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Synthesis, characterization and cytotoxic activity studies on cancer cell lines of new paraben-decorated monospiro-cyclotriphosphazenes

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What this work says

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

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Comparison of the global gene expression profiles produced by methylparaben, n‐butylparaben and 17β‐oestradiol in MCF7 human breast cancer cells
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Paraben esters: review of recent studies of endocrine toxicity, absorption, esterase and human exposure, and discussion of potential human health risks
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Estrogenic Effects ofp-Hydroxybenzoic Acid in CD1 Mice
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Some Alkyl Hydroxy Benzoate Preservatives (Parabens) Are Estrogenic
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Characterization of paraben substituted cyclotriphosphazenes, and a DNA interaction study with a real-time electrochemical profiling based biosensor
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Novel hexapodal triazole linked to a cyclophosphazene core rhodamine-based chemosensor for selective determination of Hg2+ ions
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Phosphorus–nitrogen compounds
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Cyclophosphazenes as novel potential antitumor agents: x-ray crystal structure of the octapyrrolidinocyclotetraphosphazene, N4P4(NC4 H8)8
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Cyclophosphazenes as novel antitumor agents: X-ray crystal structure and donor properties of the hexaziridinocyclotriphosphazene, N3P3(NC2H4)6
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Raman studies on anticancer inorganic ring–dna interactions
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Reactions of N-methyl 1,3-diaminopropane with N3P3Cl6 and GEM-N3P3Cl4Ph2 leading to spirocyclic products
inferredcites →https://doi.org/10.1016/b978-0-12-050560-9.x5001-3openalex-snapshot
Phosphorus-nitrogen Compounds
inferredcites →https://doi.org/10.1016/j.bios.2016.01.061openalex-snapshot
First paraben substituted cyclotetraphosphazene compounds and DNA interaction analysis with a new automated biosensor
inferredcites →https://doi.org/10.1016/j.cclet.2009.12.020openalex-snapshot
Synthesis and characterization of six-arm star-shaped liquid crystalline cyclotriphosphazenes
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Benzimidazolyl-substituted cyclotriphosphazene derivative as latent flame-retardant curing agent for one-component epoxy resin system with excellent comprehensive performance
inferredcites →https://doi.org/10.1016/j.ejmech.2012.03.018openalex-snapshot
Synthesis, cytotoxicity and apoptosis of cyclotriphosphazene compounds as anti-cancer agents
inferredcites →https://doi.org/10.1016/j.ejmech.2014.10.005openalex-snapshot
Phosphorus–nitrogen compounds. Part 29. Syntheses, crystal structures, spectroscopic and stereogenic properties, electrochemical investigations, antituberculosis, antimicrobial and cytotoxic activities and DNA interactions of ansa-spiro-ansa cyclotetraphosphazenes
inferredcites →https://doi.org/10.1016/j.ejpb.2010.03.001openalex-snapshot
Degradation of parabens by Pseudomonas beteli and Burkholderia latens
inferredcites →https://doi.org/10.1016/j.envres.2020.110488openalex-snapshot
Controversy around parabens: Alternative strategies for preservative use in cosmetics and personal care products
inferredcites →https://doi.org/10.1016/j.fct.2011.12.045openalex-snapshot
Systemic exposure to parabens: Pharmacokinetics, tissue distribution, excretion balance and plasma metabolites of [14C]-methyl-, propyl- and butylparaben in rats after oral, topical or subcutaneous administration
inferredcites →https://doi.org/10.1016/j.ica.2014.06.040openalex-snapshot
Synthesis, characterization and antiproliferative activity of hexa arm star shaped thiosemicarbazones derived from cyclotriphosphazene core
inferredcites →https://doi.org/10.1016/j.ica.2018.02.035openalex-snapshot
DNA interaction analysis of fluorenylidene double bridged cyclotriphosphazene derivatives
inferredcites →https://doi.org/10.1016/j.ica.2018.04.028openalex-snapshot
A high selective “Turn-Off” aminopyrene based cyclotriphosphazene fluorescent chemosensors for Fe3+/Cu2+ ions
inferredcites →https://doi.org/10.1016/j.ica.2019.119158openalex-snapshot
Thiazole substituted dispiromonoansa and monospiro cyclotriphosphazenes: Design, synthesis and biological activity
inferredcites →https://doi.org/10.1016/j.ica.2020.120005openalex-snapshot
2-Hydroxyanthraquinone substituted cyclotriphosphazenes: Synthesis and cytotoxic activities in cancer cell lines
inferredcites →https://doi.org/10.1016/j.inoche.2004.01.012openalex-snapshot
Stereogenic properties of 1,3-disubstituted derivatives of cyclotriphosphazene: cis (meso) and trans (racemic) isomers
inferredcites →https://doi.org/10.1016/j.jinorgbio.2005.04.019openalex-snapshot
Selective tumor targeting by enhanced permeability and retention effect. Synthesis and antitumor activity of polyphosphazene–platinum (II) conjugates
inferredcites →https://doi.org/10.1016/j.molstruc.2013.06.036openalex-snapshot
Phosphorus–nitrogen compounds: Part 28. Syntheses, structural characterizations, antimicrobial and cytotoxic activities, and DNA interactions of new phosphazenes bearing vanillinato and pendant ferrocenyl groups
inferredcites →https://doi.org/10.1016/j.poly.2010.08.035openalex-snapshot
Spiro, ansa-derivatives of cyclotetraphosphazenes with a tetrafluorobutane-1,4-diol
inferredcites →https://doi.org/10.1016/j.poly.2011.05.041openalex-snapshot
Structural properties of new spiro-1,3-propanediaminocyclotriphosphazene derivatives
inferredcites →https://doi.org/10.1016/j.polymdegradstab.2016.08.013openalex-snapshot
Synthesis of a novel bridged-cyclotriphosphazene flame retardant and its application in epoxy resin
inferredcites →https://doi.org/10.1016/j.reprotox.2009.03.003openalex-snapshot
Estrogenicity of parabens revisited: Impact of parabens on early pregnancy and an uterotrophic assay in mice
inferredcites →https://doi.org/10.1016/j.saa.2019.117232openalex-snapshot
New perylenebisimide decorated cyclotriphosphazene heavy atom free conjugate as singlet oxygen generator
inferredcites →https://doi.org/10.1016/j.snb.2016.08.029openalex-snapshot
Voltammetric determination of methylparaben and its DNA interaction using a novel platform based on carbon nanofibers and cobalt-nickel-palladium nanoparticles
inferredcites →https://doi.org/10.1016/j.taap.2017.04.001openalex-snapshot
Butyl paraben and propyl paraben modulate bisphenol A and estradiol concentrations in female and male mice
inferredcites →https://doi.org/10.1016/j.tet.2012.12.027openalex-snapshot
Synthesis and characterization of new cyclotriphosphazene compounds
inferredcites →https://doi.org/10.1016/s0020-1693(01)00557-6openalex-snapshot
AIDS-related lymphoma screen results and molecular structure determination of a new crown ether bearing aziridinylcyclophosphazene, potentially capable of ion-regulated DNA cleavage action
inferredcites →https://doi.org/10.1016/s0168-3659(03)00199-8openalex-snapshot
Synthesis and antitumor activity of novel thermosensitive platinum(II)–cyclotriphosphazene conjugates
inferredcites →https://doi.org/10.1016/s0960-0760(01)00174-1openalex-snapshot
Oestrogenic activity of parabens in MCF7 human breast cancer cells
inferredcites →https://doi.org/10.1021/acs.inorgchem.9b03031openalex-snapshot
Electrophoresis and Biosensor-Based DNA Interaction Analysis of the First Paraben Derivatives of Spermine-Bridged Cyclotriphosphazenes
inferredcites →https://doi.org/10.1021/cr00002a002openalex-snapshot
Regio- and stereochemical control in substitution reactions of cyclophosphazenes
inferredcites →https://doi.org/10.1021/ic100781vopenalex-snapshot
Phosphorus−Nitrogen Compounds. 21. Syntheses, Structural Investigations, Biological Activities, and DNA Interactions of New N/O Spirocyclic Phosphazene Derivatives. The NMR Behaviors of Chiral Phosphazenes with Stereogenic Centers upon the Addition of Chiral Solvating Agents
inferredcites →https://doi.org/10.1021/ic901039kopenalex-snapshot
Phosphorus−Nitrogen Compounds. 18. Syntheses, Stereogenic Properties, Structural and Electrochemical Investigations, Biological Activities, and DNA Interactions of New Spirocyclic Mono- and Bisferrocenylphosphazene Derivatives
inferredcites →https://doi.org/10.1021/jm0490078openalex-snapshot
Synthesis and in Vitro Antileukemic Activity of Some New 1,3-(Oxytetraethylenoxy)cyclotriphosphazene Derivatives
inferredcites →https://doi.org/10.1021/ma951830dopenalex-snapshot
Preparation of a New Type of Phosphazene High Polymers Containing 2,2‘-Dioxybiphenyl Groups
inferredcites →https://doi.org/10.1021/mp4000184openalex-snapshot
Original Multivalent Copper(II)-Conjugated Phosphorus Dendrimers and Corresponding Mononuclear Copper(II) Complexes with Antitumoral Activities
inferredcites →https://doi.org/10.1039/d0nj02723eopenalex-snapshot
Synthesis of the first 2-hydroxyanthraquinone substituted cyclotriphosphazenes and their cytotoxic properties
inferredcites →https://doi.org/10.1039/d0nj03908jopenalex-snapshot
Novel paraben derivatives of tetracyclic spermine cyclotriphosphazenes: synthesis, characterization and biosensor based DNA interaction analysis
inferredcites →https://doi.org/10.1080/02678292.2013.773093openalex-snapshot
Synthesis of a series of triple-bridged cyclotriphosphazene hexa-alkoxy derivatives and investigation of their structural and mesomorphic properties
inferredcites →https://doi.org/10.1080/10426508908046081openalex-snapshot
THE REACTIONS OF PHOSPHAZENES WITH DIFUNCTIONAL AND POLYFUNCTIONAL NUCLEOPHILIC REAGENTS
inferredcites →https://doi.org/10.1107/s002188980600731xopenalex-snapshot
Mercury : visualization and analysis of crystal structures
inferredcites →https://doi.org/10.1107/s090744490804362xopenalex-snapshot
Structure validation in chemical crystallography
inferredcites →https://doi.org/10.1107/s2053229614024218openalex-snapshot
Crystal structure refinement with SHELXL
inferredcites →https://doi.org/10.1107/s2053229614024929openalex-snapshot
PLATON SQUEEZE: a tool for the calculation of the disordered solvent contribution to the calculated structure factors
inferredcites →https://doi.org/10.1107/s2053273314026370openalex-snapshot
SHELXT – Integrated space-group and crystal-structure determination
inferredcites →https://doi.org/10.1111/j.1365-2605.2007.00841.xopenalex-snapshot
Urinary excretion of phthalates and paraben after repeated whole‐body topical application in humans
inferredcites →https://doi.org/10.1111/j.1468-2494.2011.00698.xopenalex-snapshot
In vitro induction of apoptosis, necrosis and genotoxicity by cosmetic preservatives: application of flow cytometry as a complementary analysis by NRU
inferredcites →https://doi.org/10.1191/0748233701th093oaopenalex-snapshot
Effects of butylparaben on the male reproductive system in rats
inferredcites →https://doi.org/10.1292/jvms.71.1027openalex-snapshot
Maternal Isobutyl-Paraben Exposure decreases the Plasma Corticosterone Level in Dams and Sensitivity to Estrogen in Female Offspring Rats
inferredcites →https://doi.org/10.17776/csj.66838openalex-snapshot
Etil Paraben ve Metil Parabenin Caenorhabditis Elegans’ta Yumurta Verimi, Yaşama Yüzdesi ve Fiziksel Büyüme Üzerine Olan Etkilerinin Araştırılması
inferredcites →https://doi.org/10.3109/10408444.2010.515563openalex-snapshot
Personal care products and endocrine disruption: A critical review of the literature

What points at this work

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

inferred← citeshttps://doi.org/10.2139/ssrn.4816439openalex-extracted
Cyclotriphosphazenes: Pre-Harvest Foliar Applications Improve Antioxidant Activity by Increasing Phenolic Compounds in Lavandula Angustifolia Mill
inferred← citeshttps://doi.org/10.1007/s11164-023-04984-xopenalex-snapshot
Phosphorus-nitrogen compounds: Part 69—Unsymmetrical dispiro(N/N)cyclotriphosphazenes containing different pendant arms: syntheses, characterization, stereogenism, photophysical and bioactivity studies
inferred← citeshttps://doi.org/10.1016/j.fbio.2024.104826openalex-snapshot
Cyclotriphosphazenes: Pre-harvest foliar applications improve antioxidant activity by increasing phenolic compounds in Lavandula angustifolia Mill.
inferred← citeshttps://doi.org/10.1016/j.ica.2022.121144openalex-snapshot
Nucleophilic substitution pathways in the reactions of 3-amino-1-propanol with mono substituted cyclotriphosphazene derivatives
inferred← citeshttps://doi.org/10.1016/j.microc.2026.118699openalex-snapshot
Fluorometric determination of Fe3+ in water samples using naphthylamine-functionalized cyclotriphosphazene probes and paper-based analytical platforms
inferred← citeshttps://doi.org/10.1016/j.molstruc.2024.138213openalex-snapshot
New type paraben decorated mono- and dispirocyclotriphosphazene compounds: Synthesis, characterization and DNA binding studies
inferred← citeshttps://doi.org/10.1016/j.molstruc.2024.140100openalex-snapshot
Novel Schiff base decorated cyclotriphosphazene chemosensors for Fe and Cu ions detection
inferred← citeshttps://doi.org/10.1016/j.molstruc.2025.143993openalex-snapshot
Design and synthesis of cyclotriphosphazene derivatives bearing hydroxyflavone groups: Antioxidant properties and cytotoxic effects in breast cancer cells
inferred← citeshttps://doi.org/10.1016/j.molstruc.2026.146154openalex-snapshot
Synthesis, characterization of tetra-paraben substituted monospiro cyclotriphosphazenes and their cytotoxic activities in breast cancer (MCF-7)
inferred← citeshttps://doi.org/10.1016/j.pmatsci.2024.101232openalex-snapshot
Cyclotriphosphazene based materials: Structure, functionalization and applications
inferred← citeshttps://doi.org/10.1016/j.poly.2024.117252openalex-snapshot
Synthesis and characterization of novel spiro-(2,2′-dioxybiphenyl)-cyclotriphosphazene derivatives bearing butylated oxyanisole groups and their antioxidant and antimicrobial activities
inferred← citeshttps://doi.org/10.1039/d2nj02280jopenalex-snapshot
Phosphorus–nitrogen compounds. Part 64. Comparative reactions of spiro and ansa (N/O) cyclotetraphosphazenes with bulky (4-fluorobenzyl) N/N and N/O donor type bidentate reagents: structure, stereogenic properties and cytotoxic activity studies
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