In this work a novel synthetic approach to 4-anilinoquinazoline derivatives analogues of Erlotinib as EGFR inhibitors is described. Synthesized compounds have been evaluated for their citotoxicity against specific cell lines. Moereover, a novel computational approach to study several tyrosin kinase inhibitors and related targets based on Complex Networks - QSAR strategy is reported.In questa tesi è descritto un nuovo approccio per la sintesi di derivati 4-anilinochinazolinici analoghi di Erlotinib come potenziali inibitori di EGFR. I composti sintetizzati sono stati valutati per la loro attività citotossica nei confronti di specifiche linee cellulari. E' inoltre descritto un nuovo approccio computazione di tipo Complex Network - QSAR per lo...
In this paper, a set of 3-methylquniazolinone derivatives were designed, synthesised, and studied th...
Cancer is a disease characterized by the anarchistic and uncontrolled proliferation of cells having ...
A series of quinazoline derivatives with benzylidene hydrazine carboxamide were designed and synthes...
This paper is an attempt to design 4-anilinoquinazoline compounds having promising anticancer activi...
In the last decade, some progresses have been reached in the cancer treatment, mainly through the ap...
Identification of novel targets critical for cancer growth and progression, and development of inhib...
4-Anilinoquinazolines have been widely studied as anticancer agents. Despite the widespread utility ...
In the last few years, among various suitable biological targets for cancer treatment, special atten...
Quinazoline is one of the most widespread scaffolds amongst natural and synthetic bioactive compound...
Receptor tyrosine kinases (RTKs) play key roles in signal transduction pathways, thereby affecting m...
The discovery of the anticancer drugs erlotinib and gefitinib in the early 2000\u2019s prompted inte...
On the basis of combination strategy, a novel series of EGFR inhibitors were designed and synthesize...
The aim of this project was to synthesize new PET tracers for the imaging of the EGFR/HER-2 expressi...
4-Anilinoquinazolines as an important class of protein kinase inhibitor are widely investigated for ...
4-Anilinoquinazolines as an important class of protein kinase inhibitor are widely investigated for ...
In this paper, a set of 3-methylquniazolinone derivatives were designed, synthesised, and studied th...
Cancer is a disease characterized by the anarchistic and uncontrolled proliferation of cells having ...
A series of quinazoline derivatives with benzylidene hydrazine carboxamide were designed and synthes...
This paper is an attempt to design 4-anilinoquinazoline compounds having promising anticancer activi...
In the last decade, some progresses have been reached in the cancer treatment, mainly through the ap...
Identification of novel targets critical for cancer growth and progression, and development of inhib...
4-Anilinoquinazolines have been widely studied as anticancer agents. Despite the widespread utility ...
In the last few years, among various suitable biological targets for cancer treatment, special atten...
Quinazoline is one of the most widespread scaffolds amongst natural and synthetic bioactive compound...
Receptor tyrosine kinases (RTKs) play key roles in signal transduction pathways, thereby affecting m...
The discovery of the anticancer drugs erlotinib and gefitinib in the early 2000\u2019s prompted inte...
On the basis of combination strategy, a novel series of EGFR inhibitors were designed and synthesize...
The aim of this project was to synthesize new PET tracers for the imaging of the EGFR/HER-2 expressi...
4-Anilinoquinazolines as an important class of protein kinase inhibitor are widely investigated for ...
4-Anilinoquinazolines as an important class of protein kinase inhibitor are widely investigated for ...
In this paper, a set of 3-methylquniazolinone derivatives were designed, synthesised, and studied th...
Cancer is a disease characterized by the anarchistic and uncontrolled proliferation of cells having ...
A series of quinazoline derivatives with benzylidene hydrazine carboxamide were designed and synthes...