http://rdf.ncbi.nlm.nih.gov/pubchem/patent/ES-2529075-T3

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filingDate 2011-02-08-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2015-02-16-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_88393d0e89747783bceac6dec0087f04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_4626592dc7703e1c33bc24bc55cd5d9e
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publicationDate 2015-02-16-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber ES-2529075-T3
titleOfInvention Progesterone receptor antagonist agents
abstract Compounds of the formula I ** Formula ** wherein R1 represents either a radical Y or a phenyl ring substituted with Y, ** Formula ** Y represents a group R2 and R3 are the same or different and represent hydrogen, a C1-C6 alkyl radical, optionally substituted with N (CH3) 2, ** Formula ** or - NHC (O) CH3, ** Formula ** a radical or a 6-10 membered aryl radical, which is eventually substituted once, twice or multiple times with halogen (-F, -Cl, -Br, -I), -OH, -O-alkyl, -C (O) OH, -C (O) O-alkyl, -C (O) NH2, -C (O) NH-alkyl, -C (O) N-dialkyl, -C (O) NH-aryl, -C (O) NH-heteroaryl, -NH2, -NH (C1 alkyl -C6), -N (C1-C6 alkyl) 2, in particular with -N (CH3) 2, -NHC (O) -alkyl, -NO2, -N3, -CN, -C1-C6 alkyl, - perfluoro-C1-C6 alkyl, -C1-C6 acyl, -C1-C6 acyloxy, -SO2NH2, -SO2NH-alkyl or -SO2N-dialkyl, a 5-10 membered heteroaryl radical, which is eventually substituted once , twice or multiple times with the substituents of the aryl radical d e 6-10 members mentioned above, a C1-C6 arylalkyl radical, which is optionally substituted next to the aryl ring once, twice or multiple times with the substituents of the 6-10 member aryl radical which more above, or a C1-C6 heteroarylalkyl radical, which is optionally substituted by the heteroaryl ring once, twice or multiple times with the 6-10 membered aryl radical substituents mentioned above, or but R2 and R3 in common are a component part of a 3-10 membered ring that is optionally substituted by a carbon with alkyl, carboxyl, alkoxycarbonyl, alkylcarbonyl, aminocarbonyl, aryl, in particular with phenyl, arylalkyl, heteroaryl, heteroarylalkyl, aminoalkyl or dimethylaminoalkyl, or respectively together with a nitrogen with alkyl, alkanoyl, carboxyl, alkoxycarbonyl, aryl, in particular with phenyl, pyridinyl, pyrimidinyl, pyrazinyl, sul Fonyl, benzoyl, alkylsulfonyl, arylsulfonyl, aminocarbonyl, dimethylaminocarbonyl, aminocarbonylalkyl, alkylaminocarbonylalkyl, arylalkyl, in particular with phenylalkyl, heterocyclylalkyl, heteroarylalkyl, aminoalkyl or, ** Formula which may eventually be nitrogen, which may be oxygen, which may be nitrogen, which may be oxygen, which may be oxygen, which may be oxygen, which may be oxygen, which may be oxygen oxidized to give the sulfoxide or the sulfone, possibly an aromatic radical being condensed next to the 3-10 membered ring, X means an oxygen atom, NOR4 or NNHSO2R4 and R4 is chosen from the group comprising hydrogen, C1- alkyl C6 and aryl, and their salts, solvates or solvates of the salts including all crystalline modifications (the * symbolizes the site of attachment to the fundamental framework).
priorityDate 2010-02-10-04:00^^<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/compound/CID10553
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID424411548
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID55245
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID6230
http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCP70091
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID449982031
http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCP19098
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID451567981
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID31398787
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID11954
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID220407
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID7150
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID415841605
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419536462
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419523300
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID40973
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID602506
http://rdf.ncbi.nlm.nih.gov/pubchem/gene/GID13075
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419556970
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID412298159
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID84266
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID68294
http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCQ29605
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID454557040
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID12680363
http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCF1NRL7
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID458393376
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID5991
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID6440511
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID12113982
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID416116656

Total number of triples: 313.