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filingDate 2011-04-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2016-06-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_df73b0a55ed69fe4fb23077d572d5930
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_91144dc309c6d37215013676f3da77fa
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_797cf19ff2bfb390464919b20c31d121
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f8b6f646330ecc9c263bb463167c061f
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publicationDate 2016-06-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber RU-2586219-C2
titleOfInvention Arginase inhibitors and therapeutic use thereof
abstract FIELD: chemistry. n SUBSTANCE: invention relates to compound of formula I (I), wherein R 1 is selected from group consisting of-OH and OR a ; R a is selected from group consisting of hydrogen, linear or branched (C 1 -C 6 )alkyl, (C 3 -C 14 )aryl, (C 3 -C 14 )heterocycloalkyl-(C 1 -C 6 )alkylene-, containing 1-4 heteroatoms selected from O, S and N, (C 3 -C 14 )heteroaryl-(C 1 -C 6 )alkylene-, containing 1-4 heteroatoms selected from O, S and N, and (C 3 -C 14 )aryl(C 1 -C 6 )alkylene-; and where (A) R 2 is selected from group consisting of (C 3 -C 14 )heterocycloalkyl-(C 1 -C 6 )alkylene-, containing 1-4 heteroatoms selected from O, S and N, and -(CH 2 ) m -(X) u -(CH 2 ) n -(Y) v -R f where u is 1; v represents 0; each m and n independently equal to 0, 1, 2, 3, 4, 5 or 6, where m + n≥1, each X and Y is -NH-; R f is (C 3 -C 14 )aryl; and R 5 represents linear or branched (C 1 -C 6 )alkyl; or where (B) R 2 is (C 3 -C 14 )heterocycloalkyl-(C 1 -C 2 )alkylene, containing 1-4 heteroatoms selected from O, S and N, and R 5 is selected from group consisting of n and linear or branched (C 1 -C 6 )alkyl; and where each R 3 and R 4 is hydrogen; D is -CH 2 CH 2 CH 2 CH 2 -; and where any alkyl or alkylene optionally contains one or more substitutes selected from group consisting of halogen,-OH and (C 1 -C 6 )alkoxy; and where any aryl, heteroaryl or heterocycloalkyl, possibly containing one or more substitutes selected from a group consisting of halogen,-OH, oxo,-COOH, (C 3 -C 14 )aryl(C 1 -C 6 )alkylene-, (C 3 -C 14 )aryl, (C 3 -C 14 )heteroaryl containing 1-4 heteroatoms selected from O, S and N, (C 1 -C 6 )alkyl, (C 1 -C 6 )alkoxy, (C 1 -C 6 )halogen alkyl and (C 1 -C 6 )hydroxy alkyl; or its pharmaceutically acceptable salt, stereoisomer, tautomer or prodrug is revealed. Invention also discloses compound of formula II, pharmaceutical composition, method of inhibiting arginase I, arginase II or their combination in cell, method of treating or preventing disease or condition associated with expression or activity of arginase I, arginase II or their combination, and compound specified in table. n EFFECT: compound of formula I and formula II represent high-activity arginase I and II inhibitors. n 30 cl, 6 tbl, 255 ex
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Total number of triples: 2267.