JP6546596B2 - Nr2bの選択的オクタヒドロ−シクロペンタ[c]ピロール負調節因子 - Google Patents
Nr2bの選択的オクタヒドロ−シクロペンタ[c]ピロール負調節因子 Download PDFInfo
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- JP6546596B2 JP6546596B2 JP2016545243A JP2016545243A JP6546596B2 JP 6546596 B2 JP6546596 B2 JP 6546596B2 JP 2016545243 A JP2016545243 A JP 2016545243A JP 2016545243 A JP2016545243 A JP 2016545243A JP 6546596 B2 JP6546596 B2 JP 6546596B2
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- pyrrol
- octahydrocyclopenta
- hydroxy
- benzyl
- pyrrole
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- 0 **C(*)(CC1)CCN1I* Chemical compound **C(*)(CC1)CCN1I* 0.000 description 6
- MTOYTLBXGAYODC-UHFFFAOYSA-N C=CC/N=N\N[Br]=C Chemical compound C=CC/N=N\N[Br]=C MTOYTLBXGAYODC-UHFFFAOYSA-N 0.000 description 1
- LSQWMEZEZKNSLA-NOLUUDBRSA-N CC(C(CCO)c(cc1)ccc1O)N1C[C@H](C[C@](Cc2ccccc2)(C2)F)[C@H]2C1 Chemical compound CC(C(CCO)c(cc1)ccc1O)N1C[C@H](C[C@](Cc2ccccc2)(C2)F)[C@H]2C1 LSQWMEZEZKNSLA-NOLUUDBRSA-N 0.000 description 1
- MECAHFSQQZQZOI-UHFFFAOYSA-N CC(C)(C)OC(N(C1)CC1=C)=O Chemical compound CC(C)(C)OC(N(C1)CC1=C)=O MECAHFSQQZQZOI-UHFFFAOYSA-N 0.000 description 1
- QOFLPTJYZWTYNE-FVCICTRLSA-N CC(C)(C)c1ccc([C@@](C2)(C[C@@H](C3)[C@H]2CN3F)O)cc1 Chemical compound CC(C)(C)c1ccc([C@@](C2)(C[C@@H](C3)[C@H]2CN3F)O)cc1 QOFLPTJYZWTYNE-FVCICTRLSA-N 0.000 description 1
- MYTWNIBEFOQJBS-FVCICTRLSA-N CC(C)(C)c1ccc([C@@](C2)(C[C@@H]3[C@H]2CNC3)O)cc1 Chemical compound CC(C)(C)c1ccc([C@@](C2)(C[C@@H]3[C@H]2CNC3)O)cc1 MYTWNIBEFOQJBS-FVCICTRLSA-N 0.000 description 1
- QWVHZZVJXVHVHK-UHFFFAOYSA-N CC(C)(c(cc1)ccc1C(CBr)=O)O Chemical compound CC(C)(c(cc1)ccc1C(CBr)=O)O QWVHZZVJXVHVHK-UHFFFAOYSA-N 0.000 description 1
- XZIUKEJTWSKJBW-UHFFFAOYSA-N CC(c1ccc2[nH]nnc2c1)=O Chemical compound CC(c1ccc2[nH]nnc2c1)=O XZIUKEJTWSKJBW-UHFFFAOYSA-N 0.000 description 1
- PDEYDCVFGMWDBQ-UHFFFAOYSA-N CN(C(c(cc1)cc2c1[nH]nn2)=O)OC Chemical compound CN(C(c(cc1)cc2c1[nH]nn2)=O)OC PDEYDCVFGMWDBQ-UHFFFAOYSA-N 0.000 description 1
- SDZLYPFMASMVQF-UHFFFAOYSA-N FC(c1cc(C2OC2)ccc1)(F)F Chemical compound FC(c1cc(C2OC2)ccc1)(F)F SDZLYPFMASMVQF-UHFFFAOYSA-N 0.000 description 1
- WFLBQFSWPJODCW-IHRRRGAJSA-N N[C@]1(C[C@](Cc2ccccc2)(C2)O)[C@@H]2CNC1 Chemical compound N[C@]1(C[C@](Cc2ccccc2)(C2)O)[C@@H]2CNC1 WFLBQFSWPJODCW-IHRRRGAJSA-N 0.000 description 1
- GUOVBFFLXKJFEE-UHFFFAOYSA-N OC(c(cc1)cc2c1[nH]nn2)=O Chemical compound OC(c(cc1)cc2c1[nH]nn2)=O GUOVBFFLXKJFEE-UHFFFAOYSA-N 0.000 description 1
- XCEHEPNIWGDJSA-NGRWLJPCSA-N O[C@@](Cc1ccccc1)(C1)C[C@@H]2[C@H]1CN(CC(c(cc1)ccc1O)=O)C2 Chemical compound O[C@@](Cc1ccccc1)(C1)C[C@@H]2[C@H]1CN(CC(c(cc1)ccc1O)=O)C2 XCEHEPNIWGDJSA-NGRWLJPCSA-N 0.000 description 1
- NNIRHUJLEYJPPW-WDNDVIMCSA-N O[C@@](Cc1ccccc1)(C1)C[C@@H]2[C@H]1CNC2 Chemical compound O[C@@](Cc1ccccc1)(C1)C[C@@H]2[C@H]1CNC2 NNIRHUJLEYJPPW-WDNDVIMCSA-N 0.000 description 1
- XCEHEPNIWGDJSA-HATOLVCRSA-N O[C@](Cc1ccccc1)(C1)C[C@@H]2[C@H]1CN(CC(c(cc1)ccc1O)=O)C2 Chemical compound O[C@](Cc1ccccc1)(C1)C[C@@H]2[C@H]1CN(CC(c(cc1)ccc1O)=O)C2 XCEHEPNIWGDJSA-HATOLVCRSA-N 0.000 description 1
- HPFVHVCEUGWDMQ-UHFFFAOYSA-N Oc(c(F)cc(C(CBr)=O)c1)c1F Chemical compound Oc(c(F)cc(C(CBr)=O)c1)c1F HPFVHVCEUGWDMQ-UHFFFAOYSA-N 0.000 description 1
- LJYOFQHKEWTQRH-UHFFFAOYSA-N Oc(cc1)ccc1C(CBr)=O Chemical compound Oc(cc1)ccc1C(CBr)=O LJYOFQHKEWTQRH-UHFFFAOYSA-N 0.000 description 1
- SPBWTPSYDUTQIM-UHFFFAOYSA-N Oc1ccc(C(CBr)=O)nc1 Chemical compound Oc1ccc(C(CBr)=O)nc1 SPBWTPSYDUTQIM-UHFFFAOYSA-N 0.000 description 1
- YBMKFUSPXPIFMT-UHFFFAOYSA-N Oc1ncc(C(CBr)=O)nc1 Chemical compound Oc1ncc(C(CBr)=O)nc1 YBMKFUSPXPIFMT-UHFFFAOYSA-N 0.000 description 1
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- A61K31/40—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
- A61K31/403—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil condensed with carbocyclic rings, e.g. carbazole
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- C07D205/02—Heterocyclic compounds containing four-membered rings with one nitrogen atom as the only ring hetero atom not condensed with other rings
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- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/04—Ortho-condensed systems
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Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201361883050P | 2013-09-26 | 2013-09-26 | |
| US61/883,050 | 2013-09-26 | ||
| PCT/US2014/057800 WO2015048507A1 (en) | 2013-09-26 | 2014-09-26 | Selective octahydro-cyclopenta[c] pyrrole negative modulators of nr2b |
Publications (3)
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| JP2016536348A JP2016536348A (ja) | 2016-11-24 |
| JP2016536348A5 JP2016536348A5 (https=) | 2017-11-24 |
| JP6546596B2 true JP6546596B2 (ja) | 2019-07-17 |
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| TW (1) | TW201605791A (https=) |
| UY (1) | UY35750A (https=) |
| WO (1) | WO2015048507A1 (https=) |
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| WO2015048507A1 (en) | 2013-09-26 | 2015-04-02 | Mnemosyne Pharmaceuticals, Inc. | Selective octahydro-cyclopenta[c] pyrrole negative modulators of nr2b |
| JO3579B1 (ar) * | 2014-09-26 | 2020-07-05 | Luc Therapeutics Inc | مُعدِلات تفاغرية سالبة لمستقبل nr2b من المركب n-ألكيل أريل-5-أوكسي أريل-ثامن هيدرو-خماسي الحلقة [c] بيرول |
| HK1250029A1 (zh) | 2015-08-05 | 2018-11-23 | Indivior Uk Limited | 具有双环结构的多巴胺d3受体拮抗剂 |
| WO2018232158A1 (en) * | 2017-06-15 | 2018-12-20 | Belite Bio, Inc. | Methods of treating metabolic diseases with fused bicyclic pyrroles |
| CA3121850A1 (en) | 2019-01-03 | 2020-07-09 | Avive Solutions, Inc. | Defibrillator communications architecture |
| MX2023006567A (es) * | 2020-12-04 | 2023-06-16 | Novartis Ag | Regimen de dosificacion para un nam del receptor nr2b-nmda para el tratamiento de la depresion. |
| CN117120053A (zh) * | 2021-03-26 | 2023-11-24 | 诺华股份有限公司 | 新的环戊二烯并[c]吡咯NR2B负变构调节剂 |
| EP4313041A4 (en) * | 2021-03-26 | 2025-01-15 | Novartis AG | NEW CYCLOPENTAL[C PYRROL NEGATIVE ALLOSTERIC MODULATORS OF NR2B |
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| DE4341403A1 (de) * | 1993-12-04 | 1995-06-08 | Basf Ag | N-substituierte 3-Azabicycloalkan-Derivate, ihre Herstellung und Verwendung |
| US5541217A (en) * | 1995-05-17 | 1996-07-30 | Ortho Pharmaceutical Corporation | 4-arylcyclopenta[c]pyrrole analgesics |
| US6369076B1 (en) * | 1999-10-29 | 2002-04-09 | Merck & Co. Inc. | 5-benzyl-octahydroindole and 6-benzyl-decahydroquinoline NMDA/NR2B antagonists |
| CA2440803A1 (en) * | 2001-03-07 | 2002-09-12 | Pfizer Products Inc. | Modulators of chemokine receptor activity |
| EP1394152A4 (en) | 2001-04-19 | 2005-02-02 | Eisai Co Ltd | 2-IMINOIMIDAZOLE DERIVATIVES (1) |
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| US7696241B2 (en) | 2004-03-04 | 2010-04-13 | Bristol-Myers Squibb Company | Bicyclic compounds as modulators of androgen receptor function and method |
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| US20070270417A1 (en) | 2004-07-22 | 2007-11-22 | Glaxo Group Limited | Antibacterial Agents |
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| WO2007128458A1 (en) | 2006-04-28 | 2007-11-15 | Laboratorios Del Dr. Esteve, S.A. | Bicyclic tetrahydropyrrole compounds |
| CN101230058A (zh) * | 2007-01-23 | 2008-07-30 | 上海恒瑞医药有限公司 | 双环氮杂烷类衍生物、其制备方法及其在医药上的用途 |
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| KR101469306B1 (ko) * | 2008-01-23 | 2014-12-04 | 장쑤 한서 파마슈티칼 캄파니 리미티드 | 다이사이클로아자알칸 유도체, 이의 제조 방법 및 의학적 용도 |
| US8691865B2 (en) * | 2008-11-26 | 2014-04-08 | Abbvie Inc. | Substituted octahydrocyclopenta[C]pyrrol-4-amines as calcium channel blockers |
| CA2746444A1 (en) | 2008-12-12 | 2010-06-17 | Vanderbilt University | 3.3.0 bicyclic glyt1 inhibitors and methods of making and using same |
| FR2945533B1 (fr) | 2009-05-12 | 2011-05-27 | Sanofi Aventis | Derives de cyclopenta°c!pyrrolyl-alkylcarbamates d'heterocycles a 5 chainons, leur preparation et leur application en therapeutique |
| FR2945534B1 (fr) * | 2009-05-12 | 2012-11-16 | Sanofi Aventis | DERIVES DE CYCLOPENTAL[c]PYRROLE-2-CARBOXYLATES, LEUR PREPARATION ET LEUR APPLICATION EN THERAPEUTIQUE |
| BR112012016733A2 (pt) | 2010-01-07 | 2015-09-01 | Du Pont | "composto, composição fungicida e método" |
| US8796470B2 (en) | 2010-05-25 | 2014-08-05 | Abbvie Inc. | Substituted octahydrocyclopenta[c]pyrroles as calcium channel modulators |
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| JO3611B1 (ar) | 2011-08-10 | 2020-08-27 | Janssen Sciences Ireland Uc | سايكلو بنتا (سي (بيرول 4,3 ثاني هيدرو 1 hمستبدله [8,1] نافثيريدينونات مضادة للجراثيم |
| KR102032934B1 (ko) | 2011-12-21 | 2019-10-16 | 지앙수 헨그루이 메디슨 컴퍼니 리미티드 | 피롤 6원 헤테로아릴 고리 유도체, 그의 제조 방법, 및 그의 의약 용도 |
| KR102179599B1 (ko) * | 2012-09-25 | 2020-11-19 | 에프. 호프만-라 로슈 아게 | 이환형 유도체 |
| AR095079A1 (es) * | 2013-03-12 | 2015-09-16 | Hoffmann La Roche | Derivados de octahidro-pirrolo[3,4-c]-pirrol y piridina-fenilo |
| WO2015048507A1 (en) | 2013-09-26 | 2015-04-02 | Mnemosyne Pharmaceuticals, Inc. | Selective octahydro-cyclopenta[c] pyrrole negative modulators of nr2b |
| CN106103446B (zh) | 2014-03-26 | 2019-07-30 | 豪夫迈·罗氏有限公司 | 作为自分泌运动因子(atx)和溶血磷脂酸(lpa)生产抑制剂的二环化合物 |
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2014
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- 2014-09-26 CN CN201480058773.3A patent/CN105916843B/zh active Active
- 2014-09-26 UY UY0001035750A patent/UY35750A/es not_active Application Discontinuation
- 2014-09-26 JP JP2016545243A patent/JP6546596B2/ja active Active
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2016
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| EP3461827B1 (en) | 2022-02-23 |
| UY35750A (es) | 2015-04-30 |
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| US9540324B2 (en) | 2017-01-10 |
| US10052306B2 (en) | 2018-08-21 |
| ES2707739T3 (es) | 2019-04-04 |
| US20170071906A1 (en) | 2017-03-16 |
| US20230012073A1 (en) | 2023-01-12 |
| ES2910848T3 (es) | 2022-05-13 |
| EP3036221A4 (en) | 2017-01-25 |
| EP3461827A1 (en) | 2019-04-03 |
| US20150225342A1 (en) | 2015-08-13 |
| TW201605791A (zh) | 2016-02-16 |
| JP2016536348A (ja) | 2016-11-24 |
| AR097794A1 (es) | 2016-04-13 |
| CN105916843A (zh) | 2016-08-31 |
| US20180325868A1 (en) | 2018-11-15 |
| EP3036221B1 (en) | 2018-11-07 |
| US11116749B2 (en) | 2021-09-14 |
| EP3036221A1 (en) | 2016-06-29 |
| WO2015048507A1 (en) | 2015-04-02 |
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