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BMC Bioinformatics. 2008 Sep 24;9:396. doi: 10.1186/1471-2105-9-396.

FAF-Drugs2: free ADME/tox filtering tool to assist drug discovery and chemical biology projects.

Author information

1
INSERM U648, MTi team, Paris Descartes University, Paris Diderot University, Paris, France. david.lagorce@univ-paris-diderot.fr

Abstract

BACKGROUND:

Drug discovery and chemical biology are exceedingly complex and demanding enterprises. In recent years there are been increasing awareness about the importance of predicting/optimizing the absorption, distribution, metabolism, excretion and toxicity (ADMET) properties of small chemical compounds along the search process rather than at the final stages. Fast methods for evaluating ADMET properties of small molecules often involve applying a set of simple empirical rules (educated guesses) and as such, compound collections' property profiling can be performed in silico. Clearly, these rules cannot assess the full complexity of the human body but can provide valuable information and assist decision-making.

RESULTS:

This paper presents FAF-Drugs2, a free adaptable tool for ADMET filtering of electronic compound collections. FAF-Drugs2 is a command line utility program (e.g., written in Python) based on the open source chemistry toolkit OpenBabel, which performs various physicochemical calculations, identifies key functional groups, some toxic and unstable molecules/functional groups. In addition to filtered collections, FAF-Drugs2 can provide, via Gnuplot, several distribution diagrams of major physicochemical properties of the screened compound libraries.

CONCLUSION:

We have developed FAF-Drugs2 to facilitate compound collection preparation, prior to (or after) experimental screening or virtual screening computations. Users can select to apply various filtering thresholds and add rules as needed for a given project. As it stands, FAF-Drugs2 implements numerous filtering rules (23 physicochemical rules and 204 substructure searching rules) that can be easily tuned.

PMID:
18816385
PMCID:
PMC2561050
DOI:
10.1186/1471-2105-9-396
[Indexed for MEDLINE]
Free PMC Article

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