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Flavans with cytotoxic activity from the stem and root bark of Daphne giraldii

https://doi.org/10.1039/c6ra08537g
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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/cbdv.201000117openalex-snapshot
Phytochemical and Biological Studies of the Plants from the Genus Daphne
inferredcites →https://doi.org/10.1007/s11010-016-2686-1openalex-snapshot
Physalin A induces G2/M phase cell cycle arrest in human non-small cell lung cancer cells: involvement of the p38 MAPK/ROS pathway
inferredcites →https://doi.org/10.1016/0031-9422(88)80455-2openalex-snapshot
Flavonoid and other constituents of Bauhinia manca
inferredcites →https://doi.org/10.1016/0031-9422(94)00738-fopenalex-snapshot
Flavonoids of dragon's blood from Dracaena cinnabari
inferredcites →https://doi.org/10.1016/j.bmcl.2010.04.064openalex-snapshot
New estrogenic compounds isolated from Broussonetia kazinoki
inferredcites →https://doi.org/10.1016/j.bmcl.2016.01.076openalex-snapshot
Two novel phenanthraquinones with anti-cancer activity isolated from Bletilla striata
inferredcites →https://doi.org/10.1016/j.intimp.2006.07.010openalex-snapshot
Total flavonoids of Daphne genkwa root significantly inhibit the growth and metastasis of Lewis lung carcinoma in C57BL6 mice
inferredcites →https://doi.org/10.1016/j.intimp.2006.07.011openalex-snapshot
Antitumor activity of daphnodorins from Daphne genkwa roots
inferredcites →https://doi.org/10.1016/j.phytochem.2005.02.002openalex-snapshot
Circular dichroism, a powerful tool for the assessment of absolute configuration of flavonoids
inferredcites →https://doi.org/10.1016/j.phytochem.2011.11.013openalex-snapshot
Daphnane-type diterpene esters with cytotoxic and anti-HIV-1 activities from Daphne acutiloba Rehd.
inferredcites →https://doi.org/10.1016/j.phytol.2012.05.006openalex-snapshot
Chemical constituents of Trilepisium madagascariense (Moraceae) and their antimicrobial activity
inferredcites →https://doi.org/10.1016/s0165-6147(03)00026-9openalex-snapshot
Cell-cycle dysregulation and anticancer therapy
inferredcites →https://doi.org/10.1016/s0304-3835(02)00102-7openalex-snapshot
In vitro cytotoxic potential and mechanism of action of selected coumarins, using human renal cell lines
inferredcites →https://doi.org/10.1021/acs.jnatprod.5b00117openalex-snapshot
Ibogan, Tacaman, and Cytotoxic Bisindole Alkaloids from Tabernaemontana. Cononusine, an Iboga Alkaloid with Unusual Incorporation of a Pyrrolidone Moiety
inferredcites →https://doi.org/10.1021/jm0704090openalex-snapshot
Natural Products as Leads to Potential Drugs: An Old Process or the New Hope for Drug Discovery?
inferredcites →https://doi.org/10.1021/np010288lopenalex-snapshot
Aromatase Inhibitors from Broussonetia papyrifera
inferredcites →https://doi.org/10.1021/np200906sopenalex-snapshot
Natural Products As Sources of New Drugs over the 30 Years from 1981 to 2010
inferredcites →https://doi.org/10.1039/c4ra13167copenalex-snapshot
Neogenkwanines A–H: daphnane-type diterpenes containing 4,7 or 4,6-ether groups from the flower bud of Daphne genkwa
inferredcites →https://doi.org/10.1039/c5ob00695copenalex-snapshot
Glycosmisines A and B: isolation of two new carbazole–indole-type dimeric alkaloids from Glycosmis pentaphylla and an evaluation of their antiproliferative activities
inferredcites →https://doi.org/10.1039/c5ra15074dopenalex-snapshot
(−) and (+)-Merrilliaquinone, a pair of new quinone enantiomers from Illicium merrillianum and their distinctive effect on human hepatoma and hepatic cells
inferredcites →https://doi.org/10.1039/c5ra16796eopenalex-snapshot
Ganocochlearic acid A, a rearranged hexanorlanostane triterpenoid, and cytotoxic triterpenoids from the fruiting bodies of Ganoderma cochlear
inferredcites →https://doi.org/10.1074/jbc.m113.513960openalex-snapshot
The Chinese Herb Isolate Yuanhuacine (YHL-14) Induces G2/M Arrest in Human Cancer Cells by Up-regulating p21 Protein Expression through an p53 Protein-independent Cascade
inferredcites →https://doi.org/10.1080/1028602042000204126openalex-snapshot
A new meta-homoisoflavane from the fresh stems of dracaena cochinchinensis
inferredcites →https://doi.org/10.1080/10286020801966641openalex-snapshot
Three new flavanols from Daphne giraldii
inferredcites →https://doi.org/10.1080/14786410701371603openalex-snapshot
Two new flavanes and bioactive compounds fromDaphne tanguticaMaxim
inferredcites →https://doi.org/10.1248/cpb.55.1287openalex-snapshot
Daphnogirins A and B, Two Biflavones from Daphne giraldii
inferredcites →https://doi.org/10.2174/157340707780126499openalex-snapshot
Podophyllotoxin: Current Perspectives
inferredcites →https://doi.org/10.3390/molecules200813563openalex-snapshot
Isolation and Identification of Cytotoxic Compounds from Aeschynomene fascicularis, a Mayan Medicinal Plant

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.2021.112791zenodo-depositor-declared
Structural characterization of prenylated compounds from Broussonetia kazinoki and their antiosteoclastogenic activity
inferred← citeshttps://doi.org/10.1016/j.phytochem.2021.112895zenodo-depositor-declared
A comprehensive review: Biological activity, modification and synthetic methodologies of prenylated flavonoids
inferred← citeshttps://doi.org/10.1007/s12272-023-01443-4openalex-snapshot
Phytochemistry and pharmacology of natural prenylated flavonoids
inferred← citeshttps://doi.org/10.1007/s13659-019-0197-yopenalex-snapshot
Anti-oral Microbial Flavanes from Broussonetia papyrifera Under the Guidance of Bioassay
inferred← citeshttps://doi.org/10.1016/j.arabjc.2020.102962openalex-snapshot
Flavonoids with anti-inflammatory activities from Daphne giraldii
inferred← citeshttps://doi.org/10.1016/j.bioorg.2019.103233openalex-snapshot
Anti-inflammatory flavonoids from root bark of Broussonetia papyrifera in LPS-stimulated RAW264.7 cells
inferred← citeshttps://doi.org/10.1016/j.biopha.2018.08.141openalex-snapshot
Daphnegiravone D from Daphne giraldii Nitsche induces p38-dependent apoptosis via oxidative and nitrosative stress in hepatocellular carcinoma cells
inferred← citeshttps://doi.org/10.1016/j.bse.2019.103958openalex-snapshot
Chemical constituents with prenyl substitution from the stem and root of Daphne giraldii Nitsche. (Thymelaeaceae)
inferred← citeshttps://doi.org/10.1016/j.bse.2020.104055openalex-snapshot
Chemical constituents from the flower buds of Daphne genkwa (Thymelaeaceae)
inferred← citeshttps://doi.org/10.1016/j.bse.2021.104352openalex-snapshot
Chemical constituents from the stem and root bark of Daphne giraldii Nitsche (Thymelaeaceae)
inferred← citeshttps://doi.org/10.1016/j.bse.2025.105097openalex-snapshot
Chemical constituents from the branches of Broussonetia papyrifera and their chemotaxonomic significance
inferred← citeshttps://doi.org/10.1016/j.cbi.2018.04.014openalex-snapshot
Flavan enantiomers from Daphne giraldii selectively induce apoptotic cell death in p53-null hepatocarcinoma cells in vitro
inferred← citeshttps://doi.org/10.1016/j.ejmech.2017.03.072openalex-snapshot
Autophagy antagonizes apoptosis induced by flavan enantiomers from Daphne giraldii in hepatic carcinoma cells in vitro
inferred← citeshttps://doi.org/10.1016/j.ejmech.2022.115006openalex-snapshot
Prenylated flavonoids with significant anti-hepatoma activity from Daphne giraldii and effects on Fibroblast Growth Factor Receptor 1 (FGFR1)
inferred← citeshttps://doi.org/10.1016/j.fitote.2018.11.011openalex-snapshot
Prenylated flavans from Daphne giraldii and their cytotoxic activities
inferred← citeshttps://doi.org/10.1016/j.fitote.2020.104540openalex-snapshot
The genus Daphne: A review of its traditional uses, phytochemistry and pharmacology
inferred← citeshttps://doi.org/10.1016/j.jfutfo.2025.03.007openalex-snapshot
Dual-Action Antimicrobials: Prenylated Flavonoids from Paper Mulberry Fruit Targeting Staphylococcus aureus Fatty Acid Synthesis
inferred← citeshttps://doi.org/10.1016/j.phytochem.2019.112231openalex-snapshot
Daphne giraldii Nitsche (Thymelaeaceae): Phytochemistry, pharmacology and medicinal uses
inferred← citeshttps://doi.org/10.1038/s41598-020-78785-2openalex-snapshot
Flavonoids and alkaloids from the rhizomes of Zephyranthes ajax Hort. and their cytotoxicity
inferred← citeshttps://doi.org/10.1515/psr-2021-0033openalex-snapshot
Anticancer properties of arylchromenes and arylchromans: an overview
inferred← citeshttps://doi.org/10.25135/rnp.475.2405.3230openalex-snapshot
Phytochemistry, Pharmacology and Clinical Applications of Cortex Daphnes：A Review
inferred← citeshttps://doi.org/10.33263/lianbs124.109openalex-snapshot
Investigation on the Phytochemical Analysis and Biological Activity of Daphne papyracea Wall. ex Steud. Leaf Extracts from Kumaun Himalaya
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