Search Results - "Zonta, Nicola"
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Design, synthesis and structure–activity relationship of 2-(3′,4′,5′-trimethoxybenzoyl)-benzo[ b]furan derivatives as a novel class of inhibitors of tubulin polymerization
Published in Bioorganic & medicinal chemistry (01-10-2009)“…The biological importance of microtubules in mitosis and cell division makes them an interesting target for the development of anticancer agents. Small…”
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Synthesis and Biological Evaluation of 1-Methyl-2-(3′,4′,5′-trimethoxybenzoyl)-3-aminoindoles as a New Class of Antimitotic Agents and Tubulin Inhibitors
Published in Journal of medicinal chemistry (13-03-2008)“…The 2-(3,4,5-trimethoxybenzoyl)-2-aminoindole nucleus was used as the fundamental structure for the synthesis of compounds modified with respect to positions…”
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Advanced in silico Approaches in Antiviral Research
Published in Antiviral chemistry & chemotherapy (01-04-2010)“…Computer-aided drug design has seen constantly increasing application over the past two decades in every area of drug discovery. It can offer significant…”
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Computer-aided identification, design and synthesis of a novel series of compounds with selective antiviral activity against chikungunya virus
Published in Antiviral research (01-04-2013)“…► A homology model for the CHIKV nsP2 protease was constructed and validated. ► A new class of inhibitors of CHIKV replication was identified by virtual…”
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Design, synthesis and evaluation of a novel double pro-drug: INX-08189. A new clinical candidate for hepatitis C virus
Published in Bioorganic & medicinal chemistry letters (15-08-2010)“…Phosphoramidate ProTides of 2′-C-Me-6-MeOG are up to 500-fold more potent versus HCV than the 2′-C-MeG parent, being active at nanomolar levels. The lead has…”
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Design, synthesis, and biological evaluation of thiophene analogues of chalcones
Published in Bioorganic & medicinal chemistry (15-05-2008)“…Chalcones are characterized by possessing an enone moiety between two aromatic rings. A series of chalcone-like agents, in which the double bond of the enone…”
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Synthesis and Antiviral Activity of the Carbocyclic Analogue of the Highly Potent and Selective Anti-VZV Bicyclo Furano Pyrimidines
Published in Journal of medicinal chemistry (27-12-2007)“…Carbocyclic nucleoside analogues are catabolically stable since they are resistant to phosphorolytic cleavage by pyrimidine nucleoside phosphorylase enzymes…”
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Accessible haptic technology for drug design applications
Published in Journal of molecular modeling (01-02-2009)“…Structure-based drug design is a creative process that displays several features that make it closer to human reasoning than to machine automation. However,…”
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Virtual Reality Applications in Antiviral Drug Design
Published in Antiviral research (01-05-2009)Get full text
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Development and application of modelling techniques in drug design
Published 01-01-2009“…Structure-based drug design is a creative process that displays several features that make it closer to human reasoning than to machine automation. However,…”
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Dissertation