Search results for "Oxazole"

showing 10 items of 227 documents

CCDC 707422: Experimental Crystal Structure Determination

2009

Related Article: L.Kiss, M.Nonn, E.Forro, R.Sillanpaa, F.Fulop|2009|Tetrahedron Lett.|50|2605|doi:10.1016/j.tetlet.2009.03.119

Space GroupCrystallographyCrystal SystemEthyl 4-(benzoylamino)-3-ethyl-4566a-tetrahydro-3aH-cyclopenta[d][12]oxazole-5-carboxylateCrystal StructureCell ParametersExperimental 3D Coordinates
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CCDC 707423: Experimental Crystal Structure Determination

2009

Related Article: L.Kiss, M.Nonn, E.Forro, R.Sillanpaa, F.Fulop|2009|Tetrahedron Lett.|50|2605|doi:10.1016/j.tetlet.2009.03.119

Space GroupCrystallographyCrystal SystemEthyl 6-(benzoylamino)-3-ethyl-4566a-tetrahydro-3aH-cyclopenta[d][12]oxazole-5-carboxylateCrystal StructureCell ParametersExperimental 3D Coordinates
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Identification and quantification of phosphatidylcholines containing very-long-chain polyunsaturated fatty acid in bovine and human retina using liqu…

2010

The retina is one of the vertebrate tissues with the highest content in polyunsaturated fatty acids (PUFA). A large proportion of retinal phospholipids, especially those found in photoreceptor membranes, are dipolyunsaturated molecular species. Among them, dipolyunsaturated phosphatidylcholine (PC) molecular species are known to contain very-long-chain polyunsaturated fatty acids (VLC-PUFA) from the n-3 and n-6 series having 24-36 carbon atoms (C24-C36) and four to six double bonds. Recent interest in the role played by VLC-PUFA arose from the findings that a protein called elongation of very-long-chain fatty acids 4 (ELOVL4) is involved in their biosynthesis and that mutations in the ELOVL…

Spectrometry Mass Electrospray IonizationChimie analytiquePhospholipidChromosome DisordersTandem mass spectrometry01 natural sciencesBiochemistryHigh-performance liquid chromatographyRetinaAnalytical Chemistry03 medical and health scienceschemistry.chemical_compoundMacular Degeneration[CHIM.ANAL]Chemical Sciences/Analytical chemistryTandem Mass SpectrometryPhosphatidylcholineQUANTITATIVE ANALYSISAnimalsHumansOxazolesChromatography High Pressure Liquid030304 developmental biologychemistry.chemical_classificationPhosphatidylethanolamine0303 health sciencesVERY LONG CHAIN POLYUNSATURATED FATTY ACIDSChromatography010401 analytical chemistryOrganic ChemistryPHOSPHATIDYLCHOLINES;QUANTITATIVE ANALYSIS;LC-ESI-MS/MS;VERY LONG CHAIN POLYUNSATURATED FATTY ACIDS;RETINAGeneral MedicineLC-ESI-MS/MSeye diseases0104 chemical scienceschemistryBiochemistryDocosahexaenoic acidFatty Acids UnsaturatedPhosphatidylcholines[ CHIM.ANAL ] Chemical Sciences/Analytical chemistrylipids (amino acids peptides and proteins)CattleChromosomes Human Pair 6SphingomyelinPolyunsaturated fatty acidJournal of chromatography. A
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Phenotypic and genotypic study on antibiotic resistance and pathogenic factors of Staphylococcus aureus isolates from small ruminant mastitis milk in…

2021

Staphyloccoccus aureus is the major cause of mastitis in small ruminants in the Mediterranean farms causing severe losses to dairy industry. Antibiotic treatment has been the most common approach to control these infections. Aim of this study was to investigate antimicrobial resistance (AMR), virulence factors and biofilm-related genes of 84 Sicilian strains of S. aureus isolated from sheep and goats milk during two different periods δT1 (2006-2009) and δT2 (2013-2015). Kirby Bauer method and Polymerase Chain Reaction (PCR) were utilized to monitor AMR and related genes (mecA, tetK, tetM, ermA, ermC). Moreover, toxin genes (tsst-1, sea-see, seg-sej, and sep) and biofilm genes (bap, ica, sas…

Staphylococcus aureusStaphylococcus aureus; Antimicrobial resistance; Virulence factors BiofilmVirulence factorsTetracyclineSulfamethoxazoleSCCmecBiofilmBiologyTP368-456medicine.disease_causemedicine.diseaseAntimicrobial resistanceFood processing and manufactureArticleMicrobiologyMastitisMultiple drug resistanceAntibiotic resistanceStaphylococcus aureusmedicineStaphylococcus aureuVancomycinFood Sciencemedicine.drugItalian Journal of Food Safety
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Synthesis and Structural Characterization of Substituted 2-Phenacylbenzoxazoles

2013

1 H and 13C NMR spectra of eleven 2-phenacylbenzoxazoles (ketimine form) show that their CDCl3-solutions contains also (Z)-2-(benzo[d]oxazol-2-yl)-1-phenylethenols (enolimine form). Intramolecular hydrogen bonding in the latter tautomer was found to be significantly weaker than that one in respective (Z)-2-(2-hydroxy-2-phenylvinyl)pyridines. Integrals of the 1 H NMR signals were used to evaluate the molar ratio of the tautomers. Strong electron-donating substituents were found to stabilize the ketimine tautomer. pKT (negative logarithm of the equilibrium constant, KT = [ketimine]/[enolimine]) was found to be linearly dependent on the Hammett substituent constant σ. The results of the MP2 ab…

Stereochemistry2-phenyacylbenzoxazoleSubstituent2-fenasyylibentsoksatsoli010402 general chemistry01 natural sciencesArticleCatalysisInorganic Chemistrylcsh:Chemistryresonance interactionchemistry.chemical_compoundAb initio quantum chemistry methods2-phenacylbenzoxazolePhysical and Theoretical Chemistryta116Molecular Biologylcsh:QH301-705.5SpectroscopyEquilibrium constanthydrogen bond010405 organic chemistryHydrogen bondOrganic Chemistryquantum-chemical calculationsGeneral MedicineCarbon-13 NMRTautomerNMR0104 chemical sciencesComputer Science ApplicationsCrystallographytautomerismchemistrylcsh:Biology (General)lcsh:QD1-999Intramolecular forceProton NMRsubstituent effect
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Unique regioselectivity in the C(sp3)-H α-alkylation of amines: the benzoxazole moiety as a removable directing group.

2014

The benzoxazol-2-yl- substituent was found to act as a removable activating and directing group in the Ir-catalyzed alkylation of C(sp(3))-H bonds adjacent to nitrogen in secondary amines. It can be easily introduced by oxidative coupling or by an SNAr reaction, and it can be removed by hydroxide or by hydride reduction. For 1,2,3,4-tetrahydroisoquinolines, activation exclusively takes place in the 3-position. A variety of activated as well as unactivated terminal olefins are suitable reaction partners.

StereochemistryHydrideOrganic ChemistrySubstituentRegioselectivityAlkylationBenzoxazoleBiochemistryMedicinal chemistrychemistry.chemical_compoundchemistryNucleophilic aromatic substitutionMoietyOxidative coupling of methanePhysical and Theoretical ChemistryOrganic letters
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Mononuclear heterocyclic rearrangements—vi

1974

Publisher Summary This chapter discusses the mononuclear heterocyclic rearrangements. The chapter discusses the ring conversion of type 1→2 characterized by nucleophilic attack from a Z atom on a sp 2 -nitrogen atom with displacement of an atom. On this basis, the known ring conversions are tabulated. Taking into account the reactivities observed in the rearrangements, results are presented for 1,2,4-oxadiazole, isoxazole, and 1,2,5-oxadiazole. The sequence involving an oxime group in the side chain is discussed. The chapter presents several attempts for inducing rearrangements in which the reaction center of the starting ring is an atom other than nitrogen. Rearrangement of arylhydrazones …

StereochemistryOrganic ChemistryAtom (order theory)OximeRing (chemistry)Biochemistrychemistry.chemical_compoundchemistryNucleophileDrug DiscoverySide chainIsoxazoleBenzeneIsomerizationTetrahedron
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Inhibition of B2 receptor internalization delays its dephosphorylation

1997

SucroseReceptor Bradykinin B2Immunoprecipitationmedia_common.quotation_subjectBradykininBradykininCell LineDephosphorylationRadioligand Assaychemistry.chemical_compoundOkadaic AcidConcanavalin APhosphoprotein PhosphatasesHumansEnzyme InhibitorsPhosphorylationInternalizationOxazolesBradykinin Receptor AntagonistsSkinmedia_commonPharmacologyChemistryReceptors BradykininOkadaic acidFibroblastsPrecipitinPrecipitin TestsRadioligand AssayBiochemistryCantharidinIrritantsAutoradiographyPhosphorylationElectrophoresis Polyacrylamide GelMarine ToxinsImmunopharmacology
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Molecular and physiological characterization of in vivo Sulfamethoxazole response in Procambarus clarkii

2013

Sulfamethoxazole and Mass spectrometry
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Molecular Search of New Active Drugs AgainstToxoplasma Gondii

1999

Molecular connectivity has been applied to the search of new compounds with activity against the protozoan Toxoplasma gondii, using a stepwise linear discriminant analysis (SLDA) which is able to classify a compound according its activity either as active or as inactive. Among the selected compounds, andrographolide and dibenzotiophene sulfone stand out, both with IC50 values lower than 1 microgram/ml, which are comparable to these of drugs such as sulfamethoxazole, pyrimethamine and trimethoprim, with IC50 values equal to 1.1, 0.04 and 2.31 micrograms/ml, respectively. These results confirm the usefulness of our topological approach for the selection and design of new-lead drugs active aga…

SulfamethoxazoleAndrographolideAntiprotozoal AgentsToxoplasma gondiiBioengineeringGeneral MedicinePharmacologyBiologybiology.organism_classificationVirologyTrimethoprimSulfonechemistry.chemical_compoundPyrimethaminechemistryparasitic diseasesDrug DiscoveryIc50 valuesmedicineAnimalsMolecular MedicineToxoplasmamedicine.drugSAR and QSAR in Environmental Research
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