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

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.
12-dic-2017
Area 06 - Scienze mediche
pirrolidine, oxazolidin-2-imine and mercaptoketones, HCV, HIV, HDAC inhibitors
Università degli Studi di Catania
Italy
File in questo prodotto:
File Dimensione Formato  
MNCGLI88E68C351Z.pdf

accesso solo da BNCF e BNCR

Tipologia: Altro materiale allegato
Dimensione 4.44 MB
Formato Adobe PDF
4.44 MB Adobe PDF

I documenti in UNITESI sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.

Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.14242/145877
Il codice NBN di questa tesi è URN:NBN:IT:UNICT-145877