3D QSAR studies on ketoamides of human cathepsin K inhibitors based on two different alignment methods.

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Pan X, Tan N, Zeng G, Huang H, Yan H

3D QSAR studies on ketoamides of human cathepsin K inhibitors based on two different alignment methods.

Eur J Med Chem. 2010 Feb;45(2):667-81. doi: 10.1016/j.ejmech.2009.11.010. Epub 2009 Nov 11.

PubMed ID

19962796 [ View in PubMed

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Abstract

Comparative molecular field analysis (CoMFA) and comparative molecular similarity indices analysis (CoMSIA) were performed on 64 ketoamides as human cathepsin K (CatK) inhibitors, using ROCS ligand-based alignment and receptor-based alignment. Results generated from the ligand-based model were found to be superior to those obtained by the receptor-based model. CoMFA and CoMSIA field distributions are in good agreement with the structural characteristics of the binding groove of CatK, suggesting moderate substitutes at the P1, P2, P3 and P1' may favor the inhibitory activity of ketoamides. These results provide useful information in understanding the structural and chemical features of CatK in designing and finding novel potential CatK inhibitors as osteoporosis therapeutic agents.

DrugBank Data that Cites this Article

Binding Properties

Drug	Target	Property	Measurement	pH	Temperature (°C)
[1-(4-Fluorobenzyl)Cyclobutyl]Methyl (1s)-1-[Oxo(1h-Pyrazol-5-Ylamino)Acetyl]Pentylcarbamate	Cathepsin K	IC 50 (nM)	0.832	N/A	N/A	Details