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Hepatoprotective Effects of Triterpenoids from Ganoderma cochlear

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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1007/s13659-011-0026-4openalex-snapshot

New alkaloids from the fruiting bodies of Ganoderma sinense

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Structure determination of inonotsuoxides A and B and in vivo anti-tumor promoting activity of inotodiol from the sclerotia of Inonotus obliquus

inferredcites →https://doi.org/10.1016/j.ejmech.2008.01.037openalex-snapshot

Lanostane-type triterpenoids from the sclerotia of Inonotus obliquus possessing anti-tumor promoting activity

inferredcites →https://doi.org/10.1016/j.phytochem.2006.07.004openalex-snapshot

Ganoderma – A therapeutic fungal biofactory

inferredcites →https://doi.org/10.1016/j.tetlet.2004.02.056openalex-snapshot

Two novel 3,4-seco-trinorlanostane triterpenoids isolated from Ganoderma fornicatum

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Triterpenoid Content of Berries and Leaves of Bilberry Vaccinium myrtillus from Finland and Poland

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Colossolactones, New Triterpenoid Metabolites from a Vietnamese Mushroom Ganoderma colossum

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Cytotoxicity of Ganoderma lucidum Triterpenes

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Chemical Constituents of the Ascomycete Daldinia concentrica

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Antiviral Terpenoid Constituents of Ganoderma pfeifferi

inferredcites →https://doi.org/10.1021/np100031copenalex-snapshot

Antiplasmodial Lanostanes from the Ganoderma lucidum Mushroom

inferredcites →https://doi.org/10.1021/np50102a021openalex-snapshot

The Absolute Stereochemistry of Senexdiolic Acid at C-22

inferredcites →https://doi.org/10.1021/np8001139openalex-snapshot

Anti-HIV-1 Protease Activity of Lanostane Triterpenes from the Vietnamese Mushroom Ganoderma colossum

inferredcites →https://doi.org/10.1021/ol100062bopenalex-snapshot

Three New Triterpenoids Containing Four-Membered Ring from the Fruiting Body of Ganoderma sinense

inferredcites →https://doi.org/10.1055/s-0031-1280441openalex-snapshot

Isolation and Bioactivity Evaluation of Terpenoids from the Medicinal FungusGanoderma sinense

What points at this work

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

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Highly Oxygenated Chemical Constitutes and Rearranged Derivate with Neurotrophic Activity from Ganoderma Cochlear

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Secondary Metabolites from Higher Fungi

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Recent Advance on Bioactive Compounds from the Edible and Medicinal Fungi in China

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Preventive and Therapeutic Effect of Ganoderma (Lingzhi) on Brain Injury

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Fungal Biomolecules as Nutraceuticals

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Chemical constituents from Inonotus obliquus and their antitumor activities

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Ganoderma boninense mycelia for phytochemicals and secondary metabolites with antibacterial activity

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Biophysical characterization of antibacterial compounds derived from pathogenic fungi Ganoderma boninense

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Historical and current perspectives on therapeutic potential of higher basidiomycetes: an overview

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Structural Diversity, Natural Sources and Pharmacological Potential of Naturally Occurring A-Seco-Triterpenoids

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Steroids from Ganoderma sinense as new natural inhibitors of cancer-associated mutant IDH1

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Triterpenoids and meroterpenoids with α-glucosidase inhibitory activities from the fruiting bodies of Ganoderma australe

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Highly oxygenated lanostane triterpenoids from Ganoderma applanatum and their anti-liver fibrosis effects

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Biological and chemical diversity go hand in hand: Basidiomycota as source of new pharmaceuticals and agrochemicals

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Two pairs of farnesyl phenolic enantiomers as natural nitric oxide inhibitors from Ganoderma sinense

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The triterpenes and steroids from the fruiting body Ganoderma duripora

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Two pairs of alkaloid enantiomers from Ganoderma luteomarginatum

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Hepatoprotective natural triterpenoids

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A review of pentacyclic triterpenoids derived from macrofungi and their biological activities

inferred← citeshttps://doi.org/10.1016/j.fitote.2018.01.001openalex-snapshot

New natural inhibitors of hexokinase 2 (HK2): Steroids from Ganoderma sinense

inferred← citeshttps://doi.org/10.1016/j.fitote.2018.06.023openalex-snapshot

Triterpene saponins with neuroprotective effects from the leaves of Diospyros kaki Thunb

inferred← citeshttps://doi.org/10.1016/j.fitote.2020.104733openalex-snapshot

Tropolone derivatives with hepatoprotective and antiproliferative activities from the aerial parts of Chenopodium album Linn

inferred← citeshttps://doi.org/10.1016/j.fitote.2025.106543openalex-snapshot

Triterpenoids from Ganoderma cochlear against inflammation and renal fibrosis

inferred← citeshttps://doi.org/10.1016/j.fitote.2025.106585openalex-snapshot

Triterpenoids with inhibitory effects on lipid accumulation from Ganoderma lucidum

inferred← citeshttps://doi.org/10.1016/j.foodchem.2018.07.115openalex-snapshot

Hepatoprotective activity of Ganoderma lucidum triterpenoids in alcohol-induced liver injury in mice, an iTRAQ-based proteomic analysis

inferred← citeshttps://doi.org/10.1016/j.jep.2019.112218openalex-snapshot

Identification of novel phytocannabinoids from Ganoderma by label-free dynamic mass redistribution assay

inferred← citeshttps://doi.org/10.1016/j.jep.2022.115393openalex-snapshot

Highly oxygenated chemical constitutes and rearranged derivatives with neurotrophic activity from Ganoderma cochlear

inferred← citeshttps://doi.org/10.1016/j.molstruc.2025.144558openalex-snapshot

Lanostane triterpenoids from medicinal fungi Ganoderma cochlear and their antiatherosclerotic activity

inferred← citeshttps://doi.org/10.1016/j.phytochem.2015.03.010openalex-snapshot

Secondary metabolites from Ganoderma

inferred← citeshttps://doi.org/10.1016/j.phytochem.2018.01.007openalex-snapshot

Lanostane triterpenes from the mushroom Ganoderma resinaceum and their inhibitory activities against α-glucosidase

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Lanostane triterpenoids from Ganoderma luteomarginatum and their cytotoxicity against four human cancer cell lines

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Lanostane triterpenoids with anti-inflammatory activities from Ganoderma lucidum

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Cardioprotective 22-hydroxylanostane triterpenoids from the fruiting bodies of Phellinus igniarius

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New sesquiterpenoid derivatives from Ganoderma sinense with nitric oxide inhibitory activity

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inferred← citeshttps://doi.org/10.1016/j.tet.2024.134240openalex-snapshot

Anti-inflammatory 3,4-seco-triterpenoids from Ganoderma cochlear

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Phosteoid A, a highly oxygenated norsteroid from the deep-sea-derived fungus Phomopsis tersa FS441

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Semisynthesis of 22,25-Epoxylanostane Triterpenoids: Structure Revision and Protective Effects against Oxygen-Glucose Deprivation/Reoxygenation Injury in H9c2 Cells

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Lanostane Triterpenes from the Tibetan Medicinal Mushroom Ganoderma leucocontextum and Their Inhibitory Effects on HMG-CoA Reductase and α-Glucosidase

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Diastereoselective Formal Synthesis of Polycyclic Meroterpenoid (±)-Cochlearol A

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Ganolearic Acid A, a Hexanorlanostane Triterpenoid with a 3/5/6/5-Fused Tetracyclic Skeleton from Ganoderma cochlear

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Astracondensatol D: A 6/6/5/6 Cycloartane Triterpenoid from Astragalus condensatus

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Lupane Triterpenes with Antileukemia Activity from Maytenus quadrangulata

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Four New Polycyclic Meroterpenoids from Ganoderma cochlear

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Cochlearols A and B, Polycyclic Meroterpenoids from the Fungus Ganoderma cochlear That Have Renoprotective Activities

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Biosynthesis of mushroom-derived type II ganoderic acids by engineered yeast

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Ganocochlearic acid A, a rearranged hexanorlanostane triterpenoid, and cytotoxic triterpenoids from the fruiting bodies of Ganoderma cochlear

inferred← citeshttps://doi.org/10.1039/c8np00029hopenalex-snapshot

Triterpenoids

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Rearranged lanostane-type triterpenoids with anti-hepatic fibrosis activities from Ganoderma applanatum

inferred← citeshttps://doi.org/10.1039/d0ra07219bopenalex-snapshot

Traditional uses, chemical components and pharmacological activities of the genus Ganoderma P. Karst.: a review

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Novel A- seco -nortriterpenoids from Ganoderma cochlear inhibiting Tau pathology by activating AMPK-ULK1-mediated autophagy

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A new lanostane triterpenoid from Ganoderma resinaceum

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Polysaccharide-Rich Fractions from Ganoderma resinaceum (Ganodermataceae) as Chemopreventive Agents in N-Diethylnitrosamine-Induced Hepatocellular Carcinoma in Wistar Rats

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Farnesyl phenolic enantiomers as natural MTH1 inhibitors from Ganoderma sinense

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