Evidence map›Paper›PMID 38341468›Full record

ArticleScientific reports2024

Synthesis, molecular docking and DFT analysis of novel bis-Schiff base derivatives with thiobarbituric acid for α-glucosidase inhibition assessment.

Saba Gul, Faheem Jan, Aftab Alam, Abdul Shakoor, Ajmal Khan, Abdullah F AlAsmari, Fawaz Alasmari, Momin Khan, Li Bo

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2024. 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
31.8field-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

24 citing papers in PubMed, 89 citations in OpenAlex.

  1. Article
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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 6 institutions in 4 countries.

Saba Gul *Department of Chemistry, Abdul Wali Khan University, Mardan, 23200, Pakistan.
Faheem Jan *Shenyang National Laboratory for Materials Science, Institute of Metal Research, Chineses Academy of Sciences, Shenyang, 110016, Liaoning, China.
Aftab AlamDepartment of Chemistry, University of Malakand, P.O. Box 18800, Dir Lower, Pakistan.
Abdul ShakoorDepartment of Chemistry, Abdul Wali Khan University, Mardan, 23200, Pakistan.
Ajmal KhanNatural and Medical Sciences Research Center, University of Nizwa, 616 Birkat Al Mauz, PO Box 33, Nizwa, Oman.
Abdullah F AlAsmariDepartment of Pharmacology and Toxicology, College of Pharmacy, King Saud University, 11451, Riyadh, Saudi Arabia.
Fawaz AlasmariDepartment of Pharmacology and Toxicology, College of Pharmacy, King Saud University, 11451, Riyadh, Saudi Arabia.
Momin KhanDepartment of Chemistry, Abdul Wali Khan University, Mardan, 23200, Pakistan. mominkhan@awkum.edu.pk.
Li BoInstitute of Catalysis for Energy and Environment, College of Chemistry and Chemical Engineering, Shenyang Normal University, Shenyang, 110034, China. boli@synu.edu.cn.
Abdul Wali Khan University Mardan · PKKing Saud University · SAShenyang Normal University · CNUniversity of Malakand · PKUniversity of Nizwa · OMUniversity of Science and Technology of China · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A library of novel bis-Schiff base derivatives based on thiobarbituric acid has been effectively synthesized by multi-step reactions as part of our ongoing pursuit of novel anti-diabetic agents. All these derivatives were subjected to in vitro α-glucosidase inhibitory potential testing after structural confirmation by modern spectroscopic techniques. Among them, compound 8 (IC

Indexed as

alpha-GlucosidasesGlycoside Hydrolase InhibitorsThiobarbituratesMolecular Docking SimulationMolecular StructureSchiff BasesStructure-Activity Relationshipalpha-GlucosidasesGlycoside Hydrolase InhibitorsSchiff BasesThiobarbituratesthiobarbituric acidbis-Schiff basesDFTMolecular dockingNMR spectroscopyThiobarbituric acidα-Glucosidase inhibition

Identifiers

PMID38341468
PMCPMC10858901
OpenAlexW4391723774

What OpenQuestion holds

Textmetadata
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.