno v:
Spectrochimica Acta Part A : Molecular Spectroscopy [1967-1993]
Spectrochimica Acta Part A : Molecular Spectroscopy [1967-1993], Elsevier, 2005, 62 (1-3), pp.353-363. ⟨10.1016/j.saa.2005.01.002⟩
Spectrochimica Acta Part A : Molecular Spectroscopy [1967-1993], Elsevier, 2005, 62 (1-3), pp.353-363. ⟨10.1016/j.saa.2005.01.002⟩
{[1-(3-Chloro-4-fluorobenzoyl)-4-fluoropiperidin-4yl]methyl}[(5-methylpyridin-2-yl)methyl]amine, fumaric acid salt (C(20)H(22)ClF(2)N(3)O, C(4)H(4)O(4)) (1) was synthesized and characterized by the complete (1)H, (13)C and (19)F NMR analyses. The con
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e4180eceaa3abbc26c3ff919fe5b65af
https://hal.archives-ouvertes.fr/hal-00383121
https://hal.archives-ouvertes.fr/hal-00383121
Publikováno v:
Journal of neurochemistry. 79(1)
To better understand the neurotrophic function of the neurotransmitter noradrenaline, we have developed a model of mesencephalic cultures in which we find low concentrations (0.3-10 microM) of noradrenaline to be remarkably effective in promoting lon
Publikováno v:
British Journal of Cancer
F 11782 is a novel inhibitor of topoisomerases I and II, with an original mechanism of action (Perrin et al, 2000). This study, aimed to define its anticancer efficacy against a series of murine and human tumour models, has provided evidence of major
Publikováno v:
European journal of cancer (Oxford, England : 1990). 35(3)
The antitumour activity of vinflunine, 20',20'-dichloro-3',4'-dihydrovinorelbine, a fluorinated Vinca alkaloid obtained by reaction in superacid media, was evaluated in comparison with vinorelbine against a series of subcutaneously-implanted human tu
Autor:
N. De Kimpe, Jan-Willem Thuring, F. Colpaert, F. Deroose, R. Surmont, Gregor James Macdonald, Guido Verniest
Publikováno v:
Synfacts. 2009:0487-0487