Search results for "stereo"

showing 10 items of 6147 documents

New evidence for the multiplicity of ubiquinone- and inhibitor-binding sites in the mitochondrial complex I.

2000

Determination of the number of ubiquinone- and inhibitor-binding sites in the mitochondrial complex I (NADH:ubiquinone oxidoreductase) is a controversial question with a direct implication for elaborating a suitable model to explain the bioenergetic mechanism of this complicated enzyme. We have used combinations of both selective inhibitors and common ubiquinone-like substrates to demonstrate the multiplicity of the reaction centers in the complex I in contrast with competition studies that have suggested the existence of a unique binding site for ubiquinone. Our results provide new evidence for the existence of at least two freely exchangeable ubiquinone-binding sites with different specif…

BioenergeticsStereochemistryUbiquinoneSubmitochondrial ParticlesBiophysicsBiologyIn Vitro TechniquesBiochemistryModels BiologicalMitochondria HeartSubstrate SpecificityOxidoreductaseAnimalsNADH NADPH OxidoreductasesBinding siteMultiplicity (chemistry)Molecular Biologychemistry.chemical_classificationNADH-Ubiquinone OxidoreductaseBinding SitesElectron Transport Complex IKineticsEnzymechemistryBiochemistryCattleEnergy MetabolismMitochondrial Complex IArchives of biochemistry and biophysics
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Conformational Isomerism: Influence of the Z / E Isomerism on the Pathway Complexity of a Squaramide‐Based Macrocycle (Small 7/2021)

2021

BiomaterialsSupramolecular polymerschemistry.chemical_classificationChemistryStereochemistryHydrogen bondSquaramideGeneral Materials ScienceGeneral ChemistryConformational isomerismBiotechnologySmall
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Manganese(II) complexes of scorpiand-like azamacrocycles as MnSOD mimics.

2011

Mn(II) complexes of scorpiand-type azamacrocycles constituted by a tretrazapyridinophane core appended with an ethylamino tail including 2- or 4-quinoline functionalities show very appealing in vitro SOD activity. The observed behaviour is related to structural and electrochemical parameters.

Biomimetic materialsAza CompoundsManganeseMacrocyclic CompoundsStereochemistrySuperoxide DismutaseMetals and AlloysMolecular Conformationchemistry.chemical_elementGeneral ChemistryManganeseElectrochemistryCrystallography X-RayCatalysisMolecular conformationSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialschemistryBiomimetic MaterialsCoordination ComplexesMaterials ChemistryCeramics and CompositesQuinolinesAza CompoundsChemical communications (Cambridge, England)
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Novel bile acid conjugates with aryl/alkenyl linker: Synthesis and characterization

2008

Abstract Eight potential precursors for the design of bile acid derived receptors viz. 2,6-bis[dimethyl(3α-hydroxy-5β-cholan-24-amidoethyl)ammonio-methyl]naphthalene dibromide (1), 3,3′-bis[dimethyl(3α-hydroxy-5β-cholan-24-amidoethyl)ammoniomethyl]biphenyl dibromide (2), 3,3′-bis[dimethyl(3α,7α,12α-trihydroxy-5β-cholan-24-amidoethyl)ammoniomethyl]biphenyl dibromide (3), 4,4′-bis[dimethyl(3α-hydroxy-5β-cholan-24-amidoethyl)ammoniomethyl]stilbene dibromide (4), 4,4′-bis[dimethyl(3α,7α,12α-trihydroxy-5β-cholan-24-amidoethyl)ammoniomethyl]stilbene dibromide (5), allyl-dimethyl(3α,7α,12α-trihydroxy-5β-cholan-24-amidoethyl)ammonium bromide (6), 1,4′-bis[dimethyl(3α-hydroxy-5β-cholan-24-amidoethyl…

BiphenylAmmonium bromidePhotoisomerizationChemistryStereochemistryArylOrganic ChemistryMedicinal chemistryAnalytical ChemistryInorganic ChemistryNMR spectra databasechemistry.chemical_compoundLinkerIsomerizationSpectroscopyNaphthaleneJournal of Molecular Structure
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The magnetic properties of ferrocene based macromolecules

1993

Abstract Magnetic susceptibility data for conjugatively linked biferrocenes and a methylene bridged ferrocene polymer are presented. In 9,10-di((2-ferrocenyl)vinyl)anthracene a rigid divinylanthracene bridge is connecting two ferrocene units, and the oxidation of both iron centers leads to an antiferromagnetic coupling. In contrast, ferromagnetic coupling between iron centers is indicated for 2,2'-cis,trans-di((2-ferrocenyl)vinyl)biphenyl, where a twist around the phenyl-phenyl bond in the divinylbiphenyl bridging molecule is likely to occur.

BiphenylAnthraceneStereochemistryMechanical EngineeringMetals and AlloysCondensed Matter PhysicsMagnetic susceptibilityElectronic Optical and Magnetic Materialschemistry.chemical_compoundCrystallographychemistryFerroceneFerromagnetismMechanics of MaterialsMaterials ChemistryMoleculeMethyleneMacromoleculeSynthetic Metals
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SUBSTRATE-ELICITED DISSOCIATION OF THE ISOSAFROLE METABOLITE-CYTOCHROME P-450 COMPLEX AND THE CONSEQUENTIAL REACTIVATION OF MONOOXYGENATION

1977

ABSTRACT The present study was initiated to determine whether the substrate-elicited dissociation of the isosafrole metabolite-cytochrome P-450 complex resulted in increased monooxygenase activity. It was found that the substrates p -nitroanisole and ethoxycoumarin would elicit dissociation, furthermore this dissociation was accompanied by increased dealkylation of the substrates. Benzo(a)pyrene was found not to effect the dissociation of the complex, while biphenyl, which undergoes a similar hydroxylation, was effective.

BiphenylCytochromebiologyChemistryStereochemistryMetaboliteAlkylationhumanitiesDissociation (chemistry)Hydroxylationchemistry.chemical_compoundIsosafrolebiology.proteinPyrene
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Magnetoelectrochemistry of 4,4′-bis(dimethylamino)biphenyl and 4,4′-dinitrobiphenyl azacrown macrocyclic lactams

2005

Abstract The voltammetric behaviour at carbon fibre microelectrodes under the application of static magnetic fields of two series of macrolactams containing in their structure 4,4′-bis(dimethylamino)biphenyl or 4,4′-dinitrobiphenyl groups in MeCN solution is described. The response of 4,4′-dinitrobiphenyl receptors is dominated by two successive one-electron reduction processes at −0.9 and −1.6 V versus AgCl/Ag. 4,4′-bis(dimethylamino)biphenyl-containing receptors display two one-electron oxidations above +0.8 and +1.0 V. In both cases, a dihedral/planar interconversion precedes the second electron transfer step. Upon application of moderate (0.05–0.2 T) static magnetic fields to the electr…

BiphenylStereochemistryGeneral Chemical EngineeringReaction intermediateDihedral angleElectrochemistrychemistry.chemical_compoundElectron transferCrystallographychemistryElectrochemistryCyclic voltammetryAcetonitrileConformational isomerismElectrochimica Acta
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Sterically crowded triazenides as novel ancillary ligands in copper chemistry

2011

Abstract We have synthesized copper salts MN3RR′ derived from the biphenyl- or m-terphenyl-substituted triazenes Tph2N3H (1a) and Dmp(Tph)N3H (1b) (Dmp = 2,6-Mes2C6H3 with Mes = 2,4,6-Me3C6H2; Tph = 2-TripC6H4 with Trip = 2,4,6-i-Pr3C6H2). The homoleptic copper triazenide [CuN3Tph2] (2a) was obtained in high yield from the metallation of 1a with mesityl copper in n-heptane, while the complex [CuN3(Dmp)Tph] (2b) was generated by the same method in situ only. Reaction of 2a with triphenylphosphane gave the 2:1 adduct [CuN3Tph2(PPh3)2] (3a), regardless of the used complex/donor ratio, while reaction of 2a or 2b with a stochiometric amount of t-butylisonitrile afforded the 1:1 adducts [Tph2N3Cu…

BiphenylSteric effectsStereochemistryInfrared spectroscopychemistry.chemical_elementCarbon-13 NMRMedicinal chemistryCopperAdductInorganic Chemistrychemistry.chemical_compoundchemistryMaterials ChemistryProton NMRPhysical and Theoretical ChemistryHomolepticInorganica Chimica Acta
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Biphenyl macrolactams in anion complexation. Selective naked-eye fluoride recognition

2004

Two colorimetric anion sensors 1 and 2 allow for the selective differentiation of fluoride in the presence of other anions. Two different types of species have been observed in the complexation process, one of them is a co-ordination complex and the other is a salt generated by ligand deprotonation. The deprotonation reaction induces a conformational change, giving rise to a symmetrical species. This species is responsible for colour development. Ligand 3 has a similar structure and does not give rise to any colour modification due to presence of the dimethylamino groups in the biphenyl moiety. The X-ray structure of ligand 2 is also reported and compared with that of ligand 1, that had bee…

Biphenylchemistry.chemical_classificationConformational changeStereochemistryLigandOrganic ChemistrySalt (chemistry)BiochemistryMedicinal chemistrychemistry.chemical_compoundDeprotonationchemistryDrug DiscoveryMoietyNaked eyeFluorideTetrahedron
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A polyazacyclophane containing two biphenyl subunits as a versatile cation and anion receptor

2002

Abstract The synthesis, protonation behaviour and coordination capabilities towards Cu 2+ , Zn 2+ and towards the nucleotides ATP and ADP of a cyclophane ditopic receptor 2,6,10,23,27,31-hexaaza[11,11](2,2′)biphenylophane containing two 2,2′-biphenylene spacers linked to the ends of 1,5,9-triazanonane chains are presented.

Biphenylchemistry.chemical_classificationStereochemistryOrganic ChemistryProtonationGeneral ChemistryInorganic Chemistrychemistry.chemical_compoundchemistryMaterials ChemistryNucleotideReceptorAnion receptorCyclophaneJournal of Supramolecular Chemistry
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