Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Gilbert Regnier"'
Autor:
Jean-Pierre Bizzari, Alain Dhainaut, Nicolas Guilbaud, Maryse Berlion, Suzy Cros, Theresa A. Dunn, Ghanem Atassi, Gilbert Regnier
Publikováno v:
Cancer Chemotherapy and Pharmacology. 30:491-494
S 9788, a new triazinoaminopiperidine derivative, was found to be a potent reversant of vincristine resistance in the in vivo murine leukemic P388/VCR model. In two treatment regimens (Q4D days 1, 5 and 9 and QD days 1-9), S 9788 enhanced the antitum
Autor:
Andre Tizot, Alain Dhainaut, Laurence Kraus-Berthier, Stéphane Léonce, Nicolas Guilbaud, Ghanem Atassi, Gilbert Regnier, Alain Pierré
Publikováno v:
Journal of medicinal chemistry. 39(20)
A series of 36 purine and purine analog derivatives have been synthesized and tested for their ability to modulate multidrug resistance in vitro (P388/VCR-20 and KB-A1 cells) and in vivo (P388/VCR leukemia). Compounds were compared to S9788, a triazi
Autor:
Albert Lenaers, Gilbert Regnier, Catherine Thollon, Frédéric Robin, Christine Cambarrat, Jean-Paul Vilaine, Claude Guillonneau, Jean-Pierre Iliou
Publikováno v:
European journal of pharmacology. 248(3)
Oxidative stress induced by reactive oxygen species is one aspect of the deleterious mechanisms involved in myocardial post-ischemic reperfusion injury. The antioxidant properties of the new molecule S12340 (8-[3-(3,5-diterbutyl-4-hydroxyphenyl-thio)
Autor:
Alain Dhainaut, Gilbert Regnier, Jean Francois Prost, Stéphane Léonce, Ghanem Atassi, Laurence Kraus-Berthier, Alain Pierré
Publikováno v:
Journal of medicinal chemistry. 35(13)
A series of 70 triazine derivatives have been synthesized and tested for their capacity to modulate multidrug resistance (MDR) in DC-3F/AD and KB-A1 tumor cells in vitro, in comparison with verapamil (VRP), a calcium channel antagonist currently used
Autor:
Françoise P Tisserand, Claude Guillonneau, Sophie M Holstorp, Guy Saint-Romas, Jacques Duhault, Gilbert Regnier
Publikováno v:
European Journal of Medicinal Chemistry. 22:243-250
Twenty eight new derivatives of 8-aminoalkyl substituted xanthine have been synthesized. They all have demonstrated a potent anti-bronchoconstrictive effect in the guinea pig and some of them have a very long duration of action (> 48 h). Among them,
Publikováno v:
Journal of Medicinal Chemistry. 11:1151-1155
Autor:
Jacques Duhault, Gilbert Regnier, Sophie M Holstorp, Claude Guillonneau, Guy Saint-Romas, Françoise P Tisserand
Publikováno v:
ChemInform. 18
Twenty eight new derivatives of 8-aminoalkyl substituted xanthine have been synthesized. They all have demonstrated a potent anti-bronchoconstrictive effect in the guinea pig and some of them have a very long duration of action (> 48 h). Among them,
Publikováno v:
Chemischer Informationsdienst. Organische Chemie. 2