On the public citation graph
Proversilins A–E, Drimane-Type Sesquiterpenoids from the Endophytic Aspergillus versicolor
0 signed · 73 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known work and none has been retracted — and get a dated CiteStamped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.201506264openalex-snapshot
Asperchalasine A, a Cytochalasan Dimer with an Unprecedented Decacyclic Ring System, from Aspergillus flavipes
inferredcites →https://doi.org/10.1002/anie.201601967openalex-snapshot
Artemisinin—A Gift from Traditional Chinese Medicine to the World (Nobel Lecture)
inferredcites →https://doi.org/10.1002/anie.201701125openalex-snapshot
Asperflavipine A: A Cytochalasan Heterotetramer Uniquely Defined by a Highly Complex Tetradecacyclic Ring System from Aspergillus flavipes QCS12
inferredcites →https://doi.org/10.1002/anie.201905966openalex-snapshot
Bipolarolides A–G: Ophiobolin‐Derived Sesterterpenes with Three New Carbon Skeletons from Bipolaris sp. TJ403‐B1
inferredcites →https://doi.org/10.1002/chin.200447248openalex-snapshot
Occurrence, Biological Activity and Synthesis of Drimane Sesquiterpenoids
inferredcites →https://doi.org/10.1002/ejoc.201900383openalex-snapshot
Asperteramide A, an Unusual N ‐Phenyl‐Carbamic Acid Methyl Ester Trimer Isolated from the Coral‐Derived Fungus Aspergillus Terreus
inferredcites →https://doi.org/10.1016/0031-9422(92)90042-oopenalex-snapshot
Cryptoporic acids A-G, drimane-type sesquiterpenoid ethers of isocitric acid from the fungus Cryptoporus volvatus
inferredcites →https://doi.org/10.1016/0031-9422(94)00708-2openalex-snapshot
Phytotoxic sesquiterpenoids from Canella winterana
inferredcites →https://doi.org/10.1016/j.fitote.2017.09.012openalex-snapshot
Atrichodermones A–C, three new secondary metabolites from the solid culture of an endophytic fungal strain, Trichoderma atroviride
inferredcites →https://doi.org/10.1016/j.phytochem.2012.09.008openalex-snapshot
Sesquiterpenoids from Curcuma wenyujin with anti-influenza viral activities
inferredcites →https://doi.org/10.1016/j.phytochem.2016.07.008openalex-snapshot
Bioactive sesquiterpenoids from the flowers of Inula japonica
inferredcites →https://doi.org/10.1016/j.phytochem.2018.10.006openalex-snapshot
Brasilane sesquiterpenoids and dihydrobenzofuran derivatives from Aspergillus terreus [CFCC 81836]
inferredcites →https://doi.org/10.1016/j.phytochem.2019.05.014openalex-snapshot
Anti-BACE1 and anti-AchE activities of undescribed spiro-dioxolane-containing meroterpenoids from the endophytic fungus Aspergillus terreus Thom
inferredcites →https://doi.org/10.1016/j.phytochem.2019.05.015openalex-snapshot
Highly oxygenated meroterpenoids from the Antarctic fungus Aspergillus terreus
inferredcites →https://doi.org/10.1016/s0014-2999(98)00514-7openalex-snapshot
Dialdehyde sesquiterpenes and other terpenoids as vanilloids
inferredcites →https://doi.org/10.1017/s0007485300039973openalex-snapshot
Antifeedant and insecticidal activity of compounds fromPseudowintera colorata(Winteraceae) on the webbing clothes moth,Tineola bisselliella(Lepidoptera: Tineidae) and the Australian carpet beetle,Anthrenocerus australis(Coleoptera: Dermestidae)
inferredcites →https://doi.org/10.1021/acs.jnatprod.9b00183openalex-snapshot
HPLC-DAD-Directed Isolation of Linearly Fused Prenylated Indole Alkaloids from a Soil-Derived Aspergillus versicolor
inferredcites →https://doi.org/10.1021/acs.joc.8b01087openalex-snapshot
Asperversiamides, Linearly Fused Prenylated Indole Alkaloids from the Marine-Derived Fungus Aspergillus versicolor
inferredcites →https://doi.org/10.1021/acs.orglett.5b02080openalex-snapshot
Pestaloporonins: Caryophyllene-Derived Sesquiterpenoids from a Fungicolous Isolate of Pestalotiopsis sp.
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/acs.orglett.7b02559openalex-snapshot
Nicotabin A, a Sesquiterpenoid Derivative from Nicotiana tabacum
inferredcites →https://doi.org/10.1021/acs.orglett.7b03050openalex-snapshot
Illisimonin A, a Caged Sesquiterpenoid with a Tricyclo[5.2.1.01,6]decane Skeleton from the Fruits of Illicium simonsii
inferredcites →https://doi.org/10.1021/acs.orglett.7b04035openalex-snapshot
Rhodium-Catalyzed Enantioselective Decarboxylative Alkynylation of Allenes with Arylpropiolic Acids
inferredcites →https://doi.org/10.1021/acs.orglett.8b02137openalex-snapshot
Fusicoccane-Derived Diterpenoids from Alternaria brassicicola: Investigation of the Structure–Stability Relationship and Discovery of an IKKβ Inhibitor
inferredcites →https://doi.org/10.1021/acs.orglett.9b00581openalex-snapshot
Niduterpenoids A and B: Two Sesterterpenoids with a Highly Congested Hexacyclic 5/5/5/5/3/5 Ring System from the Fungus Aspergillus nidulans
inferredcites →https://doi.org/10.1021/acs.orglett.9b03270openalex-snapshot
Periconiastone A, an Antibacterial Ergosterol with a Pentacyclo[8.7.0.01,5.02,14.010,15]heptadecane System from Periconia sp. TJ403-rc01
inferredcites →https://doi.org/10.1021/ja209700jopenalex-snapshot
Rigid P-Chiral Phosphine Ligands with tert -Butylmethylphosphino Groups for Rhodium-Catalyzed Asymmetric Hydrogenation of Functionalized Alkenes
inferredcites →https://doi.org/10.1021/jo991740xopenalex-snapshot
Illudalane Sesquiterpenoids from the Soft Coral Alcyonium paessleri: The First Natural Nitrate Esters
inferredcites →https://doi.org/10.1021/np030074zopenalex-snapshot
Africane-Type Sesquiterpenoids from the Argentine Liverwort Porella swartziana and Their Antibacterial Activity
inferredcites →https://doi.org/10.1038/srep42434openalex-snapshot
Flavichalasines A–M, cytochalasan alkaloids from Aspergillus flavipes
inferredcites →https://doi.org/10.1039/b311170aopenalex-snapshot
Occurrence, biological activity and synthesis of drimane sesquiterpenoids
inferredcites →https://doi.org/10.1039/c5np00133aopenalex-snapshot
Artemisinin, a miracle of traditional Chinese medicine
inferredcites →https://doi.org/10.1039/c6sc02464eopenalex-snapshot
Asperterpenes A and B, two unprecedented meroterpenoids from Aspergillus terreus with BACE1 inhibitory activities
inferredcites →https://doi.org/10.1039/c8ob02741bopenalex-snapshot
New 3,5-dimethylorsellinic acid-based meroterpenoids with BACE1 and AchE inhibitory activities from Aspergillus terreus
inferredcites →https://doi.org/10.1039/c9np00062copenalex-snapshot
Natural disesquiterpenoids: an update
inferredcites →https://doi.org/10.1039/np9910800309openalex-snapshot
The occurrence and biological activity of drimane sesquiterpenoids
inferredcites →https://doi.org/10.1590/s0074-02762001000600016openalex-snapshot
Polygodial, the fungitoxic component from the Brazilian medicinal plant Polygonum punctatum
inferredcites →https://doi.org/10.3390/ijms140612780openalex-snapshot
Sesquiterpenoids Lactones: Benefits to Plants and People
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.2022.113130zenodo-depositor-declared
Bioactive terpenoids derived from plant endophytic fungi: An updated review (2011–2020)
inferred← citeshttps://doi.org/10.1002/ange.202108970openalex-snapshot
Biosynthesis of Fungal Drimane‐Type Sesquiterpene Esters
inferred← citeshttps://doi.org/10.1002/anie.202108970openalex-snapshot
Biosynthesis of Fungal Drimane‐Type Sesquiterpene Esters
inferred← citeshttps://doi.org/10.1002/ejoc.202001409openalex-snapshot
Phase‐Transfer Catalytic Strategy: Rapid Synthesis of Spiro‐Fused Heterocycles, Integrated with Four Pharmacophores‐Succinimide, Pyrrolidine, Oxindole, and Trifluoromethyl Group
inferred← citeshttps://doi.org/10.1002/ejoc.202400983openalex-snapshot
Recent Advances in Sustainable Total Synthesis and Chiral Pool Strategies with Emphasis on (−)‐Sclareol in Natural Products Synthesis
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/s00253-021-11312-zopenalex-snapshot
Peculiarities of meroterpenoids and their bioproduction
inferred← citeshttps://doi.org/10.1007/s00253-021-11554-xopenalex-snapshot
Biotransformation ability of endophytic fungi: from species evolution to industrial applications
inferred← citeshttps://doi.org/10.1007/s13659-024-00480-wopenalex-snapshot
Quadriliterpenoids A − I, nine new 4,4-dimethylergostane and oleanane triterpenoids from Aspergillus quadrilineatus with immunosuppressive inhibitory activity
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/10.1016/j.crphar.2021.100050openalex-snapshot
Endophytic fungi: A treasure trove of novel anticancer compounds
inferred← citeshttps://doi.org/10.1016/j.phytochem.2023.113958openalex-snapshot
Salvirrane A-F, six undescribed nordrimane sesquiterpene derivatives from Salvia castanea Diels f. tomentosa Stib and their cytotoxic activities
inferred← citeshttps://doi.org/10.1016/j.phytochem.2025.114744openalex-snapshot
Polyketides and drimane sesquiterpenoids from kiwi plant endophytic fungus Aspergillus flavus J302-03 with antibacterial and anti-inflammatory activities
inferred← citeshttps://doi.org/10.1016/j.phytol.2021.03.019openalex-snapshot
New azaphthalide and phthalide derivatives from the marine coral-derived fungus Aspergillus sp. SCSIO41405
inferred← citeshttps://doi.org/10.1016/j.steroids.2025.109629openalex-snapshot
New secondary metabolites from the soil-derived Aspergillus versicolor QC812
inferred← citeshttps://doi.org/10.1016/j.tet.2021.132599openalex-snapshot
Nigerin and ochracenes J−L, new sesquiterpenoids from the marine sponge symbiotic fungus Aspergillus niger
inferred← citeshttps://doi.org/10.1021/acs.jafc.4c04989openalex-snapshot
Genomic and Untargeted Metabolomic Analysis of Secondary Metabolites in the Streptomyces griseoaurantiacus Strain MH191 Shows Media-Based Dependency for the Production of Bioactive Compounds with Potential Antifungal Activity
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.3c00215openalex-snapshot
Astellolides R–W, Drimane-Type Sesquiterpenoids from an Aspergillus parasiticus Strain Associated with an Isopod
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.5c00431openalex-snapshot
Spinulactones A–F: Bioactive Drimane-Type Sesquiterpenes from the Endophytic Penicillium spinulosum 9-1
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/d4ra06721eopenalex-snapshot
Drimane-type sesquiterpenoids and triterpenoids from the whole plant of Limonium sinense with their antiproliferative and anti-inflammatory activities
inferred← citeshttps://doi.org/10.1080/10286020.2023.2230895openalex-snapshot
Two new quinazoline alkaloids produced by Aspergillus versicolor and their antimicrobial activities
inferred← citeshttps://doi.org/10.1080/14786419.2025.2487687openalex-snapshot
A new insecticidal sesquiterpene from a mangrove endophytic fungus Aspergillus strain sp. GXNU R1
inferred← citeshttps://doi.org/10.1080/14786419.2026.2666669openalex-snapshot
A new sesquiterpene and two new benzoic derivatives from the marine-derived fungus Aspergillus versicolour SCSIO41697
inferred← citeshttps://doi.org/10.1111/jam.15489openalex-snapshot
The endophytic Aspergillus strains: A bountiful source of natural products
inferred← citeshttps://doi.org/10.3390/agriculture10110533openalex-snapshot
Biodiversity, Ecology, and Secondary Metabolites Production of Endophytic Fungi Associated with Amaryllidaceae Crops
inferred← citeshttps://doi.org/10.3390/ijms231911935openalex-snapshot
Diversity and Biological Activities of Endophytic Fungi from the Flowers of the Medicinal Plant Vernonia anthelmintica
inferred← citeshttps://doi.org/10.3390/ijms241311184openalex-snapshot
Fungal BGCs for Production of Secondary Metabolites: Main Types, Central Roles in Strain Improvement, and Regulation According to the Piano Principle
inferred← citeshttps://doi.org/10.3390/molecules28114381openalex-snapshot
Natural Bacterial and Fungal Peptides as a Promising Treatment to Defeat Lung Cancer Cells
inferred← citeshttps://doi.org/10.3390/molecules31040645openalex-snapshot
Drimane Sesquiterpenes Isolated from the Fruiting Body of the Clavarioid Fungus Ramaria botrytoides
inferred← citeshttps://doi.org/10.64187/mm.2026.v2.i2.004openalex-snapshot
Research Progress on Natural Products from the Fungus Aspergillus versicolor
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.