Evidence mapPaperPMID 36559028Full record

ArticlePharmaceuticals (Basel, Switzerland)2022

Antidiabetic Potential of Novel 1,3,5-Trisubstituted-2-Thioxoimidazloidin-4-One Analogues: Insights into α-Glucosidase, α-Amylase, and Antioxidant Activities.

Salma M Khirallah, Heba M M Ramadan, Hossam Aladl Aladl Aladl, Najla O Ayaz, Lina A F Kurdi, Mariusz Jaremko, Samar Zuhair Alshawwa, Essa M Saied

Open access · goldAbstract read
In one paragraph

Article in Pharmaceuticals (Basel, Switzerland), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
4.0field-weighted citation impact, top 5% 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

28 citing papers in PubMed, 37 citations in OpenAlex.

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  9. Design, synthesis,RSC advances · 2026
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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

8 authors at 6 institutions in 3 countries.

Salma M KhirallahBiochemistry Department, Faculty of Science, Port Said University, Port Said 42526, Egypt.ORCID 0000-0002-7631-6840
Heba M M RamadanChemistry Department, Faculty of Science, Port Said University, Port Said 42526, Egypt.
Hossam Aladl Aladl AladlDepartment of Internal Medicine, Faculty of Medicine, AL-Azhar University, Nasr City, Cairo 11651, Egypt.
Najla O AyazDepartment of Biochemistry, College of Science, University of Jeddah, Jeddah 80327, Saudi Arabia.
Lina A F KurdiDepartment of Biology, College of Science, University of Jeddah, Jeddah 80327, Saudi Arabia.
Mariusz JaremkoSmart-Health Initiative and Red Sea Research Center, Division of Biological and Environmental Sciences and Engineering, King Abdullah University of Science and Technology, Thuwal 23955, Saudi Arabia.
Samar Zuhair AlshawwaDepartment of Pharmaceutical Sciences, College of Pharmacy, Princess Nourah bint Abdulrahman University, P.O. Box 84428, Riyadh 11671, Saudi Arabia.ORCID 0000-0001-9232-7956
Essa M SaiedChemistry Department, Faculty of Science, Suez Canal University, Ismailia 41522, Egypt.ORCID 0000-0002-7342-6200
Port Said University · EGUniversity of Jeddah · SAAl-Azhar University · EGKing Abdullah University of Science and Technology · SAPrincess Nourah bint Abdulrahman University · SASuez Canal University · EG

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

As the ninth leading cause of death globally, diabetes mellitus (DM) is considered to be the worst chronic metabolic disease requiring an enormous need for healthcare with over 578 million expected cases by 2023. Several recent findings have demonstrated that mediating the activity of carbohydrate-hydrolyzing enzymes, including α-amylase and α-glucosidase, could be a potential strategy for managing the development of DM. In the presented study, a novel set of 1,3,5-trisubstituted-2-thioxoimidazolidin-4-ones was designed, synthesized, and characterized. The antidiabetic activity of the synthesized compounds was explored by assessing their inhibitory activity toward α-amylase and α-glucosidase enzymes. The results demonstrated that this class of compounds exhibits considerable inhibitory activity toward both α-amylase and α-glucosidase enzymes. Among the synthesized compounds, compound

Indexed as

antidiabetic activityantioxidant activitycytotoxicitydiabetes mellitusmolecular docking simulationsubstituted-2-thiohydantoinsα-amylase activityα-glucosidase activity

Identifiers

PMID36559028
PMCPMC9785777
OpenAlexW4312212132

What Socratic 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 Socratic graph.