Search results for " AMINO"

showing 10 items of 789 documents

Memantine does not block antiaggressive effects of morphine in mice.

2002

The action of the noncompetitive N-methyl-D-aspartate (NMDA) receptor blocker memantine (5, 10, 20 and 40 mg/kg) was evaluated during social encounters in mice. Although a dose-dependent increase in locomotion was observed, only with the highest dose did it reach statistical significance. Aggressive behavior was decreased with 20 and 40 mg/kg of memantine, social contacts being increased only with 20 mg/kg. Subsequently, the effect of these memantine doses on the antiaggressive actions of morphine (10 mg/kg) was evaluated. None of the doses affected the antiaggressive action of morphine. As memantine administration produced an antiaggressive effect only at doses that affected locomotion, it…

PharmacologyMaleNarcoticsMorphinebusiness.industryMemantinePharmacologyReceptors N-Methyl-D-AspartateAggressionPsychiatry and Mental healthGlutamatergicMiceMemantineAdaptation PsychologicalMorphineMedicineNMDA receptorAnimalsbusinessExcitatory Amino Acid Antagonistsmedicine.drugBehavioural pharmacology
researchProduct

A phosphonamidate containing aromatic N-terminal amino group as inhibitor of leucine aminopeptidase-design, synthesis and stability.

2006

Fully deprotected phosphonamidate dipeptides, predicted as effective inhibitors of cytosolic leucine aminopeptidase, showed unexpected instability in water solution at pH below 12. Their hydrolysis rate was strictly correlated with basicity of the N-terminal amino group. To improve this feature a phosphonamidate analogue containing less basic, aromatic 2-aminophenylphosphonate residue in P1 position of the inhibitor was designed. The target compound was synthesised starting from diethyl 2-nitrophosphonate in several step procedure. The decrease in basicity of the terminal amino moiety of the modified analogue in fact resulted in satisfactory improvement of hydrolytic stability of the P–N bo…

PharmacologyModels MolecularMagnetic Resonance SpectroscopyChemistryStereochemistryphosphonamidateLAP inhibitorsOrganic ChemistryGeneral MedicineAminopeptidaseChemical synthesisResidue (chemistry)HydrolysisLeucyl AminopeptidaseOrganophosphorus CompoundsDrug StabilityDrug DesignDrug Discoveryhydrolytic stabilityMoietyChemical stabilityProtease InhibitorsLeucineLeucyl aminopeptidaseEuropean journal of medicinal chemistry
researchProduct

Phenylalanine Hydroxylase Participation in the Synthesis of Serotonin and Pteridines in Drosophila melanogaster

1997

Abstract Phenylalanine hydroxylase is involved in the synthesis of serotonin and pteridines, probably catalysing the hydroxylation of tryptophan and a tetrahydropterin oxidase reaction, respectively. Supplementation of the wild-type Drosophila diet with either L-Phe or L-Trp induced a significant increase in the phenylalanine hydroxylase concentration, while L-Tyr supplementation had no effect. The level of serotonin in adult heads of the PAH-defective mutant Henna recessive-3 was significantly lower than that obtained for the wild-type strain. A 4-fold increase in the concentration of phenylalanine hydroxylase is observed during the pharate adult head development. It occurs in parallel wit…

PharmacologyPhenylalanine hydroxylasebiologyTyrosine hydroxylaseImmunologyTryptophanTryptophan hydroxylaseHydroxylationchemistry.chemical_compoundchemistryBiochemistrybiology.proteinAromatic amino acidsSerotonin5-HydroxytryptophanComparative Biochemistry and Physiology Part C: Pharmacology, Toxicology and Endocrinology
researchProduct

Der Einflu� von Adrenalektomie und Nebennierenrindenhormonen auf die renalen Clearancen von Inulin, p-Aminohippurat, echtem endogenen Kreatinin und H…

1959

Pharmacologymedicine.medical_specialtyPara aminohippurateAdrenal cortex hormonesAdrenalectomymedicine.medical_treatmentInulinRenal functionEndogenyGeneral Medicinechemistry.chemical_compoundEndocrinologychemistryInternal medicinemedicineCreatinine ureaClearanceNaunyn-Schmiedebergs Archiv f�r Experimentelle Pathologie und Pharmakologie
researchProduct

Structure of the phenylalanine hydroxylase gene in Drosophila melanogaster and evidence of alternative promoter usage.

1996

The complete Drosophila melanogaster phenylalanine hydroxylase gene isolated from a genomic library was sequenced. Gene structure consisted of five exons covering a region of around 3 kb. Position of introns in the C-terminal domain was conserved with mammalian aromatic amino acid hydroxylase genes. Putative promoter sequences in the 5'UTR and intron 1 were identified. A novel transcript was detected differing from that previously reported by the inclusion of a part of the intron 1 sequence. It could be produced using an alternative promoter. The deduced open reading frame would code a protein with a small difference at the N-terminus. Expression of the alternative transcripts was examined …

Phenylalanine hydroxylaseTranscription GeneticMolecular Sequence DataBiophysicsGenes InsectBiochemistryPolymerase Chain ReactionExonchemistry.chemical_compoundAromatic amino acidsAnimalsGenomic libraryAmino Acid SequenceRNA MessengerPromoter Regions GeneticMolecular BiologyGeneDNA PrimersGeneticsGenomic LibrarybiologyBase SequenceIntronPhenylalanine HydroxylaseCell BiologyExonsbiology.organism_classificationMolecular biologyIntronsOpen reading frameDrosophila melanogasterchemistrybiology.proteinDrosophila melanogasterBiochemical and biophysical research communications
researchProduct

Regulation of pteridine biosynthesis and aromatic amino acid hydroxylation in Drosophila melanogaster

1989

The relationship between high dietary levels of aromatic amino acid and regulation of pteridines in Drosophila eyes was examined by measuring changes in pool levels of six pterins in the wild type and mutants and amino acid pool levels in flies that carry mutations for pteridine biosynthesis. The effect upon relative viability and developmental times was also analyzed; relative viability was affected by L-phenylalanine, L-tryptophan, and L-tyrosine in decreasing order and the D-amino acids had little or no effect. The changes in concentration of biopterin, dihydrobiopterin, pterin, sepiapterin, drosopterins, and isoxanthopterin showed a characteristic pattern of increased and/or decreased a…

PhenylalanineBiopterinPhenylalanineBiologyHydroxylationBiochemistrychemistry.chemical_compoundDihydrobiopterinGeneticsmedicineAromatic amino acidsAnimalsAmino AcidsPterinMolecular BiologyEcology Evolution Behavior and Systematicschemistry.chemical_classificationPteridinesTryptophanGeneral MedicineTetrahydrobiopterinAmino acidDrosophila melanogasterchemistryBiochemistryMutationTyrosinePteridinemedicine.drug
researchProduct

A structural insight into the P1 S1 binding mode of diaminoethylphosphonic and phosphinic acids, selective inhibitors of alanine aminopeptidases

2016

Abstract N′-substituted 1,2-diaminoethylphosphonic acids and 1,2-diaminoethylphosphinic dipeptides were explored to unveil the structural context of the unexpected selectivity of these inhibitors of M1 alanine aminopeptidases (APNs) versus M17 leucine aminopeptidase (LAP). The diaminophosphonic acids were obtained via aziridines in an improved synthetic procedure that was further expanded for the phosphinic pseudodipeptide system. The inhibitory activity, measured for three M1 and one M17 metalloaminopeptidases of different sources (bacterial, human and porcine), revealed several potent compounds (e.g., K i  = 65 nM of 1u for Hs APN). Two structures of an M1 representative (APN from Neisser…

Phosphorous AcidsSwineStereochemistryNeisseria meningitidisCD13 AntigensCrystallography X-RayLigands010402 general chemistry01 natural sciencesAminopeptidaseArticleAminopeptidase NPhosphonic and phosphinic acidsLeucyl AminopeptidaseStructure-Activity RelationshipS1 binding modeDrug DiscoveryAnimalsHumansProtease InhibitorsPharmacologyAlanineBinding Sitesbiology010405 organic chemistryChemistryAminopeptidase NOrganic ChemistryActive siteStructural contextAPN-inhibitor complex structuresDipeptidesGeneral MedicinePhosphinic Acids0104 chemical sciencesMetalloaminopeptidasesPhosphinic Acidsbiology.proteinLeucineSelectivityEuropean Journal of Medicinal Chemistry
researchProduct

F-type lectin from serum of the Antarctic teleost fish Trematomus bernacchii (Boulenger, 1902): Purification, structural characterization, and bacter…

2021

Abstract The increasing availability of sequenced genomes has enabled a deeper understanding of the complexity of fish lectin repertoires involved in early development and immune recognition. The teleost fucose-type lectin (FTL) family includes proteins that preferentially bind fucose and display tandemly arrayed carbohydrate-recognition domains (CRDs) or are found in mosaic combinations with other domains. They function as opsonins, promoting phagocytosis and the clearance of microbial pathogens. The Antarctic fish Trematomus bernacchii is a Perciforme living at extremely low temperatures (−1.68 °C) which is considered a model for studying adaptability to the variability of environmental w…

PhysiologyAntarctic fishLectins F-type lectin Antarctic fish Trematomus bernacchii Bacterial agglutinationAntarctic RegionsTrematomus bernacchiiBiochemistryAntarctic fish; Bacterial agglutination; F-type lectin; Lectins; Trematomus bernacchii; Amino Acid Sequence; Animals; Antarctic Regions; Bacteria; Base Sequence; Fucose; Lectins; Perciformes; PhylogenyFucose03 medical and health scienceschemistry.chemical_compound0302 clinical medicineAffinity chromatographyWestern blotLectinsTrematomusmedicineAnimalsAmino Acid SequenceSea bassPerciformeMolecular BiologyOpsoninPhylogeny030304 developmental biologyFucoseAntarctic Region0303 health sciencesbiologyMolecular massmedicine.diagnostic_testBacteriaBase SequenceAnimalLectinBacterial agglutinationbiology.organism_classificationPerciformesBiochemistrychemistrybiology.proteinLectinF-type lectin030215 immunologyComparative biochemistry and physiology. Part B, Biochemistrymolecular biology
researchProduct

Review: How was metazoan threshold crossed? The hypothetical Urmetazoa.

2001

The origin of Metazoa remained — until recently — the most enigmatic of all phylogenetic problems. Sponges [Porifera] as ‘living fossils’, positioned at the base of multicellular animals, have been used to answer basic questions in metazoan evolution by molecular biological techniques. During the last few years, cDNAs/genes coding for informative proteins have been isolated and characterized from sponges, especially from the marine demosponges Suberites domuncula and Geodia cydonium. The analyses of their deduced amino acid sequences allowed a molecular biological resolution of the monophyly of Metazoa. Molecules of the extracellular matrix/basal lamina, with the integrin receptor, fibronec…

PhysiologyMolecular Sequence DataBiochemistryReceptor tyrosine kinaseMyotrophinMorphogenesisAnimalsAmino Acid SequenceeducationMolecular BiologyGeneGalectineducation.field_of_studybiologySequence Homology Amino AcidCell adhesion moleculebiology.organism_classificationBiological EvolutionInvertebratesCell biologyPoriferaSuberites domunculaIntracellular signal transductionGerm Cellsbiology.proteinSignal transductionCell Adhesion MoleculesSignal TransductionComparative biochemistry and physiology. Part A, Molecularintegrative physiology
researchProduct

Thermostability of Two Cyanobacterial GrpE Thermosensors

2011

GrpE proteins act as co-chaperones for DnaK heat-shock proteins. The dimeric protein unfolds under heat stress conditions, which results in impaired interaction with a DnaK protein. Since interaction of GrpE with DnaK is crucial for the DnaK chaperone activity, GrpE proteins act as a thermosensor in bacteria. Here we have analyzed the thermostability and function of two GrpE homologs of the mesophilic cyanobacterium Synechocystis sp. PCC 6803 and of the thermophilic cyanobacterium Thermosynechococcus elongatus BP1. While in Synechocystis an N-terminal helix pair of the GrpE dimer appears to be the thermosensing domain and mainly mediates GrpE dimerization, the C-terminal four-helix bundle i…

PhysiologyMolecular Sequence DataProtein domainPlant SciencePlasma protein bindingCyanobacteriaProtein structureBacterial ProteinsHeat shock proteinEscherichia coliAmino Acid SequencePeptide sequenceHeat-Shock ProteinsThermostabilitySequence Homology Amino AcidbiologyProtein StabilityChemistryCircular DichroismGenetic Complementation TestSynechocystisSynechocystisTemperatureCell BiologyGeneral Medicinebiology.organism_classificationProtein Structure TertiaryCross-Linking ReagentsChaperone (protein)Biophysicsbiology.proteinbacteriaProtein MultimerizationProtein BindingPlant and Cell Physiology
researchProduct