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Cytotoxic Arylnaphthalene Lignans from a Vietnamese Acanthaceae, Justicia patentiflora

https://doi.org/10.1021/np050028u
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Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1007/s002800050764openalex-snapshot
Preclinical in vivo antitumor activity of vinflunine, a novel fluorinated Vinca alkaloid
inferredcites →https://doi.org/10.1016/0031-9422(84)83096-4openalex-snapshot
Lignans of haplophyllum tuberculatum
inferredcites →https://doi.org/10.1017/cbo9780511983665openalex-snapshot
Lignans
inferredcites →https://doi.org/10.1021/jo952048eopenalex-snapshot
Hindered Rotation in Arylnaphthalene Lignans
inferredcites →https://doi.org/10.1093/emboj/17.16.4668openalex-snapshot
The requirement for the p53 proline‐rich functional domain for mediation of apoptosis is correlated with specific PIG3 gene transactivation and with transcriptional repression

What points at this work

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

inferred← citeshttps://doi.org/10.3897/pharmacia.71.e117690zenodo-depositor-declared
Arylnaphthalene lignans with a focus Linum species: a review on phytochemical, biotechnological and pharmacological potential
inferred← citeshttps://doi.org/10.1002/9781118682784.ch11openalex-snapshot
Biological Properties of Lignans
inferred← citeshttps://doi.org/10.1002/cbdv.202500312openalex-snapshot
New Phenolic Compounds from Eucalyptus tereticornis with Antioxidant Activity
inferred← citeshttps://doi.org/10.1002/chem.201500978openalex-snapshot
A Combined Transition‐Metal‐Catalyzed and Photopromoted Process: Synthesis of 2,3‐Fused 4‐Phenylnaphthalen‐1‐yl Carboxylates from 1,7‐Diaryl‐1,6‐diynes
inferred← citeshttps://doi.org/10.1002/cjoc.200790127openalex-snapshot
First Synthesis of Bioactive Diphyllin Glycosides Isolated from Justicia patentiflor Hemsl
inferred← citeshttps://doi.org/10.1002/cjoc.200890014openalex-snapshot
Total Synthesis of 4′′‐O‐Acetylmananthoside B Part II: Synthesis of the Disaccharide Fragment
inferred← citeshttps://doi.org/10.1002/ejoc.201700556openalex-snapshot
First Total Synthesis of the Bioactive Arylnaphthyl Lignan 4‐O‐Glycosides Phyllanthusmin D and 4′′‐O‐Acetylmananthoside B
inferred← citeshttps://doi.org/10.1007/978-3-031-35155-6_2openalex-snapshot
The Bioactive Components of Plants
inferred← citeshttps://doi.org/10.1007/978-3-319-93506-5_1openalex-snapshot
The Search for Anticancer Agents from Tropical Plants
inferred← citeshttps://doi.org/10.1007/s00044-011-9937-1openalex-snapshot
Synthesis and in vitro anticancer activities of novel aryl-naphthalene lignans
inferred← citeshttps://doi.org/10.1007/s10637-010-9425-3openalex-snapshot
D11, a novel glycosylated diphyllin derivative, exhibits potent anticancer activity by targeting topoisomerase IIα
inferred← citeshttps://doi.org/10.1007/s11101-020-09668-7openalex-snapshot
Update on naturally occurring novel arylnaphthalenes from plants
inferred← citeshttps://doi.org/10.1007/s11101-020-09735-zopenalex-snapshot
Arylnaphthalene lactones: structures and pharmacological potentials
inferred← citeshttps://doi.org/10.1016/b978-0-444-59603-1.00006-0openalex-snapshot
Progress in the Syntheses of Dibenzocyclooctadiene Lignans
inferred← citeshttps://doi.org/10.1016/j.bmc.2018.03.033openalex-snapshot
Synthesis and antiproliferative activity of derivatives of the phyllanthusmin class of arylnaphthalene lignan lactones
inferred← citeshttps://doi.org/10.1016/j.bmc.2025.118197openalex-snapshot
Antitumor and immunomodulatory activities of diphyllin and its derivatives
inferred← citeshttps://doi.org/10.1016/j.chroma.2009.04.017openalex-snapshot
Qualitative and quantitative analysis of diterpenoids in Salvia species by liquid chromatography coupled with electrospray ionization quadrupole time-of-flight tandem mass spectrometry
inferred← citeshttps://doi.org/10.1016/j.ebiom.2019.08.060openalex-snapshot
Glycosylated diphyllin as a broad-spectrum antiviral agent against Zika virus
inferred← citeshttps://doi.org/10.1016/j.ejmech.2011.11.011openalex-snapshot
Design, synthesis and biological evaluation of novel glycosylated diphyllin derivatives as topoisomerase II inhibitors
inferred← citeshttps://doi.org/10.1016/j.ejphar.2012.09.029openalex-snapshot
Cleistanthoside A tetraacetate-induced DNA damage leading to cell cycle arrest and apoptosis with the involvement of p53 in lung cancer cells
inferred← citeshttps://doi.org/10.1016/j.fitote.2019.104198openalex-snapshot
Synthesis, cytotoxicity and anti-invasion activity of three natural diphyllin L-arabinopyranosides
inferred← citeshttps://doi.org/10.1016/j.jep.2008.09.014openalex-snapshot
Selection methodology with scoring system: Application to Mexican plants producing podophyllotoxin related lignans
inferred← citeshttps://doi.org/10.1016/j.phytochem.2009.05.016openalex-snapshot
Glycosides of arylnaphthalene lignans from Acanthus mollis having axial chirality
inferred← citeshttps://doi.org/10.1016/j.tet.2021.132214openalex-snapshot
Triflic acid catalysed regioselective synthesis of substituted naphthalenes by benzannulation of carbonyls with alkynes
inferred← citeshttps://doi.org/10.1016/j.tetlet.2026.156149openalex-snapshot
Indium chloride catalysed annulation of arylmethyl carbonyls & arylalkynes for the synthesis of naphthalene derivatives
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.7b00004openalex-snapshot
Potent Inhibitor of Drug-Resistant HIV-1 Strains Identified from the Medicinal Plant Justicia gendarussa
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.9b00018openalex-snapshot
Potential Anticancer Agents Characterized from Selected Tropical Plants
inferred← citeshttps://doi.org/10.1021/acs.orglett.5b01477openalex-snapshot
Silver(I)-Catalyzed Regioselective Construction of Highly Substituted α-Naphthols and Its Application toward Expeditious Synthesis of Lignan Natural Products
inferred← citeshttps://doi.org/10.1021/np1005357openalex-snapshot
Caffeic Acid Esters and Lignans from Piper sanguineispicum
inferred← citeshttps://doi.org/10.1021/np5002785openalex-snapshot
Potent Cytotoxic Arylnaphthalene Lignan Lactones from Phyllanthus poilanei
inferred← citeshttps://doi.org/10.1039/c8cs00209fopenalex-snapshot
Gold-catalyzed glycosylation in the synthesis of complex carbohydrate-containing natural products
inferred← citeshttps://doi.org/10.1055/s-2007-993754openalex-snapshot
Reversal of P-Glycoprotein-Mediated Drug Efflux by Eudesmin from Haplophyllum perforatum and Cytotoxicity Pattern versus Diphyllin, Podophyllotoxin and Etoposide
inferred← citeshttps://doi.org/10.1080/00397910600948104openalex-snapshot
Total Synthesis of 4″‐O‐Acetylmananthoside B, Part I: Synthesis and Tentative Ozonolysis of a Cyclohexadiene Derivative
inferred← citeshttps://doi.org/10.1080/00397910902978023openalex-snapshot
Polyphosphoric Acid–Mediated, One-Pot, Novel Reactions to Build Polymethoxyarylnaphthalene Lignans
inferred← citeshttps://doi.org/10.1080/07328300802030860openalex-snapshot
Synthesis of Per‐acetyl d ‐fucopyranosyl Bromide and Its Use in Preparation of Diphyllin d ‐fucopyranosyl Glycoside
inferred← citeshttps://doi.org/10.1080/14786419.2022.2098495openalex-snapshot
Patulinervones A and B, two novel α -glucosidase inhibitory spiro -lignans from Melicope patulinervia (Merr. & Chun) C.C. Huang
inferred← citeshttps://doi.org/10.1135/cccc20071214openalex-snapshot
Iodine/Toluenesulfonic Acid: A Novel Catalyst for Isopropylidenation in Carbohydrate Chemistry
inferred← citeshttps://doi.org/10.1158/1535-7163.mct-14-0960openalex-snapshot
Daurinol Enhances the Efficacy of Radiotherapy in Lung Cancer via Suppression of Aurora Kinase A/B Expression
inferred← citeshttps://doi.org/10.1359/jbmr.070613openalex-snapshot
Diphyllin, a Novel and Naturally Potent V-ATPase Inhibitor, Abrogates Acidification of the Osteoclastic Resorption Lacunae and Bone Resorption
inferred← citeshttps://doi.org/10.1371/journal.pone.0093516openalex-snapshot
Evaluation and Structure-Activity Relationship Analysis of a New Series of Arylnaphthalene lignans as Potential Anti-Tumor Agents
inferred← citeshttps://doi.org/10.1515/tjb-2020-0180openalex-snapshot
Therapeutic approaches on the interaction between SARS-CoV2 and ACE2: a biochemical perspective
inferred← citeshttps://doi.org/10.1590/s0102-695x2011005000196openalex-snapshot
Chemical constituents and biological activities of species of Justicia: a review
inferred← citeshttps://doi.org/10.1593/neo.11972openalex-snapshot
A Novel Topoisomerase Inhibitor, Daurinol, Suppresses Growth of HCT116 Cells with Low Hematological Toxicity Compared to Etoposide
inferred← citeshttps://doi.org/10.2174/1389557522666220117122718openalex-snapshot
Antiviral, Anticancer and Hypotensive Potential of Diphyllin Glycosides and their Mechanisms of Action
inferred← citeshttps://doi.org/10.22159/ajpcr.2022.v15i3.43953openalex-snapshot
CLEISTANTHIN B SHOWS A POTENT CYTOTOXIC ACTIVITY AGAINST COLORECTAL CANCER CELLS
inferred← citeshttps://doi.org/10.3184/030823408x282677openalex-snapshot
Laxanol, a new 2,5-Diaryl-3,4-Dihydroxymethyltetrahydrofuran Type Lignan from Justicia Laxa
inferred← citeshttps://doi.org/10.3389/fchem.2022.1103554openalex-snapshot
Total synthesis of justicidin B, justicidin E, and taiwanin C: A general and flexible approach toward the synthesis of natural arylnaphthalene lactone lignans
inferred← citeshttps://doi.org/10.3390/app12178699openalex-snapshot
Chemical Analysis of Essential Oils of Cymbopogon schoenanthus (L.) Spreng. and Nepeta azurea R.Br. ex Benth from Djbouti, In-Vitro Cytotoxicity against Cancer Cell Lines and Antibacterial Activities
inferred← citeshttps://doi.org/10.3390/molecules23040941openalex-snapshot
Anti-Inflammatory and Antinociceptive Studies of Hydroalcoholic Extract from the Leaves of Phyllanthus brasiliensis (Aubl.) Poir. and Isolation of 5-O-β-d-Glucopyranosyljusticidin B and Six Other Lignans
inferred← citeshttps://doi.org/10.3390/molecules24020220openalex-snapshot
9-Norlignans: Occurrence, Properties and Their Semisynthetic Preparation from Hydroxymatairesinol
inferred← citeshttps://doi.org/10.3390/molecules25010183openalex-snapshot
Lignans and Their Derivatives from Plants as Antivirals
inferred← citeshttps://doi.org/10.3390/molecules25010197openalex-snapshot
Nor-Lignans: Occurrence in Plants and Biological Activities—A Review
inferred← citeshttps://doi.org/10.3390/molecules26061775openalex-snapshot
Medicinal Plants, Phytochemicals, and Herbs to Combat Viral Pathogens Including SARS-CoV-2
inferred← citeshttps://doi.org/10.3390/molecules28237874openalex-snapshot
Bioactivities and Mechanisms of Action of Diphyllin and Its Derivatives: A Comprehensive Systematic Review
inferred← citeshttps://doi.org/10.3390/ph16020250openalex-snapshot
Identification of a Family of Glycoside Derivatives Biologically Active against Acinetobacter baumannii and Other MDR Bacteria Using a QSPR Model
inferred← citeshttps://doi.org/10.3748/wjg.v12.i44.7143openalex-snapshot
Elenoside increases intestinal motility
inferred← citeshttps://doi.org/10.70675/48cfd5e7z542dz4aebz8922z3b14d21430d3openalex-snapshot
Synthèse et évaluation pharmacologique de composés originaux de la famille des méthoxynaphtalènes et lignanes arylnaphtalènes à visée antitumorale
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