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http://purl.uniprot.org/citations/19773165http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/19773165http://www.w3.org/2000/01/rdf-schema#comment"A crystal structure of 1 bound to a Cys25Ser mutant of cathepsin S helped to elucidate the binding mode of a previously disclosed series of pyrazole-based CatS inhibitors and facilitated the design of a new class of arylalkyne analogs. Optimization of the alkyne and tetrahydropyridine portions of the pharmacophore provided potent CatS inhibitors (IC50=40-300 nM), and an X-ray structure of 32 revealed that the arylalkyne moiety binds in the S1 pocket of the enzyme."xsd:string
http://purl.uniprot.org/citations/19773165http://purl.org/dc/terms/identifier"doi:10.1016/j.bmcl.2009.09.014"xsd:string
http://purl.uniprot.org/citations/19773165http://purl.uniprot.org/core/author"Gu Y."xsd:string
http://purl.uniprot.org/citations/19773165http://purl.uniprot.org/core/author"Zhu J."xsd:string
http://purl.uniprot.org/citations/19773165http://purl.uniprot.org/core/author"Sun S."xsd:string
http://purl.uniprot.org/citations/19773165http://purl.uniprot.org/core/author"Randal M."xsd:string
http://purl.uniprot.org/citations/19773165http://purl.uniprot.org/core/author"Karlsson L."xsd:string
http://purl.uniprot.org/citations/19773165http://purl.uniprot.org/core/author"Thurmond R.L."xsd:string
http://purl.uniprot.org/citations/19773165http://purl.uniprot.org/core/author"Axe F.U."xsd:string
http://purl.uniprot.org/citations/19773165http://purl.uniprot.org/core/author"Edwards J.P."xsd:string
http://purl.uniprot.org/citations/19773165http://purl.uniprot.org/core/author"Ameriks M.K."xsd:string
http://purl.uniprot.org/citations/19773165http://purl.uniprot.org/core/author"Bembenek S.D."xsd:string
http://purl.uniprot.org/citations/19773165http://purl.uniprot.org/core/date"2009"xsd:gYear
http://purl.uniprot.org/citations/19773165http://purl.uniprot.org/core/name"Bioorg Med Chem Lett"xsd:string
http://purl.uniprot.org/citations/19773165http://purl.uniprot.org/core/pages"6131-6134"xsd:string
http://purl.uniprot.org/citations/19773165http://purl.uniprot.org/core/title"Pyrazole-based cathepsin S inhibitors with arylalkynes as P1 binding elements."xsd:string
http://purl.uniprot.org/citations/19773165http://purl.uniprot.org/core/volume"19"xsd:string
http://purl.uniprot.org/citations/19773165http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/19773165
http://purl.uniprot.org/citations/19773165http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/19773165
http://purl.uniprot.org/uniprot/#_P25774-mappedCitation-19773165http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/19773165
http://purl.uniprot.org/uniprot/P25774http://purl.uniprot.org/core/mappedCitationhttp://purl.uniprot.org/citations/19773165