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Cheminformatics toolkits are software development kits that allow cheminformaticians to develop custom computer applications for use in virtual screening, chemical database mining, and structure-activity studies. Toolkits are often used for experimentation with new methodologies. Their most important functions deal with the manipulation of chemical structures and comparisons between structures. Programmatic access is provided to properties of individual bonds and atoms. == Functionality == Toolkits provide the following functionality: * Read and save structures in various chemistry file formats. * Determine if one structure is a substructure of another (substructure matching). * Determine if two structures are equal (exact matching). * Identification of substructures common to structures in a set (maximal common substructure, MCS). * Disassemble molecules, splitting into fragments. * Assemble molecules from elements or submolecules. * Apply reactions on input reactant structures, resulting in output of reaction product structures. * Generate molecular fingerprints. Fingerprints are bit-vectors where individual bits correspond to the presence or absence of structural features. The most important use of fingerprints is in indexing of chemistry databases. 抄文引用元・出典: フリー百科事典『 ウィキペディア（Wikipedia）』 ■ウィキペディアで「Cheminformatics toolkits」の詳細全文を読む スポンサード リンク
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