Search results for "Phenanthrene"

showing 10 items of 101 documents

Left, Right, or Both? On the Configuration of the Phenanthroindolizidine Alkaloid Tylophorine from Tylophora indica

2013

The alkaloid (-)-tylophorine was isolated from a sample of Tylophora indica, and the crude extract was analyzed by HPLC/MS(n) and chiral HPLC/MS. While the literature states that the naturally occurring form of this alkaloid is the R-enantiomer and that its S-antipode is usually not found in nature, we confirmed the hypothesis of Govindachari and Nagarajan that natural levorotatory tylophorine is indeed a nearly racemic mixture with a slight excess of the R-enantiomer.

PharmacologyMolecular StructureChemistryAlkaloidOrganic ChemistryIndolizinesPharmaceutical ScienceTylophoraPhenanthrenesHigh-performance liquid chromatographyLevorotatoryAnalytical ChemistryChiral column chromatographyAlkaloidsTylophora indicaComplementary and alternative medicineDrug DiscoveryMolecular MedicineOrganic chemistryRacemic mixturePhenanthrolinesJournal of Natural Products
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Regio- and stereoselectivity in the metabolism of benzo[c]phenanthrene mediated by genetically engineered V79 Chinese hamster cells expressing rat an…

1998

Regio- and stereoselective metabolism mediated by cytochrome P450 (CYP) and metabolite-dependent cytotoxicity of benzo[c]phenanthrene (B[c]Ph) and its trans-3,4-dihydrodiol, the metabolic precursor of the carcinogenic fjord-region B[c]Ph-3,4-dihydrodiol 1,2-epoxides (B[c]PhDE), were investigated with V79 Chinese hamster cells genetically engineered for three rat and six human CYP isoforms. The order of the capabilities of the CYP isoforms to metabolize B[c]Ph was as follows: h1A1>r1A1>r1A2>h1B1>h1A2>r2B1>>h2E1>h2A6>h3A4. Regardless of the species, all individual CYP isoforms preferentially catalyzed the oxidation of B[c]Ph at the 5,6-position (K-region) except human CYP1A1 and human CYP1A2,…

PharmacologybiologyChemistryStereochemistryHealth Toxicology and MutagenesisBenzo(c)phenanthreneCYP1A2Cytochrome P450General MedicineMetabolismrespiratory systemToxicologybiology.organism_classificationChinese hamsterchemistry.chemical_compoundCell culturepolycyclic compoundsbiology.proteinStereoselectivityCarcinogenEnvironmental toxicology and pharmacology
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Global patterns of polycyclic aromatic hydrocarbons (PAHs) in soil

2007

Abstract Recent findings suggest a higher natural contribution to PAH concentrations in soil than previously thought. I hypothesized that the PAH pattern in soil is dominated by two main types, which are indicative of background conditions on the one side (i.e., by biological and diffuse PAHs) and a strong impact by atmospheric deposition of anthropogenic emissions on the other side. To test this hypothesis, concentrations of 20 PAHs in 225 topsoil samples from 12 geographic regions were evaluated. The Σ20PAHs concentrations ranged between 4.8 and 186,000 μg kg− 1. In soils with low concentrations of Σ20PAHs, naphthalene (NAPH), phenanthrene (PHEN), and perylene (PERY), together defined as …

PollutionPollutantTopsoilmedia_common.quotation_subjectSoil SciencePhenanthrenechemistry.chemical_compoundchemistryEnvironmental chemistrySoil waterGeographic regionsEnvironmental scienceVolume concentrationmedia_commonNaphthaleneGeoderma
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DNA Polymerase Action on Oligonucleotide Templates from Human Ha-rasProtooncogene Containing N6-Deoxyadenosine Adducts Derived from Trans Addition of…

1996

Abstract In the present work we have used a DNA polymerase assay to investigate the primer extension with T7 DNA polymerase (Sequenase 2.0) and the Klenow fragment of Escherichia coli DNA polymerase I (exo − KF) on chemically synthesized 21mer templates representing partial sequences of the human Ha-ras protooncogene with site-specifically positioned trans-N 6-dA adducts of (-)- (adduct 1) and (+)-anti-benzo[c]phenanthrene 3,4-dihydrodiol 1,2-epoxides (adduct 2) at codon 61 (CA∗G; A∗ indicates the adducted position). With Sequenase 2.0 a complete block of primer extension opposite both adduct 1 and 2 was noted using a 10mer primer reaching the (n-1)-position of the adduct. A detailed analys…

Polymers and PlasticsbiologyChemistryDNA polymeraseOrganic ChemistryBenzo(c)phenanthreneT7 DNA polymeraseMolecular biologyPrimer extensionchemistry.chemical_compoundMaterials Chemistrybiology.proteinPrimer (molecular biology)DNA polymerase IPolymeraseKlenow fragmentPolycyclic Aromatic Compounds
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Enantioselective alkynylation of benzo[e][1,2,3]-oxathiazine 2,2-dioxides catalysed by (R)-VAPOL-Zn complexes: synthesis of chiral propargylic cyclic…

2015

[EN] (R)-VAPOL-Zn(II) complexes catalysed the enantioselective addition of terminal alkynes to cyclic benzoxathiazine 2,2-dioxides, providing the corresponding chiral propargylic sulfamidates with high yields (up to 93%) and good enantiomeric excesses (up to 87%).

PropylaminesPropanolsStereochemistryChemistryOrganic ChemistryThiazinesEnantioselective synthesisStereoisomerismPhenanthrenesCrystallography X-RayLigandsAmidesBiochemistryCatalysisZincCatàlisiPargylineAlkynylationAlkynesFISICA APLICADAPhysical and Theoretical ChemistryEnantiomerQuímica orgànicaChromatography High Pressure Liquid
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Retene, pyrene and phenanthrene cause distinct molecular-level changes in the cardiac tissue of rainbow trout (Oncorhynchus mykiss) larvae, Part 2 – …

2020

Polycyclic aromatic hydrocarbons (PAHs) are global contaminants of concern. Despite several decades of research, their mechanisms of toxicity are not very well understood. Early life stages of fish are particularly sensitive with the developing cardiac tissue being a main target of PAHs toxicity. The mechanisms of cardiotoxicity of the three widespread model polycyclic aromatic hydrocarbons (PAHs) retene, pyrene and phenanthrene were explored in rainbow trout (Oncorhynchus mykiss) early life stages. Newly hatched larvae were exposed to sublethal doses of each individual PAH causing no detectable morphometric alterations. Changes in the cardiac proteome and metabolome were assessed after 7 o…

Proteomicsbiologiset vaikutuksetEnvironmental Engineering010504 meteorology & atmospheric sciencestoksiinitDevelopmental toxicitycardiotoxicity010501 environmental sciencesmyrkyllisyys01 natural sciencesproteomiikkaTranscriptomechemistry.chemical_compoundMetabolomicsproteomicsMetabolomeEnvironmental ChemistryAnimalsMetabolomicsdevelopmental toxicityaquatic toxicology14. Life underwaterPolycyclic Aromatic HydrocarbonsWaste Management and Disposal0105 earth and related environmental scienceskalatRetenevesistötPyrenesbiologyChemistryPhenanthrenePhenanthrenesAryl hydrocarbon receptorPollutionmetabolomicsekotoksikologiaBiochemistryLarvaOncorhynchus mykisspolycyclic aromatic hydrocarbons (PAHs)biology.proteinPyrenearomaattiset hiilivedytepäpuhtaudet
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Estimation of the environmental hazard of organochlorines in pulp mill biosludge used as soil fertilizer

1993

Abstract Contents of total organic chlorine and polychlorinated phenols, guaiacols, catechols, benzenes, cymenes, cymenenes, naphthalenes, toxic dibenzodioxins, toxic dibenzofurans, toxic PCB congener 77, alkylated dibenzofurans, alkylated bibenzyls and alkylated phenanthrenes in spent biosludges from activated sludge treatment plants of chlorobleaching kraft pulp mills are reported. Some estimations of hazard caused by these organochlorines to humans and wildlife from the use of biosludge as soil fertilizer are constructed and discussed.

Pulp millEnvironmental EngineeringChemistryHealth Toxicology and MutagenesisPublic Health Environmental and Occupational Healthchemistry.chemical_elementGeneral MedicineGeneral Chemistryengineering.materialPollutionCymenesCongenerKraft processEnvironmental chemistryengineeringChlorineEnvironmental ChemistrySewage treatmentFertilizerPhenanthrenesChemosphere
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Mutagenicity of N-substituted phenanthrene 9,10-imines in Salmonella typhimurium and Chinese hamster V79 cells.

1986

We previously showed that some (nonsubstituted) aziridines derived from polycyclic aromatic hydrocarbons (arene imines) elicit various mutagenic and genotoxic effects in bacteria and mammalian cells and that these arene imines are active at much lower concentrations than the corresponding epoxide analogues. In the present study, N-substituted derivatives of phenanthrene 9,10-imine were investigated. All 10 derivatives studied showed direct mutagenicity in Salmonella typhimurium TA100. Some of the compounds additionally exhibited weak effects in the strains TA98 and TA1537. Most N-substituted derivatives were weaker mutagens than unsubstituted phenanthrene 9,10-imine but stronger mutagens th…

Salmonella typhimuriumendocrine systemStereochemistryHealth Toxicology and MutagenesisAziridinesEpoxideHamsterGene mutationChinese hamsterCell Linechemistry.chemical_compoundStructure-Activity RelationshipCricetulusCricetinaeGeneticsAnimalsbiologyAzirinesMutagenicity Testsfood and beveragesAziridinePhenanthrenePhenanthrenesbiology.organism_classificationEnterobacteriaceaechemistryBacteriaMutagensEnvironmental mutagenesis
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Photocatalysis in dimethyl carbonate green solvent: degradation and partial oxidation of phenanthrene on supported TiO2

2014

Dimethyl carbonate (DMC) is here proposed – for the first time – as a green organic solvent for photocatalytic synthesis. In this work, the photocatalytic partial oxidation of phenanthrene in dimethyl carbonate (DMC) by using anatase TiO2 as the photocatalyst is described as paradigmatic example of a green synthetic process starting from polycyclic aromatic hydrocarbons (PAHs). For comparison, the same reaction carried out also in ethanol, 1-propanol or 2-propanol is reported. The use of DMC as the solvent allowed us to achieve 19% and 23% selectivity towards 9-fluorenone and 6H-benzo[c]chromen- 6-one, respectively. The proposed approach may represent both a new green synthetic process and …

Settore ING-IND/24 - Principi Di Ingegneria ChimicaAnataseGeneral Chemical EngineeringGeneral ChemistryPhenanthreneaaSolventchemistry.chemical_compoundchemistryPhotocatalysisDegradation (geology)Organic chemistrySettore CHIM/07 - Fondamenti Chimici Delle TecnologiePartial oxidationDimethyl carbonatephenanthrene supported TiO2 partial oxidation green solventSelectivityRSC Adv.
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CCDC 103195: Experimental Crystal Structure Determination

2002

Related Article: A.Caneschi, A.Dei, F.F.de Biani, P.Gutlich, V.Ksenofontov, G.Levchenko, A.Hoefer, F.Renz|2001|Chem.-Eur.J.|7|3926|doi:10.1002/1521-3765(20010917)7:18<3926::AID-CHEM3926>3.0.CO;2-6

Space GroupCrystallographyCrystal SystemCrystal StructureCell Parameters(dl-577121414-Hexamethyl-14811-tetra-azacyclotetradecane NN'N''N''')-(910-dioxophenanthrene-OO')-cobalt(ii) hexafluorophosphate dichloromethane solvateExperimental 3D Coordinates
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