Evidence map›Paper›PMID 38253844›Full record

ReviewMolecular diversity2024

Antidiabetic potential of thiazolidinedione derivatives with efficient design, molecular docking, structural activity relationship, and biological activity: an update review (2021-2023).

Anchal Sharma, Nitish Kumar, Harmandeep Kaur Gulati, Rupali Rana, Jyoti, Aanchal Khanna, Muskan, Jatinder Vir Singh, Preet Mohinder Singh Bedi

Abstract readReview
PubMed Publisher
In one paragraph

Review in Molecular diversity, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
2.5field-weighted citation impact, top 12% 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

2 citing papers in PubMed, 10 citations in OpenAlex.

  1. Synthesis, crystal structure, andFuture medicinal chemistry · 2025
    Article
  2. 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 1 institution in 1 country.

Anchal SharmaDepartment of Pharmaceutical Sciences, Guru Nanak Dev University, Amritsar, Punjab, 143005, India. anchalsharma4619@gmail.com.
Nitish KumarDepartment of Pharmaceutical Sciences, Guru Nanak Dev University, Amritsar, Punjab, 143005, India.
Harmandeep Kaur GulatiDepartment of Pharmaceutical Sciences, Guru Nanak Dev University, Amritsar, Punjab, 143005, India.
Rupali RanaDepartment of Pharmaceutical Sciences, Guru Nanak Dev University, Amritsar, Punjab, 143005, India.
JyotiDepartment of Pharmaceutical Sciences, Guru Nanak Dev University, Amritsar, Punjab, 143005, India.
Aanchal KhannaDepartment of Pharmaceutical Sciences, Guru Nanak Dev University, Amritsar, Punjab, 143005, India.
MuskanDepartment of Pharmaceutical Sciences, Guru Nanak Dev University, Amritsar, Punjab, 143005, India.
Jatinder Vir SinghDepartment of Pharmaceutical Sciences, Guru Nanak Dev University, Amritsar, Punjab, 143005, India.
Preet Mohinder Singh BediDepartment of Pharmaceutical Sciences, Guru Nanak Dev University, Amritsar, Punjab, 143005, India. preet.pharma@gndu.ac.in.
Guru Nanak Dev University · IN

Funding

Nitish Kumar ICMR-BMI (BMI/11(04)/2022)
6 · The paper itself

Abstract

Thiazolidinedione has been used successfully by medicinal chemists all over the world in the development of potent antidiabetic derivatives. The few compounds with excellent antidiabetic potency that we have identified in this review could be used as a lead for further research into additional antidiabetic mechanisms. The information provided in this review regarding the design, biological activity, structure-activity relationships, and docking studies may be useful for scientists who wish to further explore this scaffold in order to fully utilize its biological potential and develop antidiabetic agents that would overcome the limitations of currently available medications for the treatment of diabetes. This review outlines the antidiabetic potential of Thiazolidinedione-based derivatives that have been published in the year 2021- till date.

Indexed as

Drug DesignHypoglycemic AgentsMolecular Docking SimulationThiazolidinedionesAnimalsHumansStructure-Activity RelationshipHypoglycemic AgentsThiazolidinedionesAntidiabeticDiabetes mellitusMolecular dockingStructure activity relationship (SAR)Thiazolidinedioneα-glucosidase

Identifiers

PMID38253844
OpenAlexW4391116085

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.