On the public citation graph

Cytotoxic Ergosteroids from a Strain of the Fungus Talaromyces adpressus

0 signed · 42 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 See whether every reference in this work resolves to a known work and none has been retracted — and get a dated CiteStamped badge you can embed.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/10.1002/cbdv.201200415openalex-snapshot
Two New Steroids from an Endophytic Fungus Phomopsis sp.
inferredcites →https://doi.org/10.1002/chir.20733openalex-snapshot
ECD cotton effect approximated by the Gaussian curve and other methods
inferredcites →https://doi.org/10.1002/wcms.81openalex-snapshot
The ORCA program system
inferredcites →https://doi.org/10.1007/s13659-012-0058-4openalex-snapshot
Six novel steroids from culture of basidiomycete Polyporus ellisii
inferredcites →https://doi.org/10.1016/0031-9422(94)00740-kopenalex-snapshot
Two steroids from Calvatia cyathiformis
inferredcites →https://doi.org/10.1016/0031-9422(94)85028-3openalex-snapshot
Steroids from Calvatia cyathiformis
inferredcites →https://doi.org/10.1016/j.bioorg.2019.103011openalex-snapshot
Strophasterols E and F: Rearranged ergostane-type sterols from Pleurotus eryngii
inferredcites →https://doi.org/10.1016/j.phytochem.2020.112374openalex-snapshot
Structurally diverse and bioactive alkaloids from an insect-derived fungus Neosartorya fischeri
inferredcites →https://doi.org/10.1016/j.phytochem.2021.112816openalex-snapshot
Five undescribed steroids from Talaromyces stipitatus and their cytotoxic activities against hepatoma cell lines
inferredcites →https://doi.org/10.1016/j.phytochem.2021.112910openalex-snapshot
Spectanoids A−H: Eight undescribed sesterterpenoids from Aspergillus spectabilis
inferredcites →https://doi.org/10.1016/j.phytol.2018.04.005openalex-snapshot
Polyoxygenated ergosteroids from the macrofungus Omphalia lapidescens and the structure-cytotoxicity relationship in a human gastric cancer cell line
inferredcites →https://doi.org/10.1016/j.phytol.2019.02.007openalex-snapshot
Cytotoxic ergosteroids from the fungus Stereum hirsutum
inferredcites →https://doi.org/10.1016/j.tetlet.2020.151737openalex-snapshot
Four new ergostane-type steroids from Lasiodiplodia pseudotheobromae
inferredcites →https://doi.org/10.1021/acs.orglett.6b03557openalex-snapshot
Phomopsterones A and B, Two Functionalized Ergostane-Type Steroids from the Endophytic Fungus Phomopsis sp. TJ507A
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/ja01022a027openalex-snapshot
Pyridine-induced solvent shifts in the nuclear magnetic resonance spectra of hydroxylic compounds
inferredcites →https://doi.org/10.1021/np070165mopenalex-snapshot
Variation in Cytostatic Constituents of a Sponge-Derived Gymnascella dankaliensis by Manipulating the Carbon Source
inferredcites →https://doi.org/10.1021/ol5030579openalex-snapshot
Bioactive Acylphloroglucinols with Adamantyl Skeleton from Hypericum sampsonii
inferredcites →https://doi.org/10.1039/c8ob02325eopenalex-snapshot
Rearranged ergostane-type natural products: chemistry, biology, and medicinal aspects
inferredcites →https://doi.org/10.1107/s0021889811043202openalex-snapshot
ShelXle : a Qt graphical user interface for SHELXL
inferredcites →https://doi.org/10.1271/bbb.100918openalex-snapshot
Ganodermasides C and D, Two New Anti-Aging Ergosterols from Spores of the Medicinal MushroomGanoderma lucidum
inferredcites →https://doi.org/10.3390/md16050150openalex-snapshot
Two New Terpenoids from Talaromyces purpurogenus

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.4647946openalex-extracted
inferred← citeshttps://doi.org/10.1007/s11596-024-2922-yopenalex-snapshot
Michael Acceptor Pyrrolidone Derivatives and Their Activity against Diffuse Large B-cell Lymphoma
inferred← citeshttps://doi.org/10.1016/j.bioorg.2023.107025openalex-snapshot
Penicimides A and B, two novel diels–alder [4 + 2] cycloaddition ergosteroids from Penicillium herquei
inferred← citeshttps://doi.org/10.1016/j.bioorg.2024.107280openalex-snapshot
New diarylcyclopentenone enantiomers and biphenyl derivatives from the fungus Talaromyces adpressus
inferred← citeshttps://doi.org/10.1016/j.cclet.2026.112771openalex-snapshot
Discovery of α-pyrone heteropolymers with immunosuppressive targeting PKCθ from the fungus Talaromyces adpressus
inferred← citeshttps://doi.org/10.1016/j.ejmech.2026.119074openalex-snapshot
Anticancer natural products derived from fungi: A review of promising lead compounds
inferred← citeshttps://doi.org/10.1016/j.fitote.2025.106537openalex-snapshot
Microascusteroids A and B, two 5,6-seco-9,10-seco steroids with a C-ring rearranged ergostane skeleton from the marine-derived fungus Microascus sp. SCSIO 41821
inferred← citeshttps://doi.org/10.1016/j.indcrop.2025.120507openalex-snapshot
Caesalactones A-I, rare 8,15-seco-ent-kaurane diterpenoids from the leaves and stems of Caesalpinia enneaphylla with cytotoxic activities
inferred← citeshttps://doi.org/10.1016/j.phytochem.2024.114303openalex-snapshot
Bipolaristeroid A, a 5,6-seco-9,10-seco-steroid with cytotoxic activity from the fungus Bipolaris maydis
inferred← citeshttps://doi.org/10.1016/j.phytochem.2026.114816openalex-snapshot
Seven undescribed metabolites from Ganoderma lucidum-derived endophytic Talaromyces sp. GLQ04 and their anti-DLBCL (diffuse large B-cell lymphoma) activities
inferred← citeshttps://doi.org/10.1016/j.phytochem.2026.114952openalex-snapshot
Antimicrobial specialized metabolites from the marine coral-derived fungus Talaromyces variabilis
inferred← citeshttps://doi.org/10.1016/j.phytochem.2026.114977openalex-snapshot
Immunosuppressive ergosterol-emodin hybrids from the endophytic Penicillium sp. XB152
inferred← citeshttps://doi.org/10.1016/j.tet.2025.135031openalex-snapshot
Talapolyketide A-E, polyketone derivatives from the marine-derived fungus Talaromyces sp. 6B3
inferred← citeshttps://doi.org/10.1016/s1875-5364(25)60928-9openalex-snapshot
(±)-Talapyrones A−F: six pairs of dimeric polyketide enantiomers with unusual 6/6/6 and 6/6/6/5 ring systems from Talaromyces adpressus
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.4c00742openalex-snapshot
Talauromides A–G, Nitrogen-Containing Heptacyclic Oligophenalenone Dimers from the Soil Fungus Talaromyces stipitatus BMC-16
inferred← citeshttps://doi.org/10.1039/d4qo02057jopenalex-snapshot
Bipolarsterol A, a steroid with an unprecedented 6/5/6/5 carbon skeleton from the phytopathogenic fungus Bipolaris oryzae
inferred← citeshttps://doi.org/10.1080/21501203.2024.2354302openalex-snapshot
New bioactive secondary metabolites from fungi: 2023
inferred← citeshttps://doi.org/10.1186/s40643-025-00864-xopenalex-snapshot
Uncovering a novel biosynthetic gene cluster for sordarin through genome mining in the fungus Talaromyces adpressus
inferred← citeshttps://doi.org/10.2139/ssrn.5465443openalex-snapshot
Antimicrobial and Antioxidative Secondary Metabolites from the Marine Coral-Derived Fungus Talaromyces variabilis
inferred← citeshttps://doi.org/10.3390/md22060237openalex-snapshot
New Secondary Metabolites from Marine-Derived Fungus Talaromyces minnesotensis BTBU20220184
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.