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

https://doi.org/10.1021/acs.joc.8b01906
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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/cbdv.201700567openalex-snapshot
Triterpenes and Meroterpenes with Neuroprotective Effects from Ganoderma leucocontextum
inferredcites →https://doi.org/10.1002/hlca.19820650221openalex-snapshot
Structures of Ganoderic Acid A and B, Two New Lanostane Type Bitter Triterpenes from Ganoderma lucidum (FR.) K ARST .
inferredcites →https://doi.org/10.1007/s10637-017-0526-0openalex-snapshot
Ganoderic acid, lanostanoid triterpene: a key player in apoptosis
inferredcites →https://doi.org/10.1016/0009-2614(96)00349-1openalex-snapshot
Ab initio study of solvated molecules: a new implementation of the polarizable continuum model
inferredcites →https://doi.org/10.1016/0301-0104(82)85072-6openalex-snapshot
Approximate evaluations of the electrostatic free energy and internal energy changes in solution processes
inferredcites →https://doi.org/10.1016/0301-0104(84)85133-2openalex-snapshot
Proton and carbon-13 chemical shifts: Comparison between theory and experiment
inferredcites →https://doi.org/10.1016/j.fitote.2014.05.019openalex-snapshot
Cytotoxic 9,19-cycloartane triterpenes from the aerial parts of Cimicifuga yunnanensis
inferredcites →https://doi.org/10.1016/j.fitote.2018.08.009openalex-snapshot
Eight new triterpenoids with inhibitory activity against HMG-CoA reductase from the medical mushroom Ganoderma leucocontextum collected in Tibetan plateau
inferredcites →https://doi.org/10.1016/j.phytochem.2012.11.022openalex-snapshot
Lanostane triterpenes from cultures of the Basidiomycete Ganoderma orbiforme BCC 22324
inferredcites →https://doi.org/10.1016/j.phytochem.2015.02.017openalex-snapshot
Anti-diabetic effects of Ganoderma lucidum
inferredcites →https://doi.org/10.1016/j.phytochem.2015.03.010openalex-snapshot
Secondary metabolites from Ganoderma
inferredcites →https://doi.org/10.1016/j.phytochem.2017.07.015openalex-snapshot
Lanostane-type triterpenoids from the fruiting body of Ganoderma calidophilum
inferredcites →https://doi.org/10.1016/j.phytol.2016.07.024openalex-snapshot
New cytotoxic lanostanoid triterpenes from Ganoderma lingzhi
inferredcites →https://doi.org/10.1016/j.tetlet.2004.02.056openalex-snapshot
Two novel 3,4-seco-trinorlanostane triterpenoids isolated from Ganoderma fornicatum
inferredcites →https://doi.org/10.1021/acs.jafc.5b05931openalex-snapshot
Anti-inflammatory Cerebrosides from Cultivated Cordyceps militaris
inferredcites →https://doi.org/10.1021/acs.jnatprod.7b00166openalex-snapshot
Inhibition Potential of Cycloartane-Type Glycosides from the Roots ofCimicifuga dahuricaagainst Soluble Epoxide Hydrolase
inferredcites →https://doi.org/10.1021/ja00179a005openalex-snapshot
Efficient implementation of the gauge-independent atomic orbital method for NMR chemical shift calculations
inferredcites →https://doi.org/10.1021/ja011785ropenalex-snapshot
Computational Analysis of the Potential Energy Surfaces of Glycerol in the Gas and Aqueous Phases: Effects of Level of Theory, Basis Set, and Solvation on Strongly Intramolecularly Hydrogen-Bonded Systems
inferredcites →https://doi.org/10.1021/np400323uopenalex-snapshot
Hepatoprotective Effects of Triterpenoids from Ganoderma cochlear
inferredcites →https://doi.org/10.1021/np400846kopenalex-snapshot
Triterpene Lactones from Cultures of Ganoderma sp. KM01
inferredcites →https://doi.org/10.1021/np500249vopenalex-snapshot
Cycloartane Triterpenoids and Their Glycosides from the Rhizomes of Cimicifuga foetida
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/10.1039/c5ra16796eopenalex-snapshot
Ganocochlearic acid A, a rearranged hexanorlanostane triterpenoid, and cytotoxic triterpenoids from the fruiting bodies of Ganoderma cochlear
inferredcites →https://doi.org/10.1063/1.440864openalex-snapshot
Statistical analysis of polyatomic quantum beats using the properties of random matrices
inferredcites →https://doi.org/10.1080/00268977400100711openalex-snapshot
Self-consistent perturbation theory of diamagnetism
inferredcites →https://doi.org/10.1080/01635581.2011.601845openalex-snapshot
Ganoderma lucidum (Reishi) Inhibits Cancer Cell Growth and Expression of Key Molecules in Inflammatory Breast Cancer

What points at this work

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

inferred← citeshttps://doi.org/10.2139/ssrn.4010863openalex-extracted
Highly Oxygenated Chemical Constitutes and Rearranged Derivate with Neurotrophic Activity from Ganoderma Cochlear
inferred← citeshttps://doi.org/10.2139/ssrn.4868939openalex-extracted
inferred← citeshttps://doi.org/10.1002/cjoc.202200318openalex-snapshot
Applanoids A—E as the First Examples of C‐15/C‐20 Michael Adducts in Ganoderma Triterpenoids and Their PXR Agonistic Activity
inferred← citeshttps://doi.org/10.1002/cjoc.202300275openalex-snapshot
Natural Sesquiterpenoids, Diterpenoids, Sesterterpenoids, and Triterpenoids with Intriguing Structures from 2017 to 2022
inferred← citeshttps://doi.org/10.1016/j.bioorg.2023.106375openalex-snapshot
Ganoapplins A and B with an unprecedented 6/6/6/5/6-fused pentacyclic skeleton from Ganoderma inhibit Tau pathology through activating autophagy
inferred← citeshttps://doi.org/10.1016/j.bioorg.2025.108497openalex-snapshot
Highly oxygenated lanostane triterpenoids from Ganoderma applanatum and their anti-liver fibrosis effects
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.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.2019.112109openalex-snapshot
C28 steroids from the fruiting bodies of Ganoderma resinaceum with potential anti-inflammatory activity
inferred← citeshttps://doi.org/10.1016/j.phytochem.2024.114201openalex-snapshot
Daldiconoids A-G: 3,4-Secolanostane triterpenoids from the fruiting bodies of Daldinia concentrica and their anti-inflammatory activity
inferred← citeshttps://doi.org/10.1016/j.tet.2024.134240openalex-snapshot
Anti-inflammatory 3,4-seco-triterpenoids from Ganoderma cochlear
inferred← citeshttps://doi.org/10.1021/acs.joc.8b02764openalex-snapshot
Irpexolidal Represents a Class of Triterpenoid from the Fruiting Bodies of the Medicinal Fungus Irpex lacteus
inferred← citeshttps://doi.org/10.1039/c8np90046aopenalex-snapshot
Hot off the press
inferred← citeshttps://doi.org/10.1039/d3qo02000bopenalex-snapshot
Novel A- seco -nortriterpenoids from Ganoderma cochlear inhibiting Tau pathology by activating AMPK-ULK1-mediated autophagy
inferred← citeshttps://doi.org/10.1080/10286020.2019.1684474openalex-snapshot
Survey of natural products reported by Asian research groups in 2018
inferred← citeshttps://doi.org/10.3390/biomedicines12051021openalex-snapshot
Naturally Occurring Norsteroids and Their Design and Pharmaceutical Application
inferred← citeshttps://doi.org/10.3390/md19060324openalex-snapshot
Antitumor Profile of Carbon-Bridged Steroids (CBS) and Triterpenoids
inferred← citeshttps://doi.org/10.3390/molecules31152705openalex-snapshot
Ganoderic Acid A Reverses Ultraviolet B Induced Hyperpigmentation via Multi-Targeted Regulation of Mitochondrial Homeostasis and Inflammation
inferred← citeshttps://doi.org/10.3762/bjoc.22.21openalex-snapshot
Ring contraction and ring expansion reactions in terpenoid biosynthesis and their application to total synthesis
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