http://rdf.ncbi.nlm.nih.gov/pubchem/patent/ES-2559679-T3

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filingDate 2007-06-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2016-02-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ed0e7cf4fde1d4b4f7e8fd194f1ade13
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_abef2506527e5cd487c20d51d01ffcf3
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publicationDate 2016-02-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber ES-2559679-T3
titleOfInvention Pyrazoloquinazolinones as PARP inhibitors
abstract A compound of Formula (I) ** Formula ** or a pharmaceutically acceptable salt thereof, in which R1, R2, R3 and R4 are independently selected from the group consisting of hydrogen, alkenyl, alkoxy, alkoxycarbonyl, alkyl, alkynyl , cyano, haloalkoxy, haloalkyl, halogen, hydroxy, hydroxyalkyl, nitro, NRARB, and (NRARB) carbonyl; X is heterocycloalkyl, where X is unsubstituted or substituted with 1, 2, 3, 4, or 5 substituents, Z, independently selected from the group consisting of alkyl, alkenyl, alkynyl, nitro, -CN, halogen, haloalkyl , alkoxy, alkylcarbonyl, alkylcarbonylalkyl, alkoxyalkyl, alkoxycarbonyl, alkoxycarbonylalkyl, aryl, arylalkyl, arylalkoxy, arylalkoxycarbonyl, arylalkylcarbonyl, carboxy, carboxyalkyl, cycloalkyl, cycloalkylalkyl, cycloalkylalkoxy, cycloalkylcarbonyl, heteroaryl, heteroarylalkyl, heteroarylcarbonyl, heteroarilcarbonilalquilo, heterocycle, heterocycloalkyl, heterocycloalkylcarbonyl, heterocyclocarbonyl , heterocyclocarbonylalkyl, hydroxy, hydroxyalkyl, NRCRD, (NRCRD) alkyl, (NRCRD) carbonyl, (NRCRD) carbonylalkyl, and oxo; wherein the aryl and heteroaryl residues of Z are independently unsubstituted or substituted with 1, 2, 3, 4, or 5 substituents selected from the group consisting of alkyl, formyl, halogen, and haloalkyl, and the heterocycle and cycloalkyl residues Z's are independently unsubstituted or substituted with 1, 2, 3, 4, or 5 substituents selected from the group consisting of alkyl, oxo, formyl, halogen, and haloalkyl; RC and RD are independently selected from the group consisting of hydrogen, alkyl, alkylcarbonyl, alquilcarboniloxialquilcarbonilo, arylcarbonyl, aryl, arylalkyl, arylalkylcarbonyl, carboxyalkyl, carboxyalkylcarbonyl, cycloalkyl, cycloalkylalkyl, haloalkyl, haloalkylcarbonyl, heteroaryl, heteroarylalkyl, heteroarylcarbonyl, heterocycle, heterocyclealkyl, heterocyclecarbonyl , heterocycloalkylcarbonyl, (NRARB) alkyl, and (NRARB) alkylcarbonyl; wherein if RC or RD are aryl, arylalkyl, arylalkylcarbonyl, arylcarbonyl, cycloalkyl, cycloalkylalkyl, heteroaryl, heteroarylalkyl, heteroarylcarbonyl, heterocycle, heterocycloalkyl, heterocyclocarbonyl, or heterocycloalkylcarbonyl, then RC or RD may be unsubstituted or substituted, 3, 4, or 5 substituents independently selected from the group consisting of alkyl, alkenyl, alkynyl, nitro, -CN, halogen, haloalkyl, oxo, alkoxy, alkylcarbonyl, alkylcarbonylalkyl, alkoxyalkyl, alkoxycarbonyl, alkoxycarbonylalkyl, aryl, arylalkyl, arylalkyl arylalkylcarbonyl, and arylalkoxycarbonyl; wherein RA and RB are independently selected from the group consisting of hydrogen, alkyl, haloalkyl, and alkylcarbonyl; and n is 1.
priorityDate 2006-06-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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Total number of triples: 397.