Beschreibung
Virtual screening has become an integral part of the drug discovery process. Through the two main streams of VS, ligand based and structure based, various interesting new scaffolds could be defined. Many interesting detailed studies were implemented in this field of research. A comparative computational study of pharmacophore model generation was explored, mentioning the advantage and disadvantage of each method. Also, an employed comparison between the two main streams was mentioned using CDK-2 as representative example with detection of the most acceptable pharmacophore model. A promising linking between the direct (ligand docking) and indirect (pharmacophore model) methods to identify the successful scaffold was explored. This linking approach using pharmacophore post filtering aims to increase the hit rates with minimizing the time used in VS process. Further, different programs that handled direct ligand docking approach was mentioned with mapping of their algorithm.
Autorenporträt
Heba Elzahabi is an associate professor in College of Pharmacy, Al-Azhar University. Her research focused on searching new anticancer and antiviral agents. Now she is working in organometallic field, to investigate the effect of metal chelation on bioactivity of the organic ligands, with handling full thermal analysis of organometallic compounds.
Herstellerkennzeichnung:
OmniScriptum SRL
Str. Armeneasca 28/1, office 1
2012 Chisinau
MD
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