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Spiroindole Alkaloids and Spiroditerpenoids from Aspergillus duricaulis and Their Potential Neuroprotective Effects

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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

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Curcumin has potent anti‐amyloidogenic effects for Alzheimer's β‐amyloid fibrils in vitro
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Time-Dependent Density Functional Response Theory for Electronic Chiroptical Properties of Chiral Molecules
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Alpha-tocopherol quinine ameliorates spatial memory deficits by reducing beta-amyloid oligomers, neuroinflammation and oxidative stress in transgenic mice with Alzheimer's disease
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Alzheimer Mechanisms and Therapeutic Strategies
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Alzheimer’s disease pathogenesis and therapeutic interventions
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Rutin inhibits β-amyloid aggregation and cytotoxicity, attenuates oxidative stress, and decreases the production of nitric oxide and proinflammatory cytokines
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Extracts of Actinidia arguta stems inhibited LPS-induced inflammatory responses through nuclear factor–κB pathway in Raw 264.7 cells
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The case for soluble Aβ oligomers as a drug target in Alzheimer's disease
inferredcites →https://doi.org/10.1016/s0031-9422(99)00132-6openalex-snapshot
A chromene and prenylated benzoic acid from Piper aduncum
inferredcites →https://doi.org/10.1016/s0040-4020(99)00337-3openalex-snapshot
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inferredcites →https://doi.org/10.1021/jo0011078openalex-snapshot
Novel Bioactive Breviane Spiroditerpenoids from Penicillium brevicompactum Dierckx
inferredcites →https://doi.org/10.1021/jo9622791openalex-snapshot
Conversion of Marcfortine A to Paraherquamide A via Paraherquamide B. The First Formal Synthesis of Paraherquamide A
inferredcites →https://doi.org/10.1021/np200954vopenalex-snapshot
Fungal Origins of the Bicyclo[2.2.2]diazaoctane Ring System of Prenylated Indole Alkaloids
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The Magnitude of Dementia Occurrence in the World
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inferredcites →https://doi.org/10.3233/jad-142136openalex-snapshot
Amyloid-β Oligomers Relate to Cognitive Decline in Alzheimer's Disease
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inferredcites →https://doi.org/10.7164/antibiotics.46.1355openalex-snapshot
Further novel metabolites of the paraherquamide 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.2021.113011zenodo-depositor-declared
Recent studies on terpenoids in Aspergillus fungi: Chemical diversity, biosynthesis, and bioactivity
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inferred← citeshttps://doi.org/10.1002/cbdv.202500019openalex-snapshot
Eight Breviane‐type Spiroditerpenoids From the Deep‐Sea‐Derived Fungus Penicillium olsonii SCSIO41803
inferred← citeshttps://doi.org/10.1002/chem.202404250openalex-snapshot
What Factors Determine the Brevione B Desaturation Mechanism in the Nonheme Iron Dioxygenase BrvJ?
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Bicyclic Heterocycles from Levulinic Acid through a Fast and Operationally Simple Diversity‐Oriented Multicomponent Approach
inferred← citeshttps://doi.org/10.1007/978-3-031-42422-9_1openalex-snapshot
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Biomedical features and therapeutic potential of rosmarinic acid
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inferred← citeshttps://doi.org/10.1016/b978-0-12-824467-8.00012-7openalex-snapshot
Neuroprotective effects of phytonutrients at gene level
inferred← citeshttps://doi.org/10.1016/b978-0-443-18611-0.00002-4openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.bioorg.2021.105012openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.bioorg.2021.105064openalex-snapshot
Chemical constituents from basidiomycete Basidioradulum radula culture medium and their cytotoxic effect on human prostate cancer DU-145 cells
inferred← citeshttps://doi.org/10.1016/j.bioorg.2021.105128openalex-snapshot
Microwave-assisted rapid synthesis of spirooxindole-pyrrolizidine analogues and their activity as anti-amyloidogenic agents
inferred← citeshttps://doi.org/10.1016/j.bmc.2021.116270openalex-snapshot
Natural spirocyclic alkaloids and polyphenols as multi target dementia leads
inferred← citeshttps://doi.org/10.1016/j.ejmcr.2023.100112openalex-snapshot
Discovery and current developments of isoindolinone-based fungal natural products
inferred← citeshttps://doi.org/10.1016/j.fitote.2016.07.017openalex-snapshot
Characterization of diterpenoids from Caesalpinia decapetala and their anti-TMV activities
inferred← citeshttps://doi.org/10.1016/j.fitote.2024.106251openalex-snapshot
Aculeaquamides B and C, two new paraherquamides from the co-culture of Aspergillus aculeatinus WHUF0198 and Penicillium sp. DM27
inferred← citeshttps://doi.org/10.1016/j.fitote.2026.107441openalex-snapshot
Aspergillus-derived indole diketopiperazines (IDKPs): chemical diversity, biosynthetic logics, and therapeutic potential
inferred← citeshttps://doi.org/10.1016/j.lfs.2018.07.036openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.phytochem.2022.113336openalex-snapshot
Neolignans and amide alkaloids from the stems of Piper kadsura and their neuroprotective activity
inferred← citeshttps://doi.org/10.1021/acs.chemrev.4c00250openalex-snapshot
The Mutually Inspiring Biological and Chemical Synthesis of Fungal Bicyclo[2.2.2]diazaoctane Indole Alkaloids
inferred← citeshttps://doi.org/10.1021/acs.jafc.1c02200openalex-snapshot
Clerodane Diterpenoids Identified from Polyalthia longifolia Showing Antifungal Activity against Plant Pathogens
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.4c00782openalex-snapshot
Immunosuppressive Breviane Spiroditerpenoids from Penicillium bialowiezense Isolated from a Medicinal Plant
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.4c00997openalex-snapshot
Breviane Spiroditerpenoids with Anti-inflammatory and Antiviral Activities from Deep-Sea-Derived Fungus Penicillium sp. F59
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.9b00559openalex-snapshot
Xylodon flaviporus-Derived Drimane Sesquiterpenoids That Inhibit Osteoclast Differentiation
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.9b01161openalex-snapshot
Higginsianins D and E, Cytotoxic Diterpenoids Produced by Colletotrichum higginsianum
inferred← citeshttps://doi.org/10.1021/acs.joc.9b02608openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/acs.orglett.7b00193openalex-snapshot
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Molecular and Computational Bases for Spirofuranone Formation in Setosusin Biosynthesis
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Asymmetric domino 1,6-addition/annulation reaction of 3-cyano-4-alkenyl-2 H -chromen-2-ones with isatin-derived MBH carbonates: enantioselective synthesis of 3,3′-cyclopentenylspirooxindoles bearing 2 H -chromen-2-ones
inferred← citeshttps://doi.org/10.1039/d0ob02162hopenalex-snapshot
The chemistry and biology of fungal meroterpenoids (2009–2019)
inferred← citeshttps://doi.org/10.1039/d0ob02166kopenalex-snapshot
Stereoselective synthesis of trifluoroethyl 3,2′-spirooxindole γ-lactam through the organocatalytic cascade reaction of 3-((2,2,2-trifluoroethyl)amino)indolin-2-one
inferred← citeshttps://doi.org/10.1039/d1qo01952jopenalex-snapshot
An unexpected photoinduced cyclization to synthesize fully substituted γ-spirolactones via intramolecular hydrogen abstraction with allyl acrylates
inferred← citeshttps://doi.org/10.1039/d5np00046gopenalex-snapshot
Discovery, bioactivities and biosynthesis of spirooxindole alkaloids
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Traditional Ayurvedic and herbal remedies for Alzheimer’s disease: from bench to bedside
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Aculeaquamide A, cytotoxic paraherquamide from the marine fungus Aspergillus aculeatinus WHUF0198
inferred← citeshttps://doi.org/10.1080/17568919.2026.2719228openalex-snapshot
Latest developments of spirooxindoles and their derivatives in medicinal chemistry
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A Biosynthetic Numbering System for Diterpene Pyrones
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Unlocking the Impact of Phyto-bioactive Compounds against Neurodegenerative Disorders
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Piperidine Nucleus as a Promising Scaffold for Alzheimer’s Disease: Current Landscape and Future Perspective
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Chemistry and Biology of Secondary Metabolites from Aspergillus Genus
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A Review on Nonviral, Nonbacterial Infectious Agents Toxicity Involved in Neurodegenerative Diseases
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Research progress on new alkaloids of the genus Aspergillus from 2019 to 2024
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A New Breviane Spiroditerpenoid from the Marine-Derived Fungus Penicillium sp. TJ403-1
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Role of Plant Derived Alkaloids and Their Mechanism in Neurodegenerative Disorders
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