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Amaryllidaceae Alkaloids of Norbelladine-Type as Inspiration for Development of Highly Selective Butyrylcholinesterase Inhibitors: Synthesis, Biological Activity Evaluation, and Docking Studies

https://doi.org/10.3390/ijms22158308
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Outgoing claims: the papers this work cites, builds on, or argues with.

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Acetylcholinesterase Inhibitors from Plants and Fungi
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The Natural Product Berberine is a Human Prolyl Oligopeptidase Inhibitor
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UCSF Chimera—A visualization system for exploratory research and analysis
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AutoDock4 and AutoDockTools4: Automated docking with selective receptor flexibility
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AutoDock Vina: Improving the speed and accuracy of docking with a new scoring function, efficient optimization, and multithreading
inferredcites →https://doi.org/10.1002/med.21745openalex-snapshot
Structure and therapeutic uses of butyrylcholinesterase: Application in detoxification, Alzheimer's disease, and fat metabolism
inferredcites →https://doi.org/10.1007/s11101-020-09675-8openalex-snapshot
The Amaryllidaceae alkaloids haemanthamine, haemanthidine and their semisynthetic derivatives as potential drugs
inferredcites →https://doi.org/10.1016/0006-2952(61)90145-9openalex-snapshot
A new and rapid colorimetric determination of acetylcholinesterase activity
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Rapid colorimetric assay for cellular growth and survival: Application to proliferation and cytotoxicity assays
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The modification of natural products for medical use
inferredcites →https://doi.org/10.1016/j.bioorg.2019.103455openalex-snapshot
Water-soluble betaines and amines based on thiacalix[4]arene scaffold as new cholinesterase inhibitors
inferredcites →https://doi.org/10.1016/j.biotechadv.2016.12.005openalex-snapshot
Natural products against Alzheimer's disease: Pharmaco-therapeutics and biotechnological interventions
inferredcites →https://doi.org/10.1016/j.ejmech.2016.05.004openalex-snapshot
5,10b-Ethanophenanthridine amaryllidaceae alkaloids inspire the discovery of novel bicyclic ring systems with activity against drug resistant cancer cells
inferredcites →https://doi.org/10.1016/j.ejmech.2016.09.078openalex-snapshot
Design, synthesis and biological evaluation of new phthalimide and saccharin derivatives with alicyclic amines targeting cholinesterases, beta-secretase and amyloid beta aggregation
inferredcites →https://doi.org/10.1016/j.ejmech.2018.07.033openalex-snapshot
Multi-target-directed ligands for treating Alzheimer's disease: Butyrylcholinesterase inhibitors displaying antioxidant and neuroprotective activities
inferredcites →https://doi.org/10.1016/j.ejmech.2020.112257openalex-snapshot
Design, synthesis and biological evaluation of novel naturally-inspired multifunctional molecules for the management of Alzheimer’s disease
inferredcites →https://doi.org/10.1016/j.ejmech.2020.112766openalex-snapshot
Structure-activity relationship study of tryptophan-based butyrylcholinesterase inhibitors
inferredcites →https://doi.org/10.1016/j.ejmech.2020.113112openalex-snapshot
2-Propargylamino-naphthoquinone derivatives as multipotent agents for the treatment of Alzheimer’s disease
inferredcites →https://doi.org/10.1016/j.jmgm.2005.12.005openalex-snapshot
Automatic atom type and bond type perception in molecular mechanical calculations
inferredcites →https://doi.org/10.1016/j.nbd.2015.04.008openalex-snapshot
The role of type 2 diabetes in neurodegeneration
inferredcites →https://doi.org/10.1016/j.neuroscience.2012.12.054openalex-snapshot
Butyrylcholinesterase and the cholinergic system
inferredcites →https://doi.org/10.1016/j.sajb.2018.09.011openalex-snapshot
Acetylcholinesterase inhibitors from southern African plants: An overview of ethnobotanical, pharmacological potential and phytochemical research including and beyond Alzheimer's disease treatment
inferredcites →https://doi.org/10.1016/j.softx.2015.06.001openalex-snapshot
GROMACS: High performance molecular simulations through multi-level parallelism from laptops to supercomputers
inferredcites →https://doi.org/10.1016/j.tet.2004.03.087openalex-snapshot
Synthesis of Amaryllidaceae alkaloids, siculine, oxocrinine, epicrinine, and buflavine
inferredcites →https://doi.org/10.1016/j.toxlet.2005.07.001openalex-snapshot
In vitro cytotoxicity assays: Comparison of LDH, neutral red, MTT and protein assay in hepatoma cell lines following exposure to cadmium chloride
inferredcites →https://doi.org/10.1016/s0006-2952(02)01514-9openalex-snapshot
β-Amyloid aggregation induced by human acetylcholinesterase: inhibition studies
inferredcites →https://doi.org/10.1016/s0140-6736(76)91936-xopenalex-snapshot
SELECTIVE LOSS OF CENTRAL CHOLINERGIC NEURONS IN ALZHEIMER'S DISEASE
inferredcites →https://doi.org/10.1016/s0896-6273(00)80108-7openalex-snapshot
Acetylcholinesterase Accelerates Assembly of Amyloid-β-Peptides into Alzheimer's Fibrils: Possible Role of the Peripheral Site of the Enzyme
inferredcites →https://doi.org/10.1016/s1474-4422(18)30403-4openalex-snapshot
Global, regional, and national burden of Alzheimer's disease and other dementias, 1990–2016: a systematic analysis for the Global Burden of Disease Study 2016
inferredcites →https://doi.org/10.1021/acs.accounts.9b00248openalex-snapshot
Metal Ions in Alzheimer’s Disease: A Key Role or Not?
inferredcites →https://doi.org/10.1021/acs.chemrev.8b00504openalex-snapshot
Structural Simplification of Natural Products
inferredcites →https://doi.org/10.1021/acs.jmedchem.9b01220openalex-snapshot
The Blood–Brain Barrier (BBB) Score
inferredcites →https://doi.org/10.1021/acs.jnatprod.5b01055openalex-snapshot
Natural Products as Sources of New Drugs from 1981 to 2014
inferredcites →https://doi.org/10.1021/acs.jnatprod.8b00592openalex-snapshot
Isoquinoline Alkaloids from Berberis vulgaris as Potential Lead Compounds for the Treatment of Alzheimer’s Disease
inferredcites →https://doi.org/10.1021/acschemneuro.7b00461openalex-snapshot
Design, Synthesis, and Biological Evaluation of 1-Benzylamino-2-hydroxyalkyl Derivatives as New Potential Disease-Modifying Multifunctional Anti-Alzheimer’s Agents
inferredcites →https://doi.org/10.1021/cr078198uopenalex-snapshot
Chemistry, Biology, and Medicinal Potential of Narciclasine and its Congeners
inferredcites →https://doi.org/10.1021/jm501195eopenalex-snapshot
Discovery, Biological Evaluation, and Crystal Structure of a Novel Nanomolar Selective Butyrylcholinesterase Inhibitor
inferredcites →https://doi.org/10.1021/jp003020wopenalex-snapshot
Structure and Dynamics of the TIP3P, SPC, and SPC/E Water Models at 298 K
inferredcites →https://doi.org/10.1039/b508966mopenalex-snapshot
Acetylcholinesterase inhibitors from plants and fungi
inferredcites →https://doi.org/10.1039/c4ra14666bopenalex-snapshot
Biological and pharmacological activities of amaryllidaceae alkaloids
inferredcites →https://doi.org/10.1039/c9cc01330jopenalex-snapshot
Tryptophan-derived butyrylcholinesterase inhibitors as promising leads against Alzheimer's disease
inferredcites →https://doi.org/10.1039/d0nj00282hopenalex-snapshot
Synthesis, biological evaluation and molecular modeling studies of substituted N -benzyl-2-phenylethanamines as cholinesterase inhibitors
inferredcites →https://doi.org/10.1046/j.1432-1033.2002.03297.xopenalex-snapshot
Modulation of inositol 1,4,5‐triphosphate concentration by prolyl endopeptidase inhibition
inferredcites →https://doi.org/10.1056/nejmra040223openalex-snapshot
Alzheimer's Disease
inferredcites →https://doi.org/10.1073/pnas.0508575102openalex-snapshot
Selective butyrylcholinesterase inhibition elevates brain acetylcholine, augments learning and lowers Alzheimer β-amyloid peptide in rodent
inferredcites →https://doi.org/10.1093/brain/awy132openalex-snapshot
The cholinergic system in the pathophysiology and treatment of Alzheimer’s disease
inferredcites →https://doi.org/10.1097/00001756-199503000-00012openalex-snapshot
Cholinesterase inhibitors increase secretion of APPs in rat brain cortex
inferredcites →https://doi.org/10.1097/nen.0b013e31823cc7a6openalex-snapshot
Butyrylcholinesterase Is Associated With β-Amyloid Plaques in the Transgenic APP SWE /PSEN1dE9 Mouse Model of Alzheimer Disease
inferredcites →https://doi.org/10.1097/nen.0b013e318288a8ddopenalex-snapshot
Rapid β-Amyloid Deposition and Cognitive Impairment After Cholinergic Denervation in APP/PS1 Mice
inferredcites →https://doi.org/10.1111/j.1471-4159.2006.04347.xopenalex-snapshot
Excessive hippocampal acetylcholine levels in acetylcholinesterase‐deficient mice are moderated by butyrylcholinesterase activity
inferredcites →https://doi.org/10.1186/1476-511x-4-18openalex-snapshot
Serum butyrylcholinesterase in type 2 diabetes mellitus: a biochemical and bioinformatics approach
inferredcites →https://doi.org/10.1186/1758-2946-3-33openalex-snapshot
Open Babel: An open chemical toolbox
inferredcites →https://doi.org/10.1186/1758-2946-4-17openalex-snapshot
Avogadro: an advanced semantic chemical editor, visualization, and analysis platform
inferredcites →https://doi.org/10.1517/14740338.2014.914168openalex-snapshot
Outcomes of Alzheimer's disease therapy with acetylcholinesterase inhibitors and memantine
inferredcites →https://doi.org/10.15252/emmm.201606210openalex-snapshot
The amyloid hypothesis of Alzheimer's disease at 25 years
inferredcites →https://doi.org/10.2174/1568026619666190201153257openalex-snapshot
Small Molecule Natural Products and Alzheimer’s Disease
inferredcites →https://doi.org/10.3233/jad-2011-101425openalex-snapshot
Increased Protein and Lipid Oxidative Damage in Mitochondria Isolated from Lymphocytes from Patients with Alzheimer's Disease: Insights into the Role of Oxidative Stress in Alzheimer's Disease and Initial Investigations into a Potential Biomarker for this Dementing Disorder
inferredcites →https://doi.org/10.3390/biom10050800openalex-snapshot
Amaryllidaceae Alkaloids of Belladine-Type from Narcissus pseudonarcissus cv. Carlton as New Selective Inhibitors of Butyrylcholinesterase
inferredcites →https://doi.org/10.3390/ijms22073444openalex-snapshot
Synthesis and Hybrid SAR Property Modeling of Novel Cholinesterase Inhibitors
inferredcites →https://doi.org/10.3390/molecules23020347openalex-snapshot
Design, Synthesis, and Biological Evaluation of 2-(Benzylamino-2-Hydroxyalkyl)Isoindoline-1,3-Diones Derivatives as Potential Disease-Modifying Multifunctional Anti-Alzheimer Agents
inferredcites →https://doi.org/10.3390/molecules25102337openalex-snapshot
Chemical and Biological Aspects of Montanine-Type Alkaloids Isolated from Plants of the Amaryllidaceae Family
inferredcites →https://doi.org/10.3390/molecules25245891openalex-snapshot
New Multifunctional Agents Based on Conjugates of 4-Amino-2,3-polymethylenequinoline and Butylated Hydroxytoluene for Alzheimer’s Disease Treatment

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.4633265openalex-extracted
Carltonine-Derived Compounds for Targeted Butyrylcholinesterase Inhibition
inferred← citeshttps://doi.org/10.1016/j.bioorg.2026.109894openalex-snapshot
Carltonine B derivatives: Synthesis and structure-activity relationship insights for selective butyrylcholinesterase inhibition
inferred← citeshttps://doi.org/10.1016/j.ejmech.2023.115301openalex-snapshot
Highly selective butyrylcholinesterase inhibitors related to Amaryllidaceae alkaloids - Design, synthesis, and biological evaluation
inferred← citeshttps://doi.org/10.1016/j.prenap.2024.100099openalex-snapshot
Natural products as a source of cholinesterase inhibitors
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.5c00841openalex-snapshot
Total Syntheses of the Amaryllidaceae Alkaloids Carltonines A–C and the Neuroprotective and Immunomodulatory Evaluation of Carltonine B
inferred← citeshttps://doi.org/10.1038/s41598-024-66424-zopenalex-snapshot
Synthesis, biological evaluation, molecular docking, and MD simulation of novel 2,4-disubstituted quinazoline derivatives as selective butyrylcholinesterase inhibitors and antioxidant agents
inferred← citeshttps://doi.org/10.1039/d2ob00553kopenalex-snapshot
Synthesis and cholinesterase inhibitory activity study of Amaryllidaceae alkaloid analogues with N -methyl substitution
inferred← citeshttps://doi.org/10.1039/d4md00060aopenalex-snapshot
Carltonine-derived compounds for targeted butyrylcholinesterase inhibition
inferred← citeshttps://doi.org/10.14710/ik.ijms.28.3.225-230openalex-snapshot
α-Glucosidase, Angiotensin-converting Enzyme, and Acetylcholinesterase Inhibitory Activities of a Marine Red Alga Galaxaura oblongata
inferred← citeshttps://doi.org/10.3390/molecules26175240openalex-snapshot
Recent Progress on Biological Activity of Amaryllidaceae and Further Isoquinoline Alkaloids in Connection with Alzheimer’s Disease
inferred← citeshttps://doi.org/10.3390/molecules27175621openalex-snapshot
Chemical Synthesis and Biological Activities of Amaryllidaceae Alkaloid Norbelladine Derivatives and Precursors
inferred← citeshttps://doi.org/10.3390/molecules29184442openalex-snapshot
Synthesis, Characterization, and Biological Evaluation of N-Methyl Derivatives of Norbelladine
inferred← citeshttps://doi.org/10.3390/plants11243447openalex-snapshot
Biochemical Analyses of Bioactive Extracts from Plants Native to Lampedusa, Sicily Minor Island
inferred← citeshttps://doi.org/10.3390/plants15081186openalex-snapshot
Alkaloids from In Vitro Cultured Rhodophiala pratensis Display Neuroprotective Effects in Murine Microglial Cell Models of Inflammation
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