Evidence map›Paper›PMID 39519721›Full record

ReviewMolecules (Basel, Switzerland)2024

Antimicrobial Potential of Scorpion-Venom-Derived Peptides.

Zhiqiang Xia, Lixia Xie, Bing Li, Xiangyun Lv, Hongzhou Zhang, Zhijian Cao

Abstract readReview
In one paragraph

Review in Molecules (Basel, Switzerland), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing 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

16 citing papers in PubMed.

  1. Scorpion Peptides in Antiviral Drug Discovery: An In-depth Review.Probiotics and antimicrobial proteins · 2026
    Review
  2. Review
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  4. Article
  5. Article
  6. Review
  7. Article
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  11. Review
  12. Characterization ofToxins · 2025
    Article
  13. Review
  14. Article
  15. Characterization ofFrontiers in pharmacology · 2025
    Article
  16. Article
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

6 authors.

Zhiqiang XiaSchool of Biological and Food Processing Engineering, Huanghuai University, Zhumadian 463000, China.ORCID 0009-0007-3379-9022
Lixia XieSchool of Biological and Food Processing Engineering, Huanghuai University, Zhumadian 463000, China.
Bing LiZhumadian Huazhong Chia Tai Co., Ltd., Zhumadian 463000, China.
Xiangyun LvZhumadian Huazhong Chia Tai Co., Ltd., Zhumadian 463000, China.
Hongzhou ZhangHenan Topfond Pharmaceutical Company Limited, Zhumadian 463000, China.
Zhijian CaoCenter for Evolution and Conservation Biology, Southern Marine Science and Engineering Guangdong Laboratory (Guangzhou), Guangzhou 511458, China.

Funding

Huanghuai University National research Project Cultivation Fund XKPY-2022010PI Project of Southern Marine Science and Engineering Guangdong Laboratory (Guangzhou) BYQ20240101the Key Research and Development and Promotion of Special Scientific and Technological Projects in Henan Province 242102231059the National Natural Science Fund of China 32370547the Shenzhen Science and Technology Program JCYJ20220530140800001 and JCYJ20230807090212024Zhumadian Comprehensive Test Station of Edible Fungi Industry Technology System of Henan Province HARS-22-08-Z5
6 · The paper itself

Abstract

The frequent and irrational use of antibiotics by humans has led to the escalating rise of antimicrobial resistance (AMR) with a high rate of morbidity-mortality worldwide, which poses a challenge to the development of effective treatments. A large number of host defense peptides from different organisms have gained interest due to their broad antibacterial spectrum, rapid action, and low target resistance, implying that these natural sources might be a new alternative to antimicrobial drugs. As important effectors of prey capture, defense against other animal attacks, and competitor deterrence, scorpion venoms have been developed as important candidate sources for modern drug development. With the rapid progress of bioanalytical and high throughput sequencing techniques, more and more scorpion-venom-derived peptides, including disulfide-bridged peptides (DBPs) and non-disulfide-bridged peptides (NDBPs), have been recently identified as having massive pharmacological activities in channelopathies, pathogen infections, and cancer treatments. In this review, we summarize the molecular diversity and corresponding structural classification of scorpion venom peptides with antibacterial, antifungal, and/or antiparasitic activity. We also aim to improve the understanding of the underlying mechanisms by which scorpion-venom-derived peptides exert these antimicrobial functions, and finally highlight their key aspects and prospects for antimicrobial therapeutic or pharmaceutical application.

Indexed as

Scorpion VenomsAnimalsAnti-Infective AgentsAntimicrobial PeptidesHumansPeptidesScorpionsAnti-Infective AgentsAntimicrobial PeptidesPeptidesScorpion Venomsantimicrobial activitydrug developmentscorpionsscorpion-venom-derived peptideunderlying mechanism

Identifiers

PMID39519721
PMCPMC11547508

What OpenQuestion holds

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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.