patent/CA-2387357-A1

http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CA-2387357-A1

Outgoing Links

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filingDate	2000-10-11-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor	http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a896269e3df8f001f95d32d3940c8d35 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_762720dcd72b5701191c1169014f7639 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_acce251fbec1d041acbc4101e16885d3 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ffa4c9bc2e63d64bc3fea97c83bd6562 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_7c923c30a424aef185c5ddde23edeaaa http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_272b50a2c11dccc66a38212527dfd8d0 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_06c8d5b9e23a7faa8503a0f1a9a46b43 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_49e7955b9006f8d845141ccab62f6c78
publicationDate	2001-04-19-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber	CA-2387357-A1
titleOfInvention	Derivatives of pyrazolo[4,3-d]pyrimidin-7-ones which inhibit cyclic guanosine 3',5'-monophosphate phosphodiesterase
abstract	Compounds of formula (I) wherein R1, R2, R4 and R13 are as defined or a pharmaceutically or veterinarily acceptable salt or polymorph thereof, or a pharmaceutically or veterinarily acceptable solvate or pro-drug thereof: are potent and selective inhibitors of type 5 cyclic guanosine 3', 5'-monophosphate phosphodiesterase (cGMP PDE5) and have utility in the treatment of, inter alia, male erectile dysfunction (MED) and female sexual dysfunction (FSD).
priorityDate	1999-10-11-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type	http://data.epo.org/linked-data/def/patent/Publication

Incoming Links

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Total number of triples: 100.