Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Ronan Dirr"'
Autor:
Yohann Bernard, Nigel Ribeiro, Frédéric Thuaud, Gülen Türkeri, Ronan Dirr, Mounia Boulberdaa, Canan G Nebigil, Laurent Désaubry
Publikováno v:
PLoS ONE, Vol 6, Iss 10, p e25302 (2011)
BackgroundDespite its effectiveness in the treatment of various cancers, the use of doxorubicin is limited by a potentially fatal cardiomyopathy. Prevention of this cardiotoxicity remains a critical issue in clinical oncology. We hypothesized that fl
Externí odkaz:
https://doaj.org/article/97ec74df58f24b0f91c10728b83b956b
Publikováno v:
Tetrahedron Letters. 49:4588-4590
An efficient approach to unsymmetrical halogenated resorcinol diethers has been developed. This synthesis consists of two subsequent nucleophilic aromatic substitutions (S N Ar) of unsymmetrical difluoroarenes by alkoxides. The novelty of this approa
Autor:
Ronan Dirr, Laurent Désaubry, Yohann Bernard, Nigel Ribeiro, Frédéric Thuaud, Canan G. Nebigil, Mounia Boulberdaa, Gulen Turkeri
Publikováno v:
PLoS ONE, Vol 6, Iss 10, p e25302 (2011)
PLoS ONE
PLoS ONE, Public Library of Science, 2011, 6 (10), pp.e25302. ⟨10.1371/journal.pone.0025302⟩
PLoS ONE
PLoS ONE, Public Library of Science, 2011, 6 (10), pp.e25302. ⟨10.1371/journal.pone.0025302⟩
BackgroundDespite its effectiveness in the treatment of various cancers, the use of doxorubicin is limited by a potentially fatal cardiomyopathy. Prevention of this cardiotoxicity remains a critical issue in clinical oncology. We hypothesized that fl
Autor:
Yohann Bernard, Laurent Désaubry, Canan G. Nebigil, Ronan Dirr, Catherine Tomasetto, Frédéric Thuaud, Nahum Sonenberg, Aurélie Baguet, Geneviève Aubert, Gulen Turkeri, Yuri V. Svitkin, Thierry Cresteil
Publikováno v:
Journal of Medicinal Chemistry
Journal of Medicinal Chemistry, American Chemical Society, 2009, 52 (16), pp.5176-5187. ⟨10.1021/jm900365v⟩
Journal of Medicinal Chemistry, American Chemical Society, 2009, 52 (16), pp.5176-5187. ⟨10.1021/jm900365v⟩
Flavaglines constitute a family of natural anticancer compounds. We present here 3 (FL3), the first synthetic flavagline that inhibits cell proliferation and viability (IC(50) approximately 1 nM) at lower doses than did the parent compound, racemic r
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ef0c0ad6bf0d644a505fefe2ccb42cbb
https://hal.archives-ouvertes.fr/hal-00467437
https://hal.archives-ouvertes.fr/hal-00467437
Publikováno v:
ChemInform. 39
An efficient approach to unsymmetrical halogenated resorcinol diethers has been developed. This synthesis consists of two subsequent nucleophilic aromatic substitutions (S N Ar) of unsymmetrical difluoroarenes by alkoxides. The novelty of this approa
Publikováno v:
Tetrahedron Letters. 49:7083
0040-4039/$ - see front matter 2008 Elsevier Ltd. All rights reserved.doi:10.1016/j.tetlet.2008.09.121DOI of original article: 10.1016/j.tetlet.2008.05.091* Corresponding author. Tel.: +33 90 244 141; fax: +33 390 244 310.E-mail address: desaubry@chi
Autor:
Frédéric Thuaud, Yohann Bernard, Gülen Türkeri, Ronan Dirr, Geneviève Aubert, Thierry Cresteil, Aurélie Baguet, Catherine Tomasetto, Yuri Svitkin, Nahum Sonenberg, Canan G. Nebigil, Laurent Désaubry
Publikováno v:
Journal of Medicinal Chemistry; Aug2009, Vol. 52 Issue 16, p5176-5187, 12p