Zobrazeno 1 - 10
of 105
pro vyhledávání: '"H. Sentenac-Roumanou"'
Autor:
J. D. Laval, Ghassoub Rima, H. Sentenac-Roumanou, Jacques Satge, M. Fatome, Claude Lion, Rodolphe Dagiral
Publikováno v:
Applied Organometallic Chemistry. 10:113-123
Further to our work concerning organometallic compounds active in chemical radioprotection, we report the synthesis and pharmacological study (radioprotective activity, toxicity) of new germathiazolidines and germadithioacetals derived from cysteamin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2952e69dc8375da4ab7cfd8f79610fbf
https://doi.org/10.1002/(sici)1099-0739(199603)10:2<113::aid-aoc486>3.0.co
https://doi.org/10.1002/(sici)1099-0739(199603)10:2<113::aid-aoc486>3.0.co
Autor:
Ghassoub Rima, Claude Lion, H. Sentenac-Roumanou, Jacques Satge, P. Chabertier, O. Alazard, M. Fatome, J. D. Laval
Publikováno v:
Applied Organometallic Chemistry. 8:481-490
New germa- and silathiazolidines or germa- and siladithioacetals with N-allyl-substituted cysteamine and methylcysteamine ligands have been synthesized and their pharmacological properties (toxicity, radioprotective activity) have been studied. A not
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f0ee89c553b9bc0833e2e0ab161f7987
https://doi.org/10.1002/aoc.590080508
https://doi.org/10.1002/aoc.590080508
Autor:
Laurent Dubois, G. Blanchet, Robert H. Dodd, H. Garrigue, M. Dekhane, H. Sentenac-Roumanou, Pierre Potier
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 3:2831-2836
Alkyl β-carboline-3-carboxylate derivatives (e.g. β-CCM and β-CCB), known to interact with the central benzodiazepine receptor, were quaternized at the N-2 position using methyl iodide. The products strongly inhibited acetylcholinesterase in vitro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8ec123bd2c489ada6d16b54cfb1ac0ed
https://doi.org/10.1016/s0960-894x(01)80774-5
https://doi.org/10.1016/s0960-894x(01)80774-5
Publikováno v:
European Journal of Medicinal Chemistry. 28:761-767
This work concerns the synthesis and pharmacological study (toxicity, radioprotective activity) of the N -substituted organogermylated compounds by naphthylmethylimidazoline hydrochloride and imidazoline. These new organometallic derivatives have qui
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5a69b7d2d512be24812f18f87e645beb
https://doi.org/10.1016/0223-5234(93)90111-q
https://doi.org/10.1016/0223-5234(93)90111-q
Publikováno v:
ChemInform. 25
This work concerns the synthesis and pharmacological study (toxicity, radioprotective activity) of the N -substituted organogermylated compounds by naphthylmethylimidazoline hydrochloride and imidazoline. These new organometallic derivatives have qui
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ccd405a3777242919b31c434d85671b5
https://doi.org/10.1002/chin.199407239
https://doi.org/10.1002/chin.199407239
Publikováno v:
ChemInform. 28
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4545ce26c3f3fa9bf8fc64bd72ec10ca
https://doi.org/10.1002/chin.199742300
https://doi.org/10.1002/chin.199742300
Autor:
H. Sentenac-Roumanou, Ghassoub Rima, Jacques Satge, M. Istin, Christian Pradel, C. Lion, J. M. Grognet
Publikováno v:
Synthesis and Reactivity in Inorganic and Metal-Organic Chemistry. 22:277-288
New organophosphorus compounds utilized as haptens in immunology against organophosphorus compounds, inhibitors of acetylcholinesterase, have been synthesized. These compounds have structures similar to that of the organophosphorus nerve agent VX : [
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bae213b2d71d5114b845cde63b8f522f
https://doi.org/10.1080/00945719208021389
https://doi.org/10.1080/00945719208021389
Autor:
Jean-Claude Maurizis, Annie Veyre, H. Sentenac-Roumanou, P. Demerseman, Jean-Claude Madelmont, H. Garrigue, C. Nicolas, J. M. Meyniel
Publikováno v:
Journal of Labelled Compounds and Radiopharmaceuticals. 28:1375-1383
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1c3132483c607cce3ff5af7bdd80c303
https://doi.org/10.1002/jlcr.2580281204
https://doi.org/10.1002/jlcr.2580281204
Autor:
Jean-Claude Maurizis, P. Demerseman, J. M. Meyniel, C. Nicolas, J. M. Dupuy, H. Garrigue, H. Sentenac-Roumanou, Et A. Veyre, Jean-Claude Madelmont
Publikováno v:
Journal of Labelled Compounds and Radiopharmaceuticals. 28:1385-1392
The two compounds were labelled by 14C on the hydroxyimino methyl group substituted on the 2 positions of the pyridinium ring. The convenient pyridinium lithiated intermediates were formylated with N-methyl 14C-formanilide. The hydroxyimino methyl gr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::36be3477952a6c2653fcc0263c49d67c
https://doi.org/10.1002/jlcr.2580281205
https://doi.org/10.1002/jlcr.2580281205
Autor:
H, Sentenac-Roumanou
Publikováno v:
Annales pharmaceutiques francaises. 58(1)
The reasons underlying our fear of the use of toxins as new weapons different from chemical agents are discussed together with the conditions required for their use on the battlefield. The undeniable scientific contribution of toxins as pharmacologic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::abf7e81c232eef63f10ffe83afb90a54
https://pubmed.ncbi.nlm.nih.gov/10669809
https://pubmed.ncbi.nlm.nih.gov/10669809