Cited by 55Protein Degradation and InhibitorsUbiquitin and proteasome pathwaysCancer-related Molecular Pathways

Prospecting for molecular glues

den Besten, Willem, Lipford, J. Russell·2020·Nature Chemical Biology

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Crossref · 10.1038/s41589-020-0620-z

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  • Unlike PROTACs, molecular glues possess a dual-ligand structure for both E3 ubiquitin ligase and target proteins, enabling ubiquitination and degradation of previously undruggable targets and PPIs.

    “Unlike PROTACs, molecular glues possess a dual-ligand structure for both E3 ubiquitin ligase and target proteins, enabling the ubiquitination and degradation of previously undruggable targets and PPIs.”
  • Molecular glues are small molecules that promote interaction between E3 ubiquitin ligase, substrate receptors, and target proteins, leading to ubiquitination and degradation by the proteasome.

    “Molecular glues are a class of small molecules that promote interaction between E3 ubiquitin ligase, substrate receptors, and target proteins, leading to ubiquitination and degradation by the proteasome.”

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References 6 · Cited by 55

Authors
den Besten, W., & Lipford, J. R.
Affiliations
Amgen (United States) (US)
Corresponding author
Lipford, J. Russell
Venue
Nature Chemical Biology
Published
2020-08-03
Volume
16
Issue
11
Pages
1157-1158
ISSN
  • 1552-4450 (ISSN-L)
  • 1552-4469
OpenAlex
W3046680580
Cited by
55
References
6
Citations by year
2026: 1 · 2025: 6 · 2024: 9 · 2023: 12 · 2022: 17 · 2021: 10
FWCI
3.41
Type
journal article
Language
en
Open access
closed
Locations
  • Nature Chemical Biology (publishedVersion)
  • PubMed (publishedVersion)
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Protein Degradation and Inhibitors
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Ubiquitin and proteasome pathways
  • Health Sciences › Medicine › Oncology › Cancer-related Molecular Pathways
Keywords
molecular glues, CDK12 inhibitors, protein degradation, ubiquitination, small molecule inhibitors
MeSH terms
Cyclins

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