Evidence map›Paper›PMID 36219380›Full record

ArticleMolecular diversity2023

Exploration of NMI-MsCl mediated amide bond formation for the synthesis of novel 3,5-substituted-1,2,4-oxadiazole derivatives: synthesis, evaluation of anti-inflammatory activity and molecular docking studies.

B Kulkarni, K Manjunatha, Muthipeedika Nibin Joy, Ayyiliath Meleveetil Sajith, Sougata Santra, Grigory V Zyryanov, C N Prashantha, Mohammed B Alshammari, K Sunil

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Article in Molecular diversity, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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1citing papers in PubMed
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1 · What the graph read from it

What it found

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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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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

9 authors.

B KulkarniResearch and Development Centre, Bharathiar University, Coimbatore, Tamilnadu, 641046, India.
K ManjunathaResearch and Development Centre, Bharathiar University, Coimbatore, Tamilnadu, 641046, India. manju.kumsi@ncetmail.com.
Muthipeedika Nibin JoyInstitute of Chemical Technology, Ural Federal University, 19 Mira Street, Yekaterinburg, Russia, 620002.
Ayyiliath Meleveetil SajithDepartment of Chemistry, SSIT, Sri Siddhartha Academy of Higher Education, Tumkur, Karnataka, 572107, India.
Sougata SantraInstitute of Chemical Technology, Ural Federal University, 19 Mira Street, Yekaterinburg, Russia, 620002.
Grigory V ZyryanovInstitute of Chemical Technology, Ural Federal University, 19 Mira Street, Yekaterinburg, Russia, 620002.
C N PrashanthaDepartment of Biotechnology, School of Applied Sciences, Reva University, Bengaluru, Karnataka, 560064, India.
Mohammed B AlshammariChemistry Department, College of Science and Humanities, Prince Sattam Bin Abdulaziz University, P.O. Box 83, Al-Kharj, 11942, Saudi Arabia.
K SunilDepartment of Chemistry, SSIT, Sri Siddhartha Academy of Higher Education, Tumkur, Karnataka, 572107, India.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We herein report the facile synthesis of a series of 3,5-substituted-1,2,4-oxadiazole derivatives 9a-e and 10a-e in good to excellent yields by employing NMI-MsCl mediated amide bond formation reaction. The anti-inflammatory potential of the newly synthesized compounds were evaluated by anti-denaturation assay using diclofenac sodium as the reference drug. The compounds 9a and 9d demonstrated promising activity profile when compared to the reference standard. The SAR and molecular docking studies were also carried out for obtaining more details about the profound activity profile of the synthesized molecules. The synthesized compounds were docked against two target proteins TGF-β and IL-1 by AutoDock vina and Auto Dock 4.2.

Indexed as

Anti-Inflammatory AgentsOxadiazolesAmidesMolecular Docking SimulationMolecular StructureStructure-Activity RelationshipAmidesAnti-Inflammatory AgentsOxadiazolesAnti-inflammatory activityMesyl chlorideMolecular dockingN-MethylimidazoleOxadiazoleSAR

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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.