Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Marie-José Egron"'
Publikováno v:
ChemInform. 33
Autor:
M. Idriss Bennani-Baiti, Françoise Leclercq, Kostas Antonakis, Charles Frayssinet, Marie-José Egron
Publikováno v:
Carbohydrate Research. 228:95-102
The title compound 5 was synthesized by direct oxidation of the fluoro precursor and not from an epoxyketo intermediate according to the Paulsen procedure, which has been used until now to obtain bromo- and chloro-ketonucleosides. Antineoplastic acti
Autor:
Marie-José Egron, Jean Herscovici, Dimitri Komiotis, Abraham P. Ollapally, Ismet Dorange, Kostas Antonakis
Publikováno v:
Nucleosides, nucleotidesnucleic acids. 24(4)
The proposed short synthesis involves two key steps: Oxidation of the isopropylidene derivative of the 3-fluoronucleoside possessing a free hydroxyl group in 2-position and acetylation of deprotected 3-fluoro-2-ketonucleoside which, after a beta-elim
Publikováno v:
Bioorganicmedicinal chemistry letters. 12(11)
Starting from long chain alkylamino-alkan-1-ol a series of amino glycolipids were synthesized. This procedure allows a short and convenient preparation of glycosylated cationic lipids for gene delivery.
Autor:
Jean Herscovici, Clara Uriel, Monique Santarromana, Kostas Antonakis, Daniel Scherman, Marie-José Egron
Publikováno v:
Bioorganicmedicinal chemistry. 4(12)
The design, synthesis, cytotoxicity, and biological evaluation of carbohydrate/C-glycoside conjugates are described. The design concept is predicted on the idea that physiological barriers like the blood brain barrier could be crossed selectively by
Publikováno v:
ChemInform. 21
Publikováno v:
Carbohydrate Research. 142:324-328
Autor:
Marie José Egron, Michel Bessodes, Moulay Abdellah Alaoui-Jamali, Ivan Chouroulinkov, Kostas Antonakis
Publikováno v:
European Journal of Medicinal Chemistry. 22:305-310
The synthesis and cytotoxic activity of 14 ketonucleosides on 8 normal, transformed and leukemic cell lines are described. Compounds 1, 2, 3, 4, 5 and 6 proved to be the most cytotoxic for transformed and leukemic cells; compound 7 presents an interm
Publikováno v:
Carbohydrate Research. 112:301-306
Autor:
Kostas Antonakis, Ivan Chouroulinkov, Moulay Abdellah Alaoui-Jamali, Michel Bessodes, Marie José Egron
Publikováno v:
ChemInform. 18
The synthesis and cytotoxic activity of 14 ketonucleosides on 8 normal, transformed and leukemic cell lines are described. Compounds 1, 2, 3, 4, 5 and 6 proved to be the most cytotoxic for transformed and leukemic cells; compound 7 presents an interm