Biased Complement Diversity Selection for Effective Exploration of Chemical Space in Hit-Finding Campaigns

J Chem Inf Model. 2019 May 28;59(5):1709-1714. doi: 10.1021/acs.jcim.9b00048. Epub 2019 Apr 3.

Abstract

The success of hit-finding campaigns relies on many factors, including the quality and diversity of the set of compounds that is selected for screening. This paper presents a generalized workflow that guides compound selections from large compound archives with opportunities to bias the selections with available knowledge in order to improve hit quality while still effectively sampling the accessible chemical space. An optional flag in the workflow supports an explicit complement design function where diversity selections complement a given core set of compounds. Results from three project applications as well as a literature case study exemplify the effectiveness of the approach, which is available as a KNIME workflow named Biased Complement Diversity (BCD).

MeSH terms

  • Animals
  • Anti-Bacterial Agents / pharmacology
  • Antimalarials / pharmacology
  • Drug Discovery / methods*
  • Drug Evaluation, Preclinical / methods
  • Gram-Negative Bacteria / drug effects
  • Gram-Negative Bacterial Infections / drug therapy
  • High-Throughput Screening Assays / methods
  • Humans
  • Malaria, Falciparum / drug therapy
  • Plasmodium falciparum / drug effects
  • Protein Interaction Maps / drug effects
  • Small Molecule Libraries / pharmacology
  • Workflow

Substances

  • Anti-Bacterial Agents
  • Antimalarials
  • Small Molecule Libraries