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Potent Cytotoxic Arylnaphthalene Lignan Lactones from Phyllanthus poilanei

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What this work says

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

inferredcites →https://doi.org/10.1002/ardp.201200035openalex-snapshot

Synthesis and Bioevaluation of Diphyllin Glycosides as Novel Anticancer Agents

inferredcites →https://doi.org/10.1002/hlca.200690033openalex-snapshot

A New Lignan and Four New Lignan Glycosides from Mananthes patentiflora

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Rapid screening of lignans from Phyllanthus myrtifolius and stilbenoids from Syagrus romanzoffiana by HPLC‐SPE‐NMR

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Use of the Hollow Fiber Assay for the Discovery of Novel Anticancer Agents from Fungi

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Cellular responses to etoposide: cell death despite cell cycle arrest and repair of DNA damage

inferredcites →https://doi.org/10.1016/0031-9422(95)00195-dopenalex-snapshot

Antifungal aryltetralin lignans from leaves of Podophyllum hexandrum

inferredcites →https://doi.org/10.1016/0031-9422(96)00061-1openalex-snapshot

Minor lignans from haplophyllum cappadocicum

inferredcites →https://doi.org/10.1016/0147-619x(83)90019-7openalex-snapshot

Determination of plasmid copy number by fluorescence densitometry

inferredcites →https://doi.org/10.1016/j.carres.2004.05.023openalex-snapshot

The gel-forming polysaccharide of psyllium husk (Plantago ovata Forsk)

inferredcites →https://doi.org/10.1016/j.ejmech.2011.11.011openalex-snapshot

Design, synthesis and biological evaluation of novel glycosylated diphyllin derivatives as topoisomerase II inhibitors

inferredcites →https://doi.org/10.1016/j.fitote.2009.05.005openalex-snapshot

A new arylnaphthalene lignan from Knema furfuracea

inferredcites →https://doi.org/10.1016/j.immuni.2006.03.016openalex-snapshot

Pro- and Antiinflammatory Cytokine Signaling: Reciprocal Antagonism Regulates Interferon-gamma Production by Human Natural Killer Cells

inferredcites →https://doi.org/10.1016/j.phytochem.2009.05.016openalex-snapshot

Glycosides of arylnaphthalene lignans from Acanthus mollis having axial chirality

inferredcites →https://doi.org/10.1016/s0031-9422(98)00222-2openalex-snapshot

A arylnaphthalene lignan from Haplophyllum buxbaumii

inferredcites →https://doi.org/10.1016/s0040-4020(01)93074-1openalex-snapshot

The isolation and structure of three new lignans from Justicia procumbens Linn. var. leucantha honda

inferredcites →https://doi.org/10.1016/s0092-8674(04)00031-5openalex-snapshot

Mitochondrial activation of apoptosis

inferredcites →https://doi.org/10.1021/jo952048eopenalex-snapshot

Hindered Rotation in Arylnaphthalene Lignans

inferredcites →https://doi.org/10.1021/jo971176vopenalex-snapshot

NMR Chemical Shifts of Common Laboratory Solvents as Trace Impurities

inferredcites →https://doi.org/10.1021/ml300065zopenalex-snapshot

Synthesis and Antitumor Activity of Ellagic Acid Peracetate

inferredcites →https://doi.org/10.1021/np0101651openalex-snapshot

Potent Cytotoxic Lignans from Justicia procumbens and Their Effects on Nitric Oxide and Tumor Necrosis Factor-α Production in Mouse Macrophages

inferredcites →https://doi.org/10.1021/np050028uopenalex-snapshot

Cytotoxic Arylnaphthalene Lignans from a Vietnamese Acanthaceae, Justicia patentiflora

inferredcites →https://doi.org/10.1021/np060022kopenalex-snapshot

Production of Justicidin B, a Cytotoxic Arylnaphthalene Lignan from Genetically Transformed Root Cultures of Linum l eonii

inferredcites →https://doi.org/10.1021/np200051jopenalex-snapshot

Cytotoxic and NF-κB Inhibitory Constituents of the Stems of Cratoxylum cochinchinense and Their Semisynthetic Analogues

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Natural Products As Sources of New Drugs over the 30 Years from 1981 to 2010

inferredcites →https://doi.org/10.1021/np3007414openalex-snapshot

Alkaloids from Microcos paniculata with Cytotoxic and Nicotinic Receptor Antagonistic Activities

inferredcites →https://doi.org/10.1021/np50044a030openalex-snapshot

Antitumor Agents, 81. Justicidin-A and Diphyllin, Two Cytotoxic Principles from Justicia procumbens

inferredcites →https://doi.org/10.1021/np50071a003openalex-snapshot

Chemical Constituents of the Flora of Jordan, Part V-B. Three New Arylnaphthalene Lignan Glucosides from Haplophyllum buxbaumii

inferredcites →https://doi.org/10.1021/np50100a011openalex-snapshot

Cytotoxic Constituents from Hyptis verticillata

inferredcites →https://doi.org/10.1021/np50116a013openalex-snapshot

Phyllamyricins A-C, Three Novel Lignans from Phyllanthus myrtifolius

inferredcites →https://doi.org/10.1021/np7007347openalex-snapshot

Dichapetalin-Type Triterpenoids and Lignans from the Aerial Parts of Phyllanthus acutissima

inferredcites →https://doi.org/10.1021/np800767aopenalex-snapshot

Use of the in Vivo Hollow Fiber Assay in Natural Products Anticancer Drug Discovery

inferredcites →https://doi.org/10.1021/np9900167openalex-snapshot

Cytotoxic Lignans of Justicia ciliata

inferredcites →https://doi.org/10.1023/a:1008138230896openalex-snapshot

Production of podophyllotoxin from Podophyllum hexandrum: a potential natural product for clinically useful anticancer drugs

inferredcites →https://doi.org/10.1038/sj.onc.1204402openalex-snapshot

Defective caspase-3 relocalization in non-small cell lung carcinoma

inferredcites →https://doi.org/10.1055/s-2003-39706openalex-snapshot

Antifungal, Antiprotozoal, Cytotoxic and Piscicidal Properties of Justicidin B and a New Arylnaphthalide Lignan fromPhyllanthus piscatorum

inferredcites →https://doi.org/10.1055/s-2005-873141openalex-snapshot

Cytotoxic Arylnaphthalide Lignan Glycosides from the Aerial Parts of Phyllanthus taxodiifolius

inferredcites →https://doi.org/10.1080/1057563031000122095openalex-snapshot

Cytotoxicity ofin vitroproduced podophyllotoxin frompodophyllum hexandrumon human cancer cell line

inferredcites →https://doi.org/10.1093/mutage/11.6.553openalex-snapshot

Cytotoxic and genotoxic effects of cleistanthin B in normal and tumour cells

inferredcites →https://doi.org/10.1101/gad.12.6.806openalex-snapshot

Essential contribution of caspase 3/CPP32 to apoptosis and its associated nuclear changes

inferredcites →https://doi.org/10.1107/s002188980403225xopenalex-snapshot

SIR2004: an improved 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/10.1107/s0108767307043930openalex-snapshot

A short history of SHELX

inferredcites →https://doi.org/10.1124/mol.104.004416openalex-snapshot

Biochemical and Proteomics Approaches to Characterize Topoisomerase IIα Cysteines and DNA as Targets Responsible for Cisplatin-Induced Inhibition of Topoisomerase IIα

inferredcites →https://doi.org/10.1196/annals.1397.047openalex-snapshot

Resveratrol Induces Apoptosis in Chemoresistant Cancer Cells via Modulation of AMPK Signaling Pathway

inferredcites →https://doi.org/10.1248/cpb.50.844openalex-snapshot

Patavine, a New Arylnaphthalene Lignan Glycoside from Shoot Cultures of Haplophyllum patavinum.

inferredcites →https://doi.org/10.1248/cpb.51.1299openalex-snapshot

Arylnaphthalide Lignans from Cleistanthus collinus

inferredcites →https://doi.org/10.1248/cpb.54.1223openalex-snapshot

Cytotoxic Arylnaphthalene Lignans from Phyllanthus oligospermus

inferredcites →https://doi.org/10.1351/pac-con-08-10-16openalex-snapshot

Discovery of anticancer agents of diverse natural origin

inferredcites →https://doi.org/10.1593/neo.11972openalex-snapshot

A Novel Topoisomerase Inhibitor, Daurinol, Suppresses Growth of HCT116 Cells with Low Hematological Toxicity Compared to Etoposide

inferredcites →https://doi.org/10.2174/0929867043364531openalex-snapshot

Etoposide: Discovery and Medicinal Chemistry

inferredcites →https://doi.org/10.3390/ijerph9072444openalex-snapshot

Secondary Leukemia Associated with the Anti-Cancer Agent, Etoposide, a Topoisomerase II Inhibitor

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/asia.202301013openalex-snapshot

An Open‐Air Palladium‐Catalyzed Stereoselective O‐Glycosylation of Glycals via in‐situ Generation of gem‐Disubstituted Methanols from p‐Quinone Methides

inferred← citeshttps://doi.org/10.1002/asia.70583openalex-snapshot

Recent Advances in Palladium‐Catalyzed Functionalization of Carbohydrate Frameworks

inferred← citeshttps://doi.org/10.1002/cbdv.202402071openalex-snapshot

Isolation of Novel Compounds from Lepidium sativum Seeds and Evaluation of Their Potential Anti‐Tumor Activity

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/10.1007/978-3-030-81404-5_15-1openalex-snapshot

Lignans

inferred← citeshttps://doi.org/10.1007/978-3-031-28109-9_15openalex-snapshot

Lignans

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/10.1007/978-3-642-36202-6_245-1openalex-snapshot

Current Status and Future Prospects of Bioactive Phytolignans

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/10.1007/s13659-019-0198-xopenalex-snapshot

Bioactivity-Guided Isolation of Totarane-Derived Diterpenes from Podocarpus neriifolius and Structure Revision of 3-Deoxy-2α-hydroxynagilactone E

inferred← citeshttps://doi.org/10.1016/b978-0-12-802104-0.00012-3openalex-snapshot

Other Plant Metabolites

inferred← citeshttps://doi.org/10.1016/b978-0-12-816675-8.00003-8openalex-snapshot

Bioactive C-glycosides inspired from natural products towards therapeutics

inferred← citeshttps://doi.org/10.1016/b978-0-443-15269-6.00013-4openalex-snapshot

Semisynthesis of lignans

inferred← citeshttps://doi.org/10.1016/b978-0-443-18657-8.00014-1openalex-snapshot

Other plant metabolites

inferred← citeshttps://doi.org/10.1016/j.bioelechem.2022.108133openalex-snapshot

A c-MWCNTs/AuNPs-based electrochemical cytosensor to evaluate the anticancer activity of pinoresinol from Cinnamomum camphora against HeLa cells

inferred← citeshttps://doi.org/10.1016/j.biopha.2019.108645openalex-snapshot

Phyllanthus taxodiifolius Beille suppresses microtubule dynamics and restricts glioblastoma aggressiveness

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.2023.117486openalex-snapshot

The mechanisms of multidrug resistance of breast cancer and research progress on related reversal agents

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.bse.2024.104901openalex-snapshot

Cytotoxicity of endemic Haplophyllum megalanthum Bornm. and its newly isolated alkaloids and lignans

inferred← citeshttps://doi.org/10.1016/j.bse.2026.105357openalex-snapshot

Chemical constituents from the root extract of Phyllanthus reticulatus and their chemotaxonomic significance

inferred← citeshttps://doi.org/10.1016/j.chempr.2018.11.007openalex-snapshot

Site-Selective C–H Functionalization of (Hetero)Arenes via Transient, Non-symmetric Iodanes

inferred← citeshttps://doi.org/10.1016/j.fitote.2018.05.006openalex-snapshot

Phenylacetylene-bearing 3,4-seco-cleistanthane diterpenoids from the roots of Phyllanthus glaucus

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.indcrop.2026.124204openalex-snapshot

Spatiotemporal dynamics and a proposed biosynthetic framework for multi-bioactive arylnaphthalene lignans in Taiwania flousiana Gaussen

inferred← citeshttps://doi.org/10.1016/j.phytochem.2014.12.014openalex-snapshot

Cytotoxic and natural killer cell stimulatory constituents of Phyllanthus songboiensis

inferred← citeshttps://doi.org/10.1016/j.phytochem.2017.01.005openalex-snapshot

Anti-HIV diphyllin glycosides from Justicia gendarussa

inferred← citeshttps://doi.org/10.1016/j.phytol.2023.09.007openalex-snapshot

Justicidin B and related lignans from two South African Monsonia species with potent activity against HeLa cervical cancer cells

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

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Indium chloride catalysed annulation of arylmethyl carbonyls & arylalkynes for the synthesis of naphthalene derivatives

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Discovery of Anticancer Agents of Diverse Natural Origin

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Cytotoxic Barrigenol-like Triterpenoids from an Extract of Cyrilla racemiflora Housed in a Repository

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Cardiac Glycoside Constituents of Streblus asper with Potential Antineoplastic Activity

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Potent Inhibitor of Drug-Resistant HIV-1 Strains Identified from the Medicinal Plant Justicia gendarussa

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Crystal Structures and Human Leukemia Cell Apoptosis Inducible Activities of Parthenolide Analogues Isolated from Piptocoma rufescens

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Potential Anticancer Agents Characterized from Selected Tropical Plants

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Stereoselective O-Glycosylation of Glycals with Arylboronic Acids Using Air as the Oxygen Source

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Phainanolide A, Highly Modified and Oxygenated Triterpenoid from Phyllanthus hainanensis

inferred← citeshttps://doi.org/10.1021/acscatal.9b04260openalex-snapshot

Designing Synergistic Nanocatalysts for Multiple Substrate Activation: Interlattice Ag–Fe3O4 Hybrid Materials for CO2-Inserted Lactones

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NCI Program for Natural Product Discovery: A Publicly-Accessible Library of Natural Product Fractions for High-Throughput Screening

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Phainanoids A–F, A New Class of Potent Immunosuppressive Triterpenoids with an Unprecedented Carbon Skeleton from Phyllanthus hainanensis

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Oleanane Triterpenes from the Flowers of Camellia japonica Inhibit Porcine Epidemic Diarrhea Virus (PEDV) Replication

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(±)-Quassidines I and J, Two Pairs of Cytotoxic Bis-β-carboline Alkaloid Enantiomers fromPicrasma quassioides

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PHY34 inhibits autophagy through V-ATPase V0A2 subunit inhibition and CAS/CSE1L nuclear cargo trafficking in high grade serous ovarian cancer

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Enantiomeric Lignans and Neolignans from Phyllanthus glaucus: Enantioseparation and Their Absolute Configurations

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Recent advances in research on lignans and neolignans

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Deconjugative alkylation/Heck reaction as a simple platform for dihydronaphthalene synthesis

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Arylnaphthalene lactone analogues: synthesis and development as excellent biological candidates for future drug discovery

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Strategies for the discovery of potential anticancer agents from plants collected from Southeast Asian tropical rainforests as a case study

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Discovery and development of botanical natural products and their analogues as therapeutics for ovarian cancer

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The dichapetalins and dichapetalin-type compounds: structural diversity, bioactivity, and future research perspectives

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The Genus Phyllanthus: An Ethnopharmacological, Phytochemical, and Pharmacological Review

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Phyllanthusmin Derivatives Induce Apoptosis and Reduce Tumor Burden in High-Grade Serous Ovarian Cancer by Late-Stage Autophagy Inhibition

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Extractives elucidation of Taiwania cryptomerioides sapwood

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Lignans: a versatile source of anticancer drugs

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Inhibition of DNA Topoisomerases I and II and Cytotoxicity of Compounds from Polygonum aviculare L .

inferred← citeshttps://doi.org/10.2139/ssrn.4823138openalex-snapshot

Phytochemical Characterization and Cytotoxic Activity of Haplophyllum Megalanthum: An Endemic Plant from Turkey

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Immune Modulation of Asian Folk Herbal Medicines and Related Chemical Components for Cancer Management

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/10.21873/anticanres.11146openalex-snapshot

Discovery of Anticancer Agents of Diverse Natural Origin

inferred← citeshttps://doi.org/10.3389/fchem.2020.00628openalex-snapshot

Transition Metal-Mediated Annulation Approaches for Synthesis of Arylnaphthalene Lignan Lactones

inferred← citeshttps://doi.org/10.3389/fimmu.2018.01509openalex-snapshot

A Synthetic Disaccharide Derivative of Diphyllin, TAARD, Activates Human Natural Killer Cells to Secrete Interferon-Gamma via Toll-Like Receptor-Mediated NF-κB and STAT3 Signaling Pathways

inferred← citeshttps://doi.org/10.3390/horticulturae10020195openalex-snapshot

Phyllanthus Lignans: A Review of Biological Activity and Elicitation

inferred← citeshttps://doi.org/10.3390/molecules28237874openalex-snapshot

Bioactivities and Mechanisms of Action of Diphyllin and Its Derivatives: A Comprehensive Systematic Review

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Cytokines, the Tumor Microenvironment, and Selected Plant-Derived Natural Products

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Bioactive small-molecule constituents of Lao plants

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