On the public citation graph

Cytotoxic Alkaloids from the Whole Plants of Zephyranthes candida

0 signed · 116 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 See whether every reference in this work resolves to a known work and none has been retracted — and get a dated CiteStamped badge you can embed.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/cber.19550881019openalex-snapshot

Alkaloide von Sprekelia formosissima, Galanthus Elwesii, Zephyranthes candida und Crinum Powellii (VIII. Mitteil. über Amaryllidaceen‐Alkaloide1))

inferredcites →https://doi.org/10.1007/s10600-010-9564-yopenalex-snapshot

Another two novel ceramides from Zephyranthes candida

inferredcites →https://doi.org/10.1007/s11745-008-3246-6openalex-snapshot

Two Novel Ceramides with a Phytosphingolipid and a Tertiary Amide Structure from Zephyranthes candida

inferredcites →https://doi.org/10.1016/0022-1759(83)90303-4openalex-snapshot

Rapid colorimetric assay for cellular growth and survival: Application to proliferation and cytotoxicity assays

inferredcites →https://doi.org/10.1016/0031-9422(83)83051-9openalex-snapshot

1H and 13c nmr analysis of lycorine and α-dihydrolycorine

inferredcites →https://doi.org/10.1016/0031-9422(90)80157-copenalex-snapshot

Ismine and related alkaloids from Lapiedra martinezii

inferredcites →https://doi.org/10.1016/0031-9422(90)85448-oopenalex-snapshot

Alkaloids from Narcissus bicolor

inferredcites →https://doi.org/10.1016/j.canlet.2008.08.029openalex-snapshot

Lycorine induces apoptosis and down-regulation of Mcl-1 in human leukemia cells

inferredcites →https://doi.org/10.1016/j.febslet.2004.10.095openalex-snapshot

Effects of lycorine on HL‐60 cells via arresting cell cycle and inducing apoptosis

inferredcites →https://doi.org/10.1016/s0031-9422(00)83001-0openalex-snapshot

Crinum alkaloids: their chemistry and biology

inferredcites →https://doi.org/10.1016/s0031-9422(02)00206-6openalex-snapshot

A dinitrogenous alkaloid from Cyrtanthus obliquus

inferredcites →https://doi.org/10.1016/s0031-9422(98)00651-7openalex-snapshot

Two novel dinitrogenous alkaloids from Galanthus plicatus subsp. byzantinus (Amaryllidaceae)

inferredcites →https://doi.org/10.1021/ja01001a024openalex-snapshot

Structure of 6-hydroxycrinamine

inferredcites →https://doi.org/10.1021/jm901031hopenalex-snapshot

Lycorine, the Main Phenanthridine Amaryllidaceae Alkaloid, Exhibits Significant Antitumor Activity in Cancer Cells That Display Resistance to Proapoptotic Stimuli: An Investigation of Structure−Activity Relationship and Mechanistic Insight

inferredcites →https://doi.org/10.1021/np030529kopenalex-snapshot

New Crinine-Type Alkaloids with Inhibitory Effect on Induction of Inducible Nitric Oxide Synthase from Crinum yemense

inferredcites →https://doi.org/10.1021/np50067a026openalex-snapshot

Antineoplastic Agents, 162. Zephyranthes candida

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/10.1039/b718044fopenalex-snapshot

Amaryllidaceae and Sceletium alkaloids

inferredcites →https://doi.org/10.1039/c0np00073fopenalex-snapshot

Amaryllidaceae and Sceletium alkaloids

inferredcites →https://doi.org/10.1039/jr9650002001openalex-snapshot

358. Proton magnetic resonance studies of some amaryllidaceae alkaloids of the 5,10b-ethanophenanthridine series and of criwelline and tazettine

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/10.1055/s-2002-32068openalex-snapshot

Antiproliferative Amaryllidaceae Alkaloids Isolated from the Bulbs of Sprekelia formosissima and Hymenocallis × festalis

inferredcites →https://doi.org/10.1055/s-2006-958007openalex-snapshot

Cytotoxic Activity of Amaryllidaceae Alkaloids

inferredcites →https://doi.org/10.1107/s0108270198006933openalex-snapshot

AmaryllidaceaeAlkaloids: (+)-Tazettine, (+)-3-O-Demethylcriwelline and (+)-3-Epimacronine at 173 K

inferredcites →https://doi.org/10.1107/s0108767383001762openalex-snapshot

On enantiomorph-polarity estimation

inferredcites →https://doi.org/10.1248/yakushi1947.84.12_1194openalex-snapshot

Studies on the Alkaloids of Zephyranthes candida HERB. I

inferredcites →https://doi.org/10.1248/yakushi1947.85.8_699openalex-snapshot

Studies on the Alkaloids of Zephyranthes candida HERB. IV

inferredcites →https://doi.org/10.3987/com-00-9132openalex-snapshot

Four New Amaryllidaceae Alkaloids from Galanthus gracilis andÅ@Galanthus plicatus Subsp. byzantinus

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/adsc.201800606openalex-snapshot

Synthesis and Reactivity of o‐Enoyl Arylisocyanides: Access to Phenanthridine‐8‐Carboxylate Derivatives

inferred← citeshttps://doi.org/10.1002/ange.202206064openalex-snapshot

Oxidation Potential Gap (ΔEox): The Hidden Parameter in Redox Chemistry

inferred← citeshttps://doi.org/10.1002/anie.202206064openalex-snapshot

Oxidation Potential Gap (ΔEox): The Hidden Parameter in Redox Chemistry

inferred← citeshttps://doi.org/10.1002/cjoc.202100582openalex-snapshot

Au(I)‐Catalyzed 6‐ endo ‐ dig Cyclizations of Aromatic 1, 5‐Enynes to 2‐(Naphthalen‐2‐yl)anilines Leading to Divergent Syntheses of Benzo[ α ]carbazole, Benzo[ c , h ]cinnoline and Dibenzo[ i ]phenanthridine Derivatives

inferred← citeshttps://doi.org/10.1002/ejoc.202001404openalex-snapshot

Five‐Membered Nitrogen Heterocycles Synthesis through 1,3‐Dipolar Cycloaddition of Non‐Stabilized Azomethine Ylides with 2‐Pyridone Heteroaromatic Systems as Dipolarophiles

inferred← citeshttps://doi.org/10.1002/ejoc.202101511openalex-snapshot

Total Syntheses of the Imidazo[1,2‐f]phenanthridine‐Containing Alkaloid Zephycandidine A

inferred← citeshttps://doi.org/10.1002/jhet.2725openalex-snapshot

Facile Synthesis of Phenanthridinone Alkaloids via Suzuki–Miyaura Cross‐coupling

inferred← citeshttps://doi.org/10.1002/rcm.9506openalex-snapshot

Gas chromatography–mass spectrometry of some homolycorine‐type Amaryllidaceae alkaloids

inferred← citeshttps://doi.org/10.1007/978-3-030-83350-3_14-1openalex-snapshot

Herbal Drugs Against Polio Infections: Ethnopharmacology, Chemistry, and Clinical and Preclinical Studies

inferred← citeshttps://doi.org/10.1007/978-3-031-12199-9_14openalex-snapshot

Herbal Drugs Against Polio Infections: Ethnopharmacology, Chemistry, and Clinical and Preclinical Studies

inferred← citeshttps://doi.org/10.1007/978-3-031-29006-0_14-1openalex-snapshot

Bioactive Compounds and Biological Activities of Zephyranthes Species

inferred← citeshttps://doi.org/10.1007/978-3-031-44746-4_14openalex-snapshot

Bioactive Compounds and Biological Activities of Zephyranthes Species

inferred← citeshttps://doi.org/10.1007/978-3-031-77900-8_22openalex-snapshot

Genetic Landscape of Zephyranthes: Insights into Breeding and Propagation

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/s11101-024-09931-1openalex-snapshot

Specialized metabolites of the genus Zephyranthes Herb.: a critical review on taxonomy and phytochemistry

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/s11418-014-0819-yopenalex-snapshot

Four new Amaryllidaceae alkaloids from Zephyranthes candida

inferred← citeshttps://doi.org/10.1016/b978-0-444-63601-0.00003-xopenalex-snapshot

Cytotoxic Alkaloid Constituents of the Amaryllidaceae

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.bioorg.2020.104261openalex-snapshot

Antiproliferative abietane quinone diterpenoids from the roots of Salvia deserta

inferred← citeshttps://doi.org/10.1016/j.bioorg.2020.104567openalex-snapshot

Alkaloids of Zephyranthes citrina (Amaryllidaceae) and their implication to Alzheimer's disease: Isolation, structural elucidation and biological activity

inferred← citeshttps://doi.org/10.1016/j.bioorg.2021.104693openalex-snapshot

Chaetocochin J, an epipolythiodioxopiperazine alkaloid, induces apoptosis and autophagy in colorectal cancer via AMPK and PI3K/AKT/mTOR pathways

inferred← citeshttps://doi.org/10.1016/j.bmcl.2016.10.081openalex-snapshot

Flavans with potential anti-inflammatory activities from Zephyranthes candida

inferred← citeshttps://doi.org/10.1016/j.ejmech.2016.10.057openalex-snapshot

Amaryllidaceae alkaloids with new framework types from Zephyranthes candida as potent acetylcholinesterase inhibitors

inferred← citeshttps://doi.org/10.1016/j.fitote.2017.06.021openalex-snapshot

Secondary metabolites from endophytic fungus Chaetomium sp. induce colon cancer cell apoptotic death

inferred← citeshttps://doi.org/10.1016/j.fitote.2020.104546openalex-snapshot

New triterpenoids, steroids and lignan from the stem barks of Entandrophragma utile

inferred← citeshttps://doi.org/10.1016/j.fitote.2020.104704openalex-snapshot

Peraksine derivatives with potential anti-inflammatory activities from the stems of Rauvolfia vomitoria

inferred← citeshttps://doi.org/10.1016/j.fitote.2021.104873openalex-snapshot

Chisosiamens A–E, five new ring-intact limonoids with isomerized furan ring from the fruit of Chisocheton siamensis

inferred← citeshttps://doi.org/10.1016/j.fitote.2024.106309openalex-snapshot

Bioactive phenolics from the bulbs of Hymenocallis littoralis

inferred← citeshttps://doi.org/10.1016/j.jff.2014.02.001openalex-snapshot

Production of nigragillin and dihydrophaseic acid by biotransformation of litchi pericarp with Aspergillus awamori and their antioxidant activities

inferred← citeshttps://doi.org/10.1016/j.jpba.2019.06.047openalex-snapshot

Simultaneous quantification and identification of Amaryllidaceae alkaloids in Narcissus tazetta by ultra performance liquid chromatography-diode array detector-electrospray ionisation tandem mass spectrometry

inferred← citeshttps://doi.org/10.1016/j.molstruc.2024.137692openalex-snapshot

Synthesis and characterization of copper(II) norcraugsodine complexes: Their in vitro binding studies with therapeutic targets (ct-DNA/tRNA/BSA), cleavage, and cytotoxicity profile

inferred← citeshttps://doi.org/10.1016/j.phytochem.2018.03.012openalex-snapshot

Hebecarposides A−K, antiproliferative lanostane-type triterpene glycosides from the leaves of Lyonia ovalifolia var. hebecarpa

inferred← citeshttps://doi.org/10.1016/j.phytochem.2018.04.004openalex-snapshot

Trijugin- and mexicanolide-type limonoids from the fruits of Heynea trijuga that reverse multidrug resistance in MCF-7/DOX cells

inferred← citeshttps://doi.org/10.1016/j.phytochem.2018.09.010openalex-snapshot

Norditerpenoid alkaloids from Delphinium pseudoaemulans C. Y. Yang et B. Wang

inferred← citeshttps://doi.org/10.1016/j.phytochem.2024.114198openalex-snapshot

Immunosuppressive alkaloids from Narcissus tazetta subsp. Chinensis and the mechanism of (+)-narciclasine in vitro and in vivo

inferred← citeshttps://doi.org/10.1016/j.phytol.2015.08.004openalex-snapshot

Cytotoxic activities of Amaryllidaceae alkaloids against gastrointestinal cancer cells

inferred← citeshttps://doi.org/10.1016/j.phytol.2019.06.009openalex-snapshot

Three new diterpenoid alkaloids from Delphinium naviculare var. lasiocarpum W. T. Wang

inferred← citeshttps://doi.org/10.1016/j.plantsci.2020.110764openalex-snapshot

Abscisic acid-mediated induction of FLAVIN-CONTAINING MONOOXYGENASE 2 leads to reduced accumulation of methylthioalkyl glucosinolates in Arabidopsis thaliana

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.taap.2014.08.009openalex-snapshot

N-methylhemeanthidine chloride, a novel Amaryllidaceae alkaloid, inhibits pancreatic cancer cell proliferation via down-regulating AKT activation

inferred← citeshttps://doi.org/10.1016/j.tetlet.2020.151785openalex-snapshot

Synthesis of zephycandidine A from haemanthamine

inferred← citeshttps://doi.org/10.1016/j.tetlet.2026.156039openalex-snapshot

Visible light-mediated synthesis of phenanthridine derivative via imine intermediates

inferred← citeshttps://doi.org/10.1021/acs.jnatprod.0c01180openalex-snapshot

Structurally Diverse Diterpenoids from the Roots of Salvia deserta Based on Nine Different Skeletal Types

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.5b00681openalex-snapshot

Galanthamine, Plicamine, and Secoplicamine Alkaloids from Zephyranthes candida and Their Anti-acetylcholinesterase and Anti-inflammatory Activities

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.joc.5b02903openalex-snapshot

Kinetic Control of Rh(III)-Catalyzed Annulation of C–H Bonds with Quinones: Chemoselective Synthesis of Hydrophenanthridinones and Phenanthridinones

inferred← citeshttps://doi.org/10.1021/acs.orglett.1c00709openalex-snapshot

Iridium-Catalyzed Asymmetric Cascade Allylation/Pictet–Spengler Cyclization Reaction for the Enantioselective Synthesis of 1,3,4-Trisubstituted Tetrahydroisoquinolines

inferred← citeshttps://doi.org/10.1021/acscatal.3c00063openalex-snapshot

Divergent Rh Catalysis: Asymmetric Dearomatization Versus C–H Activation Initiated by C–C Activation

inferred← citeshttps://doi.org/10.1021/np400600copenalex-snapshot

Cytotoxic ent-Kaurane Diterpenoids from Salvia cavaleriei

inferred← citeshttps://doi.org/10.1038/srep09294openalex-snapshot

Indole diketopiperazines from endophytic Chaetomium sp 88194 induce breast cancer cell apoptotic death

inferred← citeshttps://doi.org/10.1038/srep20045openalex-snapshot

Cytotoxic Rocaglate Derivatives from Leaves of Aglaia perviridis

inferred← citeshttps://doi.org/10.1038/srep26510openalex-snapshot

Small molecule activation of NOTCH signaling inhibits acute myeloid leukemia

inferred← citeshttps://doi.org/10.1038/srep33990openalex-snapshot

Zephycandidine A, the First Naturally Occurring Imidazo[1,2-f]phenanthridine Alkaloid from Zephyranthes candida, Exhibits Significant Anti-tumor and Anti-acetylcholinesterase Activities

inferred← citeshttps://doi.org/10.1039/c4ob00797bopenalex-snapshot

A new synthetic approach to 6-unsubstituted phenanthridine and phenanthridine-like compounds under mild and metal-free conditions

inferred← citeshttps://doi.org/10.1039/c4ra11675eopenalex-snapshot

Hyperattenins A–I, bioactive polyprenylated acylphloroglucinols from Hypericum attenuatum Choisy

inferred← citeshttps://doi.org/10.1039/c6cc09430aopenalex-snapshot

Organocatalyzed aerobic oxidative Robinson-type annulation of 2-isocyanochalcones: expedient synthesis of phenanthridines

inferred← citeshttps://doi.org/10.1039/c6np00068aopenalex-snapshot

Amaryllidaceae and Sceletium alkaloids

inferred← citeshttps://doi.org/10.1039/c8np00055gopenalex-snapshot

Amaryllidaceae and Sceletium alkaloids

inferred← citeshttps://doi.org/10.1039/c9ra04747fopenalex-snapshot

Cytotoxic and antimicrobial indole alkaloids from an endophytic fungus Chaetomium sp. SYP-F7950 of Panax notoginseng

inferred← citeshttps://doi.org/10.1039/d0cc00300jopenalex-snapshot

Expeditious synthesis of phenanthridines through a Pd/MnO 2 -mediated C–H arylation/oxidative annulation cascade from aldehydes, aryl iodides and amino acids

inferred← citeshttps://doi.org/10.1039/d0qo00735hopenalex-snapshot

Spirodesertols A and B, two highly modified spirocyclic diterpenoids with an unprecedented 6-isopropyl-3 H -spiro[benzofuran-2,1′-cyclohexane] motif from Salvia deserta

inferred← citeshttps://doi.org/10.1039/d0sc05763kopenalex-snapshot

Metal-free tandem carbene N–H insertions and C–C bond cleavages

inferred← citeshttps://doi.org/10.1039/d4sc03907fopenalex-snapshot

Visible light-induced Mallory reaction of tertiary benzanilides via iminium intermediates

inferred← citeshttps://doi.org/10.1039/d5ra06934copenalex-snapshot

Dual fluorescent phenanthridinones and crinasiadine derivatives by consecutive palladium-catalyzed three-component syntheses

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-1957-4343openalex-snapshot

Tf2O-Promoted Morgan–Walls Reaction: From a Flexible Approach to Functionalized Phenanthridines and Quinazolines to the Short and Divergent Total Syntheses of Alkaloids

inferred← citeshttps://doi.org/10.1080/10286020.2013.864639openalex-snapshot

Two new alkaloids from the bulbs of Lycoris sprengeri

inferred← citeshttps://doi.org/10.1080/10286020.2016.1198332openalex-snapshot

Phytochemical and biological investigations of Amaryllidaceae alkaloids: a review

inferred← citeshttps://doi.org/10.1080/10826076.2016.1204615openalex-snapshot

Comparison of different HPLC systems for analysis of galantamine and lycorine in various species of Amaryllidaceae family

inferred← citeshttps://doi.org/10.1080/14786419.2019.1598989openalex-snapshot

Profiling of acetylcholinesterase inhibitory alkaloids from some Crinum, Habranthus and Zephyranthes species by GC–MS combined with multivariate analyses and in silico studies

inferred← citeshttps://doi.org/10.1080/14786419.2021.1872568openalex-snapshot

Armochaetoglasins J and K: new cytochalasans from Chaetomium globosum

inferred← citeshttps://doi.org/10.1093/nar/gky202openalex-snapshot

ZYH005, a novel DNA intercalator, overcomes all-trans retinoic acid resistance in acute promyelocytic leukemia

inferred← citeshttps://doi.org/10.1177/1934578x1400900834openalex-snapshot

Cytotoxicity Studies of Lycorine Alkaloids of the Amaryllidaceae

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/10.20944/preprints202406.0855.v1openalex-snapshot

Potential Distribution of 11 Species of the Genus Zephyranthes Herb. (Amaryllidaceae) in Mexico

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/10.3184/174751917x14894997017496openalex-snapshot

Rapid Synthesis of Ismine, a Bioactive Amaryllidaceae Alkaloid

inferred← citeshttps://doi.org/10.3390/ecologies5040034openalex-snapshot

Prediction of Environmentally Suitable Areas for Zephyranthes (Amaryllidaceae) in Mexico

inferred← citeshttps://doi.org/10.3390/molecules25235621openalex-snapshot

Advances in the Chemical and Biological Characterization of Amaryllidaceae Alkaloids and Natural Analogues Isolated in the Last Decade

inferred← citeshttps://doi.org/10.3390/plants13050569openalex-snapshot

Influence of Sucrose and Activated Charcoal on Phytochemistry and Vegetative Growth in Zephyranthes irwiniana (Ravenna) Nic. García (Amaryllidaceae)

inferred← citeshttps://doi.org/10.3390/plants13243577openalex-snapshot

Phytochemical and Cytotoxic Aspects of Amaryllidaceae Alkaloids in Galanthus Species: A Review

inferred← citeshttps://doi.org/10.4103/0973-1296.210176openalex-snapshot

In vitro cell viability by CellProfiler®software as equivalent to MTT assay

inferred← citeshttps://doi.org/10.4172/2167-0412.1000212openalex-snapshot

Phytochemistry and Pharmacology of Genus Zephyranthes

inferred← citeshttps://doi.org/10.5772/intechopen.92596openalex-snapshot

Plant-Derived Compounds against Microbial Infections and Cancers

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.