Evidence map›Paper›PMID 29672633›Full record

ArticlePloS one2018

Design, synthesis, DFT, docking studies and ADME prediction of some new coumarinyl linked pyrazolylthiazoles: Potential standalone or adjuvant antimicrobial agents.

Sunil Kumar, Vikram Saini, Indresh K Maurya, Jayant Sindhu, Mukesh Kumari, Ramesh Kataria, Vinod Kumar

Abstract read
In one paragraph

Article in PloS one, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing 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

34 citing papers in PubMed.

  1. Assessment and Density Functional Theory of Bioactive Compounds ofPharmaceuticals (Basel, Switzerland) · 2026
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  3. Green synthesis,Future medicinal chemistry · 2025
    Article
  4. Synthesis,Future medicinal chemistry · 2025
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  5. Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Direct synthesis, characterization,Royal Society open science · 2024
    Article
  11. Article
  12. Article
  13. Review
  14. Review
  15. Article
  16. Article
  17. Article
  18. Theoretical and Anti-Molecules (Basel, Switzerland) · 2023
    Article
  19. Article
  20. 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

7 authors.

Sunil KumarDepartment of Chemistry & Centre of Advance Studies in Chemistry, Panjab University, Chandigarhs, India.
Vikram SainiDepartment of Biotechnology, AIIMS- New Delhi, Delhi, India.
Indresh K MauryaDepartment of Microbial Biotechnology, Panjab University, Chandigarh, India.
Jayant SindhuK.M. Government College, Narwana, India.
Mukesh KumariDepartment of Chemistry, Kurukshetra University, Kurukshetra, India.
Ramesh KatariaDepartment of Chemistry & Centre of Advance Studies in Chemistry, Panjab University, Chandigarhs, India.ORCID 0000-0002-4279-4801
Vinod KumarDepartment of Chemistry, M. M. University, Mullana-Ambala, India.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The control of antimicrobial resistance (AMR) seems to have come to a dead end. The major consequences of the use and abuse of antibacterial drugs are the development of resistant strains due to genetic mutability of both pathogenic and nonpathogenic microorganisms. We, herein, report the synthesis, characterization and biological activities of coumarin-thiazole-pyrazole (CTP) molecular hybrids with an effort to explore and overcome the increasing antimicrobial resistance. The compounds were characterized by analyzing their IR, Mass, 1H and13C NMR spectral data and elemental analysis. The in vitro antimicrobial activity of the synthesized compounds was investigated against various pathogenic strains; the results obtained were further explained with the help of DFT and molecular orbital calculations. Compound 1b and 1f displayed good antimicrobial activity and synergistic effects when used with kanamycin and amphotericin B. Furthermore, in vitro cytotoxicity of compounds 1b and 1f were studied against HeLa cells (cervical cancer cell) and Hek-293 cells. The results of molecular docking study were used to better rationalize the action and prediction of the binding modes of these compounds.

Indexed as

Chemistry Techniques, SyntheticDrug DesignMolecular Docking SimulationAnti-Bacterial AgentsCell LineDNA GyraseHumansMagnetic Resonance SpectroscopyMicrobial Sensitivity TestsMolecular Dynamics SimulationMolecular StructureStructure-Activity RelationshipThiazolesAnti-Bacterial AgentsDNA GyraseThiazoles

Identifiers

PMID29672633
PMCPMC5908142

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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.