Evidence map›Paper›PMID 42259899›Full record

ArticleCommunications chemistry2026

Generative pretraining for drug molecule design with bidirectional structure-property optimization.

Yingying Song, Song He, Xiaochen Bo, Zhongnan Zhang

Abstract read
In one paragraph

Article in Communications chemistry, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
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1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors.

Yingying SongSchool of Informatics, Xiamen University, Xiamen, China.
Song HeDepartment of Advanced & Interdisciplinary Biotechnology, Academy of Military Medical Sciences, Beijing, China. hes1224@163.com.ORCID http://orcid.org/0000-0002-4136-6151
Xiaochen BoDepartment of Advanced & Interdisciplinary Biotechnology, Academy of Military Medical Sciences, Beijing, China. boxiaoc@163.com.ORCID http://orcid.org/0000-0003-3490-5812
Zhongnan ZhangSchool of Informatics, Xiamen University, Xiamen, China. zhongnan_zhang@xmu.edu.cn.ORCID http://orcid.org/0000-0002-7227-3943

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Designing drug-like molecules that satisfy both properties requirements and structural constraints remains challenging. Current generative approaches typically reduce properties to numerical constraints and treat molecular structures as deterministic functions of properties, failing to capture complex, nonlinear structure-property relationships and limiting generative diversity and controllability. Therefore, we propose BiSP-GP, a bidirectional structure-property generative pretraining framework that unifies molecular generation and property prediction as a single sequence modeling task. BiSP-GP serializes continuous properties into semantic token sequences for joint modeling with molecular structures in a shared sequence space. Molecular generation and property prediction are cast as autoregressive sequence modeling tasks, with a cross-modal decoder supporting bidirectional mapping. The framework also incorporates scaffolds as conditional inputs to guide structure generation. Experiments demonstrate that BiSP-GP achieves strong performance gconditional molecular generation, property prediction, and downstream tasks. A case study on PAK1 further validates the model's generative ability and shows improved binding capacity in molecular docking evaluation.

Identifiers

PMID42259899
PMCPMC13582974

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.