http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CA-2647932-C

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K31-519
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filingDate 2006-04-04-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2011-06-07-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_1c8b5fe4832c6c5def5c79ac99c913a3
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b893e8ef34926ef2da9d4c10f1e60290
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_71ecb7b40e6705c3e8796d065a09d23e
publicationDate 2011-06-07-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CA-2647932-C
titleOfInvention Agent for the prevention and treatment of prostatic hyperplasia comprising pyrazolopyrimidinone compound
abstract The present invention relates to an agent for preventing and treating benign prostatic hyperplasia (BPH) and lower urinary tract symptoms (LUTS) associated with BPH and a relaxant for relaxing urethral smooth muscle or prostatic smooth muscle comprising a pyrazolopyrimidinone compound as an effective ingredient. The agent in accordance with the present invention can provide nitric oxides by inhibiting the activity of PDE-5 that decomposes c-GMP, and the provided nitric oxides relax the urethral smooth muscle or the prostatic smooth muscle to lower the intraurethral pressure (IUP), thus treating BPH and LUTS associated with BPH. Furthermore, the time required for reaching a maximum blood concentration is shorter and the half-life is longer than the other PDE-5 inhibitors, thus reducing the frequency of administration. Moreover, the agent of the invention causing few side effects can be efficiently used as a safe drug.
priorityDate 2006-04-04-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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