Evidence map›Paper›PMID 29275696›Full record

ArticlePharmaceutical biology2018

Potential of rare actinomycetes in the production of metabolites against multiple oxidant agents.

Fatemeh Mohammadipanah, Mana Momenilandi

Abstract read
In one paragraph

Article in Pharmaceutical biology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing 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

10 citing papers in PubMed.

  1. Actinomycetes: A Source of Anticancer Metabolites.Current medicinal chemistry · 2025
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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

2 authors.

Fatemeh Mohammadipanaha Microbial Biotechnology Laboratory, Department of Microbiology , School of Biology and Center of Excellence in Phylogeny of Living Organisms, College of Science, University of Tehran , Tehran , Iran.
Mana Momenilandia Microbial Biotechnology Laboratory, Department of Microbiology , School of Biology and Center of Excellence in Phylogeny of Living Organisms, College of Science, University of Tehran , Tehran , Iran.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

contextActinobacteria are a precious source of novel bioactive metabolites with potential pharmaceutical applications.

objectivesRepresentatives of 11 genera of rare Actinobacteria were selected for the evaluation of antioxidant activity. MATERIAL AND

methodsFermentation broths of the Actinobacteria were extracted and dosage of 10 to 2000 µg/mL were applied for in vitro antioxidant-related bioassays. Cytotoxicity was assessed at the concentration of 2.5-20 µg/mL.

resultsIn the DPPH scavenging activity, 15 out of 52 extracts showed 17.0-26.8% activity in quantitative evaluation. Metabolites of five prominent antioxidant producing strains protected the DNA (pUC19) against UV-induced photolyzed H

conclusionsThe presence of nonidentical metabolites might be responsible for antioxidant and enzyme inhibitory activities of S. ecbatanensis, newly described actinobacterium in family Pseudonocardiaceae. The scavenging of the free electrons, protection of DNA and model yeast cells against oxidative stress, in addition to the inhibition of the oxidating enzymes are the main mechanisms of the antioxidant effect of the introduced resource in this study.

Indexed as

ActinobacteriaAnimalsAntioxidantsArtemiaCell SurvivalEnzyme InhibitorsFree Radical ScavengersHumansHuman Umbilical Vein Endothelial CellsOxidantsAntioxidantsEnzyme InhibitorsFree Radical ScavengersOxidantsenzyme inhibitionnatural antioxidantsradical scavenging agentsSecondary metabolites

Identifiers

PMID29275696
PMCPMC6130666

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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.