Literature DB >> 19012570

RelACCS-FP: a structural minimalist approach to fingerprint design.

Ye Hu1, Eugen Lounkine, José Batista, Jürgen Bajorath.   

Abstract

The design and evaluation of structural key-type fingerprints is reported that consist of only 10-30 substructures isolated from randomly generated fragment populations of different classes of active compounds. To identify minimal sets of fragments that carry substantial compound class-specific information, fragment frequency calculations are applied to guide fingerprint generation. These compound class-directed and extremely small structural fingerprints push the design of so-called mini-fingerprints to the limit and are the shortest bit string fingerprints reported to date. For the application of relative frequency-based activity class characteristic substructure fingerprints, a bit density-dependent similarity metric is introduced that makes it possible to adjust similarity coefficients for individual compound classes and balance the recall of active compounds with database selection size. In similarity search trials, these small compound class-directed fingerprints enrich active compounds in relatively small database selection sets and approach or exceed the performance of widely used structural fingerprints of much larger size and higher complexity.

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Year:  2008        PMID: 19012570     DOI: 10.1111/j.1747-0285.2008.00723.x

Source DB:  PubMed          Journal:  Chem Biol Drug Des        ISSN: 1747-0277            Impact factor:   2.817


  1 in total

1.  Introducing a Chemically Intuitive Core-Substituent Fingerprint Designed to Explore Structural Requirements for Effective Similarity Searching and Machine Learning.

Authors:  Tiago Janela; Kosuke Takeuchi; Jürgen Bajorath
Journal:  Molecules       Date:  2022-04-04       Impact factor: 4.411

  1 in total

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