http://rdf.ncbi.nlm.nih.gov/pubchem/patent/RU-2418803-C2

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filingDate 2006-10-17^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2011-05-20^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_312ce78fa555c536fa05e4e15b43e511
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_03db210029f66c60967960b4faec53ad
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_2dd191cf836f29324b61ad79a5bf8e4d
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_6f5dcdfc6dd2aa91229151249acc34cf
publicationDate 2011-05-20^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber RU-2418803-C2
titleOfInvention Condensed heterocyclic derivative, therapeutic composition which contains it and its application in medicine
abstract FIELD: medicine, pharmaceutics. n SUBSTANCE: invention relates to condensed heterocyclic derivative, represented by formula (I): where ring A represents 5-member monocyclic heteroaryl, containing 1 or 2 heteroatoms, selected from N or S; R A represents lower alkyl group, optionally substituted with hydroxyl group, COW 1 , COOW 1 or CONW 2 W 3 , in which W 1 -W 3 independently represent a hydrogen atom or lower alkyl group; m represents integer 0 or 2; ring B represents benzene ring or thiophene ring; R B represents halogen atom, cyano group, lower alkyl group or OW 4 , in which W 4 represents a hydrogen atom or lower alkyl group; n represents integer 0-2; E 1 represents an oxygen atom; E 2 represents an oxygen atom; U represents a single bond or lower alkelene group; X represents group, represented by Y, -CO-Y, -SO 2 -Y, -S-L-Y, -O-L-Y, -CO-L-Y, -SO-L-Y, -SO 2 -L-Y, -S-Z or -O-Z, in which L represents a lower alkylene group optionally substituted with halogen or hydroxy group; Y represents group, represented by Z or -NW 7 W 8 , where W 7 and W 8 independently represent a hydrogen atom, lower alkyl group or Z on condition that W 7 and W 8 are not simultaneously hydrogen atoms, or W 7 and W 8 can bind together with adjacent nitrogen atom with formation of cyclic amino group; Z represents cycloalkyl group, optionally condensed with phenyl and optionally substituted with phenyl group, optionally substituted with halogen or alkoxy group; 6-8-member heterocycoalkyl group, which has 1 heteroatom, selected from nitrogen atom or oxygen atom, optionally condensed with phenyl and optionally substituted with phenyl; phenyl group optionally substituted with a substituent, selected from group, consisting of a halogen atom, cyano group, alkyl group, optionally substituted with halogen atom, hydroxy group or alkoxy group, alkoxy group, optionally substituted with halogen atom, hydroxy group, alkoxy group, alkoxy-carbonyl-oxy group or acyloxy group, alkylthio group, carboxy group and alkoxy-carbonyl group; pyridyl; or its pharmaceutically acceptable salt. Invention also relates to pharmaceutical composition possessing antagonistic activity with respect to gonatotropin-releasing hormone, based on the claimed compound. n EFFECT: obtained are novel compounds and based on them pharmaceutical composition, which can be applied in medicine for prevention or treatment of a disease depending on sex hormones, which is selected from group, consisting of benign prostatic hypertrophy, hysteromyoma, endometriosis, premature puberty, prostate cancer, ovarian cancer and breast cancer. n 29 cl, 112 tbl, 428 ex
priorityDate 2005-10-19^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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