http://rdf.ncbi.nlm.nih.gov/pubchem/patent/SK-35097-A3
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_5c24684033fba97d1ad845ce453a57e3 http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_69ece09bafee7e0c49d1f7951a3faa2c |
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D405-14 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P19-08 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D471-04 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D471-10 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D401-12 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D403-12 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D307-80 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D233-36 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D249-14 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D233-96 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D235-30 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P9-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P9-08 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P9-10 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P27-02 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D233-52 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P29-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D233-72 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P3-08 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P3-14 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P35-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P43-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D239-18 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P13-02 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P13-12 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P15-00 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D471-10 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D471-04 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D233-24 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P3-08 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P29-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P15-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P13-02 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D491-04 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P35-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P27-02 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P43-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P9-08 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P9-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P9-10 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-41 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-415 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-4166 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-435 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-505 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D233-76 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D405-14 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D403-12 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D233-96 |
| filingDate | 1997-03-18-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_3346c3f0fb6cf6de026b30795ded3b1c http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_63fc84f4cdf91ed3ed04e7a6285170c7 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a257a45b7e6c125d9049f3f0abfb8cd7 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f9d7c44789b09a7a3720fc6281cae450 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_5fb4743d4ae59b710dac235ba60a3c0c http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_541ee2271d6a071958685cc2151505de http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_54fed6578b8ecdb8fc0584df1fe43496 |
| publicationDate | 1997-10-08-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | SK-35097-A3 |
| titleOfInvention | Fivemembered heterocycles, preparation method thereof, pharmaceutical compositions containing them, and their use as bone resorption inhibitors and antagonists of the vintronectin receptor |
| abstract | 5-Membered azacyclic derivatives (I) and their salts are new. W = C(R<16>)-D-B-A-R<1> (a), C=C(R<16>)-D-B-A-R<1> (b) or a group of formula (c) or (d); the ring of formula (e) is saturated or partly or fully unsaturated, and optionally contains 1 or 2 N, O and/or S atoms and is optionally mono-, di- or trisubstituted by R<16> or mono- or disubstituted by =Q; Y = CQ or CH2; Z = N(R<0>), Q or CH2; A = bond, 1-8C alkanediyl, CR<2>=NNR<2>, NR<2>CQNR<2>, QCQ'NR<2>, NR<2>S(O)nNR<2>, OS(O)nNR<2>, S(O)nNR<2>, 3-12 cycloalkanediyl, C IDENTICAL C, NR<2>CO, CONR<2>, NR<2>CO-5-14C arylene, O, S(O)n, 5-14C arylene, CO, CO-5-14C arylene, NR<2>, NR<2>SO2, OCO, COO, N=CR<2> CR<2>=N, CR<2>=CR<3> or S(O)n-5-14C arylene (all optionally substituted by NR<2> and/or by 1 or 2 1-8C alkanediyl); Q, Q' = O or S; B = bond, 1-8C alkanediyl, 5-10C arylene, 3-8C cycloalkanediyl, C IDENTICAL C, NR<2>, CO, CONR<2>, NR<2>CO, NR<2>-CQ-NR<2>, OCO, COO, SO, SO2, SONR<2>, SO2NR<2>, NR<2>SO, NR<2>SO2, Q or CR<2>=CR<3> (all optionally mono- or disubstitute d by 1-6C alkanediyl) or a divalent residue of a 5-6 membered saturated or unsaturated ring containing 1 or 2 N atoms (optionally mono- or disubstituted substituted by 1-6C alkyl or =Q); D, F = bond, 1-8C alkanediyl, 5-10C arylene, Q, NR<2>, CONR<2>, NR<2>CO, NR<2>CQNR<2>, OCO, COO, CQ, SO, SO2, SO2NR<2>, NR<2>SO, NR<2>SO2, CR<2>=CR<3>, C IDENTICAL C, CR<2>=NNR<2>, N=CR<2>, CR<2>=N or CHOH (all optionally mono- or disubstituted by 1-8C alkanediyl, CR<2>=CR<3> or 5-6C arylene); E = bond, 1-6C alkanediyl, 2-6C alkenediyl, 2-6C alkynediyl, phenylene, phenylene-1-3C alkanediyl or 1-3C alkanediyl-phenylene; G = CR<4>R<5)<CR<6>R<7>)p(CH2)qR<10>; L = C(R<16>) or N; R<0> = H, 1-8C alkyl (optionally substituted by 3-12C cycloalkyl or 5-14C aryl), 1-8C alkylcarbonyl, 3-12C cycloalkyl-carbonyl, (3-12C cycloalkyl- or 5-14C aryl-substituted) 1-6C alkylcarbonyl, 5-14C aryl-carbonyl, 3-12C cycloalkyl or 5-14C aryl (where all alkyl are optionally substituted by 1 or more F); R<1> = NR<2>CR<2)<=NR<2>), C(=NR<2>)NR<2>R<3>, NR<2>C(=NR<2>)NR<2>R<3>, or a 4-14 membered mono- or polycyclic optionally aromatic ring (optionally containing 1-4 N, O and/or S and optionally substituted by R<12>-R<15>); R<2>, R<3> = H. 1-10C alkyl (optionally substituted by 1 or more F), 3-12C cycloalkyl, 3-12C cycloalkyl-1-8C alkyl, 5-14C aryl, 5-14C aryl-1-8C alkyl, NH2; NR<9>OR<8>, R<9>OR<8>, R<9>COOR<8>, R<9>-5-14C aryl-R<8>, R<9>N(R<8>)2, R<9>-NR<8>-(1-8C hydroxyalkyl), R<9>CON(R<8>)2, R<9>NR<8>COR<8>, R<9>COR8, C(=NR<8>)N(R<8>)2; NR<8>C(=NR<8>)N(R<8>)2 or (1-18C alkyl)-COO-1-6C alkoxycarbonyl; R<4>-R<7> = H, F, OH, 1-8C alkyl, 3-12C cycloalkyl, 3-12C cycloalkyl-1-8C alkyl, R<9>QR<8>, R<9>OCOR<8>, R<9>COOR<8>, R<9>-5-14C aryl-R<8>, R<9>N(R<2>)R<8>, R<9>N(R<8>)2, R<9>OCONR<8>R<2>, R<9>N(R<2>)S(O)nR<8>, R<9>NR<2>COQR<8>, R<9>NR<2>COR<8>, R<9>N(R<2>)CON(R<2>)R<8>, R<9>N(R<2>)S(O)nNR<2>R<8>, R<9>S(O)nR<8>, R<9>NR<2>COSR<8>, R<9>COR<8>, R<9>CONR<2>R<8> or R<9>S(O)nNR<2>R<8>; R<8> = H, 1-8C alkyl (optionally substituted by 3-12C cycloalkyl or 5-14C aryl), 3-12C cycloalkyl or 5-14C aryl (where all alkyl are optionally substituted by 1 or more F); R<9> = bond or 1-8C alkanediyl; R<10> = CQR<11>, S(O)nR<11>, P(O)nR<11> or a 4-8 membered saturated or unsaturated heterocycle containing 1-4 N, O and/or S atoms; R<11> = OH, 1-8C alkoxy, 5-14C aryl-1-8C alkoxy, 5-14C aryloxy, 1-8C alkylcarbonyloxy-1-4C alkoxy, 5-14C aryl-1-8C alkylcarbonyloxy-1-4C alkoxy, NH2, mono- or di-1-8C alkylamino, 5-14C aryl-1-8C alkylamino, 1-8C dialkylaminocarbonylmethoxy, 5-14C aryl-1-8C dialkylaminocarbonylmethoxy, 5-14C arylamino or a D- or L-amino acid; R<12>-R<15> = H, 1-10C alkyl (optionally substituted by one or more F), 3-12C cycloalkyl, 3-12C cycloalkyl-1-8C alkyl, 5-14C aryl, 5-14C aryl-1-8C alkyl, NH2, R<9>OR<8>, R<9>COOR<8>, R<9>N(R<8>)2, R<9>-5-14C aryl-R<8>; R<9>-NR<2> (1-8C hydroxyalkyl), R<9>CON(R<2>)R<8>, R<9>N(R<2>)COR<8>, R<9>COR<8>, NR<2>C(=NR<3>)-NR<2>R<3>, C(=NR<2>)NR<2>R<3> or Q; or 2 of R<12>-R<15> which are adjacent form -OCH2O-, -OCH2CH2O- or -OC(CH3)2O-; R<16> = H, 1-10C alkyl optionally substituted by 1 or more F, 3-12C cycloalkyl, 3-12C cycloalkyl-1-8C alkyl, 5-14C aryl, 5-14C aryl-1-8C alkyl, 2-20C alkenyl or 2-10C alkynyl; m = 1-6; n = 1 or 2; p, q = 0 or 1; with provisos. |
| priorityDate | 1996-03-20-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
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Total number of triples: 462.