dc.contributor.author | Morretta, Elva | |
dc.date.accessioned | 2023-04-20T16:53:31Z | |
dc.date.available | 2023-04-20T16:53:31Z | |
dc.date.issued | 2020-10-24 | |
dc.identifier.uri | http://elea.unisa.it:8080/xmlui/handle/10556/6579 | |
dc.identifier.uri | http://dx.doi.org/10.14273/unisa-4644 | |
dc.description | 2018 - 2019 | it_IT |
dc.description.abstract | The 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.iso | en | it_IT |
dc.publisher | Universita degli studi di Salerno | it_IT |
dc.subject | Proteomica | it_IT |
dc.subject | Spettrometria di massa | it_IT |
dc.title | Interactome analysis of bioactive molecules: optimization of a functional proteomics platform | it_IT |
dc.type | Doctoral Thesis | it_IT |
dc.subject.miur | CHIM/06 CHIMICA ORGANICA | it_IT |
dc.contributor.coordinatore | Sbardella, Gianluca | it_IT |
dc.description.ciclo | XXXII ciclo | it_IT |
dc.contributor.tutor | Casapullo, Agostino | it_IT |
dc.identifier.Dipartimento | Farmacia | it_IT |