Search results for "sulfonamide"

showing 10 items of 258 documents

Copper(II) complexes with sulfonamides derived from 2-picolylamine and their use as chemical nucleases

2006

Reaction between 2-picolylamine (2-aminomethylpyridine) with 2-mesitylenesulfonyl and 4- tert -butylbenzene sulfonyl chlorides leads to the formation of 2,4,6-trimethyl- N -[pyridin-2-ilmethyl]benzenesulfonamide (Hpmesa) and 4-ter-butyl- N -[pyridin-2-ilmethyl]benzenesulfonamide (Hptbsa). These compounds react with Cu(II) salts to yield coordination compounds with CuL 2 stoichiometry. The immediate environment of the metal ion is a highly distorted tetrahedron, the sulfonamide ligands acting in a bidentate fashion. Compound Hpmesa crystallizes in monoclinic space group P 2 1 /c (number 14), with Z  = 4; complex [Cu(pmesa) 2 ] crystallizes in monoclinic space group P 1 ¯ (number 2), with Z  …

chemistry.chemical_classificationSulfonylDenticityStereochemistryCoordination complexSulfonamidelaw.inventionInorganic ChemistryCrystallographychemistryUnpaired electronlawMaterials ChemistrySinglet statePhysical and Theoretical ChemistryElectron paramagnetic resonanceMonoclinic crystal systemInorganica Chimica Acta
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N-p-Amino- and N-p-nitro-phenylsulfonyl derivatives of dipeptides, a new family of ligands for copper(II). Potentiometric and spectroscopic studies

1995

The co-ordination ability of four dipeptide analogues substituted on the N-terminal amino group with p-nitrophenylsulfonyl (nps-Ala-Ala and nps-Ala-His) and p-aminophenylsulfonyl (aps-Ala-Ala and aps-Ala-His) groups was studied by potentiometric and spectroscopic (UV/VIS absorption, CD and EPR) techniques. The N-terminal sulfonyl substituent drastically changes the acidity of the sulfonamide proton making nitrogen very efficient in binding to CuII. The sulfonamide nitrogen having pK between 9 and 11 does not need any anchoring binding group to form complexes with CuII. The para substituent on the phenyl ring (amino or nitro) influences very strongly the acidity of the sulfonamide proton. Th…

chemistry.chemical_classificationSulfonylDipeptideChemistryStereochemistryPotentiometric titrationSubstituentGeneral Chemistrylaw.inventionSulfonamidechemistry.chemical_compoundMonomerlawNitroElectron paramagnetic resonanceDalton Transactions
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Carbonic anhydrase inhibitors

1999

Reaction of 20 aromatic/heterocyclic sulfonamides containing a free amino, imino, hydrazino or hydroxyl group, with 8-quinoline-sulfonyl chloride afforded a series of water-soluble (as hydrochloride or triflate salts) compounds. The new derivatives were assayed as inhibitors of the zinc enzyme carbonic anhydrase (CA), and more precisely of three of its isozymes, CA I, II (cytosolic forms) and IV (membrane-bound form), involved in important physiological processes. Efficient inhibition was observed against all three isozymes, but especially against CA II (in nanomolar range), which is the isozyme known to play a critical role in aqueous humor secretion within the ciliary processes of the eye…

chemistry.chemical_classificationSulfonylbiologyChemistryHydrochlorideOrganic ChemistryClinical BiochemistryQuinolinePharmaceutical ScienceBiochemistryMedicinal chemistrySulfonamidechemistry.chemical_compoundDorzolamideEnzyme inhibitorCarbonic anhydraseDrug Discoverybiology.proteinmedicineMolecular MedicineMoietyOrganic chemistryMolecular Biologymedicine.drugBioorganic & Medicinal Chemistry
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A novel and selective fluoride opening of aziridines by XtalFluor-E. synthesis of fluorinated diamino acid derivatives.

2015

The selective introduction of fluorine onto the skeleton of an aminocyclopentane or cyclohexane carboxylate has been developed through a novel and efficient fluoride opening of an activated aziridine ring with XtalFluor-E. The reaction proceeded through a stereoselective aziridination of the olefinic bond of a bicyclic lactam and regioselective aziridine ring opening with difluorosulfiliminium tetrafluoroborate with the neighboring group assistance of the sulfonamide moiety to yield fluorinated diamino acid derivatives. The method based on the selective aziridine opening by fluoride has been generalized to afford access to mono- or bicyclic fluorinated substances.

chemistry.chemical_classificationTetrafluoroborateBicyclic moleculesynthesisOrganic ChemistryRegioselectivitycarboxylatesAziridineBiochemistryMedicinal chemistrySulfonamidechemistry.chemical_compoundchemistryaziridinesfluorineLactamMoietyOrganic chemistryPhysical and Theoretical ChemistryFluorideta116Organic letters
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Mit Donorzentren versehener korbförmiger Molekülhohlraum — Darstellung, Struktur, Eigenschaften

1991

Basket-shaped Molecular Cavity-Containing Donor Centres — Synthesis, Structure, Properties The macrocyclic basket-shaped molecule 2, composed of three 4-donor-substituted pyridine units, is synthesized by cyclisation of the chloromethyl compound 7 with sulfonamide 8. The X-ray structure analysis of 2 gives an impression of the shape of the molecular basket. Furthermore it demonstrates that the toluenesulfonamide residues interlink, creating dimeric units of 2 in the crystal.

chemistry.chemical_classificationanimal structuresStructure analysisChemistryStereochemistryEtherCrystal structureCondensation reactionSulfonamidebody regionsInorganic Chemistrychemistry.chemical_compoundnervous systemembryonic structuresX-ray crystallographyPyridineMoleculeChemische Berichte
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Amino Acid derivatives as new zinc binding groups for the design of selective matrix metalloproteinase inhibitors.

2012

A number of matrix metalloproteinases (MMPs) are important medicinal targets for conditions ranging from rheumatoid arthritis to cardiomyopathy, periodontal disease, liver cirrhosis, multiple sclerosis, and cancer invasion and metastasis, where they showed to have a dual role, inhibiting or promoting important processes involved in the pathology. MMPs contain a zinc (II) ion in the protein active site. Small-molecule inhibitors of these metalloproteins are designed to bind directly to the active site metal ions. In an effort to devise new approaches to selective inhibitors, in this paper, we describe the synthesis and preliminary biological evaluation of amino acid derivatives as new zinc b…

chemistry.chemical_classificationbiologyArticle SubjectMatrix metalloproteinase inhibitorbusiness.industryActive sitechemistry.chemical_elementGeneral MedicineZincMatrix metalloproteinaseBioinformaticsBiochemistrySulfonamideAmino acidEnzymeBiochemistrychemistrybiology.proteinMetalloproteinMedicinebusinessMolecular BiologyResearch ArticleJournal of amino acids
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Structural and functional models for the dinuclear copper active site in catechol oxidases

2003

Two new mu-methoxo-bridged dinuclear copper(II) complexes with a N-substituted sulfonamide, [Cu(mu-OMe)(L)(NH(3))](2) (1) and [Cu(mu-OMe)(L)(DMSO)](2) (2) [HL, N-2-(4-methylbenzothiazole)benzenesulfonamide], have been prepared and characterized by single-crystal X-ray difraction analyses. Compound 1 crystallizes in the monoclinic space group C(2)/c with a=22.0678(18), b=7.9134(7), c=21.1186(18)A, beta=113.788(4) degrees and Z=8. Compound 2 crystallizes in the monoclinic space group C(2)/c with a=18.0900(10), b=9.5720(10), c=24.2620(10) A, beta=98.7120(10) degrees and Z=8. In both complexes the copper atoms have square-planar environments bridged by two oxygen atoms from methoxide groups. Ma…

chemistry.chemical_classificationbiologyStereochemistryActive sitechemistry.chemical_elementNuclear magnetic resonance spectroscopyCrystal structureMethoxideBiochemistryCopperlaw.inventionSulfonamideInorganic ChemistryCrystallographychemistry.chemical_compoundchemistrylawbiology.proteinElectron paramagnetic resonanceMonoclinic crystal systemJournal of Inorganic Biochemistry
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Mechanismus und Reaktionswege der Xanthenylierung an ambidenten nukleophilen Arzneistoffen

1986

Am Beispiel der ambidenten nukleophilen Arzneistoffe 4-Aminobenzolsulfonamid (3), Indometacin (7) und Phenylbutazon (10) werden Aralkylierungen mit dem SN1-aktiven Reagens Xanthydrol (1) vorgestellt. Mechanism and Reaction Path of the Xanthenylation of Ambident Nucleophilic Drugs The aralkylation of ambident nucleophilic drugs, e.g. 4-aminobenzenesulfonamide (3), indometacine (7) and phenylbutazone (10), with SN1-active xanthydrol (1) is described.

chemistry.chemical_classificationchemistry.chemical_compoundSN1 reactionNucleophileBicyclic moleculechemistryStereochemistryDrug DiscoveryPharmaceutical ScienceReaction pathXanthydrolSulfonamideArchiv der Pharmazie
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A new access to 2′-amino-substituted vinylindoles as donor-activated heterocyclic dienes and their first diels-alder reactions

1992

Abstract Reactions of the 3-acylindoles 5, 10 , and 15 with α-amino-α′-diphenylphosphinoyl-substituted carbanions gave rise to the 2′-amino-substituted 3− and 2-vinylindoles 7, 12 , and 17 by way of the isolable carbinols 6 , 11 , and 16 . The heterocyclic dienes 7 , 12 , and 17 readily underwent Diels-Alder reactions with N -phenylmaleimide.

chemistry.chemical_classificationchemistry.chemical_compoundTertiary amineBicyclic moleculeChemistryOrganic ChemistryDrug DiscoveryDiels alderOrganic chemistryImideBiochemistryCarbanionSulfonamideTetrahedron
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A novel heterocyclic sulfonamide: N-benzyl-5-[N-benzyl-N-(tert-butyloxycarbonyl)amino]-N-(tert-butyloxycarbonyl)-1,3,4-thiadiazole-2-sulfonamide

2000

The title compound, C(26)H(32)N(4)O(6)S(2), is a heterocyclic sulfonamide which is a 1,3,4-thiadiazole derivative. Structural data for this compound are compared with those of related compounds.

chemistry.chemical_classificationchemistry.chemical_compoundchemistryStereochemistryCrystal structureGeneral MedicineDerivative (chemistry)General Biochemistry Genetics and Molecular BiologySulfonamideActa Crystallographica Section C Crystal Structure Communications
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