Search results for "Acridone"

showing 5 items of 5 documents

Crystal structure of disordered nanocrystalline $\alpha^{II}$-quinacridone determined by electron diffraction

2016

CrystEngComm 18(4), 529 - 535(2016). doi:10.1039/C5CE01855B

DiffractionMaterials scienceGas electron diffractionStacking02 engineering and technologyGeneral ChemistryCrystal structure010402 general chemistry021001 nanoscience & nanotechnologyCondensed Matter Physics54001 natural sciencesNanocrystalline material0104 chemical scienceschemistry.chemical_compoundCrystallographychemistryElectron diffractionQuinacridoneddc:540General Materials Science0210 nano-technologyElectron backscatter diffraction
researchProduct

Flow-injection analysis study of the chemiluminescent behaviour of proflavine and acriflavine

2001

Abstract The chemiluminescent behaviour of the amino acridines like acriflavine, and proflavin is reported. Different strong oxidants (potassium permanganate, cerium(IV), hexacyanoferrate(III), hydrogen peroxide in different media) were tested, and potassium permanganate in sulphuric acid medium was selected. The study of the experimental parameters affecting the oxidation and detection was performed with the aid of a FIA assembly. The calibration graph was applied over the range 0.05–12.0 μg ml −1 of acriflavine (regression coefficient 0.9957, and the calculated relative standard deviation (R.S.D., %) was 0.9; LOD 10 ng ml −1 and the sample throughput 48 h −1 . The study of interfering com…

Flow injection analysisCalibration curveInorganic chemistryAnalytical chemistryBiochemistryAnalytical Chemistrylaw.inventionAcridonechemistry.chemical_compoundPotassium permanganatechemistrylawEnvironmental ChemistryAcriflavineHydrogen peroxideSpectroscopyProflavineChemiluminescenceAnalytica Chimica Acta
researchProduct

Synthesis of novel xanthone and acridone carboxamides with potent antiproliferative activities

2020

Abstract Several new amino-substituted acridone and xanthone derivatives have been designed and synthesized, using an efficient methodology from suitable acridone- or xanthone-carboxylic acid intermediates. The antiproliferative activity of the target compounds has been evaluated against four cancer cell lines, namely breast adenocarcinoma MCF-7, acute lymphocytic leukemia CCRF-CEM, and its doxorubicin-resistant variant CEM/ADR5000 and prostate cancer PC-3 cell lines. Selected derivatives have also been tested against the urinary bladder T24 and metastatic melanoma WM266-4 cancer cell lines. Two nitro substituted acridones, bearing a basic side chain as well, were endowed with a remarkable …

General Chemical Engineering02 engineering and technologyAntiproliferative activityXanthone010402 general chemistry01 natural sciencesCell cycle arrestlcsh:Chemistrychemistry.chemical_compoundProstate cancerAcute lymphocytic leukemiaXanthonemedicineAutophagyAcridoneAutophagyGeneral Chemistry021001 nanoscience & nanotechnologymedicine.disease0104 chemical sciencesAcridonechemistrylcsh:QD1-999Cell cultureApoptosisCancer researchNitro0210 nano-technologyArabian Journal of Chemistry
researchProduct

Cytotoxicity of a naturally occurring furoquinoline alkaloid and four acridone alkaloids towards multi-factorial drug-resistant cancer cells

2015

Abstract Introduction Chemotherapy is one of the preferred mode of treatment of malignancies, but is complicated by the expression of diverse resistance mechanisms of cancer cells. Methods In the present study, we investigated the cytotoxicity of five alkaloids including a furoquinoline montrofoline (1) and four acridones namely 1-hydroxy-4-methoxy-10-methylacridone (2), norevoxanthine (3), evoxanthine (4), 1,3-dimethoxy-10-methylacridone (5) against 9 drug-sensitive and multidrug-resistant (MDR) cancer cell lines. The resazurin reduction assay was used to evaluate the cytotoxicity of these compounds, whilst caspase-Glo assay was used to detect caspase activation. Cell cycle, mitochondrial …

Pharmaceutical ScienceApoptosisPharmacologyBiologyFuroquinoline alkaloidFlow cytometryInhibitory Concentration 50chemistry.chemical_compoundAlkaloidsCell Line TumorDrug DiscoverymedicineHumansCytotoxic T cellCytotoxicityMembrane Potential MitochondrialPharmacologyMolecular Structuremedicine.diagnostic_testCell Cyclemedicine.diseaseAntineoplastic Agents PhytogenicMolecular biologyDrug Resistance MultipleAcridoneLeukemiaComplementary and alternative medicinechemistryDrug Resistance NeoplasmApoptosisCaspasesCancer cellMolecular MedicineReactive Oxygen SpeciesAcridonesPhytomedicine
researchProduct

Design, synthesis and biological evaluation of new oligopyrrole carboxamides linked with tricyclic DNA-intercalators as potential DNA ligands or topo…

2007

In the context of the design and synthesis of minor groove binding and intercalating DNA ligands some new oligopyrrole carboxamides were synthesized. These hybrid molecules (combilexins) possess a variable and conformatively flexible spacer at the N-terminal end. As intercalating tricyclic systems acridone, acridine, anthraquinones and in a special case iminostilbene terminate the N-terminal end of the pyrrole chain. The cytotoxicity was examined by the NCI antitumor screening, furthermore, biophysical as well as biochemical studies were performed in order to get some information about the DNA binding properties and topoisomerase inhibition effect of this new series of molecules.

Stereochemistrymedicine.drug_classTopoisomerase InhibitorsDNA FootprintingContext (language use)Antineoplastic AgentsLigandschemistry.chemical_compoundStructure-Activity RelationshipCell Line TumorDrug DiscoverymedicineStructure–activity relationshipHumansPyrrolesPharmacologybiologyMolecular StructureChemistryTopoisomeraseOrganic ChemistryDistamycinsNetropsinGeneral MedicineDNADNA Minor Groove BindingIntercalating AgentsAcridoneDrug DesignAcridinebiology.proteinTopoisomerase inhibitorDNAEuropean journal of medicinal chemistry
researchProduct