Evidence map›Paper›PMID 42404710›Full record

ArticleDrug design, development and therapy2026

Design, Synthesis and Biological Evaluation of New Oxazolidinone Antimicrobial Agents with Low Monoamine Oxidase A Inhibition.

Jie Zhang, Yuhua Hu, Hao Tian, Chuang Li, Zihe Liang, Yuhe Yuan, Fangfang Lai, Wenxuan Zhang, Song Wu

Abstract read
In one paragraph

Article in Drug design, development and therapy, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

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

9 authors.

Jie Zhang *State Key Laboratory of Bioactive Substance and Function of Natural Medicines, Institute of Materia Medica, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing, 100050, People's Republic of China.ORCID 0009-0000-4671-0786
Yuhua Hu *State Key Laboratory of Bioactive Substance and Function of Natural Medicines, Institute of Materia Medica, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing, 100050, People's Republic of China.ORCID 0009-0004-6004-2576
Hao TianState Key Laboratory of Bioactive Substance and Function of Natural Medicines, Institute of Materia Medica, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing, 100050, People's Republic of China.ORCID 0009-0008-2599-7659
Chuang LiState Key Laboratory of Bioactive Substance and Function of Natural Medicines, Institute of Materia Medica, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing, 100050, People's Republic of China.ORCID 0009-0003-4043-8955
Zihe LiangState Key Laboratory of Bioactive Substance and Function of Natural Medicines, Institute of Materia Medica, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing, 100050, People's Republic of China.
Yuhe YuanState Key Laboratory of Bioactive Substance and Function of Natural Medicines, Institute of Materia Medica, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing, 100050, People's Republic of China.
Fangfang LaiState Key Laboratory of Bioactive Substance and Function of Natural Medicines, Institute of Materia Medica, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing, 100050, People's Republic of China.
Wenxuan ZhangState Key Laboratory of Bioactive Substance and Function of Natural Medicines, Institute of Materia Medica, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing, 100050, People's Republic of China.
Song WuState Key Laboratory of Bioactive Substance and Function of Natural Medicines, Institute of Materia Medica, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing, 100050, People's Republic of China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Linezolid is an oxazolidinone antibacterial agent that acts by binding to the 23S rRNA of the bacterial 50S ribosomal subunit to inhibit protein synthesis and exhibits potent activity against Gram-positive pathogens and Methods: We applied a rational drug design strategy based on the distinct binding models of linezolid within human MAO-A and the ribosomal large subunit of Results & Discussion: This strategy led to the identification of compound Conclusion: These results closely validated our rational design strategy.

Indexed as

Anti-Bacterial AgentsDrug DesignMonoamine OxidaseMonoamine Oxidase InhibitorsOxazolidinonesDose-Response Relationship, DrugGram-Positive BacteriaHumansMicrobial Sensitivity TestsMolecular Docking SimulationMolecular StructureMycobacterium tuberculosisStaphylococcus aureusStructure-Activity RelationshipAnti-Bacterial AgentsMonoamine Oxidasemonoamine oxidase A, humanMonoamine Oxidase InhibitorsOxazolidinonesantibacterial activityhuman MAO-Aoxazolidinone derivativesrational drug designstructural modifications

Identifiers

PMID42404710
PMCPMC13332732

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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.