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http://purl.uniprot.org/citations/21996520http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/21996520http://www.w3.org/2000/01/rdf-schema#comment"Design, synthesis, and SAR of 7-oxopyrrolopyridine-derived DPP4 inhibitors are described. The preferred stereochemistry of these atropisomeric biaryl analogs has been identified as Sa. Compound (+)-3t, with a K(i) against DPP4, DPP8, and DPP9 of 0.37 nM, 2.2, and 5.7 μM, respectively, showed a significant improvement in insulin response after single doses of 3 and 10 μmol/kg in ob/ob mice."xsd:string
http://purl.uniprot.org/citations/21996520http://purl.org/dc/terms/identifier"doi:10.1016/j.bmcl.2011.09.074"xsd:string
http://purl.uniprot.org/citations/21996520http://purl.uniprot.org/core/author"Sun L."xsd:string
http://purl.uniprot.org/citations/21996520http://purl.uniprot.org/core/author"Wang W."xsd:string
http://purl.uniprot.org/citations/21996520http://purl.uniprot.org/core/author"Wang A."xsd:string
http://purl.uniprot.org/citations/21996520http://purl.uniprot.org/core/author"Li Y.X."xsd:string
http://purl.uniprot.org/citations/21996520http://purl.uniprot.org/core/author"Fura A."xsd:string
http://purl.uniprot.org/citations/21996520http://purl.uniprot.org/core/author"Hamann L.G."xsd:string
http://purl.uniprot.org/citations/21996520http://purl.uniprot.org/core/author"Kish K."xsd:string
http://purl.uniprot.org/citations/21996520http://purl.uniprot.org/core/author"Kirby M.S."xsd:string
http://purl.uniprot.org/citations/21996520http://purl.uniprot.org/core/author"Klei H.E."xsd:string
http://purl.uniprot.org/citations/21996520http://purl.uniprot.org/core/author"Zahler R."xsd:string
http://purl.uniprot.org/citations/21996520http://purl.uniprot.org/core/author"Harrity T."xsd:string
http://purl.uniprot.org/citations/21996520http://purl.uniprot.org/core/author"Morgan N."xsd:string
http://purl.uniprot.org/citations/21996520http://purl.uniprot.org/core/author"Weigelt C."xsd:string
http://purl.uniprot.org/citations/21996520http://purl.uniprot.org/core/author"Egan D."xsd:string
http://purl.uniprot.org/citations/21996520http://purl.uniprot.org/core/author"Devasthale P."xsd:string
http://purl.uniprot.org/citations/21996520http://purl.uniprot.org/core/author"Cap M."xsd:string
http://purl.uniprot.org/citations/21996520http://purl.uniprot.org/core/author"Levesque P."xsd:string
http://purl.uniprot.org/citations/21996520http://purl.uniprot.org/core/date"2011"xsd:gYear
http://purl.uniprot.org/citations/21996520http://purl.uniprot.org/core/name"Bioorg Med Chem Lett"xsd:string
http://purl.uniprot.org/citations/21996520http://purl.uniprot.org/core/pages"6646-6651"xsd:string
http://purl.uniprot.org/citations/21996520http://purl.uniprot.org/core/title"7-Oxopyrrolopyridine-derived DPP4 inhibitors-mitigation of CYP and hERG liabilities via introduction of polar functionalities in the active site."xsd:string
http://purl.uniprot.org/citations/21996520http://purl.uniprot.org/core/volume"21"xsd:string