Evidence map›Paper›PMID 25871371›Full record

ArticleMolecules (Basel, Switzerland)2015

A facile synthesis and antimicrobial activity evaluation of sydnonyl-substituted thiazolidine derivatives.

Mei-Hsiu Shih, Yu-Yuan Xu, Yu-Sheng Yang, Guan-Ling Lin

Open access · goldAbstract read
In one paragraph

Article in Molecules (Basel, Switzerland), 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.5field-weighted citation impact, top 33% 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

6 citing papers in PubMed, 13 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Crystal structures of two substituted thia-zolidine derivatives.Acta crystallographica. Section E, Crystallographic communications · 2016
    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 at 1 institution in 1 country.

Mei-Hsiu ShihDepartment of Chemical and Materials Engineering, Southern Taiwan University of Science and Technology, Tainan City 71005, Taiwan. meihsius@mail.stust.edu.tw.
Yu-Yuan XuDepartment of Chemical and Materials Engineering, Southern Taiwan University of Science and Technology, Tainan City 71005, Taiwan. ma140107@stust.edu.tw.
Yu-Sheng YangDepartment of Chemical and Materials Engineering, Southern Taiwan University of Science and Technology, Tainan City 71005, Taiwan. ma140201@stust.edu.tw.
Guan-Ling LinDepartment of Chemical and Materials Engineering, Southern Taiwan University of Science and Technology, Tainan City 71005, Taiwan. lynnlin0221@yahoo.com.tw.
Southern Taiwan University of Science and Technology · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Some new sydnonyl-substituted thiazolidine derivatives were synthesized in high yields by the modified Knoevenagel condensation of 3-aryl-4-formylsydnones with thiazolidine-2,4-dione and 2-thioxo-thiazolidine-4-one, respectively. All the synthesized thiazolidine derivatives were screened by paper-disc method to identify their antimicrobial activities against three bacteria viz. Staphylococcus aureus, Proteus vulgaris and Escherichia coli, and two fungal cultures viz. Aspergillus niger and Penicillium citrinum. The reference drugs were Norfloxacin and Griseofulvin, respectively. The screening data indicated that the tested sydnonyl-substituted thiazolidine derivatives exhibited no obvious antibacterial activity compared with the standard drug Norfloxacin. However, thiazolidine derivatives displayed significant antifungal activities against Penicillium citrinum and Aspergillus niger. Notably, all of the tested compounds showed growth inhibitory activity 1.5-4.4 times higher than that of the standard drug Griseofulvin against the two fungi.

Indexed as

Anti-Infective AgentsBacteriaChemistry Techniques, SyntheticFungiMicrobial Sensitivity TestsMolecular StructureSydnonesThiazolidinesAnti-Infective AgentsSydnonesThiazolidines

Identifiers

PMID25871371
PMCPMC6272598
OpenAlexW2026277545

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

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.