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Cytotoxic and Antimalarial Alkaloids from the Bulbs of Crinum amabile

https://doi.org/10.1021/np50098a017
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Alkaloids with cholinesterase inhibitory activities from the bulbs of Crinum × amabile Donn ex Ker Gawl
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(−)‐Augustamine and (−)‐Amabiline
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Alkaloids from Zephyranthes robusta Baker and Their Acetylcholinesterase‐ and Butyrylcholinesterase‐Inhibitory Activity
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Exploring the Anti‐Inflammatory Potential of Australian Native Plants Based on their Ethnopharmacological Knowledge
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Bulbispermine: A Crinine‐Type Amaryllidaceae Alkaloid Exhibiting Cytostatic Activity toward Apoptosis‐Resistant Glioma Cells
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Alkaloids from the Bulbs of Lycoris aurea
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CGC‐MS of alkaloids in Leucojum aestivum plants and their in vitro cultures
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Antimalarial activity of some plants traditionally used in Meru district of Kenya
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Inhibitory effects of Korean plants on HIV‐1 activities
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The potential of alkaloids in drug discovery
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Efficient Enantioselective Syntheses of Chiral Natural Products Facilitated by Ligand Design
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Purification of the Alkaloid Lycorine and Simultaneous Analysis of Ascorbic Acid and Lycorine by Micellar Electrokinetic Capillary Chromatography
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Amaryllidaceae Alkaloid Accumulation by Plant In Vitro Systems
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Amaryllidaceae Alkaloid Accumulation by Plant In Vitro Systems
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Trichomonas vaginalis NTPDase inhibited by lycorine modulates the parasite-neutrophil interaction
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The Amaryllidaceae alkaloids haemanthamine, haemanthidine and their semisynthetic derivatives as potential drugs
inferred← citeshttps://doi.org/10.1007/s11745-008-3246-6openalex-snapshot
Two Novel Ceramides with a Phytosphingolipid and a Tertiary Amide Structure from Zephyranthes candida
inferred← citeshttps://doi.org/10.1016/0031-9422(95)00191-9openalex-snapshot
Alkaloids from Boophane flava
inferred← citeshttps://doi.org/10.1016/0031-9422(95)00375-hopenalex-snapshot
Further alkaloids from Brunsvigia josephinae
inferred← citeshttps://doi.org/10.1016/0031-9422(95)00565-xopenalex-snapshot
Alkaloids from Crinum firmifolium var. hygrophilum
inferred← citeshttps://doi.org/10.1016/b978-0-12-405927-6.00017-5openalex-snapshot
Antimalarial and Other Antiprotozoal Products from African Medicinal Plants
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Cytotoxic Alkaloid Constituents of the Amaryllidaceae
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Chemodiversity, chemotaxonomy and chemoecology of Amaryllidaceae alkaloids
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Pressurized liquid extraction and anticholinesterase activity-based thin-layer chromatography with bioautography of Amaryllidaceae alkaloids
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Synthesis and antiplasmodial activity of lycorine derivatives
inferred← citeshttps://doi.org/10.1016/j.bmc.2024.118051openalex-snapshot
Targeting glioma with heteroaromatic alkaloids: A review of potential therapeutics
inferred← citeshttps://doi.org/10.1016/j.bmcl.2009.04.086openalex-snapshot
Selective cytochrome P450 3A4 inhibitory activity of Amaryllidaceae alkaloids
inferred← citeshttps://doi.org/10.1016/j.bmcl.2009.08.032openalex-snapshot
Structure–activity studies on seco-pancratistatin analogs: Potent inhibitors of human cytochrome P450 3A4
inferred← citeshttps://doi.org/10.1016/j.bmcl.2010.01.157openalex-snapshot
Potent and selective inhibition of human cytochrome P450 3A4 by seco-pancratistatin structural analogs
inferred← citeshttps://doi.org/10.1016/j.bmcl.2011.09.097openalex-snapshot
Ungeremine effectively targets mammalian as well as bacterial type I and type II topoisomerases
inferred← citeshttps://doi.org/10.1016/j.bmcl.2012.08.005openalex-snapshot
Apoptosis-inducing effects of distichamine and narciprimine, rare alkaloids of the plant family Amaryllidaceae
inferred← citeshttps://doi.org/10.1016/j.bse.2005.08.002openalex-snapshot
An antimalarial abietane diterpene from Fuerstia africana T.C.E. Fries
inferred← citeshttps://doi.org/10.1016/j.bse.2011.01.012openalex-snapshot
Amaryllidaceae alkaloids from the Australasian tribe Calostemmateae with acetylcholinesterase inhibitory activity
inferred← citeshttps://doi.org/10.1016/j.bse.2013.09.015openalex-snapshot
Phytochemical investigation of Galanthus woronowii
inferred← citeshttps://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
inferred← citeshttps://doi.org/10.1016/j.exppara.2010.11.004openalex-snapshot
Investigation of some medicinal plants traditionally used for treatment of malaria in Kenya as potential sources of antimalarial drugs
inferred← citeshttps://doi.org/10.1016/j.fct.2013.08.042openalex-snapshot
Pharmacological and toxicological insights to the South African Amaryllidaceae
inferred← citeshttps://doi.org/10.1016/j.fitote.2014.03.006openalex-snapshot
Alkaloids from Lycoris aurea and their cytotoxicities against the head and neck squamous cell carcinoma
inferred← citeshttps://doi.org/10.1016/j.fitote.2015.01.003openalex-snapshot
Amaryllidaceae alkaloids from the bulbs of Lycoris radiata with cytotoxic and anti-inflammatory activities
inferred← citeshttps://doi.org/10.1016/j.fitote.2019.02.009openalex-snapshot
The Amaryllidaceae as a source of antiplasmodial crinane alkaloid constituents
inferred← citeshttps://doi.org/10.1016/j.indcrop.2018.06.082openalex-snapshot
Aphicidal activities of Amaryllidaceae alkaloids from bulbs of Lycoris radiata against Aphis citricola
inferred← citeshttps://doi.org/10.1016/j.indcrop.2020.112667openalex-snapshot
Comparative antioxidant and antimicrobial potentials of leaf successive extract fractions of poison bulb, Crinum asiaticum L.
inferred← citeshttps://doi.org/10.1016/j.jchromb.2011.03.002openalex-snapshot
Determination of pseudolycorine in the bulb of lycoris radiata by capillary electrophoresis combined with online electrochemiluminescence using ultrasonic-assisted extraction
inferred← citeshttps://doi.org/10.1016/j.jep.2005.03.011openalex-snapshot
Evaluation of plants used for antimalarial treatment by the Maasai of Kenya
inferred← citeshttps://doi.org/10.1016/j.jep.2012.07.011openalex-snapshot
Cytotoxicity and acetylcholinesterase inhibitory activity of an isolated crinine alkaloid from Boophane disticha (Amaryllidaceae)
inferred← citeshttps://doi.org/10.1016/j.jep.2013.10.053openalex-snapshot
Traditional usage, phytochemistry and pharmacology of the South African medicinal plant Boophone disticha (L.f.) Herb. (Amaryllidaceae)
inferred← citeshttps://doi.org/10.1016/j.jep.2016.10.046openalex-snapshot
A review of ethnoboatany, therapeutic value, phytochemistry and pharmacology of Crinum macowanii Baker: A highly traded bulbous plant in Southern Africa
inferred← citeshttps://doi.org/10.1016/j.jep.2022.115359openalex-snapshot
ANTIMALARIAL activities and alkaloids from Crinum jagus (Thomps) DANDY
inferred← citeshttps://doi.org/10.1016/j.jsps.2023.06.017openalex-snapshot
Design of semisynthetic derivatives of the Amaryllidaceae alkaloid ambelline and exploration of their in vitro cytotoxic activities
inferred← citeshttps://doi.org/10.1016/j.phymed.2017.12.020openalex-snapshot
Cholinesterase-inhibitory effect and in silico analysis of alkaloids from bulbs of Hieronymiella species
inferred← citeshttps://doi.org/10.1016/j.phytochem.2003.12.013openalex-snapshot
Intraspecific variability in the alkaloid metabolism of Galanthus elwesii
inferred← citeshttps://doi.org/10.1016/j.phytochem.2004.10.004openalex-snapshot
Augustamine type alkaloids from Crinum kirkii
inferred← citeshttps://doi.org/10.1016/j.phytochem.2007.01.006openalex-snapshot
Selective apoptosis-inducing activity of crinum-type Amaryllidaceae alkaloids
inferred← citeshttps://doi.org/10.1016/j.phytochem.2007.03.025openalex-snapshot
Alkaloids from Galanthus nivalis
inferred← citeshttps://doi.org/10.1016/j.phytochem.2009.04.012openalex-snapshot
Structure-activity studies on the lycorine pharmacophore: A potent inducer of apoptosis in human leukemia cells
inferred← citeshttps://doi.org/10.1016/j.phytochem.2023.113929openalex-snapshot
Amaryllidaceae alkaloids from the bulbs of Crinum latifolium L. and their cholinesterase inhibitory activities
inferred← citeshttps://doi.org/10.1016/j.phytochem.2025.114383openalex-snapshot
Amaryllidaceae alkaloids with nitric oxide inhibitory activity from the leaves of Crinum asiaticum L. var. asiaticum
inferred← citeshttps://doi.org/10.1016/j.phytol.2010.06.004openalex-snapshot
In vitro antiprotozoal activity of alkaloids from Phaedranassa dubia (Amaryllidaceae)
inferred← citeshttps://doi.org/10.1016/j.phytol.2016.10.009openalex-snapshot
Cognate and cognitive ecopharmacognosy — in an anthropogenic era
inferred← citeshttps://doi.org/10.1016/j.phytol.2020.03.006openalex-snapshot
Alkaloids with anti-human carbonic anhydrase isozyme II activity from the bulbs of Crinum asiaticum L. var. asiaticum
inferred← citeshttps://doi.org/10.1016/j.sajb.2012.11.008openalex-snapshot
Acetylcholinesterase inhibitory effects of the bulb of Ammocharis coranica (Amaryllidaceae) and its active constituent lycorine
inferred← citeshttps://doi.org/10.1016/j.sajb.2018.07.021openalex-snapshot
Alkaloids isolated from indigenous South African Amaryllidaceae: Crinum buphanoides (Welw. ex Baker), Crinum graminicola (I. Verd.), Cyrtanthus mackenii (Hook. f) and Brunsvigia grandiflora (Lindl)
inferred← citeshttps://doi.org/10.1016/j.sajb.2020.07.026openalex-snapshot
Antimicrobial secondary metabolites from the medicinal plant Crinum glaucum A. Chev. (Amaryllidaceae)
inferred← citeshttps://doi.org/10.1016/j.sajb.2020.08.014openalex-snapshot
Organ-specific production of alkaloids from bulbs and seeds of Crinum stuhlmannii subsp. delagoense (Amaryllidaceae)
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.2021.07.047openalex-snapshot
Acute and sub-acute toxicity studies of the chloroform extract of Crinum asiaticum bulbs in mice.
inferred← citeshttps://doi.org/10.1016/j.sajb.2021.09.034openalex-snapshot
Chemical profile and biological activity of Crinum americanum L. (Amaryllidaceae)
inferred← citeshttps://doi.org/10.1016/j.sajb.2021.11.027openalex-snapshot
Alkaloids from the Crinum variabile (Amaryllidaceae)- including a full house of lycorine and its acylated derivatives
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.tet.2006.07.005openalex-snapshot
Total syntheses of crinine and related alkaloids
inferred← citeshttps://doi.org/10.1016/j.tet.2006.07.027openalex-snapshot
A general approach to crinine-type Amaryllidaceae alkaloids: total syntheses of (±)-haemanthidine, (±)-pretazettine, (±)-tazettine, and (±)-crinamine
inferred← citeshttps://doi.org/10.1016/j.tet.2007.05.041openalex-snapshot
Total synthesis of Amaryllidaceae alkaloids, (+)-vittatine and (+)-haemanthamine, starting from d-glucose
inferred← citeshttps://doi.org/10.1016/j.tet.2010.03.096openalex-snapshot
‘Aromatic ring umpolung’, a rapid access to the main core of several natural products
inferred← citeshttps://doi.org/10.1016/s0021-9673(01)00624-0openalex-snapshot
Screening for acetylcholinesterase inhibitors from Amaryllidaceae using silica gel thin-layer chromatography in combination with bioactivity staining
inferred← citeshttps://doi.org/10.1016/s0031-9422(00)00039-xopenalex-snapshot
Alkaloids and triterpenoids from Ammocharis coranica (Amaryllidaceae)
inferred← citeshttps://doi.org/10.1016/s0031-9422(00)00128-xopenalex-snapshot
Alkaloids from Crinum macowanii
inferred← citeshttps://doi.org/10.1016/s0031-9422(96)00506-7openalex-snapshot
Alkaloids from Brunsvigia orientalis
inferred← citeshttps://doi.org/10.1016/s0031-9422(97)00125-8openalex-snapshot
7-O-methylgarcinone e from Garcinia cowa
inferred← citeshttps://doi.org/10.1016/s0031-9422(97)00797-8openalex-snapshot
Two alkaloids from Zephyranthes carinata
inferred← citeshttps://doi.org/10.1016/s0031-9422(97)01081-9openalex-snapshot
Alkaloids from Crinum amabile
inferred← citeshttps://doi.org/10.1016/s0031-9422(98)00245-3openalex-snapshot
Alkaloids from Crinum delagoense
inferred← citeshttps://doi.org/10.1016/s0031-9422(98)00498-1openalex-snapshot
Alkaloids from Narcissus bujei (Amaryllidaceae)1Part 25 in the series “Narcissus alkaloids”. For part 24 see Viladomat et al., 1997 [Viladomat, F., Sellés, M., Codina, C. and Bastida, J., Planta Medica, 1997, 63, 583.].1
inferred← citeshttps://doi.org/10.1016/s0031-9422(99)00118-1openalex-snapshot
Alkaloids from Ammocharis tinneana
inferred← citeshttps://doi.org/10.1016/s0031-9422(99)00255-1openalex-snapshot
Alkaloids from Crinum bulbispermum
inferred← citeshttps://doi.org/10.1016/s0031-9422(99)00575-0openalex-snapshot
Bioactive alkaloids from Brunsvigia radulosa
inferred← citeshttps://doi.org/10.1016/s0065-308x(01)50032-9openalex-snapshot
Antiparasitic properties of medicinal plants and other naturally occurring products
inferred← citeshttps://doi.org/10.1016/s0099-9598(08)60008-5openalex-snapshot
The Amaryllidaceae Alkaloids
inferred← citeshttps://doi.org/10.1016/s0162-3109(98)00040-xopenalex-snapshot
The inhibitory effect of lycorine on tumor cell apoptosis induced by polymorphonuclear leukocyte-derived calprotectin
inferred← citeshttps://doi.org/10.1016/s0254-6299(15)30157-5openalex-snapshot
Lupane triterpenoid and alkaloid isolates from Cyrtanthus breviflorus (Amaryllidaceae)
inferred← citeshttps://doi.org/10.1016/s0254-6299(15)30447-6openalex-snapshot
Bulb alkaloids of the reputedly psychoactive Brunsvigia radulosa (Amaryllidaceae)
inferred← citeshttps://doi.org/10.1016/s0305-1978(02)00222-3openalex-snapshot
Variation among three Crinum species in alkaloid content
inferred← citeshttps://doi.org/10.1016/s0305-1978(03)00129-7openalex-snapshot
Alkaloids of Hippeastrum glaucescens
inferred← citeshttps://doi.org/10.1016/s0367-326x(02)00068-0openalex-snapshot
Crinum L. (Amaryllidaceae)
inferred← citeshttps://doi.org/10.1016/s0378-8741(01)00295-1openalex-snapshot
Enhanced antifungal activity of ketoconazole by Euphorbia characias latex against Candida albicans
inferred← citeshttps://doi.org/10.1016/s0378-8741(01)00305-1openalex-snapshot
Crinum species in traditional and modern medicine
inferred← citeshttps://doi.org/10.1016/s0378-8741(02)00147-2openalex-snapshot
Anti-nociceptive and anti-inflammatory activity caused by Cistanche deserticola in rodents
inferred← citeshttps://doi.org/10.1016/s0378-8741(02)00184-8openalex-snapshot
Medicinal bulbous plants of South Africa and their traditional relevance in the control of infectious diseases
inferred← citeshttps://doi.org/10.1016/s0378-8741(02)00245-3openalex-snapshot
Evaluation of selected Sudanese medicinal plants for their in vitro activity against hemoflagellates, selected bacteria, HIV-1-RT and tyrosine kinase inhibitory, and for cytotoxicity
inferred← citeshttps://doi.org/10.1016/s0378-8741(99)00090-2openalex-snapshot
Antimalarial activity of 20 crude extracts from nine African medicinal plants used in Kinshasa, Congo
inferred← citeshttps://doi.org/10.1016/s0731-7085(03)00283-8openalex-snapshot
Disposable electrochemical biosensor for the detection of the interaction between DNA and lycorine based on guanine and adenine signals
inferred← citeshttps://doi.org/10.1016/s0735-8210(01)80017-0openalex-snapshot
Chapter Three Recent Advances in the Total Synthesis of Amaryllidaceae Alkaloids
inferred← citeshttps://doi.org/10.1016/s1099-4831(06)63003-4openalex-snapshot
Chapter 3 Chemical and Biological Aspects of Narcissus Alkaloids
inferred← citeshttps://doi.org/10.1016/s1099-4831(08)00202-2openalex-snapshot
Chapter 2 Alkaloids with Antiprotozoal Activity
inferred← citeshttps://doi.org/10.1016/s1567-5769(01)00140-0openalex-snapshot
Aqueous extracts of Crinum latifolium (L.) and Camellia sinensis show immunomodulatory properties in human peripheral blood mononuclear cells
inferred← citeshttps://doi.org/10.1016/s1572-5995(97)80034-8openalex-snapshot
Narcissus alkaloids
inferred← citeshttps://doi.org/10.1016/s1572-5995(97)80037-3openalex-snapshot
In vitro models of human disease states
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.5b00785openalex-snapshot
Alkaloids fromHippeastrum argentinumand Their Cholinesterase-Inhibitory Activities: An in Vitro and in Silico Study
inferred← citeshttps://doi.org/10.1021/acs.joc.5c01480openalex-snapshot
Total Synthesis of Naturally Occurring Amaryllidaceae Alkaloids, (−)-Elwesine and (−)-epi-Crinine
inferred← citeshttps://doi.org/10.1021/acs.joc.8b01368openalex-snapshot
Diversity-Oriented Approach Toward the Syntheses of Amaryllidaceae Alkaloids via a Common Chiral Synthon
inferred← citeshttps://doi.org/10.1021/jo8008353openalex-snapshot
Total Syntheses of (±)-Crinine, (±)-Crinamine, and (±)-6a-epi-Crinamine via the Regioselective Synthesis and Diels−Alder Reaction of 3-Aryl-5-bromo-2-pyrone
inferred← citeshttps://doi.org/10.1021/np0702077openalex-snapshot
Benzylphenethylamine Alkaloids from Hosta plantaginea with Inhibitory Activity against Tobacco Mosaic Virus and Acetylcholinesterase
inferred← citeshttps://doi.org/10.1021/ol300466aopenalex-snapshot
Enantioselective Total Synthesis of (+)-Amabiline
inferred← citeshttps://doi.org/10.1021/ol901230wopenalex-snapshot
A Chemoenzymatic Total Synthesis of (+)-Amabiline
inferred← citeshttps://doi.org/10.1021/ol902000jopenalex-snapshot
An Unprecedented Oxidative Wagner−Meerwein Transposition
inferred← citeshttps://doi.org/10.1039/b008980jopenalex-snapshot
Antimalarial activity of plant metabolitesElectronic Supplementary Information (ESI) available: IC50 values of plant metabolites. See http://www.rsc.org/suppdata/np/b0/b008980j/
inferred← citeshttps://doi.org/10.1039/c4qo00353eopenalex-snapshot
Synthesis of (−)-mesembrine using the quaternary carbon-constructing allylic substitution
inferred← citeshttps://doi.org/10.1039/c7sc02112gopenalex-snapshot
Bioinspired enantioselective synthesis of crinine-type alkaloids via iridium-catalyzed asymmetric hydrogenation of enones
inferred← citeshttps://doi.org/10.1039/c9ra01181aopenalex-snapshot
Solvent-driven structural topology involving energetically significant intra- and intermolecular chelate ring contacts and anticancer activities of Cu( ii ) phenanthroline complexes involving benzoates: experimental and theoretical studies
inferred← citeshttps://doi.org/10.1039/np9941100329openalex-snapshot
Amaryllidaceae and Sceletium alkaloids
inferred← citeshttps://doi.org/10.1055/a-0880-5414openalex-snapshot
Antiplasmodial Lycorane Alkaloid Principles of the Plant Family Amaryllidaceae
inferred← citeshttps://doi.org/10.1055/a-1585-5877openalex-snapshot
Flavanols and Flavanes from Crinum asiaticum and Their Effects on LPS Signaling Pathway Through the Inhibition of NF-κB Activation
inferred← citeshttps://doi.org/10.1055/a-2788-6538openalex-snapshot
Synthesis of (+)-Dehydrobulbispermine Analogs
inferred← citeshttps://doi.org/10.1055/s-2001-11495openalex-snapshot
Crinane and Lycorane Type Alkaloids from Zephyranthes citrina
inferred← citeshttps://doi.org/10.1080/13880200600592301openalex-snapshot
Selective Anticancer Activity of Pure Licamichauxiioic-B Acid in Cultured Cell Lines
inferred← citeshttps://doi.org/10.1080/14786410802263758openalex-snapshot
Isolation of acetylcholinesterase inhibitory alkaloids from Nerine bowdenii
inferred← citeshttps://doi.org/10.1080/14786419.2019.1693561openalex-snapshot
Amabiloid A from Crinum × amabile Donn ex Ker Gawl
inferred← citeshttps://doi.org/10.1080/14786419.2026.2690079openalex-snapshot
An undescribed alkaloid from Crinum latifolium L.: structural elucidation and evaluation of its biological activity
inferred← citeshttps://doi.org/10.1134/s199542122303036xopenalex-snapshot
Isoquinoline Alkaloids of Amaryllidaceae Crinane Alkaloids
inferred← citeshttps://doi.org/10.1155/2014/972853openalex-snapshot
In VitroandIn VivoAntimalarial Activity ofFicus thonningiiBlume (Moraceae) andLophira alataBanks (Ochnaceae), Identified from the Ethnomedicine of the Nigerian Middle Belt
inferred← citeshttps://doi.org/10.1155/2019/7521504openalex-snapshot
Cytostatic and Antiproliferative Activities of F5 Fraction ofCrinum amabileLeaf Chloroform Extract Showed Its Potential as Cancer Chemotherapeutic Agent
inferred← citeshttps://doi.org/10.1177/1934578x0900400408openalex-snapshot
Structure Activity Studies on the Crinane Alkaloid Apoptosis-inducing Pharmacophore
inferred← citeshttps://doi.org/10.1177/1934578x1000500809openalex-snapshot
Cytochrome P450 3A4 Inhibitory Activity Studies within the Lycorine series of Alkaloids
inferred← citeshttps://doi.org/10.1177/1934578x1200700741openalex-snapshot
Acetylcholinesterase Inhibition within the Lycorine Series of Amaryllidaceae Alkaloids
inferred← citeshttps://doi.org/10.1177/1934578x1200701234openalex-snapshot
Cytotoxic Agents of the Crinane Series of Amaryllidaceae Alkaloids
inferred← citeshttps://doi.org/10.1177/1934578x1300800501openalex-snapshot
Cytotoxic Agents of the Crinane Series of Amaryllidaceae Alkaloids
inferred← citeshttps://doi.org/10.1177/1934578x1300801110openalex-snapshot
Alkaloids from Chlidanthus fragrans and their Acetylcholinesterase, Butyrylcholinesterase and Prolyl Oligopeptidase Activities
inferred← citeshttps://doi.org/10.1177/1934578x1300801211openalex-snapshot
Alkaloids from Boophone haemanthoides (Amaryllidaceae)
inferred← citeshttps://doi.org/10.1177/1934578x1400900834openalex-snapshot
Cytotoxicity Studies of Lycorine Alkaloids of the Amaryllidaceae
inferred← citeshttps://doi.org/10.1177/1934578x19872931openalex-snapshot
Antiplasmodial Studies Within the Plant Family Amaryllidaceae
inferred← citeshttps://doi.org/10.1177/1934578x261493255openalex-snapshot
Traditional Antimalarial Medicinal Plants of Sudan: A Review of Ethnopharmacology, Antiplasmodial Extracts and Phytochemicals, Toxicology, and Future Prospects
inferred← citeshttps://doi.org/10.1186/s43094-023-00490-4openalex-snapshot
Crinum jagus: antiproliferative studies of extracts on HepG2 cell line and in silico assessment of phytoconstituents as potential inhibitors of p53–mortalin interaction
inferred← citeshttps://doi.org/10.1248/bpb.25.223openalex-snapshot
Inhibition of Cell Cycle Progression through Specific Phase by Pancratistatin Derivatives.
inferred← citeshttps://doi.org/10.1248/bpb.29.2140openalex-snapshot
Crinamine from Crinum asiaticum var. japonicum Inhibits Hypoxia Inducible Factor-1 Activity But Not Activity of Hypoxia Inducible Factor-2
inferred← citeshttps://doi.org/10.1248/cpb.49.1217openalex-snapshot
Cytotoxic Alkaloids and a Flavan from the Bulbs of Crinum asiaticum var. japonicum.
inferred← citeshttps://doi.org/10.1248/cpb.51.315openalex-snapshot
Alkaloids from Eucharis amazonica (Amaryllidaceae).
inferred← citeshttps://doi.org/10.1300/j044v13n01_09openalex-snapshot
Antimalarial Activity in Tropical Plants: A Review
inferred← citeshttps://doi.org/10.13040/ijpsr.0975-8232.3(7).1883-90openalex-snapshot
inferred← citeshttps://doi.org/10.13040/ijpsr.0975-8232.3(9).3091-00openalex-snapshot
inferred← citeshttps://doi.org/10.13040/ijpsr.0975-8232.4(4).1239-52openalex-snapshot
inferred← citeshttps://doi.org/10.1515/znc-2013-3-407openalex-snapshot
GC-MS Investigation and Acetylcholinesterase Inhibitory Activity of Galanthus rizehensis
inferred← citeshttps://doi.org/10.1590/s2175-97902022e20459openalex-snapshot
Anti-Acanthamoeba castellanii activity of alkaloid-enriched extracts and lycorine from the Amaryllidaceae species
inferred← citeshttps://doi.org/10.2139/ssrn.5050464openalex-snapshot
Structural Determination and Anti-Bacterial Activity of Calotropis Procera Milky Latex
inferred← citeshttps://doi.org/10.2174/1570180819666220701103553openalex-snapshot
The Role of Aquatic Plants in Natural Products and Drug Discovery
inferred← citeshttps://doi.org/10.2174/1871520619666190118122523openalex-snapshot
Cytotoxic and Genotoxic Activities of Alkaloids from the Bulbs of Griffinia gardneriana and Habranthus itaobinus (Amaryllidaceae)
inferred← citeshttps://doi.org/10.2306/scienceasia1513-1874.2022.059openalex-snapshot
Cytotoxic compounds from Goniothalamus repevensis Pierre ex Finet & Gagnep
inferred← citeshttps://doi.org/10.32911/as.2023.v16.n2.1049openalex-snapshot
Comparativo morfométrico entre adultos de Taeniopoda varipennis Rehn, 1905 (Orthoptera: Romaleidae) en Chiriquí, Panamá
inferred← citeshttps://doi.org/10.3390/12071430openalex-snapshot
Revised NMR data for Incartine: an Alkaloid from Galanthus elwesii
inferred← citeshttps://doi.org/10.3390/biom11091298openalex-snapshot
Isolation and Biological Characterization of Homoisoflavanoids and the Alkylamide N-p-Coumaroyltyramine from Crinum biflorum Rottb., an Amaryllidaceae Species Collected in Senegal
inferred← citeshttps://doi.org/10.3390/biom9090494openalex-snapshot
Crinamine Induces Apoptosis and Inhibits Proliferation, Migration, and Angiogenesis in Cervical Cancer SiHa Cells
inferred← citeshttps://doi.org/10.3390/ijms140611713openalex-snapshot
Towards a Molecular Understanding of the Biosynthesis of Amaryllidaceae Alkaloids in Support of Their Expanding Medical Use
inferred← citeshttps://doi.org/10.3390/molecules18032458openalex-snapshot
Cytotoxic and Antimalarial Amaryllidaceae Alkaloids from the Bulbs of Lycoris radiata
inferred← citeshttps://doi.org/10.3390/molecules190811453openalex-snapshot
An Unusual Piceatannol Dimer from Rheum austral D. Don with Antioxidant Activity
inferred← citeshttps://doi.org/10.3390/molecules23061277openalex-snapshot
N-oxide alkaloids from Crinum amabile (Amaryllidaceae)
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/plants13243577openalex-snapshot
Phytochemical and Cytotoxic Aspects of Amaryllidaceae Alkaloids in Galanthus Species: A Review
inferred← citeshttps://doi.org/10.4314/tjpr.v15i11.27openalex-snapshot
Ethnobotanical, phytochemical and pharmacological properties of Crinum bulbispermum (Burm f) Milne-Redh and Schweick (Amaryllidaceae)
inferred← citeshttps://doi.org/10.5487/tr.2008.24.1.029openalex-snapshot
The Effects of Crinum asiaticum on the Apoptosis Induction and the Reversal of Multidrug Resistance in HL-60/MX2
inferred← citeshttps://doi.org/10.5530/pj.2021.13.135openalex-snapshot
Chemical Composition and In Vitro Antiplasmodial Activity of the Total Alkaloids of the Bulbs of Two Amaryllidaceae Species from Northern Peru
inferred← citeshttps://doi.org/10.5772/28798openalex-snapshot
The Genus Galanthus: A Source of Bioactive Compounds
inferred← citeshttps://doi.org/10.5897/ajb2009.000-9459openalex-snapshot
The importance of including toxicity assays when screening plant extracts for antimalarial activity
inferred← citeshttps://doi.org/10.66563/mz03ka36openalex-snapshot
Antioxidant, acetylcholinesterase inhibitory activity, and cytotoxicity assessment of the crude extracts of Boophane disticha
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