http://rdf.ncbi.nlm.nih.gov/pubchem/patent/RU-2727198-C2

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filingDate 2016-11-02-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2020-07-21-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f06a91309547053a18d2482fde98baa4
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_bf34919982acea79464251dd9bafd853
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publicationDate 2020-07-21-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber RU-2727198-C2
titleOfInvention Benzofuran derivative, a method for production thereof and use thereof in medicine
abstract FIELD: medicine; pharmaceuticals. n SUBSTANCE: invention relates to a benzofuran derivative of general formula (I), or a pharmaceutically acceptable salt thereof, in which ring A is selected from a group consisting of heterocyclyl, which is 5–6 membered saturated monocyclic hydrocarbon group having one heteroatom selected from N, O and S, and 3–6-member cycloalkyl; each R 1 is identical to or different from the other, and each is independently selected from a group consisting of a hydrogen atom, a halogen atom, C 1-6 -alkyl, halo-C 1-6 -alkyl, cyano, 3–6-member cycloalkyl, 5–6 membered saturated or partially unsaturated monocyclic hydrocarbon group having one N atom and -(CH 2 ) x R a , where 5–6 membered saturated or partially unsaturated monocyclic hydrocarbon group is optionally substituted with one or more groups selected from group, consisting of C 1-6 -alkyl; R a is selected from a group consisting of heterocyclyl which is 5–6 membered saturated monocyclic hydrocarbon group having one or two heteroatoms selected from N and O, and -NR 7 R 8 , where each heterocyclyl is independently and optionally substituted with one or more groups selected from a group consisting of C 1-6 -alkyl, a halogen atom and hydroxy-C 1-6 -alkyl; R 2 is C 1-6 -alkyl, where alkyl is optionally substituted with one or more groups selected from a group consisting of 3–6-member cycloalkyl; R 3 is selected from a group consisting of C 1-6 -alkyl, a halogen atom and halo-C 1-6 -alkyl; each R 4 is identical to the other or different from it, and each is independently selected from a group consisting of a hydrogen atom, C 1-6 -alkyl and C 1-6 -alkoxy; each R 5 is identical to the other or different from it, and each is independently selected from a group, consisting of a hydrogen atom, oxo, a halogen atom, halo-C 1-6 -alkyl, -C(O)R 6 , -S(O) m R 6 and -NR 7 R 8 ; R 6 is selected from C 1-6 -alkyl; R 7 and R 8 are identical or different from each other, and each is independently selected from a group consisting of C 1-6 -alkyl; m equals 2; n equals 2; p is 0, 1 or 2; q equals 0 or 1; and x is equal to 1, 2 or 3. Invention also relates to a method of producing a compound of formula (I) and a pharmaceutical composition having inhibitory activity on EZH2 based thereon. n n n n EFFECT: technical result is obtaining a novel compound and a pharmaceutical composition based thereon, which can be used in medicine for preventing and/or treating diseases, such as tumors and cancer. n 13 cl, 4 tbl, 34 ex
priorityDate 2015-11-19-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID425559426
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID135332326
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID430235034
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID140943034
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID430235036
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID430234948
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID140943035
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID421072085
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID430234856
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID140943032
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID1146
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID457561146
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID140943033
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID421651418
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID420368670
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID53629922
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID152774289
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419508115
http://rdf.ncbi.nlm.nih.gov/pubchem/gene/GID2146
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID429547330
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID67518
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID430234897
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID450418934
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID547667
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID458393672
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID429547331
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID120273
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID430234883
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID71310626
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID135332302
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID458393660
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID135332258
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID450350652
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419891701
http://rdf.ncbi.nlm.nih.gov/pubchem/gene/GID768133
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID2758351

Total number of triples: 318.