StereoMolGraph: Stereochemistry-Aware Molecular and Reaction Graphs

Conventional molecular graphs are often unable to reliably encode stereochemistry, especially for symmetric molecules, nontetrahedral centers, and transition states. To overcome this, we present StereoMolGraph, an open-source Python library implementing a stereochemistry-aware graph representation for molecules and condensed graphs of reactions. Our method uses permutation-invariant local stereodescriptors, grounded in group theory, to provide an extensible representation of chirality. Based on this we introduce methods allowing for robust comparison of stereoisomers, including the identification of enantiomerism and diastereomerism, and support fleeting stereochemistry in transition states. We demonstrate the library's utility for complex organic molecules and metal complexes and analysis of distinct chiral reaction pathways. With RDKit interoperability and visualization features, StereoMolGraph offers a practical and transparent tool for advanced stereochemically aware chemoinformatics workflows.

Authors

Institutions

Publication Details

Journal
Journal of Chemical Information and Modeling
Published
2026-03-27
DOI
https://doi.org/10.1021/acs.jcim.5c02523
Primary Topic
Graph theory and applications
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

StereoMolGraph: Stereochemistry-Aware Molecular and Reaction Graphs

Maxim Papusha, Kai Leonhard
Journal of Chemical Information and Modeling
Graph theory and applications
article

StereoMolGraph: Stereochemistry-Aware Molecular and Reaction Graphs

Maxim Papusha, Kai Leonhard
article en

Abstract

Conventional molecular graphs are often unable to reliably encode stereochemistry, especially for symmetric molecules, nontetrahedral centers, and transition states. To overcome this, we present StereoMolGraph, an open-source Python library implementing a stereochemistry-aware graph representation for molecules and condensed graphs of reactions. Our method uses permutation-invariant local stereodescriptors, grounded in group theory, to provide an extensible representation of chirality. Based on this we introduce methods allowing for robust comparison of stereoisomers, including the identification of enantiomerism and diastereomerism, and support fleeting stereochemistry in transition states. We demonstrate the library's utility for complex organic molecules and metal complexes and analysis of distinct chiral reaction pathways. With RDKit interoperability and visualization features, StereoMolGraph offers a practical and transparent tool for advanced stereochemically aware chemoinformatics workflows.

Journal of Chemical Information and Modeling
RWTH Aachen University (DE)
Openalex Percentile: Top 4%
Graph theory and applications
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.