Evidence map›Paper›PMID 32206929›Full record

ReviewTopics in current chemistry (Cham)2020

Saturated Five-Membered Thiazolidines and Their Derivatives: From Synthesis to Biological Applications.

Nusrat Sahiba, Ayushi Sethiya, Jay Soni, Dinesh K Agarwal, Shikha Agarwal

Abstract readReview
In one paragraph

Review in Topics in current chemistry (Cham), 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing 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

24 citing papers in PubMed.

  1. Article
  2. Graphitic Carbon Nitride (g-CMolecules (Basel, Switzerland) · 2026
    Review
  3. Article
  4. Article
  5. d‑Glucose-Conjugated Benzo[ACS medicinal chemistry letters · 2025
    Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Copper-Catalyzed One-Pot Synthesis of Thiazolidin-2-imines.The Journal of organic chemistry · 2024
    Article
  12. Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. 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

5 authors.

Nusrat SahibaDepartment of Chemistry, Synthetic Organic Chemistry Laboratory, MLSU, Udaipur, 313001, India.
Ayushi SethiyaDepartment of Chemistry, Synthetic Organic Chemistry Laboratory, MLSU, Udaipur, 313001, India.
Jay SoniDepartment of Chemistry, Synthetic Organic Chemistry Laboratory, MLSU, Udaipur, 313001, India.
Dinesh K AgarwalDepartment of Pharmacy, B. N. University, MLSU, Udaipur, 313001, India.
Shikha AgarwalDepartment of Chemistry, Synthetic Organic Chemistry Laboratory, MLSU, Udaipur, 313001, India. shikha_urj@yahoo.com.ORCID http://orcid.org/0000-0003-2946-0409

Funding

Council of Scientific and Industrial Research, India 09/172(0088)/2018-EMR-I
6 · The paper itself

Abstract

In past decades, interdisciplinary research has been of great interest for scholars. Thiazolidine motifs behave as a bridge between organic synthesis and medicinal chemistry and compel researchers to explore new drug candidates. Thiazolidine motifs are very intriguing heterocyclic five-membered moieties present in diverse natural and bioactive compounds having sulfur at the first position and nitrogen at the third position. The presence of sulfur enhances their pharmacological properties, and, therefore, they are used as vehicles in the synthesis of valuable organic combinations. They show varied biological properties viz. anticancer, anticonvulsant, antimicrobial, anti-inflammatory, neuroprotective, antioxidant activity and so on. This diversity in the biological response makes it a highly prized moiety. Based on literature studies, various synthetic approaches like multicomponent reaction, click reaction, nano-catalysis and green chemistry have been employed to improve their selectivity, purity, product yield and pharmacokinetic activity. In this review article, we have summarized systematic approaches for the synthesis of thiazolidine and its derivatives, along with their pharmacological activity, including advantages of green synthesis, atom economy, cleaner reaction profile and catalyst recovery which will help scientists to probe and stimulate the study of these scaffolds.

Indexed as

Chemistry Techniques, SyntheticMolecular StructureThiazolidinesThiazolidinesAnticancerAntimicrobialAntitubercular activityBiological profileSynthesisThiazolidineThiazolidinone

Identifiers

PMID32206929
PMCPMC7101601

What OpenQuestion holds

Textmetadata
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.