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filingDate 2012-08-08-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_42f011511e435edc8d2eec5d9f0b747b
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_3753974421cf6a171bd488ad10cec83a
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_d9ff4a2f9f1f3ef43c0024012bea48ce
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a72a3e0463a2ba7d939b0269c61eb198
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_626042acf26d258e958249d6b015573b
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_79a13029f82827a86ea7ffad05482384
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_750aab2fa1a86d9b92a2314badd1b849
publicationDate 2014-06-18-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-2743256-A1
titleOfInvention Cyclopropaneamine compound
abstract The present invention provides a compound having a lysine-specific demethylase 1 inhibitory action, and useful as a medicament such as a prophylactic or therapeutic agent for cancer, and central nervous system diseases, and the like. The present invention relates to a compound represented by the formulan nwherein A is a hydrocarbon group or heterocyclic group optionally having substituent(s); R is H, a hydrocarbon group or heterocyclic group optionally having substituent(s); A and R are optionally bonded to each other to form a ring optionally having substituent(s); Q 1 , Q 2 , Q 3 and Q 4 are each a hydrogen atom or a substituent; Q 1 and Q 2 , and Q 3 and Q 4 , are each optionally bonded to each other to form a ring optionally having substituent(s); X is H, an acyclic hydrocarbon group or saturated cyclic group optionally having substituent(s); Y 1 , Y 2 and Y 3 are each H, a hydrocarbon group or heterocyclic group optionally having substituent(s); X and Y 1 , and Y 1 and Y 2 , are each optionally bonded to each other to form a ring optionally having substituent(s); and Z 1 , Z 2 and Z 3 are each H or a substituent, or a salt thereof.
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Total number of triples: 3927.