On the public citation graph
Sesquiterpenes from an Endophytic Aspergillus flavus
0 signed · 62 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known work and none has been retracted — and get a dated CiteStamped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/cbdv.201100026openalex-snapshot
Terpenoid and Phenolic Metabolites from the Fungus Xylaria sp. Associated with Termite Nests
inferredcites →https://doi.org/10.1002/mrc.2748openalex-snapshot
Steroids and an oxylipin from an algicolous isolate of Aspergillus flavus
inferredcites →https://doi.org/10.1007/s10068-016-0199-zopenalex-snapshot
Furan, phenolic, and heptelidic acid derivatives produced by Aspergillus oryzae
inferredcites →https://doi.org/10.1007/s10600-013-0447-xopenalex-snapshot
Biologically active metabolites of the facultative marine fungus Penicillium citrinum
inferredcites →https://doi.org/10.1016/j.foodchem.2017.08.065openalex-snapshot
Development of an analytical method for identification of Aspergillus flavus based on chemical markers using HPLC-MS
inferredcites →https://doi.org/10.1016/s0031-9422(00)83034-4openalex-snapshot
Sesquiterpenes from pernettya furens
inferredcites →https://doi.org/10.1016/s0031-9422(01)00340-5openalex-snapshot
Biotransformation of 4β-hydroxyeudesmane-1,6-dione by Gliocladium roseum and Exserohilum halodes
inferredcites →https://doi.org/10.1016/s0953-7562(09)80939-8openalex-snapshot
Metabolites toxic to spruce budworm from balsam fir needle endophytes
inferredcites →https://doi.org/10.1021/acs.orglett.6b00919openalex-snapshot
Structural Characterization of Kadcoccinin A: A Sesquiterpenoid with a Tricyclo[4.4.0.0 3,10 ]decane Scaffold from Kadsura coccinea
inferredcites →https://doi.org/10.1021/jo00305a030openalex-snapshot
Aflavazole: a new antiinsectan carbazole metabolite from the sclerotia of Aspergillus flavus
inferredcites →https://doi.org/10.1021/np050141kopenalex-snapshot
Aspirochlorine Class Compounds from Aspergillus flavus Inhibit Azole-Resistant Candida albicans
inferredcites →https://doi.org/10.1038/s41598-017-07436-wopenalex-snapshot
Aspergillus Secondary Metabolite Database, a resource to understand the Secondary metabolome of Aspergillus genus
inferredcites →https://doi.org/10.1039/c2np00084aopenalex-snapshot
Advances in Aspergillus secondary metabolite research in the post-genomic era
inferredcites →https://doi.org/10.1080/14786410600899084openalex-snapshot
New calamenene sesquiterpenes fromTarenna madagascariensis
inferredcites →https://doi.org/10.1111/j.1365-2621.1991.tb05406.xopenalex-snapshot
Aflatoxin and Cyclopiazonic Acid Production by Aspergillus flavus Isolated from Contaminated Maize
inferredcites →https://doi.org/10.1146/annurev-phyto-072910-095221openalex-snapshot
Aspergillus flavus
inferredcites →https://doi.org/10.1271/bbb.90843openalex-snapshot
Novel Terpenoids, Trichoderonic Acids A and B Isolated fromTrichoderma virens, Are Selective Inhibitors of Family X DNA Polymerases
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.2021.113011zenodo-depositor-declared
Recent studies on terpenoids in Aspergillus fungi: Chemical diversity, biosynthesis, and bioactivity
inferred← citeshttps://doi.org/10.1002/cbdv.202000036openalex-snapshot
Trichodermaloids A–C, Cadinane Sesquiterpenes from a Marine Sponge Symbiotic Trichoderma sp. SM16 Fungus
inferred← citeshttps://doi.org/10.1002/cbdv.202300424openalex-snapshot
Cyclohexenone Derivative and Drimane Sesquiterpenes from the Seagrass‐Derived Fungus Aspergillus insuetus
inferred← citeshttps://doi.org/10.1007/978-3-642-36202-6_199-1openalex-snapshot
Biology and Chemistry of Secondary Metabolites from Endophytic Fungi
inferred← citeshttps://doi.org/10.1007/978-981-15-9371-0_3openalex-snapshot
Recent Update on Novel Anticancer Compounds from Endophytes
inferred← citeshttps://doi.org/10.1007/978-981-97-7312-1_10openalex-snapshot
Endophytic Fungal Terpenoids: Biosynthesis and Biological Activity
inferred← citeshttps://doi.org/10.1007/s10600-020-03256-zopenalex-snapshot
Secondary Metabolites from the Endophytic Fungus Stemphylium lycopersici and Their Antibacterial Activities
inferred← citeshttps://doi.org/10.1007/s10600-022-03651-8openalex-snapshot
Isolation and Characterization of Hepatoprotective Xanthones from the Fruits of Hovenia acerba
inferred← citeshttps://doi.org/10.1007/s10600-026-05011-2openalex-snapshot
A New Antibacterial Sesquiterpene Alkaloid from the Cigar-Tobacco-Derived Aspergillus ustus
inferred← citeshttps://doi.org/10.1007/s10658-026-03183-9openalex-snapshot
Mass spectrometry-based metabolomics and chemometric analysis reveal host tissue-level classification of Aspergillus flavus isolates
inferred← citeshttps://doi.org/10.1007/s11418-024-01832-zopenalex-snapshot
Isolation of C-29 oxygenated oleanane triterpenoids and a (+)-muurolene type sesquiterpenoid from the fruiting bodies of Fuscoporia torulosa and their bioactivities
inferred← citeshttps://doi.org/10.1007/s11802-022-4959-5openalex-snapshot
A New α-Cyclopiazonic Acid Alkaloid Identified from the Weizhou Island Coral-Derived Fungus Aspergillus flavus GXIMD 02503
inferred← citeshttps://doi.org/10.1007/s12010-021-03702-wopenalex-snapshot
Antimicrobial, Antioxidant, Cytotoxic Activities and Phytochemical Analysis of Fungal Endophytes Isolated from Ocimum Basilicum
inferred← citeshttps://doi.org/10.1007/s13205-023-03675-zopenalex-snapshot
Biocontrol potential of endophytic fungi originated from grapevine leaves for management of anthracnose disease caused by Colletotrichum gloeosporioides
inferred← citeshttps://doi.org/10.1007/s13659-025-00501-2openalex-snapshot
Newly isolated terpenoids (covering 2019–2024) from Aspergillus species and their potential for the discovery of novel antimicrobials
inferred← citeshttps://doi.org/10.1007/s42770-021-00502-6openalex-snapshot
Chromolaena laevigata (Asteraceae) as a source of endophytic non-aflatoxigenic Aspergillus flavus: chemical profile in different culture conditions and biological applications
inferred← citeshttps://doi.org/10.1016/j.bioorg.2019.103288openalex-snapshot
Dihydro-β-agarofuran sesquiterpenoid derivatives with anti-inflammatory activity from the leaves of Tripterygium wilfordii
inferred← citeshttps://doi.org/10.1016/j.bioorg.2020.103630openalex-snapshot
Structural characterization, neuroprotective and hepatoprotective activities of flavonoids from the bulbs of Heleocharis dulcis
inferred← citeshttps://doi.org/10.1016/j.bioorg.2020.103645openalex-snapshot
Antibacterial sesquiterpenes from the stems and roots of Thuja sutchuenensis
inferred← citeshttps://doi.org/10.1016/j.bioorg.2020.104622openalex-snapshot
Isolation and characterization of neolignan derivatives with hepatoprotective and neuroprotective activities from the fruits of Citrus medica L. var. Sarcodactylis Swingle
inferred← citeshttps://doi.org/10.1016/j.bioorg.2021.104866openalex-snapshot
Oxygenated pentacyclic triterpenoids from the stems and branches of Enkianthus chinensis
inferred← citeshttps://doi.org/10.1016/j.bse.2022.104415openalex-snapshot
Anti-Pathogenic Depsidones and its Derivatives from a Coral-Derived Fungus Aspergillus Sp. Scsio Sx7s7
inferred← citeshttps://doi.org/10.1016/j.cpb.2020.100189openalex-snapshot
Plant-microbial endophytes interactions: Scrutinizing their beneficial mechanisms from genomic explorations
inferred← citeshttps://doi.org/10.1016/j.fitote.2020.104812openalex-snapshot
Structurally diverse coumarin-homoisoflavonoid derivatives with hepatoprotective activities from the fruits of Cucumis bisexualis
inferred← citeshttps://doi.org/10.1016/j.fitote.2022.105165openalex-snapshot
Dihydro-β-agarofuran-type sesquiterpenoids from the seeds of Celastrus virens with lifespan-extending effect on the nematode Caenorhabditis elegans
inferred← citeshttps://doi.org/10.1016/j.heliyon.2024.e35270openalex-snapshot
Eudesmane-type sesquiterpenoids: Structural diversity and biological activity
inferred← citeshttps://doi.org/10.1016/j.jenvman.2024.121875openalex-snapshot
Advanced photocatalytic disinfection mechanisms and their challenges
inferred← citeshttps://doi.org/10.1016/j.pestbp.2023.105613openalex-snapshot
Extraction and characterization of anti-virus anthraquinones from Nicotiana tabacum-derived Aspergillus oryzae YNCA1220
inferred← citeshttps://doi.org/10.1016/s1875-5364(26)61181-8openalex-snapshot
Penicipenoids A−G, antioxidant and anti-inflammatory cadinane sesquiterpenoids with rearranged carbon skeletons from the marine sponge symbiotic Penicillium sp. 5975
inferred← citeshttps://doi.org/10.1021/acs.jafc.9b04053openalex-snapshot
Sesquiterpenes with Phytopathogenic Fungi Inhibitory Activities from Fungus Trichoderma virens from Litchi chinensis Sonn.
inferred← citeshttps://doi.org/10.1021/acsomega.5c10614openalex-snapshot
Unveiling Valuable Secondary Metabolites from the Bioconversion of Banana ( Musa balbisiana ) Peel-Derived Biomass with Aspergillus niger . Metabolomic Insights into the Chemical Profiles
inferred← citeshttps://doi.org/10.1039/c9np00062copenalex-snapshot
Natural disesquiterpenoids: an update
inferred← citeshttps://doi.org/10.1039/d0ra04290kopenalex-snapshot
Natural product diversity from the endophytic fungi of the genus Aspergillus
inferred← citeshttps://doi.org/10.1039/d3sc04172gopenalex-snapshot
Rapid discovery of terpene tailoring enzymes for total biosynthesis
inferred← citeshttps://doi.org/10.1039/d4ra01055hopenalex-snapshot
Comparative metabolomics study on the secondary metabolites of the red alga, Corallina officinalis and its associated endosymbiotic fungi
inferred← citeshttps://doi.org/10.1080/14786419.2020.1747456openalex-snapshot
New cadinene-sesquiterpene from Chromolaena laevigata (lam.) R. M. King & H. Rob (Asteraceae) aerial parts and biological activities
inferred← citeshttps://doi.org/10.1080/14786419.2023.2209820openalex-snapshot
Three new isocoumarin analogues from an endolichenic fungus Aspergillus flavus CPCC 400810
inferred← citeshttps://doi.org/10.1080/14786419.2023.2286602openalex-snapshot
Two new seco-abietane type diterpenoids from the leaves of Isodon serra
inferred← citeshttps://doi.org/10.1177/1934578x20937204openalex-snapshot
Progress on Terpenoids With Biological Activities Produced by Plant Endophytic Fungi in China Between 2017 and 2019
inferred← citeshttps://doi.org/10.1186/s12934-023-02118-xopenalex-snapshot
Bioactive compounds and biomedical applications of endophytic fungi: a recent review
inferred← citeshttps://doi.org/10.1515/znc-2019-0202openalex-snapshot
Bioactivity-guided isolation of aurone derivatives with hepatoprotective activities from the fruits of Cucumis bisexualis
inferred← citeshttps://doi.org/10.2478/fzm-2021-0006openalex-snapshot
Tridepsides from the endophytic fungus colletotrichum gloeosporioides associated with a toxic medicinal plant tylophora ovata
inferred← citeshttps://doi.org/10.3390/ijms21175958openalex-snapshot
Diversity and Antimicrobial Activity of Endophytic Fungi Isolated from Chloranthus japonicus Sieb in Qinling Mountains, China
inferred← citeshttps://doi.org/10.3390/microorganisms10020339openalex-snapshot
Endophytic Fungal Terpenoids: Natural Role and Bioactivities
inferred← citeshttps://doi.org/10.3390/ph17050656openalex-snapshot
Unveiling the Multifaceted Capabilities of Endophytic Aspergillus flavus Isolated from Annona squamosa Fruit Peels against Staphylococcus Isolates and HCoV 229E—In Vitro and In Silico Investigations
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.