On the public citation graph
Meroterpenoids from the Fungus Ganoderma sinensis and First Absolute Configuration Clarification of Zizhine H
0 signed · 39 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known work and none has been retracted — and get a dated CiteStamped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/pst.426openalex-snapshot
Guidelines for accurate EC50/IC50 estimation
inferredcites →https://doi.org/10.1007/s13659-011-0026-4openalex-snapshot
New alkaloids from the fruiting bodies of Ganoderma sinense
inferredcites →https://doi.org/10.1007/s13659-018-0164-zopenalex-snapshot
Meroterpenoids from Ganoderma Species: A Review of Last Five Years
inferredcites →https://doi.org/10.1016/j.bmcl.2018.12.011openalex-snapshot
Ganocapenoids A–D: Four new aromatic meroterpenoids from Ganoderma capense
inferredcites →https://doi.org/10.1016/j.carbpol.2009.03.030openalex-snapshot
Modulatory effect of Ganoderma lucidum polysaccharides on serum antioxidant enzymes activities in ovarian cancer rats
inferredcites →https://doi.org/10.1016/j.ejmech.2018.08.088openalex-snapshot
Nature-inspired development of unnatural meroterpenoids as the non-toxic anti-colon cancer agents
inferredcites →https://doi.org/10.1016/j.fitote.2016.03.003openalex-snapshot
Meroterpenoid enantiomers from Ganoderma sinensis
inferredcites →https://doi.org/10.1016/j.fitote.2018.11.005openalex-snapshot
Meroterpenoids isolated from Arnebia euchroma (Royle) Johnst. and their cytotoxic activity in human hepatocellular carcinoma cells
inferredcites →https://doi.org/10.1016/j.fitote.2019.03.016openalex-snapshot
Zizhines G–O, AchE inhibitory meroterpenoids from Ganoderma sinensis
inferredcites →https://doi.org/10.1016/j.foodchem.2014.08.127openalex-snapshot
Unusual prenylated phenols with antioxidant activities from Ganoderma cochlear
inferredcites →https://doi.org/10.1016/j.leukres.2005.12.015openalex-snapshot
Ganoderma lucidum in cancer research
inferredcites →https://doi.org/10.1016/j.lfs.2005.07.017openalex-snapshot
Ganoderma lucidum polysaccharides peptide inhibits the growth of vascular endothelial cell and the induction of VEGF in human lung cancer cell
inferredcites →https://doi.org/10.1016/j.tet.2014.12.052openalex-snapshot
Isolation and identification of renoprotective substances from the mushroom Ganoderma lucidum
inferredcites →https://doi.org/10.1016/s0065-2164(08)70253-3openalex-snapshot
Medicinal Benefits of the Mushroom Ganoderma
inferredcites →https://doi.org/10.1021/acs.jnatprod.7b00435openalex-snapshot
Meroterpenoids with Protein Tyrosine Phosphatase 1B Inhibitory Activity from a Hyrtios sp. Marine Sponge
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/ja00011a006openalex-snapshot
High-field FT NMR application of Mosher's method. The absolute configurations of marine terpenoids
inferredcites →https://doi.org/10.1021/np030372wopenalex-snapshot
Biologically Active Compounds from Aphyllophorales (Polypore) Fungi
inferredcites →https://doi.org/10.1021/np800687topenalex-snapshot
Triterpene-Farnesyl Hydroquinone Conjugates from Ganoderma sinense
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/10.1080/10286020.2014.960858openalex-snapshot
Two new compounds from Ganoderma lucidum
inferredcites →https://doi.org/10.1080/87559120600694739openalex-snapshot
Recent Advances on Triterpenes fromGanodermaMushroom
inferredcites →https://doi.org/10.1096/fasebj.1.5.3315805openalex-snapshot
Fitting curves to data using nonlinear regression: a practical and nonmathematical review
inferredcites →https://doi.org/10.1142/s0192415x07005065openalex-snapshot
Ganodermataceae: Natural Products and Their Related Pharmacological Functions
inferredcites →https://doi.org/10.1517/13543784.2013.805202openalex-snapshot
Anti-cancer properties of triterpenoids isolated from Ganoderma lucidum – a review
inferredcites →https://doi.org/10.3390/molecules23071797openalex-snapshot
Cytotoxic and N-Acetyltransferase Inhibitory Meroterpenoids from Ganoderma cochlear
inferredcites →https://doi.org/10.3892/or_00001070openalex-snapshot
A novel polysaccharide from Se-enriched Ganoderma lucidum induces apoptosis of human breast cancer cells
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.2022.113184zenodo-depositor-declared
Meroterpenoids containing benzopyran or benzofuran motif from Ganoderma cochlear
inferred← citeshttps://doi.org/10.1002/cbdv.202300022openalex-snapshot
Isolation and Characterization of trans‐p‐Hydroxycinnamoyl Meroterpenoids from Ganoderma sinensis
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/s11011-025-01702-xopenalex-snapshot
The therapeutic effects of various tonic traditional Chinese medicines on demyelinating diseases
inferred← citeshttps://doi.org/10.1016/j.bioorg.2021.104706openalex-snapshot
Gancochlearols E − I, meroterpenoids from Ganoderma cochlear against COX-2 and triple negative breast cancer cells and the absolute configuration assignment of ganomycin K
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.jff.2021.104758openalex-snapshot
Direct determination of E and Z configurations for double bond in bioactive meroterpenoids from Ganoderma mushrooms by diagnostic 1H NMR chemical shifts and structure revisions of previous analogues
inferred← citeshttps://doi.org/10.1039/d0ob02162hopenalex-snapshot
The chemistry and biology of fungal meroterpenoids (2009–2019)
inferred← citeshttps://doi.org/10.1039/d3np00006kopenalex-snapshot
Structural diversity, hypothetical biosynthesis, chemical synthesis, and biological activity of Ganoderma meroterpenoids
inferred← citeshttps://doi.org/10.1080/0028825x.2024.2375996openalex-snapshot
Exploring the health benefits of Ganoderma : bioactive compounds and mechanisms of action; immunomodulatory, and anti-tumour activities
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.