Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Jean Louis Maurel"'
Publikováno v:
Thermochimica Acta. 408:85-96
Thermogravimetric analysis was used to study the sublimation and vaporisation processes of S(−) efaroxan hydrochloride, a potent and highly selective α-2-adrenoreceptor antagonist. The kinetic parameters of the sublimation were investigated by con
Publikováno v:
Journal of Thermal Analysis and Calorimetry. 53:123-131
We have shown that efaxoran hydrochloride and efaxoran hydrobromide form solid solution over the entire range of compositions. The small values of enthalpy of mixing indicate that the system is close to ideality. Consequently, Oonk's method was used
Publikováno v:
Journal of Thermal Analysis and Calorimetry. 53:697-709
The phase diagram of R(+)-S(-) efaroxan hydrochloride (Tfus.(R)=245.1±0.3°C. ΔHfus.(R)=119.6±3.0 J g-1) shows a racemic compound. The melting temperature and melting enthalpy of the compound are: Tfus.(RS)=247.8±0.2°C and ΔHfus. (RS)=124.6±2.
Autor:
Laure Monconduit, Jean-Louis Maurel, Claude Belin, Monique Tillard, Serge Brunel, Jean-Paul Ribet
Publikováno v:
Scopus-Elsevier
The title compound, C 11 H 13 N 2 O 2 + .Br - , crystallizes in the P2 1 2 1 2 1 space group. The absolute configuration of the therapeutically active molecule idazoxan [2-(1,4-benzodioxan-2-yl)imidazoline] could be resolved in this hydrobromide salt
Autor:
Adrian Newman-Tancredi, Bernard Vacher, Francis Colpaert, Jean Louis Maurel, Philippe Funes, Jean-Marie Autin
Publikováno v:
Journal of medicinal chemistry. 50(20)
We report the discovery of novel 5-HT1A receptor agonists and describe the process that led to the antidepressant candidate 9 (F 15599). 9 has nanomolar affinity for 5-HT1A binding sites and is over 1000-fold selective with respect to the other 5-HT1
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:
Acta Crystallographica Section C Crystal Structure Communications. 51:2439-2441
The isomorphous structures of 2-[2-(2-ethyl-2,3-dihydro-2-benzofuranyl)]-2-imidazolinium [(+)-efaroxan cation] chloride, C 13 H 17 N 2 O + .Cl - , and bromide, C 13 H 17 N 2 O + .-Br-, have been determined. The absolute configuration of the active mo
Publikováno v:
Acta crystallographica. Section C, Crystal structure communications. 57(Pt 4)
The title compound, C(12)H(14)FN(2)O(3)(+).Br(-), crystallizes in the non-centrosymmetric P2(1)2(1)2(1) space group. The absolute configuration of the pharmacologically active molecule could be resolved in the hydrobromide salt, the structure of whic
Autor:
Jean-Marie Autin, Alain Chauvet, Jean-François Patoiseau, Joël Jaud, Jacqueline Masse, D C Bigg, Jean-Louis Maurel, Jean-Paul Ribet
Publikováno v:
Journal of pharmaceutical sciences. 81(8)
The characterization of two polymorphs of the title compound (F2692; 1) by differential scanning calorimetry (DSC), microanalysis, proton nuclear magnetic resonance spectroscopy, thermogravimetry, thermomicroscopy, infrared spectroscopy, and X-ray di
Publikováno v:
Acta Crystallographica Section C Crystal Structure Communications. 54:IUC9800004
In the title compound, C13H17N2O+.Cl−, homochiral cationic molecules are linked to form chains in the b-direction of the triclinic cell by N—H⋯Cl hydrogen bonds. The dihydro-2-furanyl groups are nearly parallel to the a axis [81.7 (1)° between