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dc.provenanceCONICET-
dc.creatorVelappan, Anand Babu-
dc.creatorCharan Raja, Mamilla R.-
dc.creatorDatta, Dhrubajyoti-
dc.creatorTsai, Yi Ting-
dc.creatorHalloum, Iman-
dc.creatorWan, Baojie-
dc.creatorKremer, Laurent-
dc.creatorGramajo, Hugo Cesar-
dc.creatorFranzblau, Scott G.-
dc.creatorKar Mahapatra, Santanu-
dc.creatorDebnath, Joy-
dc.date2018-07-19T20:42:49Z-
dc.date2018-07-19T20:42:49Z-
dc.date2016-09-
dc.date2018-07-18T20:48:34Z-
dc.date.accessioned2019-04-29T15:37:53Z-
dc.date.available2019-04-29T15:37:53Z-
dc.date.issued2016-09-
dc.identifierVelappan, Anand Babu; Charan Raja, Mamilla R.; Datta, Dhrubajyoti; Tsai, Yi Ting; Halloum, Iman; et al.; Attenuation of Mycobacterium species through direct and macrophage mediated pathway by unsymmetrical diaryl urea; Elsevier France-editions Scientifiques Medicales Elsevier; European Journal of Medical Chemistry; 125; 9-2016; 825-841-
dc.identifier0223-5234-
dc.identifierhttp://hdl.handle.net/11336/52712-
dc.identifierCONICET Digital-
dc.identifierCONICET-
dc.identifier.urihttp://rodna.bn.gov.ar:8080/jspui/handle/bnmm/298098-
dc.descriptionTuberculosis is a major threat for mankind and the emergence of resistance strain of Mycobacterium tuberculosis (Mtb) against first line antibiotics makes it lethal for human civilization. In this study, we have synthesized different diaryl urea derivatives targeting the inhibition of mycolic acid biosynthesis. Among the 39 synthesized molecules, compounds 46, 57, 58 and 86 showed MIC values ≤ 10 μg/ml against H37Rv and mc26030 strains. The best molecule with a methyl at ortho position of the first aromatic ring and prenyl group at the meta position of the second aromatic ring showed the MIC value of 5.2 μg/ml and 1 μg/ml against H37Rv and mc26030 respectively, with mammalian cytotoxicity of 163.4 μg/ml. The effective compounds showed selective inhibitory effect on mycolic acid (epoxy mycolate) biosynthesis in14C-radiolabelled assay. At the same time these molecules also executed their potent immunomodulatory activity by up-regulation of IFN-γ and IL-12 and down-regulation of IL-10.-
dc.descriptionFil: Velappan, Anand Babu. Sastra University; India-
dc.descriptionFil: Charan Raja, Mamilla R.. Sastra University; India-
dc.descriptionFil: Datta, Dhrubajyoti. Indian Institute of Science Education and Research Pune; India-
dc.descriptionFil: Tsai, Yi Ting. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Rosario. Instituto de Biología Molecular y Celular de Rosario. Universidad Nacional de Rosario. Facultad de Ciencias Bioquímicas y Farmacéuticas. Instituto de Biología Molecular y Celular de Rosario; Argentina-
dc.descriptionFil: Halloum, Iman. Université de Montpellier; Francia. Centre National de la Recherche Scientifique; Francia-
dc.descriptionFil: Wan, Baojie. University of Illinois; Estados Unidos-
dc.descriptionFil: Kremer, Laurent. Université de Montpellier; Francia. Inserm; Francia. Centre National de la Recherche Scientifique; Francia-
dc.descriptionFil: Gramajo, Hugo Cesar. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Rosario. Instituto de Biología Molecular y Celular de Rosario. Universidad Nacional de Rosario. Facultad de Ciencias Bioquímicas y Farmacéuticas. Instituto de Biología Molecular y Celular de Rosario; Argentina-
dc.descriptionFil: Franzblau, Scott G.. University of Illinois; Estados Unidos-
dc.descriptionFil: Kar Mahapatra, Santanu. Sastra University; India-
dc.descriptionFil: Debnath, Joy. Sastra University; India-
dc.formatapplication/pdf-
dc.formatapplication/pdf-
dc.formatapplication/pdf-
dc.languageeng-
dc.publisherElsevier France-editions Scientifiques Medicales Elsevier-
dc.relationinfo:eu-repo/semantics/altIdentifier/doi/http://dx.doi.org/10.1016/j.ejmech.2016.09.083-
dc.relationinfo:eu-repo/semantics/altIdentifier/url/https://www.sciencedirect.com/science/article/pii/S0223523416308170-
dc.rightsinfo:eu-repo/semantics/openAccess-
dc.rightshttps://creativecommons.org/licenses/by-nc-nd/2.5/ar/-
dc.sourcereponame:CONICET Digital (CONICET)-
dc.sourceinstname:Consejo Nacional de Investigaciones Científicas y Técnicas-
dc.sourceinstacron:CONICET-
dc.source.urihttp://hdl.handle.net/11336/52712-
dc.subjectANTIMYCOBACTERIAL ACTIVITY-
dc.subjectCYTOKINES-
dc.subjectCYTOTOXICITY-
dc.subjectDIARYL UREA-
dc.subjectMYCOLIC ACID-
dc.subjectSTRUCTURE-ACTIVITY RELATIONSHIP-
dc.subjectTUBERCULOSIS-
dc.subjectOtras Ciencias Químicas-
dc.subjectCiencias Químicas-
dc.subjectCIENCIAS NATURALES Y EXACTAS-
dc.titleAttenuation of Mycobacterium species through direct and macrophage mediated pathway by unsymmetrical diaryl urea-
dc.typeinfo:eu-repo/semantics/article-
dc.typeinfo:eu-repo/semantics/publishedVersion-
dc.typeinfo:ar-repo/semantics/articulo-
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