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dc.contributor.authorRusso, Alessandra
dc.date.accessioned2018-12-13T12:38:15Z
dc.date.available2018-12-13T12:38:15Z
dc.date.issued2018-04-05
dc.identifier.urihttp://hdl.handle.net/10556/3037
dc.identifier.urihttp://dx.doi.org/10.14273/unisa-1325
dc.description2016 - 2017it_IT
dc.description.abstractCancer development is a complex pathological process that exploits a variety of biological actors. The identification of new molecular entities able to interfere with new biological targets, involved in tumorigenesis, is strongly needed, both for the development of new promising drug candidates, and, as chemical probes useful to further investigate less understood biological aspects. Two main targets, involved at different levels, in cancer development, have been thoroughly investigated: Macrodomain proteins, MacroD1 and MacroD2, and the Bcl-2 associated athanogene 3, BAG3 protein... [edited by Author]it_IT
dc.language.isoenit_IT
dc.publisherUniversita degli studi di Salernoit_IT
dc.subjectBAG3it_IT
dc.subjectMacrodomainsit_IT
dc.subjectAntitumoralit_IT
dc.titleDesign, synthesis and biological activity of new target selective antitumoral agentsit_IT
dc.typeDoctoral Thesisit_IT
dc.subject.miurCHIM/06 CHIMICA ORGANICAit_IT
dc.contributor.coordinatoreSbardella, Gianlucait_IT
dc.description.cicloXXX cicloit_IT
dc.contributor.tutorBruno, Inesit_IT
dc.identifier.DipartimentoFarmaciait_IT
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