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http://purl.uniprot.org/citations/21506569http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/21506569http://www.w3.org/2000/01/rdf-schema#comment"Aromatic amides comprising branched aliphatic carboxylic acids and 4-aminobenzenesulfonamide were evaluated for their inhibition of carbonic anhydrase (CA) isoforms. Of the most anticonvulsant-active compounds (2, 4, 13, 16, and 17), only 13, 16, and 17 were potent inhibitors of CAs VII and XIV. Compounds 9, 14, and 19 inhibited CA II, while 10 and 12 inhibited all isoforms. Structural studies suggest that differences in the active sites' hydrophobicity modulate the affinity of the inhibitors."xsd:string
http://purl.uniprot.org/citations/21506569http://purl.org/dc/terms/identifier"doi:10.1021/jm200209n"xsd:string
http://purl.uniprot.org/citations/21506569http://purl.uniprot.org/core/author"McKenna R."xsd:string
http://purl.uniprot.org/citations/21506569http://purl.uniprot.org/core/author"Robbins A.H."xsd:string
http://purl.uniprot.org/citations/21506569http://purl.uniprot.org/core/author"Maresca A."xsd:string
http://purl.uniprot.org/citations/21506569http://purl.uniprot.org/core/author"Scozzafava A."xsd:string
http://purl.uniprot.org/citations/21506569http://purl.uniprot.org/core/author"Supuran C.T."xsd:string
http://purl.uniprot.org/citations/21506569http://purl.uniprot.org/core/author"Aggarwal M."xsd:string
http://purl.uniprot.org/citations/21506569http://purl.uniprot.org/core/author"Bialer M."xsd:string
http://purl.uniprot.org/citations/21506569http://purl.uniprot.org/core/author"Hen N."xsd:string
http://purl.uniprot.org/citations/21506569http://purl.uniprot.org/core/author"Yagen B."xsd:string
http://purl.uniprot.org/citations/21506569http://purl.uniprot.org/core/date"2011"xsd:gYear
http://purl.uniprot.org/citations/21506569http://purl.uniprot.org/core/name"J Med Chem"xsd:string
http://purl.uniprot.org/citations/21506569http://purl.uniprot.org/core/pages"3977-3981"xsd:string
http://purl.uniprot.org/citations/21506569http://purl.uniprot.org/core/title"Anticonvulsant 4-aminobenzenesulfonamide derivatives with branched-alkylamide moieties: X-ray crystallography and inhibition studies of human carbonic anhydrase isoforms I, II, VII, and XIV."xsd:string
http://purl.uniprot.org/citations/21506569http://purl.uniprot.org/core/volume"54"xsd:string
http://purl.uniprot.org/citations/21506569http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/21506569
http://purl.uniprot.org/citations/21506569http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/21506569
http://purl.uniprot.org/uniprot/#_P00918-mappedCitation-21506569http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/21506569
http://purl.uniprot.org/uniprot/P00918http://purl.uniprot.org/core/mappedCitationhttp://purl.uniprot.org/citations/21506569