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http://purl.uniprot.org/citations/17350258http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/17350258http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/17350258http://www.w3.org/2000/01/rdf-schema#comment"A series of aryl sulfonamides of 5,6-disubstituted anthranilic acids were identified as potent inhibitors of methionine aminopeptidase-2 (MetAP2). Small alkyl groups and 3-furyl were tolerated at the 5-position of anthranilic acid, while -OCH(3), CH(3), and Cl were found optimal for the 6-position. Placement of 2-aminoethoxy group at the 6-position enabled interaction with the second Mn(2+) but did not result in enhancement in potency. Introduction of a tertiary amino moiety at the ortho-position of the sulfonyl phenyl ring gave reduced protein binding and improved cellular activity, but led to lower oral bioavailability."xsd:string
http://purl.uniprot.org/citations/17350258http://purl.org/dc/terms/identifier"doi:10.1016/j.bmcl.2007.02.062"xsd:string
http://purl.uniprot.org/citations/17350258http://purl.org/dc/terms/identifier"doi:10.1016/j.bmcl.2007.02.062"xsd:string
http://purl.uniprot.org/citations/17350258http://purl.uniprot.org/core/author"Park C."xsd:string
http://purl.uniprot.org/citations/17350258http://purl.uniprot.org/core/author"Park C."xsd:string
http://purl.uniprot.org/citations/17350258http://purl.uniprot.org/core/author"Zhang Q."xsd:string
http://purl.uniprot.org/citations/17350258http://purl.uniprot.org/core/author"Zhang Q."xsd:string
http://purl.uniprot.org/citations/17350258http://purl.uniprot.org/core/author"Wang J."xsd:string
http://purl.uniprot.org/citations/17350258http://purl.uniprot.org/core/author"Wang J."xsd:string
http://purl.uniprot.org/citations/17350258http://purl.uniprot.org/core/author"Wang G.T."xsd:string
http://purl.uniprot.org/citations/17350258http://purl.uniprot.org/core/author"Wang G.T."xsd:string
http://purl.uniprot.org/citations/17350258http://purl.uniprot.org/core/author"Kawai M."xsd:string
http://purl.uniprot.org/citations/17350258http://purl.uniprot.org/core/author"Kawai M."xsd:string
http://purl.uniprot.org/citations/17350258http://purl.uniprot.org/core/author"Sheppard G.S."xsd:string
http://purl.uniprot.org/citations/17350258http://purl.uniprot.org/core/author"Sheppard G.S."xsd:string
http://purl.uniprot.org/citations/17350258http://purl.uniprot.org/core/author"Yates M."xsd:string
http://purl.uniprot.org/citations/17350258http://purl.uniprot.org/core/author"Yates M."xsd:string
http://purl.uniprot.org/citations/17350258http://purl.uniprot.org/core/author"Lesniewski R."xsd:string
http://purl.uniprot.org/citations/17350258http://purl.uniprot.org/core/author"Lesniewski R."xsd:string
http://purl.uniprot.org/citations/17350258http://purl.uniprot.org/core/author"Lou P."xsd:string
http://purl.uniprot.org/citations/17350258http://purl.uniprot.org/core/author"Lou P."xsd:string
http://purl.uniprot.org/citations/17350258http://purl.uniprot.org/core/author"Barnes D.M."xsd:string
http://purl.uniprot.org/citations/17350258http://purl.uniprot.org/core/author"Barnes D.M."xsd:string