Zobrazeno 1 - 10
of 27
pro vyhledávání: '"Tchirioua Ekou"'
Publikováno v:
E-Journal of Chemistry, Vol 8, Iss 3, Pp 1394-1400 (2011)
Inhibitors of histone deacetylases (HDACs) are patent inducers of differentiation and bear considerable potential as drugs for chemoprevention and treatment of cancer. In this paper, we have investigated three synthetic, inhibitors A1a,b, A2a. Analog
Externí odkaz:
https://doaj.org/article/82c3704bd4b24635a20202a526a83e50
Publikováno v:
E-Journal of Chemistry, Vol 8, Iss S1, Pp S79-S84 (2011)
The inhibition of HDAC (histone deacetylase) activity by specific inhibitors induces growth arrest, differentiation and apoptosis of transformed or several cancer cells. Some of these inhibitors are in clinical trial at phase I or phase II. The disco
Externí odkaz:
https://doaj.org/article/995007e3bd534c1cb5cd67c62251c4ac
Autor:
Zoungranan, Yacouba *, Lynda, Ekou, Dobi-Brice, Kouassi Kouadio, Tchirioua, Ekou, Bakary, Coulibaly, Yannick, Dje Daniel
Publikováno v:
In Journal of Environmental Chemical Engineering October 2020 8(5)
Publikováno v:
Rasayan Journal of chemistry. 13:1933-1943
Publikováno v:
European Journal of Engineering Research and Science. 4:45-49
Several studies have been carried out on the structure of hydroxamic acids as histone deacetylase inhibitors. Scientists discovered that the (-CONHOH) moiety of hydroxamic acids was responsible for the chelation of the zinc ion into the active site o
Autor:
Nahossé Ziao, Lynda Ekou, Tchirioua Ekou, Bafétigué Ouattara, Doh Soro, Mamadou Guy-Richard Koné
Publikováno v:
Computational Molecular Bioscience. :63-80
In this work, we conducted a QSAR study on 18 molecules using descriptors from the Density Functional Theory (DFT) in order to predict the inhibitory activity of hydroxamic acids on histone deacetylase 7. This study is performed using the principal c
Autor:
Elvina Barré, Lynda Ekou, Mireia Rodriguez-Zubiri, Ehu Camille Aka, François-Xavier Felpin, Daniel Cortés-Borda, Eric Wimmer, Tchirioua Ekou
Publikováno v:
Organic Process Research and Development
Organic Process Research and Development, American Chemical Society, 2020, 24 (5), pp.745-751. ⟨10.1021/acs.oprd.9b00525⟩
Organic Process Research and Development, American Chemical Society, 2020, 24 (5), pp.745-751. ⟨10.1021/acs.oprd.9b00525⟩
The hazardous nature of molecular oxygen can be mitigated with the use of flow reactors of small size, which in turn accelerate the gas-to-liquid mass transfer rate. In this contribution, we describe a reconfigurable automated flow platform integrati
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::803eea9bf7ed00c3d89fcb9d3337aafa
https://hal.archives-ouvertes.fr/hal-03003776/file/Manuscript-Felpin-10012020.pdf
https://hal.archives-ouvertes.fr/hal-03003776/file/Manuscript-Felpin-10012020.pdf
Autor:
Medy C. Nongbe, Guillaume Bretel, Tchirioua Ekou, Lynda Ekou, Erwan Le Grognec, Benjamin K. Yao, François-Xavier Felpin
Publikováno v:
Cellulose
Cellulose, 2018, 25 (7), pp.4043-4055. ⟨10.1007/s10570-018-1833-0⟩
Cellulose, 2018, 25 (7), pp.4043-4055. ⟨10.1007/s10570-018-1833-0⟩
International audience; The preparation of new adsorbents for heavy metals consisting of cellulose paper grafted with polyamine moieties is described. The tosylation of pristine cellulose paper allowed the subsequent displacement of the tosylated lea
Autor:
Mamadou Guy-Richard Koné, Tchirioua Ekou, Doh Soro, Nahossé Ziao, Sopi Thomas Affi, Lamoussa Ouattara, Lynda Ekou
Publikováno v:
International Research Journal of Pure and Applied Chemistry. 16:1-13
Autor:
Medy C. Nongbe, Tchirioua Ekou, Lynda Ekou, Ehu Camille Aka, Vincent Coeffard, François-Xavier Felpin
Publikováno v:
Journal of Environmental Sciences
Journal of Environmental Sciences, Elsevier, 2019, 84, pp.174-183. ⟨10.1016/j.jes.2019.05.006⟩
Journal of Environmental Sciences, Elsevier, 2019, 84, pp.174-183. ⟨10.1016/j.jes.2019.05.006⟩
International audience; The fabrication of a fully bio-sourced adsorbent of Cd(II) by covalent immobilization of quinine on cellulose paper is described. The double bond of commercially available quinine was converted to a terminal alkyne function wh