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Fungal Metabolites Antagonists towards Plant Pests and Human Pathogens: Structure-Activity Relationship Studies
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Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/cbdv.201200358openalex-snapshot
Cyclopaldic Acid, Seiridin, and Sphaeropsidin A as Fungal Phytotoxins, and Larvicidal and Biting Deterrents against Aedes aegypti (Diptera: Culicidae): StructureActivity Relationships
inferredcites →https://doi.org/10.1002/cbdv.201600145openalex-snapshot
Fusaproliferin, Terpestacin and Their Derivatives Display Variable Allelopathic Activity Against Some Ascomycetous Fungi
inferredcites →https://doi.org/10.1002/chir.22744openalex-snapshot
Pyriculins A and B, two monosubstituted hex‐4‐ene‐2,3‐diols and other phytotoxic metabolites produced by Pyricularia grisea isolated from buffelgrass ( Cenchrus ciliaris )
inferredcites →https://doi.org/10.1002/med.21348openalex-snapshot
Toward a Cancer Drug of Fungal Origin
inferredcites →https://doi.org/10.1002/nt.2620020103openalex-snapshot
Fusapyrone and deoxyfusapyrone, two antifungal α‐Pyrones From Fusarium semitectum
inferredcites →https://doi.org/10.1002/nt.2620030307openalex-snapshot
Biological activity of cyclopaldic acid, a major toxin of Seiridium cupressi, its six derivatives, and iso‐cyclopaldic acid
inferredcites →https://doi.org/10.1002/ps.3744openalex-snapshot
Natural products for pest control: an analysis of their role, value and future
inferredcites →https://doi.org/10.1002/ps.4206openalex-snapshot
Dung‐inhabiting fungi: a potential reservoir of novel secondary metabolites for the control of plant pathogens
inferredcites →https://doi.org/10.1002/ps.4596openalex-snapshot
Differences in the progress of the biopesticide revolution between the EU and other major crop‐growing regions
inferredcites →https://doi.org/10.1007/978-3-642-11458-8_7openalex-snapshot
Insecticidal and Nematicidal Metabolites from Fungi
inferredcites →https://doi.org/10.1007/s00018-015-1902-6openalex-snapshot
Sphaeropsidin A shows promising activity against drug-resistant cancer cells by targeting regulatory volume increase
inferredcites →https://doi.org/10.1007/s00044-015-1439-0openalex-snapshot
Papyracillic acid and its derivatives as biting deterrents against Aedes aegypti (Diptera: Culicidae): structure–activity relationships
inferredcites →https://doi.org/10.1007/s00280-017-3293-xopenalex-snapshot
Computed determination of the in vitro optimal chemocombinations of sphaeropsidin A with chemotherapeutic agents to combat melanomas
inferredcites →https://doi.org/10.1007/s10295-015-1723-5openalex-snapshot
Natural product discovery: past, present, and future
inferredcites →https://doi.org/10.1007/s11557-013-0942-2openalex-snapshot
Formation of 6-n-pentyl-2H-pyran-2-one (6-PAP) and other volatiles by different Trichoderma species
inferredcites →https://doi.org/10.1016/0031-9422(90)89018-5openalex-snapshot
Cytochalasins: Structure-activity relationships
inferredcites →https://doi.org/10.1016/0031-9422(96)00206-3openalex-snapshot
A phytotoxic pimarane diterpene of Sphaeropsis sapinea f. sp. Cupressi, the pathogen of a canker disease of cypress
inferredcites →https://doi.org/10.1016/0040-4020(96)00559-5openalex-snapshot
Papyracillic acid, a new penicillic acid analogue from the ascomycete Lachnum papyraceum
inferredcites →https://doi.org/10.1016/b978-0-444-59514-0.00010-9openalex-snapshot
Bioactive Natural Products as Potential Candidates to Control Aedes aegypti, the Vector of Dengue
inferredcites →https://doi.org/10.1016/c2009-0-03073-6openalex-snapshot
Handbook of Toxic Fungal Metabolites
inferredcites →https://doi.org/10.1016/j.coph.2014.09.006openalex-snapshot
Update on the antibiotic resistance crisis
inferredcites →https://doi.org/10.1016/j.drudis.2008.07.004openalex-snapshot
Natural products in drug discovery
inferredcites →https://doi.org/10.1016/j.ejmech.2011.07.057openalex-snapshot
Natural products: An evolving role in future drug discovery
inferredcites →https://doi.org/10.1016/j.fitote.2016.11.007openalex-snapshot
Sarniensine, a mesembrine-type alkaloid isolated from Nerine sarniensis, an indigenous South African Amaryllidaceae, with larvicidal and adulticidal activities against Aedes aegypti
inferredcites →https://doi.org/10.1016/j.foodcont.2014.05.047openalex-snapshot
Natural products as antimicrobial agents
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.phytochem.2003.11.006openalex-snapshot
Studies on structure–activity relationship of sphaeropsidins A–F, phytotoxins produced by Sphaeropsis sapinea f. sp. cupressi
inferredcites →https://doi.org/10.1016/j.phytochem.2005.10.010openalex-snapshot
Stimulation of Orobanche ramosa seed germination by fusicoccin derivatives: A structure–activity relationship study
inferredcites →https://doi.org/10.1016/j.phytochem.2007.11.003openalex-snapshot
Nonenolides and cytochalasins with phytotoxic activity against Cirsium arvense and Sonchus arvensis: A structure–activity relationships study
inferredcites →https://doi.org/10.1016/j.phytochem.2012.01.011openalex-snapshot
Afritoxinones A and B, dihydrofuropyran-2-ones produced by Diplodia africana the causal agent of branch dieback on Juniperus phoenicea
inferredcites →https://doi.org/10.1016/j.phytochem.2012.03.010openalex-snapshot
Agropyrenol and agropyrenal, phytotoxins from Ascochyta agropyrina var. nana, a fungal pathogen of Elitrigia repens
inferredcites →https://doi.org/10.1016/j.phytochem.2015.07.008openalex-snapshot
Phytotoxins produced by Phoma chenopodiicola, a fungal pathogen of Chenopodium album
inferredcites →https://doi.org/10.1016/j.phytol.2012.08.011openalex-snapshot
Evaluation of in vitro anticancer activity of sphaeropsidins A–C, fungal rearranged pimarane diterpenes, and semisynthetic derivatives
inferredcites →https://doi.org/10.1016/j.phytol.2014.07.005openalex-snapshot
Bioactivity studies of oxysporone and several derivatives
inferredcites →https://doi.org/10.1016/j.tet.2013.06.031openalex-snapshot
Fischerindoline, a pyrroloindole sesquiterpenoid isolated from Neosartorya pseudofischeri, with in vitro growth inhibitory activity in human cancer cell lines
inferredcites →https://doi.org/10.1016/j.tet.2013.12.056openalex-snapshot
Spirostaphylotrichin W, a spirocyclic γ-lactam isolated from liquid culture of Pyrenophora semeniperda, a potential mycoherbicide for cheatgrass (Bromus tectorum) biocontrol
inferredcites →https://doi.org/10.1016/j.tet.2016.09.008openalex-snapshot
Further secondary metabolites produced by Diplodia corticola, a fungal pathogen involved in cork oak decline
inferredcites →https://doi.org/10.1016/j.tetlet.2016.08.098openalex-snapshot
Crystal structure and absolute configuration of sphaeropsidin A and its 6-O-p-bromobenzoate
inferredcites →https://doi.org/10.1016/s0031-9422(02)00379-5openalex-snapshot
Meroterpenes from Penicillium sp found in association with Melia azedarach
inferredcites →https://doi.org/10.1016/s0031-9422(97)00006-xopenalex-snapshot
Sphaeropsidins B and C, phytotoxic pimarane diterpenes from Sphaeropsis sapinea f. sp. Cupressi and Diplodia mutila
inferredcites →https://doi.org/10.1016/s0040-4020(97)00277-9openalex-snapshot
The Reactivity of the Fungal Toxin Papyracillic Acid 1
inferredcites →https://doi.org/10.1016/s0195-9255(02)00002-1openalex-snapshot
Environmental risk assessment for pesticides
inferredcites →https://doi.org/10.1021/acs.jafc.5b05170openalex-snapshot
Bioactive Secondary Metabolites Produced by the Oak PathogenDiplodia corticola
inferredcites →https://doi.org/10.1021/acs.jafc.6b01910openalex-snapshot
Induction of Haustorium Development by Sphaeropsidones in Radicles of the Parasitic WeedsStrigaandOrobanche. A Structure–Activity Relationship Study
inferredcites →https://doi.org/10.1021/acs.jnatprod.5b01055openalex-snapshot
Natural Products as Sources of New Drugs from 1981 to 2014
inferredcites →https://doi.org/10.1021/acs.jnatprod.6b00696openalex-snapshot
Cochliotoxin, a Dihydropyranopyran-4,5-dione, and Its Analogues Produced by Cochliobolus australiensis Display Phytotoxic Activity against Buffelgrass (Cenchrus ciliaris)
inferredcites →https://doi.org/10.1021/acs.jnatprod.7b00583openalex-snapshot
Chloromonilinic Acids C and D, Phytotoxic Tetrasubstituted 3-Chromanonacrylic Acids Isolated fromCochliobolus australiensiswith Potential Herbicidal Activity against Buffelgrass (Cenchrus ciliaris)
inferredcites →https://doi.org/10.1021/acschembio.7b00878openalex-snapshot
Biosynthesis and Structure–Activity Relationship Studies of Okaramines That Target Insect Glutamate-Gated Chloride Channels
inferredcites →https://doi.org/10.1021/jf034708jopenalex-snapshot
Viridepyronone, a New Antifungal 6-Substituted 2H-Pyran-2-one Produced by Trichoderma viride
inferredcites →https://doi.org/10.1021/jf035233zopenalex-snapshot
Structure−Activity Relationships of Derivatives of Fusapyrone, an Antifungal Metabolite of Fusarium semitectum
inferredcites →https://doi.org/10.1021/jf300146nopenalex-snapshot
Metabolites from Aspergillus fumigatus , an Endophytic Fungus Associated with Melia azedarach , and Their Antifungal, Antifeedant, and Toxic Activities
inferredcites →https://doi.org/10.1021/jf304933zopenalex-snapshot
Agropyrenol, a Phytotoxic Fungal Metabolite, and Its Derivatives: A Structure–Activity Relationship Study
inferredcites →https://doi.org/10.1021/jf4030618openalex-snapshot
Phomentrioloxin, a Fungal Phytotoxin with Potential Herbicidal Activity, and its Derivatives: A Structure–Activity Relationship Study
inferredcites →https://doi.org/10.1021/jf5035515openalex-snapshot
Pyrenophoric Acids B and C, Two New Phytotoxic Sesquiterpenoids Produced by Pyrenophora semeniperda
inferredcites →https://doi.org/10.1021/jf504252nopenalex-snapshot
Biopesticides: State of the Art and Future Opportunities
inferredcites →https://doi.org/10.1021/jf801727yopenalex-snapshot
Stimulation of Seed Germination of Orobanche Species by Ophiobolin A and Fusicoccin Derivatives
inferredcites →https://doi.org/10.1021/jf903499yopenalex-snapshot
Papyracillic Acid, a Phytotoxic 1,6-Dioxaspiro[4,4]nonene Produced by Ascochyta agropyrina Var.nana, a Potential Mycoherbicide for Elytrigia repens Biocontrol
inferredcites →https://doi.org/10.1021/np100837ropenalex-snapshot
Sphaeropsidones, Phytotoxic Dimedone Methyl Ethers Produced by Diplodia cupressi: A Structure−Activity Relationship Study
inferredcites →https://doi.org/10.1021/np200625mopenalex-snapshot
In Vitro Antibacterial Activity of Sphaeropsidins and Chemical Derivatives toward Xanthomonas oryzae pv. oryzae, the Causal Agent of Rice Bacterial Blight
inferredcites →https://doi.org/10.1021/np300103wopenalex-snapshot
Antibacterial Anthraquinone Derivatives from a Sea Anemone-Derived Fungus Nigrospora sp.
inferredcites →https://doi.org/10.1021/np300200jopenalex-snapshot
Phomentrioloxin: A Phytotoxic Pentasubstituted Geranylcyclohexentriol Produced by Phomopsis sp., a Potential Mycoherbicide for Carthamus lanatus Biocontrol
inferredcites →https://doi.org/10.1021/np400218zopenalex-snapshot
Chenopodolin: A Phytotoxic Unrearranged ent-Pimaradiene Diterpene Produced by Phoma chenopodicola, a Fungal Pathogen for Chenopodium album Biocontrol
inferredcites →https://doi.org/10.1021/np4009915openalex-snapshot
Pyrenophoric Acid, a Phytotoxic Sesquiterpenoid Penta-2,4-dienoic Acid Produced by a Potential Mycoherbicide, Pyrenophora semeniperda
inferredcites →https://doi.org/10.1021/np5000457openalex-snapshot
Spiromastixones A–O, Antibacterial Chlorodepsidones from a Deep-Sea-Derived Spiromastix sp. Fungus
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/10.1021/np50046a006openalex-snapshot
Structure Determination of Seiridin and Isoseiridin, Phytotoxic Butenolides from Culture Filtrate of Seiridium cardinale
inferredcites →https://doi.org/10.1038/emi.2014.23openalex-snapshot
Molecular basis of host specificity in human pathogenic bacteria
inferredcites →https://doi.org/10.1038/nrd4510openalex-snapshot
The re-emergence of natural products for drug discovery in the genomics era
inferredcites →https://doi.org/10.1038/srep06190openalex-snapshot
GluCl a target of indole alkaloid okaramines: a 25 year enigma solved
inferredcites →https://doi.org/10.1039/b903913aopenalex-snapshot
The chemistry and biology of cytochalasans
inferredcites →https://doi.org/10.1039/b914961aopenalex-snapshot
Natural products as antifungal agents against clinically relevant pathogens
inferredcites →https://doi.org/10.1039/c4ob01494dopenalex-snapshot
Antibacterial epipolythiodioxopiperazine and unprecedented sesquiterpene from Pseudallescheria boydii, a beetle (coleoptera)-associated fungus
inferredcites →https://doi.org/10.1039/c5np00081eopenalex-snapshot
Fungal phytotoxins with potential herbicidal activity: chemical and biological characterization
inferredcites →https://doi.org/10.1046/j.1472-765x.1998.00437.xopenalex-snapshot
Trichoderma /pathogen interactions: measurement of antagonistic chemicals produced at the antagonist/pathogen interface using a tubular bioassay
inferredcites →https://doi.org/10.1046/j.1472-765x.1998.t01-9-00449.xopenalex-snapshot
Trichoderma/pathogen interactions: measurement of antagonistic chemicals produced at the antagonist/pathogen interface using a tubular bioassay
inferredcites →https://doi.org/10.1080/00021369.1989.10869287openalex-snapshot
Structure and Insecticidal Activity of New Indole Alkaloids, Okaramines A and B, fromPenicillium simplicissimumAK-40
inferredcites →https://doi.org/10.1080/09583157.2013.844769openalex-snapshot
Effect of strain and cultural conditions on the production of cytochalasin B by the potential mycoherbicidePyrenophora semeniperda(Pleosporaceae, Pleosporales)
inferredcites →https://doi.org/10.1094/phi-a-2006-1117-02openalex-snapshot
Biological Control of Plant Pathogens
inferredcites →https://doi.org/10.1098/rstb.2007.2182openalex-snapshot
Biological control and sustainable food production
inferredcites →https://doi.org/10.1104/pp.114.239061openalex-snapshot
Natural Compounds as Next-Generation Herbicides
inferredcites →https://doi.org/10.1111/j.1364-3703.2012.00804.xopenalex-snapshot
Top 10 plant pathogenic bacteria in molecular plant pathology
inferredcites →https://doi.org/10.1111/j.1365-3059.1992.tb02454.xopenalex-snapshot
Cyclopaldic acid, a major phytotoxic metabolite of Seiridium cupressi , the pathogen of a canker disease of cypress
inferredcites →https://doi.org/10.1111/j.1439-0434.2009.01657.xopenalex-snapshot
Status of Streptomycin Resistance Development inXanthomonas oryzaepv.oryzaeandXanthomonas oryzaepv.oryzicolain China and their Resistance Characters
inferredcites →https://doi.org/10.1111/j.1469-8137.2005.01358.xopenalex-snapshot
Impacts of parasitic plants on natural communities
inferredcites →https://doi.org/10.1111/j.1476-5381.1995.tb15896.xopenalex-snapshot
Actions of the insecticide fipronil, on dieldrin‐sensitive and ‐resistant GABA receptors of Drosophila melanogaster
inferredcites →https://doi.org/10.1111/j.1552-6909.2009.01092.xopenalex-snapshot
Pesticides and Health Risks
inferredcites →https://doi.org/10.1111/ppa.12377openalex-snapshot
Mycelial growth rate and toxin production in the seed pathogen Pyrenophora semeniperda : resource trade‐offs and temporally varying selection
inferredcites →https://doi.org/10.1126/science.257.5073.1064openalex-snapshot
The Crisis in Antibiotic Resistance
inferredcites →https://doi.org/10.1146/annurev-ecolsys-102209-144634openalex-snapshot
Changing Geographic Distributions of Human Pathogens
inferredcites →https://doi.org/10.1201/b15333-47openalex-snapshot
Biological.Control.of.Plant.Pathogens
inferredcites →https://doi.org/10.1271/bbb1961.53.461openalex-snapshot
Structure and insecticidal activity of new indole alkaloids, okaramines A and B, from Penicillium simplicissimum AK-40.
inferredcites →https://doi.org/10.1515/chem-2017-0019openalex-snapshot
A survey of bacterial, fungal and plant metabolites against Aedes aegypti (Diptera: Culicidae), the vector of yellow and dengue fevers and Zika virus
inferredcites →https://doi.org/10.15562/medicina.v47i2.78openalex-snapshot
Faktor-faktor yang memengaruhi status imunisasi pada anak dengan infeksi human immunodeficiency virus
inferredcites →https://doi.org/10.2174/0929867324666170314145159openalex-snapshot
Bioactive Metabolites from Pathogenic and Endophytic Fungi of Forest Trees
inferredcites →https://doi.org/10.22270/ajprd.v11i5.1321openalex-snapshot
The Antibiotic Resistance Crisis
inferredcites →https://doi.org/10.2478/v10102-009-0001-7openalex-snapshot
Impact of pesticides use in agriculture: their benefits and hazards
inferredcites →https://doi.org/10.3389/fmicb.2017.01113openalex-snapshot
Fungal and Bacterial Pigments: Secondary Metabolites with Wide Applications
inferredcites →https://doi.org/10.3390/insects7040052openalex-snapshot
Biological Control of Mosquito Vectors: Past, Present, and Future
inferredcites →https://doi.org/10.3390/md12115657openalex-snapshot
Exploring the Chemodiversity and Biological Activities of the Secondary Metabolites from the Marine Fungus Neosartorya pseudofischeri
inferredcites →https://doi.org/10.3390/md13106352openalex-snapshot
Spiromastixones Inhibit Foam Cell Formation via Regulation of Cholesterol Efflux and Uptake in RAW264.7 Macrophages
inferredcites →https://doi.org/10.3390/medicina47030019openalex-snapshot
Antibiotic Resistance Mechanisms of Clinically Important Bacteria
inferredcites →https://doi.org/10.3390/molecules21111432openalex-snapshot
Alkaloids with Activity against the Zika Virus Vector Aedes aegypti (L.)—Crinsarnine and Sarniensinol, Two New Crinine and Mesembrine Type Alkaloids Isolated from the South African Plant Nerine sarniensis
inferredcites →https://doi.org/10.3390/molecules22122026openalex-snapshot
Structural Diversity and Biological Activities of the Cyclodipeptides from Fungi
inferredcites →https://doi.org/10.3390/molecules23020333openalex-snapshot
The Fungal Metabolite Eurochevalierine, a Sequiterpene Alkaloid, Displays Anti-Cancer Properties through Selective Sirtuin 1/2 Inhibition
inferredcites →https://doi.org/10.4236/pp.2013.43a003openalex-snapshot
The Success of Natural Products in Drug Discovery
inferredcites →https://doi.org/10.5495/wjcid.v1.i1.11openalex-snapshot
Antibiotic-resistant bugs in the 21st century: A public health challenge
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Incoming claims: where this work appears in other papers’ reference lists and arguments.
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inferred← citeshttps://doi.org/10.31038/jppr.2020324openalex-snapshot
Cytotoxic Meroterpenes: A Review
inferred← citeshttps://doi.org/10.3389/fagro.2025.1578915openalex-snapshot
Biological control agents: mechanisms of action, selection, formulation and challenges in agriculture
inferred← citeshttps://doi.org/10.3390/agriculture13102022openalex-snapshot
Journey of Trichoderma from Pilot Scale to Mass Production: A Review
inferred← citeshttps://doi.org/10.3390/agriculture16080860openalex-snapshot
Evaluation of Fungal Parasitic Activity Under Field Conditions: A Soil Simulation Test
inferred← citeshttps://doi.org/10.3390/agronomy10111637openalex-snapshot
The Influence of Trichoderma harzianum Rifai T-22 and Other Biostimulants on Rhizosphere Beneficial Microorganisms of Carrot
inferred← citeshttps://doi.org/10.3390/antibiotics10020148openalex-snapshot
Farnesane-Type Sesquiterpenoids with Antibiotic Activity from Chiliadenus lopadusanus
inferred← citeshttps://doi.org/10.3390/biom10010081openalex-snapshot
Isolation and Bioactivity of Secondary Metabolites from Solid Culture of the Fungus, Alternaria sonchi
inferred← citeshttps://doi.org/10.3390/biom11121902openalex-snapshot
The Assignment of the Absolute Configuration of Non-Cyclic Sesquiterpenes by Vibrational and Electronic Circular Dichroism: The Example of Chiliadenus lopadusanus Metabolites
inferred← citeshttps://doi.org/10.3390/jof7050331openalex-snapshot
In Vitro Antibacterial, Antifungal, Nematocidal and Growth Promoting Activities of Trichoderma hamatum FB10 and Its Secondary Metabolites
inferred← citeshttps://doi.org/10.3390/plants11233382openalex-snapshot
Phytotoxic Metabolites Produced by Fungi Involved in Grapevine Trunk Diseases: Progress, Challenges, and Opportunities
inferred← citeshttps://doi.org/10.3390/plants9060762openalex-snapshot
Trichoderma: The “Secrets” of a Multitalented Biocontrol Agent
inferred← citeshttps://doi.org/10.3390/su16010145openalex-snapshot
Potential Biopesticides from Seed Extracts: A Sustainable Way to Protect Cotton Crops from Bollworm Damage
inferred← citeshttps://doi.org/10.3390/toxins12020126openalex-snapshot
Phytotoxic Metabolites Isolated from Neufusicoccum batangarum, the Causal Agent of the Scabby Canker of Cactus Pear (Opuntia ficus-indica L.)
inferred← citeshttps://doi.org/10.3390/toxins13110805openalex-snapshot
In Vitro and In Vivo Toxicity Evaluation of Natural Products with Potential Applications as Biopesticides
inferred← citeshttps://doi.org/10.47371/mycosci.2020.11.002openalex-snapshot
Characterization and phytotoxicity of ophiobolins produced by Bipolaris setariae
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