On the public citation graph

Four New Crinine-Type Alkaloids from Sternbergia Species

https://doi.org/10.1021/np50064a020
0 signed · 56 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 See whether every reference in this work resolves to a known work and none has been retracted — and get a dated CiteStamped badge you can embed.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 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.2020.112485zenodo-depositor-declared
Streamlined targeting of Amaryllidaceae alkaloids from the bulbs of Crinum scillifolium using spectrometric and taxonomically-informed scoring metabolite annotations
inferred← citeshttps://doi.org/10.1016/j.phytochem.2022.113473zenodo-depositor-declared
Alkaloids with cholinesterase inhibitory activities from the bulbs of Crinum × amabile Donn ex Ker Gawl
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/cbdv.200890031openalex-snapshot
Phytochemical and Biological Investigation of Hymenocallis littoralis Salisb .
inferred← citeshttps://doi.org/10.1002/chir.22719openalex-snapshot
Amaryllidaceae alkaloids: Absolute configuration and biological activity
inferred← citeshttps://doi.org/10.1002/pca.1157openalex-snapshot
Analysis of metabolic variation and galanthamine content in Narcissus bulbs by 1H NMR
inferred← citeshttps://doi.org/10.1002/rcm.70019openalex-snapshot
GC–MS of Some Haemanthamine‐ and Crinine‐Type Amaryllidaceae Alkaloids
inferred← citeshttps://doi.org/10.1007/s12272-014-0397-2openalex-snapshot
Alkaloids from the bulbs of Lycoris longituba and their neuroprotective and acetylcholinesterase inhibitory activities
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)00448-gopenalex-snapshot
Alkaloids from Narcissus cantabricus
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.bse.2011.01.012openalex-snapshot
Amaryllidaceae alkaloids from the Australasian tribe Calostemmateae with acetylcholinesterase inhibitory activity
inferred← citeshttps://doi.org/10.1016/j.fitote.2004.11.007openalex-snapshot
Antimicrobial activity of Sternbergia sicula and Sternbergia lutea
inferred← citeshttps://doi.org/10.1016/j.phytochem.2014.03.007openalex-snapshot
Crinine-type alkaloids from Hippeastrum aulicum and H. calyptratum
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.2012.03.004openalex-snapshot
Alkaloids from Galanthus rizehensis
inferred← citeshttps://doi.org/10.1016/j.phytol.2016.07.016openalex-snapshot
Alkaloids from Galanthus fosteri
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.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.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.2004.03.087openalex-snapshot
Synthesis of Amaryllidaceae alkaloids, siculine, oxocrinine, epicrinine, and buflavine
inferred← citeshttps://doi.org/10.1016/s0031-9422(96)00506-7openalex-snapshot
Alkaloids from Brunsvigia orientalis
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/s0040-4020(98)00491-8openalex-snapshot
4,4′-Disubstituted 1,2,3,4-tetrahydroisoquinolines from alkylation of a chiral non racemic lactam. An approach to the crinine-type alkaloids
inferred← citeshttps://doi.org/10.1016/s0099-9598(08)60008-5openalex-snapshot
The Amaryllidaceae Alkaloids
inferred← citeshttps://doi.org/10.1016/s0367-326x(00)00313-0openalex-snapshot
Alkaloids from Cyrtanthus elatus
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(10)06801-xopenalex-snapshot
Chemistry and Biology of Pancratium Alkaloids
inferred← citeshttps://doi.org/10.1016/s1572-5995(97)80034-8openalex-snapshot
Narcissus alkaloids
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/10.1021/acsptsci.6c00139openalex-snapshot
From Daffodils to Drug Leads: Amaryllidaceae Alkaloids Target Protein Translation in Chronic Lymphocytic Leukemia to Induce Selective Apoptosis
inferred← citeshttps://doi.org/10.1021/np100819nopenalex-snapshot
Comprehensive Study of Alkaloids from Crinum asiaticum var. sinicum Assisted by HPLC-DAD-SPE-NMR
inferred← citeshttps://doi.org/10.1039/b106369nopenalex-snapshot
π-Allyl cation cyclisations initiated by electrocyclic ring-opening of gem-dihalocyclopropanes: application to the first total syntheses of the crinine-type alkaloids maritinamine and epi-maritinamine
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/np9941100329openalex-snapshot
Amaryllidaceae and Sceletium alkaloids
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/10.1074/jbc.m116.717827openalex-snapshot
Identification of a Noroxomaritidine Reductase with Amaryllidaceae Alkaloid Biosynthesis Related Activities
inferred← citeshttps://doi.org/10.1080/10286020.2013.864639openalex-snapshot
Two new alkaloids from the bulbs of Lycoris sprengeri
inferred← citeshttps://doi.org/10.1080/10286020.2023.2269541openalex-snapshot
Acetylcholinesterase inhibition studies of alkaloid components from Crinum asiaticum var. sinicum : in vitro assessments by molecular docking and molecular dynamics simulations
inferred← citeshttps://doi.org/10.1080/14786419.2025.2592267openalex-snapshot
Phytochemical investigation of Crinum asiaticum L.: isolation and characterisation of a new dimeric alkaloid and evaluation of acetylcholinesterase inhibition with molecular docking
inferred← citeshttps://doi.org/10.1134/s199542122303036xopenalex-snapshot
Isoquinoline Alkaloids of Amaryllidaceae Crinane Alkaloids
inferred← citeshttps://doi.org/10.12991/201014446openalex-snapshot
Quality control and anticholinesterase activity determinations on Sternbergia sicula
inferred← citeshttps://doi.org/10.12991/mpj.81757openalex-snapshot
Quality control and anticholinesterase activity determinations on Sternbergia sicula
inferred← citeshttps://doi.org/10.1351/pac200880040669openalex-snapshot
New processes for the synthesis of biologically relevant heterocycles
inferred← citeshttps://doi.org/10.1515/znc-2009-5-601openalex-snapshot
Alkaloids from Sternbergia colchiciflora
inferred← citeshttps://doi.org/10.20307/nps.2024.30.4.304openalex-snapshot
Alkaloids with Acetylcholinesterase Inhibitory Activities from Crinum latifolium L.
inferred← citeshttps://doi.org/10.3390/molecules26030765openalex-snapshot
The Chemical Synthesis of the Crinine and Haemanthamine Alkaloids: Biologically Active and Enantiomerically-Related Systems that Serve as Vehicles for Showcasing New Methodologies for Molecular Assembly
inferred← citeshttps://doi.org/10.3390/plants11223034openalex-snapshot
Amaryllidaceae Alkaloids from Clivia miniata (Lindl.) Bosse (Amaryllidaceae): Isolation, Structural Elucidation, and Biological Activity
inferred← citeshttps://doi.org/10.3390/plants14131935openalex-snapshot
The Occurrence and Bioactivities of Amaryllidaceae Alkaloids from Plants: A Taxonomy-Guided Genera-Wide Review
inferred← citeshttps://doi.org/10.3390/toxins14040262openalex-snapshot
Cytotoxicity and Antiviral Properties of Alkaloids Isolated from Pancratium maritimum
inferred← citeshttps://doi.org/10.70675/578e81f8zc8cbz4f56z9399z3d106e1a6047openalex-snapshot
Synthèse totale d'alcaloïdes de type Lycorine par métathèse tandem
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.