Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Salomé El Hage"'
Autor:
Jeanne Trognon, Gonzalo Vera, Maya Rima, Jean-Luc Stigliani, Laurent Amielet, Salomé El Hage, Barbora Lajoie, Christine Roques, Fatima El Garah
Publikováno v:
Pharmaceuticals, Vol 15, Iss 4, p 417 (2022)
Biofilm formation is considered a major cause of therapeutic failure because bacteria in biofilms have higher protection against antimicrobials. Thus, biofilm-related infections are extremely challenging to treat and pose major concerns for public he
Externí odkaz:
https://doaj.org/article/c3ae9fd1c30244b2837250f9a0421635
Autor:
Geneviève Baziard, Alaa Hamdar, Barbora Lajoie, Christine Roques, Fatima El Garah, Salomé El Hage
Publikováno v:
Process Biochemistry
Process Biochemistry, Elsevier, 2019, 77, pp.18-22. ⟨10.1016/j.procbio.2018.11.011⟩
Process Biochemistry, Elsevier, 2019, 77, pp.18-22. ⟨10.1016/j.procbio.2018.11.011⟩
Description of the relationship between protein structure and function remains a primary focus in molecular biology, biochemistry, protein engineering and bioelectronics. Moreover, the investigation of the protein conformational changes after adhesio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e532f820503f26c0d88abdfb0e10fd18
https://doi.org/10.1016/j.procbio.2018.11.011
https://doi.org/10.1016/j.procbio.2018.11.011
Autor:
Fatima Bousejra-El Garah, Salomé El Hage, Jean-Pierre Souchard, Jalloul Bouajila, Geneviève Baziard, Barbora Lajoie Halova
Publikováno v:
Medicinal Chemistry Research
Medicinal Chemistry Research, Springer Verlag, 2016, 25 (11), pp.2547-2556. ⟨10.1007/s00044-016-1691-y⟩
Medicinal Chemistry Research, Springer Verlag, 2016, 25 (11), pp.2547-2556. ⟨10.1007/s00044-016-1691-y⟩
International audience; In the present study, we prepared a series of 21 chromone carboxamide derivatives bearing diverse amide side chains. Their potency to inhibit the proliferation of breast (MCF-7), ovarian (OVCAR and IGROV), and colon (HCT-116)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::39e10bee2a5261266cf777d387995510
https://doi.org/10.1007/s00044-016-1691-y
https://doi.org/10.1007/s00044-016-1691-y
Publikováno v:
Archiv der Pharmazie. 344:402-410
Two series of chlorinated benzhydryl imidazole and triazole derivatives were synthesized and tested in vitro against representative strains of potent pathogenic bacteria (Staphylococcus aureus CIP 4.83, Escherichia hirae CIP 5855, Pseudomonas aerugin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::04a7b43d09a82980bc421c1429ff7242
https://doi.org/10.1002/ardp.201000304
https://doi.org/10.1002/ardp.201000304
Autor:
Salomé El Hage, Christine Roques, Jean-Luc Stigliani, Geneviève Baziard, Barbora Lajoie, Aurélie Furiga-Chusseau
Publikováno v:
Journal of Applied Biomedicine
Journal of Applied Biomedicine, University of South Bohemia in České Budějovice, 2014, 12 (4), pp.245-253. ⟨10.1016/j.jab.2014.02.002⟩
Journal of Applied Biomedicine, 2014, 12 (4), pp.245-253. ⟨10.1016/j.jab.2014.02.002⟩
Journal of Applied Biomedicine, University of South Bohemia in České Budějovice, 2014, 12 (4), pp.245-253. ⟨10.1016/j.jab.2014.02.002⟩
Journal of Applied Biomedicine, 2014, 12 (4), pp.245-253. ⟨10.1016/j.jab.2014.02.002⟩
International audience; Quaternary ammonium salts (chloride, bromide and iodide; QUATs) with n-alkyl chain lengths between C8 and C18 have been synthesized under optimized experimental conditions. These compounds were tested in vitro for antimicrobia
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6e326c47b3f312b837f246485837c79c
https://oatao.univ-toulouse.fr/20234/
https://oatao.univ-toulouse.fr/20234/
Autor:
Jean Luc Stigliani, Salomé El Hage, Marc Payard, Jean-Guy Bizot-Espiard, Louis Crane, Daniel-Henri Caignard, Jean-Michel Léger, Labssita Youssef, Alain Ktorza, Maria Anastassiadou, Pierre Renard
Publikováno v:
Bioorganicmedicinal chemistry. 14(22)
Imidazoline derivatives have been reported to show antihyperglycemic activity in vivo. In the present study, we first showed that there was no correlation between the in vivo antidiabetic activity and the in vitro affinities for the I1/I2 binding sit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dbdf4e6180dc311842e0920ba5d87608
https://pubmed.ncbi.nlm.nih.gov/16889967
https://pubmed.ncbi.nlm.nih.gov/16889967