Zobrazeno 1 - 10
of 88
pro vyhledávání: '"Daniel Dauzonne"'
Publikováno v:
AIMS Molecular Science, Vol 3, Iss 3, Pp 368-385 (2016)
Leukemia cells from patients with acute myeloid leukemia (AML) display high proliferative capacity and are resistant to death. Membrane-anchored aminopeptidase-N/CD13 is a potential drug target in AML. Clinical research efforts are currently focusing
Externí odkaz:
https://doaj.org/article/a3cbedf537344e4a959ff5dbe895b997
Autor:
Marianne Lucas-Hourani, Daniel Dauzonne, Pierre Jorda, Gaëlle Cousin, Alexandru Lupan, Olivier Helynck, Grégory Caignard, Geneviève Janvier, Gwénaëlle André-Leroux, Samira Khiar, Nicolas Escriou, Philippe Desprès, Yves Jacob, Hélène Munier-Lehmann, Frédéric Tangy, Pierre-Olivier Vidalain
Publikováno v:
PLoS Pathogens, Vol 9, Iss 10, p e1003678 (2013)
Searching for stimulators of the innate antiviral response is an appealing approach to develop novel therapeutics against viral infections. Here, we established a cell-based reporter assay to identify compounds stimulating expression of interferon-in
Externí odkaz:
https://doaj.org/article/50f5357168b6455188060f26593ac8fd
Publikováno v:
European Journal of Medicinal Chemistry
European Journal of Medicinal Chemistry, Elsevier, 2020, pp.111829. ⟨10.1016/j.ejmech.2019.111829⟩
European Journal of Medicinal Chemistry, 2020, pp.111829. ⟨10.1016/j.ejmech.2019.111829⟩
European Journal of Medicinal Chemistry, Elsevier, 2020, pp.111829. ⟨10.1016/j.ejmech.2019.111829⟩
European Journal of Medicinal Chemistry, 2020, pp.111829. ⟨10.1016/j.ejmech.2019.111829⟩
International audience; The implication of DNA methylation in cancer is today clearly established. Despite that nucleoside analogues are currently used for leukaemia treatment, their low stability in physiological conditions and their lack of selecti
Publikováno v:
AIMS Molecular Science, Vol 3, Iss 3, Pp 368-385 (2016)
Leukemia cells from patients with acute myeloid leukemia (AML) display high proliferative capacity and are resistant to death. Membrane-anchored aminopeptidase-N/CD13 is a potential drug target in AML. Clinical research efforts are currently focusing
Autor:
Daniel Dauzonne, Damien Bonne, Diana Becerra, Jean Rodriguez, Thierry Constantieux, Wilfried Raimondi
Publikováno v:
SYNTHESIS
SYNTHESIS, Georg Thieme Verlag, 2016, 49 (01), pp.195-201. ⟨10.1055/s-0035-1562446⟩
SYNTHESIS, Georg Thieme Verlag, 2016, 49 (01), pp.195-201. 〈10.1055/s-0035-1562446〉
Synthesis: Journal of Synthetic Organic Chemistry
Synthesis: Journal of Synthetic Organic Chemistry, 2016, 49 (01), pp.195-201. ⟨10.1055/s-0035-1562446⟩
Illustration. France. 2016
SYNTHESIS, Georg Thieme Verlag, 2016, 49 (01), pp.195-201. ⟨10.1055/s-0035-1562446⟩
SYNTHESIS, Georg Thieme Verlag, 2016, 49 (01), pp.195-201. 〈10.1055/s-0035-1562446〉
Synthesis: Journal of Synthetic Organic Chemistry
Synthesis: Journal of Synthetic Organic Chemistry, 2016, 49 (01), pp.195-201. ⟨10.1055/s-0035-1562446⟩
Illustration. France. 2016
International audience; Alkyl 4,5-dihydrofuran-2-carboxylates can be efficiently ob- tained via an enantioselective organocatalyzed consecutive reaction between _-keto esters and (Z)-(2-chloro-2-nitroethenyl)benzenes. The overall sequence combines a
Publikováno v:
Anti-Cancer Drugs
Anti-Cancer Drugs, Lippincott, Williams & Wilkins, 2016, 27 (5), pp.398-406. ⟨10.1097/CAD.0000000000000341⟩
Anti-Cancer Drugs, Lippincott, Williams & Wilkins, 2016, 27 (5), pp.398-406. ⟨10.1097/CAD.0000000000000341⟩
International audience; Flavone-8-acetic acid (FAA) has been proved to be a potent vascular-disrupting agent in mice. Unfortunately, FAA did not produce any anticancer activity in clinical trials. Previously, we had reported that FAA is metabolized b
Autor:
Marianne Lucas-Hourani, Philippe V. Afonso, Julien Dairou, Frédéric Tangy, Olivier Helynck, Sébastien Nisole, Daniel Dauzonne, Hélène Munier-Lehmann, Samira Khiar, Pierre-Olivier Vidalain
Publikováno v:
Antimicrobial Agents and Chemotherapy
Antimicrobial Agents and Chemotherapy, American Society for Microbiology, 2017, 61 (10), pp.e00383-17. ⟨10.1128/AAC.00383-17⟩
Antimicrobial Agents and Chemotherapy, 2017, 61 (10), pp.e00383-17. ⟨10.1128/AAC.00383-17⟩
Antimicrobial Agents and Chemotherapy, American Society for Microbiology, 2017, 61 (10), pp.e00383-17. ⟨10.1128/AAC.00383-17⟩
Antimicrobial Agents and Chemotherapy, 2017, 61 (10), pp.e00383-17. ⟨10.1128/AAC.00383-17⟩
De novo pyrimidine biosynthesis is a key metabolic pathway involved in multiple biosynthetic processes. Here, we identified an original series of 3-(1 H -indol-3-yl)-2,3-dihydro-4 H -furo[3,2- c ]chromen-4-one derivatives as a new class of pyrimidine
Autor:
Evelyne Ségal-Bendirdjian, Daniel Dauzonne, Marie-Paule Teulade-Fichou, Vanessa Masson, Florent Dingli, Guillaume Kellermann, Damarys Loew, Sophie Bombard
Publikováno v:
FEBS letters. 591(6)
Telomerase is an almost universal cancer target that consists minimally of a core protein human telomerase reverse transcriptase (hTERT) and a RNA component human telomerase RNA (hTR). Some inhibitors of this enzyme are thought to function by the cov
Publikováno v:
International Reviews in Physical Chemistry. 32:393-434
A large number of molecules referred to here as M, several of which are extracted from plants, belong to different chemical classes and exhibit chemoprotective activity against carcinogenesis and inflammation in rodents and in vitro cell culture. The
Autor:
Minh Hien, Pham, Nicolas, Auzeil, Anne, Regazzetti, Daniel, Scherman, Johanne, Seguin, Nathalie, Mignet, Daniel, Dauzonne, Guy G, Chabot
Publikováno v:
Anticancer research. 36(8)
Flavone-8-acetic acid (FAA) is a potent antivascular agent in mice but not in humans. Assuming that FAA was bioactivated in mice, we previously demonstrated that 6-OH-FAA was formed from FAA by mouse microsomes but not by human microsomes; its antiva