Evidence map›Paper›PMID 42770064›Full record

ArticleSmart molecules : open access2026

Molecular glues: Recent advances in cereblon substrate identification and mechanistic insights.

Qingyun Guan, Xiaoyu Shi, Qian Yang, Xiangyi Jiang, Xinyong Liu, Peng Zhan

Abstract read
In one paragraph

Article in Smart molecules : open access, 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
–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

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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

6 authors.

Qingyun GuanDepartment of Medicinal Chemistry, State Key Laboratory of Discovery and Utilization of Functional Components in Traditional Chinese Medicine, Shandong Key Laboratory of Druggability Optimization and Evaluation for Lead Compounds, Shandong Basic Science Special Academic Zone (Pharmacy) School of Pharmaceutical Sciences Shandong University Jinan Shandong China.ORCID https://orcid.org/0009-0002-3161-2280
Xiaoyu ShiDepartment of Medicinal Chemistry, State Key Laboratory of Discovery and Utilization of Functional Components in Traditional Chinese Medicine, Shandong Key Laboratory of Druggability Optimization and Evaluation for Lead Compounds, Shandong Basic Science Special Academic Zone (Pharmacy) School of Pharmaceutical Sciences Shandong University Jinan Shandong China.
Qian YangDepartment of Medicinal Chemistry, State Key Laboratory of Discovery and Utilization of Functional Components in Traditional Chinese Medicine, Shandong Key Laboratory of Druggability Optimization and Evaluation for Lead Compounds, Shandong Basic Science Special Academic Zone (Pharmacy) School of Pharmaceutical Sciences Shandong University Jinan Shandong China.
Xiangyi JiangDepartment of Medicinal Chemistry, State Key Laboratory of Discovery and Utilization of Functional Components in Traditional Chinese Medicine, Shandong Key Laboratory of Druggability Optimization and Evaluation for Lead Compounds, Shandong Basic Science Special Academic Zone (Pharmacy) School of Pharmaceutical Sciences Shandong University Jinan Shandong China.ORCID https://orcid.org/0000-0001-6224-2513
Xinyong LiuDepartment of Medicinal Chemistry, State Key Laboratory of Discovery and Utilization of Functional Components in Traditional Chinese Medicine, Shandong Key Laboratory of Druggability Optimization and Evaluation for Lead Compounds, Shandong Basic Science Special Academic Zone (Pharmacy) School of Pharmaceutical Sciences Shandong University Jinan Shandong China.ORCID https://orcid.org/0000-0002-7302-2214
Peng ZhanDepartment of Medicinal Chemistry, State Key Laboratory of Discovery and Utilization of Functional Components in Traditional Chinese Medicine, Shandong Key Laboratory of Druggability Optimization and Evaluation for Lead Compounds, Shandong Basic Science Special Academic Zone (Pharmacy) School of Pharmaceutical Sciences Shandong University Jinan Shandong China.ORCID https://orcid.org/0000-0002-9675-6026

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

This highlight summarizes the recent advances in cereblon (CRBN) substrate discovery and mechanisms of action within the field of molecular glues. It emphasizes that molecular glue technology has transitioned from the stage of monofunctional targeted protein degradation to that of rational design and multidimensional regulation. Key recent breakthroughs include: (1) overcoming the limitations of canonical CRBN recognition motifs, identifying extensive novel substrates and unconventional recognition modes independent of fixed specific secondary structures; (2) reconceptualizing G protein-coupled receptor (GPCR) signal transduction theory by demonstrating that molecular glues can stabilize GPCR megacomplexes to achieve sustained signal modulation, providing a novel strategy to overcome the challenge of traditional drug tolerance; (3) pioneering the concept of orthosteric molecular glue inhibitors, which expands the mechanistic modalities of molecular glues. Furthermore, this highlight delineates the therapeutic potential and mechanistic basis of molecular glues in antiviral therapies against HIV and the mpox virus, corroborating their core essence of inducing or stabilizing protein-protein interactions. Finally, it summarizes current challenges facing the field, including target discovery, rational design, and druggability optimization, aiming to provide a theoretical reference for innovative research and development of molecular glues and their applications in chronic diseases and antiviral therapies.

Indexed as

CRBNmechanisms of actionmolecular gluesprotein‐protein interactionssubstrate discovery

Identifiers

PMID42770064
PMCPMC13592437

What OpenQuestion holds

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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.