Evidence map›Paper›PMID 31671653›Full record

ReviewMolecules (Basel, Switzerland)2019

Guanidine-Containing Polyhydroxyl Macrolides: Chemistry, Biology, and Structure-Activity Relationship.

Xiaoyuan Song, Ganjun Yuan, Peibo Li, Sheng Cao

Abstract readReview
In one paragraph

Review in Molecules (Basel, Switzerland), 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing 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

15 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Isopropoxy Benzene Guanidine AmelioratesInternational journal of molecular sciences · 2023
    Article
  6. Review
  7. Article
  8. Antimicrobial Activity of Lactones.Antibiotics (Basel, Switzerland) · 2022
    Review
  9. Article
  10. Article
  11. Bacterial marginolactones trigger formation of algal gloeocapsoids, protective aggregates on the verge of multicellularity.Proceedings of the National Academy of Sciences of the United States of America · 2021
    Article
  12. Article
  13. Review
  14. Article
  15. Azalomycin FInternational journal of molecular sciences · 2020
    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

4 authors.

Xiaoyuan SongCollege of Bioscience and Bioengineering, Jiangxi Agricultural University, Nanchang 330045, China. 18700585380@163.com.
Ganjun YuanCollege of Bioscience and Bioengineering, Jiangxi Agricultural University, Nanchang 330045, China. gyuan@jxau.edu.cn.ORCID 0000-0002-4944-1144
Peibo LiSchool of Life Sciences, Sun Yat-sen University, 135 Xingang Road, Guangzhou 510275, China. lipb73@126.com.ORCID 0000-0002-2163-2045
Sheng CaoCollege of Bioscience and Bioengineering, Jiangxi Agricultural University, Nanchang 330045, China. 18322801808@163.com.

Funding

National Natural Science Foundation of China 81660578, 81960636 and 81460529
6 · The paper itself

Abstract

Antimicrobial resistance has been seriously threatening human health, and discovering new antimicrobial agents from the natural resource is still an important pathway among various strategies to prevent resistance. Guanidine-containing polyhydroxyl macrolides, containing a polyhydroxyl lactone ring and a guanidyl side chain, can be produced by many actinomycetes and have been proved to possess many bioactivities, especially broad-spectrum antibacterial and antifungal activities. To explore the potential of these compounds to be developed into new antimicrobial agents, a review on their structural diversities, spectroscopic characterizations, bioactivities, acute toxicities, antimicrobial mechanisms, and the structure-activity relationship was first performed based on the summaries and analyses of related publications from 1959 to 2019. A total of 63 guanidine-containing polyhydroxyl macrolides were reported, including 46 prototype compounds isolated from 33 marine and terrestrial actinomycetes and 17 structural derivatives. Combining with their antimicrobial mechanisms, structure-activity relationship analyses indicated that the terminal guanidine group and lactone ring of these compounds are vital for their antibacterial and antifungal activities. Further, based on their bioactivities and toxicity analyses, the discovery of guanidyl side-chain targeting to lipoteichoic acid of

Indexed as

GuanidineMacrolidesPhylogenySpectrum AnalysisStructure-Activity RelationshipToxicity Tests, AcuteGuanidineMacrolidesantibacterialantifungalantimicrobialazalomycin Fbioactivityguanidinemacrolidestructural diversitystructure-activity relationshiptoxicity

Identifiers

PMID31671653
PMCPMC6864768

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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.