Search results for "Cyclic compound"

showing 10 items of 819 documents

In vitro activity of scorpiand-like azamacrocycle derivatives in promastigotes and intracellular amastigotes of Leishmania infantum and Leishmania br…

2012

The activity of a family scorpiand-like azamacrocycles against Leishmania infantum and Leishmania braziliensis was studied using promastigotes, axenic and intracellular amastigotes forms. All the compounds are more active and less toxic than meglumine antimoniate (Glucantime). Moreover, the data on infection rates and amastigotes showed that compounds P2Py, PN and P3Py are the most active against both species of Leishmania. On the other hand, studies on the inhibitory effect of these compounds on SOD enzymes showed that while the inhibition of the Fe-SOD enzyme of the promastigote forms of the parasites is remarkable, the inhibition of human CuZn-SOD and Mn-SOD from Escherichia coli is negl…

Macrocyclic CompoundsMeglumine antimoniateAntiprotozoal AgentsLeishmania braziliensisMicrobiologyStructure-Activity RelationshipParasitic Sensitivity TestsDrug DiscoverymedicineLeishmania infantumAmastigoteAxenicPharmacologychemistry.chemical_classificationAza CompoundsbiologyDose-Response Relationship DrugMolecular StructureOrganic ChemistryGeneral MedicineLeishmaniabiology.organism_classificationLeishmania braziliensisEnzymechemistryLeishmania infantumIntracellularmedicine.drugEuropean journal of medicinal chemistry
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Synthesis and coordination properties of an azamacrocyclic Zn(II) chemosensor containing pendent methylnaphthyl groups

2008

The synthesis of a polyazamacrocycle constituted by two diethylenetriamine bridges functionalized at their central nitrogen with naphth-2-ylmethyl units and interconnected through 2,6-dimethylpyridine spacers (L1) is reported. The protonation behaviour of the new macrocycle in water and in water-ethanol 70/30 v/v mixed solvent has been examined by means of pH-metric, UV-Vis and steady-state fluorescence techniques. The fluorescence emission is slightly quenched following the deprotonation of the central tertiary amines and more deeply quenched upon deprotonation of the secondary amino groups. pH-Metric titrations show that in water-ethanol 70/30 v/v L1 forms stable mononuclear complexes wit…

Macrocyclic CompoundsMetal ions in aqueous solutionProtonationNaphthalenesLigandsPhotochemistryChemistry Techniques AnalyticalFluorescenceDivalentInorganic Chemistrychemistry.chemical_compoundDeprotonationOrganometallic CompoundsTransition ElementsQualitative inorganic analysischemistry.chemical_classificationAza CompoundsTemperatureHydrogen-Ion ConcentrationPhotochemical ProcessesFluorescenceZincCrystallographychemistryDiethylenetriamineTitrationProtonsDalton Transactions
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Zn(II)-coordination and fluorescence studies of a new polyazamacrocycle incorporating 1H-pyrazole and naphthalene units.

2010

The synthesis and Zn(2+) coordination properties of a new macrocycle (L1) obtained by dipodal (2 + 2) condensation of the polyamine 3-(naphthalen-2-ylmethyl)pentane-1,5-diamine with 1H-pyrazole-3,5-dicarbaldehyde are reported. pH-metric studies show that L1 bears five measurable protonation steps in the 2.0-11.0 pH range. Fluorescence emission studies indicate that the removal of the first proton from the H(5)L1(5+) species leads to a significant decrease in the emission due to a photoinduced electron transfer process. Addition of Zn(2+) promotes a boat-like conformation that approaches both fluorophores and facilitates the formation of an excimer which reaches its highest emission for a 1 …

Macrocyclic CompoundsMolecular ConformationProtonationPyrazoleNaphthalenesPhotochemistryExcimerPhotoinduced electron transferFluorescenceInorganic Chemistrychemistry.chemical_compoundOrganometallic CompoundsPolyaminesMoietyFluorescent DyesMolecular StructureChemistryHydrogen bondHydrogen BondingElectrochemical TechniquesHydrogen-Ion ConcentrationFluorescenceZincPyrazolesDensity functional theoryProtonsCopperDalton transactions (Cambridge, England : 2003)
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Total synthesis of two potent anti-inflammatory macrolactones of the oxacyclododecindione type

2015

An esterification/Friedel-Crafts-cyclization approach permitted the first successful synthetic entry into the oxacyclododecindione subclass of the dihydroxyphenylacetic acid lactone-type natural products. This route allowed the preparation of two highly active anti-inflammatory fungal secondary metabolites 14-deoxyoxacyclododecindione and 14-deoxy-4-dechlorooxacyclododecindione as well as their 14-desmethyl analogues.

Macrocyclic CompoundsMolecular StructureChemistrymedicine.drug_classDihydroxyphenylacetic acidStereochemistryAnti-Inflammatory Agents Non-SteroidalOrganic ChemistryTotal synthesisBiochemistrySubclassAnti-inflammatoryLactonesBiochemistryCyclizationmedicineOxacyclododecindionePhysical and Theoretical ChemistryOrganic & Biomolecular Chemistry
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Total synthesis and biological evaluation of seven new anti-inflammatory oxacyclododecindione-type macrolactones

2020

Through variation of our previously published total synthesis of two highly active anti-inflammatory macrolactones from the oxacyclododecindione family (J. Tauber, M. Rohr, T. Walter, G. Erkel and T. Opatz, Org. Biomol. Chem., 2015, 13, 7813-7821), seven new representatives of this compound class were prepared. Substitution of the 14-hydroxy group in oxacyclododecindione with a methyl substituent provided a readily accessible non-natural analogue which has similar pharmacological properties to the scarcely available natural product. Since the producible amount of substance is therefore no longer restricted by low fermentation yields, extensive in vivo studies become possible for the first t…

Macrocyclic CompoundsNatural productStereochemistryOrganic ChemistrySubstituentTotal synthesisBiochemistrychemistry.chemical_compoundchemistryIn vivoSide chainBioassayFermentationPhysical and Theoretical ChemistryIC50Organic & Biomolecular Chemistry
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Bifunctional Gallium-68 Chelators: Past, Present, and Future

2016

This article reviews the development of bifunctional chelates for synthesising (68)Ga radiopharmaceuticals. It structures the chelates into groups of macrocycles, nonmacrocycles, and chimeric derivatives. The most relevant bifunctional chelates are discussed in chelate structure, parameters of (68)Ga-labeling, and stability of the (68)Ga-chelate complexes. Furthermore those derivatives are included, where (67)Ga was applied instead of (68)Ga. A particular feature discussed is the ability of certain bifunctional chelate structures to function in kit-type preparation of the (68)Ga radiopharmaceuticals. Currently, nonmacrocyclic and chimeric derivates attract particular attention such as THP-d…

Macrocyclic CompoundsRadiochemistry010405 organic chemistrybusiness.industrychemistry.chemical_elementGallium Radioisotopes010402 general chemistry01 natural sciencesCombinatorial chemistry0104 chemical scienceschemistry.chemical_compoundchemistryBifunctional chelateMedicineRadiology Nuclear Medicine and imagingChelationGalliumbusinessBifunctionalChelating AgentsSeminars in Nuclear Medicine
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MK801 blocks hypoxic blood-brain-barrier disruption and leukocyte adhesion.

2008

The aim of the present study was to examine the signaling pathways of hypoxia followed by reoxygenation (H/R)-induced disruption of the blood-brain-barrier (BBB) in a co-culture of astrocytes and brain endothelial cells (BEC) in vitro. We analyzed the possible stabilizing effect of MK801, a highly selective N-methyl-d-aspartate receptor (NMDAR) antagonist, on BBB integrity. Levels of reactive oxygen species (ROS), glutamate (Glut) release and monocyte adhesion were measured under normoxia and H/R. BBB integrity was monitored measuring the trans-endothelial electrical resistance (TEER). TEER values dropped under H/R conditions which was abolished by MK801. Glut release from astrocytes, but n…

Macrocyclic CompoundsSwineGlutamic AcidBiologyBlood–brain barrierchemistry.chemical_compoundmedicineExtracellularCell AdhesionElectric ImpedanceLeukocytesAnimalsEnzyme InhibitorsOxazolesCells Culturedchemistry.chemical_classificationReactive oxygen speciesRyanodine receptorRyanodineGeneral NeuroscienceEndoplasmic reticulumGlutamate receptorAcetophenonesBrainEndothelial CellsCell HypoxiaCoculture TechniquesCell biologyOxygenmedicine.anatomical_structurechemistryBlood-Brain BarrierAstrocytesApocyninCalciumNAD+ kinaseDizocilpine MaleateReactive Oxygen SpeciesExcitatory Amino Acid AntagonistsNeuroscience letters
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4-Dechloro-14-deoxy-oxacyclododecindione and 14-deoxy-oxacylododecindione, two inhibitors of inducible connective tissue growth factor expression fro…

2015

Connective tissue growth factor (CTGF/CCN2), a member of the CCN superfamily of secreted cysteine-rich glycoproteins, is a central mediator of tissue remodeling and fibrosis. CTGF is suggested to be an important down-stream effector of transforming growth factor-beta (TGF-β) signaling and has therefore reached considerable pathophysiological relevance because of its involvement in the pathogenesis of fibrotic diseases, atherosclerosis, skin scarring, and other conditions with excess production of connective tissue. In a search for inhibitors of inducible CTGF expression from fungi, two new macrocyclic lactones, namely 4-dechloro-14-deoxy-oxacyclododecindione (1) and 14-deoxy-oxacylododecind…

Macrocyclic Compoundsmedicine.medical_treatmentClinical BiochemistryPharmaceutical ScienceConnective tissueBiochemistryAscomycotaFibrosisDrug DiscoverymedicineHumansMolecular BiologyTube formationintegumentary systemEffectorChemistryGrowth factorOrganic ChemistryConnective Tissue Growth FactorHep G2 CellsTransfectionmedicine.diseaseMolecular biologyCTGFmedicine.anatomical_structureBiochemistryMolecular MedicineTransforming growth factorBioorganic & Medicinal Chemistry
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Synthesis of Lamellarin U and Lamellarin G Trimethyl Ether by Alkylation of a Deprotonated α-Aminonitrile

2008

1,2,3,4-Tetrahydroisoquinoline-1-carbonitriles can serve as starting materials for the one-pot synthesis of 5,6-dihydropyrrolo[2,1 a]isoquinolines and 1-benzyl-3,4-dihydroisoquinolines. The latter compounds were transformed to lamellarin G trimethyl ether and lamellarin U in short reaction sequences. This method allows the introduction of acid-sensitive protecting groups for the phenolic hydroxy functions which would be cleaved under the harsh conditions of the classical Bischler-Napieralski reaction.

Magnetic Resonance SpectroscopyAlkylationSpectrophotometry InfraredNitrileStereochemistryOrganic ChemistryEtherNuclear magnetic resonance spectroscopyAlkylationIsoquinolinesHeterocyclic Compounds 4 or More RingsChemical synthesisMass Spectrometrychemistry.chemical_compoundDeprotonationchemistryCoumarinsNitrilesProtecting groupBischler–Napieralski reactionThe Journal of Organic Chemistry
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Circumdatin H, a new inhibitor of mitochondrial NADH oxidase, from Aspergillus ochraceus

2005

Circumdatin H (1), a new alkaloid from the culture broth of Aspergillus ochraceus, has been isolated, together with a known circumdatin, circumdatin E (2) and other known compounds: flavacol (3) and stephacidin A (4). The structure of 1 was established on the basis of chemical and spectral evidence. All of these alkaloids showed biological activity as inhibitors of the mammalian mitochondrial respiratory chain.

Magnetic Resonance SpectroscopyChemical PhenomenaSpectrophotometry InfraredStereochemistryCircumdatin HMass SpectrometryElectron Transportchemistry.chemical_compoundMultienzyme ComplexesDrug Discoveryheterocyclic compoundsNADH NADPH OxidoreductasesEnzyme InhibitorsPharmacologyAspergillus ochraceusBenzodiazepinonesbiologyChemistry PhysicalAlkaloidStephacidinBiological activityGeneral Medicinebiology.organism_classificationMitochondriaCircumdatin EMitochondrial respiratory chainchemistryBiochemistryFermentationNADH oxidaseSpectrophotometry UltravioletAspergillus ochraceus
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