The main objective of this thesis was the synthesis of modified azanucleosides potential ihibitors of non-structural proteins of HCV virus ((NS) NS3/4A, NS4B, NS5A and NS5B). Moreover the research project included the synthesis of pyrimidine-1,3-oxazolidin-2-arylimino hybrids as HIV ihibitors and the synthesis of mercaptoketone deriatives as antitumor agents potential HDAC's inhibitor.

Synthesis and biological evaluation of pirrolidine, oxazolidin-2-imine and mercaptoketones derivates as HCV, HIV and HDAC inhibitors

MONCIINO, GIULIA
2017

Abstract

The main objective of this thesis was the synthesis of modified azanucleosides potential ihibitors of non-structural proteins of HCV virus ((NS) NS3/4A, NS4B, NS5A and NS5B). Moreover the research project included the synthesis of pyrimidine-1,3-oxazolidin-2-arylimino hybrids as HIV ihibitors and the synthesis of mercaptoketone deriatives as antitumor agents potential HDAC's inhibitor.
29-nov-2017
Inglese
CHIACCHIO, Ugo
LIBRA, Massimo
Università degli studi di Catania
Catania
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.14242/77643
Il codice NBN di questa tesi è URN:NBN:IT:UNICT-77643