Evidence map›Paper›PMID 37593578›Full record

ReviewRSC medicinal chemistry2023

Antibacterial activities of anthraquinones: structure-activity relationships and action mechanisms.

Tang Qun, Tiantian Zhou, Jiongkai Hao, Chunmei Wang, Keyu Zhang, Jing Xu, Xiaoyang Wang, Wen Zhou

Open access · hybridAbstract readReview
In one paragraph

Review in RSC medicinal chemistry, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 46 papers.

0numbers the graph read from it
0cells of the map it votes in
46citing papers in PubMed
36.9field-weighted citation impact, top 1% of its field
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

46 citing papers in PubMed, 93 citations in OpenAlex.

  1. Natural Product-Based Therapeutic Potential ofPharmaceuticals (Basel, Switzerland) · 2026
    Article
  2. Article
  3. Physcion isolated fromRSC advances · 2026
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  4. Article
  5. Article
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  7. Article
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  9. Article
  10. Review
  11. Classification and Anti-Pathogens (Basel, Switzerland) · 2026
    Review
  12. Review
  13. Current pharmaceutical biotechnology · 2026
    Article
  14. Article
  15. Article
  16. Review
  17. Article
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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 at 2 institutions in 1 country.

Tang QunShanghai Veterinary Research Institute, Chinese Academy of Agricultural Sciences 200241 Shanghai China wxy@shvri.ac.cn zhouwen60@126.com.ORCID https://orcid.org/0009-0000-4682-5663
Tiantian ZhouSchool of Chinese Materia Medica, Guangdong Pharmaceutical University 440113 Guangzhou China.
Jiongkai HaoShanghai Veterinary Research Institute, Chinese Academy of Agricultural Sciences 200241 Shanghai China wxy@shvri.ac.cn zhouwen60@126.com.
Chunmei WangShanghai Veterinary Research Institute, Chinese Academy of Agricultural Sciences 200241 Shanghai China wxy@shvri.ac.cn zhouwen60@126.com.
Keyu ZhangShanghai Veterinary Research Institute, Chinese Academy of Agricultural Sciences 200241 Shanghai China wxy@shvri.ac.cn zhouwen60@126.com.
Jing XuHuanghua Agricultural and Rural Development Bureau Bohai New Area 061100 Hebei China.
Xiaoyang WangShanghai Veterinary Research Institute, Chinese Academy of Agricultural Sciences 200241 Shanghai China wxy@shvri.ac.cn zhouwen60@126.com.
Wen ZhouShanghai Veterinary Research Institute, Chinese Academy of Agricultural Sciences 200241 Shanghai China wxy@shvri.ac.cn zhouwen60@126.com.ORCID https://orcid.org/0000-0002-3961-1816
Shanghai Veterinary Research Institute · CNGuangdong Pharmaceutical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

With the increasing prevalence of untreatable infections caused by antibiotic-resistant bacteria, the discovery of new drugs from natural products has become a hot research topic. The antibacterial activity of anthraquinones widely distributed in traditional Chinese medicine has attracted much attention. Herein, the structure and activity relationships (SARs) of anthraquinones as bacteriostatic agents are reviewed and elucidated. The substituents of anthraquinone and its derivatives are closely related to their antibacterial activities. The stronger the polarity of anthraquinone substituents is, the more potent the antibacterial effects appear. The presence of hydroxyl groups is not necessary for the antibacterial activity of hydroxyanthraquinone derivatives. Substitution of di-isopentenyl groups can improve the antibacterial activity of anthraquinone derivatives. The rigid plane structure of anthraquinone lowers its water solubility and results in the reduced activity. Meanwhile, the antibacterial mechanisms of anthraquinone and its analogs are explored, mainly including biofilm formation inhibition, destruction of the cell wall, endotoxin inhibition, inhibition of nucleic acid and protein synthesis, and blockage of energy metabolism and other substances.

Identifiers

PMID37593578
PMCPMC10429894
OpenAlexW4383738618

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.