Evidence map›Paper›PMID 39950292›Full record

ArticleCurrent organic synthesis2025

Design, Synthesis, and Biological Evaluation of Some Novel o-aminophenol Derivatives.

Dat Van Nguyen, Ly Duou Tran, Phuong Uyen Ngoc Vu, Luc Van Meervelt, Mai Ngoc Thi Nguyen, Anh Lan Ngo, Hoan Quoc Duong

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Article in Current organic synthesis, 2025. 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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1 · What the graph read from it

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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

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0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Dat Van NguyenDepartment of Chemistry, Hanoi National University of Education, Hanoi, Vietnam.ORCID 0009-0007-4623-6819
Ly Duou TranDepartment of Chemistry, Hanoi National University of Education, Hanoi, Vietnam.ORCID 0009-0008-0728-9325
Phuong Uyen Ngoc VuDepartment of Chemistry, Hanoi National University of Education, Hanoi, Vietnam.ORCID 0009-0000-3224-4665
Luc Van MeerveltDepartment of Chemistry, KU Leuven, Celestijnenlaan, 200F, B-3001 Leuven, Belgium.
Mai Ngoc Thi NguyenDepartment of Science, Hong Duc University, Thanh Hoa, Vietnam.ORCID 0000-0002-9639-1696
Anh Lan NgoDepartment of Chemistry, Hanoi National University of Education, Hanoi, Vietnam.
Hoan Quoc DuongDepartment of Chemistry, Hanoi National University of Education, Hanoi, Vietnam.ORCID 0000-0001-7540-6142

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundo-Aminophenol derivatives are of particular interest for their diverse biological activities and potential therapeutic applications. Such as, antioxidant, antibacterial, and cytotoxic activities.

objectivesThis study aimed to design and synthesize a series of novel o-aminophenol derivatives through an efficient multi-step process, characterize them using modern spectroscopic techniques, and evaluate their antimicrobial, antioxidant, and cytotoxic activities.

methodsA series of novel derivatives of o-aminophenol have been successfully synthesized with very high efficiency through a simple six-step process using readily available chemicals and straightforward reactions. The structures of all products were accurately determined using modern spectroscopic methods such as 1D and 2D NMR, as well as IR, MS spectroscopy, and X-ray methods. The antimicrobial activities of eight o-nitrophenol derivatives were assessed against Gram (-) and Gram (+) bacteria as well as fungi. In comparison, antioxidant activities were tested for two o-nitrophenol and 11 o-aminophenol derivatives using SC

resultsSix synthesized compounds 5b, 5c, 5g, 6b, 6c, 6g exhibited unusual doublet signals in the H8 region of the

conclusionDesign, synthesis, antimicrobial activity, DPPH Radical Scavenging, Cytotoxic activity, Evaluation of H8 signal anomalies in certain compounds, and Single crystal X-ray diffraction analysis.

Indexed as

AminophenolsAnti-Bacterial AgentsAnti-Infective AgentsAntineoplastic AgentsAntioxidantsDrug DesignBiphenyl CompoundsCell Line, TumorDrug Screening Assays, AntitumorFungiHumansMicrobial Sensitivity TestsMolecular StructureStructure-Activity Relationship2-aminophenolAminophenolsAnti-Bacterial AgentsAnti-Infective AgentsAntineoplastic AgentsAntioxidantsBiphenyl Compoundsantibacterial activityantioxidant activityatropisomercytotoxic activity.N-acetylo-aminophenolo-nitrophenolvanillin

Identifiers

PMID39950292

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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.