On the public citation graph

Aspochalasins I, J, and K: Three New Cytotoxic Cytochalasans of Aspergillus flavipes from the Rhizosphere of Ericameria laricifolia of the Sonoran Desert

0 signed · 87 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 See whether every reference in this work resolves to a known work and none has been retracted — and get a dated CiteStamped badge you can embed.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/mrc.1260310315openalex-snapshot

Gradient selection in inverse heteronuclear correlation spectroscopy

inferredcites →https://doi.org/10.1016/s0006-2952(96)00389-9openalex-snapshot

Altered actin polymerization dynamics in various malignant cell types: evidence for differential sensitivity to cytochalasin B

inferredcites →https://doi.org/10.1016/s0040-4020(01)85632-5openalex-snapshot

Two new cytotoxic cytochalasins from Xylaria obovata

inferredcites →https://doi.org/10.1093/jnci/82.13.1113openalex-snapshot

Comparison of In Vitro Anticancer-Drug-Screening Data Generated With a Tetrazolium Assay Versus a Protein Assay Against a Diverse Panel of Human Tumor Cell Lines

inferredcites →https://doi.org/10.1093/jnci/82.13.1118openalex-snapshot

Two-Year Carcinogenicity Study of Sodium Fluoride in Rats

inferredcites →https://doi.org/10.7164/antibiotics.50.919openalex-snapshot

Two New Components of the Aspochalasins Produced by Aspergillus sp.

inferredcites →https://doi.org/10.7164/antibiotics.54.379openalex-snapshot

Selective Cytotoxicity and Stereochemistry of Aspochalasin D.

inferredcites →https://doi.org/10.7164/antibiotics.55.666openalex-snapshot

Structure of Aspochalasin H, a New Member of the Aspochalasin Family.

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.2022.113264zenodo-depositor-declared

Undescribed diphenyl ethers betaethrins A-I from a desert plant endophytic strain of the fungus Phoma betae A.B. Frank (Didymellaceae)

inferred← citeshttps://doi.org/10.1002/9781118260005.ch1openalex-snapshot

Natural Products in Drug Discovery: Recent Advances

inferred← citeshttps://doi.org/10.1002/ejoc.200801085openalex-snapshot

Spicochalasin A and New Aspochalasins from the Marine‐Derived Fungus Spicaria elegans

inferred← citeshttps://doi.org/10.1002/ejoc.201200053openalex-snapshot

Trichoderones A and B: Two Pentacyclic Cytochalasans from the Plant Endophytic Fungus Trichoderma gamsii

inferred← citeshttps://doi.org/10.1002/ejoc.201403678openalex-snapshot

Armochaetoglobins K–R, Anti‐HIV Pyrrole‐Based Cytochalasans from Chaetomium globosum TW1‐1

inferred← citeshttps://doi.org/10.1002/jms.3922openalex-snapshot

Biosynthesis and mass spectral fragmentation pathways of 13C and 15N labeled cytochalasin D produced by Xylaria arbuscula

inferred← citeshttps://doi.org/10.1007/978-3-030-59444-2_1openalex-snapshot

Progress in the Chemistry of Cytochalasans

inferred← citeshttps://doi.org/10.1007/978-981-16-4497-9_8openalex-snapshot

Genetic Basis of Fungal Endophytic Bioactive Compounds Synthesis, Modulation, and Their Biotechnological Application

inferred← citeshttps://doi.org/10.1007/978-981-16-4907-3_15openalex-snapshot

Biotechnological Application of Extremophilic Fungi

inferred← citeshttps://doi.org/10.1007/978-981-99-5696-8_16openalex-snapshot

Uncovering the Desert Fungal Enigma: An Attractive Resource for Biopharmaceuticals

inferred← citeshttps://doi.org/10.1007/s00253-020-10399-0openalex-snapshot

Fungi from the extremes of life: an untapped treasure for bioactive compounds

inferred← citeshttps://doi.org/10.1007/s00253-023-12501-8openalex-snapshot

Enhanced production of aspochalasin D through genetic engineering of Aspergillus flavipes

inferred← citeshttps://doi.org/10.1007/s00253-024-13338-5openalex-snapshot

Biotechnological potential of salt tolerant and xerophilic species of Aspergillus

inferred← citeshttps://doi.org/10.1007/s10600-017-2102-4openalex-snapshot

Cytochalasins from the Gorgonian-Derived Fungus Aspergillus sp. XS-2009-0B15

inferred← citeshttps://doi.org/10.1007/s11101-009-9123-yopenalex-snapshot

Nature: a vital source of leads for anticancer drug development

inferred← citeshttps://doi.org/10.1016/b978-0-12-374194-3.00008-1openalex-snapshot

Natural Products as Pharmaceuticals and Sources for Lead Structures

inferred← citeshttps://doi.org/10.1016/b978-0-444-63601-0.00005-3openalex-snapshot

Bioactive Secondary Metabolites From Endophytic Fungi

inferred← citeshttps://doi.org/10.1016/b978-008045382-8.00057-5openalex-snapshot

Nature as Source of Medicines; Novel Drugs from Nature; Screening for Antitumor Activity

inferred← citeshttps://doi.org/10.1016/j.bbagen.2013.02.008openalex-snapshot

Natural products: A continuing source of novel drug leads

inferred← citeshttps://doi.org/10.1016/j.bioorg.2019.103167openalex-snapshot

Iizukines C−E from a saline soil fungus Aspergillus iizukae

inferred← citeshttps://doi.org/10.1016/j.biotechadv.2019.107462openalex-snapshot

A critical review on exploiting the pharmaceutical potential of plant endophytic fungi

inferred← citeshttps://doi.org/10.1016/j.fitote.2014.03.021openalex-snapshot

New phenyl derivatives from endophytic fungus Aspergillus flavipes AIL8 derived of mangrove plant Acanthus ilicifolius

inferred← citeshttps://doi.org/10.1016/j.fitote.2020.104722openalex-snapshot

1-Isoindolinone scaffold-based natural products with a promising diverse bioactivity

inferred← citeshttps://doi.org/10.1016/j.phytol.2019.05.002openalex-snapshot

Two new cytochalasans from the marine sediment-derived fungus Westerdykella dispersa and their antibacterial activities

inferred← citeshttps://doi.org/10.1016/j.tet.2020.131475openalex-snapshot

Phomopsisins A–C: Three new cytochalasans from the plant endophytic fungus Phomopsis sp. sh917

inferred← citeshttps://doi.org/10.1016/j.tetlet.2014.04.027openalex-snapshot

Facile synthesis of 3H,3′H-spiro[benzofuran-2,1′-isoindole]-3,3′-diones using monobromomalononitrile (MBM) as an efficient organo-brominating agent

inferred← citeshttps://doi.org/10.1016/j.tetlet.2014.06.064openalex-snapshot

Synthesis of different isoindolone embedded heterocycles with phenolic subunits from a common intermediate, 3-(2′-hydroxyaroyl)-2,3-dihydroisoindol-1-ones

inferred← citeshttps://doi.org/10.1016/j.tetlet.2015.12.099openalex-snapshot

Flaviphenalenones A–C, three new phenalenone derivatives from the fungus Aspergillus flavipes PJ03-11

inferred← citeshttps://doi.org/10.1016/j.tetlet.2017.04.071openalex-snapshot

Aspochalazine A, a novel polycyclic aspochalasin from the fungus Aspergillus sp. Z4

inferred← citeshttps://doi.org/10.1016/j.tetlet.2018.03.077openalex-snapshot

Cytotoxic cytochalasans from Aspergillus flavipes PJ03-11 by OSMAC method

inferred← citeshttps://doi.org/10.1016/j.tetlet.2021.153207openalex-snapshot

New cytochalasan alkaloids and cyclobutane dimer from an endophytic fungus Cytospora chrysosperma in Hippophae rhamnoides and their antimicrobial activities

inferred← citeshttps://doi.org/10.1021/acs.joc.1c00425openalex-snapshot

Bisaspochalasins D and E: Two Heterocycle-Fused Cytochalasan Homodimers from an Endophytic Aspergillus flavipes

inferred← citeshttps://doi.org/10.1021/acs.joc.9b00440openalex-snapshot

Amiaspochalasins A–H, Undescribed Aspochalasins with a C-21 Ester Carbonyl from Aspergillus micronesiensis

inferred← citeshttps://doi.org/10.1021/acs.orglett.0c02860openalex-snapshot

Bisaspochalasins A–C: Three Cytochalasan Homodimers with Highly Fused Ring System from an Endophytic Aspergillus flavipes

inferred← citeshttps://doi.org/10.1021/acscatal.9b05608openalex-snapshot

Organocatalyzed Kinetic Resolution of α-Functionalized Ketones: The Malonate Unit Leads the Way

inferred← citeshttps://doi.org/10.1021/acsomega.2c00544openalex-snapshot

Insights into the Chemical Diversity of Selected Fungi from the Tza Itzá Cenote of the Yucatan Peninsula

inferred← citeshttps://doi.org/10.1021/cr900019jopenalex-snapshot

Impact of Natural Products on Developing New Anti-Cancer Agents

inferred← citeshttps://doi.org/10.1021/np058128nopenalex-snapshot

Natural Products from Plant-Associated Microorganisms: Distribution, Structural Diversity, Bioactivity, and Implications of Their Occurrence

inferred← citeshttps://doi.org/10.1021/np200958ropenalex-snapshot

Aflaquinolones A–G: Secondary Metabolites from Marine and Fungicolous Isolates of Aspergillus spp.

inferred← citeshttps://doi.org/10.1021/np500324bopenalex-snapshot

γ-Butyrolactone, Cytochalasin, Cyclic Carbonate, Eutypinic Acid, and Phenalenone Derivatives from the Soil Fungus Aspergillus sp. PSU-RSPG185

inferred← citeshttps://doi.org/10.1038/ja.2005.34openalex-snapshot

A Novel Aspochalasin with HIV-1 Integrase Inhibitory Activity from Aspergillus flavipes

inferred← citeshttps://doi.org/10.1038/ja.2011.124openalex-snapshot

Cytochalasans with different amino-acid origin from the plant endophytic fungus Trichoderma gamsii

inferred← citeshttps://doi.org/10.1038/ja.2011.97openalex-snapshot

Aspochalasin U, a moderate TNF-α inhibitor from Aspergillus sp.

inferred← citeshttps://doi.org/10.1038/s41598-026-39382-xopenalex-snapshot

Diversity of specialized metabolites in Phaeoacremonium species revealed by untargeted metabolomics and bioactivity assays

inferred← citeshttps://doi.org/10.1038/srep18711openalex-snapshot

Nine new cytochalasan alkaloids from Chaetomium globosum TW1-1 (Ascomycota, Sordariales)

inferred← citeshttps://doi.org/10.1038/srep42434openalex-snapshot

Flavichalasines A–M, cytochalasan alkaloids from Aspergillus flavipes

inferred← citeshttps://doi.org/10.1039/b413523gopenalex-snapshot

Equisetin biosynthesis in Fusarium heterosporum

inferred← citeshttps://doi.org/10.1039/b903913aopenalex-snapshot

The chemistry and biology of cytochalasans

inferred← citeshttps://doi.org/10.1039/c4np00144copenalex-snapshot

Marine natural products

inferred← citeshttps://doi.org/10.1039/np9900700269openalex-snapshot

Marine natural products

inferred← citeshttps://doi.org/10.1080/08927014.2020.1864343openalex-snapshot

Marine natural products as antifouling molecules – a mini-review (2014–2020)

inferred← citeshttps://doi.org/10.1080/10286020.2024.2311150openalex-snapshot

A gene cluster encoding a nonribosomal peptide synthetase-like enzyme catalyzes γ-aromatic butenolides

inferred← citeshttps://doi.org/10.1080/14786419.2014.902945openalex-snapshot

A new cyclopeptide metabolite of marine gut fungus from Ligia oceanica

inferred← citeshttps://doi.org/10.1080/14786419.2015.1136910openalex-snapshot

Induced production of cytochalasans in co-culture of marine fungus Aspergillus flavipes and actinomycete Streptomyces sp.

inferred← citeshttps://doi.org/10.1080/14786419.2025.2566463openalex-snapshot

Antifungal cytochalasans from the co-culture of two endophytic fungi Aspergillus spelaeus and Xylaria sp

inferred← citeshttps://doi.org/10.1099/mgen.0.001658openalex-snapshot

Genomic features and the transcriptional regulation of secondary metabolite biosynthesis of endophytic fungus Xylaria sp. VDL4 isolated from Vaccinium dunalianum

inferred← citeshttps://doi.org/10.1186/s13065-019-0624-5openalex-snapshot

Secondary metabolites from the Aspergillus sp. in the rhizosphere soil of Phoenix dactylifera (Palm tree)

inferred← citeshttps://doi.org/10.1186/s13568-016-0272-2openalex-snapshot

Antifouling phenyl ethers and other compounds from the invertebrates and their symbiotic fungi collected from the South China Sea

inferred← citeshttps://doi.org/10.1201/b13868-5openalex-snapshot

Bioactive Secondary Metabolites from Marine-Derived Fungi

inferred← citeshttps://doi.org/10.1371/journal.pone.0144304openalex-snapshot

Transcriptional and Proteomic Profiling of Aspergillus flavipes in Response to Sulfur Starvation

inferred← citeshttps://doi.org/10.2478/acph-2013-0040openalex-snapshot

Lipid-based systems as a promising approach for enhancing the bioavailability of poorly water-soluble drugs

inferred← citeshttps://doi.org/10.3390/md11062054openalex-snapshot

Bioactive Phenylalanine Derivatives and Cytochalasins from the Soft Coral-Derived Fungus, Aspergillus elegans

inferred← citeshttps://doi.org/10.3390/md12105124openalex-snapshot

Methylthio-Aspochalasins from a Marine-Derived Fungus Aspergillus sp.

inferred← citeshttps://doi.org/10.3390/md13010237openalex-snapshot

New Meroterpenoids from the Endophytic Fungus Aspergillus flavipes AIL8 Derived from the Mangrove Plant Acanthus ilicifolius

inferred← citeshttps://doi.org/10.3390/md16100343openalex-snapshot

Two Novel Aspochalasins from the Gut Fungus Aspergillus sp. Z4

inferred← citeshttps://doi.org/10.3390/md17080483openalex-snapshot

Secondary Metabolites with α-Glucosidase Inhibitory Activity from the Mangrove Fungus Mycosphaerella sp. SYSU-DZG01

inferred← citeshttps://doi.org/10.3390/md23070285openalex-snapshot

Discovery of Secondary Metabolites from the Sponge-Derived Fungus Aspergillus templicola

inferred← citeshttps://doi.org/10.3390/md9040561openalex-snapshot

Phylogenetic Identification of Fungi Isolated from the Marine Sponge Tethya aurantium and Identification of Their Secondary Metabolites

inferred← citeshttps://doi.org/10.3390/molecules171214091openalex-snapshot

Isolation, Identification and Antimicrobial Activities of Two Secondary Metabolites of Talaromyces verruculosus

inferred← citeshttps://doi.org/10.3390/molecules19079786openalex-snapshot

Isolation, Structural Analyses and Biological Activity Assays against Chronic Lymphocytic Leukemia of Two Novel Cytochalasins — Sclerotionigrin A and B

inferred← citeshttps://doi.org/10.3390/molecules26113227openalex-snapshot

Species Diversity and Secondary Metabolites of Sarcophyton-Associated Marine Fungi

inferred← citeshttps://doi.org/10.3762/bjoc.9.243openalex-snapshot

The chemistry of isoindole natural products

inferred← citeshttps://doi.org/10.3852/14-059openalex-snapshot

Revision of Aspergillus section Flavipedes : seven new species and proposal of section Jani sect. nov.

inferred← citeshttps://doi.org/10.4014/jmb.0806.389openalex-snapshot

Aspochalasin I, a Melanogenesis Inhibitor from Aspergillus sp.

inferred← citeshttps://doi.org/10.70675/87adaea7z1f12z4553za4f1z65a3b2079c89openalex-snapshot

Exploration de la chimiodiversité d'un Penicillium restrictum d'origine marine par approches métabolomique et lipidomique

inferred← citeshttps://doi.org/10.7164/antibiotics.57.341openalex-snapshot

A New Anthraquinone and Cytotoxic Curvularins of a Penicillium sp. from the Rhizosphere of Fallugia paradoxa of the Sonoran Desert

inferred← citeshttps://doi.org/10.7164/antibiotics.57.541openalex-snapshot

Isolation, Optimization of Production and Structure-Activity Relationship Studies of Monocillin I, the Cytotoxic Constituent of Paraphaeosphaeria quadriseptata

inferred← citeshttps://doi.org/10.7164/antibiotics.57.707openalex-snapshot

Aspochalamins A-D and Aspochalasin Z Produced by the Endosymbiotic Fungus Aspergillus niveus LU 9575: I. Taxonomy, Fermentation, Isolation and Biological Activities

inferred← citeshttps://doi.org/10.7164/antibiotics.57.715openalex-snapshot

Aspochalamins A-D and Aspochalasin Z Produced by the Endosymbiotic Fungus Aspergillus niveus LU 9575: II. Structure Elucidation

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.