JP2013505946A5 - - Google Patents
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- Publication number
- JP2013505946A5 JP2013505946A5 JP2012531043A JP2012531043A JP2013505946A5 JP 2013505946 A5 JP2013505946 A5 JP 2013505946A5 JP 2012531043 A JP2012531043 A JP 2012531043A JP 2012531043 A JP2012531043 A JP 2012531043A JP 2013505946 A5 JP2013505946 A5 JP 2013505946A5
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- JP
- Japan
- Prior art keywords
- substituted
- unsubstituted
- moiety
- cycloalkyl
- alkyl
- 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.)
- Granted
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- 125000000217 alkyl group Chemical group 0.000 claims description 64
- 125000003545 alkoxy group Chemical group 0.000 claims description 52
- -1 perhaloalkyl Chemical group 0.000 claims description 52
- 125000001475 halogen functional group Chemical group 0.000 claims description 50
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 48
- 229910052799 carbon Inorganic materials 0.000 claims description 45
- 125000001072 heteroaryl group Chemical group 0.000 claims description 41
- 125000003118 aryl group Chemical group 0.000 claims description 40
- 125000000623 heterocyclic group Chemical group 0.000 claims description 39
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims description 36
- 150000001875 compounds Chemical class 0.000 claims description 36
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 35
- 125000004442 acylamino group Chemical group 0.000 claims description 34
- OKTJSMMVPCPJKN-UHFFFAOYSA-N carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 33
- 150000003839 salts Chemical class 0.000 claims description 33
- 239000011780 sodium chloride Substances 0.000 claims description 33
- 125000005102 carbonylalkoxy group Chemical group 0.000 claims description 32
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 32
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 30
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 28
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 28
- 125000004648 C2-C8 alkenyl group Chemical group 0.000 claims description 24
- 125000000266 alpha-aminoacyl group Chemical group 0.000 claims description 20
- 125000004649 C2-C8 alkynyl group Chemical group 0.000 claims description 16
- 125000004423 acyloxy group Chemical group 0.000 claims description 16
- 125000004001 thioalkyl group Chemical group 0.000 claims description 16
- 125000000392 cycloalkenyl group Chemical group 0.000 claims description 15
- 125000006552 (C3-C8) cycloalkyl group Chemical group 0.000 claims description 14
- 125000002252 acyl group Chemical group 0.000 claims description 12
- 125000003710 aryl alkyl group Chemical group 0.000 claims description 12
- 125000004104 aryloxy group Chemical group 0.000 claims description 12
- 125000005589 carbonylalkylenealkoxy group Chemical group 0.000 claims description 12
- 125000004432 carbon atoms Chemical group C* 0.000 claims description 10
- 125000000325 methylidene group Chemical group [H]C([H])=* 0.000 claims description 8
- 150000003573 thiols Chemical class 0.000 claims description 8
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 claims description 6
- 206010057668 Cognitive disease Diseases 0.000 claims description 5
- 206010061920 Psychotic disease Diseases 0.000 claims description 5
- 201000010099 disease Diseases 0.000 claims description 5
- 230000001404 mediated Effects 0.000 claims description 5
- 239000002858 neurotransmitter agent Substances 0.000 claims description 5
- 208000009025 Nervous System Disease Diseases 0.000 claims description 4
- 206010029305 Neurological disorder Diseases 0.000 claims description 4
- 125000000304 alkynyl group Chemical group 0.000 claims description 4
- 125000006598 aminocarbonylamino group Chemical group 0.000 claims description 4
- 239000003937 drug carrier Substances 0.000 claims description 3
- 239000008194 pharmaceutical composition Substances 0.000 claims description 3
- 125000005111 carboxyalkoxy group Chemical group 0.000 claims description 2
- 239000000203 mixture Substances 0.000 claims 2
- 125000003107 substituted aryl group Chemical group 0.000 claims 1
- 206010029331 Neuropathy peripheral Diseases 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 201000001119 neuropathy Diseases 0.000 description 1
- 239000000546 pharmaceutic aid Substances 0.000 description 1
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US24514809P | 2009-09-23 | 2009-09-23 | |
US61/245,148 | 2009-09-23 | ||
PCT/US2010/050079 WO2011038162A1 (en) | 2009-09-23 | 2010-09-23 | Pyrido(3,4-b)indoles and methods of use |
Publications (3)
Publication Number | Publication Date |
---|---|
JP2013505946A JP2013505946A (ja) | 2013-02-21 |
JP2013505946A5 true JP2013505946A5 (US07981874-20110719-C00313.png) | 2013-11-07 |
JP5791611B2 JP5791611B2 (ja) | 2015-10-07 |
Family
ID=43796210
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2012531043A Expired - Fee Related JP5791611B2 (ja) | 2009-09-23 | 2010-09-23 | ピリド[3,4−b]インドールおよび使用方法 |
Country Status (8)
Families Citing this family (32)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
RU2007139634A (ru) | 2007-10-25 | 2009-04-27 | Сергей Олегович Бачурин (RU) | Новые тиазол-, триазол- или оксадиазол-содержащие тетрациклические соединения |
RU2544856C2 (ru) * | 2008-01-25 | 2015-03-20 | Сергей Олегович Бачурин | НОВЫЕ ПРОИЗВОДНЫЕ 2,3,4,5-ТЕТРАГИДРО-1-ПИРИДО[4,3-b]ИНДОЛА И СПОСОБЫ ИХ ПРИМЕНЕНИЯ |
CA2719412A1 (en) | 2008-03-24 | 2009-10-01 | Medivation Technologies, Inc. | Pyrido[3,4-b]indoles and methods of use |
WO2009120720A1 (en) | 2008-03-24 | 2009-10-01 | Medivation Technologies,Inc. | Bridged heterocyclic compounds and methods of use |
TWI477503B (zh) | 2008-10-31 | 2015-03-21 | Medivation Technologies Inc | 含有剛性部分之吡啶并〔4,3-b〕吲哚 |
EP2348847A4 (en) * | 2008-10-31 | 2012-05-23 | Medivation Technologies Inc | AZEPINO [4, 5-B] INDOLE AND USE PROCESS |
US9962368B2 (en) | 2009-01-09 | 2018-05-08 | Board Of Regents Of The University Of Texas System | Pro-neurogenic compounds |
US9162980B2 (en) | 2009-01-09 | 2015-10-20 | Board Of Regents Of The University Of Texas System | Anti-depression compounds |
US8362277B2 (en) | 2009-01-09 | 2013-01-29 | Board Of Regents Of The University Of Texas System | Pro-neurogenic compounds |
US8604074B2 (en) | 2009-01-09 | 2013-12-10 | Board Of Regents Of The University Of Texas System | Pro-neurogenic compounds |
JP5711725B2 (ja) | 2009-04-29 | 2015-05-07 | メディベイション テクノロジーズ, インコーポレイテッド | ピリド[4,3−b]インドールおよびその使用方法 |
AU2010282990B2 (en) | 2009-04-29 | 2015-11-05 | Medivation Technologies, Inc. | Pyrido [4, 3-b] indoles and methods of use |
CA2775328A1 (en) | 2009-09-23 | 2011-03-31 | Medivation Technologies, Inc. | Pyrido[4,3-b]indoles and methods of use |
EP2480080A4 (en) | 2009-09-23 | 2014-01-08 | Medivation Technologies Inc | PYRIDO [3,4-B] INDOLES AND METHODS OF USE |
CN102711466A (zh) | 2009-09-23 | 2012-10-03 | 梅迪维新技术公司 | 桥连杂环化合物及其使用方法 |
US9034865B2 (en) | 2010-02-18 | 2015-05-19 | Medivation Technologies, Inc. | Pyrido [4,3-B] indole and pyrido [3,4-B] indole derivatives and methods of use |
WO2011103460A1 (en) | 2010-02-18 | 2011-08-25 | Medivation Technologies, Inc. | Fused tetracyclic pyrido[4,3-b]indole and pyrido[3,4-b]ondole derivatives and methods of use |
WO2011103485A1 (en) | 2010-02-18 | 2011-08-25 | Medivation Technologies, Inc. | Fused tetracyclic pyrido[4,3-b]indole and pyrido[3,4-b]indole derivatives and methods of use |
WO2011103430A1 (en) | 2010-02-19 | 2011-08-25 | Medivation Technologies, Inc. | Pyrido[4,3-b]indole and pyrido[3,4-b]indole derivatives and methods of use |
EP2590647B1 (en) | 2010-07-07 | 2017-11-08 | Board of Regents of the University of Texas System | Pro-neurogenic compounds |
US9035056B2 (en) | 2011-02-18 | 2015-05-19 | Medivation Technologies, Inc. | Pyrido[4,3-b]indole and pyrido[3,4-b]indole derivatives and methods of use |
WO2012112966A1 (en) | 2011-02-18 | 2012-08-23 | Medivation Technologies, Inc. | Compounds and methods for treatment of hypertension |
WO2012112963A1 (en) | 2011-02-18 | 2012-08-23 | Medivation Technologies, Inc. | Compounds and methods for treatment of hypertension |
WO2012112961A1 (en) | 2011-02-18 | 2012-08-23 | Medivation Technologies, Inc. | Compounds and methods of treating hypertension |
US9701676B2 (en) | 2012-08-24 | 2017-07-11 | Board Of Regents Of The University Of Texas System | Pro-neurogenic compounds |
WO2015070237A1 (en) | 2013-11-11 | 2015-05-14 | Board Of Regents Of The University Of Texas System | Neuroprotective chemicals and methods for identifying and using same |
EP3068388A4 (en) | 2013-11-11 | 2017-04-12 | Board of Regents of the University of Texas System | Neuroprotective compounds and use thereof |
US10092550B2 (en) | 2014-10-21 | 2018-10-09 | Ions Pharmaceutical S.À R.L. | Therapeutic compositions containing curcumin, harmine, and isovanillin components, and methods of use thereof |
US9907786B2 (en) | 2014-10-21 | 2018-03-06 | Ions Pharmaceutical S.À R.L. | Therapeutic compositions containing harmine and isovanillin components, and methods of use thereof |
CN104839184A (zh) * | 2015-04-18 | 2015-08-19 | 广东中迅农科股份有限公司 | 含有氯吡嘧磺隆和氯氨吡啶酸以及烟嘧磺隆的农药组合物 |
EP3703716A4 (en) | 2017-11-02 | 2021-12-01 | California Institute of Technology | EXPRESSION OF NEUROPEPTIDES |
EP3704271A4 (en) * | 2017-11-02 | 2021-09-08 | California Institute of Technology | NEUROKININ ANTAGONISTS AND RELATED USES |
Family Cites Families (30)
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US2642438A (en) * | 1949-07-15 | 1953-06-16 | Hoffmann La Roche | Pyridindoles and method of manufacture |
GB721171A (en) * | 1951-04-30 | 1954-12-29 | Bayer Ag | Derivatives of ª‰- and ª†- carbolines |
JPS3922979B1 (US07981874-20110719-C00313.png) * | 1962-04-10 | 1964-10-15 | ||
JPS3920857B1 (US07981874-20110719-C00313.png) * | 1962-05-17 | 1964-09-24 | ||
JPS412713B1 (US07981874-20110719-C00313.png) * | 1963-08-30 | 1966-02-21 | ||
US4754038A (en) * | 1987-02-26 | 1988-06-28 | American Home Products Corporation | Carboline histamine H1 antagonists |
US5817756A (en) * | 1993-09-09 | 1998-10-06 | Scios Inc. | Pseudo- and non-peptide bradykinin receptor antagonists |
CA2171446C (en) * | 1993-09-09 | 2004-11-23 | Donald James Kyle | Pseudo- and non-peptide bradykinin receptor antagonists |
JPH09510216A (ja) * | 1994-03-11 | 1997-10-14 | イーライ・リリー・アンド・カンパニー | 5−ht▲下2b▼受容体に関連する病態を治療するための方法 |
US5688807A (en) * | 1994-03-11 | 1997-11-18 | Eli Lilly And Company | Method for treating 5HT2B receptor related conditions |
JPH11505217A (ja) * | 1995-05-05 | 1999-05-18 | ノボ ノルディスク アクティーゼルスカブ | 新規複素環の化学 |
GB9604996D0 (en) * | 1996-03-08 | 1996-05-08 | Black James Foundation | Benzodiazonine derivatives |
AU1407399A (en) * | 1997-11-14 | 1999-06-07 | Eli Lilly And Company | Treatment for alzheimer's disease |
FR2771095B1 (fr) * | 1997-11-14 | 1999-12-17 | Adir | Nouveaux inhibiteurs de metalloproteases, leur procede de preparation et les compositions pharmaceutiques qui les contiennent |
EP1057814B1 (en) * | 1997-12-25 | 2005-03-09 | Meiji Seika Kaisha, Ltd. | Tetrahydrobenzindole derivatives |
FR2796644B1 (fr) * | 1999-07-23 | 2001-09-07 | Adir | Nouveaux derives de beta-carboline, leur procede de preparation et les compositions pharmaceutiques qui les contiennent |
UA74826C2 (en) * | 2000-05-17 | 2006-02-15 | Ortho Mcneil Pharm Inc | ?-carboline derivatives as phosphodiesterase inhibitors |
US20060235012A1 (en) * | 2003-06-16 | 2006-10-19 | Chroma Therapeutics Limited | Carboline and betacarboline derivatives for use as hdac enzyme inhibitors |
EP1637521B1 (en) * | 2003-06-23 | 2013-06-19 | Ono Pharmaceutical Co., Ltd. | Novel tricyclic heterocycle compound |
EP1714961B1 (en) * | 2004-02-12 | 2015-12-09 | Mitsubishi Tanabe Pharma Corporation | Indazole compound and pharmaceutical use thereof |
WO2006011750A1 (en) * | 2004-07-27 | 2006-02-02 | C & C Research Laboratories | Tetrahydro-beta-carbolinone derivatives and process for preparing the same |
EP1851219A1 (en) * | 2005-02-14 | 2007-11-07 | Miikana Therapeutics, Inc. | Fused heterocyclic compounds useful as inhibitors of histone deacetylase |
JP5287257B2 (ja) * | 2007-02-07 | 2013-09-11 | アステラス製薬株式会社 | アシルグアニジン誘導体 |
DE102007009264A1 (de) * | 2007-02-26 | 2008-08-28 | Ellneuroxx Ltd. | 9-Alkyl-ß-Carboline zur Behandlung von neurodegenerativen Erkrankungen |
CA2683453C (en) * | 2007-04-05 | 2013-06-11 | Alla Chem, Llc | Substituted 2,3,4,5-tetrahydro-1h-pyrido[4,3-.beta.]indoles, methods for the production and use thereof |
RU2007139634A (ru) * | 2007-10-25 | 2009-04-27 | Сергей Олегович Бачурин (RU) | Новые тиазол-, триазол- или оксадиазол-содержащие тетрациклические соединения |
JP5366211B2 (ja) * | 2007-12-18 | 2013-12-11 | 国立大学法人富山大学 | アルドース還元酵素阻害活性を有する縮合三環化合物 |
RU2544856C2 (ru) * | 2008-01-25 | 2015-03-20 | Сергей Олегович Бачурин | НОВЫЕ ПРОИЗВОДНЫЕ 2,3,4,5-ТЕТРАГИДРО-1-ПИРИДО[4,3-b]ИНДОЛА И СПОСОБЫ ИХ ПРИМЕНЕНИЯ |
CA2719412A1 (en) * | 2008-03-24 | 2009-10-01 | Medivation Technologies, Inc. | Pyrido[3,4-b]indoles and methods of use |
TW201038569A (en) * | 2009-02-16 | 2010-11-01 | Abbott Gmbh & Co Kg | Heterocyclic compounds, pharmaceutical compositions containing them, and their use in therapy |
-
2010
- 2010-09-23 CN CN2010800528027A patent/CN102711467A/zh active Pending
- 2010-09-23 CA CA2775129A patent/CA2775129A1/en not_active Abandoned
- 2010-09-23 EP EP10819491.1A patent/EP2480079A4/en not_active Withdrawn
- 2010-09-23 WO PCT/US2010/050079 patent/WO2011038162A1/en active Application Filing
- 2010-09-23 US US13/498,099 patent/US20130137705A1/en not_active Abandoned
- 2010-09-23 AU AU2010298167A patent/AU2010298167B2/en not_active Ceased
- 2010-09-23 BR BR112012006644A patent/BR112012006644A2/pt not_active IP Right Cessation
- 2010-09-23 JP JP2012531043A patent/JP5791611B2/ja not_active Expired - Fee Related
-
2013
- 2013-01-04 US US13/734,873 patent/US20130123277A1/en not_active Abandoned