http://rdf.ncbi.nlm.nih.gov/pubchem/patent/ES-2324535-T3

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_b6d6b0a9721d7b7ca7d5f368df0f3658
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D249-08
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filingDate 2004-02-06-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2009-08-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_9809c7577fe4b6d81fc2b95db022c3ce
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b741be7d69ee7d8fbb31f60785442cab
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_8b0cb4be7d37eb50758d9867de053503
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_6195c9383dd221ce7e80bf38742da20e
publicationDate 2009-08-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber ES-2324535-T3
titleOfInvention DERIVATIVES OF PIPERAZINA-2-CARBOXAMIDA.
abstract Use of a compound according to formula (I) ** see formula ** as well as its geometric isomers, its optically active forms such as enantiomers, diastereomers and its racemate forms, as well as pharmaceutically acceptable salts and pharmaceutically active derivatives thereof, wherein A and B are each independently selected from the group consisting of C1-C6 alkyl, C3-C8 cycloalkyl, linear or branched 3-8 membered heterocycloalkyl, linear C1-C6-heterocycloalkyl (3-8 membered) alkyl or branched, aryl, linear or branched (C 1-C 6) alkyl, C 2 -C 6-aryl alkenyl, C 2 -C 6-aryl alkynyl, heteroaryl, (C 1-C 6) -heteroaryl alkyl group linear or branched, C 2 -C 6-heteroaryl alkenyl, C 2 -C 6-heteroaryl alkynyl, an acyl, C 1- C6 alkoxy, wherein said cycloalkyl, heterocycloalkyl, aryl or heteroaryl can be fused with cycloalkyl, aryl groups or heteroaryl; X is selected from the group consisting of -CO- or -SO 2-; And it is selected in the group consisting of -SO2-, -CO-, -CO-NR 3 where R 3 is as defined below; R 1 and R 2 independently of each other are selected from the group consisting of hydrogen, hydroxy, sulfonyl, amino, C 1 -C 6 alkyl, C 2 -C 6 alkenyl, C 2 -C 6 alkynyl wherein said alkyl chains , alkenyl, alkynyl can be interrupted by a heteroatom selected from N, O or S, aryl, heteroaryl, cycloalkyl (C3-C8), heterocycloalkyl, wherein said heterocycloalkyl, aryl or heteroaryl cycloalkyl groups can be fused with 1-2 other groups cycloalkyl, heterocycloalkyl, aryl or heteroaryl, an acyl moiety, C1-C6 alkyl aryl, C1-C6 alkyl heteroaryl, C2-C6 aryl alkenyl, C2-C6 alkenyl heteroaryl, C2-C6 alkynyl aryl, C2 alkynyl -C 6 heteroaryl, C 1 -C 6 alkyl cycloalkyl, C 1- C 6 alkyl heterocycloalkyl, C 2 -C 6 alkenyl cycloalkyl, C 2-C 6-heterocycloalkyl alkenyl, C 2-C 6 alkynyl cycloalkyl, C2 alkynyl -C6 heterocycloalkyl, alkoxycarbonyl, aminocarbonyl, C1-C6 carboxy alkyl, C1-C6 acyl alkyl, aryl acyl, heteroaryl ac il, (hetero) -C3-C8 acylcycloalkyl, C1-C6 alkyl acyloxy, C1-C6 alkyl alkoxy, C1-C6 alkyl alkoxycarbonyl, C 1-C 6 aminocarbonyl alkyl, C 1-C 6 alkyl acylamino, acylamino, C alkyl 1-C 6 ureido, C 1-C 6 alkyl carbamate, C 1-C 6 amino alkyl, C 1-C 6 ammonium alkyl, C 1-C 6 sulfonyloxy alkyl, C 1-C 6 sulfonyl alkyl, C 1- alkyl C 6 sulfinyl, C1-C6 alkyl sulfanyl, C1-C6 alkyl sulfonylamino or C1-C6 alkyl aminosulfonyl and R 1 and R 2 can together form a 3-8 membered heterocycle which optionally comprises a heteroatom selected from O, N or S; R 3 is selected from the group consisting of a linear or branched C 1 -C 6 alkyl; for the preparation of a medicament for the prophylaxis and / or treatment of dysmenorrhea, premature labor, premature birth and to stop labor before cesarean delivery.
priorityDate 2003-02-14-04:00^^<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: 515.