Search results for "BIP"

showing 10 items of 1908 documents

Synthesis and copper-mediated nuclease activity of a tetracationic tris(2,2′-bipyridine) ligand

2009

Abstract We report herein the synthesis of a novel tetracationic tris(2,2′-bipyridine) ligand 4 . We show that this ligand metalated with copper(II), and in the presence of ascorbate as a reducing agent, strongly damages pUC18 plasmid DNA. Copper complex formation was demonstrated by ESI-MS (electrospray ionization-mass spectrum) at a 1:3 ligand to metal ratio. Binding of both 4 and its copper(II) complex to CT-DNA (calf thymus DNA) was characterized by viscosimetry, thermal denaturation and fluorescence-based competition assays. The viscosimetric data indicated that 4 and its copper(II) complex bind DNA through partial intercalation and thermal denaturation studies revealed a significant i…

TrisSpectrometry Mass Electrospray IonizationDeoxyribonucleasesChemistryIntercalation (chemistry)chemistry.chemical_elementDNALigandsPhotochemistryLigand (biochemistry)BiochemistryCopper22'-BipyridineInorganic Chemistrychemistry.chemical_compound22'-DipyridylPolymer chemistryAnimalsHydroxyl radicalDNA CleavageEthidium bromideCopperDNAJournal of Inorganic Biochemistry
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A New Macrobicyclic Tris-bipyridine Ligand and Its Cu2I and Ag3I Complexes

1991

Trischemistry.chemical_compoundBipyridineChemistryLigandPolymer chemistryGeneral MedicineGeneral ChemistryCatalysisAngewandte Chemie International Edition in English
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Emotional Processing in Bipolar Disorder: Behavioral and Eye-movement Evidence

2014

El estado de ánimo modula cómo se procesa la información emocionalmente relevante. El Trastorno Bipolar (TB) se caracteriza precisamente por la pérdida de control de las emociones, por lo que el procesamiento emocional podría estar cualitativamente sesgado. Este trabajo examina las variaciones patológicas de las emociones mediante la caracterización de los sesgos atencionales en el TB como factores de vulnerabilidad comunes a todos los estados del TB (i.e., sesgos-rasgo) o como factores de mantenimiento que sólo están presentes durante los episodios agudos (i.e., sesgos-estado). Para ello, se comparan pacientes con TB en cada uno de los posibles episodios (manía, depresión, eutimia) junto c…

UNESCO::CIENCIAS MÉDICAS ::Psiquiatríasesgos atencionales:CIENCIAS MÉDICAS ::Psiquiatría [UNESCO]:PSICOLOGÍA [UNESCO]movimientos ocularestrastorno bipolarUNESCO::PSICOLOGÍA
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Oxovanadium(V) complexes with tripodal bisphenolate and monophenolate ligands: Syntheses, structures and catalytic activities

2019

Abstract The reactions between [VO(acac)2] (acac– = acetylacetonate) and the tripodal amino bisphenols 6,6′-(((2-morpholinoethyl)azanediyl)bis(methylene))bis(2,4-di-tert-butylphenol) (H2L1) and 6,6′-(((thiophen-2-ylmethyl)azanediyl)bis(methylene))bis(2,4-di-tert-butylphenol) (H2L2) as well as the tetradentate amino phenol 2,2′-((3,5-di-tert-butyl-2-hydroxybenzyl)azanediyl)bis(ethan-1-ol) (H3L3) afford the complexes [VO(L1)(OMe)] (1), [VO(L2)(acac)] (2) and [VO(L3)] (3), correspondingly. Complexes 1 and 3 can also be prepared using VOSO4·xH2O or [VO(OPr)3] as vanadium precursors. When [VO(acac)2] or VOSO4·xH2O is used, mononuclear oxovanadium(V) complexes are formed upon oxidation of the met…

Vanadiumchemistry.chemical_element010402 general chemistry01 natural sciencesMedicinal chemistrysulfoxidationCatalysisInorganic ChemistryMetalchemistry.chemical_compoundepoxidationcalculationsMaterials ChemistryPhysical and Theoretical ChemistryMethyleneta116Vanadium (V) complexes010405 organic chemistryChemistryThioanisolekompleksiyhdisteet0104 chemical sciencesTrigonal bipyramidal molecular geometryOctahedronvisual_artvisual_art.visual_art_mediumSingle crystalInorganica Chimica Acta
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Synthesis of honokiol analogues and evaluation of their modulating action on VEGF protein secretion and telomerase-related gene expressions

2017

A group of 36 biphenyl derivatives structurally related to honokiol were synthesized by means of Suzuki coupling reactions. Their cytotoxicities were evaluated and compared to that of honokiol. Some of the compounds were then evaluated for their ability to downregulate the secretion of the VEGF protein and the expression of the VEGF, hTERT, and c-Myc genes; the two latter involved in the activation of telomerase in tumoral cells. Some of the synthetized derivatives showed promising pharmacological features as they exhibited IC50 values in low micromolar range, good therapeutic margins, and a multiple mode of action on tumor cells based on the inhibition of VEGF and, at the same time, of the…

Vascular Endothelial Growth Factor A0301 basic medicineHonokiolTelomeraseAngiogenesishonokiol analoguesGene ExpressionEnzyme-Linked Immunosorbent AssayBiologytelomeraseBiochemistryLignans03 medical and health scienceschemistry.chemical_compoundangiogenesisDownregulation and upregulationDrug DiscoveryHumansSecretionTelomerase reverse transcriptaseTelomerasePharmacologyRegulation of gene expressionBiphenyl CompoundsOrganic ChemistryVEGFHEK293 Cells030104 developmental biologySecretory proteinc-MycchemistryMCF-7 CellsCancer researchMolecular Medicinegene regulationhTERTHT29 Cells
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Identification and optimization of small molecule antagonists of vasoactive intestinal peptide receptor-1 (VIPR1).

2012

Identification, synthesis and structure-activity relationship of small-molecule VIPR1 antagonists encompassing two chemical series are described.

Vasoactive intestinal peptide (VIP)Settore MED/09 - Medicina InternaReceptors Vasoactive Intestinal Polypeptide Type IClinical BiochemistryVasoactive intestinal peptidePharmaceutical ScienceAntineoplastic AgentsThiophenesBiochemistrySmall Molecule LibrariesStructure-Activity RelationshipCell Line TumorDrug DiscoveryStructure–activity relationshipHumansReceptorMolecular BiologyChemistryVasoactive intestinal peptide receptorOrganic ChemistryBiphenyl CompoundsSmall Molecule LibrariesSmall moleculeHigh-Throughput Screening AssaysBiochemistryCell cultureVasoactive intestinal peptide receptor (VIPR)Molecular MedicineDrug Screening Assays AntitumorVIPR1Bioorganicmedicinal chemistry letters
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A time course investigation of vitamin A level and lipid composition of the liver endoplasmic reticulum in rats following treatment with congeneric p…

1990

Abstract The drug metabolizing enzyme activities, the vitamin A content and the fatty acid composition in the endoplasmic reticulum membrane were studied in rat liver after a single injection of the polychlorobiphenyls (PCBs) 3,3′,4,4′-tetrachlorobiphenyl [(3,4)2Cl] or 2,2′,4,4′,5,5′-hexachlorobiphenyl [(2,4,5)2Cl], 300 μ mol/kg each. The microsomal vitamin A level was markedly lowered 3 days after treatment with (3,4)2Cl, a coplanar type inducer of cytochrome P-450. A marked increase in microsomal AHH and UDPGT activities occurred within 3 days after injection of (3,4)2Cl whereas (2,4,5,)2Cl treatment enhanced APDM activity only. Arachidonic, stearic and linoleic acid microsomal contents w…

VitaminMalemedicine.medical_specialtyCytochromeLinoleic acidToxicologyEndoplasmic Reticulumchemistry.chemical_compoundInternal medicinemedicineAnimalsVitamin APhospholipidsbiologyEndoplasmic reticulumFatty AcidsRetinolRats Inbred Strainsbiology.organism_classificationPolychlorinated BiphenylsRatsEndocrinologyMicrosomaBiochemistrychemistryDocosahexaenoic acidMicrosomebiology.proteinMicrosomes LiverAryl Hydrocarbon HydroxylasesToxicology
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A time-course investigation of vitamin A levels and drug metabolizing enzyme activities in rats following a single treatment with prototypic polychlo…

1987

Xenobiotics previously characterized as selective inducers of drug-metabolizing enzymes were chosen to probe possible relationships between enzyme induction and vitamin A metabolism. Liver, kidney and serum retinol and retinyl palmitate levels were investigated in male Sprague--Dawley rats receiving a single i.p. injection of the polychlorinated biphenyls (PCBs), 2,2',5,5'-tetrachlorobiphenyl, 3,3',4,4'-tetrachlorobiphenyl or 2,2',4,4',5,5'-hexachlorobiphenyl (300 mumol/kg) or 1,1,1-trichloro-2,2-bis-(4-chlorophenyl)-ethane (DDT) (150 mumol/kg). While 2,2',5,5'-tetrachlorobiphenyl, a weak or non-inducer, and 2,2',4,4',5,5'-hexaclorobiphenyl and DDT, phenobarbital-type inducers of cytochrome…

VitaminMalemedicine.medical_specialtyInternational unit10050 Institute of Pharmacology and Toxicology610 Medicine & healthToxicologyKidneyDDTMixed Function Oxygenaseschemistry.chemical_compoundInternal medicineRetinyl palmitatemedicineAnimalsEnzyme inducerVitamin AbiologyChemistryRetinolCytochrome P4503005 ToxicologyRats Inbred StrainsPolychlorinated BiphenylsRatsKineticsEndocrinologyLiverEnzyme InductionToxicitybiology.protein570 Life sciences; biologyXenobiotic
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[Cu(P^P)(N^N)][PF6] compounds with bis(phosphane) and 6-alkoxy, 6-alkylthio, 6-phenyloxy and 6-phenylthio-substituted 2,2'-bipyridine ligands for lig…

2018

We report a series of [Cu(P^P)(N^N)][PF6] complexes with P^P = bis(2-(diphenylphosphino)phenyl)ether (POP) or 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene (xantphos) and N^N = 6-methoxy-2,2′-bipyridine (MeObpy), 6-ethoxy-2,2′-bipyridine (EtObpy), 6-phenyloxy-2,2′-bipyridine (PhObpy), 6-methylthio-2,2′-bipyridine (MeSbpy), 6-ethylthio-2,2′-bipyridine (EtSbpy) and 6-phenylthio-2,2′-bipyridine (PhSbpy). The single crystal structures of all twelve compounds have been determined and confirm chelating modes for each N^N and P^P ligand, and a distorted tetrahedral geometry for copper(I). For the xantphos-containing complexes, the asymmetrical bpy ligand is arranged with the 6-substituent lying …

XantheneMaterials scienceXantphosLigandTetrahedral molecular geometryEther02 engineering and technologyGeneral Chemistry010402 general chemistry021001 nanoscience & nanotechnology01 natural sciencesMedicinal chemistry22'-Bipyridine0104 chemical scienceschemistry.chemical_compoundchemistryMaterials ChemistryAlkoxy group0210 nano-technologySingle crystal
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Shine bright or live long: substituent effects in [Cu(N^N)(P^P)]+-based light-emitting electrochemical cells where N^N is a 6-substituted 2,2'-bipyri…

2016

We report [Cu(P^P)(N^N)][PF6] complexes with P^P = bis(2-(diphenylphosphino)phenyl)ether (POP) or 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene (xantphos) and N^N = 6-methyl-2,2′-bipyridine (Mebpy), 6-ethyl-2,2′-bipyridine (Etbpy), 6,6′-dimethyl-2,2′-bipyridine (Me2bpy) or 6-phenyl-2,2′-bipyridine (Phbpy). The crystal structures of [Cu(POP)(Phbpy)][PF6]·Et2O, [Cu(POP)(Etbpy)][PF6]·Et2O, [Cu(xantphos)(Me2bpy)][PF6], [Cu(xantphos)(Mebpy)][PF6]·CH2Cl2·0.4Et2O, [Cu(xantphos)(Etbpy)][PF6]·CH2Cl2·1.5H2O and [Cu(xantphos)(Phbpy)][PF6] are described; each copper(I) centre is distorted tetrahedral. In the crystallographically determined structures, the N^N domain in [Cu(xantphos)(Phbpy)]+ and [Cu(…

XantphosLigand02 engineering and technologyGeneral ChemistryCrystal structureNuclear magnetic resonance spectroscopy010402 general chemistry021001 nanoscience & nanotechnology01 natural sciences22'-Bipyridine0104 chemical scienceschemistry.chemical_compoundCrystallographyElectron transferchemistryExcited stateMaterials ChemistrySinglet state0210 nano-technology
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