Search results for "Oxamide"

showing 10 items of 227 documents

Evaluation of Fused Pyrrolothiazole Systems as Correctors of Mutant CFTR Protein.

2021

Cystic fibrosis (CF) is a genetic disease caused by mutations that impair the function of the CFTR chloride channel. The most frequent mutation, F508del, causes misfolding and premature degradation of CFTR protein. This defect can be overcome with pharmacological agents named “correctors”. So far, at least three different classes of correctors have been identified based on the additive/synergistic effects that are obtained when compounds of different classes are combined together. The development of class 2 correctors has lagged behind that of compounds belonging to the other classes. It was shown that the efficacy of the prototypical class 2 corrector, the bithiazole corr-4a, could be impr…

Yellow fluorescent proteinProtein FoldingCystic FibrosisMutantPharmaceutical ScienceCystic Fibrosis Transmembrane Conductance RegulatorCarboxamidemedicine.disease_cause01 natural sciencesAnalytical Chemistrychemistry.chemical_compoundMutant ProteinDrug DiscoveryMoietyCFTR potentiatorCFTRchemistry.chemical_classification0303 health sciencesMutationbiologyChemistryChemistry (miscellaneous)Chloride channelMolecular MedicineHumanStereochemistrymedicine.drug_classCFTR correctorArticleF508del-CFTRlcsh:QD241-44103 medical and health scienceslcsh:Organic chemistrymedicineHumansBenzodioxolesPhysical and Theoretical ChemistryThiazoleCystic Fibrosi030304 developmental biology010405 organic chemistryOrganic ChemistryAminoimidazole Carboxamide0104 chemical sciencesThiazolesMutationbiology.proteinMutant ProteinsBenzodioxoleTricyclicMolecules (Basel, Switzerland)
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CCDC 1823433: Experimental Crystal Structure Determination

2018

Related Article: Rajendhraprasad Tatikonda, Evgeny Bulatov, Zülal Özdemir, Nonappa, Matti Haukka|2019|Soft Matter|15|442|doi:10.1039/C8SM02006J

catena-((mu-acetato)-[mu-N-(pyridin-3-yl)pyridine-4-carboxamide]-silver)Space GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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CCDC 1451174: Experimental Crystal Structure Determination

2017

Related Article: Thais Grancha, Jesús Ferrando-Soria, Joan Cano, Pedro Amoros , Beatriz Seoane, Jorge Gascon, Montse Bazaga-García, Enrique R. Losilla, Aurelio Cabeza, Donatella Armentano, Emilio Pardo|2016|Chem.Mater.|28|4608|doi:10.1021/acs.chemmater.6b01286

catena-[tris(mu-NN'-bis((S)-2-propanoato)oxamide)-(mu-aqua)-bis(mu-hydroxy)-calcium(ii)-hexa-copper(ii) hydrate]Space GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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Anticancer study of heterobimetallic platinum(II)-ruthenium(II) and platinum(II)-rhodium(III) complexes with bridging dithiooxamide ligand

2019

Abstract Three heterobimetallic platinum (II)/ruthenium (II) and platinum (II)/rhodium (III) complexes, A: Pt{S–S2C2(NR)2H}{μ-S2C2(NR)2}-[Ru (p-cymene)Cl], R = isoamyl; B: Pt{S–S2C2(NR)2H}{μ-S2C2(NR)2}[Rh (phpy)2], R = isoamyl; C: [Pt{S–S2C2(NR)2H}{μ-S2C2(NR)2}-[Rh(C5Me5)Cl]], R = benzyl, were prepared from mononuclear complexes 1 and 2, 1: [Pt (H-isoamyl2DTO)2]; 2: [Pt (H-benzyl2DTO)2], DTO = dithiooxamide, by reaction of 1 or 2 with the corresponding chlorido-bridged dimers, [Rh(C5Me5)Cl (μ-Cl)]2, [Ru (p-cymene)Cl (μ-Cl)]2 or [Rh (phpy)2 (μ-Cl)]2, and then evaluated as anticancer agents for the inhibition of the three proteolytic activities of human 20S proteasome, one of the main target …

chemistry.chemical_classification010405 organic chemistryChemistryOrganic Chemistrychemistry.chemical_element010402 general chemistrymedicine.disease01 natural sciencesBiochemistryMedicinal chemistry0104 chemical sciencesRhodiumRutheniumAnticancer; Dithiooxamide; Heterobimetallic; Platinum complexes; Rhodium; RutheniumInorganic Chemistrychemistry.chemical_compoundEnzymeDithiooxamideApoptosisNeuroblastomaMaterials ChemistrymedicinePhysical and Theoretical ChemistryPlatinumCytotoxicityJournal of Organometallic Chemistry
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N-[3-(5-Oxo-10,11-dihydro-5H-dibenzo[a,d]cyclohepten-2-ylamino)phenyl]furan-3-carboxamide

2010

In the title compound, C26H20N2O3, the two aromatic rings of the tricyclic unit are oriented at a dihedral angle of 54.53 (9)°. The crystal structure displays intermolecular N—H...O hydrogen bonding.

chemistry.chemical_classificationChemistrymedicine.drug_classHydrogen bondCarboxamideAromaticityGeneral ChemistryCrystal structureDihedral angleCondensed Matter PhysicsBioinformaticsMedicinal chemistryOrganic Paperslcsh:Chemistrychemistry.chemical_compoundlcsh:QD1-999FuranmedicineGeneral Materials ScienceTricyclicActa Crystallographica Section E
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Reaktionen bei der Bestrahlung von poly(N-chloramid)en

1980

On irradiating poly(N-chloroamide)s in films or in solution in the range of 325–375 nm carboxamide groups are formed. The irradiated polymer contains chlorine which is linked to C-atoms. This reaction can certainly not be explained with an intramolecular photorearrangement but with a sequence of photoreactions and dark reactions satisfactorily accounting for all observations.

chemistry.chemical_classificationChemistrymedicine.drug_classIntramolecular forcePolymer chemistrymedicineChlorinechemistry.chemical_elementCarboxamidePolymerIrradiationDie Makromolekulare Chemie
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Development of competitive enzyme-linked immunosorbent assays for boscalid determination in fruit juices

2012

Abstract Boscalid is a modern, broad-spectrum carboxamide pesticide highly efficient against most fungal diseases affecting valuable crops. In this study, a boscalid-mimicking derivative with a six-carbon spacer arm replacing the chlorine atom at the pyridine ring of the target molecule was synthesized and coupled to carrier proteins. Following rabbit immunization, antibodies against this agrochemical were obtained for the first time, and they were characterised in terms of affinity and specificity, tolerance to solvents, and robustness to changes in buffer pH and ionic strength, using two assay formats. Both of the optimised immunoassays showed limits of detection below 0.1 μg/L. Moreover,…

chemistry.chemical_classificationDetection limitChromatographymedicine.diagnostic_testPesticide residuemedicine.drug_classCarboxamideGeneral MedicinePesticideAnalytical ChemistryEnzymechemistryIonic strengthImmunoassaymedicineHaptenFood ScienceFood Chemistry
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First Electrophilic Substitutions of 3-Substituted Indoles with Diethoxycarbenium Tetrafluoroborate: Functionalized Indole Derivatives

1990

The indoles 2a-2c react with diethoxycarbenium tetrafluoroborate (1) to furnish the indolecarbaldehydes 3a-3d. In the thermodynamically controlled reaction of 3-methylindole (2a) with 1 the tris(indolyl)methane 4 and diskatole (5), are formed in addition. The limitations of these reactions are discussed and evidence is presented for a C-3-ipso-attack and a Wagner-Meerwein rearrangement, respectively, leading to the formation of 3b or 3d. Erste elektrophile Substitution von 3-substituierten Indolen mit Diethoxycarbenium-Tetrafluoroborat: Funktionalisierte Indol-Derivate Die Indole 2a-2c reagieren mit dem per se synthetisierten Diethoxycarbenium-Tetrafluoroborat (1) zu den Indolcarbaldehyden …

chemistry.chemical_classificationIndole testWagner–Meerwein rearrangementTetrafluoroborateBicyclic moleculeChemistrymedicine.drug_classStereochemistryPharmaceutical ScienceCarboxamideAldehydechemistry.chemical_compoundElectrophilic substitutionDrug DiscoveryElectrophilemedicineArchiv der Pharmazie
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Chemistry with Roataxanes: Intra- and Intermolecularly Covalently Linked Rotaxanes

2006

The direct introduction of sulfonamide units (cf. 9) into carboxamide-based rotaxanes allows us to intramolecularly bridge the “wheel” and the “axle” of such species for the first time as is shown by the bridged bissulfonamide rotaxane 11. Due to its stronger acidity the SO2-NH proton can be selectively abstracted by mild bases even in the presence of CO.NH and then be substituted by treatment with suitable iodo compounds. This leads intramolecularly to 11 (71% yield) and intermolecularly to bis[2]rotaxane 16 (76% yield). The iodo-substituted rotaxane 15 isolated as a remarkably stable byproduct offers a new synthetic potential demonstrated by the preparation of 16.

chemistry.chemical_classificationRotaxaneStereochemistryChemistrymedicine.drug_classOrganic ChemistryCarboxamideGeneral ChemistrySulfonamideCovalent bondYield (chemistry)Polymer chemistrymedicinePhysical and Theoretical ChemistryLiebigs Annalen
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H2-Antihistaminika, 33. Mitt. Synthese und H2-antagonistische Aktivität heteroaromatischer (Thio)Carboxamide und Triazol(thi)on-Derivate des Piperidi…

1987

Die Zyklisierung der (Thio)Semicarbazide la, b mit N-Cyan-diphenylimidocarbonat, N-Cyan-dimethyldithioimidocarbonat, Aminocrotonsaurenitril und Acetessigester gibt die heteroaromatischen (Thio)Carboxamide 5a, b und 7–9. Beim Einwirken von NaOH auf die (Thio)Biharnstoffe 12 und 13 sowie die (Oxa)Thiadiazoldiamine 19 und 20 werden die Triazol(thi)one 15 und 17 erhalten. Am Vorhof des Meerschweinchens zeigen 5a, 7 und 8 eine mit Cimetidin vergleichbare Histamin-H2-antagonistische Wirkung. H2-Antihistaminics, XXXIII: Synthesis and H2-Antagonistic Activity of Heteroaromatic (Thio)Carboxamides and Triazole(thi)one-Derivatives of Piperidinomethylphenoxypropylamine The (thio)semicarbazides la, b ar…

chemistry.chemical_classificationSemicarbazideSemicarbazidesStereochemistrymedicine.drug_classTriazolePharmaceutical ScienceThio-Carboxamidechemistry.chemical_compoundchemistryEthyl acetoacetateDrug DiscoverymedicineAliphatic compoundThioamideArchiv der Pharmazie
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