Evidence map›Paper›PMID 41703061›Full record

ArticleCommunications biology2026

De novo covalent drug generation with enhanced drug-likeness and safety.

Wenbo Zhang, Tianxiao Liu, Xiaoying Dong, Saisai Sun, Xiaojun Yao, Pengyong Li, Lin Gao

Abstract read
In one paragraph

Article in Communications biology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
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

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

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

1 citing paper in PubMed.

  1. Article
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

7 authors.

Wenbo Zhang *School of Computer Science and Technology, Xidian University, Xi'an, Shaanxi, China.
Tianxiao Liu *School of Computer Science and Technology, Xidian University, Xi'an, Shaanxi, China.
Xiaoying DongSchool of Computer Science and Technology, Xidian University, Xi'an, Shaanxi, China.
Saisai SunSchool of Computer Science and Technology, Xidian University, Xi'an, Shaanxi, China.
Xiaojun YaoCentre for Artificial Intelligence Driven Drug Discovery, Faculty of Applied Sciences, Macao Polytechnic University, Macao, China.
Pengyong LiSchool of Computer Science and Technology, Xidian University, Xi'an, Shaanxi, China. lipengyong@xidian.edu.cn.ORCID http://orcid.org/0000-0001-5971-046X
Lin GaoSchool of Computer Science and Technology, Xidian University, Xi'an, Shaanxi, China. lgao@mail.xidian.edu.cn.ORCID http://orcid.org/0000-0001-6396-0787

Funding

National Natural Science Foundation of China (National Science Foundation of China) 62132015National Natural Science Foundation of China (National Science Foundation of China) 62202353National Natural Science Foundation of China (National Science Foundation of China) 62572374National Natural Science Foundation of China (National Science Foundation of China) U22A2037
6 · The paper itself

Abstract

Covalent drugs have long played an essential role in therapeutics, yet computational design approaches remain largely confined to virtual screening of existing libraries. Despite recent advances in deep generative models for drug discovery, methods specifically tailored to de novo covalent drug generation are still lacking. Here we introduce CovaGEN, a conditional latent diffusion framework for the de novo design of covalent inhibitors with enhanced drug-likeness and safety. CovaGEN generates ligands from a drug-like latent space while conditioning on target sequences and employing a classifier to guide the formation of desirable covalent warheads. A reinforcement learning strategy further optimizes the safety profiles of generated molecules. Experimental results demonstrate that CovaGEN effectively generates covalent drugs with the desired covalent warheads, exhibiting strong target protein affinity, favorable drug-likeness, and low toxicity. When applied to EGFR T790M and Mpro, the generated compounds exhibit higher probabilities of covalent binding. Overall, CovaGEN offers a pioneering approach for the de novo design of covalent inhibitors, advancing the discovery of covalent drugs with improved properties.

Indexed as

Drug DesignDrug DiscoveryProtein Kinase InhibitorsErbB ReceptorsGenerative Artificial IntelligenceHumansLigandsReinforcement Machine LearningErbB ReceptorsLigandsProtein Kinase Inhibitors

Identifiers

PMID41703061
PMCPMC13022440

What OpenQuestion holds

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Registered trials

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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.