http://rdf.ncbi.nlm.nih.gov/pubchem/patent/RU-2328484-C2

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filingDate 2003-11-03-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2008-07-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_dee3931b16601373919eb62af3258a4c
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ddea5095e894f8d2c384b0f170316399
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publicationDate 2008-07-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber RU-2328484-C2
titleOfInvention Indoles useful in treatment androgen receptors bound deseases
abstract FIELD: chemistry. n SUBSTANCE: invention relates to the novel indole derivatives with the formula , where X means S, SO, SO 2 ; R 1 means 6-membered mono-homocyclic saturated or unsaturated ring structure or 5-, 6-membered monohetercyclic saturated or unsaturated ring structure with one or two heteratoms, chosen from N, O, S, and each of the said structures is not necessarily substituted with one or more substituters, chosen from the group, consisting of halogen, CN, (1C-4C)fluoroalkyl, NO 2 , (1C-4C)alkyl, (1C-4C)alkoxi or (1C-4C)fluoroalkoxi; R 2 means 2-nitorphenyl, 2-cyanophenyl, 2-hydroxymethylphenyl, pyridine-2-il, pyridine-2-il-N-oxide, 2-benzamide, methylic ether of the 2-benzoic acid or 2-methoxyphenyl; R 3 means H, halogen or (1C-4C)alkyl; R 4 means H, OH, (1C-4C) alkoxy or halogen; R 5 means H, OH, (1C-4C) alkoxy, NH 2 CN, halogen, (1C-4C)fluoroalkyl, NO 2 , hydroxy(1C-4C)alkyl, CO 2 H, CO 2 (1C-6C)alkyl, or R 5 means NHR 6 , where R 6 means (1C-6C)acyl, not necessarily substituted with one or more halogens, S(O) 2 (1C-4C)alkyl or S(O) 2 heteroaryl, not necessarily substituted with (1C-4C)alkyl or one or more halogens, where heteroaryl is the 5-membered mono-heterocyclic unsaturated ring structure with one S atom or two N atoms, or R 5 means C(O)N(R 8 ,R 9 ), where R 8 and R 9 , each independently, mean H, (3C-6C)cycloalkyl or CH 2 R 10 , where R 10 means H, (1C-5C)alkyl, hydroxy(1C-3C)alkyl, complex (1C-4C)alkyl ether of the carboxy(1C-4C)alkyl, (1C-3C)alkoxy(1C-3C)alkyl, (mono- or di(1C-4C)alkyl)aminomethyl, (mono- or di1C-4C)alkyl)aminocarbonyl or pyhenyl, where R 8 and R 9 together with N form 5- or 6-membered saturated aor unsaturated heterocyclic ring, not necessarily containing N or O as the second heteroatom, not necessarily substituted with (1C-4C)alkyl; or its saline or hydrated form. n EFFECT: allows using indoles for producing pharmaceutical agent and in method for inhibiting 5α-dihydrosterone activity. n 17 cl, 7 dwg, 5 tbl, 25 ex
priorityDate 2002-11-07-04:00^^<http://www.w3.org/2001/XMLSchema#date>
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http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCP45376
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID412954018
http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCP23901
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID408582474
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID518896
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID421833817
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID91649
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID458394811
http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCQ54KG7
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID449984280
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID421069987
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID59463835
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419839321
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID66775531
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID10318031
http://rdf.ncbi.nlm.nih.gov/pubchem/taxonomy/TAXID11757
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419839325
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419511530
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID10452790
http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCQ6GCZ8
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID428171817
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID59463837
http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCQ5HKG6
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID66775533
http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCQ61578
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID2733207
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID426070774
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID66775938
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID428055769
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID59463840
http://rdf.ncbi.nlm.nih.gov/pubchem/anatomy/ANATOMYID11757
http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCQ5HJP2
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID76659
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID59463839
http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCQ48436
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID458394314
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID59463842
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID15466386
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID9979674
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID421071796

Total number of triples: 321.