On the public citation graph
(+/−)-Lucidumone, a COX-2 Inhibitory Caged Fungal Meroterpenoid from Ganoderma lucidum
0 signed · 77 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known work and none has been retracted — and get a dated CiteStamped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/10.1002/anie.201814581openalex-snapshot
Lugdunomycin, an Angucycline‐Derived Molecule with Unprecedented Chemical Architecture
inferredcites →https://doi.org/10.1016/j.ejmech.2016.11.015openalex-snapshot
A novel class of α-glucosidase and HMG-CoA reductase inhibitors from Ganoderma leucocontextum and the anti-diabetic properties of ganomycin I in KK-A y mice
inferredcites →https://doi.org/10.1021/acs.orglett.5b00448openalex-snapshot
(±)-Sinensilactam A, a Pair of Rare Hybrid Metabolites with Smad3 Phosphorylation Inhibition from Ganoderma sinensis
inferredcites →https://doi.org/10.1021/acs.orglett.5b01353openalex-snapshot
Two New Classes of T-Type Calcium Channel Inhibitors with New Chemical Scaffolds from Ganoderma cochlear
inferredcites →https://doi.org/10.1021/acs.orglett.6b00542openalex-snapshot
An approach to (±)-Lingzhiol
inferredcites →https://doi.org/10.1021/acs.orglett.8b00380openalex-snapshot
Total Synthesis of Sinensilactam A
inferredcites →https://doi.org/10.1021/acs.orglett.8b01608openalex-snapshot
Mangelonoids A and B, Two Pairs of Macrocyclic Diterpenoid Enantiomers from Croton mangelong
inferredcites →https://doi.org/10.1021/acs.orglett.8b04123openalex-snapshot
(+)- and (−)-Preuisolactone A: A Pair of Caged Norsesquiterpenoidal Enantiomers with a Tricyclo[4.4.01,6.02,8]decane Carbon Skeleton from the Endophytic Fungus Preussia isomera
inferredcites →https://doi.org/10.1021/acs.orglett.9b00108openalex-snapshot
Isolation, Structure Elucidation, and Total Synthesis of Myrtuspirone A from Myrtus communis
inferredcites →https://doi.org/10.1021/acs.orglett.9b00312openalex-snapshot
(±)-Xylaridines A and B, Highly Conjugated Alkaloids from the Fungus Xylaria longipes
inferredcites →https://doi.org/10.1021/acs.orglett.9b01440openalex-snapshot
Meroindenon and Merochlorins E and F, Antibacterial Meroterpenoids from a Marine-Derived Sediment Bacterium of the Genus Streptomyces
inferredcites →https://doi.org/10.1021/acs.orglett.9b01901openalex-snapshot
Total Synthesis of Applanatumol B
inferredcites →https://doi.org/10.1021/ja305665fopenalex-snapshot
Merochlorins A–D, Cyclic Meroterpenoid Antibiotics Biosynthesized in Divergent Pathways with Vanadium-Dependent Chloroperoxidases
inferredcites →https://doi.org/10.1021/ol4026364openalex-snapshot
Lingzhiols, Unprecedented Rotary Door-Shaped Meroterpenoids as Potent and Selective Inhibitors of p-Smad3 from Ganoderma lucidum
inferredcites →https://doi.org/10.1038/ncomms13083openalex-snapshot
Non-enzymatic pyridine ring formation in the biosynthesis of the rubrolone tropolone alkaloids
inferredcites →https://doi.org/10.1038/ncomms6707openalex-snapshot
Asymmetric total synthesis of (−)-lingzhiol via a Rh-catalysed [3+2] cycloaddition
inferredcites →https://doi.org/10.1038/nrd.2016.39openalex-snapshot
Resolution of inflammation: a new therapeutic frontier
inferredcites →https://doi.org/10.1038/nrd.2018.97openalex-snapshot
Targeting the NLRP3 inflammasome in inflammatory diseases
inferredcites →https://doi.org/10.1039/c5np00090dopenalex-snapshot
Biosynthesis of fungal meroterpenoids
inferredcites →https://doi.org/10.1039/c8ob00615fopenalex-snapshot
A concise total synthesis of cochlearoid B
inferredcites →https://doi.org/10.1074/jbc.m116.725713openalex-snapshot
Substrate-selective Inhibition of Cyclooxygeanse-2 by Fenamic Acid Derivatives Is Dependent on Peroxide Tone
inferredcites →https://doi.org/10.1136/bmj.329.7471.867openalex-snapshot
Lessons from the withdrawal of rofecoxib: ***
inferredcites →https://doi.org/10.1194/jlr.r800042-jlr200openalex-snapshot
Cyclooxygenases: structural and functional insights
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.2021.112970zenodo-depositor-declared
Chemical constituents from the flowers of Hypericum monogynum L. with COX-2 inhibitory activity
inferred← citeshttps://doi.org/10.1002/ajoc.202300633openalex-snapshot
Total Synthesis of Ganoderma Meroterpenoids – Progresses since 2014
inferred← citeshttps://doi.org/10.1002/ajoc.202500116openalex-snapshot
Recent Developments in Prins Cyclization Toward the Synthesis of Spirocyclic Scaffolds
inferred← citeshttps://doi.org/10.1002/ange.202304132openalex-snapshot
Total Synthesis of Lucidumone through Convenient One‐pot Preparation of the Tetracyclic Skeleton by Claisen Rearrangement and Subsequent Intramolecular Aldol Reaction
inferred← citeshttps://doi.org/10.1002/anie.202304132openalex-snapshot
Total Synthesis of Lucidumone through Convenient One‐pot Preparation of the Tetracyclic Skeleton by Claisen Rearrangement and Subsequent Intramolecular Aldol Reaction
inferred← citeshttps://doi.org/10.1002/cjoc.202300231openalex-snapshot
Meroterpenoids Possessing Diverse Rearranged Skeletons with Anti‐inflammatory Activity from the Mangrove‐Derived Fungus Penicillium sp. HLLG ‐122
inferred← citeshttps://doi.org/10.1002/ejoc.70395openalex-snapshot
Recent Approaches for the Synthesis of Lucidumone
inferred← citeshttps://doi.org/10.1002/med.22006openalex-snapshot
Insights into Ganoderma fungi meroterpenoids opening a new era of racemic natural products in mushrooms
inferred← citeshttps://doi.org/10.1007/978-3-032-09901-3_1openalex-snapshot
The Diels–Alder Reaction as a Key Step in Natural Product Synthesis
inferred← citeshttps://doi.org/10.1007/978-981-99-5696-8_13openalex-snapshot
Fungal Enzyme Inhibitors: Potent Repository of Lead Compounds to Curb Cancer
inferred← citeshttps://doi.org/10.1016/j.bioorg.2021.104774openalex-snapshot
Lucidumones B-H, racemic meroterpenoids that inhibit tumor cell migration from Ganoderma lucidum
inferred← citeshttps://doi.org/10.1016/j.chmed.2025.03.003openalex-snapshot
From natural laboratory to drug discovery: Chemical structures, bioactivities, and biosynthesis of meroterpenoids from Ganoderma species
inferred← citeshttps://doi.org/10.1016/j.ejmech.2020.112860openalex-snapshot
Meroterpenoids produced by fungi: Occurrence, structural diversity, biological activities, and their molecular targets
inferred← citeshttps://doi.org/10.1016/j.fitote.2022.105390openalex-snapshot
COX-2 and iNOS inhibitory epimeric meroterpenoids from Ganoderma cochlear and structure revision of cochlearol Q
inferred← citeshttps://doi.org/10.1016/j.phytol.2025.104072openalex-snapshot
New 6/6/6/6 tetracyclic Rhododendron chromane meroterpenoids from flowers of Rhododendron rubiginosum Franch. var. rubiginosum with COX-2 inhibitory activity
inferred← citeshttps://doi.org/10.1016/j.tet.2025.135101openalex-snapshot
Diels-Alder reaction: A versatile synthetic tool for the synthesis of terpenoids and alkaloids: A review
inferred← citeshttps://doi.org/10.1016/j.tetlet.2020.152715openalex-snapshot
(±)-Pabmaragramin, a scalemic meroterpenoid produced by Marasmius graminum via precursor-assisted biosynthesis
inferred← citeshttps://doi.org/10.1021/acs.joc.0c00842openalex-snapshot
Meroapplanins A–E: Five Meroterpenoids with a 2,3,4,5-Tetrahydropyridine Motif from Ganoderma applanatum
inferred← citeshttps://doi.org/10.1021/acs.orglett.0c00452openalex-snapshot
Ganoderma cochlear Metabolites as Probes to Identify a COX-2 Active Site and as in Vitro and in Vivo Anti-Inflammatory Agents
inferred← citeshttps://doi.org/10.1021/acs.orglett.2c02023openalex-snapshot
Construction of the Skeleton of Lucidumone
inferred← citeshttps://doi.org/10.1021/acs.orglett.4c00411openalex-snapshot
Asymmetric Total Synthesis of (+)-Chuanxiongnolide L1 via a Stereoselective Oxidative Dearomatization/Diels–Alder Strategy
inferred← citeshttps://doi.org/10.1021/acs.orglett.5c03142openalex-snapshot
Chizhiaroterpenoids A–C: Benzofused Rearranged Lanostane-Type Triterpenoids from Ganoderma lucidum
inferred← citeshttps://doi.org/10.1021/acs.orglett.5c03633openalex-snapshot
Enantioselective Total Synthesis of (+)-Lucidumone via Organocatalytic Double Michael Addition
inferred← citeshttps://doi.org/10.1021/acs.orglett.9b04666openalex-snapshot
Revision of the Structure of Hypatulone A by NMR, Computations, and Biosynthetic Considerations
inferred← citeshttps://doi.org/10.1021/jacs.0c06179openalex-snapshot
Catalytic Hydroxycyclopropanol Ring-Opening Carbonylative Lactonization to Fused Bicyclic Lactones
inferred← citeshttps://doi.org/10.1021/jacs.0c06306openalex-snapshot
Bisketene Equivalents as Diels–Alder Dienes
inferred← citeshttps://doi.org/10.1021/jacs.2c08760openalex-snapshot
Gram-Scale Enantioselective Synthesis of (+)-Lucidumone
inferred← citeshttps://doi.org/10.1038/s41467-024-46896-3openalex-snapshot
Enantioselective total synthesis of (‒)-lucidumone enabled by tandem prins cyclization/cycloetherification sequence
inferred← citeshttps://doi.org/10.1038/s41467-024-54117-0openalex-snapshot
Photoinduced formal [4 + 2] cycloaddition of two electron-deficient olefins and its application to the synthesis of lucidumone
inferred← citeshttps://doi.org/10.1039/d0ob02162hopenalex-snapshot
The chemistry and biology of fungal meroterpenoids (2009–2019)
inferred← citeshttps://doi.org/10.1039/d0ra05532hopenalex-snapshot
Fused multicyclic polyketides with a two-spiro-carbon skeleton from mangrove-derived endophytic fungus Epicoccum nigrum SCNU-F0002
inferred← citeshttps://doi.org/10.1039/d1qo00294eopenalex-snapshot
Applanmerotic acids A and B, two meroterpenoid dimers with an unprecedented polycyclic skeleton from Ganoderma applanatum that inhibit formyl peptide receptor 2
inferred← citeshttps://doi.org/10.1039/d3np00006kopenalex-snapshot
Structural diversity, hypothetical biosynthesis, chemical synthesis, and biological activity of Ganoderma meroterpenoids
inferred← citeshttps://doi.org/10.1039/d4sc06010eopenalex-snapshot
Biosynthesis of a bacterial meroterpenoid reveals a non-canonical class II meroterpenoid cyclase
inferred← citeshttps://doi.org/10.1039/d5ra09257dopenalex-snapshot
Total synthesis of natural products facilitated by prins reaction: a review
inferred← citeshttps://doi.org/10.1055/s-0042-1751412openalex-snapshot
Retro-[4+2]/Intramolecular Diels–Alder Cascade Allows a Concise Total Synthesis of Lucidumone
inferred← citeshttps://doi.org/10.1055/s-0042-1751529openalex-snapshot
Total Synthesis of Lucidumone: Attempted Shortcuts, Dead Ends and Lessons Learnt
inferred← citeshttps://doi.org/10.1080/10286020.2020.1844675openalex-snapshot
Survey of natural products reported by Asian research groups in 2019
inferred← citeshttps://doi.org/10.1142/s0192415x23500878openalex-snapshot
A Comprehensive Review on the Chemical Composition, Pharmacology and Clinical Applications of Ganoderma
inferred← citeshttps://doi.org/10.3389/fchem.2021.772740openalex-snapshot
Meroterpenoids From Ganoderma lucidum Mushrooms and Their Biological Roles in Insulin Resistance and Triple-Negative Breast Cancer
inferred← citeshttps://doi.org/10.3390/molecules27041279openalex-snapshot
Natural Enantiomers: Occurrence, Biogenesis and Biological Properties
inferred← citeshttps://doi.org/10.3390/molecules27072346openalex-snapshot
Computational Analysis and Biological Activities of Oxyresveratrol Analogues, the Putative Cyclooxygenase-2 Inhibitors
inferred← citeshttps://doi.org/10.3390/molecules28124668openalex-snapshot
Design, Synthesis, and Evaluation of the COX-2 Inhibitory Activities of New 1,3-Dihydro-2H-indolin-2-one Derivatives
inferred← citeshttps://doi.org/10.3390/ph15121520openalex-snapshot
Ganoaustralins A and B, Unusual Aromatic Triterpenes from the Mushroom Ganoderma australe
inferred← citeshttps://doi.org/10.3724/abbs.2026162openalex-snapshot
Wogonin combined with cinnamaldehyde synergistically induces ferroptosis by increasing PTGS2 in breast cancer
inferred← citeshttps://doi.org/10.5059/yukigoseikyokaishi.82.348openalex-snapshot
Collective Synthesis of Meroterpenoids Derived from Ganoderma Family
inferred← citeshttps://doi.org/10.59761/rcr5237openalex-snapshot
Stereoselective reactions of nitro compounds in the synthesis of natural compound analogs and active pharmaceutical ingredients: recent advances
inferred← citeshttps://doi.org/10.6023/a25040131openalex-snapshot
Total Synthesis of Complex Natural Products Via Radical-Mediated Formal Diels-Alder Reaction
inferred← citeshttps://doi.org/10.6023/cjoc202409039openalex-snapshot
Advances in the Total Synthesis of Ganoderma Meroterpenoids
inferred← citeshttps://doi.org/10.6023/cjoc202509001openalex-snapshot
Study on Dearomatization [4＋2] Reactions of Allene Substrates
inferred← citeshttps://doi.org/10.70675/7a39ae48z55f0z4d97z82c6z274c76ec1d02openalex-snapshot
Asymmetric inverse-electron-demand Diels-Alder cycloaddition between 2-pyrones and acyclic enol ethers : gram-scale total synthesis of (+)-lucidumone
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.