Evidence map›Paper›PMID 39487898›Full record

ArticleMolecular diversity2025

Screening for antimicrobial and antioxidant activities of quinazolinone based isoxazole and isoxazoline derivatives, synthesis and In silico studies.

Nagaraju Myakala, Vishnu Thumma, Kotaiah Kandula, Nagamani Rayala, Lakshmi Satya Boddu, Kanaka Durga Bhavani Anagani

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Article in Molecular diversity, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
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

The trial behind it

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3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Nagaraju MyakalaDepartment of Chemistry, University College of Science, Osmania University, Hyderabad, Telangana, 500007, India.
Vishnu ThummaDepartment of Sciences and Humanities, Matrusri Engineering College, Hyderabad, Telangana, 500059, India.
Kotaiah KandulaDepartment of Chemistry, University College of Science, Osmania University, Hyderabad, Telangana, 500007, India.
Nagamani RayalaDepartment of Chemistry, University College of Science, Osmania University, Hyderabad, Telangana, 500007, India.
Lakshmi Satya BodduDepartment of Pharmaceutics, Vishnu Institute of Pharmaceutical Education and Research, Narsapur, Telangana, 502313, India.
Kanaka Durga Bhavani AnaganiDepartment of Chemistry, University College of Science, Osmania University, Hyderabad, Telangana, 500007, India. durgabhavani237@gmail.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Two novel series of quinazolinone based isoxazole and isoxazoline hybrid compounds were synthesized from 6-aminoquinazolinone as a key precursor. The title compounds were achieved in synthetic routes via propargylation and allylation reactions of the precursor followed by cyclization with various chloroximes. The new compounds 4a-g and 6a-g were screened for their antimicrobial activity against two Gram-positive bacteria, two Gram-negative bacteria and two fungi by employing Ampicillin and Itraconazole as standard reference. Among all, the 4-bromosubstituted analogues in isoxazole series 4d and in isoxazoline series 6d demonstrated potent activity against all bacterial and fungal strains compared to Ampicillin as well as Itraconazole. The MIC of these compounds were determined as 0.012 μM. The antioxidant investigation revealed that compounds 4f and 6f with dimethyl substitution, exhibited significant activity. Their respective IC

Indexed as

Anti-Infective AgentsAntioxidantsIsoxazolesQuinazolinonesFungiMicrobial Sensitivity TestsMolecular Docking SimulationStructure-Activity RelationshipAnti-Infective AgentsAntioxidantsIsoxazolesQuinazolinonesAntimicrobial agentIsoxazoleIsoxazolineMolecular dockingQuinazolinone

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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 Socratic graph.