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DESCRIBE <http://purl.uniprot.org/SHA-384/D58AD2A62E2CC78C1B7281EDB5B50817F3E5626270CE88D439FCD5C8EEE13AFA43E7F7AA54ED9F7E3602FB4B75FBFE7C>
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http://purl.uniprot.org/SHA-384/D58AD2A62E2CC78C1B7281EDB5B50817F3E5626270CE88D439FCD5C8EEE13AFA43E7F7AA54ED9F7E3602FB4B75FBFE7C
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/D58AD2A62E2CC78C1B7281EDB5B50817F3E5626270CE88D439FCD5C8EEE13AFA43E7F7AA54ED9F7E3602FB4B75FBFE7C
http://www.w3.org/2000/01/rdf-schema#comment
"the p-substituted benzyl side chain at N2-position helps to enhance the PDE1 inhibitory profile. Depending on these observations some new molecules are predicted that may possess better PDE1 inhibition"
xsd:string
http://purl.uniprot.org/uniprot/#_B76C7C0CB42149393E4EEFCEE809C500711BCAA6CAF253E3A5644E9F71BF96AD727D3FF837222D8B9F6DEDFD30CFDB89
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/D58AD2A62E2CC78C1B7281EDB5B50817F3E5626270CE88D439FCD5C8EEE13AFA43E7F7AA54ED9F7E3602FB4B75FBFE7C
http://purl.uniprot.org/uniprot/Q9Y633
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/D58AD2A62E2CC78C1B7281EDB5B50817F3E5626270CE88D439FCD5C8EEE13AFA43E7F7AA54ED9F7E3602FB4B75FBFE7C
http://purl.uniprot.org/uniprot/#_Q9Y633-mappedCitation-28132591
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/D58AD2A62E2CC78C1B7281EDB5B50817F3E5626270CE88D439FCD5C8EEE13AFA43E7F7AA54ED9F7E3602FB4B75FBFE7C