Evidence map›Paper›PMID 37857636›Full record

ArticleScientific reports2023

One-pot synthesis, computational chemical study, molecular docking, biological study, and in silico prediction ADME/pharmacokinetics properties of 5-substituted 1H-tetrazole derivatives.

Ahmed El-Sewedy, Eman A El-Bordany, Naglaa F H Mahmoud, Kholoud A Ali, Sayed K Ramadan

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
5.4field-weighted citation impact, top 3% 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

17 citing papers in PubMed, 36 citations in OpenAlex.

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  12. Synthesis and Antimicrobial Activity of (Molecules (Basel, Switzerland) · 2024
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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 1 institution in 1 country.

Ahmed El-SewedyChemistry Department, Faculty of Science, Ain Shams University, Cairo, 11566, Egypt.
Eman A El-BordanyChemistry Department, Faculty of Science, Ain Shams University, Cairo, 11566, Egypt.ORCID http://orcid.org/0000-0001-9224-4800
Naglaa F H MahmoudChemistry Department, Faculty of Science, Ain Shams University, Cairo, 11566, Egypt.ORCID http://orcid.org/0000-0002-6655-5741
Kholoud A AliZoology Department, Faculty of Science, Ain Shams University, Cairo, 11566, Egypt.
Sayed K RamadanChemistry Department, Faculty of Science, Ain Shams University, Cairo, 11566, Egypt. sayed.karam2008@sci.asu.edu.eg.ORCID http://orcid.org/0000-0003-2743-6544
Ain Shams University · EG

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

An efficient synthesis of 5-substituted 1H-tetrazoles was successfully achieved through one-pot multi-component condensation reactions of some aromatic aldehydes or indolin-2,3-dione with malononitrile and sodium azide using diverse reaction conditions to obtain considerable product yields. Furthermore, it has been achieved for the first time to construct desired products under neat condition. Molecular docking studies with CSNK2A1 receptor disclosed the lowest binding energy displayed by the dimethoxyphenyl derivative 4c with - 6.8687 kcal/mol. The synthesized tetrazoles were screened for their in-vitro cytotoxic activity against epidermoid cancer cell line (A431) and colon cancer line (HCT116) with respect to normal skin fibroblast cell line (BJ-1) using MTT assay, and antimicrobial activity against the bacteria: K. pneumonia, S. aureus, and the fungi: Candida albicans, as well as their antioxidant activity using 2,2-diphenyl-1-picrylhydrazyl assay. In addition, the toxicity of tetrazole derivative was assessed by determination of their approximate lethal dose fifty (LD

Indexed as

AntioxidantsStaphylococcus aureusAnimalsMolecular Docking SimulationMolecular StructureRatsStructure-Activity RelationshipTetrazoles1H-tetrazoleAntioxidantsTetrazoles

Identifiers

PMID37857636
PMCPMC10587066
OpenAlexW4387781629

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.