Search results for "Pyrimidine"

showing 10 items of 589 documents

[39] DNA damage induced by ultraviolet and visible light and its wavelength dependence

2000

Publisher Summary DNA damage induced by solar radiation in mammalian cells consists largely of two types of modification: pyrimidine dimers and oxidative modifications. Pyrimidine dimmers that can be subdivided into cyclobutane pyrimidine dimmers, (CPDs) and (6-4) photoproducts are the characteristic and most abundant modifications after direct excitation of DNA, although they can also be formed indirectly by energy transfer from other excited molecules such as carbonyl compounds. Oxidative DNA damage, which includes various pyrimidine and purine modifications, sites of base loss (AP sites), and strand breaks, is generated in only low yield after direct excitation of DNA (except at very sho…

chemistry.chemical_compoundchemistryPyrimidineSinglet oxygenDNA damagemedicinePyrimidine dimerFree radical damage to DNAmedicine.disease_causePhotochemistryDNAUltravioletCyclobutane
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Cyclobutane Pyrimidine Photodimerization of DNA/RNA Nucleobases in the Triplet State

2010

The photoinduced formation of cyclobutane pyrimidine dimers in the triplet excited state of the DNA/RNA pyrimidine nucleobases pairs has been studied at the CASPT2 level of theory. A stepwise mechanism through the triplet state of the homodimer is proposed for the pairs of nucleobases cytosine, thymine, and uracil involving a singlet−triplet crossing intermediary structure of biradical character representing the most favorable triplet state conformation of the nucleobases as found in the DNA environment. The efficiency of the mechanism will be modulated by two factors: the effectiveness of the triplet−triplet energy transfer process from a donor photosensitizer molecule, which relates to th…

congenital hereditary and neonatal diseases and abnormalitiesPhysics::Biological PhysicsQuantitative Biology::BiomoleculesPyrimidineStereochemistryPyrimidine dimerUracilPhotochemistryQuantitative Biology::GenomicsNucleobaseThymineCyclobutanechemistry.chemical_compoundIntersystem crossingchemistryGeneral Materials SciencePhysical and Theoretical ChemistryCytosineThe Journal of Physical Chemistry Letters
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Organotin(IV) Adducts of 5,7-Diphenyl-1,2,4-triazolo[1,5-a] pyrimidine and 5,7-Ditertbutyl-1,2,4-triazolo[1,5-a] pyrimidine

2007

diorganotin(IV) chlorides 124-triazolo[15-a] pyrimidine
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One-pot synthesis of fluorinated 2-amino-pyrimidine-N-oxides. Competing pathways in the four-atom side-chain rearrangements of 1,2,4-oxadiazoles

2006

Abstract Trifluoromethylated 2-amino-pyrimidine N-oxides have been synthesized by reaction of the 3-amino-5-methyl-1,2,4-oxadiazole with trifluoromethyl-β-diketones in the presence of perchloric acid, followed by hydrolysis. In this ring-to-ring transformation an initial formation of (unisolated) 1,2,4-oxadiazole-pyrimidinium salts, and subsequent ring-opening at the oxadiazole moiety occurs. Isolation of 2-(hydroxyamino)-pyrimidine from the reaction mixture evidenced the presence of a competing pathway where the N(4) nitrogen of the oxadiazole is involved in the formation of a regioisomeric pyrimidinium salt. The effect of the trifluoromethyl group on the product distribution is discussed.…

fluoropyrimidine derivativecrystal structurepyrimidine N-oxidePyrimidinesynthesisStereochemistryOne-pot synthesisOxadiazoleX ray analysis3 diketoneBiochemistryMedicinal chemistryperchloric acidnitrogenchemistry.chemical_compoundside-chain rearrangementDrug DiscoveryStructural isomerSide chainMoietyPerchloric acidring openingfluorinated heterocycle3 diketone fluoropyrimidine derivative ketone derivative nitrogen oxide perchloric acid; article crystal structure hydrolysis priority journal reaction analysis ring opening synthesis X ray analysisTrifluoromethylChemistryOrganic Chemistryarticle124-oxadiazoleketone derivativereaction analysishydrolysispriority journaloxide
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V gamma 9V delta 2 T lymphocytes efficiently recognize and kill zoledronate-sensitized, imatinib-sensitive, and imatinib-resistant chronic myelogenou…

2010

Abstract Imatinib mesylate (imatinib), a competitive inhibitor of the BCR-ABL tyrosine kinase, is highly effective against chronic myelogenous leukemia (CML) cells. However, because 20–30% of patients affected by CML display either primary or secondary resistance to imatinib, intentional activation of Vγ9Vδ2 T cells by phosphoantigens or by agents that cause their accumulation within cells, such as zoledronate, may represent a promising strategy for the design of a novel and highly innovative immunotherapy capable to overcome imatinib resistance. In this study, we show that Vγ9Vδ2 T lymphocytes recognize, trogocytose, and efficiently kill imatinib-sensitive and -resistant CML cell lines pre…

gamma delta T cells Imatinib Leukemia cellsAdultmedicine.medical_treatmentImmunologyMice SCIDLymphocyte ActivationZoledronic AcidPiperazinesMicehemic and lymphatic diseasesLeukemia Myelogenous Chronic BCR-ABL PositivemedicineImmunology and AllergyAnimalsHumansneoplasmsCells CulturedDiphosphonatesbusiness.industryImidazolesImatinibReceptors Antigen T-Cell gamma-deltaImmunotherapymedicine.diseaseIn vitroCoculture TechniquesDrug Resistance MultipleLeukemiaImatinib mesylatePyrimidinesCell cultureDrug Resistance NeoplasmImmunologyBenzamidesCancer researchImatinib MesylatebusinessK562 CellsTyrosine kinasemedicine.drugChronic myelogenous leukemiaT-Lymphocytes CytotoxicJournal of immunology (Baltimore, Md. : 1950)
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CCDC 732637: Experimental Crystal Structure Determination

2010

Related Article: E.Colacio, H.Aouryaghal, A.J.Mota, J.Cano, R.Sillanpaa, A.Rodriguez-Dieguez|2009|CrystEngComm|11|2054|doi:10.1039/b906382j

hexakis((mu~2~-Pyrimidine-2-carboxylato)-(NNN'N'-tetramethyl-ethylene-12-diamine))-hexa-cobalt hexaperchlorate tetrahydrateSpace GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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CCDC 725441: Experimental Crystal Structure Determination

2010

Related Article: E.Colacio, H.Aouryaghal, A.J.Mota, J.Cano, R.Sillanpaa, A.Rodriguez-Dieguez|2009|CrystEngComm|11|2054|doi:10.1039/b906382j

hexakis((mu~2~-Pyrimidine-2-carboxylato)-(NNN'N'-tetramethyl-ethylene-12-diamine))-hexa-nickel hexakis(tetrafluoroborate) tetrahydrateSpace GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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CCDC 725440: Experimental Crystal Structure Determination

2010

Related Article: E.Colacio, H.Aouryaghal, A.J.Mota, J.Cano, R.Sillanpaa, A.Rodriguez-Dieguez|2009|CrystEngComm|11|2054|doi:10.1039/b906382j

hexakis((mu~2~-Pyrimidine-2-carboxylato)-(NNN'N'-tetramethyl-ethylene-12-diamine))-hexa-nickel hexaperchlorate tetrahydrateSpace GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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Synthesis of a Novel Hydrazone of Thieno[2,3-d]pyrimidine Clubbed with Ninhydrin: X-ray Crystal Structure and Computational Investigations

2023

The novel hydrazone-containing thieno[2,3-d]pyrimidine, namely, N′-(1,3-dioxo-1,3-dihydro-2H-inden-2-ylidene)-2-(4-oxo-5,6,7,8-tetrahydrobenzo[4,5]thieno[2,3-d]pyrimidin-3(4H)-yl)acetohydrazide 4 was synthesized in a very good yield from the reaction of the triketoester 1 or ninhydrin 2 with the exocyclic acetohydrazide 3 in methanol. Good-quality crystals of 4 were obtained by recrystallization of the compound from the DMF/MeOH solvent mixture. The target product 4 crystallized in the triclinic crystal system and P-1 space group. The topology analysis of molecular packing indicated that the H…H (30.4%), O…H (22.0%) and H…C (17.0%) contacts are the most dominant i…

kemiallinen synteesiGeneral Chemical EngineeringX-ray crystal structureCondensed Matter Physicsthieno[23-d]pyrimidinethieno[23-<i>d</i>]pyrimidineHirshfeldInorganic Chemistryhydrazonex-ray crystal structureGeneral Materials Scienceninhydrinheterosykliset yhdisteetCrystals
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X-Ray characterization of 3-methyl-6,8-di(2-pyridyl)-[1,2,3]triazolo[5',1':6,1]pyrido[2,3-d]pyrimidine

2005

Abarca Gonzalez, Belen. Belen.Abarca@uv.es ; Ballesteros Campos, Rafael, Rafael.Ballesteros@uv.es ; Chadlaoui, Mimoun, michad@alumni.uv.es ; Ramirez de Arellano Sanchez, Maria del Carmen, Ramirezdearellano@uv.es

lcsh:QD241-441Crystallographychemistry.chemical_compoundPyrimidinelcsh:Organic chemistryChemistryStereochemistryOrganic ChemistryX-ray crystallographyX-rayCharacterization (materials science)ARKIVOC
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