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dc.contributor.authorMorretta, Elva
dc.date.accessioned2023-04-20T16:53:31Z
dc.date.available2023-04-20T16:53:31Z
dc.date.issued2020-10-24
dc.identifier.urihttp://elea.unisa.it:8080/xmlui/handle/10556/6579
dc.identifier.urihttp://dx.doi.org/10.14273/unisa-4644
dc.description2018 - 2019it_IT
dc.description.abstractThe identification of natural products (NPs) target proteins is pivotal to understand their mechanism of action, in order to develop molecular probes and/or potential drugs. In the last 15 years, affinity chromatography-coupled to mass spectrometry (AP-MS) has been the top-choice technique in the Drug Target Deconvolution field, having brought brilliant results in the targetome profiling of a multitude of bioactive compounds. Unfortunately, since a chemical modification of the molecule to be investigated is mandatory, AP MS is not suitable for compounds that do not exhibit properly reactive structural feature. .. [edited by the Author]it_IT
dc.language.isoenit_IT
dc.publisherUniversita degli studi di Salernoit_IT
dc.subjectProteomicait_IT
dc.subjectSpettrometria di massait_IT
dc.titleInteractome analysis of bioactive molecules: optimization of a functional proteomics platformit_IT
dc.typeDoctoral Thesisit_IT
dc.subject.miurCHIM/06 CHIMICA ORGANICAit_IT
dc.contributor.coordinatoreSbardella, Gianlucait_IT
dc.description.cicloXXXII cicloit_IT
dc.contributor.tutorCasapullo, Agostinoit_IT
dc.identifier.DipartimentoFarmaciait_IT
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