Search results for "stereo"

showing 10 items of 6147 documents

Receptor-mediated uptake of boron-rich neuropeptide y analogues for boron neutron capture therapy.

2014

Peptidic ligands selectively targeting distinct G protein-coupled receptors that are highly expressed in tumor tissue represent a promising approach in drug delivery. Receptor-preferring analogues of neuropeptide Y (NPY) bind and activate the human Y1 receptor subtype (hY1 receptor), which is found in 90% of breast cancer tissue and in all breast-cancer-derived metastases. Herein, novel highly boron-loaded Y1 -receptor-preferring peptide analogues are described as smart shuttle systems for carbaboranes as (10) B-containing moieties. Various positions in the peptide were screened for their susceptibility to carbaborane modification, and the most promising positions were chosen to create a mu…

inorganic chemicalsStereochemistrymedia_common.quotation_subjectMolecular Sequence Datachemistry.chemical_elementPeptideBoron Neutron Capture TherapyBreast NeoplasmsBiochemistrySolid-phase synthesisDrug DiscoveryChlorocebus aethiopsAnimalsHumansNeuropeptide YAmino Acid SequenceGeneral Pharmacology Toxicology and PharmaceuticsReceptorInternalizationBoronBoranesmedia_commonPharmacologychemistry.chemical_classificationChemistryOrganic ChemistryReceptor-mediated endocytosisNeuropeptide Y receptorReceptors Neuropeptide YHEK293 CellsDrug deliveryCOS CellsMolecular MedicineFemaleChemMedChem
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ChemInform Abstract: Synthesis and anti-Staphylococcal Activity of New Halogenated Pyrroles Related to Pyrrolomycins F.

2008

The chemical synthesis of new halogenated pyrroles related to pyrrolomycins F is described and the anti-staphylococcal activity compared. The replacement of 4′-bromo atom of parent compounds with two chloro atoms at 3′ and 5′ position increase the antibacterial activity against a reference strain of S. aureus.

inorganic chemicalsStrain (chemistry)StereochemistryChemistryStructure–activity relationshipGeneral MedicineAntibacterial activityChemical synthesisPyrrole derivativesChemInform
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Impact of α,β-dehydroamino acid residues on the binding abilities of di-, tri- and tetra-peptides

2000

Insertion of a dehydroamino acid residue into a sequence of di-, tri- or tetra-peptide changed considerably the binding abilities of peptide ligands towards copper(II) ions. Potentiometric and spectroscopic (EPR, UV-VIS and CD) data have shown that the amide nitrogen of the dehydroamino acid residue is more effective in co-ordination than its parent analogue. In the case of the bulky ΔPhe residue also the (Z–E) isomerisation has a critical impact on the co-ordination equilibria in the system studied.

inorganic chemicalsbiologyStereochemistryPotentiometric titrationchemistry.chemical_elementGeneral Chemistrybiology.organism_classificationCopperCatalysislaw.inventionchemistry.chemical_compoundResidue (chemistry)chemistrylawAmideMaterials ChemistryTetraElectron paramagnetic resonanceIsomerizationPeptide ligandNew Journal of Chemistry
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CO2 Fixation by Copper(II) Complexes of a Terpyridinophane Aza Receptor

2004

CO2 is fixed by a Cu2+ complex of a macrocyclic terpyridinophane ligand forming a carbamate group. Several features of the structure mimic the enzyme rubisco.

inorganic chemicalschemistry.chemical_classificationCarbamateReaction mechanismbiologyChemistryStereochemistrymedicine.medical_treatmentfungiCarbon fixationRuBisCOfood and beverageschemistry.chemical_elementmacromolecular substancesGeneral ChemistryLigand (biochemistry)BiochemistryCopperCatalysisColloid and Surface ChemistryEnzymemedicinebiology.proteinReceptorJournal of the American Chemical Society
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A DFT study on the NHC catalysed Michael addition of enols to α,β-unsaturated acyl-azoliums. A base catalysed C–C bond-formation step

2013

The NHC catalysed nucleophilic additions of enols to α,β-unsaturated acyl-azolium intermediates have been investigated using DFT methods at the MPWB1K/6-31G** computational level. In the direct and the conjugate additions, formation of a hydrogen bond (HB) with the carboxyl oxygen is not sufficient to favour the C-C bond formation as a consequence of the low nucleophilic character of enols. Interestingly, when enols form a HB with the chloride counterion, the activation energies associated with the conjugate addition decrease as a consequence of the increased nucleophilic character of enols and the increased electrophilic character of the 'acyl-azolium + Cl' ion pair. Analysis of the DFT re…

inorganic chemicalschemistry.chemical_classificationHydrogen bondChemistryStereochemistryOrganic ChemistryBiochemistryChlorideMedicinal chemistryNucleophileElectrophileMichael reactionmedicineReactivity (chemistry)Physical and Theoretical ChemistryCounterionmedicine.drugConjugateOrg. Biomol. Chem.
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Synthese und pharmakologische Wirkung von carbocyclischen Muskarinanalogen

1974

Als carbocyclische Muskarinanaloga wurden das (3-Hydroxycyclopentylmethyl)trimethyl-ammonium-jodid und dessen Acetat dargestellt und am isolierten Ileum des Meerschweinchens untersucht. Synthesis and Pharmacological Activity of Carbocyclic Analogs of Muscarine As carbocyclic analogs of muscarine (3-hydroxycyclopentylmethyl)trimethylammonium iodide and (3-acetoxycyclopentylmethyl)trimethylammonium iodide were synthesized and tested on the isolated guinea pig ileum.

inorganic chemicalschemistry.chemical_classificationMuscarineChemistryStereochemistryIodidetechnology industry and agriculturePharmaceutical ScienceBiological activityIleumchemistry.chemical_compoundmedicine.anatomical_structureDrug Discoverymedicinelipids (amino acids peptides and proteins)Guinea pig ileumArchiv der Pharmazie
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Synthesis, characterization and antimicrobial activity of palladium(II) complexes with some alkyl derivates of thiosalicylic acids: Crystal structure…

2012

Abstract S-Alkyl (R = benzyl, methyl, ethyl, propyl and butyl) derivatives of thiosalicylic acid and the corresponding palladium(II) complexes were prepared and their structures were proposed on the basis of infrared, 1H and 13C NMR spectroscopy. The cis geometrical configurations of the isolated complexes were proposed on the basis of an X-ray structural study of the bis(S-benzyl-thiosalicylate)–palladium(II), [Pd(S-bz-thiosal)2] complex. Antimicrobial activity of the tested compounds was evaluated by determining the minimum inhibitory concentration (MIC) and minimum microbicidal concentration (MMC) in relation to 26 species of microorganisms. The tested ligands, with a few exceptions, sho…

inorganic chemicalschemistry.chemical_classificationThiosalicylic acidbiologyStereochemistrychemistry.chemical_elementCrystal structurebiology.organism_classificationAntimicrobialMedicinal chemistryAspergillus fumigatusInorganic Chemistrychemistry.chemical_compoundMinimum inhibitory concentrationchemistryMaterials ChemistryPhysical and Theoretical ChemistryAntibacterial activityta116AlkylPalladiumPolyhedron
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Enantioselective transport of amino acid through supported chiral liquid membranes

1993

Abstract Two chiral alcohols, nopol and (2S)-(−)-methyl-1-butanol, immobilized in the pores of a polyethylene film were used for the anantioselective transport of amino acid hydrochloride. The degree of stereoselectivity of the permeation process varied from 0.39 to 1.52 depending on both the type of the chiral membrane phase and the properties of the amino acid. The evaluation of the membrane ability to separate stereoisomers was performed by the step-by-step analysis by considering the effect of amino acids' hydrophobicity, polarity and degree of chirality. For the purpose of this paper, the chirality measure was introduced. It was demonstrated that the enantioselectivity was affected mai…

inorganic chemicalschemistry.chemical_classificationamino acidschiral discriminationStereochemistryHydrochlorideorganic chemicalsEnantioselective synthesisFiltration and SeparationPermeationBiochemistryAmino acidsupported liquid membraneschemistry.chemical_compoundMembranechemistryPhase (matter)Organic chemistryheterocyclic compoundsGeneral Materials ScienceStereoselectivityPhysical and Theoretical ChemistryChirality (chemistry)Journal of Membrane Science
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Crystal structure ofN-(tert-butoxycarbonyl)glycyl-(Z)-β-bromodehydroalanine methyl ester [Boc–Gly–(β-Br)(Z)ΔAla–OMe]

2014

In a de­hydro­amino acid with a C=C bond between the α- and β-C atoms, the amino acid residues are linked trans to each other and there are no strong intra­molecular hydrogen bonds. The torsion angles indicate a non-helical conformation of the mol­ecule.

inorganic chemicalscrystal structureStereochemistryeducationCrystal structurebehavioral disciplines and activitiesResearch CommunicationsSteric repulsionlcsh:Chemistrychemistry.chemical_compoundde­hydro­amino acidβ-bromo­dehydro­alaninedehydroamino acidnon-helical conformationGeneral Materials Science[beta]-bromo­dehydro­alanineAmino acid residuehealth care economics and organizationsQuantitative Biology::BiomoleculesDipeptideChemistryHydrogen bondGeneral Chemistryhydrogen bondingCondensed Matter Physicshumanitieslcsh:QD1-999β-bromodehydroalanineAlanine methyl esterActa Crystallographica Section E Structure Reports Online
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Diastereomeric control of enantioselectivity: evidence for metal cluster catalysis

2014

Enantioselective hydrogenation of tiglic acid effected by diastereomers of the general formula [(μ-H)2Ru3(μ3-S)(CO)7(μ-P–P*)] (P–P* = chiral Walphos diphosphine ligand) strongly supports catalysis by intact Ru3 clusters. A catalytic mechanism involving Ru3 clusters has been established by DFT calculations. peerReviewed

intactLigandStereochemistryMetals and AlloysEnantioselective synthesisDiastereomerTiglic acidGeneral Chemistryhydrogenation catalysisCatalysisSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsCatalysisMetalchemistry.chemical_compoundchemistryvisual_artMaterials ChemistryCeramics and Compositesvisual_art.visual_art_mediumCluster (physics)triruthenium clustersta116Chemical Communications
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