Systematic Extraction of Analogue Series from Large Compound Collections Using a New Computational Compound–Core Relationship Method
Abstract
Chemical optimization of organic compounds produces a series of analogues. In addition to considering an analogue series (AS) or multiple series on a case-by-case basis, which is often done in the practice of chemistry, the extraction of analogues from compound repositories is of high interest in organic and medicinal chemistry. In organic chemistry, ASs are a source of alternative synthetic routes and also aid in exploring relationships between compounds from different sources including synthetic vs. naturally occurring molecules. In medicinal chemistry, ASs are the major source of structure–activity relationship information and of hits or leads for drug development. ASs might be identified in different ways. For a given reference compound, a substructure search can be carried out using its scaffold. Alternatively, matched molecular pairs can be calculated to retrieve analogues from a compound repository. However, if no query compounds are used, the identification of ASs in databases is a difficult task. Herein, we introduce a computational approach to systematically identify ASs in collections of organic compounds. The approach involves compound decomposition on the basis of well-established retrosynthetic rules, organization of compound–core relationships, and identification of analogues sharing the same core. The method was applied on a large scale to extract ASs from the ChEMBL database, yielding more than 30 000 distinct series.
Read the paper
Related studies
- eggNOG 5.0: a hierarchical, functionally and phylogenetically annotated orthology resource based on 5090 organisms and 2502 viruses
- Online Survival Analysis Software to Assess the Prognostic Value of Biomarkers Using Transcriptomic Data in Non-Small-Cell Lung Cancer
- OptiType: precision HLA typing from next-generation sequencing data
- Nicotinic Cholinergic System and COVID-19: In Silico Identification of an Interaction between SARS-CoV-2 and Nicotinic Receptors with Potential Therapeutic Targeting Implications
- Saccharomyces cerevisiae cells have three Omega class glutathione S-transferases acting as 1-Cys thiol transferases
- Hemolysis at low blood flow rates: in-vitro and in-silico evaluation of a centrifugal blood pump
Go deeper in Evidence Hub
Evidence Hub adds a study data sheet (design, sample size, evidence level, key numbers), an AI summary and a chat grounded in the paper's text.