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Hyfraxinic Acid, a Phytotoxic Tetrasubstituted Octanoic Acid, Produced by the Ash (Fraxinus excelsior L.) Pathogen Hymenoscyphus fraxineus Together with Viridiol and Some of Its Analogues
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/anie.201402290openalex-snapshot
A Volatile Lactone of Hymenoscyphus pseudoalbidus, Pathogen of European Ash Dieback, Inhibits Host Germination
inferredcites →https://doi.org/10.1002/cbdv.201700325openalex-snapshot
Fraxitoxin, a New Isochromanone Isolated from Diplodia fraxini
inferredcites →https://doi.org/10.1002/ppp3.11openalex-snapshot
Estimating mortality rates of European ash (Fraxinus excelsior) under the ash dieback (Hymenoscyphus fraxineus) epidemic
inferredcites →https://doi.org/10.1007/s10530-015-0911-6openalex-snapshot
Genetic population structure of the invasive ash dieback pathogen Hymenoscyphus fraxineus in its expanding range
inferredcites →https://doi.org/10.1016/j.funeco.2013.09.006openalex-snapshot
Vegetative incompatibility in the ash dieback pathogen Hymenoscyphus pseudoalbidus and its ecological implications
inferredcites →https://doi.org/10.1016/j.jpba.2017.02.037openalex-snapshot
Application of Mosher’s method for absolute configuration assignment to bioactive plants and fungi metabolites
inferredcites →https://doi.org/10.1016/j.pbi.2009.06.004openalex-snapshot
Fungal phytotoxins as mediators of virulence
inferredcites →https://doi.org/10.1016/j.phytochem.2012.09.012openalex-snapshot
Viridin-like steroids from Hymenoscyphus pseudoalbidus
inferredcites →https://doi.org/10.1016/j.phytochem.2014.01.018openalex-snapshot
Hymenosetin, a 3-decalinoyltetramic acid antibiotic from cultures of the ash dieback pathogen, Hymenoscyphus pseudoalbidus
inferredcites →https://doi.org/10.1016/j.steroids.2018.03.007openalex-snapshot
Hyfraxins A and B, cytotoxic ergostane-type steroid and lanostane triterpenoid glycosides from the invasive ash dieback ascomycete Hymenoscyphus fraxineus
inferredcites →https://doi.org/10.1016/s0031-9422(00)98644-8openalex-snapshot
Desmethoxyviridiol, a new toxin from Nodulisporium hinnuleum
inferredcites →https://doi.org/10.1021/jacs.7b02829openalex-snapshot
Enantioselective Chemical Syntheses of the Furanosteroids (−)-Viridin and (−)-Viridiol
inferredcites →https://doi.org/10.1021/np500258ropenalex-snapshot
Diplopimarane, a 20-nor-ent-Pimarane Produced by the Oak Pathogen Diplodia quercivora
inferredcites →https://doi.org/10.1038/s41467-018-04298-2openalex-snapshot
Biosynthetic pathway for furanosteroid demethoxyviridin and identification of an unusual pregnane side-chain cleavage
inferredcites →https://doi.org/10.1038/s41579-018-0121-1openalex-snapshot
Fungal secondary metabolism: regulation, function and drug discovery
inferredcites →https://doi.org/10.1039/c2969000839aopenalex-snapshot
Viridiol, a steroid-like product from Trichoderma viride
inferredcites →https://doi.org/10.1039/np9951200381openalex-snapshot
The viridin family of steroidal antibiotics
inferredcites →https://doi.org/10.1039/p19750000943openalex-snapshot
Demethoxyviridin and demethoxyviridiol: new fungal metabolites
inferredcites →https://doi.org/10.1039/p29720000760openalex-snapshot
Crystal and molecular structure of viridin
inferredcites →https://doi.org/10.1046/j.1439-0329.2002.00301.xopenalex-snapshot
Fungi associated with necrotic apical parts of Fraxinus excelsior shoots
inferredcites →https://doi.org/10.1093/forestry/cpx059openalex-snapshot
Evidence from mortality dating of Fraxinus excelsior indicates ash dieback (Hymenoscyphus fraxineus) was active in England in 2004–2005
inferredcites →https://doi.org/10.1094/phyto-74-1346openalex-snapshot
Phytotoxicity to Crop Plants and Herbicidal Effects on Weeds of Viridiol Produced byGliocladium virens
inferredcites →https://doi.org/10.1107/s0021889807067908openalex-snapshot
Mercury CSD 2.0 – new features for the visualization and investigation of crystal structures
inferredcites →https://doi.org/10.1107/s0021889812029111openalex-snapshot
WinGX and ORTEP for Windows : an update
inferredcites →https://doi.org/10.1107/s0021889898007717openalex-snapshot
SIR 97: a new tool for crystal structure determination and refinement
inferredcites →https://doi.org/10.1107/s2053229614024218openalex-snapshot
Crystal structure refinement with SHELXL
inferredcites →https://doi.org/10.1111/efp.12066openalex-snapshot
H ymenoscyphus pseudoalbidus and H ymenoscyphus albidus: viridiol concentration and virulence do not correlate
inferredcites →https://doi.org/10.1111/j.1439-0329.2006.00453.xopenalex-snapshot
Chalara fraxinea sp. nov. associated with dieback of ash (Fraxinus excelsior) in Poland
inferredcites →https://doi.org/10.1111/j.1439-0329.2009.00605.xopenalex-snapshot
Isolation, identification and necrotic activity of viridiol from Chalara fraxinea, the fungus responsible for dieback of ash
inferredcites →https://doi.org/10.1111/ppa.13014openalex-snapshot
Life at the edge – the cytology and physiology of the biotroph to necrotroph transition in Hymenoscyphus fraxineus during lesion formation in ash
inferredcites →https://doi.org/10.1139/m92-210openalex-snapshot
Characterization of major secondary metabolites produced in soilless mix by a formulated strain of the biocontrol fungus Gliocladium virens
inferredcites →https://doi.org/10.1524/zpch.1997.198.part_1_2.281openalex-snapshot
100 and More Basic NMR Experiments, A Practical Course
inferredcites →https://doi.org/10.2174/0929867324666170314145159openalex-snapshot
Bioactive Metabolites from Pathogenic and Endophytic Fungi of Forest Trees
inferredcites →https://doi.org/10.3389/fpls.2015.00573openalex-snapshot
Secondary metabolites in fungus-plant interactions
inferredcites →https://doi.org/10.3390/molecules17077769openalex-snapshot
B-norsteroids from Hymenoscyphus pseudoalbidus
inferredcites →https://doi.org/10.5598/imafungus.2014.05.01.09openalex-snapshot
Hymenoscyphus fraxineus, the correct scientific name for the fungus causing ash dieback in Europe
inferredcites →https://doi.org/10.5943/mycosphere/si/1b/5openalex-snapshot
Sardiniella urbana gen. et sp. nov., a new member of the Botryosphaeriaceae isolated from declining Celtis australis trees in Sardinian streetscapes
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1016/j.phytochem.2022.113302zenodo-depositor-declared
Diplofuranoxin, a disubstituted dihydrofuranone, was produced together with sphaeropsidin A and epi-sphaeropsidone by Diplodia subglobosa, an emerging ash (Fraxinus excelsior L.) pathogen in Europe
inferred← citeshttps://doi.org/10.1007/s41348-024-01056-zopenalex-snapshot
Priming of ash saplings with a low virulent Hymenoscyphus fraxineus strain as a possible disease control approach for reducing symptoms of ash dieback
inferred← citeshttps://doi.org/10.1016/j.funbio.2025.101646openalex-snapshot
Fungal endophytes with anti-fungal metabolites reduce symptoms of ash dieback in Fraxinus excelsior in a greenhouse experiment
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.1c00365openalex-snapshot
Pinofuranoxins A and B, Bioactive Trisubstituted Furanones Produced by the Invasive Pathogen Diplodia sapinea
inferred← citeshttps://doi.org/10.1039/d4ob00549jopenalex-snapshot
Asymmetric total syntheses of aspilactonol F and aspiketolactonol and synthetic studies toward diplofuranoxin
inferred← citeshttps://doi.org/10.1186/s12864-021-07837-2openalex-snapshot
Comparative analyses of the Hymenoscyphus fraxineus and Hymenoscyphus albidus genomes reveals potentially adaptive differences in secondary metabolite and transposable element repertoires
inferred← citeshttps://doi.org/10.29328/journal.jpsp.1001050openalex-snapshot
A Perspective on therapeutic potential of weeds
inferred← citeshttps://doi.org/10.29328/journal.jpsp.1001051openalex-snapshot
Antiviral and Antinematodal potentials of chitosan: Review
inferred← citeshttps://doi.org/10.3390/biom13111632openalex-snapshot
Bioactive Compounds from an Endophytic Pezicula sp. Showing Antagonistic Effects against the Ash Dieback Pathogen
inferred← citeshttps://doi.org/10.3390/f11080883openalex-snapshot
Diplodia fraxini and Diplodia subglobosa: The Main Species Associated with Cankers and Dieback of Fraxinus excelsior in North-Eastern Italy
inferred← citeshttps://doi.org/10.3390/microorganisms11040843openalex-snapshot
Specialized Metabolites Produced by Phytotopatogen Fungi to Control Weeds and Parasite Plants
inferred← citeshttps://doi.org/10.3390/microorganisms9122504openalex-snapshot
Priming of Resistance-Related Phenolics: A Study of Plant-Associated Bacteria and Hymenoscyphus fraxineus
inferred← citeshttps://doi.org/10.3390/toxins12070444openalex-snapshot
Anti-Biofilm Activity of the Fungal Phytotoxin Sphaeropsidin A against Clinical Isolates of Antibiotic-Resistant Bacteria
inferred← citeshttps://doi.org/10.3390/toxins13110812openalex-snapshot
Phytotoxins Produced by Two Biscogniauxia rosacearum Strains, Causal Agents of Grapevine Trunk Diseases, and Charcoal Canker of Oak Trees in Iran
inferred← citeshttps://doi.org/10.3390/toxins14080517openalex-snapshot
In Vitro Effects of Fungal Phytotoxins on Cancer Cell Viability: First Insight into Structure Activity Relationship of a Potent Metabolite of Cochliobolus australiensis Radicinin
inferred← citeshttps://doi.org/10.6084/m9.figshare.14905990openalex-snapshot
Additional file 1 of Comparative analyses of the Hymenoscyphus fraxineus and Hymenoscyphus albidus genomes reveals potentially adaptive differences in secondary metabolite and transposable element repertoires
inferred← citeshttps://doi.org/10.6084/m9.figshare.14905993openalex-snapshot
Additional file 2 of Comparative analyses of the Hymenoscyphus fraxineus and Hymenoscyphus albidus genomes reveals potentially adaptive differences in secondary metabolite and transposable element repertoires
inferred← citeshttps://doi.org/10.6084/m9.figshare.14905996openalex-snapshot
Additional file 3 of Comparative analyses of the Hymenoscyphus fraxineus and Hymenoscyphus albidus genomes reveals potentially adaptive differences in secondary metabolite and transposable element repertoires
inferred← citeshttps://doi.org/10.6084/m9.figshare.14905999openalex-snapshot
Additional file 4 of Comparative analyses of the Hymenoscyphus fraxineus and Hymenoscyphus albidus genomes reveals potentially adaptive differences in secondary metabolite and transposable element repertoires
inferred← citeshttps://doi.org/10.6084/m9.figshare.14906002openalex-snapshot
Additional file 5 of Comparative analyses of the Hymenoscyphus fraxineus and Hymenoscyphus albidus genomes reveals potentially adaptive differences in secondary metabolite and transposable element repertoires
inferred← citeshttps://doi.org/10.6084/m9.figshare.14906005openalex-snapshot
Additional file 6 of Comparative analyses of the Hymenoscyphus fraxineus and Hymenoscyphus albidus genomes reveals potentially adaptive differences in secondary metabolite and transposable element repertoires
inferred← citeshttps://doi.org/10.6084/m9.figshare.14906008openalex-snapshot
Additional file 7 of Comparative analyses of the Hymenoscyphus fraxineus and Hymenoscyphus albidus genomes reveals potentially adaptive differences in secondary metabolite and transposable element repertoires
inferred← citeshttps://doi.org/10.64898/2025.12.19.695327openalex-snapshot
Modulation of translational elongation by montanine alkaloids preferentially inhibits RNA viruses
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