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Two New Terpenoids from Talaromyces purpurogenus

https://doi.org/10.3390/md16050150
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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/hlca.201000283openalex-snapshot
Ophiobolin Sesterterpenoids and Pyrrolidine Alkaloids from the Sponge‐Derived Fungus Aspergillus ustus
inferredcites →https://doi.org/10.1002/jcc.21460openalex-snapshot
Accurate conformation‐dependent molecular electrostatic potentials for high‐throughput in silico drug discovery
inferredcites →https://doi.org/10.1016/j.ejmech.2016.10.057openalex-snapshot
Amaryllidaceae alkaloids with new framework types from Zephyranthes candida as potent acetylcholinesterase inhibitors
inferredcites →https://doi.org/10.1016/j.fitote.2013.08.002openalex-snapshot
Ophiobolins P–T, five new cytotoxic and antibacterial sesterterpenes from the endolichenic fungus Ulocladium sp.
inferredcites →https://doi.org/10.1016/j.tet.2004.05.021openalex-snapshot
Cytotoxic sesterterpenes, 6-epi-ophiobolin G and 6-epi-ophiobolin N, from marine derived fungus Emericella variecolor GF10
inferredcites →https://doi.org/10.1016/j.tet.2007.04.045openalex-snapshot
Toward breast cancer resistance protein (BCRP) inhibitors: design, synthesis of a series of new simplified fumitremorgin C analogues
inferredcites →https://doi.org/10.1016/s0031-9422(00)84893-1openalex-snapshot
Enantiomeric type sesquiterpenoids of the liverwort Marchantia polymorpha
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.6b00910openalex-snapshot
Diterpenoids of the Cassane Type from Caesalpinia decapetala
inferredcites →https://doi.org/10.1021/acs.jnatprod.7b00301openalex-snapshot
Acetylcholinesterase Inhibitory Alkaloids from the Whole Plants of Zephyranthes carinata
inferredcites →https://doi.org/10.1021/acs.jnatprod.7b00335openalex-snapshot
Ophiobolins from the Mangrove Fungus Aspergillus ustus
inferredcites →https://doi.org/10.1021/ci6005646openalex-snapshot
Generating Conformer Ensembles Using a Multiobjective Genetic Algorithm
inferredcites →https://doi.org/10.1021/jo062445xopenalex-snapshot
Practical Method for the Absolute Configuration Assignment of tert / tert 1,2-Diols Using Their Complexes with Mo 2 (OAc) 4
inferredcites →https://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
inferredcites →https://doi.org/10.1021/jo800960wopenalex-snapshot
Structure Revision of Spiroleucettadine, a Sponge Alkaloid with a Bicyclic Core Meager in H-Atoms
inferredcites →https://doi.org/10.1021/np070165mopenalex-snapshot
Variation in Cytostatic Constituents of a Sponge-Derived Gymnascella dankaliensis by Manipulating the Carbon Source
inferredcites →https://doi.org/10.1021/np2004769openalex-snapshot
Anti-influenza Virus Polyketides from the Acid-Tolerant Fungus Penicillium purpurogenum JS03-21
inferredcites →https://doi.org/10.1021/np400045zopenalex-snapshot
Roussoellols A and B, Tetracyclic Fusicoccanes from Roussoella hysterioides
inferredcites →https://doi.org/10.1021/np500110zopenalex-snapshot
Caryophyllene Sesquiterpenes from the Marine-Derived Fungus Ascotricha sp. ZJ-M-5 by the One Strain–Many Compounds Strategy
inferredcites →https://doi.org/10.1021/np700737gopenalex-snapshot
Cytotoxic Alkaloids and Antibiotic Nordammarane Triterpenoids from the Marine-Derived Fungus Aspergillus sydowi
inferredcites →https://doi.org/10.1021/ol0611346openalex-snapshot
Predicting NMR Spectra by Computational Methods: Structure Revision of Hexacyclinol
inferredcites →https://doi.org/10.1021/ol200031topenalex-snapshot
Dhilirolides A−D, Meroterpenoids Produced in Culture by the Fruit-Infecting Fungus Penicillium purpurogenum Collected in Sri Lanka
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/10.1038/ja.2011.117openalex-snapshot
Indole alkaloids from marine-derived fungus Aspergillus sydowii SCSIO 00305
inferredcites →https://doi.org/10.1039/a903840jopenalex-snapshot
Dankasterone, a new class of cytotoxic steroid produced by a Gymnascella species from a marine sponge
inferredcites →https://doi.org/10.1039/c3np70078jopenalex-snapshot
Fungal metabolites with anticancer activity
inferredcites →https://doi.org/10.1080/14786419.2014.940586openalex-snapshot
Antifungal, phytotoxic and toxic metabolites produced byPenicillium purpurogenum
inferredcites →https://doi.org/10.1080/14786419.2016.1207075openalex-snapshot
Anti-neuroinflammatory constituents from the fungus Penicillium purpurogenum MHZ 111
inferredcites →https://doi.org/10.3114/sim.2011.70.04openalex-snapshot
Phylogeny and nomenclature of the genus Talaromyces and taxa accommodated in Penicillium subgenus Biverticillium
inferredcites →https://doi.org/10.3390/md12041815openalex-snapshot
Seven New and Two Known Lipopeptides as well as Five Known Polyketides: The Activated Production of Silent Metabolites in a Marine-Derived Fungus by Chemical Mutagenesis Strategy Using Diethyl Sulphate
inferredcites →https://doi.org/10.3390/md13085219openalex-snapshot
Rare Chromones from a Fungal Mutant of the Marine-Derived Penicillium purpurogenum G59
inferredcites →https://doi.org/10.3891/acta.chem.scand.17-0738openalex-snapshot
The Chemistry of the Natural Order Cupressales. 49. The Configuration of Thujopsene.

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

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inferred← citeshttps://doi.org/10.1002/anie.202117476openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s11596-020-2168-2openalex-snapshot
Polysubstituted Phenyl Glucosides Produced by the Fungus Metarrhizium anisopliae
inferred← citeshttps://doi.org/10.1007/s12010-022-04187-xopenalex-snapshot
Isolation, Characterization, Antioxidant, and Wound Healing Activities of Extracellular Polysaccharide from Endophytic Fungus Talaromyces purpureogenus
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/j.bioorg.2024.107726openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.bioorg.2026.109549openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.ejphar.2023.175988openalex-snapshot
Dankasterone A induces prostate cancer cell death by inducing oxidative stress
inferred← citeshttps://doi.org/10.1016/j.fitote.2019.02.025openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.fitote.2026.107496openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.gresc.2025.12.006openalex-snapshot
Activation of diterpene hydrocarbon skeletons by microbial natural P450 oxidases
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Brasilane sesquiterpenoids and dihydrobenzofuran derivatives from Aspergillus terreus [CFCC 81836]
inferred← citeshttps://doi.org/10.1016/j.tetlet.2022.154224openalex-snapshot
Biosynthesis of fusicoccane-type diterpenoids featuring a 5–8–5 tricyclic carbon skeleton
inferred← citeshttps://doi.org/10.1021/acs.jafc.4c03959openalex-snapshot
New Cytotoxic γ -Lactam Alkaloids from the Mangrove-Derived Fungus Talaromyces hainanensis sp. nov. Guided by Molecular Networking Strategy
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.3c00089openalex-snapshot
Cytotoxic Ergosteroids from a Strain of the Fungus Talaromyces adpressus
inferred← citeshttps://doi.org/10.1021/acs.joc.2c00528openalex-snapshot
Talaromynoids A–E: Five New Fusicoccane Diterpenoids from the Endophytic Fungus Talaromyces sp. DC-26
inferred← citeshttps://doi.org/10.1021/acs.joc.8b02912openalex-snapshot
Uncommon Polyoxygenated Sesquiterpenoids from South China Sea Soft Coral Lemnalia flava
inferred← citeshttps://doi.org/10.1021/acs.orglett.3c03355openalex-snapshot
Total Syntheses of Brassicicenes A, R, and T
inferred← citeshttps://doi.org/10.1038/s41598-025-90304-9openalex-snapshot
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inferred← citeshttps://doi.org/10.1039/c9np00069kopenalex-snapshot
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inferred← citeshttps://doi.org/10.1039/d0qo00960aopenalex-snapshot
Talaronoids A–D: four fusicoccane diterpenoids with an unprecedented tricyclic 5/8/6 ring system from the fungus Talaromyces stipitatus
inferred← citeshttps://doi.org/10.1134/s1068162020060023openalex-snapshot
Antibiotics from Extremophilic Micromycetes
inferred← citeshttps://doi.org/10.15625/1811-4989/15613openalex-snapshot
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inferred← citeshttps://doi.org/10.2174/0929867327666200113154115openalex-snapshot
Marine Natural Products with High Anticancer Activities
inferred← citeshttps://doi.org/10.3389/fmicb.2020.609952openalex-snapshot
Bioactive Metabolites From Acid-Tolerant Fungi in a Thai Mangrove Sediment
inferred← citeshttps://doi.org/10.3389/fmicb.2022.984801openalex-snapshot
Research advances in the structures and biological activities of secondary metabolites from Talaromyces
inferred← citeshttps://doi.org/10.3390/antibiotics11020222openalex-snapshot
New Antibacterial Secondary Metabolites from a Marine-Derived Talaromyces sp. Strain BTBU20213036
inferred← citeshttps://doi.org/10.3390/biom13071021openalex-snapshot
The Outstanding Chemodiversity of Marine-Derived Talaromyces
inferred← citeshttps://doi.org/10.3390/books978-3-03897-981-4openalex-snapshot
Bioactive Compounds from Marine-Derived Aspergillus, Penicillium, Talaromyces and Trichoderma Species
inferred← citeshttps://doi.org/10.3390/f14061172openalex-snapshot
Evaluation of the Antifungal Activity of Polysubstituted Cyclic 1,2-Diketones against Colletotrichum gloeosporioides
inferred← citeshttps://doi.org/10.3390/ijms241511941openalex-snapshot
Maize Genotypes Sensitive and Tolerant to Low Phosphorus Levels Exhibit Different Transcriptome Profiles under Talaromyces purpurogenus Symbiosis and Low-Phosphorous Stress
inferred← citeshttps://doi.org/10.3390/jof8030244openalex-snapshot
Diterpenes Specially Produced by Fungi: Structures, Biological Activities, and Biosynthesis (2010–2020)
inferred← citeshttps://doi.org/10.3390/md16110408openalex-snapshot
Bioactive Compounds from Marine-Derived Aspergillus, Penicillium, Talaromyces and Trichoderma Species
inferred← citeshttps://doi.org/10.3390/md18060321openalex-snapshot
A Review of Terpenes from Marine-Derived Fungi: 2015–2019
inferred← citeshttps://doi.org/10.3390/md19020088openalex-snapshot
Metabolites of Marine Sediment-Derived Fungi: Actual Trends of Biological Activity Studies
inferred← citeshttps://doi.org/10.3390/md23030131openalex-snapshot
Diterpenoids of Marine Organisms: Isolation, Structures, and Bioactivities
inferred← citeshttps://doi.org/10.3390/molecules27072103openalex-snapshot
Structure and Biological Activity of Ergostane-Type Steroids from Fungi
inferred← citeshttps://doi.org/10.3390/molecules27238303openalex-snapshot
A Review of Diterpenes from Marine-Derived Fungi: 2009–2021
inferred← citeshttps://doi.org/10.3390/molecules28227650openalex-snapshot
New Meroterpenoid Derivatives from the Pomegranate-Derived Endophytic Fungus Talaromyces purpureogenus
inferred← citeshttps://doi.org/10.3390/su15075961openalex-snapshot
Talaromyces purpurogenus Isolated from Rhizosphere Soil of Maize Has Efficient Organic Phosphate-Mineralizing and Plant Growth-Promoting Abilities
inferred← citeshttps://doi.org/10.3762/bjoc.18.144openalex-snapshot
Characterization of a new fusicoccane-type diterpene synthase and an associated P450 enzyme
inferred← citeshttps://doi.org/10.4018/979-8-3693-6972-2.ch014openalex-snapshot
Marine World of Terpenes Targeting Specific Cancers
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