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Eur J Med Chem. 2009 Dec;44(12):4793-800. doi: 10.1016/j.ejmech.2009.07.018. Epub 2009 Jul 21.

Discovery of potential ZAP-70 kinase inhibitors: pharmacophore design, database screening and docking studies.

Author information

1
GVK Biosciences Pvt. Ltd., Informatics Division, S-1, Phase-1, T.I.E. Balanagar, Hyderabad, Andhra Pradesh 500037, India. ramadevi.sanam@gvkbio.com

Abstract

The best ZAP-70 inhibitor model consists of four-pharmacophore features, (1) one hydrogen bond acceptor, (2) one hydrogen bond donor (3) one hydrophobic aliphatic and (4) one hydrophobic aromatic features. This model was validated against 110 known ZAP-70 inhibitors with a correlation of 0.902 as well as enrichment factor of 1.61 against a maximum value of 2. This model picked 4094 hits from a database of 238,819 molecules while 358 molecules were indicated as highly active. Subsequently, docking studies were performed on the hits and novel series of potent leads were suggested based on the interactions energy between ZAP-70 and the putative inhibitors which validated not only the virtual screening potential of the model but also identified the possible new Chemotypes.

PMID:
19674816
DOI:
10.1016/j.ejmech.2009.07.018
[Indexed for MEDLINE]

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