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Learning Molecular Chirality via Chiral Determinant Kernels

About

Chirality is a fundamental molecular property that governs stereospecific behavior in chemistry and biology. Capturing chirality in machine learning models remains challenging due to the geometric complexity of stereochemical relationships and the limitations of traditional molecular representations that often lack explicit stereochemical encoding. Existing approaches to chiral molecular representation primarily focus on central chirality, relying on handcrafted stereochemical tags or limited 3D encodings, and thus fail to generalize to more complex forms such as axial chirality. In this work, we introduce ChiDeK (Chiral Determinant Kernels), a framework that systematically integrates stereogenic information into molecular representation learning. We propose the chiral determinant kernel to encode the SE(3)-invariant chirality matrix and employ cross-attention to integrate stereochemical information from local chiral centers into the global molecular representation. This design enables explicit modeling of chiral-related features within a unified architecture, capable of jointly encoding central and axial chirality. To support the evaluation of axial chirality, we construct a new benchmark for electronic circular dichroism (ECD) and optical rotation (OR) prediction. Across four tasks, including R/S configuration classification, enantiomer ranking, ECD spectrum prediction, and OR prediction, ChiDeK achieves substantial improvements over state-of-the-art baselines, most notably yielding over 7% higher accuracy on axially chiral tasks on average.

Runhan Shi, Zhicheng Zhang, Letian Chen, Gufeng Yu, Yang Yang• 2026

Related benchmarks

TaskDatasetResultRank
Molecular Property ClassificationMoleculeNet BBBP
ROC AUC68.9
41
Molecular Property ClassificationMoleculeNet BACE
ROC AUC78.1
36
Molecular Property ClassificationMoleculeNet ClinTox
ROC-AUC79.2
27
Molecular property predictionSIDER
ROC AUC0.583
21
Enantiomer rankingChIRo
Accuracy72.8
9
Optical Rotation PredictionACMP (test)
Accuracy69.2
9
R/S classificationChIRo
Accuracy99.8
9
ECD predictionCMCDS
Position RMSE2.2
9
ECD Spectrum PredictionACMP (test)
Position RMSE3.24
9
Molecular property predictionFreeSolv MoleculeNet
RMSE2.412
5
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