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Bioactive Polyhydroxanthones from Penicillium purpurogenum

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Inferred edges come from two machine sources: sweeps of open repository metadata (mostly SSRN and Zenodo), and a bulk OpenAlex citation snapshot. Every row below is labelled with the one it came from. Neither is a complete citation index — absence here is not evidence of absence.

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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.200352154openalex-snapshot
A Short, Atom‐Economical Entry to Tetrahydroxanthenones
inferredcites →https://doi.org/10.1002/anie.201311260openalex-snapshot
Total Syntheses of Secalonic Acids A and D
inferredcites →https://doi.org/10.1002/chem.200800035openalex-snapshot
New Mono‐ and Dimeric Members of the Secalonic Acid Family: Blennolides A–G Isolated from the Fungus Blennoria sp.
inferredcites →https://doi.org/10.1002/chem.200900749openalex-snapshot
Xanthones and Oxepino[2, 3‐b]chromones from Three Endophytic Fungi
inferredcites →https://doi.org/10.1002/chem.201503593openalex-snapshot
Enantioselective Total Synthesis of Secalonic Acid E
inferredcites →https://doi.org/10.1016/j.phytochem.2013.03.018openalex-snapshot
Cryptosporioptide: A bioactive polyketide produced by an endophytic fungus Cryptosporiopsis sp.
inferredcites →https://doi.org/10.1016/j.tet.2017.11.038openalex-snapshot
Prenylated indole alkaloids and chromone derivatives from the fungus Penicillium sp. SCSIO041218
inferredcites →https://doi.org/10.1016/s0040-4039(00)78501-7openalex-snapshot
The yellow toxins produced by Cercospora Beticola. Part VIII : Chemical equilibrium between beticolins ; structures of minor compounds : beticolin 6 and beticolin 8
inferredcites →https://doi.org/10.1021/acs.jnatprod.5b00636openalex-snapshot
Versixanthones A–F, Cytotoxic Xanthone–Chromanone Dimers from the Marine-Derived Fungus Aspergillus versicolor HDN1009
inferredcites →https://doi.org/10.1021/acs.orglett.5b02536openalex-snapshot
Bisacremines E–G, Three Polycyclic Dimeric Acremines Produced by Acremonium persicinum SC0105
inferredcites →https://doi.org/10.1021/cr100446hopenalex-snapshot
Xanthones from Fungi, Lichens, and Bacteria: The Natural Products and Their Synthesis
inferredcites →https://doi.org/10.1021/jo0006831openalex-snapshot
Yanuthones: Novel Metabolites from a Marine Isolate of Aspergillus niger
inferredcites →https://doi.org/10.1021/np010020uopenalex-snapshot
Dicerandrols, New Antibiotic and Cytotoxic Dimers Produced by the Fungus Phomopsis longicolla Isolated from an Endangered Mint
inferredcites →https://doi.org/10.1021/np500142gopenalex-snapshot
Cytotoxic and Antibacterial Quinone Sesquiterpenes from a Myrothecium Fungus
inferredcites →https://doi.org/10.1021/np501037xopenalex-snapshot
Bisacremines A–D, Dimeric Acremines Produced by a Soil-Derived Acremonium persicinum Strain
inferredcites →https://doi.org/10.1021/ol500418fopenalex-snapshot
Penicillitone, a Potent in Vitro Anti-inflammatory and Cytotoxic Rearranged Sterol with an Unusual Tetracycle Core Produced by Penicillium purpurogenum
inferredcites →https://doi.org/10.1039/c4np00050aopenalex-snapshot
Xanthone dimers: a compound family which is both common and privileged
inferredcites →https://doi.org/10.1039/c8sc05126gopenalex-snapshot
Structure revision of cryptosporioptides and determination of the genetic basis for dimeric xanthone biosynthesis in fungi
inferredcites →https://doi.org/10.1080/10286020.2014.938647openalex-snapshot
α-Glucosidase and lipoxygenase inhibitory derivatives of cryptosporioptide from the endophytic fungusCryptosporiopsissp.
inferredcites →https://doi.org/10.1107/s0108767307043930openalex-snapshot
A short history of SHELX
inferredcites →https://doi.org/10.2174/092986705774370691openalex-snapshot
Xanthone Derivatives: New Insights in Biological Activities
inferredcites →https://doi.org/10.3390/molecules20045825openalex-snapshot
Three New Pigment Protein Tyrosine Phosphatases Inhibitors from the Insect Parasite Fungus Cordyceps gracilioides: Terreusinone A, Pinophilin C and Cryptosporioptide A

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.2021.112762zenodo-depositor-declared
Bioactive sesterterpenoids from the fungus Penicillium roqueforti YJ-14
inferred← citeshttps://doi.org/10.1002/slct.202402965openalex-snapshot
Synthetic and Natural Xanthones as Antibacterial Agents—Review
inferred← citeshttps://doi.org/10.1007/s11030-022-10417-5openalex-snapshot
Antibacterial natural products from microbial and fungal sources: a decade of advances
inferred← citeshttps://doi.org/10.1016/j.phytochem.2022.113246openalex-snapshot
Xanthones from the stems of Calophyllum membranaceum Gardn. et Champ. and their anti-inflammatory activity
inferred← citeshttps://doi.org/10.1016/j.phytochem.2026.114820openalex-snapshot
Soil-associated microorganisms: A natural source of biologically active compounds
inferred← citeshttps://doi.org/10.1016/j.psep.2022.03.013openalex-snapshot
Biotechnological valorization of mycelium-bound lipase of Penicillium purpurogenum in hydrolysis of high content lauric acid vegetable oils
inferred← citeshttps://doi.org/10.1016/j.tetlet.2021.153354openalex-snapshot
New polyhydroxanthones from the marine-associated fungus Penicillium sp. ZZ1750
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.2c00353openalex-snapshot
Cladoxanthones A and B, Xanthone-Derived Metabolites with a Spiro[cyclopentane-1,2′-[3,9a]ethanoxanthene]-2,4′,9′,11′-tetraone Skeleton from a Cladosporium sp.
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.3c00628openalex-snapshot
Subplenones A–J: Dimeric Xanthones with Antibacterial Activity from the Endophytic Fungus Subplenodomus sp. CPCC 401465
inferred← citeshttps://doi.org/10.1039/d2ra02639bopenalex-snapshot
New dimeric chromanone derivatives from the mutant strains of Penicillium oxalicum and their bioactivities
inferred← citeshttps://doi.org/10.1039/d3ra04012gopenalex-snapshot
Cladoxanthones C–G, xanthone derivatives from Cladosporium sp.
inferred← citeshttps://doi.org/10.1039/d5np00061kopenalex-snapshot
Microbe-derived aromatic polyketides toward MRSA infection: current advances and perspectives
inferred← citeshttps://doi.org/10.1080/14786419.2020.1853725openalex-snapshot
Three new andrastin derivatives from the endophytic fungus Penicillium vulpinum
inferred← citeshttps://doi.org/10.3390/molecules30040967openalex-snapshot
Xanthone Dimers in Angiosperms, Fungi, Lichens: Comprehensive Review of Their Sources, Structures, and Pharmacological Properties
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