Search results for "carbolines"

showing 5 items of 25 documents

Monoamine Oxidase Inhibition by β-Carbolines: A Quantum Chemical Approach

1979

Monoamine oxidase inhibition by beta-carboline derivatives is related to the energy change, delta E, arising from complex formation between the inhibitor and the enzyme. The energy change was expressed in terms of electronic indexes, which were estimated for a set of aromatic beta-carbolines. The electronic indexes were correlated to the experimental activity indexes by a simplified quantum chemical perturbational treatment with a multiple regression procedure. A characteristic structure for the inhibitor-enzyme complex was derived from the correlation. The molecules are linked by two kinds of bond. One involves the lone pyridine nitrogen pair of beta-carbolines; the other is due to a pi-el…

Quantum chemicalIndole testchemistry.chemical_classificationTryptamineIndolesMonoamine Oxidase InhibitorsChemistryMonoamine oxidaseStereochemistryPharmaceutical ScienceModels BiologicalStructure-Activity Relationshipchemistry.chemical_compoundNon-competitive inhibitionEnzymePyridineQuantum TheoryThermodynamicsMoleculeCarbolinesJournal of Pharmaceutical Sciences
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DNA Oxidation Photoinduced by Norharmane Rhenium(I) Polypyridyl Complexes: Effect of the Bidentate N,N′-Ligands on the Damage Profile

2018

Re(I)--polypyridyl complexes have interesting and distinctive photochemical and photosensitizing properties. This work describes the capability to induce (or photoinduce) DNA damage of three Re(I)-complexes with a naturally occurring alkaloid called norharmane (nHo) as ligand: [Re(CO)₃ (nHo)(L)]CF₃ SO₃ where L=2,2'-bipyridine (ReBpy), phenanthroline (RePhen) or dipyrido[3,2-a:2',3'-c]phenazine (ReDppz). The interaction of the complexes with DNA was investigated by steady-state and time-resolved spectroscopy. Data show that the mode and strength of interaction depend on the chemical structure of the bidentate ligand. The complexes show a major static contribution to the overall interaction, …

Salmonella typhimuriumDenticityLightFísico-Química Ciencia de los Polímeros ElectroquímicaPhenanthrolineLigands01 natural sciences//purl.org/becyt/ford/1 [https]chemistry.chemical_compound22'-DipyridylStereochemistryCoordination ComplexesELECTRON TRANSFERSinglet OxygenCiencias QuímicasRHENIUMQuímicaChemistryRheniumPhotosensitizationPHOTOSENSITIZATIONAdductOxidation-ReductionCIENCIAS NATURALES Y EXACTASStereochemistryDNA damagePhenanthrolinePhenazineDNA CLEAVAGELigand010402 general chemistryCatalysisAdductElectron transferElectron transferAlkaloidsOxidants PhotochemicalPhenazine//purl.org/becyt/ford/1.4 [https]010405 organic chemistryLigandMutagenicity TestsDna cleavageOrganic ChemistryDenticityGeneral ChemistryDNA0104 chemical scienceschemistryALKALOIDSReactive Oxygen SpeciesDNACarbolinesDNA Damage
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Harvesting canthinones: identification of the optimal seasonal point of harvest of Zanthoxylum chiloperone leaves as a source of 5-methoxycanthin-6-o…

2015

This article is focused on the seasonal variation in the contents of 5-methoxycanthin-6-one from the leaves of Zanthoxylum chiloperone (Rutaceae). Based on the pharmacological interest presented by 5-methoxycanthin-6-one, its seasonal variation in Z. chiloperone leaves was analysed in order to determine the best time for harvesting, optimising the 5-methoxycanthin-6-one content. The seasonal dynamics of canthinone alkaloids can be the key to improve the isolation from natural sustainable sources, such as leaves. Complementarily, this study describes the phytochemistry of leaf from this Ruraceae species.

ZanthoxylumPhytochemistryPlant compositionalkylamidePlant SciencealkaloidsBiochemistryHPLC-UV-MSAnalytical ChemistryZanthoxylumMS-MSBotanymedicineRutaceaechiloperoneMolecular StructurebiologyHplc uv msseasonalityOrganic ChemistryTemperatureSeasonalitymedicine.diseasebiology.organism_classificationsustainabilityPlant LeavesHorticulturecanthinoneRutaceaebenzylisoquinoline5-methoxycanthin-6-oneelectrochemistryphytochemistrySeasonsCarbolines
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Photosensitization of DNA by β-carbolines: Kinetic analysis and photoproduct characterization

2012

β-Carbolines (βCs) are a group of alkaloids present in many plants and animals. It has been suggested that these alkaloids participate in a variety of significant photosensitized processes. Despite their well-established natural occurrence, the main biological role of these alkaloids and the mechanisms involved are, to date, poorly understood. In the present work, we examined the capability of three important βCs (norharmane, harmane and harmine) and two of its derivatives (N-methyl-norharmane and N-methyl-harmane) to induce DNA damage upon UV-A excitation, correlating the type and extent of the damage with the photophysical characteristics and DNA binding properties of the compounds. The r…

chemistry.chemical_classificationReactive oxygen speciesPhotosensitizing AgentsMolecular StructurebiologySuperoxideSinglet oxygenDNA damageStereochemistryOrganic ChemistryPyrimidine dimerDNAPhotochemical ProcessesBiochemistrySuperoxide dismutaseKineticschemistry.chemical_compoundHarminechemistrybiology.proteinPhysical and Theoretical ChemistryHarmaneReactive Oxygen SpeciesCarbolinesThymidineOrganic & Biomolecular Chemistry
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?-Carboline binding indicates the presence of benzodiazepine receptor subclasses in the bovine central nervous system

1982

Receptor binding studies were performed with tritiated propyl β-carboline-3-carboxylate ([3H]PrCC), tritiated ethyl β-carboline-3-carboxylate ([3H]ECC), and tritiated flunitrazepam ([3H]FNT) in membrane preparations from different regions of the bovine brain and retina. Specific binding in all regions investigated was associated with benzodiazepine receptor sites. However, not all benzodiazepine receptor sites. However, not all benzodiazepine receptors in the regions investigated as determined by the specific binding of tritiated flunitrazepam ([3H]FNT) are available for [3H]PrCC suggesting that specific [3H]PrCC binding labels only one subclass or subpopulation of the benzodiazepine recept…

medicine.medical_specialtyAdenosineIndolesmedicine.drug_classReceptors DrugCentral nervous systemHippocampusSubstrate Specificitychemistry.chemical_compoundInternal medicinemedicineAnimalsReceptorgamma-Aminobutyric AcidBrain ChemistryPharmacologyBenzodiazepineBinding SitesGABAA receptorChemistrybeta-CarbolineGeneral MedicineReceptors GABA-Amedicine.anatomical_structureEndocrinologyGABAergicCattleFlunitrazepamCarbolinesmedicine.drugNaunyn-Schmiedeberg's Archives of Pharmacology
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