Evidence map›Paper›PMID 34443347›Full record

ArticleMolecules (Basel, Switzerland)2021

Discovery of Amide-Functionalized Benzimidazolium Salts as Potent α-Glucosidase Inhibitors.

Imran Ahmad Khan, Matloob Ahmad, Usman Ali Ashfaq, Sadia Sultan, Magdi E A Zaki

Open access · goldAbstract read
In one paragraph

Article in Molecules (Basel, Switzerland), 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.5field-weighted citation impact, top 17% 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

7 citing papers in PubMed, 13 citations in OpenAlex.

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  6. Synthesis of NovelMolecules (Basel, Switzerland) · 2022
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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

5 authors at 3 institutions in 3 countries.

Imran Ahmad KhanDepartment of Chemistry, Government College University, Faisalabad 38000, Pakistan.
Matloob AhmadDepartment of Chemistry, Government College University, Faisalabad 38000, Pakistan.ORCID 0000-0003-1302-8056
Usman Ali AshfaqDepartment of Bioinformatics and Biotechnology, Government College University, Faisalabad 38000, Pakistan.
Sadia SultanFaculty of Pharmacy, Universiti Teknologi MARA, Puncak Alam Campus, Bandar Puncak Alam 42300, Selangor Darul Ehsan, Malaysia.
Magdi E A ZakiDepartment of Chemistry, Faculty of Science, Imam Mohammad Ibn Saud Islamic University (IMSIU), Riyadh 11623, Saudi Arabia.
Government College University, Faisalabad · PKImam Mohammad ibn Saud Islamic University · SAUniversiti Teknologi MARA · MY

Funding

Government College University, Faisalabad, PakistanHigher Education Commission, Pakistan NRPU-5614
6 · The paper itself

Abstract

α-Glucosidase inhibitors (AGIs) are used as medicines for the treatment of diabetes mellitus. The α-Glucosidase enzyme is present in the small intestine and is responsible for the breakdown of carbohydrates into sugars. The process results in an increase in blood sugar levels. AGIs slow down the digestion of carbohydrates that is helpful in controlling the sugar levels in the blood after meals. Among heterocyclic compounds, benzimidazole moiety is recognized as a potent bioactive scaffold for its wide range of biologically active derivatives. The aim of this study is to explore the α-glucosidase inhibition ability of benzimidazolium salts. In this study, two novel series of benzimidazolium salts, i.e., 1-benzyl-3-{2-(substituted) amino-2-oxoethyl}-1

Indexed as

alpha-GlucosidasesBenzimidazolesGlycoside Hydrolase InhibitorsMolecular Docking SimulationAmidesDrug DiscoveryHumansMolecular StructureSaltsStructure-Activity Relationshipalpha-GlucosidasesAmidesBenzimidazolesGlycoside Hydrolase InhibitorsSaltsanti-diabetic studiesbenzimidazole derivativesbenzimidazolium saltsmolecular dockingα-glucosidase inhibition

Identifiers

PMID34443347
PMCPMC8400806
OpenAlexW3188462936

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.