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• W2041404811 abstract "Substituted (thio)hydantoins (2-thioxoimidazolidinones and imidazolidinediones) were reported as new potential reversible inhibitors of fatty acid amide hydrolase (FAAH). Their binding mode to FAAH was explored to rationalize their activity and give idea to design highly active inhibitors. Starting from the crystal structure of one of these molecules, docking studies provide us with rational basis for the design of new inhibitors within the thiohydantoin family." @default.
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• W2041404811 date "2006-09-01" @default.
• W2041404811 modified "2023-10-16" @default.
• W2041404811 title "Binding mode of new (thio)hydantoin inhibitors of fatty acid amide hydrolase: Comparison with two original compounds, OL-92 and JP104" @default.
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• W2041404811 doi "https://doi.org/10.1016/j.bmcl.2006.06.087" @default.
• W2041404811 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/16844375" @default.
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