Data Science & Analytics
Medchem
Filters and triages small-molecule libraries with the Python medchem library (datamol-io, v2.0.5) on top of RDKit and datamol. Covers drug-likeness rules (Lipinski, Veber, CNS, lead-like) via RuleFilters, structural alerts (ChEMBL-derived sets, NIBR, PAINS, Brenk), chemical group detection, ZINC-based complexity thresholds, scaffold constraints, and the medchem query language (QueryFilter). Use when screening a compound library for drug-likeness, removing PAINS or other structural-alert compounds, prioritizing hits for hit-to-lead or lead optimization, detecting functional groups, or combining criteria in one query. Not for computing general descriptors or fingerprints; use RDKit directly.
- Publisher / source
- KalarisLabs/research-agent-skills (found on the CSV list)
- Upstream record
- KalarisLabs/research-agent-skills
- Version
- Version 2
- Published
- Publication review
- Approved for publication
- Content fingerprint
df416df8b1d3ba4249bce22c0b37cf8f8b8fe289d2d67da2e9035a7093caf374