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Griseofamines A and B: Two Indole-Tetramic Acid Alkaloids with 6/5/6/5 and 6/5/7/5 Ring Systems from Penicillium griseofulvum

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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/anie.201603312openalex-snapshot
Bacterial Alkaloids Prevent Amoebal Predation
inferredcites →https://doi.org/10.1016/j.tet.2015.10.010openalex-snapshot
Cytotoxic and antiviral tetramic acid derivatives from the deep-sea-derived fungus Trichobotrys effuse DFFSCS021
inferredcites →https://doi.org/10.1016/s0040-4020(00)00092-2openalex-snapshot
Melophlins A and B, Novel Tetramic Acids Reversing the Phenotype of ras-Transformed Cells, from the Marine Sponge Melophlus sarassinorum
inferredcites →https://doi.org/10.1021/bi901123ropenalex-snapshot
Cyclopiazonic Acid Biosynthesis in Aspergillus sp.: Characterization of a Reductase-like R* Domain in Cyclopiazonate Synthetase That Forms and Releases cyclo-Acetoacetyl- l -tryptophan
inferredcites →https://doi.org/10.1021/bi901597jopenalex-snapshot
Characterization ofcyclo-Acetoacetyl- l -Tryptophan Dimethylallyltransferase in Cyclopiazonic Acid Biosynthesis: Substrate Promiscuity and Site Directed Mutagenesis Studies
inferredcites →https://doi.org/10.1021/ol502307uopenalex-snapshot
Aspergillines A–E, Highly Oxygenated Hexacyclic Indole–Tetrahydrofuran–Tetramic Acid Derivatives from Aspergillus versicolor
inferredcites →https://doi.org/10.1039/b909987popenalex-snapshot
Prenylated indole derivatives from fungi: structure diversity, biological activities, biosynthesis and chemoenzymatic synthesis
inferredcites →https://doi.org/10.1039/c4ra09047kopenalex-snapshot
Naturally occurring tetramic acid products: isolation, structure elucidation and biological activity
inferredcites →https://doi.org/10.1039/p19800001057openalex-snapshot
Structural investigations of 3-acylpyrrolidine-2,4-diones by nuclear magnetic resonance spectroscopy and X-ray crystallography
inferredcites →https://doi.org/10.1080/23312009.2016.1181536openalex-snapshot
Small-molecule inhibitors of the tuberculosis target, phenylalanyl- t RNA synthetase from Penicillium griseofulvum CPCC-400528
inferredcites →https://doi.org/10.1139/v64-240openalex-snapshot
C13 CHEMICAL SHIFTS IN ORGANIC CARBONYL GROUPS

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.2021.112708zenodo-depositor-declared
Piperazine-2,5-dione derivatives and an α-pyrone polyketide from Penicillium griseofulvum and their immunosuppression activity
inferred← citeshttps://doi.org/10.1002/ajoc.70428openalex-snapshot
Research Progress on the Application of Donor–Acceptor Cyclopropanes in Cycloaddition/Annulation Reactions
inferred← citeshttps://doi.org/10.1007/s13659-024-00486-4openalex-snapshot
Unveiling the mechanism of action of a novel natural dual inhibitor of SARS-CoV-2 Mpro and PLpro with molecular dynamics simulations
inferred← citeshttps://doi.org/10.1016/j.bioorg.2019.01.042openalex-snapshot
Dibrefeldins A and B, A pair of epimers representing the first brefeldin A dimers with cytotoxic activities from Penicillium janthinellum
inferred← citeshttps://doi.org/10.1016/j.bioorg.2021.104927openalex-snapshot
Chromene and chromone derivatives as liver X receptors modulators from a marine-derived Pestalotiopsis neglecta fungus
inferred← citeshttps://doi.org/10.1016/j.bioorg.2023.106553openalex-snapshot
Pegriseofamines A−E: Five cyclopiazonic acid related indole alkaloids from the fungus Penicillium griseofulvum
inferred← citeshttps://doi.org/10.1016/j.bioorg.2024.108105openalex-snapshot
Nidustrin A, cysteine-retained emestrin with a unique 18-membered macrocyclic lactone from the endophytic fungus Aspergillus nidulans
inferred← citeshttps://doi.org/10.1016/j.ejmech.2019.06.078openalex-snapshot
Amino acid-oriented poly-substituted heterocyclic tetramic acid derivatives as potential antifungal agents
inferred← citeshttps://doi.org/10.1016/j.ejmech.2024.116703openalex-snapshot
Design, synthesis of griseofamine A derivatives and development of potent antibacterial agents against MRSA
inferred← citeshttps://doi.org/10.1016/j.fitote.2020.104532openalex-snapshot
New bioactive secondary metabolites from the Anoectochilus roxburghii endophytic fungus Aspergillus versicolor
inferred← citeshttps://doi.org/10.1016/j.molstruc.2026.145476openalex-snapshot
Isolation, structural elucidation, and cytotoxicity of undescribed sesquiterpenoids and polyketides from a marine-derived fungus Talaromyces stipitatus
inferred← citeshttps://doi.org/10.1016/j.phytochem.2019.112177openalex-snapshot
Prenylated quinolinone alkaloids and prenylated isoindolinone alkaloids from the fungus Aspergillus nidulans
inferred← citeshttps://doi.org/10.1016/j.phytochem.2021.113045openalex-snapshot
Isolation, absolute configurations and bioactivities of pestaphilones A–I: Undescribed methylated side chain containing-azaphilones from Pestalotiopsis oxyanthi
inferred← citeshttps://doi.org/10.1016/j.phytochem.2024.114012openalex-snapshot
Penigrines A−E: Five undescribed azepine-indole alkaloids from Penicillium griseofulvum
inferred← citeshttps://doi.org/10.1016/j.phytochem.2026.114894openalex-snapshot
Discovery of previously undescribed specialized metabolites from the endophytic fungus Penicillium griseofulvum
inferred← citeshttps://doi.org/10.1016/j.phytochem.2026.114983openalex-snapshot
Anti-inflammatory compounds from Penicillium fungi: A review
inferred← citeshttps://doi.org/10.1016/j.phytol.2019.11.009openalex-snapshot
Asperpentenone A, A novel polyketide isolated from the deep-sea derived fungus Aspergillus sp. SCSIO 41024
inferred← citeshttps://doi.org/10.1016/j.tetlet.2021.152894openalex-snapshot
An improved total synthesis of griseofamine A
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.2c00069openalex-snapshot
Asymmetric Total Synthesis of Griseofamine B and Its Three Stereoisomers
inferred← citeshttps://doi.org/10.1021/acs.joc.0c01210openalex-snapshot
Atypical Spirotetronate Polyketides Identified in the Underexplored Genus Streptacidiphilus
inferred← citeshttps://doi.org/10.1021/acs.orglett.8b04019openalex-snapshot
Septosones A–C, in Vivo Anti-inflammatory Meroterpenoids with Rearranged Carbon Skeletons from the Marine Sponge Dysidea septosa
inferred← citeshttps://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
inferred← citeshttps://doi.org/10.1021/acs.orglett.9b00672openalex-snapshot
Total Synthesis and Antibacterial Activity Evaluation of Griseofamine A and 16-epi-Griseofamine A
inferred← citeshttps://doi.org/10.1039/c8np90015aopenalex-snapshot
Hot off the Press
inferred← citeshttps://doi.org/10.1039/c9qo00820aopenalex-snapshot
Canescones A–E: aromatic polyketide dimers with PTP1B inhibitory activity from Penicillium canescens
inferred← citeshttps://doi.org/10.1039/d0np00099jopenalex-snapshot
Biosynthetic strategies for tetramic acid formation
inferred← citeshttps://doi.org/10.1080/10286020.2019.1684474openalex-snapshot
Survey of natural products reported by Asian research groups in 2018
inferred← citeshttps://doi.org/10.1186/s43094-025-00924-1openalex-snapshot
Unveiling the anti-gout potential of terpenes isolated from Penicillium sp. supported by in silico studies
inferred← citeshttps://doi.org/10.3390/molecules24081527openalex-snapshot
DP4-Assisted Structure Elucidation of Isodemethylchodatin, a New Norlichexanthone Derivative Meager in H-Atoms, from the Lichen Parmotrema tsavoense
inferred← citeshttps://doi.org/10.3390/molecules26030663openalex-snapshot
Recent Advances in the Synthesis of β-Carboline Alkaloids
inferred← citeshttps://doi.org/10.3390/molecules27217586openalex-snapshot
Indole-Containing Natural Products 2019–2022: Isolations, Reappraisals, Syntheses, and Biological Activities
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