On the public citation graph

Geopyxins A–E, ent-Kaurane Diterpenoids from Endolichenic Fungal Strains Geopyxis aff. majalis and Geopyxis sp. AZ0066: Structure–Activity Relationships of Geopyxins and Their Analogues

https://doi.org/10.1021/np200769q

0 signed · 116 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.

Claim with ORCID

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 See whether every reference in this work resolves to a known work and none has been retracted — and get a dated CiteStamped badge you can embed.

See reference health

What this work says

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

inferredcites →https://doi.org/10.1007/s00248-010-9698-2openalex-snapshot

Community Analysis Reveals Close Affinities Between Endophytic and Endolichenic Fungi in Mosses and Lichens

inferredcites →https://doi.org/10.1007/s12192-010-0206-xopenalex-snapshot

Xenohormesis: health benefits from an eon of plant stress response evolution

inferredcites →https://doi.org/10.1016/j.bmc.2008.10.091openalex-snapshot

2,3-Dihydrowithaferin A-3β-O-sulfate, a new potential prodrug of withaferin A from aeroponically grown Withania somnifera

inferredcites →https://doi.org/10.1016/j.cbpa.2010.11.003openalex-snapshot

Proteomic approaches to the characterization of protein thiol modification

inferredcites →https://doi.org/10.1016/j.cell.2007.07.020openalex-snapshot

Heat Shock Factor 1 Is a Powerful Multifaceted Modifier of Carcinogenesis

inferredcites →https://doi.org/10.1016/j.cell.2008.04.019openalex-snapshot

Xenohormesis: Sensing the Chemical Cues of Other Species

inferredcites →https://doi.org/10.1016/j.mycres.2007.03.014openalex-snapshot

A phylogenetic overview of the family Pyronemataceae (Ascomycota, Pezizales)

inferredcites →https://doi.org/10.1016/j.ympev.2005.03.010openalex-snapshot

Evolutionary relationships of the cup-fungus genus Peziza and Pezizaceae inferred from multiple nuclear genes: RPB2, β-tubulin, and LSU rDNA

inferredcites →https://doi.org/10.1016/s0040-4039(00)80593-6openalex-snapshot

Absolute configurations of cytotoxic marine cembranolides; Consideration of mosher's method

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/ja01613a080openalex-snapshot

The Effect of Ring Strain on the Ultraviolet Spectra of α,β-Unsaturated Carbonyl Compounds

inferredcites →https://doi.org/10.1021/jf070734wopenalex-snapshot

Isolation of Two Bioactiveent-Kauranoids from the Leaves ofIsodon xerophilus

inferredcites →https://doi.org/10.1021/jo00868a023openalex-snapshot

New hydroxylated ent-kauranoic acids from Eupatorium album

inferredcites →https://doi.org/10.1021/np020059eopenalex-snapshot

Cytotoxic 3,20-Epoxy-ent-Kaurane Diterpenoids from Isodon eriocalyx var. laxiflora

inferredcites →https://doi.org/10.1021/np0304114openalex-snapshot

Ponicidin and Oridonin Are Responsible for the Antiangiogenic Activity of Rabdosia rubescens, a Constituent of the Herbal Supplement PC SPES

inferredcites →https://doi.org/10.1021/np058095bopenalex-snapshot

Search for Hsp90 Inhibitors with Potential Anticancer Activity: Isolation and SAR Studies of Radicicol and Monocillin I from Two Plant-Associated Fungi of the Sonoran Desert

inferredcites →https://doi.org/10.1021/np060504wopenalex-snapshot

Cytotoxic Activity of Some Natural and Synthetic ent-Kauranes

inferredcites →https://doi.org/10.1021/np070205mopenalex-snapshot

Cytotoxic ent-Kauranoids from the Medicinal Plant Isodon xerophilus

inferredcites →https://doi.org/10.1021/np070466wopenalex-snapshot

Heptaketides from Corynespora sp. Inhabiting the Cavern Beard Lichen, Usnea cavernosa: First Report of Metabolites of an Endolichenic Fungus

inferredcites →https://doi.org/10.1021/np100071zopenalex-snapshot

Oxepinochromenones, Furochromenone, and their Putative Precursors from the Endolichenic Fungus Coniochaeta sp.

inferredcites →https://doi.org/10.1021/np100159jopenalex-snapshot

Absolute Configuration of Brevisamide and Brevisin: Confirmation of a Universal Biosynthetic Process for Karenia brevis Polyethers

inferredcites →https://doi.org/10.1021/np2000864openalex-snapshot

Smardaesidins A–G, Isopimarane and 20-nor-Isopimarane Diterpenoids from Smardaea sp., a Fungal Endophyte of the Moss Ceratodon purpureus

inferredcites →https://doi.org/10.1021/np8003062openalex-snapshot

ent-Kaurane Diterpenoids from the Liverwort Jungermannia atrobrunnea

inferredcites →https://doi.org/10.1021/np800671popenalex-snapshot

Antioxidant and Anticholinesterase Activity Evaluation of ent -Kaurane Diterpenoids from Sideritis arguta

inferredcites →https://doi.org/10.1021/np800733yopenalex-snapshot

Ambuic Acid and Torreyanic Acid Derivatives from the Endolichenic Fungus Pestalotiopsis sp.

inferredcites →https://doi.org/10.1021/np9001465openalex-snapshot

Inhibition of NF-κB Activation and iNOS Induction by ent-Kaurane Diterpenoids in LPS-Stimulated RAW264.7 Murine Macrophages

inferredcites →https://doi.org/10.1021/np900250kopenalex-snapshot

Cytotoxic Diterpenoids from Croton argyrophylloides

inferredcites →https://doi.org/10.1021/np900512kopenalex-snapshot

Allenyl and Alkynyl Phenyl Ethers from the Endolichenic Fungus Neurospora terricola

inferredcites →https://doi.org/10.1021/np9903705openalex-snapshot

New 7,20:14,20-Diepoxy ent-Kauranoids from Isodon xerophilus

inferredcites →https://doi.org/10.1021/ol102168zopenalex-snapshot

The First Naturally Occurring Thiepinols and Thienol from an Endolichenic Fungus Coniochaeta sp.

inferredcites →https://doi.org/10.1021/tx050312lopenalex-snapshot

Cytosolic and Nuclear Protein Targets of Thiol-Reactive Electrophiles

inferredcites →https://doi.org/10.1038/nature09472openalex-snapshot

Quantitative reactivity profiling predicts functional cysteines in proteomes

inferredcites →https://doi.org/10.1039/p19840002363openalex-snapshot

Carbon-13 nuclear magnetic resonance spectra of eighteen derivatives of ent-kaur-16-en-19-oic acid

inferredcites →https://doi.org/10.1046/j.1432-1327.2000.01606.xopenalex-snapshot

Investigation of the Alamar Blue (resazurin) fluorescent dye for the assessment of mammalian cell cytotoxicity

inferredcites →https://doi.org/10.1055/s-0029-1186002openalex-snapshot

Ent -Kaurane Diterpenoids from Rabdosia rubescens and Their Cytotoxic Effects on Human Cancer Cell Lines

inferredcites →https://doi.org/10.1055/s-0029-1240683openalex-snapshot

Anti-HIV‐1 Diterpenoids from Leaves and Twigs ofPolyalthia sclerophylla

inferredcites →https://doi.org/10.1055/s-0029-1240863openalex-snapshot

SIRT1 Inhibitory Diterpenoids from the Vietnamese Medicinal PlantCroton tonkinensis

inferredcites →https://doi.org/10.1055/s-2001-15808openalex-snapshot

Kaurane Diterpenes from Isodon japonicus Inhibit Nitric Oxide and Prostaglandin E2 Production and NF-κB Activation in LPS-Stimulated Macrophage RAW264.7 Cells

inferredcites →https://doi.org/10.1055/s-2005-871234openalex-snapshot

An Anti-Inflammatoryent-Kaurane from the Stems ofAnnona squamosathat Inhibits Various Human Neutrophil Functions

inferredcites →https://doi.org/10.1073/pnas.1014714108openalex-snapshot

Identity, regulation, and activity of inducible diterpenoid phytoalexins in maize

inferredcites →https://doi.org/10.1093/bioinformatics/14.9.817openalex-snapshot

MODELTEST: testing the model of DNA substitution.

inferredcites →https://doi.org/10.1271/bbb.70.583openalex-snapshot

Biochemical and Molecular Analyses of Gibberellin Biosynthesis in Fungi

inferredcites →https://doi.org/10.25911/5d6c3f290bb26openalex-snapshot

Studies in natural products chemistry

inferredcites →https://doi.org/10.3390/12030455openalex-snapshot

Occurrence, Biological Activities and Synthesis of Kaurane Diterpenes and their Glycosides

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.3352498openalex-extracted

Non-Covalent NRF2 Activation Confers Greater Cellular Protection than Covalent Activation

inferred← citeshttps://doi.org/10.1002/cbdv.201400146openalex-snapshot

Identification and Biological Evaluation of Secondary Metabolites from the Endolichenic Fungus Aspergillus versicolor

inferred← citeshttps://doi.org/10.1002/cbdv.201400279openalex-snapshot

New Metabolites from Endolichenic Fungus Pleosporales sp.

inferred← citeshttps://doi.org/10.1002/cbdv.201400317openalex-snapshot

Secondary Metabolites from Aspergillus fumigatus, an Endophytic Fungus from the Liverwort Heteroscyphus tener ( Steph .) Schiffn .

inferred← citeshttps://doi.org/10.1007/978-3-642-53971-8_32openalex-snapshot

Marine-Derived Fungal Metabolites

inferred← citeshttps://doi.org/10.1007/978-981-13-7154-7_4openalex-snapshot

Endolichenic Fungi from Common Lichens as New Sources for Valuable Bio-active Compounds

inferred← citeshttps://doi.org/10.1007/978-981-13-7268-1_5openalex-snapshot

Endolichenic Fungi: A Promising Source for Novel Bioactive Compounds

inferred← citeshttps://doi.org/10.1007/s00044-021-02835-1openalex-snapshot

Semi-synthesis and cytotoxicity evaluation of pyrimidine, thiazole, and indole analogues of argentatins A–C from guayule (Parthenium argentatum) resin

inferred← citeshttps://doi.org/10.1007/s10600-015-1305-9openalex-snapshot

A New Fatty Acid from the Endolichenic Fungus Massarina sp.

inferred← citeshttps://doi.org/10.1007/s11101-016-9473-1openalex-snapshot

Endolichenic fungi: a new source of rich bioactive secondary metabolites on the horizon

inferred← citeshttps://doi.org/10.1007/s11101-018-9577-xopenalex-snapshot

Have lichenized fungi delivered promising anticancer small molecules?

inferred← citeshttps://doi.org/10.1007/s40203-026-00633-4openalex-snapshot

Antiproliferative activity of Xylopia aethiopica extracts and molecular docking studies of their main phytochemicals

inferred← citeshttps://doi.org/10.1016/b978-0-12-809633-8.21118-7openalex-snapshot

Antitumor and Immunomodulatory Compounds from Fungi

inferred← citeshttps://doi.org/10.1016/b978-0-444-63602-7.00011-4openalex-snapshot

Endolichenic Fungi

inferred← citeshttps://doi.org/10.1016/j.bmc.2014.08.039openalex-snapshot

Altertoxins with potent anti-HIV activity from Alternaria tenuissima QUE1Se, a fungal endophyte of Quercus emoryi

inferred← citeshttps://doi.org/10.1016/j.chembiol.2019.07.011openalex-snapshot

Non-covalent NRF2 Activation Confers Greater Cellular Protection than Covalent Activation

inferred← citeshttps://doi.org/10.1016/j.fitote.2022.105160openalex-snapshot

Discovery of ent-kaurane diterpenoids, characteristic metabolites of Isodon species, from an endophytic fungal strain Geopyxis sp. XY93 inhabiting Isodon parvifolia

inferred← citeshttps://doi.org/10.1016/j.phymed.2018.01.006openalex-snapshot

Acetonic extracts of the endolichenic fungus EL002332 isolated from Endocarpon pusillum exhibits anticancer activity in human gastric cancer cells

inferred← citeshttps://doi.org/10.1016/j.phytochem.2015.08.010openalex-snapshot

Sesquiterpenes and other constituents of Xylaria sp. NC1214, a fungal endophyte of the moss Hypnum sp.

inferred← citeshttps://doi.org/10.1016/j.phytol.2013.08.011openalex-snapshot

Austdiol, fulvic acid and citromycetin derivatives from an endolichenic fungus, Myxotrichum sp.

inferred← citeshttps://doi.org/10.1016/j.phytol.2018.10.011openalex-snapshot

Modulation of polyketide biosynthetic pathway of the endophytic fungus, Anteaglonium sp. FL0768, by copper (II) and anacardic acid

inferred← citeshttps://doi.org/10.1016/j.redox.2021.101977openalex-snapshot

ent-Kaurane diterpenoids induce apoptosis and ferroptosis through targeting redox resetting to overcome cisplatin resistance

inferred← citeshttps://doi.org/10.1016/j.sajb.2019.12.008openalex-snapshot

Endolichenic fungi: A hidden source of bioactive metabolites

inferred← citeshttps://doi.org/10.1021/acs.jmedchem.5b00208openalex-snapshot

ent-Kaurane Diterpenoids from Chinese Liverworts and Their Antitumor Activities through Michael Addition As Detected in Situ by a Fluorescence Probe

inferred← citeshttps://doi.org/10.1021/acs.jnatprod.1c00662openalex-snapshot

Strobiloscyphones A–F, 6-Isopentylsphaeropsidones and Other Metabolites from Strobiloscypha sp. AZ0266, a Leaf-Associated Fungus of Douglas Fir

inferred← citeshttps://doi.org/10.1021/acs.jnatprod.5b00911openalex-snapshot

17β-Hydroxy-18-acetoxywithanolides from Aeroponically Grown Physalis crassifolia and Their Potent and Selective Cytotoxicity for Prostate Cancer Cells

inferred← citeshttps://doi.org/10.1021/acs.jnatprod.6b00197openalex-snapshot

p-Terphenyl Derivatives from the Endolichenic Fungus Floricola striata

inferred← citeshttps://doi.org/10.1021/acs.jnatprod.6b00960openalex-snapshot

Chlorinated Dehydrocurvularins and Alterperylenepoxide A from Alternaria sp. AST0039, a Fungal Endophyte of Astragalus lentiginosus

inferred← citeshttps://doi.org/10.1021/acs.jnatprod.7b00838openalex-snapshot

Cytotoxic and Noncytotoxic Metabolites from Teratosphaeria sp. FL2137, a Fungus Associated with Pinus clausa

inferred← citeshttps://doi.org/10.1021/acs.orglett.9b00385openalex-snapshot

Isocoumarindole A, a Chlorinated Isocoumarin and Indole Alkaloid Hybrid Metabolite from an Endolichenic Fungus Aspergillus sp.

inferred← citeshttps://doi.org/10.1021/acsomega.1c01714openalex-snapshot

Cycloartane- and Lanostane-Type Triterpenoids from the Resin of Parthenium argentatum AZ-2, a Byproduct of Guayule Rubber Production

inferred← citeshttps://doi.org/10.1021/np300106jopenalex-snapshot

Laxiflorolides A and B, Epimeric Bishomoditerpene Lactones from Isodon eriocalyx

inferred← citeshttps://doi.org/10.1021/np300792topenalex-snapshot

Mycoleptodiscins A and B, Cytotoxic Alkaloids from the Endophytic Fungus Mycoleptodiscus sp. F0194

inferred← citeshttps://doi.org/10.1021/np400391popenalex-snapshot

Phomapyrrolidones A–C, Antitubercular Alkaloids from the Endophytic Fungus Phoma sp. NRRL 46751

inferred← citeshttps://doi.org/10.1021/np400762kopenalex-snapshot

Secoemestrin D, a Cytotoxic Epitetrathiodioxopiperizine, and Emericellenes A–E, Five Sesterterpenoids from Emericella sp. AST0036, a Fungal Endophyte of Astragalus lentiginosus1

inferred← citeshttps://doi.org/10.1021/ol502973copenalex-snapshot

Delitschiapyrone A, a Pyrone–Naphthalenone Adduct Bearing a New Pentacyclic Ring System from the Leaf-Associated Fungus Delitschia sp. FL1581

inferred← citeshttps://doi.org/10.1038/s41429-018-0058-7openalex-snapshot

Anti-inflammatory phomalichenones from an endolichenic fungus Phoma sp.

inferred← citeshttps://doi.org/10.1038/srep41273openalex-snapshot

A compound-based proteomic approach discloses 15-ketoatractyligenin methyl ester as a new PPARγ partial agonist with anti-proliferative ability

inferred← citeshttps://doi.org/10.1039/c3np70046aopenalex-snapshot

Diterpenoids of terrestrial origin

inferred← citeshttps://doi.org/10.1039/c4np00075gopenalex-snapshot

Traversing the fungal terpenome

inferred← citeshttps://doi.org/10.1039/c6np00059bopenalex-snapshot

Diterpenoids of terrestrial origin

inferred← citeshttps://doi.org/10.1039/c7cs00431aopenalex-snapshot

Secondary metabolism in the lichen symbiosis

inferred← citeshttps://doi.org/10.1039/c7np00027hopenalex-snapshot

Diterpenoids from Isodon species: an update

inferred← citeshttps://doi.org/10.1039/c7ra07060hopenalex-snapshot

New and bioactive natural products from an endophyte of Panax notoginseng

inferred← citeshttps://doi.org/10.1055/s-0041-1730956openalex-snapshot

Synthesis and Antitumor Activity of (3-Hydroxyacrylato-O,O′) Diammineplatinum(II)

inferred← citeshttps://doi.org/10.1073/pnas.1406999111openalex-snapshot

Diversity-oriented combinatorial biosynthesis of benzenediol lactone scaffolds by subunit shuffling of fungal polyketide synthases

inferred← citeshttps://doi.org/10.1080/10286020.2015.1135906openalex-snapshot

Three new drimane-type sesquiterpenoids, chaetothyrins A–C, from an endolichenic fungus Chaetothyriales sp.

inferred← citeshttps://doi.org/10.1080/10286020.2025.2501030openalex-snapshot

Endophytic microorganisms in lichen: rising stars in the biomedicine field deserving broader recognition

inferred← citeshttps://doi.org/10.1080/14786419.2016.1190719openalex-snapshot

Activity of compounds from Taxillus sutchuenensis as inhibitors of HCV NS3 serine protease

inferred← citeshttps://doi.org/10.1080/21501203.2017.1352048openalex-snapshot

Endolichenic fungi: the lesser known fungal associates of lichens

inferred← citeshttps://doi.org/10.11005/jbm.2019.26.2.113openalex-snapshot

Extracts ofFlavoparmeliasp. Inhibit Receptor Activator of Nuclear Factor-κB Ligand-Mediated Osteoclast Differentiation

inferred← citeshttps://doi.org/10.1111/1462-2920.70112openalex-snapshot

A Biosynthetic and Taxonomic Atlas of the Global Lichen Holobiont

inferred← citeshttps://doi.org/10.1111/bph.15974openalex-snapshot

The natural product argentatin C attenuates postoperative pain via inhibition of voltage‐gated sodium and T‐type voltage‐gated calcium channels

inferred← citeshttps://doi.org/10.1111/nph.17886openalex-snapshot

Endophytism and endolichenism in Pezizomycetes: the exception or the rule?

inferred← citeshttps://doi.org/10.11606/t.60.2013.tde-27062013-101222openalex-snapshot

Caracterização fitoquímica, avaliação das atividades analgésica e anti-inflamatória e biotransformação de um composto isolado das folhas de Copaifera langsdorffii

inferred← citeshttps://doi.org/10.1177/1934578x1300800515openalex-snapshot

10′-Deoxy-10′ α-hydroxyascochlorin, a New Cell Migration Inhibitor and Other Metabolites from Acremonium sp., a Fungal Endophyte in Ephedra trifurca

inferred← citeshttps://doi.org/10.1177/1934578x1300800802openalex-snapshot

Microbial Biotransformation of 16α,17-Epoxy- Ent -kaurane-19-oic acid by Beauveria Sulfurescens ATCC 7159-F

inferred← citeshttps://doi.org/10.1177/1934578x1501001007openalex-snapshot

Cytotoxic Cytochalasins and Other Metabolites from Xylariaceae sp. FL0390, a Fungal Endophyte of Spanish Moss

inferred← citeshttps://doi.org/10.1186/s13041-020-00616-2openalex-snapshot

1-O-Acetylgeopyxin A, a derivative of a fungal metabolite, blocks tetrodotoxin-sensitive voltage-gated sodium, calcium channels and neuronal excitability which correlates with inhibition of neuropathic pain

inferred← citeshttps://doi.org/10.1186/s13065-020-00671-9openalex-snapshot

Auto-oxidation of Ent-beyer-15-en-19-al isolated from the essential oil of the heartwood of Erythroxylum monogynum Roxb.: formation of 15,16-epoxy-ent-beyeran-19-oic acid and other products

inferred← citeshttps://doi.org/10.1515/ncrs-2023-0061openalex-snapshot

Crystal structure of 7α,11α-dihydroxy-15-oxo-ent-kauran-16-en-19,6β-olide, C20H26O5

inferred← citeshttps://doi.org/10.1639/007-2745-115.3.465openalex-snapshot

Recent literature on lichens—226

inferred← citeshttps://doi.org/10.2174/0929867322666150821101047openalex-snapshot

Sesterterpenoids with Anticancer Activity

inferred← citeshttps://doi.org/10.2174/1871520619666190118121439openalex-snapshot

Synthesis of Oridonin Derivatives via Mizoroki-Heck Reaction and Click Chemistry for Cytotoxic Activity

inferred← citeshttps://doi.org/10.3389/fchem.2022.885487openalex-snapshot

Novel Triterpenoid Alkaloids With Their Potential Cytotoxic Activity From the Roots of Siraitia grosvenorii

inferred← citeshttps://doi.org/10.3389/fphar.2022.986946openalex-snapshot

An acetonic extract and secondary metabolites from the endolichenic fungus Nemania sp. EL006872 exhibit immune checkpoint inhibitory activity in lung cancer cell

inferred← citeshttps://doi.org/10.3390/ijms17091395openalex-snapshot

Oridonin, a Promising ent-Kaurane Diterpenoid Lead Compound

inferred← citeshttps://doi.org/10.3390/molecules25215058openalex-snapshot

Teratopyrones A–C, Dimeric Naphtho-γ-Pyrones and Other Metabolites from Teratosphaeria sp. AK1128, a Fungal Endophyte of Equisetum arvense

inferred← citeshttps://doi.org/10.5943/ajom/3/1/18openalex-snapshot

The diversity of endolichenic fungi – A review

inferred← citeshttps://doi.org/10.6084/m9.figshare.11984967openalex-snapshot

Additional file 1 of Auto-oxidation of Ent-beyer-15-en-19-al isolated from the essential oil of the heartwood of Erythroxylum monogynum Roxb.: formation of 15,16-epoxy-ent-beyeran-19-oic acid and other products

inferred← citeshttps://doi.org/10.6084/m9.figshare.11984976openalex-snapshot

Additional file 2 of Auto-oxidation of Ent-beyer-15-en-19-al isolated from the essential oil of the heartwood of Erythroxylum monogynum Roxb.: formation of 15,16-epoxy-ent-beyeran-19-oic acid and other products

inferred← citeshttps://doi.org/10.70675/69c906a4z8a84z4595zbe8bz1f87507c0b52openalex-snapshot

Études phytochimiques du lichen Nephroma laevigatum et de ses champignons endolichéniques. Évaluation des activités antiprolifératives et anti-biofilms.

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.