Search results for "Ficusin"

showing 4 items of 4 documents

A theoretical insight into the photophysics of psoralen

2006

Psoralen photophysics has been studied on quantum chemistry grounds using the multiconfigurational second-order perturbation method CASPT2. Absorption and emission spectra of the system have been rationalized by computing the energies and properties of the low-lying singlet and triplet excited states. The S1 ππ* state has been determined to be responsible of the lowest absorption and fluorescence bands and to initially carry the population in the photophysical processes related to the phototherapeutic properties of psoralen derivatives. The low-lying T1 ππ* state is, on the other hand, protagonist of the phosphorescence, and its prevalent role in the reactivity of psoralen is suggested to b…

LightPhotochemistryPopulationMolecular ConformationGeneral Physics and AstronomyPerturbation theoryPhotochemistryQuantum chemistryFluorescenceAbsorptionElectromagnetic FieldsTriplet state Excited statesOrganic compoundsReaction kinetics theoryEmission spectrumSinglet statePhysical and Theoretical ChemistryPerturbation theoryTriplet stateeducation:FÍSICA::Química física [UNESCO]education.field_of_studyMolecular StructureChemistryChemistry PhysicalPhosphorescenceFicusinModels TheoreticalCarbonUNESCO::FÍSICA::Química físicaSpectrometry FluorescenceModels ChemicalOrganic compounds ; Photochemistry ; Perturbation theory ; Reaction kinetics theory ; Fluorescence ; Phosphorescence ; Triplet state Excited statesExcited stateQuantum TheoryPhosphorescenceSoftware
researchProduct

Photoreactivity of Furocoumarins and DNA in PUVA Therapy: Formation of Psoralen−Thymine Adducts

2008

The mechanism of the [2 + 2] cycloaddition photoreaction of psoralen and a DNA nucleobase, thymine, cornerstone of the furocoumarin-based PUVA (psoralen + UVA radiation) phototherapy, has been studied by the quantum-chemical multiconfigurational CASPT2 method. Triplet- and singlet-mediated mono- and diadduct formations have been determined to take place via singlet-triplet crossings and conical intersections, correlated with the initially promoted triplet or singlet states in different possible reactive orientations. Pyroneside monoadducts are suggested to be formed in the triplet manifold of the system, and to be less prone to yield diadducts because of the properties of the monoadduct low…

Models MolecularMolecular StructurePhotochemistryFurocoumarinFicusinDNAConical intersectionPhotochemistrySurfaces Coatings and FilmsThymineNucleobasechemistry.chemical_compoundFurocoumarinschemistryFurocoumarinsMaterials ChemistrySinglet statePhysical and Theoretical ChemistryTriplet statePUVA TherapyThyminePsoralenThe Journal of Physical Chemistry B
researchProduct

Successful treatment of adult multisystemic Langerhans cell histiocytosis with psoralen-UV-A, prednisolone, mercaptopurine, and vinblastine.

2008

Background Langerhans cell histiocytosis (LCH) is a rare disease with a peak incidence in childhood. There is limited experience with treatment options for adult patients having multisystemic LCH involvement. We report successful treatment of a 70-year-old woman with adult onset of LCH and multisystem disease (diabetes insipidus centralis, bone marrow infiltration, and lung and skin involvement). Observations A 70-year-old woman with erythematous plaques and papules of the submammary and inguinal skin attended our outpatient clinic and was diagnosed as having LCH. Organ involvement was found in the infundibulum of the pituitary gland, associated with diabetes insipidus centralis, bone marro…

Pathologymedicine.medical_specialtyPrednisoloneDermatologyVinblastineUltraviolet therapyLangerhans cell histiocytosisBone MarrowMedicineOutpatient clinicHumansGlucocorticoidsLungHistiocyteAgedSkinPhotosensitizing Agentsbusiness.industryFicusinGeneral Medicinemedicine.diseaseMercaptopurineMagnetic Resonance ImagingHistiocytosisHistiocytosis Langerhans-CellTreatment OutcomePituitary GlandImmunologyDiabetes insipidusPrednisoloneDrug Therapy CombinationFemaleUltraviolet TherapybusinessTomography X-Ray Computedmedicine.drugFollow-Up StudiesArchives of dermatology
researchProduct

Photochemical and Photobiological Studies of a Furonaphthopyranone as a Benzo-spaced Psoralen Analog in Cell-free and Cellular DNA

1997

Photobiological activities of the benzo-spaced psoralen analog furonaphthopyranone 3 have been investigated in cell-free and cellular DNA. The molecular geometry parameters of 3 suggest that it should not form interstrand crosslinks with DNA. With cell-free DNA no evidence for crosslinking but also not for monoadduct formation was obtained; rather, the unnatural furocoumarin 3 induces oxidative DNA modifications under near-UVA irradiation. The enzymatic assay of the photosensitized damage in cell-free PM2 DNA revealed the significant formation of lesions sensitive to formamidopyrimidine DNA glycosylase (Fpg protein). In the photooxidation of calf thymus DNA by the furonaphthopyranone 3, 0.2…

PhotochemistryUltraviolet RaysDNA damageMolecular ConformationCHO CellsPhotochemistryBiochemistryOxazolonechemistry.chemical_compoundCricetinaeFurocoumarinsAnimalsDeoxyguanosinePhysical and Theoretical ChemistryPsoralenPhotosensitizing AgentsCell-Free SystemMolecular StructureMutagenicity TestsFurocoumarinFicusinDeoxyguanosineDNAGeneral MedicineFormamidopyrimidine DNA glycosylaseComet assaychemistryDNA ViralMethoxsalenCattleDNADNA DamagePhotochemistry and Photobiology
researchProduct