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Antiproliferative and Structure Activity Relationships of Amaryllidaceae Alkaloids

https://doi.org/10.3390/molecules200813854
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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/cmdc.200500057openalex-snapshot
Prins‐Type Synthesis and SAR Study of Cytotoxic Alkyl Chloro Dihydropyrans
inferredcites →https://doi.org/10.1016/j.bmc.2010.05.023openalex-snapshot
Synthesis and antiplasmodial activity of lycorine derivatives
inferredcites →https://doi.org/10.1016/j.bmc.2012.07.036openalex-snapshot
Synthesis and antimalarial activity of new haemanthamine-type derivatives
inferredcites →https://doi.org/10.1016/j.bmcl.2010.06.130openalex-snapshot
Structure–activity studies on acetylcholinesterase inhibition in the lycorine series of Amaryllidaceae alkaloids
inferredcites →https://doi.org/10.1016/j.ejmech.2013.03.018openalex-snapshot
Preparation and antimalarial activity of semisynthetic lycorenine derivatives
inferredcites →https://doi.org/10.1016/j.fitote.2011.09.008openalex-snapshot
Evaluation of analgesic, anti-inflammatory and hepatoprotective effects of lycorine from Sternbergia fisheriana (Herbert) Rupr.
inferredcites →https://doi.org/10.1016/j.jep.2005.05.011openalex-snapshot
Plants as a source of anti-cancer agents
inferredcites →https://doi.org/10.1016/j.phytochem.2004.03.020openalex-snapshot
(−)-Amarbellisine, a lycorine-type alkaloid from Amaryllis belladonna L. growing in Egypt
inferredcites →https://doi.org/10.1016/s1099-4831(10)06801-xopenalex-snapshot
Chemistry and Biology of Pancratium Alkaloids
inferredcites →https://doi.org/10.1021/cr078198uopenalex-snapshot
Chemistry, Biology, and Medicinal Potential of Narciclasine and its Congeners
inferredcites →https://doi.org/10.1021/jm8013585openalex-snapshot
Structure−Activity Relationship Analysis of Novel Derivatives of Narciclasine (an Amaryllidaceae Isocarbostyril Derivative) as Potential Anticancer Agents
inferredcites →https://doi.org/10.1021/np50048a005openalex-snapshot
Antineoplastic Agents, 120. Pancratium littorale
inferredcites →https://doi.org/10.1021/np800459dopenalex-snapshot
Pancratium canariense as an Important Source of Amaryllidaceae Alkaloids
inferredcites →https://doi.org/10.1021/np9008255openalex-snapshot
Amaryllidaceae Alkaloids Belonging to Different Structural Subgroups Display Activity against Apoptosis-Resistant Cancer Cells
inferredcites →https://doi.org/10.1021/ol900065xopenalex-snapshot
Bioactive Montanine Derivatives from Halide-induced Rearrangements of Haemanthamine-type Alkaloids. Absolute Configuration by VCD
inferredcites →https://doi.org/10.1055/s-0029-1185340openalex-snapshot
Biological Evaluation of Structurally Diverse Amaryllidaceae Alkaloids and their Synthetic Derivatives: Discovery of Novel Leads for Anticancer Drug Design
inferredcites →https://doi.org/10.1159/000441772openalex-snapshot
Signet-Ring Cell Carcinoma of the Colon: A Case Report and Review of the Literature
inferredcites →https://doi.org/10.3322/caac.21208openalex-snapshot
Cancer statistics, 2014
inferredcites →https://doi.org/10.3390/molecules19022469openalex-snapshot
Novel Lycorine Derivatives as Anticancer Agents: Synthesis and In Vitro Biological Evaluation

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

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Amaryllidaceae alkaloids from Narcissus pseudonarcissus L. cv. Dutch Master as potential drugs in treatment of Alzheimer's disease
inferred← citeshttps://doi.org/10.1007/s11101-020-09675-8openalex-snapshot
The Amaryllidaceae alkaloids haemanthamine, haemanthidine and their semisynthetic derivatives as potential drugs
inferred← citeshttps://doi.org/10.1007/s11101-025-10122-9openalex-snapshot
Cytotoxic crinane alkaloids of the Amaryllidaceae: in vitro, in vivo and in silico effects, structure–activity relationships and mechanisms of action
inferred← citeshttps://doi.org/10.1007/s42729-025-02511-yopenalex-snapshot
Phytopriming Technique for Enhancing Seed Germination and Secondary Metabolites Production in Sand Daffodil
inferred← citeshttps://doi.org/10.1016/j.arabjc.2022.103746openalex-snapshot
Semisynthetic derivatives of haemanthamine and their in vitro antiproliferative activity evaluation against a panel of human cell lines
inferred← citeshttps://doi.org/10.1016/j.bioorg.2020.103928openalex-snapshot
Functionalized aromatic esters of the Amaryllidaceae alkaloid haemanthamine and their in vitro and in silico biological activity connected to Alzheimer’s disease
inferred← citeshttps://doi.org/10.1016/j.biopha.2023.115295openalex-snapshot
Antiproliferative activity and apoptosis-inducing mechanism of Amaryllidaceae alkaloid montanine on A549 and MOLT-4 human cancer cells
inferred← citeshttps://doi.org/10.1016/j.cbi.2017.07.018openalex-snapshot
Anticancer potential of Amaryllidaceae alkaloids evaluated by screening with a panel of human cells, real-time cellular analysis and Ehrlich tumor-bearing mice
inferred← citeshttps://doi.org/10.1016/j.indcrop.2016.09.021openalex-snapshot
Determination of phenolic composition and antioxidant activities of Pancratium maritimum L. from Tunisia
inferred← citeshttps://doi.org/10.1016/j.sajb.2020.07.002openalex-snapshot
Cytotoxic tazettine alkaloids of the plant family Amaryllidaceae
inferred← citeshttps://doi.org/10.1016/j.sajb.2020.07.013openalex-snapshot
The plant family Amaryllidaceae as a source of cytotoxic homolycorine alkaloid principles
inferred← citeshttps://doi.org/10.1016/j.sajb.2020.09.007openalex-snapshot
Alkaloids of Phaedranassa dubia (Kunth) J.F. Macbr. and Phaedranassa brevifolia Meerow (Amaryllidaceae) from Ecuador and its cholinesterase-inhibitory activity
inferred← citeshttps://doi.org/10.1016/j.sajb.2020.09.015openalex-snapshot
Cytotoxic activities of selected plants of the family Amaryllidaceae on brain tumour cell lines
inferred← citeshttps://doi.org/10.1016/j.scienta.2023.112034openalex-snapshot
Zinc and phosphorus fertilization in Galanthus elwesii Hook: Changes in the total alkaloid, flavonoid, and phenolic content, and evaluation of anti-cancer, anti-microbial, and antioxidant activities
inferred← citeshttps://doi.org/10.1016/j.str.2018.01.009openalex-snapshot
The Amaryllidaceae Alkaloid Haemanthamine Binds the Eukaryotic Ribosome to Repress Cancer Cell Growth
inferred← citeshttps://doi.org/10.1016/j.tiv.2017.10.027openalex-snapshot
Toxicity and structure-activity relationship (SAR) of α,β-dehydroamino acids against human cancer cell lines
inferred← citeshttps://doi.org/10.1021/acs.joc.9b00018openalex-snapshot
Application of Electrocyclic Ring-Opening and Desymmetrizing Nucleophilic Trappings of meso-6,6-Dibromobicyclo[3.1.0]hexanes to Total Syntheses of Crinine and Haemanthamine Alkaloids
inferred← citeshttps://doi.org/10.1039/c8np00055gopenalex-snapshot
Amaryllidaceae and Sceletium alkaloids
inferred← citeshttps://doi.org/10.1055/a-1380-1888openalex-snapshot
Cytotoxic Agents in the Minor Alkaloid Groups of the Amaryllidaceae
inferred← citeshttps://doi.org/10.1055/a-2021-7944openalex-snapshot
Bioinspired Formal Synthesis of Pancracine via Selective Hydrogenation of an Indole Derivative
inferred← citeshttps://doi.org/10.1055/s-011-52170openalex-snapshot
inferred← citeshttps://doi.org/10.1177/1934578x1601101038openalex-snapshot
The Biological Activity of Alkaloids from the Amaryllidaceae: From Cholinesterases Inhibition to Anticancer Activity
inferred← citeshttps://doi.org/10.1186/s12985-022-01751-zopenalex-snapshot
Searching for plant-derived antivirals against dengue virus and Zika virus
inferred← citeshttps://doi.org/10.3390/agronomy12112786openalex-snapshot
Effect of Temperature and Sucrose on In Vitro Seed Germination and Bulblet Production of Pancratium maritimum L.
inferred← citeshttps://doi.org/10.3390/ijms22137014openalex-snapshot
Pancracine, a Montanine-Type Amaryllidaceae Alkaloid, Inhibits Proliferation of A549 Lung Adenocarcinoma Cells and Induces Apoptotic Cell Death in MOLT-4 Leukemic Cells
inferred← citeshttps://doi.org/10.3390/ijms25147640openalex-snapshot
The Structure–Antiproliferative Activity Relationship of Pyridine Derivatives
inferred← citeshttps://doi.org/10.3390/life15050719openalex-snapshot
Alkaloid Profile Characterisation and Bioactivity Evaluation of Bolivian Hippeastrum Species (Amaryllidaceae) as Cholinesterase Inhibitors
inferred← citeshttps://doi.org/10.3390/molecules23040719openalex-snapshot
Amaryllidaceae Alkaloids as Potential Glycogen Synthase Kinase-3β Inhibitors
inferred← citeshttps://doi.org/10.3390/molecules24071307openalex-snapshot
Derivatives of the β-Crinane Amaryllidaceae Alkaloid Haemanthamine as Multi-Target Directed Ligands for Alzheimer’s Disease
inferred← citeshttps://doi.org/10.3390/molecules25102337openalex-snapshot
Chemical and Biological Aspects of Montanine-Type Alkaloids Isolated from Plants of the Amaryllidaceae Family
inferred← citeshttps://doi.org/10.3390/molecules26010192openalex-snapshot
Alkaloids Analysis of Habranthus cardenasianus (Amaryllidaceae), Anti-Cholinesterase Activity and Biomass Production by Propagation Strategies
inferred← citeshttps://doi.org/10.3390/molecules28145408openalex-snapshot
Chemical and Biological Aspects of Different Species of the Genus Clinanthus Herb. (Amaryllidaceae) from South America
inferred← citeshttps://doi.org/10.3390/pharmaceutics12020122openalex-snapshot
Biological Evaluation of Naproxen–Dehydrodipeptide Conjugates with Self-Hydrogelation Capacity as Dual LOX/COX Inhibitors
inferred← citeshttps://doi.org/10.6084/m9.figshare.19219125openalex-snapshot
Additional file 1 of Searching for plant-derived antivirals against dengue virus and Zika virus
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