KR20110137377A - 치환된 스피로-아미드 화합물 - Google Patents
치환된 스피로-아미드 화합물 Download PDFInfo
- Publication number
- KR20110137377A KR20110137377A KR1020117025143A KR20117025143A KR20110137377A KR 20110137377 A KR20110137377 A KR 20110137377A KR 1020117025143 A KR1020117025143 A KR 1020117025143A KR 20117025143 A KR20117025143 A KR 20117025143A KR 20110137377 A KR20110137377 A KR 20110137377A
- Authority
- KR
- South Korea
- Prior art keywords
- diazaspiro
- carbonyl
- dihydro
- inden
- ind
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
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- 0 CN1CCN(*)CC1 Chemical compound CN1CCN(*)CC1 0.000 description 19
- AVFZOVWCLRSYKC-UHFFFAOYSA-N CN1CCCC1 Chemical compound CN1CCCC1 AVFZOVWCLRSYKC-UHFFFAOYSA-N 0.000 description 3
- PAMIQIKDUOTOBW-UHFFFAOYSA-N CN1CCCCC1 Chemical compound CN1CCCCC1 PAMIQIKDUOTOBW-UHFFFAOYSA-N 0.000 description 2
- SJRJJKPEHAURKC-UHFFFAOYSA-N CN1CCOCC1 Chemical compound CN1CCOCC1 SJRJJKPEHAURKC-UHFFFAOYSA-N 0.000 description 2
- JVVCBFHTFCFZHF-UHFFFAOYSA-N C(C1)CNCC1(CC1)CCN1c1ccncc1 Chemical compound C(C1)CNCC1(CC1)CCN1c1ccncc1 JVVCBFHTFCFZHF-UHFFFAOYSA-N 0.000 description 1
- JNVWQHJNDBJJGP-UHFFFAOYSA-N C(CC1(CC2)CCNCC1)C2Oc1ccncc1 Chemical compound C(CC1(CC2)CCNCC1)C2Oc1ccncc1 JNVWQHJNDBJJGP-UHFFFAOYSA-N 0.000 description 1
- XPTSEPHTIHPTNN-UHFFFAOYSA-N C(CC1(CCNCC1)C1)CN1c1ccncc1 Chemical compound C(CC1(CCNCC1)C1)CN1c1ccncc1 XPTSEPHTIHPTNN-UHFFFAOYSA-N 0.000 description 1
- GREMFGOCNFLAES-UHFFFAOYSA-N C(CN(C1)c2ccncc2)C11CCNCC1 Chemical compound C(CN(C1)c2ccncc2)C11CCNCC1 GREMFGOCNFLAES-UHFFFAOYSA-N 0.000 description 1
- SUEIREMUBJAJLP-UHFFFAOYSA-N C(CNCC1)C1(CC1)CCN1c1cnccn1 Chemical compound C(CNCC1)C1(CC1)CCN1c1cnccn1 SUEIREMUBJAJLP-UHFFFAOYSA-N 0.000 description 1
- GUIHWXNNSVPRBL-UHFFFAOYSA-N C(c1ccncc1)N1CCC2(CCNCC2)CC1 Chemical compound C(c1ccncc1)N1CCC2(CCNCC2)CC1 GUIHWXNNSVPRBL-UHFFFAOYSA-N 0.000 description 1
- SUGRHKFXYGMJEY-SNAWJCMRSA-N C/C(/ON=C)=N\C Chemical compound C/C(/ON=C)=N\C SUGRHKFXYGMJEY-SNAWJCMRSA-N 0.000 description 1
- BCYZYTYXBSMZMY-PLNGDYQASA-N C/C=C\NN(C)C Chemical compound C/C=C\NN(C)C BCYZYTYXBSMZMY-PLNGDYQASA-N 0.000 description 1
- PVRCPAUXRKKPEW-UHFFFAOYSA-N CC(C)(Cc(cc1)c2cc1C(O)=O)C2NC(c1ccccc1Cl)=O Chemical compound CC(C)(Cc(cc1)c2cc1C(O)=O)C2NC(c1ccccc1Cl)=O PVRCPAUXRKKPEW-UHFFFAOYSA-N 0.000 description 1
- PIMSOQGSBHTPCE-UHFFFAOYSA-N CC(C)(Cc(cc1)c2cc1C(OC)=O)C2NC(c(cccc1)c1Cl)=O Chemical compound CC(C)(Cc(cc1)c2cc1C(OC)=O)C2NC(c(cccc1)c1Cl)=O PIMSOQGSBHTPCE-UHFFFAOYSA-N 0.000 description 1
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- NPOZBHCPELPGKW-UHFFFAOYSA-N CC(C)C[n]1cncc1 Chemical compound CC(C)C[n]1cncc1 NPOZBHCPELPGKW-UHFFFAOYSA-N 0.000 description 1
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- BFBZQWQKWJTPPY-UHFFFAOYSA-N CCCC(CC(CC1)(c(cc2)ccc2F)N(C)C)C11CCNCC1 Chemical compound CCCC(CC(CC1)(c(cc2)ccc2F)N(C)C)C11CCNCC1 BFBZQWQKWJTPPY-UHFFFAOYSA-N 0.000 description 1
- MAHIJGIMXRYUMB-UHFFFAOYSA-N CN(C)c(cccc1)c1N=C Chemical compound CN(C)c(cccc1)c1N=C MAHIJGIMXRYUMB-UHFFFAOYSA-N 0.000 description 1
- CDRRCHLZTHXXAY-UHFFFAOYSA-N CN(CC1)CC1(CC1)CCC1(c1ccncc1)O Chemical compound CN(CC1)CC1(CC1)CCC1(c1ccncc1)O CDRRCHLZTHXXAY-UHFFFAOYSA-N 0.000 description 1
- NGRPMKDQZYCTAK-UHFFFAOYSA-N CN(CC1)CC1(CC1)CCN1c(cc1)ccc1Cl Chemical compound CN(CC1)CC1(CC1)CCN1c(cc1)ccc1Cl NGRPMKDQZYCTAK-UHFFFAOYSA-N 0.000 description 1
- IVMSMOWNKQAHHN-UHFFFAOYSA-N CN(CC1)CC1(CC1)CCN1c1ccccn1 Chemical compound CN(CC1)CC1(CC1)CCN1c1ccccn1 IVMSMOWNKQAHHN-UHFFFAOYSA-N 0.000 description 1
- XJGNCNRATMSRRB-UHFFFAOYSA-N CN(CC1)CC1(CC1)CCN1c1cccnc1 Chemical compound CN(CC1)CC1(CC1)CCN1c1cccnc1 XJGNCNRATMSRRB-UHFFFAOYSA-N 0.000 description 1
- KDJQEIBGIJZCBW-UHFFFAOYSA-N CN(CC1)CC1(CC1)CCN1c1ccnc(C(F)(F)F)c1 Chemical compound CN(CC1)CC1(CC1)CCN1c1ccnc(C(F)(F)F)c1 KDJQEIBGIJZCBW-UHFFFAOYSA-N 0.000 description 1
- YZIMKPVELHMYKS-UHFFFAOYSA-N CN(CC1)CC1(CC1)CN1c1ccncc1 Chemical compound CN(CC1)CC1(CC1)CN1c1ccncc1 YZIMKPVELHMYKS-UHFFFAOYSA-N 0.000 description 1
- MPNOVHORSSFHBA-UHFFFAOYSA-N CN(CC1)CC1(CCC1)CN1c1ccncc1 Chemical compound CN(CC1)CC1(CCC1)CN1c1ccncc1 MPNOVHORSSFHBA-UHFFFAOYSA-N 0.000 description 1
- MCWZMOAGSAWBAV-UHFFFAOYSA-N CN(CC1)CCC1(CC1)CCN1c1ccc(C(F)(F)F)cc1 Chemical compound CN(CC1)CCC1(CC1)CCN1c1ccc(C(F)(F)F)cc1 MCWZMOAGSAWBAV-UHFFFAOYSA-N 0.000 description 1
- SSGAPMMTTZZHFI-UHFFFAOYSA-N CN(CC1)CCC1(CC1)CCN1c1cccnc1 Chemical compound CN(CC1)CCC1(CC1)CCN1c1cccnc1 SSGAPMMTTZZHFI-UHFFFAOYSA-N 0.000 description 1
- HECNAASYBFJRIJ-UHFFFAOYSA-N CN(CC1)CCC1(CC1)CCN1c1ccncc1 Chemical compound CN(CC1)CCC1(CC1)CCN1c1ccncc1 HECNAASYBFJRIJ-UHFFFAOYSA-N 0.000 description 1
- UIISXJKQBIPGAD-UHFFFAOYSA-N CN(CC1)CCC1(CC1)CCN1c1ncccc1 Chemical compound CN(CC1)CCC1(CC1)CCN1c1ncccc1 UIISXJKQBIPGAD-UHFFFAOYSA-N 0.000 description 1
- ZBOGVZXNICFCQB-UHFFFAOYSA-N CN(CC1)CCC1N(CC1)CCC1(CC1)CCN1I Chemical compound CN(CC1)CCC1N(CC1)CCC1(CC1)CCN1I ZBOGVZXNICFCQB-UHFFFAOYSA-N 0.000 description 1
- BUCNASUOQSTXIN-UHFFFAOYSA-N CN1CCC(CN2CCC3(CCN(C)CC3)CC2)CC1 Chemical compound CN1CCC(CN2CCC3(CCN(C)CC3)CC2)CC1 BUCNASUOQSTXIN-UHFFFAOYSA-N 0.000 description 1
- GQCXXSBYRZSSKM-ZDUSSCGKSA-N COC(c(cc1)cc2c1OCC[C@H]2CNC(c(cccc1)c1Cl)=O)=O Chemical compound COC(c(cc1)cc2c1OCC[C@H]2CNC(c(cccc1)c1Cl)=O)=O GQCXXSBYRZSSKM-ZDUSSCGKSA-N 0.000 description 1
- CQYOOEXLNATOHG-KRWDZBQOSA-N COC(c1ccc(CCC[C@@H]2NC(c(cccc3)c3Cl)=O)c2c1)=O Chemical compound COC(c1ccc(CCC[C@@H]2NC(c(cccc3)c3Cl)=O)c2c1)=O CQYOOEXLNATOHG-KRWDZBQOSA-N 0.000 description 1
- QLXFRNKKBOZWNH-UHFFFAOYSA-N C[N+]1(CCC1)[SH-]C Chemical compound C[N+]1(CCC1)[SH-]C QLXFRNKKBOZWNH-UHFFFAOYSA-N 0.000 description 1
- SMZCNCDZWBWQRI-MRXNPFEDSA-N Cc(cc(CC[C@H]1NC(c(cccc2)c2Cl)=O)c1c1)c1C(O)=O Chemical compound Cc(cc(CC[C@H]1NC(c(cccc2)c2Cl)=O)c1c1)c1C(O)=O SMZCNCDZWBWQRI-MRXNPFEDSA-N 0.000 description 1
- MRXNXDNMNUHFEE-GOSISDBHSA-N Cc(cc(cc1C)OC)c1S(N[C@H]1c2cc(C(O)=O)ccc2CCC1)(=O)=O Chemical compound Cc(cc(cc1C)OC)c1S(N[C@H]1c2cc(C(O)=O)ccc2CCC1)(=O)=O MRXNXDNMNUHFEE-GOSISDBHSA-N 0.000 description 1
- UWXXWXUEQLQPSN-LJQANCHMSA-N Cc(cc(cc1C)OC)c1S(N[C@H]1c2cc(C(OC)=O)ccc2CCC1)(O)=O Chemical compound Cc(cc(cc1C)OC)c1S(N[C@H]1c2cc(C(OC)=O)ccc2CCC1)(O)=O UWXXWXUEQLQPSN-LJQANCHMSA-N 0.000 description 1
- ORKAEJVWXGHTFN-MRXNPFEDSA-N Cc(cccc1)c1C(N[C@H](CC1)c2c1ccc(C(O)=O)c2)=O Chemical compound Cc(cccc1)c1C(N[C@H](CC1)c2c1ccc(C(O)=O)c2)=O ORKAEJVWXGHTFN-MRXNPFEDSA-N 0.000 description 1
- CRDLHQNHUYIUPH-QGZVFWFLSA-N Cc(cccc1)c1C(N[C@H](CC1)c2c1ccc(C(OC)=O)c2)=O Chemical compound Cc(cccc1)c1C(N[C@H](CC1)c2c1ccc(C(OC)=O)c2)=O CRDLHQNHUYIUPH-QGZVFWFLSA-N 0.000 description 1
- YKPWOLLABDRWIW-SNVBAGLBSA-N Cc1cc(CC[C@H]2N)c2cc1C(O)=O Chemical compound Cc1cc(CC[C@H]2N)c2cc1C(O)=O YKPWOLLABDRWIW-SNVBAGLBSA-N 0.000 description 1
- RSWVDKOTHOHNSR-UHFFFAOYSA-O FC(C1)(CN1C(CC1)CCC11CC[NH2+]CC1)F Chemical compound FC(C1)(CN1C(CC1)CCC11CC[NH2+]CC1)F RSWVDKOTHOHNSR-UHFFFAOYSA-O 0.000 description 1
- NNONYXVGCAAJBP-UHFFFAOYSA-N FC(c(cc1)ccc1N1CCC2(CNCC2)CC1)(F)F Chemical compound FC(c(cc1)ccc1N1CCC2(CNCC2)CC1)(F)F NNONYXVGCAAJBP-UHFFFAOYSA-N 0.000 description 1
- MZBHQUMZBYMIJC-UHFFFAOYSA-N Fc(cc1)ccc1N(CC1)CCC1(CC1)CCN1I Chemical compound Fc(cc1)ccc1N(CC1)CCC1(CC1)CCN1I MZBHQUMZBYMIJC-UHFFFAOYSA-N 0.000 description 1
- QRIGLXXCRBPHPW-UHFFFAOYSA-O Fc(cc1)ccc1N1CCC2(C[NH2+]CC2)CC1 Chemical compound Fc(cc1)ccc1N1CCC2(C[NH2+]CC2)CC1 QRIGLXXCRBPHPW-UHFFFAOYSA-O 0.000 description 1
- VMHYWKBKHMYRNF-UHFFFAOYSA-N O=C(c1ccccc1)c1ccccc1Cl Chemical compound O=C(c1ccccc1)c1ccccc1Cl VMHYWKBKHMYRNF-UHFFFAOYSA-N 0.000 description 1
- ONIKNECPXCLUHT-UHFFFAOYSA-N O=C(c1ccccc1Cl)Cl Chemical compound O=C(c1ccccc1Cl)Cl ONIKNECPXCLUHT-UHFFFAOYSA-N 0.000 description 1
- SAIPYNSOQGKXSR-UHFFFAOYSA-N OC(C(c1ccccc1)c1ccccc1Cl)=O Chemical compound OC(C(c1ccccc1)c1ccccc1Cl)=O SAIPYNSOQGKXSR-UHFFFAOYSA-N 0.000 description 1
- JZASDHMSVHTJLZ-CQSZACIVSA-N OC(c(cc1)cc2c1OCC[C@H]2NC(c(cccc1)c1Cl)=O)=O Chemical compound OC(c(cc1)cc2c1OCC[C@H]2NC(c(cccc1)c1Cl)=O)=O JZASDHMSVHTJLZ-CQSZACIVSA-N 0.000 description 1
- QTDLEEXQXRWYLB-UHFFFAOYSA-N OC(c(cccc1)c1Cl)Cl Chemical compound OC(c(cccc1)c1Cl)Cl QTDLEEXQXRWYLB-UHFFFAOYSA-N 0.000 description 1
- CBMFHSZHCVEYME-INIZCTEOSA-N OC(c1ccc(CCC[C@@H]2NC(c(cccc3)c3Cl)=O)c2c1)=O Chemical compound OC(c1ccc(CCC[C@@H]2NC(c(cccc3)c3Cl)=O)c2c1)=O CBMFHSZHCVEYME-INIZCTEOSA-N 0.000 description 1
- AWJUIBRHMBBTKR-UHFFFAOYSA-N c(cc1)cc2c1cncc2 Chemical compound c(cc1)cc2c1cncc2 AWJUIBRHMBBTKR-UHFFFAOYSA-N 0.000 description 1
- SMWDFEZZVXVKRB-UHFFFAOYSA-N c(cc1)cc2c1nccc2 Chemical compound c(cc1)cc2c1nccc2 SMWDFEZZVXVKRB-UHFFFAOYSA-N 0.000 description 1
- XSCHRSMBECNVNS-UHFFFAOYSA-N c(cc1)cc2c1nccn2 Chemical compound c(cc1)cc2c1nccn2 XSCHRSMBECNVNS-UHFFFAOYSA-N 0.000 description 1
- GUJPOATUKJUDJT-UHFFFAOYSA-N c1ccc(C=[I]N=C2)c2c1 Chemical compound c1ccc(C=[I]N=C2)c2c1 GUJPOATUKJUDJT-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/10—Spiro-condensed systems
-
- A—HUMAN NECESSITIES
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- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
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- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/4353—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems
- A61K31/4355—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system containing a five-membered ring having oxygen as a ring hetero atom
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- A—HUMAN NECESSITIES
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- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/438—The ring being spiro-condensed with carbocyclic or heterocyclic ring systems
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- A—HUMAN NECESSITIES
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- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/439—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom the ring forming part of a bridged ring system, e.g. quinuclidine
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- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/4427—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
- A61K31/4439—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. omeprazole
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- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/4427—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
- A61K31/444—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a six-membered ring with nitrogen as a ring heteroatom, e.g. amrinone
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- A61K31/47—Quinolines; Isoquinolines
- A61K31/4709—Non-condensed quinolines and containing further heterocyclic rings
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- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/47—Quinolines; Isoquinolines
- A61K31/472—Non-condensed isoquinolines, e.g. papaverine
- A61K31/4725—Non-condensed isoquinolines, e.g. papaverine containing further heterocyclic rings
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- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/496—Non-condensed piperazines containing further heterocyclic rings, e.g. rifampin, thiothixene or sparfloxacin
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- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/4985—Pyrazines or piperazines ortho- or peri-condensed with heterocyclic ring systems
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- A—HUMAN NECESSITIES
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- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
- A61K31/506—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim not condensed and containing further heterocyclic rings
-
- A—HUMAN NECESSITIES
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- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/55—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole
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| Publication number | Priority date | Publication date | Assignee | Title |
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| CN102369186B (zh) | 2009-04-02 | 2014-07-09 | 默克专利有限公司 | 作为自分泌运动因子抑制剂的哌啶和哌嗪衍生物 |
| DK2547679T3 (en) * | 2010-03-19 | 2016-01-11 | Pfizer | 2,3 dihydro-1H-inden-1-yl-2,7-diazaspiro [3.6] nonane derivatives and their use as antagonists or inverse agonists of ghrelin receptor |
| US8809552B2 (en) * | 2011-11-01 | 2014-08-19 | Hoffmann-La Roche Inc. | Azetidine compounds, compositions and methods of use |
| CN104364239B (zh) | 2012-06-13 | 2017-08-25 | 霍夫曼-拉罗奇有限公司 | 二氮杂螺环烷烃和氮杂螺环烷烃 |
| MX368615B (es) | 2012-09-25 | 2019-10-09 | Hoffmann La Roche | Derivados bicíclicos como inhibidores de la autotaxina (atx) que son inhibidores de la producción de ácido lisofosfatídico (lpa) y el uso de los mismos. |
| AR095079A1 (es) | 2013-03-12 | 2015-09-16 | Hoffmann La Roche | Derivados de octahidro-pirrolo[3,4-c]-pirrol y piridina-fenilo |
| MX377396B (es) | 2013-09-12 | 2025-03-10 | Janssen Biopharma Inc | Compuestos de azapiridona y usos de los mismos. |
| DK3074400T3 (en) | 2013-11-26 | 2018-01-15 | Hoffmann La Roche | Octahydro-cyclobuta [1,2-c; 3,4-c '] dipyrrole derivatives as autotaxin inhibitors |
| CA2937616A1 (en) | 2014-03-26 | 2015-10-01 | F. Hoffmann-La Roche Ag | Bicyclic compounds as autotaxin (atx) and lysophosphatidic acid (lpa) production inhibitors |
| EA032357B1 (ru) | 2014-03-26 | 2019-05-31 | Ф. Хоффманн-Ля Рош Аг | Конденсированные [1,4]диазепиновые соединения в качестве ингибиторов продукции аутотаксина (atx) и лизофосфатидиловой кислоты (lpa) |
| HUE040133T2 (hu) * | 2014-07-15 | 2019-02-28 | Gruenenthal Gmbh | Szubsztituált azaspiro(4.5)dekán származékok |
| US10208045B2 (en) | 2015-03-11 | 2019-02-19 | Alios Biopharma, Inc. | Aza-pyridone compounds and uses thereof |
| CN106008503B (zh) * | 2015-03-31 | 2020-09-01 | 齐鲁制药有限公司 | 螺环芳基砜作为蛋白激酶抑制剂 |
| MA41898A (fr) | 2015-04-10 | 2018-02-13 | Hoffmann La Roche | Dérivés de quinazolinone bicyclique |
| CA2992889A1 (en) | 2015-09-04 | 2017-03-09 | F. Hoffmann-La Roche Ag | Phenoxymethyl derivatives |
| BR112017026682A2 (pt) | 2015-09-24 | 2018-08-14 | Hoffmann La Roche | novos compostos bicíclicos como inibidores de dupla ação de atx/ca |
| JP6876685B2 (ja) | 2015-09-24 | 2021-05-26 | エフ.ホフマン−ラ ロシュ アーゲーF. Hoffmann−La Roche Aktiengesellschaft | Atx阻害剤としての二環式化合物 |
| AU2016328436B2 (en) | 2015-09-24 | 2020-05-14 | F. Hoffmann-La Roche Ag | New bicyclic compounds as dual ATX/CA inhibitors |
| WO2017050732A1 (en) | 2015-09-24 | 2017-03-30 | F. Hoffmann-La Roche Ag | Bicyclic compounds as atx inhibitors |
| TW201726678A (zh) | 2015-10-30 | 2017-08-01 | 赫孚孟拉羅股份公司 | 嘧啶酮衍生物及其於治療、改善或預防病毒性疾病之用途 |
| AU2016378579A1 (en) * | 2015-12-22 | 2018-06-14 | Vitae Pharmaceuticals, Inc. | Inhibitors of the menin-MLL interaction |
| CA3011180A1 (en) | 2016-01-13 | 2017-07-20 | Grunenthal Gmbh | 3-(carboxymethyl)-8-amino-2-oxo-1,3-diaza-spiro-[4.5]-decane derivatives |
| CA3011176C (en) | 2016-01-13 | 2023-09-19 | Grunenthal Gmbh | 3-((hetero-)aryl)-8-amino-2-oxo-1,3-diaza-spiro-[4.5]-decane derivatives |
| SI3402782T1 (sl) | 2016-01-13 | 2020-11-30 | Grunenthal Gmbh | 8-amino-2-okso-1,3-diaza-spiro-(4,5)-dekanski derivati |
| PL3429591T3 (pl) | 2016-03-16 | 2023-07-17 | Kura Oncology, Inc. | Podstawione pochodne tieno[2,3-d]pirymidyny jako inhibitory meniny-mll i metody ich zastosowania |
| US11401255B2 (en) | 2016-07-28 | 2022-08-02 | Mayo Foundation For Medical Education And Research | Small molecule activators of Parkin enzyme function |
| EP3366683A1 (en) * | 2017-02-28 | 2018-08-29 | Acousia Therapeutics GmbH | Cyclic amides, acteamides and ureas useful as potassium channel openers |
| RU2019132254A (ru) | 2017-03-16 | 2021-04-16 | Ф. Хоффманн-Ля Рош Аг | Гетероциклические соединения, пригодные в качестве дуальных ингибиторов atx/ca |
| JP7090099B2 (ja) | 2017-03-16 | 2022-06-23 | エフ.ホフマン-ラ ロシュ アーゲー | Atxインヒビターとしての新規二環式化合物 |
| EP3684361A4 (en) * | 2017-09-20 | 2021-09-08 | Kura Oncology, Inc. | SUBSTITUTED INHIBITORS OF MENIN-MLL AND METHOD OF USING |
| WO2019200114A1 (en) * | 2018-04-12 | 2019-10-17 | Arbutus Biopharma Corporation | Methods for preparing substituted dihydroindene-4-carboxamide compounds |
| CN111434664A (zh) * | 2019-01-13 | 2020-07-21 | 西南大学 | 亚胺螺环哌啶类化合物的合成及应用 |
| BR112023015210A2 (pt) | 2021-01-29 | 2023-11-07 | Cedilla Therapeutics Inc | Inibidores de cdk2 e métodos de uso dos mesmos |
| CA3225439A1 (en) | 2021-06-26 | 2022-12-29 | Cedilla Therapeutics, Inc. | Cdk2 inhibitors and methods of using the same |
| CN113976072B (zh) * | 2021-11-10 | 2024-02-23 | 武汉青风凯默生物医药科技有限公司 | 一种4-甲酰基-n-cbz哌啶的制备装置及方法 |
| EP4530282A4 (en) | 2022-04-28 | 2026-05-06 | Sds Biotech Corp | Haloalkyl sulfone anilide compound and herbicide containing same |
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| WO2000012077A1 (en) * | 1998-09-01 | 2000-03-09 | Bristol-Myers Squibb Company | Potassium channel inhibitors and method |
| US6686370B2 (en) * | 1999-12-06 | 2004-02-03 | Euro-Celtique S.A. | Triazospiro compounds having nociceptin receptor affinity |
| WO2005087236A1 (en) | 2004-03-11 | 2005-09-22 | Glaxo Group Limited | Novel m3 muscarinic acetylcholine receptor antagonists |
| EP1740579B1 (en) | 2004-03-24 | 2015-08-19 | AbbVie Inc. | Tricyclic pyrazole kinase inhibitors |
| AU2005314601A1 (en) * | 2004-10-15 | 2006-06-15 | Bayer Pharmaceuticals Corporation | Indane amides with antiproliferative activity |
| CN101103016A (zh) * | 2004-11-18 | 2008-01-09 | 因塞特公司 | 11-β羟基类固醇脱氢酶1型抑制剂及其使用方法 |
| JP2008537953A (ja) * | 2005-04-15 | 2008-10-02 | エラン ファーマシューティカルズ,インコーポレイテッド | ブラジキニンb1受容体拮抗作用に有用な新規化合物 |
| DE102005030051A1 (de) * | 2005-06-27 | 2006-12-28 | Grünenthal GmbH | Substituierte 1-Oxa-3,8-diazaspiro[4,5]-decan-2-on-Verbindungen und deren Verwendung zur Herstellung von Arzneimitteln |
| WO2007011809A1 (en) * | 2005-07-19 | 2007-01-25 | Merck & Co., Inc. | Spirochromanone derivatives as acetyl coenzyme a carboxylase (acc) inhibitors |
| WO2007101007A2 (en) | 2006-02-23 | 2007-09-07 | Neurogen Corporation | Aryl sulfonyl heterocycles |
| WO2007140383A2 (en) | 2006-05-30 | 2007-12-06 | Neurogen Corporation | Spirocyclic sulfonamides and related compounds |
| RU2462464C2 (ru) | 2006-09-29 | 2012-09-27 | Грюненталь Гмбх | Замещенные сульфамидные производные |
| JP5406722B2 (ja) | 2006-10-16 | 2014-02-05 | グリュネンタール・ゲゼルシャフト・ミト・ベシュレンクテル・ハフツング | ブラジキニン1受容体モジュレータとしての置換されたスルホンアミド誘導体 |
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| MX2011010068A (es) | 2011-10-06 |
| BRPI1013614A2 (pt) | 2019-09-24 |
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| CN102365276A (zh) | 2012-02-29 |
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| PE20120833A1 (es) | 2012-07-23 |
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| US8455475B2 (en) | 2013-06-04 |
| ECSP11011390A (es) | 2012-03-30 |
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| JP2012521377A (ja) | 2012-09-13 |
| AU2010227802A1 (en) | 2011-11-10 |
| ZA201107772B (en) | 2012-07-25 |
| TW201038572A (en) | 2010-11-01 |
| RU2011142618A (ru) | 2013-04-27 |
| US20100249095A1 (en) | 2010-09-30 |
| EP2411381A1 (en) | 2012-02-01 |
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