Evidence map›Paper›PMID 26753111›Full record

ArticleSpringerPlus2015

Antibacterial activity of nineteen selected natural products against multi-drug resistant Gram-negative phenotypes.

Armelle T Mbaveng, Louis P Sandjo, Simplice B Tankeo, Ache R Ndifor, Ambassa Pantaleon, Bonaventure T Nagdjui, Victor Kuete

Abstract read
In one paragraph

Article in SpringerPlus, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed, 1 pooled it
–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

32 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Appraising the therapeutical potentials ofFrontiers in pharmacology · 2022
    Pooled it
  2. The GenusMolecules (Basel, Switzerland) · 2026
    Review
  3. Antibacterial Activity of Extract, Fractions, and Compounds fromPharmaceuticals (Basel, Switzerland) · 2026
    Article
  4. Review
  5. Article
  6. Article
  7. Bixin fromACS omega · 2025
    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

7 authors.

Armelle T MbavengDepartment of Biochemistry, Faculty of Science, University of Dschang, P.O. Box 67, Dschang, Cameroon.
Louis P SandjoDepartment of Pharmaceutical Sciences, CSS, Universitade Federal de Santa Catarina, Florianópolis, SC 88040-900 Brazil.
Simplice B TankeoDepartment of Biochemistry, Faculty of Science, University of Dschang, P.O. Box 67, Dschang, Cameroon.
Ache R NdiforDepartment of Organic Chemistry, Faculty of Science, University of Yaoundé I, Yaoundé, Cameroon.
Ambassa PantaleonDepartment of Organic Chemistry, Faculty of Science, University of Yaoundé I, Yaoundé, Cameroon.
Bonaventure T NagdjuiDepartment of Organic Chemistry, Faculty of Science, University of Yaoundé I, Yaoundé, Cameroon.
Victor KueteDepartment of Biochemistry, Faculty of Science, University of Dschang, P.O. Box 67, Dschang, Cameroon ; P.O. Box 1499, Bafoussam, Cameroon.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The present study was designed to assess the antimicrobial activity of 19 natural products belonging to terpenoids, alkaloids, thiophenes and phenolics against a panel of 14 Gram-negative multidrug-resistant (MDR) bacteria. The results demonstrated that amongst the studied compounds, alkaloids and terpenoids were less active contrary to flavonoids: neocyclomorusin (3) and candidone (6) and isoflavonoids: neobavaisoflavone (8) and daidzein (12). Thiophene, 2-(penta-1,3-diynyl)-5-(3,4-dihydroxybut-1-ynyl)thiophene (17) showed moderate and selective activities. Compounds 3, 6, 8 and 12 displayed minimal inhibitory concentration (MIC) ranged from 4 to 256 μg/mL on all the 14 tested bacteria. MIC values below 10 μg/mL were obtained with 8, 3, 6 and 12 against 50, 42.9, 35.7 and 21.4 % of the tested bacteria. The lowest MIC value of 4 μg/mL was obtained with compound 3 against Klebsiella pneumoniae ATCC11296, Enterobacter cloacae BM47, compound 6 against Escherichia coli ATCC8739, K. pneumoniae ATCC11296, E. cloacae BM47 and compound 8 against K. pneumoniae ATCC11296 and E. cloacae BM47. The activity of flavonoid 3 was better or equal to that of chloramphenicol in all tested K. pneumoniae, Providencia stuartii, E. aerogenes, E. cloacae and Pseudomonas aeruginosa strains. Within isoflavonoids, neobavaisoflavone scaffold was detected as a pharmacophoric moiety. This study indicates that natural products such as 3, 6 and 8 could be explored more to develop antimicrobial drugs to fight MDR bacterial infections.

Indexed as

AntibacterialFlavonoidsIsoflavonoidsMultidrug resistanceNatural products

Identifiers

PMID26753111
PMCPMC4695461

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.