The QDπ dataset, training data for drug-like molecules and biopolymer fragments and their interactions

The development of universal machine learning potentials (MLP) for small organic and drug-like molecules requires large, accurate datasets that span diverse chemical spaces. In this study, we introduce the QDπ dataset which incorporates data taken from several datasets. We use a query-by-committee active learning strategy to extract data from large datasets to maximize the diversity and avoid redundancy as relevant for neural network training to construct the QDπ dataset. The QDπ dataset requires only 1.6 million structures to express the chemical diversity of 13 elements from the various source datasets at the ωB97M-D3(BJ)/def2-TZVPPD level of theory. The QDπ dataset enables creation of flexible target loss functions for neural network training relevant to drug discovery, including information-dense data sets of relative conformational energies and barriers, intermolecular interactions, tautomers and relative protonation energies of drug-like compounds and biomolecular fragments. It is the hope that the high chemical information density and diversity contained in the QDπ dataset will provide a valuable resource for the development of new universal MLPs for drug discovery.

Authors

Institutions

Publication Details

Journal
Scientific Data
Published
2025-04-25
DOI
https://doi.org/10.1038/s41597-025-04972-3
Citations
5
Primary Topic
Machine Learning in Materials Science
Type
article
Field-Weighted Citation Impact
2.59

Funders

Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

The QDπ dataset, training data for drug-like molecules and biopolymer fragments and their interactions

Timothy J. Giese, Jinzhe Zeng, Andreas Goetz, Darrin M. York
5 citations
Scientific Data
Machine Learning in Materials Science
2.59
article

The QDπ dataset, training data for drug-like molecules and biopolymer fragments and their interactions

Timothy J. Giese, Jinzhe Zeng, Andreas Goetz, Darrin M. York
article en
5 citations

Abstract

The development of universal machine learning potentials (MLP) for small organic and drug-like molecules requires large, accurate datasets that span diverse chemical spaces. In this study, we introduce the QDπ dataset which incorporates data taken from several datasets. We use a query-by-committee active learning strategy to extract data from large datasets to maximize the diversity and avoid redundancy as relevant for neural network training to construct the QDπ dataset. The QDπ dataset requires only 1.6 million structures to express the chemical diversity of 13 elements from the various source datasets at the ωB97M-D3(BJ)/def2-TZVPPD level of theory. The QDπ dataset enables creation of flexible target loss functions for neural network training relevant to drug discovery, including information-dense data sets of relative conformational energies and barriers, intermolecular interactions, tautomers and relative protonation energies of drug-like compounds and biomolecular fragments. It is the hope that the high chemical information density and diversity contained in the QDπ dataset will provide a valuable resource for the development of new universal MLPs for drug discovery.

Scientific DataVol. 12(1)
Rutgers, The State University of New Jersey (US), San Diego Supercomputer Center (US), University of California San Diego (US), Quantitative BioSciences (US)
National Science Foundation, San Diego Supercomputer Center, National Institutes of Health, Office of Advanced Research Computing, Rutgers, The State University of New Jersey, Office of Advanced Cyberinfrastructure, Division of Chemistry
Openalex Percentile: Top 11%
Machine Learning in Materials Science
2.59
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.