http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-2014016789-A1

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filingDate 2013-07-24-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c7a198eaecda96cae400a280c4d689e0
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publicationDate 2014-01-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber WO-2014016789-A1
titleOfInvention Pyrazolo[3,4-d]pyrimidin-4(5h)-one derivatives as pde9 inhibitors
abstract A compound of the general formula (I) wherein R 1 is selected from the group consisting of phenyl unsubstituted or substituted with 1 to 3 substituents selected from F, Cl, Br, I, CN, -O-C1-C3-alkyl, fluorinated -O-C1-C3-alkyl, -(CH 2 ) m OH and 5-membered heterocyclic group with 1 or 2 heteroatoms selected from N, O and S; and 6- or 10-membered heteroaryl with 1 to 3 heteroatoms selected from O, N and S; R 2 and R 3 independently of each other represent H atom or straight or branched C1-C3 alkyl; R 4 is selected from the group consisting of 4- to 6- membered cycloalkyl, wherein one of carbon atoms can be replaced by O atom, and which is unsubstituted or substituted with one or two halogen atoms,and straight or branched C1-C4 alkyl; Q represents a bond or C1-C3-alkylene, which can be optionally substituted by one to three C1-C3-alkyls; X is selected from the group consisting of O, NR 5 , and S(O) p ; R 5 represents H atom or C1-C3alkyl; m is 1, 2 or 3; p is 0, 1 or 2; and salts thereof, for use as a medicament, in particular for treating cognitive function disorders and neurodegenerative diseases.
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priorityDate 2012-07-26-04:00^^<http://www.w3.org/2001/XMLSchema#date>
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Total number of triples: 723.