Evidence map›Paper›PMID 42763916›Full record

ArticleChemistry & biodiversity2026

Design, Synthesis, and Antifungal Activity of Natural Furan Carboxylic Acid Derivatives as Potential Succinate Dehydrogenase Inhibitors.

Hongxin Luo, Yusen Wang, Yanchang Shi, Chengna Dong, Yadong Song, Qilin Zhang, Zhiqiang Hu, Yukun Qin

Abstract read
In one paragraph

Article in Chemistry & biodiversity, 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

8 authors.

Hongxin LuoKey Laboratory of Optic-electric Sensing and Analytical Chemistry for Life Science, MOE, College of Chemistry and Molecular Engineering, Qingdao University of Science and Technology, Qingdao, 266042, China.ORCID https://orcid.org/0009-0002-0479-4832
Yusen WangLaboratory of Experimental Marine Biology, Institute of Oceanology, Chinese Academy of Sciences, Qingdao, 266071, China.
Yanchang ShiLaboratory of Experimental Marine Biology, Institute of Oceanology, Chinese Academy of Sciences, Qingdao, 266071, China.
Chengna DongLaboratory of Experimental Marine Biology, Institute of Oceanology, Chinese Academy of Sciences, Qingdao, 266071, China.
Yadong SongLaboratory of Experimental Marine Biology, Institute of Oceanology, Chinese Academy of Sciences, Qingdao, 266071, China.
Qilin ZhangLaboratory of Experimental Marine Biology, Institute of Oceanology, Chinese Academy of Sciences, Qingdao, 266071, China.
Zhiqiang HuKey Laboratory of Optic-electric Sensing and Analytical Chemistry for Life Science, MOE, College of Chemistry and Molecular Engineering, Qingdao University of Science and Technology, Qingdao, 266042, China.ORCID https://orcid.org/0000-0002-6029-3242
Yukun QinLaboratory of Experimental Marine Biology, Institute of Oceanology, Chinese Academy of Sciences, Qingdao, 266071, China.ORCID https://orcid.org/0000-0001-6497-462X

Funding

Central guidance for local scientific and technological development funds 2024ZY0039Modern Agro-industry Technology Research Systesm CARS-49National Natural Science Foundation of China 42076126Qingdao Science and Technology Benefit the People Demonstration Project NO.25-1-5-xdny-7-nshShandong Key R&D Plan, Major Scientific and Technological Innovation Project 2022CXGC020413Shandong Provincial Natural Science Foundation ZR2025MS456
6 · The paper itself

Abstract

In this study, a series of furan amide derivatives were designed and synthesized from natural furan carboxylic acids as starting materials, with the aim of developing potential succinate dehydrogenase (SDH) inhibitors. The antifungal activities of the target compounds against four species of plant-pathogenic fungi were evaluated using in vitro bioassays. Structure-activity relationship (SAR) analysis revealed that the introduction of a trifluoromethyl group imparted superior antifungal activity to the compounds. Notably, compound 3m exhibited the most potent inhibitory effect against Rhizoctonia solani, with an EC

Indexed as

Antifungal AgentsBiological ProductsCarboxylic AcidsDrug DesignEnzyme InhibitorsFuransSuccinate DehydrogenaseDose-Response Relationship, DrugFusariumMicrobial Sensitivity TestsMolecular Docking SimulationMolecular StructureRhizoctoniaStructure-Activity RelationshipAntifungal AgentsBiological ProductsCarboxylic AcidsEnzyme InhibitorsfuranFuransSuccinate Dehydrogenaseantifungal activityF. oxysporumnatural furan carboxylic acidsR. solaniSARs

Identifiers

PMID42763916
PMCPMC13590135

What OpenQuestion holds

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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.