Zobrazeno 1 - 10
of 19
pro vyhledávání: '"Dolor Renko"'
Autor:
Romain Darrigrand, Alison Pierson, Marine Rouillon, Dolor Renko, Mathilde Boulpicante, David Bouyssié, Emmanuelle Mouton-Barbosa, Julien Marcoux, Camille Garcia, Michael Ghosh, Mouad Alami, Sébastien Apcher
Publikováno v:
Communications Biology, Vol 4, Iss 1, Pp 1-14 (2021)
Darrigrand, Pierson et al. study the effect of mRNA splicing inhibitors on the generation of the MHC class I ligands. They developed a derivative of the spliceosome inhibitor isoginkgetin which is less toxic and more effective at enhancing antigen pr
Externí odkaz:
https://doaj.org/article/1c8392da73b6409daf3965425089b16d
Autor:
Boris Letribot, Megane Nascimento, Giulia Cerrato, Romain Darrigrand, Valerie Salgues, Dolor Renko, Alain Pruvost, Mouad Alami, Samir Messaoudi, Sebastien Apcher
Publikováno v:
Journal of Medicinal Chemistry. 65:4633-4648
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c6088dcf54b286199f6cd12482a31561
https://doi.org/10.1021/acs.jmedchem.1c01654
https://doi.org/10.1021/acs.jmedchem.1c01654
Autor:
Camille Hauguel, Sarah Ducellier, Olivier Provot, Nada Ibrahim, Diana Lamaa, Coline Balcerowiak, Boris Letribot, Megane Nascimento, Vincent Blanchard, Laurie Askenatzis, Helene Levaique, Jérôme Bignon, Francesco Baschieri, Cyril Bauvais, Guillaume Bollot, Dolor Renko, Alain Deroussent, Bastien Prost, Marie-Catherine Laisne, Sophie Michallet, Laurence Lafanechère, Sébastien Papot, Guillaume Montagnac, Christine Tran, Mouad Alami, Sebastien Apcher, Abdallah Hamze
Publikováno v:
European Journal of Medicinal Chemistry. 240:114573
A series of quinoline and quinazoline analogs were designed and synthesized as new tubulin polymerization (TP) and histone deacetylases (HDAC) inhibitors. Compounds 12a and 12d showed the best cytotoxicity activities against a panel of human cancer c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e7336a68864efb3226acaab439909276
https://doi.org/10.1016/j.ejmech.2022.114573
https://doi.org/10.1016/j.ejmech.2022.114573
Autor:
Dolor Renko, Romain Darrigrand, Marine Rouillon, Mouad Alami, Mathilde Boulpicante, Julien Marcoux, Michael Ghosh, Camille Garcia, Alison Pierson, David Bouyssié, Sébastien Apcher, Emmanuelle Mouton-Barbosa
Publikováno v:
Communications Biology
Communications Biology, Nature Publishing Group, 2021, 4 (1), ⟨10.1038/s42003-021-01801-2⟩
Communications Biology, Vol 4, Iss 1, Pp 1-14 (2021)
Communications Biology, Nature Publishing Group, 2021, 4 (1), ⟨10.1038/s42003-021-01801-2⟩
Communications Biology, Vol 4, Iss 1, Pp 1-14 (2021)
The success of cancer immunotherapy relies on the induction of an immunoprotective response targeting tumor antigens (TAs) presented on MHC-I molecules. We demonstrated that the splicing inhibitor isoginkgetin and its water-soluble and non-toxic deri
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a8b7ed2073a3b29ecd025c65e319e909
https://doi.org/10.1038/s42003-021-01801-2
https://doi.org/10.1038/s42003-021-01801-2
Autor:
Mathilde Boulpicante, Camille Garcia, Marie-Charlotte Laiguillon, Marine Rouillon, Romain Darrigrand, Camille Lobry, Michael Ghosh, Zafiarisoa Dolor Renko, Alison Pierson, Sébastien Apcher, Mouad Alami
The success of cancer immunotherapy relies on the induction of an immunoprotective response targeting tumor antigens (TAs) presented by tumor cells on MHC class I molecules. Alternative translation events emerged as a rich source of TAs and generate
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2d4d6a351cac1ab7c3911a67849b7d10
https://doi.org/10.1101/512681
https://doi.org/10.1101/512681
Autor:
Abdallah Hamze, Olivier Provot, Mouad Alami, Ling-Zhi Yuan, Dolor Renko, Jean-Daniel Brion, Ilhem Khelifi
Publikováno v:
ChemInform. 47
The reaction generally proceeds with excellent α-selectivity at the carbonyl group proximal to the more electron-rich aromatic ring.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1a5ee8d1aeffff195068eae57bded2fc
https://doi.org/10.1002/chin.201646095
https://doi.org/10.1002/chin.201646095
Autor:
Jérôme Bignon, Ilhem Khelifi, Jean-Daniel Brion, Christine Lenoir, Dolor Renko, Mouad Alami, Olivier Provot, Timothée Naret, Guillaume Bernadat, Joëlle Dubois, Abdallah Hamze
Publikováno v:
European Journal of Medicinal Chemistry
European Journal of Medicinal Chemistry, Elsevier, 2017, 127, pp.1025-1034. ⟨10.1016/j.ejmech.2016.11.012⟩
European Journal of Medicinal Chemistry, Elsevier, 2017, 127, pp.1025-1034. ⟨10.1016/j.ejmech.2016.11.012⟩
International audience; (O.P.) and/or mouad.alami@u-psud.fr (M.A.) Abstract The synthesis and evaluation of a new series of IsoCombretaQuinolines (IsoCoQuines) 2 with a 2-substituted-quinoline in place of the 3,4,5-trimethoxyphenyl ring present in is
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f31694a3754714126a9a63959d1dd805
https://pubmed.ncbi.nlm.nih.gov/28166995
https://pubmed.ncbi.nlm.nih.gov/28166995
Autor:
Dolor Renko, Jean-Daniel Brion, Mouad Alami, Ling-Zhi Yuan, Olivier Provot, Abdallah Hamze, Ilhem Khelifi
Publikováno v:
Organic Letters
Organic Letters, American Chemical Society, 2016, 18 (13), pp.3238-3241. ⟨10.1021/acs.orglett.6b01491⟩
Organic Letters, American Chemical Society, 2016, 18 (13), pp.3238-3241. ⟨10.1021/acs.orglett.6b01491⟩
International audience; For the first time, the combination of chlorotrimethylsilane with NaI is used as a selective reducting system toward 1,2-diketones. This combination is successfully evaluated with several unsymmetrically benzil derivatives, wh
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b65116d53eb89505fa38b89f4c7fb915
https://pubmed.ncbi.nlm.nih.gov/27337273
https://pubmed.ncbi.nlm.nih.gov/27337273
Autor:
Joëlle Dubois, Abdallah Hamze, Dolor Renko, Jordi Rodrigo, Mouad Alami, Jean-Daniel Brion, Jérôme Bignon, Olivier Provot, Evelia Rasolofonjatovo
Publikováno v:
ChemInform. 46
A high yield procedure for the synthesis of various functionalized 4-arylchromene derivatives [cf.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::217340f93b720fcd787df7badef25d48
https://doi.org/10.1002/chin.201523155
https://doi.org/10.1002/chin.201523155