Search results for "Nitroreductase"

showing 8 items of 8 documents

Analysis of metabolism and genotoxicity of 5-nitro-3-thiophenecarboxanilides in bacterial, mammalian and human cells

1995

5-nitro-3-thiophenecarboxanilide (NTCA3) was clearly mutagenic in Salmonella typhimurium strains TA98, YG1021 (the strain with elevated nitroreductase) and YG1024 (the strain with elevated O-acetyltransferase) and only slightly mutagenic at the gpt locus in AS52 cells. Clastogenic activity in human lymphocytes was dependent on the length of exposure : detectable chromosome aberrations were observed following a 24 h treatment period, but not after 3 h exposure. S9 increased genotoxicity in both mammalian cells and human lymphocytes. Metabolites formed by incubation of NTCA3 with the different cell systems were examined. A time-course study in cell whole extracts showed that bacterial and mam…

Salmonella typhimuriumHealth Toxicology and MutagenesisMetaboliteLymphocyteIn Vitro TechniquesBiologyToxicologymedicine.disease_causeCell LineAmes testchemistry.chemical_compoundNitroreductaseGeneticsmedicineAnimalsHumansAnilidesGenetics (clinical)Chromosome AberrationsMutagenicity TestsNitroreductasesmedicine.anatomical_structurechemistryBiochemistryCell cultureAcetyltransferaseAcyltransferaseAcetylesteraseGenotoxicityMutagensMutagenesis
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Targeting a Targeted Drug: An Approach Toward Hypoxia-Activatable Tyrosine Kinase Inhibitor Prodrugs

2016

Tyrosine kinase inhibitors (TKIs), which have revolutionized cancer therapy over the past 15 years, are limited in their clinical application due to serious side effects. Therefore, we converted two approved TKIs (sunitinib and erlotinib) into 2-nitroimidazole-based hypoxia-activatable prodrugs. Kinetics studies showed very different stabilities over 24 h; however, fast reductive activation via E. coli nitroreductase could be confirmed for both panels. The anticancer activity and signaling inhibition of the compounds against various human cancer cell lines were evaluated in cell culture. These data, together with molecular docking simulations, revealed distinct differences in the impact of …

medicine.drug_classPharmacology010402 general chemistry01 natural sciencesBiochemistryArticleTyrosine-kinase inhibitor03 medical and health sciencesNitroreductase0302 clinical medicinetyrosine kinase inhibitorsDrug DiscoverymedicinecancerEpidermal growth factor receptorGeneral Pharmacology Toxicology and PharmaceuticsPharmacologybiologyhypoxiaSunitinibChemistryOrganic ChemistryProdrugtargeted therapeutic0104 chemical sciencesSettore CHIM/03 - Chimica Generale E InorganicaCell culture030220 oncology & carcinogenesisbiology.proteinMolecular MedicineErlotinibprodrugTyrosine kinasemedicine.drugChemMedChem
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A nitroreductase and glutathione responsive nanoplatform for integration of gene delivery and near-infrared fluorescence imaging

2020

A novel platform rationally integrating indocyanine green analogues and an arginine-rich dendritic peptide with both nitroreductase (NTR) and glutathione (GSH) reduction responsive linkers was developed. This multifunctional platform can enable selective and efficient gene delivery and specific turn-on fluorescence imaging in tumors.

Indocyanine GreenGlutathione metabolismFluorescence-lifetime imaging microscopyNear-Infrared Fluorescence ImagingInfrared RaysPeptideGene deliveryCatalysischemistry.chemical_compoundNitroreductaseOptical imagingMaterials ChemistryHumansFluorescent Dyeschemistry.chemical_classificationOptical ImagingGene Transfer TechniquesMetals and Alloysfood and beveragesGeneral ChemistryGlutathioneNitroreductasesGlutathioneSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialschemistryCeramics and CompositesBiophysicsPeptidesHeLa CellsChemical Communications
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Distribution of nitroreductive activity toward nilutamide in rat.

2004

Abstract Nilutamide is a pneumotoxic and hepatotoxic nitroaromatic (R-NO 2 ) antiandrogen used in the treatment of prostate carcinoma in man. Previously, we established that in the rat lung, the drug is metabolized into the corresponding hydroxylamine (R-NHOH) and amine (R-NH 2 ) derivatives. These results evidenced a cytosolic oxygen-sensitive (type II) nitroreductase activity in lung. In the present studies, we extended the characterization of nilutamide metabolism in liver, brain, kidney, heart, blood, intestine (small, cecum, and large, and their respective luminal contents) of male Sprague–Dawley rats. Subcellular fractions for all tissues (except blood) examined (postmitochondrial, cy…

MaleBiologyToxicologyImidazolidinesKidneyRats Sprague-DawleyNitroreductaseCecumCytosolmedicineAnimalsIntestinal MucosaCells CulturedChromatography High Pressure LiquidPharmacologyKidneyBrainAndrogen AntagonistsMetabolismNitroreductasesSmall intestineRatsCytosolmedicine.anatomical_structureBiochemistryLiverNilutamideMicrosomemedicine.drugToxicology and applied pharmacology
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Influence of nitroreductase and O-acetyltransferase on the mutagenicity of substituted nitrobenzothiophenamines in Salmonella typhimurium.

1999

The mutagenic activity of 17 substituted (aryl)(2-nitrobenzo[b]thiophen-3yl)amines has been evaluated in the Ames test with different isogenic strains of Salmonella typhimurium, that varied in their expression of nitroreductase and O-acetyltransferase. Active derivatives induced frameshift mutations in TA98 strain, and differences in the chemical structure resulted in up to 15-fold changes in mutagenic activity. The non-mutagenic compounds are the unsubstituted parent compound and derivatives with para-chloro, para-fluoro, para-diethylamino, meta-bromo and para-dimethylamino groups. They do not show any activity even in strains with higher level of nitroreductase or O-acetyltransferase. The…

Salmonella typhimuriumendocrine systemStereochemistryChemical structureThiophenesToxicologyAmes testNitroreductaseAcetyltransferasesStructure–activity relationshipAnimalsAminesBiotransformationbiologyStrain (chemistry)Molecular StructureChemistryMutagenicity Testsfungifood and beveragesGeneral MedicineNitroreductasesbiology.organism_classificationRatsS9 fractionLiverAcetyltransferaseBacteriaMutagensChemico-biological interactions
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Mechanism of genotoxicity and electron density distribution by NMR of 5-nitro-3-thiophenecarboxamides, a novel group of direct-acting mutagens in Sal…

1993

Abstract The mutagenic activity of 23 5-nitro-3-thiophenecarboxanilides and of 5-nitro-3-thiophenecarboxamide, the prototype, (NTCAs) have been evaluated in the Ames test on Salmonella typhimurium strains TA100 ad TA98 with and without metabolic activation. Effects of different substituents (electron-donating and electron-withdrawing) were studied to evaluate structural features that affect the metabolism and the bacterial mutagenic potency. All the derivatives were direct-acting mutagens, the mutagenic potency ranging from 0.7 to 142 revertants (rev.)/nmol in TA100 and from 0.09 to 68 rev./nmol in TA98 strain. Results obtained with strains TA98NR and TA98/1,8-DNP 6 indicated that the mutag…

Salmonella typhimuriumendocrine systemMagnetic Resonance SpectroscopyFree RadicalsStereochemistryMutagenThiophenesToxicologymedicine.disease_causeAmes testNitroreductasechemistry.chemical_compoundStructure-Activity RelationshipAcetyltransferasesNitrationmedicinechemistry.chemical_classificationChemistrySuperoxideMutagenicity Testsfungifood and beveragesGeneral MedicineNitroreductasesEnzymeNitroGenotoxicityMutagensChemico-biological interactions
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Dual enzyme-responsive "turn-on" fluorescence sensing systems based on in situ formation of 7-hydroxy-2-iminocoumarin scaffolds.

2015

A new strategy for the simultaneous fluorogenic detection of two distinct enzyme activities namely hydrolase (amidase or esterase) and reductase is described. This innovative biosensing method is based on the powerful "covalent-assembly" principle that involves in situ synthesis of a fluorophore from a non-fluorescent caged precursor and through domino reactions triggered by the two analytes of interest. To establish this approach, penicillin G acylase (PGA) (or pig liver esterase (PLE)) and nitroreductase (NTR) were chosen as model enzymes, and original bis-O-protected 2,4-dihydroxycinnamonitrile derivatives acting as dual-reactive probes readily convertible to highly fluorescent 7-hydroxy…

In situFluorophoreMolecular StructureStereochemistryChemistryOrganic ChemistryEsterasesBiochemistryFluorescenceEsteraseFluorescenceAmidaseAmidohydrolasesNitroreductasechemistry.chemical_compoundCoumarinsHydrolasePhysical and Theoretical ChemistryOxidoreductasesBiosensorOrganicbiomolecular chemistry
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A novel water-soluble BODIPY dye as red fluorescent probe for imaging hypoxic status of human cancer cells

2020

The development of effective methods for real-time monitoring of nitroreductase (NTR) activity is of great significance for medical diagnosis and cancer research. Here, we present a novel water-soluble BODIPY-based chemodosimeter (NBB) for imaging the hypoxic status of human non-small-cell lung cancer A549 cells. We assume that ‘on–off’ response of NBB is activated by the NTRmediated reductive release of meso-phenol BODIPY dye resulting in unusual fluorescence.

A549 cell010405 organic chemistryGeneral Chemistry010402 general chemistrymedicine.disease01 natural sciencesFluorescence0104 chemical scienceschemistry.chemical_compoundNitroreductaseWater solublechemistryBiochemistrymedicineBODIPYLung cancerHuman cancerMendeleev Communications
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