On the public citation graph

Pancratium canariense as an Important Source of Amaryllidaceae Alkaloids

https://doi.org/10.1021/np800459d
0 signed · 80 inferred · view as graph

Inferred edges come from two machine sources: sweeps of open repository metadata (mostly SSRN and Zenodo), and a bulk OpenAlex citation snapshot. Every row below is labelled with the one it came from. Neither is a complete citation index — absence here is not evidence of absence.

Is this your work? Sign in with ORCID and put your name on the claims that are yours.
Claim with ORCID
Reference health. See whether every reference in this work resolves to a known work and none has been retracted — and get a dated CiteStamped badge you can embed.
See reference health

What this work says

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

inferredcites →https://doi.org/10.1002/ptr.1346openalex-snapshot
Antimalarial activity screening of some alkaloids and the plant extracts from Amaryllidaceae
inferredcites →https://doi.org/10.1002/ptr.2130openalex-snapshot
In Vitro cytotoxicity of some medicinal plants from Georgian Amaryllidaceae
inferredcites →https://doi.org/10.1007/s00280-004-0941-8openalex-snapshot
Pancratistatin causes early activation of caspase-3 and the flipping of phosphatidyl serine followed by rapid apoptosis specifically in human lymphoma cells
inferredcites →https://doi.org/10.1007/s11101-006-9019-zopenalex-snapshot
New skeletons and new concepts in Amaryllidaceae alkaloids
inferredcites →https://doi.org/10.1016/0031-9422(88)80044-xopenalex-snapshot
Alkaloid N-oxides of amaryllidaceae
inferredcites →https://doi.org/10.1016/0031-9422(91)83751-6openalex-snapshot
Alkaloid N-oxides from Lycoris sanguinea
inferredcites →https://doi.org/10.1016/0031-9422(95)00187-copenalex-snapshot
Alkaloids of Galanthus elwesii
inferredcites →https://doi.org/10.1016/0040-4020(96)00297-9openalex-snapshot
Alkaloids from Hippeastrum equestre Herb. —5. Circular dichroism studies
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/j.phytochem.2007.01.006openalex-snapshot
Selective apoptosis-inducing activity of crinum-type Amaryllidaceae alkaloids
inferredcites →https://doi.org/10.1016/j.tet.2007.05.041openalex-snapshot
Total synthesis of Amaryllidaceae alkaloids, (+)-vittatine and (+)-haemanthamine, starting from d-glucose
inferredcites →https://doi.org/10.1016/s0024-3205(02)02034-9openalex-snapshot
Acetylcholinesterase inhibitory activity of some Amaryllidaceae alkaloids and Narcissus extracts
inferredcites →https://doi.org/10.1016/s0031-9422(00)81849-xopenalex-snapshot
Alkaloids from Narcissus confusus
inferredcites →https://doi.org/10.1016/s0031-9422(02)00154-1openalex-snapshot
Alkaloids from Narcissus angustifolius subsp. transcarpathicus (Amaryllidaceae)
inferredcites →https://doi.org/10.1016/s0031-9422(98)00743-2openalex-snapshot
Two novel Amaryllidaceae alkaloids from Hippeastrum equestre Herb.: 3-O-demethyltazettine and egonine
inferredcites →https://doi.org/10.1016/s0031-9422(99)00575-0openalex-snapshot
Bioactive alkaloids from Brunsvigia radulosa
inferredcites →https://doi.org/10.1016/s0367-326x(00)00313-0openalex-snapshot
Alkaloids from Cyrtanthus elatus
inferredcites →https://doi.org/10.1016/s0378-8741(02)00014-4openalex-snapshot
Medicinal natural products. A biosynthetic approach
inferredcites →https://doi.org/10.1021/cr000665jopenalex-snapshot
The Assignment of Absolute Configuration by NMR
inferredcites →https://doi.org/10.1021/jo00069a032openalex-snapshot
Synthesis applications of cationic aza-Cope rearrangements. Part 25. Total synthesis of Amaryllidaceae alkaloids of the 5,11-methanomorphanthridine type. Efficient total syntheses of (-)-pancracine and (.+-.)-pancracine
inferredcites →https://doi.org/10.1021/jo00210a031openalex-snapshot
Alkaloids of the Amaryllidaceae. 27. Structures of 9-O-demethylhomolycorine and 5.alpha.-hydroxyhomolycorine. Alkaloids of Crinum defixum, C. scabrum, and C. latifolium. Assignment of aromatic substitution patterns from 1H-coupled carbon-13 spectra
inferredcites →https://doi.org/10.1021/jo0256989openalex-snapshot
Absolute Configuration of Secondary Alcohols by 1H NMR: In Situ Complexation of α-Methoxyphenylacetic Acid Esters with Barium(II)
inferredcites →https://doi.org/10.1021/jo030309bopenalex-snapshot
Palladium-Catalyzed Asymmetric Allylic Substitution of 2-Arylcyclohexenol Derivatives: Asymmetric Total Syntheses of (+)-Crinamine, (−)-Haemanthidine, and (+)-Pretazettine
inferredcites →https://doi.org/10.1021/np50043a028openalex-snapshot
Identification of 11-Hydroxyvittatine in Sternbergia lutea
inferredcites →https://doi.org/10.1021/np50076a033openalex-snapshot
(-)-3-O-Acetylnarcissidine, a New Alkaloid from Hippeastrum puniceum
inferredcites →https://doi.org/10.1021/np50098a030openalex-snapshot
Cytotoxicity of Hymenocallis expansa Alkaloids
inferredcites →https://doi.org/10.1021/ol9911472openalex-snapshot
Total Syntheses of (−)-Haemanthidine, (+)-Pretazettine, and (+)-Tazettine
inferredcites →https://doi.org/10.1039/b316106bopenalex-snapshot
Amaryllidaceae and Sceletium alkaloids
inferredcites →https://doi.org/10.1039/c39840001693openalex-snapshot
Isolation and structure of pancratistatin
inferredcites →https://doi.org/10.1055/s-2004-818919openalex-snapshot
Acetylcholinesterase Enzyme Inhibitory Effects of Amaryllidaceae Alkaloids
inferredcites →https://doi.org/10.1055/s-2006-957381openalex-snapshot
Cytotoxic and Antimalarial Alkaloids fromBrunsvigia littoralis
inferredcites →https://doi.org/10.1055/s-2007-969669openalex-snapshot
Phytochemical Investigation ofHippeastrum vittatum
inferredcites →https://doi.org/10.1107/s0021889898007717openalex-snapshot
SIR 97: a new tool for crystal structure determination and refinement
inferredcites →https://doi.org/10.1107/s0021889899006020openalex-snapshot
WinGX suite for small-molecule single-crystal crystallography
inferredcites →https://doi.org/10.1248/cpb.35.1070openalex-snapshot
Alkaloidal constituents of Hymenocallis rotata Herb. (Amaryllidaceae).
inferredcites →https://doi.org/10.1248/cpb.39.1849openalex-snapshot
Alkaloidal Constituents of the Flowers of Lycoris radiata Herb. Amaryllidaceae.
inferredcites →https://doi.org/10.3987/com-88-4694openalex-snapshot
New Alkaloids from Pancratium maritimum L
inferredcites →https://doi.org/10.3987/com-89-5275openalex-snapshot
New Amaryllidaceae Alkaloids from Narcissus papyraceus Ker-Gawler

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.2022.113564zenodo-depositor-declared
Structurally diverse alkaloids with nine frameworks from Zephyranthes candida and their acetylcholinesterase inhibitory and anti-inflammatory activities
inferred← citeshttps://doi.org/10.1002/9783527664610.ch7openalex-snapshot
Simplified NMR Procedures for the Assignment of the Absolute Configuration
inferred← citeshttps://doi.org/10.1002/ange.201307324openalex-snapshot
Bioinspired Total Synthesis of Montanine‐Type Amaryllidaceae Alkaloids
inferred← citeshttps://doi.org/10.1002/anie.201307324openalex-snapshot
Bioinspired Total Synthesis of Montanine‐Type Amaryllidaceae Alkaloids
inferred← citeshttps://doi.org/10.1002/ejoc.201403569openalex-snapshot
Computational NMR Methods in the Stereochemical Analysis of Organic Compounds: Are Proton or Carbon NMR Chemical Shift Data More Discriminating?
inferred← citeshttps://doi.org/10.1002/ejoc.202000942openalex-snapshot
One‐Pot Two‐Step Synthesis of Isochromene‐Fused CF3‐Substituted Pyrazoles
inferred← citeshttps://doi.org/10.1002/elsc.201100177openalex-snapshot
Galanthamine production by L eucojum aestivum L . shoot culture in a modified bubble column bioreactor with internal sections
inferred← citeshttps://doi.org/10.1002/hlca.201000176openalex-snapshot
Amaryllidaceae Alkaloids from Lycoris radiata
inferred← citeshttps://doi.org/10.1002/pca.1158openalex-snapshot
Metabolic profiling of bioactive Pancratium canariense extracts by GC‐MS
inferred← citeshttps://doi.org/10.1007/978-3-031-29006-0_12-1openalex-snapshot
Bioactive Compounds and Biological Activities of the Genus Pancratium
inferred← citeshttps://doi.org/10.1007/978-3-031-44746-4_12openalex-snapshot
Bioactive Compounds and Biological Activities of the Genus Pancratium
inferred← citeshttps://doi.org/10.1007/978-3-642-22144-6_18openalex-snapshot
Amaryllidaceae Alkaloids
inferred← citeshttps://doi.org/10.1007/978-3-642-36202-6_18-1openalex-snapshot
Amaryllidaceae Alkaloids
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/s11738-010-0622-7openalex-snapshot
Alkaloids biosynthesis by Pancratium maritimum L. shoots in liquid culture
inferred← citeshttps://doi.org/10.1007/s13562-013-0222-xopenalex-snapshot
Temporary immersion systems for Amaryllidaceae alkaloids biosynthesis by Pancratium maritimum L. shoot culture
inferred← citeshttps://doi.org/10.1007/s13659-018-0163-0openalex-snapshot
Anti-TMV Effects of Amaryllidaceae Alkaloids Isolated from the Bulbs of Lycoris radiata and Lycoricidine Derivatives
inferred← citeshttps://doi.org/10.1016/bs.alkal.2019.10.002openalex-snapshot
Chemodiversity, chemotaxonomy and chemoecology of Amaryllidaceae alkaloids
inferred← citeshttps://doi.org/10.1016/j.bmc.2010.05.023openalex-snapshot
Synthesis and antiplasmodial activity of lycorine derivatives
inferred← citeshttps://doi.org/10.1016/j.bmc.2012.07.036openalex-snapshot
Synthesis and antimalarial activity of new haemanthamine-type derivatives
inferred← citeshttps://doi.org/10.1016/j.ejmech.2013.03.018openalex-snapshot
Preparation and antimalarial activity of semisynthetic lycorenine derivatives
inferred← citeshttps://doi.org/10.1016/j.fitote.2013.05.006openalex-snapshot
Neuroprotective compounds from the bulbs of Lycoris radiata
inferred← citeshttps://doi.org/10.1016/j.jplph.2011.09.010openalex-snapshot
Alkaloid patterns in Leucojum aestivum shoot culture cultivated at temporary immersion conditions
inferred← citeshttps://doi.org/10.1016/j.phytol.2011.05.008openalex-snapshot
Antiprotozoal alkaloids from Galanthus trojanus
inferred← citeshttps://doi.org/10.1016/j.phytol.2012.03.004openalex-snapshot
Alkaloids from Galanthus rizehensis
inferred← citeshttps://doi.org/10.1016/j.sajb.2019.11.016openalex-snapshot
A comprehensive study on narcissus tazetta subsp. tazetta L.: Chemo-profiling, isolation, anticholinesterase activity and molecular docking of amaryllidaceae alkaloids
inferred← citeshttps://doi.org/10.1016/j.tetlet.2016.04.055openalex-snapshot
Multigram synthesis of an advanced nitroalkene intermediate: application in synthesis of octahydroindol-2-one derivative featuring diastereoselective Michael addition of diethylmalonate
inferred← citeshttps://doi.org/10.1016/s1099-4831(10)06801-xopenalex-snapshot
Chemistry and Biology of Pancratium Alkaloids
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.4c00825openalex-snapshot
Undescribed Amaryllidaceae Alkaloids from Zephyranthes citrina and Their Cytotoxicity
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.7b00301openalex-snapshot
Acetylcholinesterase Inhibitory Alkaloids from the Whole Plants of Zephyranthes carinata
inferred← citeshttps://doi.org/10.1021/acs.orglett.3c02310openalex-snapshot
Diastereoselective Construction of Fused Carbocyclic Pyrrolidines via a Copper-Catalyzed [3 + 2] Cycloaddition: Total Syntheses of Pancratinines B–C
inferred← citeshttps://doi.org/10.1021/jo401888fopenalex-snapshot
Halonium Ion Triggered Rearrangement of Unsaturated Benzo-Annulated Bi- and Tricyclic Sulfonamides
inferred← citeshttps://doi.org/10.1021/np200285jopenalex-snapshot
Kinetic Study of the Rearrangement of Deuterium-Labeled 4′-O-Methylnorbelladine inLeucojum aestivumShoot Cultures by Mass Spectrometry. Influence of Precursor Feeding on Amaryllidaceae Alkaloid Accumulation
inferred← citeshttps://doi.org/10.1021/ol900065xopenalex-snapshot
Bioactive Montanine Derivatives from Halide-induced Rearrangements of Haemanthamine-type Alkaloids. Absolute Configuration by VCD
inferred← citeshttps://doi.org/10.1039/c0np00073fopenalex-snapshot
Amaryllidaceae and Sceletium alkaloids
inferred← citeshttps://doi.org/10.1039/c8cy01425fopenalex-snapshot
Oxidative cross-coupling reaction of catechols with active methylene compounds in an aqueous medium using an AlPO 4 -supported Ru catalyst
inferred← citeshttps://doi.org/10.1039/d3qo01835kopenalex-snapshot
Asymmetric total synthesis of montanine-type amaryllidaceae alkaloids
inferred← citeshttps://doi.org/10.1080/10286020.2016.1198332openalex-snapshot
Phytochemical and biological investigations of Amaryllidaceae alkaloids: a review
inferred← citeshttps://doi.org/10.1080/14786419.2019.1574785openalex-snapshot
Pseudolycorine N-oxide, a new N-oxide from Narcissus tazetta
inferred← citeshttps://doi.org/10.3390/molecules200813854openalex-snapshot
Antiproliferative and Structure Activity Relationships of Amaryllidaceae Alkaloids
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/molecules26133990openalex-snapshot
Neuroprotective Activities of Crossyne flava Bulbs and Amaryllidaceae Alkaloids: Implications for Parkinson’s Disease
Editorial review for independent work. ICSAC — the Institute for Complexity Science and Advanced Computing — runs a structured editorial panel for researchers publishing outside journals, and publishes on CiteStamp rails. Submission is free and goes through ORCID: icsacinstitute.org/submit.