Evidence map›Paper›PMID 41622634›Full record

ReviewJournal of the American Chemical Society2026

From Serendipity to Strategy: Rationalizing Molecular Glue Discovery and Proximity-Induced Pharmacology through Chemical Biology.

Janine L Gray, Zhangping Xiao, Vanessa V Rogga, Xinyue Zhang, Edward W Tate

Abstract readReview
In one paragraph

Review in Journal of the American Chemical Society, 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

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

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

5 authors.

Janine L GrayDepartment of Chemistry, Molecular Sciences Research Hub, Imperial College London, London W12 0BZ, U.K.ORCID 0000-0001-8679-2499
Zhangping XiaoDepartment of Chemistry, Molecular Sciences Research Hub, Imperial College London, London W12 0BZ, U.K.
Vanessa V RoggaDepartment of Chemistry, Molecular Sciences Research Hub, Imperial College London, London W12 0BZ, U.K.
Xinyue ZhangDepartment of Chemistry, Molecular Sciences Research Hub, Imperial College London, London W12 0BZ, U.K.
Edward W TateDepartment of Chemistry, Molecular Sciences Research Hub, Imperial College London, London W12 0BZ, U.K.ORCID 0000-0003-2213-5814

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Molecular glues represent a new paradigm in drug discovery, stabilizing novel protein-protein interactions between two proteins to elicit targeted cellular outcomes. Historically discovered through serendipity, molecular glue identification is becoming increasingly systematic. In this perspective, we discuss the current advances and challenges of this field, highlighting the transition toward rational discovery through the convergence of four complementary approaches. Innovations in library design and screening platforms are expanding access to glue-relevant chemical space, guided by a deeper mechanistic understanding of proximity-induced pharmacology. These efforts are further enabled by functional genomic approaches that reveal gluable interfaces. Finally, the integration of chemical and biological data through machine learning is beginning to support rational de novo glue design.

Indexed as

Drug DiscoveryProteinsHumansProteins

Identifiers

PMID41622634
PMCPMC12903864

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.