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Bisaspochalasins A–C: Three Cytochalasan Homodimers with Highly Fused Ring System from an Endophytic Aspergillus flavipes
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/ange.201808481openalex-snapshot
Total Synthesis of Asperchalasines A, D, E, and H
inferredcites →https://doi.org/10.1002/anie.199604771openalex-snapshot
The Schenck Ene Reaction: Diastereoselective Oxyfunctionalization with Singlet Oxygen in Synthetic Applications
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.201511315openalex-snapshot
Epicochalasines A and B: Two Bioactive Merocytochalasans Bearing Caged Epicoccine Dimer Units from Aspergillus flavipes
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.201808249openalex-snapshot
Total Syntheses of Asperchalasines A–E
inferredcites →https://doi.org/10.1002/anie.201808481openalex-snapshot
Total Synthesis of Asperchalasines A, D, E, and H
inferredcites →https://doi.org/10.1002/hlca.19790620516openalex-snapshot
Stoffwechselprodukte von Mikroorganismen. 186. Mitteilung. Über die Aspochalasine A, B, C und D
inferredcites →https://doi.org/10.1016/j.bioorg.2018.10.020openalex-snapshot
Antibacterial activity against drug-resistant microbial pathogens of cytochalasan alkaloids from the arthropod-associated fungus Chaetomium globosum TW1-1
inferredcites →https://doi.org/10.1016/j.cclet.2010.02.019openalex-snapshot
Three new aspochalasin derivatives from the marine-derived fungus Spicaria elegans
inferredcites →https://doi.org/10.1016/j.fitote.2019.104278openalex-snapshot
Cytotoxic cytochalasans from fungus Xylaria longipes
inferredcites →https://doi.org/10.1016/s1875-5364(19)30121-9openalex-snapshot
Cangumycins A–F, six new angucyclinone analogues with immunosuppressive activity from Streptomyces
inferredcites →https://doi.org/10.1021/acs.chemrev.6b00697openalex-snapshot
Enzymatic Carbon–Sulfur Bond Formation in Natural Product Biosynthesis
inferredcites →https://doi.org/10.1021/acs.jafc.9b00273openalex-snapshot
Cytochalasins and an Abietane-Type Diterpenoid with Allelopathic Activities from the Endophytic Fungus Xylaria Species
inferredcites →https://doi.org/10.1021/acs.jnatprod.6b00697openalex-snapshot
Monoterpenoid Indole Alkaloids from Kopsia officinalis and the Immunosuppressive Activity of Rhazinilam
inferredcites →https://doi.org/10.1021/acs.joc.9b02968openalex-snapshot
Total Synthesis of Rhodonoids A, B, E, and F, Enabled by Singlet Oxygen Ene Reactions
inferredcites →https://doi.org/10.1021/acs.orglett.0c00141openalex-snapshot
Dimericchalasine A and Amichalasines D and E: Unexpected Cytochalasan Homodimer and Heterotrimers from Aspergillus micronesiensis PG-1
inferredcites →https://doi.org/10.1021/acs.orglett.5b02123openalex-snapshot
Pericoannosin A, a Polyketide Synthase–Nonribosomal Peptide Synthetase Hybrid Metabolite with New Carbon Skeleton from the Endophytic Fungus Periconia sp.
inferredcites →https://doi.org/10.1021/acs.orglett.7b02146openalex-snapshot
Aspergilasines A–D: Four Merocytochalasans with New Carbon Skeletons from Aspergillus flavipes QCS12
inferredcites →https://doi.org/10.1021/acs.orglett.8b02942openalex-snapshot
Cytochathiazines A–C: Three Merocytochalasans with a 2 H -1,4-Thiazine Functionality from Coculture of Chaetomium globosum and Aspergillus flavipes
inferredcites →https://doi.org/10.1021/acs.orglett.8b04066openalex-snapshot
Amichalasines A–C: Three Cytochalasan Heterotrimers from Aspergillus micronesiensis PG-1
inferredcites →https://doi.org/10.1021/acs.orglett.8b04129openalex-snapshot
Intramolecular Diels–Alder Cycloaddition Approach toward the cis-Fused Δ5,6-Hexahydroisoindol-1-one Core of Cytochalasins
inferredcites →https://doi.org/10.1021/acs.orglett.9b01065openalex-snapshot
Chamiside A, a Cytochalasan with a Tricyclic Core Skeleton from the Endophytic Fungus Chaetomium nigricolor F5
inferredcites →https://doi.org/10.1021/acs.orglett.9b01344openalex-snapshot
Targeted Gene Inactivations Expose Silent Cytochalasans in Magnaporthe grisea NI980
inferredcites →https://doi.org/10.1021/acs.orglett.9b02552openalex-snapshot
Xylarichalasin A, a Halogenated Hexacyclic Cytochalasan from the Fungus Xylaria cf. curta
inferredcites →https://doi.org/10.1021/acs.orglett.9b03372openalex-snapshot
Investigating the Function of Cryptic Cytochalasan Cytochrome P450 Monooxygenases Using Combinatorial Biosynthesis
inferredcites →https://doi.org/10.1021/cr60321a001openalex-snapshot
The reaction of singlet oxygen with olefins: the question of mechanism
inferredcites →https://doi.org/10.1021/ja072884topenalex-snapshot
Molecular Basis of Cytochalasan Biosynthesis in Fungi: Gene Cluster Analysis and Evidence for the Involvement of a PKS-NRPS Hybrid Synthase by RNA Silencing
inferredcites →https://doi.org/10.1021/ja402828wopenalex-snapshot
Combinatorial Generation of Complexity by Redox Enzymes in the Chaetoglobosin A Biosynthesis
inferredcites →https://doi.org/10.1021/np030353mopenalex-snapshot
Aspochalasins I, J, and K: Three New Cytotoxic Cytochalasans of Aspergillus flavipes from the Rhizosphere of Ericameria laricifolia of the Sonoran Desert
inferredcites →https://doi.org/10.1021/ol503666bopenalex-snapshot
Armochaeglobines A and B, Two New Indole-Based Alkaloids from the Arthropod-Derived Fungus Chaetomium globosum
inferredcites →https://doi.org/10.1039/b903913aopenalex-snapshot
The chemistry and biology of cytochalasans
inferredcites →https://doi.org/10.1039/c8qo01107aopenalex-snapshot
Naphthomycin-derived macrolactams with two new carbon skeletons from endophytic Streptomyces
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.2021.112952zenodo-depositor-declared
Asporychalasin, a bioactive cytochalasan with an unprecedented 6/6/11 skeleton from the Red Sea sediment Aspergillus oryzae
inferred← citeshttps://doi.org/10.1002/cbdv.202400794openalex-snapshot
Chemical Diversity, Pharmacology, Synthesis and Detection of Naturally Occurring Peroxides
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/s13659-025-00572-1openalex-snapshot
Harziachalasins A–G, polycyclic-fused cytochalasins from the endophytic fungus Trichoderma harzianum MLJ-4 with HIV latency reversal activity
inferred← citeshttps://doi.org/10.1007/s13659-026-00618-yopenalex-snapshot
Four new Cyclohexenone with antibacterial activity from the coral-derived fungus Aspergillus flavus
inferred← citeshttps://doi.org/10.1016/j.cclet.2022.03.063openalex-snapshot
Thiocytochalasins A−D, four sulfur-containing cytochalasans from an endophytic fungus Phoma multirostrata XJ-2-1
inferred← citeshttps://doi.org/10.1016/j.fitote.2026.107207openalex-snapshot
Aspochalaflavins A and B: Two Cytochalasans decorated with a 2,2-dimethyl-2,5-dihydrooxazole moiety from an endophytic Aspergillus flavipes
inferred← citeshttps://doi.org/10.1021/acs.jafc.4c09395openalex-snapshot
Antibacterial and Cytotoxic Methylthioether-Containing Cytochalasins from Chaetomium globosum AS-506, an Endozoic Fungus Associated with Deep-Sea Sponge of Magellan Seamounts
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.4c00489openalex-snapshot
Sucurchalasins A and B, Sulfur-Containing Heterodimers of a Cytochalasan and a Macrolide from the Endophytic Fungus Aspergillus spelaeus GDGJ-286
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.6c00375openalex-snapshot
Polycyclic-Fused Cytochalasins with Anti-Liver Fibrosis Activity Produced by the Endophytic Fungus Trichoderma harzianum
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.2c02983openalex-snapshot
Cytochalasans with Inhibitory Activity against NPC1L1 from the Endophytic Fungus Chaetomium nigricolor F5
inferred← citeshttps://doi.org/10.1021/acs.joc.3c01515openalex-snapshot
Boerelasins A–D, Four Unprecedented Cytochalasins from the Endophytic Fungus Boeremia Exigua
inferred← citeshttps://doi.org/10.1021/acs.orglett.6c00352openalex-snapshot
Bioinspired Synthesis of Curtachalasin A and Δ 6,12 -Curtachalasin N Enabled by Tandem Transannular Epoxyalkene Cyclization and α-Ketol Rearrangement
inferred← citeshttps://doi.org/10.1021/acs.orglett.6c03240openalex-snapshot
Boereguasins A–D, Cytochalasins from Boeremia exigua with Differential MAPK/NF-κB Inhibition
inferred← citeshttps://doi.org/10.1039/d2qo00309kopenalex-snapshot
Asperflavipines C–E and aspermichalasine A: three cytochalasan heterotetramers and an unusual cytochalasan monomer from Aspergillus micronesiensis
inferred← citeshttps://doi.org/10.1039/d2qo01223eopenalex-snapshot
Recent advances in the total synthesis of cytochalasan natural products using bioinspired strategies
inferred← citeshttps://doi.org/10.1039/d3qo00565hopenalex-snapshot
Amichalasines F–J: cytochalasan heterotrimers with mirror-imaged core structures from Aspergillus micronesiensis
inferred← citeshttps://doi.org/10.1039/d4np00076eopenalex-snapshot
The cytochalasans: potent fungal natural products with application from bench to bedside
inferred← citeshttps://doi.org/10.1039/d6ob00028bopenalex-snapshot
Bisaspochalasin F: a tetrahydrofuran ring-fused cytochalasan homodimer from an endophytic Aspergillus flavipes as a Ca v 3.2 inhibitor
inferred← citeshttps://doi.org/10.1080/10286020.2021.2004131openalex-snapshot
Survey of natural products reported by Asian research groups in 2020
inferred← citeshttps://doi.org/10.1111/jam.15489openalex-snapshot
The endophytic Aspergillus strains: A bountiful source of natural products
inferred← citeshttps://doi.org/10.26599/fmh.2027.9420151openalex-snapshot
Research progress on new alkaloids of the genus Aspergillus from 2019 to 2024
inferred← citeshttps://doi.org/10.3390/md21110598openalex-snapshot
Rhizoaspergillin A and Rhizoaspergillinol A, including a Unique Orsellinic Acid–Ribose–Pyridazinone-N-Oxide Hybrid, from the Mangrove Endophytic Fungus Aspergillus sp. A1E3
inferred← citeshttps://doi.org/10.3390/molecules28237789openalex-snapshot
Bioactive Alkaloids as Secondary Metabolites from Plant Endophytic Aspergillus Genus
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