On the public citation graph
Three New Polyketide−Terpenoid Hybrids from Penicillium sp.
0 signed · 59 inferred · view as graph
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.
Is this your work? Sign in with ORCID and put your name on the
claims that are yours.
Reference health. See whether every reference in this work resolves to a
known work and none has been retracted — and get a dated CiteStamped
badge you can embed.
What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
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/s0040-4020(03)00739-7openalex-snapshot
Meroterpenoids from Penicillium citreo-viride B. IFO 4692 and 6200 hybrid
inferredcites →https://doi.org/10.1016/s0040-4020(97)00015-xopenalex-snapshot
Biosynthesis of polyketide-terpenoid (meroterpenoid) metabolites andibenin B and andilesin A in Aspergillus variecolor
inferredcites →https://doi.org/10.1016/s0040-4039(00)88109-5openalex-snapshot
Paraherquonin, a new meroterpenoid from penicillium paraherquei
inferredcites →https://doi.org/10.1021/ja00437a081openalex-snapshot
Austin, a novel polyisoprenoid mycotoxin from Aspergillus ustus
inferredcites →https://doi.org/10.1021/ja00437a082openalex-snapshot
Thallium in organic synthesis. 44. Oxidative rearrangements via oxythallation with thallium(III) nitrate supported on clay
inferredcites →https://doi.org/10.1021/ja01483a040openalex-snapshot
OPTICAL ACTIVITY IN SKEWED DIENES
inferredcites →https://doi.org/10.1021/ja01483a041openalex-snapshot
NOVEL GONADOTROPHIN INHIBITORS IN THE 19-NORSTEROID SERIES
inferredcites →https://doi.org/10.1021/ol049852kopenalex-snapshot
Berkeleydione and Berkeleytrione, New Bioactive Metabolites from an Acid Mine Organism
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.2021.112974zenodo-depositor-declared
Metabolites isolated from the human intestinal fungus Penicillium oxalicum SL2 and their agonistic effects on PXR and FXR
inferred← citeshttps://doi.org/10.1002/cbdv.202200403openalex-snapshot
Two New Nor‐seco‐Isodhilarane‐Type Meroterpenoids from the Endophytic Fungus Penicillium purpurogenum
inferred← citeshttps://doi.org/10.1002/chin.200830186openalex-snapshot
ChemInform Abstract: Three New Polyketide—Terpenoid Hybrids from Penicillium sp.
inferred← citeshttps://doi.org/10.1002/ejoc.201701335openalex-snapshot
3,5‐Dimethylorsellinic Acid Derived Meroterpenoids from Eupenicillium sp. 6A‐9, a Fungus Isolated from the Marine Sponge Plakortis simplex
inferred← citeshttps://doi.org/10.1007/s13659-024-00449-9openalex-snapshot
New piperazine derivatives helvamides B–C from the marine-derived fungus Penicillium velutinum ZK-14 uncovered by OSMAC (One Strain Many Compounds) strategy
inferred← citeshttps://doi.org/10.1016/b978-0-12-409547-2.14731-6openalex-snapshot
Fungal Partially Reducing Polyketides and Related Natural Products From Aspergillus, Penicillium, and Talaromyces
inferred← citeshttps://doi.org/10.1016/b978-0-12-821734-4.00014-9openalex-snapshot
Bioactive compounds from marine-derived fungi and their potential applications
inferred← citeshttps://doi.org/10.1016/b978-0-444-62615-8.00001-1openalex-snapshot
Bioprospecting in the Berkeley Pit
inferred← citeshttps://doi.org/10.1016/b978-0-444-63473-3.00006-xopenalex-snapshot
Drimane-Related Merosesquiterpenoids, a Promising Library of Metabolites for Drug Development
inferred← citeshttps://doi.org/10.1016/j.apsb.2017.12.005openalex-snapshot
Activation of an unconventional meroterpenoid gene cluster in Neosartorya glabra leads to the production of new berkeleyacetals
inferred← citeshttps://doi.org/10.1016/j.apsb.2020.07.015openalex-snapshot
A four-protein metabolon assembled by a small peptide protein creates the pentacyclic carbonate ring of aldgamycins
inferred← citeshttps://doi.org/10.1016/j.bioorg.2019.103166openalex-snapshot
Anti-inflammatory spiroaxane and drimane sesquiterpenoids from Talaromyces minioluteus (Penicillium minioluteum)
inferred← citeshttps://doi.org/10.1016/j.bioorg.2022.106271openalex-snapshot
OSMAC strategy integrated with molecular networking discovery peniciacetals A−I, nine new meroterpenoids from the mangrove-derived fungus Penicillium sp. HLLG-122
inferred← citeshttps://doi.org/10.1016/j.biotechadv.2018.02.001openalex-snapshot
Recent advances in reconstructing microbial secondary metabolites biosynthesis in Aspergillus spp.
inferred← citeshttps://doi.org/10.1016/j.fitote.2014.06.011openalex-snapshot
Meroterpenes and azaphilones from marine mangrove endophytic fungus Penicillium 303#
inferred← citeshttps://doi.org/10.1016/j.fitote.2018.01.010openalex-snapshot
Four new hybrid polyketide-terpenoid metabolites from the Penicillium sp. SYPF7381 in the rhizosphere soil of Pulsatilla chinensis
inferred← citeshttps://doi.org/10.1016/j.phytochem.2017.11.011openalex-snapshot
Anti-inflammatory meroterpenoids from the mangrove endophytic fungus Talaromyces amestolkiae YX1
inferred← citeshttps://doi.org/10.1016/j.phytochem.2024.114344openalex-snapshot
Congested heptacyclic meroterpenoids with anti-SARS-CoV-2 and anti-inflammatory activities from mangrove endophytic fungus Talaromyces amestolkiae SCNU–F0041
inferred← citeshttps://doi.org/10.1016/j.simyco.2014.08.001openalex-snapshot
Polyphasic taxonomy of the genus Talaromyces
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.1c00681openalex-snapshot
Talaromynoids A–I, Highly Oxygenated Meroterpenoids from the Marine-Derived Fungus Talaromyces purpureogenus SCSIO 41517 and Their Lipid Accumulation Inhibitory Activities
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.1c01025openalex-snapshot
Seco and Nor-seco Isodhilarane-Type Meroterpenoids from Penicillium purpurogenum and the Configuration Revisions of Related Compounds
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.6b00160openalex-snapshot
Nitric Oxide Inhibitory Meroterpenoids from the Fungus Penicillium purpurogenum MHZ 111
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.7b00438openalex-snapshot
3,5-Dimethylorsellinic Acid Derived Meroterpenoids from Penicillium chrysogenum MT-12, an Endophytic Fungus Isolated from Huperzia serrata
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.8b00569openalex-snapshot
Metabolomics-Driven Discovery of Meroterpenoids from a Mussel-Derived Penicillium ubiquetum
inferred← citeshttps://doi.org/10.1021/cr300430eopenalex-snapshot
Organic Carbonates from Natural Sources
inferred← citeshttps://doi.org/10.1021/jacs.6b08424openalex-snapshot
Discovery of Key Dioxygenases that Diverged the Paraherquonin and Acetoxydehydroaustin Pathways in Penicillium brasilianum
inferred← citeshttps://doi.org/10.1021/jo400616ropenalex-snapshot
Copper-Catalyzed Decarboxylative Coupling of Alkynyl Carboxylates with 1,1-Dibromo-1-alkenes
inferred← citeshttps://doi.org/10.1021/jo4024039openalex-snapshot
Dhilirolides E–N, Meroterpenoids Produced in Culture by the Fungus Penicillium purpurogenum Collected in Sri Lanka: Structure Elucidation, Stable Isotope Feeding Studies, and Insecticidal Activity
inferred← citeshttps://doi.org/10.1021/jo8025127openalex-snapshot
Practical Ruthenium-Catalyzed Cyclocarbonylation of Allenyl Alcohols in 2,4,6-Collidine Leading to α,β-Unsaturated Lactones: Concise Stereoselective Synthesis of (+)-Isomintlactone
inferred← citeshttps://doi.org/10.1021/np2003066openalex-snapshot
Berkeleyones and Related Meroterpenes from a Deep Water Acid Mine Waste Fungus That Inhibit the Production of Interleukin 1-β from Induced Inflammasomes
inferred← citeshttps://doi.org/10.1021/np300377bopenalex-snapshot
Meroterpenoid and Diphenyl Ether Derivatives from Penicillium sp. MA-37, a Fungus Isolated from Marine Mangrove Rhizospheric Soil
inferred← citeshttps://doi.org/10.1021/ol200031topenalex-snapshot
Dhilirolides A−D, Meroterpenoids Produced in Culture by the Fruit-Infecting Fungus Penicillium purpurogenum Collected in Sri Lanka
inferred← citeshttps://doi.org/10.1038/s41429-022-00587-7openalex-snapshot
New meroterpenoids from a soil-derived fungus Penicillium sp. SSW03M2 GY and their anti-virulence activity
inferred← citeshttps://doi.org/10.1039/c1ob06189eopenalex-snapshot
Synthesis of enantioenriched γ-quaternary cycloheptenones using a combined allylic alkylation/Stork–Danheiser approach: preparation of mono-, bi-, and tricyclic systems
inferred← citeshttps://doi.org/10.1039/c5np00090dopenalex-snapshot
Biosynthesis of fungal meroterpenoids
inferred← citeshttps://doi.org/10.1080/14786419.2018.1452001openalex-snapshot
Two new polyketides from the fungus Penicillium oxalicum MHZ153
inferred← citeshttps://doi.org/10.1107/s2056989015013614openalex-snapshot
Crystal structure and absolute configuration of preaustinoid A1
inferred← citeshttps://doi.org/10.1177/1934578x1300800510openalex-snapshot
A New Metabolite from the Endophytic Fungus Penicillium citrinum
inferred← citeshttps://doi.org/10.1186/s12934-025-02891-xopenalex-snapshot
Antifungal activity of oily core PEGylated PLGA nanocapsules loaded with Penicillium oxalicum fungal extract: in vitro, in vivo, and in silico study
inferred← citeshttps://doi.org/10.1201/b11196-6openalex-snapshot
Recent Advances in the Application of Electronic Circular Dichroism for Studies of Bioactive Natural Products
inferred← citeshttps://doi.org/10.1515/znb-2015-0184openalex-snapshot
Two new glycosidal metabolites of endophytic fungus Penicillium sp. (NO.4) from Tapiscia sinensis
inferred← citeshttps://doi.org/10.3389/fchem.2018.00314openalex-snapshot
Brasilianoids A–F, New Meroterpenoids From the Sponge-Associated Fungus Penicillium brasilianum
inferred← citeshttps://doi.org/10.3389/fchem.2018.00605openalex-snapshot
(±)-Peniorthoesters A and B, Two Pairs of Novel Spiro-Orthoester en-antiomers With an Unusual 1,4,6-Trioxaspi-ro[4.5]decane-7-One Unit From Penicillium minioluteum
inferred← citeshttps://doi.org/10.3390/md13063567openalex-snapshot
Drimane Sesquiterpene-Conjugated Amino Acids from a Marine Isolate of the Fungus Talaromyces minioluteus (Penicillium Minioluteum)
inferred← citeshttps://doi.org/10.3390/md14020037openalex-snapshot
Bioactive Compounds Produced by Strains of Penicillium and Talaromyces of Marine Origin
inferred← citeshttps://doi.org/10.5059/yukigoseikyokaishi.77.628openalex-snapshot
Total Synthesis of a Simplest Natural Product by a Clumsy Chemist
inferred← citeshttps://doi.org/10.70675/078603c8z6e19z4e41z94c8z33e60c8f1f76openalex-snapshot
De l'analyse métabolomique par LC-HRMS de souches fongiques marines à la production, l'isolement et l'hémisynthèse de produits naturels bioactifs
inferred← citeshttps://doi.org/10.7939/r3sq8qr76openalex-snapshot
Investigation of the biosynthesis of lovastatin and cytochalasin E, two fungal polyketides assembled by iterative PKS-NRPS enzymes
Editorial review for independent work. ICSAC — the Institute for Complexity
Science and Advanced Computing — runs a structured editorial panel for researchers
publishing outside journals, and publishes on CiteStamp rails. Submission is free
and goes through ORCID: icsacinstitute.org/submit.