http://rdf.ncbi.nlm.nih.gov/pubchem/patent/RU-2602814-C2

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filingDate 2010-04-19-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2016-11-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_5ee2b3b44958414cf908a3874bd108e5
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_d344fc2a3f2761fe96d8dc355e4822fb
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publicationDate 2016-11-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber RU-2602814-C2
titleOfInvention Lysin-specific demethylase-1 inhibitors and use thereof
abstract FIELD: chemistry. n SUBSTANCE: invention relates to organic chemistry, specifically to a heterocyclic compound of general formula (I), where (A) denotes phenyl or pyridyl; each (A′), if present, is independently selected from a group consisting of phenyl, phenylC 1 -C 10 alkoxy group, phenylC 1 -C- 10 alkyl, phenyloxy group and halogen, where each (A′) contains 0, 1, 2 or 3 substitutes independently selected from a group, including halogen, halogenC 1 -C- 10 alkyl, phenyl, C 1 -C 10 alkyl and C 1 -C 10 alkoxy group; X equals 0, 1 or 2; (B) denotes cyclopropyl ring, where (A) and (Z) are covalently bonded to different carbon atoms in (B); (Z) denotes -NH-; (L) is selected from -CH 2 CH 2 -, -CH 2 CH 2 CH 2 - and -CH 2 CH 2 CH 2 CH 2 -; and (D) is selected from -N(-R1)-R2, -O-R3 and -S-R3, where R1 and R2 are bonded to each other, and together with a nitrogen atom to which R1 and R2 are bonded, form a 5- or 6-member heterocyclic ring, where said heterocyclic ring contains 0, 1 or 2 substitutes, independently selected from a group comprising -NH 2 , -NH(C 1 -C 6 -alkyl), -N(C 1 -C 6 -alkyl)(C 1 -C 6 -alkyl) and C 1 -C 10 alkyl, or R1 and R2 are independently selected from a group including -H, C 1 -C- 10 alkyl and C 3 -C 7 -cycloalkyl, where total number of substitutes in R1 and R2 is equal to 0, 1 or 2 and substitutes are independently selected from -NH 2 , -NH(C 1 -C 6 -alkyl) and -N(C 1 -C 6 -alkyl) (C 1 -C 6 -alkyl); and R3 denotes C 1 -C 10 alkyl; or its enantiomer, diastereomer or mixture thereof, or its pharmaceutically acceptable salt or solvate; provided that following compounds are excluded: N1,N1-dimethyl-N2-(2-phenylcyclopropyl)-1,3-propandiamine and N1,N1-dimethyl-N2-(2-phenylcyclopropyl)-1,2-ethanediamine. Invention also relates to a heterocyclic compound of formula (I'), a pharmaceutical composition based on compound of formula (I) and use of compound of formula (I). n EFFECT: technical result is obtaining novel heterocyclic compounds having activity as a LSD1 inhibitor. n 29 cl, 7 dwg, 1 tbl, 40 ex n (I) (I')
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/RU-2765152-C2
priorityDate 2009-09-25-04:00^^<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: 781.