3D pharmacophore signatures and fingerprints
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Updated
May 8, 2025 - Python
3D pharmacophore signatures and fingerprints
A package to identify matched molecular pairs and use them to predict property changes.
Molecular Processing Made Easy.
The Open Forcefield Toolkit provides implementations of the SMIRNOFF format, parameterization engine, and other tools. Documentation available at http://open-forcefield-toolkit.readthedocs.io
Consensus pharmacophore for Drug Design
Interface for AutoDock, molecule parameterization
ChEMBL database structure pipelines
Adds or removes hydrogen atoms to achieve the appropriate molecular protonation state for a user-specified pH range
molfeat - the hub for all your molecular featurizers
Some useful RDKit functions
a molecular descriptor calculator
Molecule Validation and Standardization
The official sources for the RDKit library
3D ligand-based pharmacophore modeling
Generate Simple Pharmacophore Models with RDKit
Plausibility checks for generated molecule poses.
Interaction Fingerprints for protein-ligand complexes and more
Descriptor computation(chemistry) and (optional) storage for machine learning
Open-source tool to generate 3D-ready small molecules for virtual screening
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