Zobrazeno 1 - 10
of 91
pro vyhledávání: '"MESH : Indoles"'
Autor:
Dorine Fournier, Stéphane Jouneau, Guillaume Bouzillé, Elisabeth Polard, Marie-Noëlle Osmont, Lucie-Marie Scailteux
Publikováno v:
Pulmonary Pharmacology and Therapeutics
Pulmonary Pharmacology and Therapeutics, 2022, 76, pp.102149. ⟨10.1016/j.pupt.2022.102149⟩
Annual Meeting of French Society of Pharmacology and Therapeutics
Annual Meeting of French Society of Pharmacology and Therapeutics, Jun 2022, Lille, France. 36, pp.77-78, 2022
Pulmonary Pharmacology and Therapeutics, 2022, 76, pp.102149. ⟨10.1016/j.pupt.2022.102149⟩
Annual Meeting of French Society of Pharmacology and Therapeutics
Annual Meeting of French Society of Pharmacology and Therapeutics, Jun 2022, Lille, France. 36, pp.77-78, 2022
Introduction: While pirfenidone and nintedanib have greatly influenced the treatment of idiopathic pulmonary fibrosis (IPF), both drugs have significant early adverse drug reactions (ADRs) and almost nothing is known of their rare and delayed ADRs. W
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::41f463e5ba0ebf3d17710bd8bdd4015b
https://univ-rennes.hal.science/hal-03954444/document
https://univ-rennes.hal.science/hal-03954444/document
Autor:
Gwenaelle Le Garff, Margaux Geier, Lionel Falchero, Jean-Bernard Auliac, A. Bizieux, Alain Vergnenegre, Charles Ricordel, Florian Guisier, Laurent Greillier, Isabelle Monnet, R. Lamy, Refract Gfpc investigators, Christos Chouaid
Publikováno v:
Lung Cancer
Lung Cancer, 2021, 161, pp.122-127. ⟨10.1016/j.lungcan.2021.09.007⟩
Lung Cancer, Elsevier, 2021, 161, pp.122-127. ⟨10.1016/j.lungcan.2021.09.007⟩
Lung Cancer, 2021, 161, pp.122-127. ⟨10.1016/j.lungcan.2021.09.007⟩
Lung Cancer, Elsevier, 2021, 161, pp.122-127. ⟨10.1016/j.lungcan.2021.09.007⟩
Introduction Advanced non-squamous non-small cell lung cancer (NsqNSCLC) progressing at the induction of a first-line of platin-based chemotherapy is a subgroup of patients with poor prognosis and few second-line treatment options. Materials and Meth
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7d1b9fe5d0e6dc748f9ad0dda55f243d
https://hal.inria.fr/hal-03524385
https://hal.inria.fr/hal-03524385
Autor:
Bruno Ragazzon, Jean-Christophe Pointud, Houda Tabbal, Pierre Val, Igor Tauveron, Coralie Drelon, M. Batisse-Lignier, Cyril Djari, Stéphanie Rodriguez, Anne-Marie Lefrançois-Martinez, Amandine Septier, Jérôme Bertherat, Guillaume Assié, Isabelle Sahut-Barnola, Mickael Mathieu, Antoine Martinez
Publikováno v:
British Journal of Cancer
British Journal of Cancer, Cancer Research UK, 2019, 121 (5), pp.384-394. ⟨10.1038/s41416-019-0538-y⟩
British Journal of Cancer, 2019, 121 (5), pp.384-394. ⟨10.1038/s41416-019-0538-y⟩
British Journal of Cancer, Cancer Research UK, 2019, 121 (5), pp.384-394. ⟨10.1038/s41416-019-0538-y⟩
British Journal of Cancer, 2019, 121 (5), pp.384-394. ⟨10.1038/s41416-019-0538-y⟩
International audience; BACKGROUND: EZH2 is overexpressed and associated with poor prognosis in adrenocortical carcinoma (ACC) and its inhibition reduces growth and aggressiveness of ACC cells in culture. Although EZH2 was identified as the methyltra
Autor:
Jessica Bertrand, Bernard Payrastre, N Gallay, Nathalie Vergnolle, Véronique Maguer-Satta, Mathieu Despeaux, Cécile Demur, Ezzeddine Bourogaa, S Joly, P Bonnevialle, F Louache, Claire Racaud-Sultan
Publikováno v:
Oncogene
Oncogene, Nature Publishing Group, 2012, 31 (6), pp.694-705. 〈10.1038/onc.2011.258〉
Oncogene, Nature Publishing Group, 2012, 31 (6), pp.694-705. ⟨10.1038/onc.2011.258⟩
Oncogene, Nature Publishing Group, 2012, 31 (6), pp.694-705. 〈10.1038/onc.2011.258〉
Oncogene, Nature Publishing Group, 2012, 31 (6), pp.694-705. ⟨10.1038/onc.2011.258⟩
International audience; Therapeutic resistance of acute myeloid leukemia stem cells, enriched in the CD34(+)38(-)123(+) progenitor population, is supported by extrinsic factors such as the bone marrow niche. Here, we report that when adherent onto fi
Autor:
Hossam M. Draz, Alexander A. Goldberg, J. Thomas Sanderson, Stephen Safe, Vladimir I. Titorenko, Emma S. Tomlinson Guns
Publikováno v:
Cellular Signalling
Cellular Signalling, Elsevier, 2017, 40, pp.172-182. ⟨10.1016/j.cellsig.2017.09.006⟩
Cellular Signalling, Elsevier, 2017, 40, pp.172-182. ⟨10.1016/j.cellsig.2017.09.006⟩
International audience; 3,3'-Diindolylmethane (DIM) and its synthetic halogenated derivatives 4,4'-Br2- and 7,7'-Cl2DIM (ring-DIMs) have recently been shown to induce protective autophagy in human prostate cancer cells. The mechanisms by which DIM an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e7331239d2af63ac200a47891a978e8b
https://hal-riip.archives-ouvertes.fr/pasteur-01854432
https://hal-riip.archives-ouvertes.fr/pasteur-01854432
Publikováno v:
Neuropharmacology
Neuropharmacology, Elsevier, 2017, 115, pp.92-99. ⟨10.1016/j.neuropharm.2016.06.001⟩
Neuropharmacology, Elsevier, 2017, 115, pp.92-99. ⟨10.1016/j.neuropharm.2016.06.001⟩
International audience; The orphan Glutamate receptor Delta2 (GluD2) intrinsic ion channel activity is indirectly triggered by glutamate through stimulation of the metabotropic glutamate receptor 1 (mGlu1), in cerebellar Purkinje cells. However, the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4e81109bd037540b03d7a019764b76ad
https://hal.archives-ouvertes.fr/hal-03109591
https://hal.archives-ouvertes.fr/hal-03109591
Autor:
Stephanie Troy-Fioramonti, Laurent Demizieux, Joseph Gresti, Tania Muller, Bruno Vergès, Pascal Degrace
Publikováno v:
Diabetes
Diabetes, American Diabetes Association, 2015, 64 (3), pp.808-18. ⟨10.2337/db14-0721⟩
Diabetes, American Diabetes Association, 2015, 64 (3), pp.808-18. 〈10.2337/db14-0721〉
Diabetes, American Diabetes Association, 2015, 64 (3), pp.808-18. ⟨10.2337/db14-0721⟩
Diabetes, American Diabetes Association, 2015, 64 (3), pp.808-18. 〈10.2337/db14-0721〉
International audience; The endocannabinoid system (ECS) is associated with an alteration of glucose homeostasis dependent on cannabinoid receptor-1 (CB1R) activation. However, very little information is available concerning the consequences of ECS a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3e025a03b2eaffb58d5ca253aa302691
https://www.hal.inserm.fr/inserm-01344501
https://www.hal.inserm.fr/inserm-01344501
Autor:
Andrea Medeiros, Laurent Meijer, Nadège Loaëc, Oliver Koch, Ricarda S. Korn, Lutz Preu, Conrad Kunick, Marcelo A. Comini, Diego Benítez, Oliver C.F. Orban
Publikováno v:
Bioorganic and Medicinal Chemistry
Bioorganic and Medicinal Chemistry, Elsevier, 2016, 24 (16), pp.3790-800. ⟨10.1016/j.bmc.2016.06.023⟩
Bioorganic and Medicinal Chemistry, Elsevier, 2016, 24 (16), pp.3790-800. ⟨10.1016/j.bmc.2016.06.023⟩
International audience; Trypanothione synthetase is an essential enzyme for kinetoplastid parasites which cause highly disabling and fatal diseases in humans and animals. Inspired by the observation that N(5)-substituted paullones inhibit the trypano
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::80e4e9673479b0f5057fd3ad369138d5
https://hal-riip.archives-ouvertes.fr/pasteur-01499026
https://hal-riip.archives-ouvertes.fr/pasteur-01499026
Autor:
Frédéric Buron, Emeline Vedrenne, Cleopatra Neagoie, Olivier Lozach, Laurent Meijer, Stéphane Bourg, Sorin Rosca, Amélie Lansiaux, Sylvain Routier, Brigitte Baldeyrou, Jean-Yves Mérour
Publikováno v:
European Journal of Medicinal Chemistry
European Journal of Medicinal Chemistry, 2012, 49, pp.379-96. ⟨10.1016/j.ejmech.2012.01.040⟩
European Journal of Medicinal Chemistry, Elsevier, 2012, 49, pp.379-96. ⟨10.1016/j.ejmech.2012.01.040⟩
European Journal of Medicinal Chemistry, Elsevier, 2012, 49, pp.379-396. ⟨10.1016/j.ejmech.2012.01.040⟩
European Journal of Medicinal Chemistry, 2012, 49, pp.379-96. ⟨10.1016/j.ejmech.2012.01.040⟩
European Journal of Medicinal Chemistry, Elsevier, 2012, 49, pp.379-96. ⟨10.1016/j.ejmech.2012.01.040⟩
European Journal of Medicinal Chemistry, Elsevier, 2012, 49, pp.379-396. ⟨10.1016/j.ejmech.2012.01.040⟩
International audience; A library of substituted chromeno[3,4-b]indoles was developed as Lamellarin isosters. Synthesis was achieved from indoles after a four-step pathway sequence involving C-3 iodination, a Suzuki cross-coupling reaction, and a one
Autor:
Olga N. Burchak, Jean-Noel Denis, Max Maurin, Carmela Giglione, Xavier Guinchard, Claude Jolivalt, Laure Maigre, Emmanuelle Le Pihive, Dominique Schneider, Pascale Bouhours, Jean-Marc Paris, Thierry Meinnel
Publikováno v:
Bioorganic and Medicinal Chemistry
Bioorganic and Medicinal Chemistry, Elsevier, 2011, 19 (10), pp.3204-15. ⟨10.1016/j.bmc.2011.03.060⟩
Bioorganic and Medicinal Chemistry, Elsevier, 2011, 19 (10), pp.3204-15. ⟨10.1016/j.bmc.2011.03.060⟩
International audience; A collection of 3-substituted indole derivatives was prepared using nucleophilic addition of indoles to nitrones. The compounds were then tested for their antibacterial activity against almost thirty bacterial strains represen