Evidence map›Paper›PMID 36770611›Full record

ReviewMolecules (Basel, Switzerland)2023

Approved Small-Molecule ATP-Competitive Kinases Drugs Containing Indole/Azaindole/Oxindole Scaffolds: R&D and Binding Patterns Profiling.

Haofan Zhang, Fengming He, Guiping Gao, Sheng Lu, Qiaochu Wei, Hongyu Hu, Zhen Wu, Meijuan Fang, Xiumin Wang

Abstract readReview
In one paragraph

Review in Molecules (Basel, Switzerland), 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing 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

13 citing papers in PubMed.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Molecular Pharmacology at the Crossroads of Precision Medicine.Current issues in molecular biology · 2025
    Article
  6. Review
  7. Structural Mechanisms of Topoisomerase-Targeting Drugs.Annual review of biochemistry · 2025
    Review
  8. Review
  9. Review
  10. Review
  11. Chemical proteomics approaches for protein post-translational modification studies.Biochimica et biophysica acta. Proteins and proteomics · 2024
    Review
  12. Article
  13. 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

9 authors.

Haofan ZhangSchool of Pharmaceutical Sciences, Xiamen University, Xiamen 361102, China.
Fengming HeSchool of Pharmaceutical Sciences, Xiamen University, Xiamen 361102, China.
Guiping GaoSchool of Pharmaceutical Sciences, Xiamen University, Xiamen 361102, China.
Sheng LuSchool of Pharmaceutical Sciences, Xiamen University, Xiamen 361102, China.
Qiaochu WeiSchool of Public Health, Xiamen University, Xiamen 361102, China.
Hongyu HuXingzhi College, Zhejiang Normal University, Lanxi 321004, China.
Zhen WuSchool of Pharmaceutical Sciences, Xiamen University, Xiamen 361102, China.
Meijuan FangSchool of Pharmaceutical Sciences, Xiamen University, Xiamen 361102, China.
Xiumin WangSchool of Pharmaceutical Sciences, Xiamen University, Xiamen 361102, China.

Funding

Natural Science Foundation of Fujian Province of China 2022Y0001Special fund for marine development of Fujian province FJHJF-L-2021-5
6 · The paper itself

Abstract

Kinases are among the most important families of biomolecules and play an essential role in the regulation of cell proliferation, apoptosis, metabolism, and other critical physiological processes. The dysregulation and gene mutation of kinases are linked to the occurrence and development of various human diseases, especially cancer. As a result, a growing number of small-molecule drugs based on kinase targets are being successfully developed and approved for the treatment of many diseases. The indole/azaindole/oxindole moieties are important key pharmacophores of many bioactive compounds and are generally used as excellent scaffolds for drug discovery in medicinal chemistry. To date, 30 ATP-competitive kinase inhibitors bearing the indole/azaindole/oxindole scaffold have been approved for the treatment of diseases. Herein, we summarize their research and development (R&D) process and describe their binding models to the ATP-binding sites of the target kinases. Moreover, we discuss the significant role of the indole/azaindole/oxindole skeletons in the interaction of their parent drug and target kinases, providing new medicinal chemistry inspiration and ideas for the subsequent development and optimization of kinase inhibitors.

Indexed as

Drug DiscoveryProtein Kinase InhibitorsAdenosine TriphosphateBinding SitesHumansOxindolesAdenosine TriphosphateOxindolesProtein Kinase Inhibitorsapproved ATP-competitive kinases drugscancerdrug designdrug discoveryindole/azaindole/oxindole derivativeskinases binding patterns

Identifiers

PMID36770611
PMCPMC9920796

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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.