Evidence map›Paper›PMID 39521808›Full record

ArticleScientific reports2024

Elaboration of newly synthesized tetrahydrobenzo[b]thiophene derivatives and exploring their antioxidant evaluation, molecular docking, and DFT studies.

Mina G Balamon, Ashraf A Hamed, Eman A El-Bordany, Ahmed E Swilem, Naglaa F H Mahmoud

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Article in Scientific reports, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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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

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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

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0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Mina G BalamonDepartment of Chemistry, Faculty of Science, Ain Shams University, Cairo, 11566, Egypt. minagirgis@sci.asu.edu.eg.
Ashraf A HamedDepartment of Chemistry, Faculty of Science, Ain Shams University, Cairo, 11566, Egypt.
Eman A El-BordanyDepartment of Chemistry, Faculty of Science, Ain Shams University, Cairo, 11566, Egypt.
Ahmed E SwilemDepartment of Chemistry, Faculty of Science, Ain Shams University, Cairo, 11566, Egypt.
Naglaa F H MahmoudDepartment of Chemistry, Faculty of Science, Ain Shams University, Cairo, 11566, Egypt.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Herein, 2-amino-6-(tert-butyl)-4,5,6,7-tetrahydrobenzo[b]thiophene-3-carbonitrile (1) was synthesized in excellent yield through gewald reaction in multi components one pot reaction. Compound 1 was utilized as a building block to synthesize a new group of tetrahydro benzo[b] thiophene congeners. The chemical structure of all the novel tetrahydro benzo[b]thiophene derivatives were elucidated through the melting point, elemental analysis, FT-IR,

Indexed as

AntioxidantsDensity Functional TheoryMolecular Docking SimulationThiophenesAscorbic AcidHumansKelch-Like ECH-Associated Protein 1Molecular StructureStructure-Activity RelationshipAntioxidantsAscorbic AcidKelch-Like ECH-Associated Protein 1Thiophenes2-amino thiophene-3-carbonitrileAntioxidantDFTDocking

Identifiers

PMID39521808
PMCPMC11550804

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Registered trials

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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.