Evidence map›Paper›PMID 36285735›Full record

ReviewChemical Society reviews2022

Applications of covalent chemistry in targeted protein degradation.

Dong Lu, Xin Yu, Hanfeng Lin, Ran Cheng, Erika Y Monroy, Xiaoli Qi, Meng C Wang, Jin Wang

Abstract readReview
In one paragraph

Review in Chemical Society reviews, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing 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

28 citing papers in PubMed.

  1. Review
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  6. Article
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  8. Article
  9. Article
  10. Review
  11. Review
  12. Targeting ubiquitination in disease and therapy.Signal transduction and targeted therapy · 2025
    Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
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  20. Review
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

8 authors.

Dong LuDepartment of Pharmacology and Chemical Biology, Baylor College of Medicine, Houston TX 77030, USA. wangj@bcm.edu.
Xin YuDepartment of Pharmacology and Chemical Biology, Baylor College of Medicine, Houston TX 77030, USA. wangj@bcm.edu.
Hanfeng LinDepartment of Pharmacology and Chemical Biology, Baylor College of Medicine, Houston TX 77030, USA. wangj@bcm.edu.ORCID http://orcid.org/0000-0002-3172-5616
Ran ChengDepartment of Pharmacology and Chemical Biology, Baylor College of Medicine, Houston TX 77030, USA. wangj@bcm.edu.
Erika Y MonroyDepartment of Pharmacology and Chemical Biology, Baylor College of Medicine, Houston TX 77030, USA. wangj@bcm.edu.ORCID http://orcid.org/0000-0003-1614-3340
Xiaoli QiDepartment of Pharmacology and Chemical Biology, Baylor College of Medicine, Houston TX 77030, USA. wangj@bcm.edu.
Meng C WangDepartment of Molecular and Human Genetics, Baylor College of Medicine, Houston TX 77030, USA.
Jin WangDepartment of Pharmacology and Chemical Biology, Baylor College of Medicine, Houston TX 77030, USA. wangj@bcm.edu.ORCID http://orcid.org/0000-0003-3625-7919

Funding

Development of First-in-Class RIPK1 Degraders to Improve Cancer ImmunotherapiesR01CA268518 · NCI · BAYLOR COLLEGE OF MEDICINE · PI Jin Wang · 2022 to 2026
$3.5M
Reversible Covalent BTK Degraders as the Next Generation Targeted Therapy to Treat B-cell MalignanciesR01CA250503 · NCI · BAYLOR COLLEGE OF MEDICINE · PI WANG, JIN, WANG, MICHAEL · 2020 to 2024
$3.4M
REAL-TIME QUANTITATIVE IMAGING OF INTRACELLULAR BIOTHIOL DYNAMICSR01GM115622 · NIGMS · BAYLOR COLLEGE OF MEDICINE · PI WANG, JIN · 2015 to 2019
$1.6M
NCI NIH HHS R01 CA250503NCI NIH HHS R01 CA268518NIGMS NIH HHS R01 GM115622
6 · The paper itself

Abstract

Proteolysis-targeting chimeras (PROTACs) and targeted covalent inhibitors (TCIs) are currently two exciting strategies in the fields of chemical biology and drug discovery. Extensive research in these two fields has been conducted, and significant progress in these fields has resulted in many clinical candidates, some of which have been approved by FDA. Recently, a novel concept termed covalent PROTACs that combine these two strategies has emerged and gained an increasing interest in the past several years. Herein, we briefly review and highlight the mechanism and advantages of TCIs and PROTACs, respectively, and the recent development of covalent PROTACs using irreversible and reversible covalent chemistry.

Indexed as

Drug DiscoveryUbiquitin-Protein LigasesProteolysisUbiquitin-Protein Ligases

Identifiers

PMID36285735
PMCPMC9669245

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.