Structure­based drug design and AutoDock study of potential protein tyrosine kinase inhibitors.

Different classes of compounds were investigated for their binding affinities into different protein tyrosine kinases (PTKs) employing a novel flexible ligand docking approach by using AutoDock 3.05 and 4. These compounds include many flavin analogs, which were developed in our group with varying de...

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Detalles Bibliográficos
Autores principales: Ali, Hamed Ismail, Nagamatsu, Tomofumi, Akaho, Eiichi
Formato: Texto
Lenguaje:English
Publicado: Biomedical Informatics 2011
Materias:
Hypothesis
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3044423/
https://www.ncbi.nlm.nih.gov/pubmed/21383902

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3044423/
https://www.ncbi.nlm.nih.gov/pubmed/21383902

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