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Matsutakone and Matsutoic Acid, Two (Nor)steroids with Unusual Skeletons from the Edible Mushroom Tricholoma matsutake
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
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Total Synthesis and Structure Assignment of (+)‐Hexacyclinol
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Strophasterols A to D with an Unprecedented Steroid Skeleton: From the Mushroom Stropharia rugosoannulata
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Novel Natural Oximes and Oxime Esters with a Vibralactone Backbone from the Basidiomycete Boreostereum vibrans
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Six novel steroids from culture of basidiomycete Polyporus ellisii
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A new and rapid colorimetric determination of acetylcholinesterase activity
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N-Containing Compounds of Macromycetes
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Natural Terphenyls: Developments since 1877
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Corner flapping: a simple and fast algorithm for exhaustive generation of ring conformations
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Calculation of Optical Rotation Using Density Functional Theory
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Panepophenanthrin, from a Mushroom Strain, a Novel Inhibitor of the Ubiquitin-Activating Enzyme
inferredcites →https://doi.org/10.1021/np100682copenalex-snapshot
A Highly Conjugated Dihydroxylated C28 Steroid from a Myxobacterium
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Prediction of the Structure of Nobilisitine A Using Computed NMR Chemical Shifts
inferredcites →https://doi.org/10.1021/ol062307uopenalex-snapshot
Vibralactone: A Lipase Inhibitor with an Unusual Fused β-Lactone Produced by Cultures of the Basidiomycete Boreostereum vibrans
inferredcites →https://doi.org/10.1039/c0np00006jopenalex-snapshot
N-Containing compounds of macromycetes
inferredcites →https://doi.org/10.1039/p29930000187openalex-snapshot
An efficient algorithm for searching low-energy conformers of cyclic and acyclic molecules
inferredcites →https://doi.org/10.1615/interjmedicmush.v5.i4.60openalex-snapshot
Studies on the Constituents of the Mycelia Produced from Fermented Culture of Flammulina velutipes (W.Curt.:Fr.) Singer (Agaricomycetideae)
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Hexacylinol, a New Antiproliferative Metabolite of Panus rudis HKI 0254.
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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Cadinane sesquiterpenoids from the fungus Antrodiella albocinnamomea and their inhibitory activity against nitric oxide production
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Chiral Building Blocks for Total Steroid Synthesis and the Use of Steroids as Chiral Building Blocks in Organic Synthesis
inferred← citeshttps://doi.org/10.1007/s13205-020-02333-yopenalex-snapshot
A critical review on submerged production of mushroom and their bioactive metabolites
inferred← citeshttps://doi.org/10.1007/s13659-021-00297-xopenalex-snapshot
Structures, Chemical Conversions, and Cytotoxicity of Tricholopardins C and D, Two Tricholoma Triterpenoids from the Wild Mushroom Tricholoma pardinum
inferred← citeshttps://doi.org/10.1016/b978-0-443-19049-0.00010-4openalex-snapshot
Nutraceutical metabolites, value addition and industrial products for developing entrepreneurship through edible fleshy fungi
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Endophytic fungus Umbelopsis sp. TM01 as high-activity alternative to Tricholoma matsutake
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Isoindolinone-containing meroterpenoids with α -glucosidase inhibitory activity from mushroom Hericium caput-medusae
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LC-MS guided isolation of gracilistones A and B, a pair of diastereomeric sesquiterpenoids with an unusual tetrahydrofuran-fused tricyclic skeleton from Acanthopanax gracilistylus and their potential anti-inflammatory activities
inferred← citeshttps://doi.org/10.1016/j.fitote.2019.104289openalex-snapshot
Cytotoxic ergosterols from cultures of the basidiomycete Psathyrella candolleana
inferred← citeshttps://doi.org/10.1016/j.fitote.2019.104362openalex-snapshot
Ochracines A-E, chamigrane-related norsesquiterpene derivatives from the basidiomycete Steccherinum ochraceum HFG119
inferred← citeshttps://doi.org/10.1016/j.fitote.2024.106084openalex-snapshot
Psathrosterols C–E, highly conjugated ergosterol derivatives from Psathyrella rogueiana with anti-inflammatory and immunosuppressive activity
inferred← citeshttps://doi.org/10.1016/j.phytochem.2018.05.002openalex-snapshot
Lanostane triterpenoids from Tricholoma pardinum with NO production inhibitory and cytotoxic activities
inferred← citeshttps://doi.org/10.1016/j.phytochem.2020.112431openalex-snapshot
Chemical constituents and their cytotoxicities from mushroom Tricholoma imbricatum
inferred← citeshttps://doi.org/10.1016/j.phytochem.2022.113554openalex-snapshot
Polyketides with antimicrobial activities from Penicillium canescens DJJ-1
inferred← citeshttps://doi.org/10.1016/j.phytochem.2024.114303openalex-snapshot
Bipolaristeroid A, a 5,6-seco-9,10-seco-steroid with cytotoxic activity from the fungus Bipolaris maydis
inferred← citeshttps://doi.org/10.1016/j.phytochem.2025.114483openalex-snapshot
Matsulongifolins A–J: (−)-longifolane-type sesquiterpenoids from the mushroom Tricholoma matsutake (S. Ito & Imai) Singer
inferred← citeshttps://doi.org/10.1016/j.phytol.2019.02.007openalex-snapshot
Cytotoxic ergosteroids from the fungus Stereum hirsutum
inferred← citeshttps://doi.org/10.1016/j.phytol.2019.05.016openalex-snapshot
Cadinane-type sesquiterpenoids and an indolizine alkaloid from the rice fermentation of the fungus Rigidoporus microporus
inferred← citeshttps://doi.org/10.1016/j.phytol.2022.06.002openalex-snapshot
Two new alliacane sesquiterpenes from the fruiting bodies of edible mushroom Gomphus purpuraceus
inferred← citeshttps://doi.org/10.1016/j.steroids.2022.109157openalex-snapshot
Tricholosterols A–D, four new ergosterol derivatives from the mushroom Tricholoma terreum
inferred← citeshttps://doi.org/10.1016/j.tetlet.2017.12.084openalex-snapshot
Pyridone alkaloids from the scale-insect pathogenic fungus Hypocrella discoidea BCC 71382
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Confluenines A–F, N -oxidized l -isoleucine derivatives from the edible mushroom Albatrellus confluens
inferred← citeshttps://doi.org/10.1016/j.tetlet.2020.151892openalex-snapshot
Cyclic dipeptides with peroxy groups from the fruiting bodies of the edible mushroom Tricholoma matsutake
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Advanced natural products chemistry research in China between 2015 and 2017
inferred← citeshttps://doi.org/10.1016/s1875-5364(24)60671-0openalex-snapshot
Ten ring-B aromatized ergosterols from Aspergillus spectabilis
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Constructing a Myxobacterial Natural Product Database to Facilitate NMR-Based Metabolomics Bioprospecting of Myxobacteria
inferred← citeshttps://doi.org/10.1021/acs.jafc.0c04460openalex-snapshot
Lanostane Triterpenoids with PTP1B Inhibitory and Glucose-Uptake Stimulatory Activities from Mushroom Fomitopsis pinicola Collected in North America
inferred← citeshttps://doi.org/10.1021/acs.jafc.5c09424openalex-snapshot
Tricholoma and Lanostane Triterpenoids from Tricholoma terreum and Their Anti-Inflammatory Assessment
inferred← citeshttps://doi.org/10.1021/acs.jafc.9b04530openalex-snapshot
C30 and C31 Triterpenoids and Triterpene Sugar Esters with Cytotoxic Activities from Edible Mushroom Fomitopsis pinicola (Sw. Ex Fr.) Krast
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Trichothecrotocins D–L, Antifungal Agents from a Potato-Associated Trichothecium crotocinigenum
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.2c01169openalex-snapshot
Aromatic Polyketides from the Mangrove-Derived Streptomyces sp. SCSIO 40069
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.5c00452openalex-snapshot
Cordycepsterols A–C, Anti-Inflammatory C30 Ergosterols with a 6/6/6/5/6-Fused Ring System from Cordyceps militaris
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.6c00334openalex-snapshot
Discovery of Rearranged Steroids from Cultures of Penicillium soli as Inhibitors of Idiopathic Pulmonary Fibrosis
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.7b00845openalex-snapshot
Irpeksins A–E, 1,10-seco-Eburicane-Type Triterpenoids from the Medicinal Fungus Irpex lacteus and Their Anti-NO Activity
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.8b00460openalex-snapshot
Tricholopardins A and B, Anti-inflammatory Terpenoids from the Fruiting Bodies of Tricholoma pardinum
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.9b00913openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/acs.joc.0c02049openalex-snapshot
Asperfloketals A and B, the First Two Ergostanes with Rearranged A and D Rings: From the Sponge-Associated Aspergillus flocculosus 16D-1
inferred← citeshttps://doi.org/10.1021/acs.joc.0c02742openalex-snapshot
Uncommon Diterpenoids from the South China Sea Soft Coral Sinularia humilis and Their Stereochemistry
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inferred← citeshttps://doi.org/10.1021/acs.joc.8b01420openalex-snapshot
Heterocyclic Compounds from the Mushroom Albatrellus confluens and Their Inhibitions against Lipopolysaccharides-Induced B Lymphocyte Cell Proliferation
inferred← citeshttps://doi.org/10.1021/acs.joc.8b02679openalex-snapshot
Asperflotone, an 8(14→15)-abeo-Ergostane from the Sponge-Derived Fungus Aspergillus flocculosus 16D-1
inferred← citeshttps://doi.org/10.1021/acs.orglett.1c03863openalex-snapshot
Aspersteroids A–C, Three Rearranged Ergostane-type Steroids from Aspergillus ustus NRRL 275
inferred← citeshttps://doi.org/10.1021/acs.orglett.6c00338openalex-snapshot
Pullenvasterols A–G: Rare 2β-Hydroxyanthrasteroids from the Australian Soil-Derived Fungi, Clonostachys rosea and Coccidioides sp.
inferred← citeshttps://doi.org/10.1021/acs.orglett.8b03530openalex-snapshot
Aspersecosteroids A and B, Two 11(9 → 10)-abeo-5,10-Secosteroids with a Dioxatetraheterocyclic Ring System from Aspergillus flocculosus 16D-1
inferred← citeshttps://doi.org/10.1021/acs.orglett.8b03735openalex-snapshot
Trichothecrotocins A–C, Antiphytopathogenic Agents from Potato Endophytic Fungus Trichothecium crotocinigenum
inferred← citeshttps://doi.org/10.1021/acsomega.1c04418openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/acsomega.3c03749openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/jacs.8b13356openalex-snapshot
Translation of a Polar Biogenesis Proposal into a Radical Synthetic Approach: Synthesis of Pleurocin A/Matsutakone and Pleurocin B
inferred← citeshttps://doi.org/10.1039/c8ob02325eopenalex-snapshot
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inferred← citeshttps://doi.org/10.1039/c8ra04226hopenalex-snapshot
Albatredines A and B, a pair of epimers with unusual natural heterocyclic skeletons from edible mushroom Albatrellus confluens
inferred← citeshttps://doi.org/10.1039/c8ra06544fopenalex-snapshot
Polyellisin, a novel polyketide from cultures of the basidiomycete Polyporus ellisii
inferred← citeshttps://doi.org/10.1039/c9qo01087dopenalex-snapshot
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inferred← citeshttps://doi.org/10.1039/d0qo00605jopenalex-snapshot
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inferred← citeshttps://doi.org/10.1039/d1ob00448dopenalex-snapshot
Contemporary advancements in the semi-synthesis of bioactive terpenoids and steroids
inferred← citeshttps://doi.org/10.1039/d3cc01009kopenalex-snapshot
Biogenetic space-guided synthesis of rearranged terpenoids
inferred← citeshttps://doi.org/10.1039/d3np00066dopenalex-snapshot
Controllable skeletal reorganizations in natural product synthesis
inferred← citeshttps://doi.org/10.1055/s-0037-1611576openalex-snapshot
Contemporary Synthetic Strategies towards Secosteroids, abeo-Steroids, and Related Triterpenes
inferred← citeshttps://doi.org/10.1080/10286020.2018.1521804openalex-snapshot
Survey of natural products reported by Asian research groups in 2017
inferred← citeshttps://doi.org/10.1080/10286020.2019.1668377openalex-snapshot
Two new compounds from cultures of the basidiomycete Daedaleopsis tricolor
inferred← citeshttps://doi.org/10.1080/10286020.2023.2279539openalex-snapshot
Two highly conjugated ergosterols from the fungus Psathyrella rogueiana and their anti-inflammatory activity
inferred← citeshttps://doi.org/10.1080/10286020.2024.2340691openalex-snapshot
Ganonorsterone A, a norsteroid from the medicinal fungus Ganoderma lingzhi
inferred← citeshttps://doi.org/10.1080/10408398.2021.2023857openalex-snapshot
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inferred← citeshttps://doi.org/10.1080/14786419.2019.1624963openalex-snapshot
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inferred← citeshttps://doi.org/10.1111/ijfs.17121openalex-snapshot
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inferred← citeshttps://doi.org/10.1177/1934578x1801300926openalex-snapshot
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inferred← citeshttps://doi.org/10.1177/1934578x19850958openalex-snapshot
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inferred← citeshttps://doi.org/10.1248/cpb.c24-00126openalex-snapshot
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inferred← citeshttps://doi.org/10.1360/ssc-2025-0067openalex-snapshot
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inferred← citeshttps://doi.org/10.3390/microbiolres17010015openalex-snapshot
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inferred← citeshttps://doi.org/10.3390/microorganisms8071049openalex-snapshot
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inferred← citeshttps://doi.org/10.3390/molecules22101675openalex-snapshot
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inferred← citeshttps://doi.org/10.3390/molecules23051198openalex-snapshot
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inferred← citeshttps://doi.org/10.3390/molecules27072103openalex-snapshot
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inferred← citeshttps://doi.org/10.3390/molecules29194719openalex-snapshot
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inferred← citeshttps://doi.org/10.3390/nu15122758openalex-snapshot
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inferred← citeshttps://doi.org/10.6023/cjoc202506022openalex-snapshot
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