| Literature DB >> 19714705 |
Britta Nisius1, Jürgen Bajorath.
Abstract
Molecular fingerprints have a long history in computational medicinal chemistry and continue to be popular tools for similarity searching. Over the years, a variety of fingerprint types have been introduced. We report an approach to identify preferred bit subsets in fingerprints of different design and "recombine" these bit segments into "hybrid fingerprints". These compound class-directed fingerprint representations are found to increase the similarity search performance of their parental fingerprints, which can be rationalized by the often complementary nature of distinct fingerprint features.Mesh:
Year: 2009 PMID: 19714705 DOI: 10.1002/cmdc.200900243
Source DB: PubMed Journal: ChemMedChem ISSN: 1860-7179 Impact factor: 3.466