Evidence map›Paper›PMID 33386071›Full record

ArticleBMC complementary medicine and therapies2021

Potential natural inhibitors of xanthine oxidase and HMG-CoA reductase in cholesterol regulation: in silico analysis.

Rishab Marahatha, Saroj Basnet, Bibek Raj Bhattarai, Prakriti Budhathoki, Babita Aryal, Bikash Adhikari, Ganesh Lamichhane, Darbin Kumar Poudel, Niranjan Parajuli

Open access · goldAbstract read
In one paragraph

Article in BMC complementary medicine and therapies, 2021. 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
10.4field-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

15 citing papers in PubMed, 102 citations in OpenAlex.

  1. Article
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  4. Biotechnologia · 2025
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  7. The Nutraceutical Properties ofInternational journal of molecular sciences · 2023
    Review
  8. Article
  9. Review
  10. Effect of Ginger on Inflammatory Diseases.Molecules (Basel, Switzerland) · 2022
    Review
  11. Review
  12. Article
  13. Alleviation of Malathion Toxicity Effect byPlants (Basel, Switzerland) · 2021
    Article
  14. Bioactive Triterpenes ofInternational journal of molecular sciences · 2021
    Article
  15. BioMed research international · 2021
    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

9 authors at 2 institutions in 1 country.

Rishab MarahathaCentral Department of Chemistry, Tribhuvan University, Kirtipur, Kathmandu, Nepal.
Saroj BasnetCenter for Drug Design and Molecular Simulation Division, Cancer Care Nepal and Research Center, Jorpati, Kathmandu, Nepal.
Bibek Raj BhattaraiCentral Department of Chemistry, Tribhuvan University, Kirtipur, Kathmandu, Nepal.
Prakriti BudhathokiCentral Department of Chemistry, Tribhuvan University, Kirtipur, Kathmandu, Nepal.
Babita AryalCentral Department of Chemistry, Tribhuvan University, Kirtipur, Kathmandu, Nepal.
Bikash AdhikariCentral Department of Chemistry, Tribhuvan University, Kirtipur, Kathmandu, Nepal.
Ganesh LamichhaneCentral Department of Chemistry, Tribhuvan University, Kirtipur, Kathmandu, Nepal.
Darbin Kumar PoudelCentral Department of Chemistry, Tribhuvan University, Kirtipur, Kathmandu, Nepal.
Niranjan ParajuliCentral Department of Chemistry, Tribhuvan University, Kirtipur, Kathmandu, Nepal. nparajuli@cdctu.edu.np.ORCID http://orcid.org/0000-0002-9233-6489
Tribhuvan University · NPNepal Cancer Hospital and Research Center · NP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundHypercholesterolemia has posed a serious threat of heart diseases and stroke worldwide. Xanthine oxidase (XO), the rate-limiting enzyme in uric acid biosynthesis, is regarded as the root of reactive oxygen species (ROS) that generate atherosclerosis and cholesterol crystals. β-Hydroxy β-methylglutaryl-coenzyme A reductase (HMGR) is a rate-limiting enzyme in cholesterol biosynthesis. Although some commercially available enzyme inhibiting drugs have effectively reduced cholesterol levels, most of them have failed to meet potential drug candidates' requirements. Here, we have carried out an in-silico analysis of secondary metabolites that have already shown good inhibitory activity against XO and HMGR in a wet lab setup.

methodsOut of 118 secondary metabolites reviewed, sixteen molecules inhibiting XO and HMGR were selected based on the IC

resultsThe molecular docking of amentoflavone (GOLD score 70.54, ∆G

conclusionThis computational analysis supports earlier experimental evidence towards the inhibition of XO and HMGR by natural products. Further study is necessary to explore the clinical efficacy of these secondary molecules, which might be alternatives for the treatment of hypercholesterolemia.

Indexed as

BiflavonoidsComputer SimulationDrug DiscoveryFungiGuaiacolHydroquinonesHydroxymethylglutaryl-CoA Reductase InhibitorsKetonesMolecular Docking SimulationPhytochemicalsSecondary MetabolismXanthine Oxidase6-paradolamentoflavoneBiflavonoidsganomycin IGuaiacolHydroquinonesHydroxymethylglutaryl-CoA Reductase InhibitorsKetonesPhytochemicalsXanthine OxidaseCholesterolEnzyme inhibitionMolecular dockingNatural products

Identifiers

PMID33386071
PMCPMC7775628
OpenAlexW3114717537

What OpenQuestion holds

Textmetadata
LicenceCC BY
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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.