JP2013505947A5 - - Google Patents
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- JP2013505947A5 JP2013505947A5 JP2012531044A JP2012531044A JP2013505947A5 JP 2013505947 A5 JP2013505947 A5 JP 2013505947A5 JP 2012531044 A JP2012531044 A JP 2012531044A JP 2012531044 A JP2012531044 A JP 2012531044A JP 2013505947 A5 JP2013505947 A5 JP 2013505947A5
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- JP
- Japan
- Prior art keywords
- substituted
- unsubstituted
- moiety
- propylene
- alkoxy
- 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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- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 claims description 98
- 125000003545 alkoxy group Chemical group 0.000 claims description 70
- 125000000217 alkyl group Chemical group 0.000 claims description 66
- 125000000383 tetramethylene group Chemical group [H]C([H])([*:1])C([H])([H])C([H])([H])C([H])([H])[*:2] 0.000 claims description 60
- 239000005977 Ethylene Substances 0.000 claims description 58
- VGGSQFUCUMXWEO-UHFFFAOYSA-N ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims description 58
- -1 perhaloalkyl Chemical group 0.000 claims description 56
- 125000001475 halogen functional group Chemical group 0.000 claims description 54
- 125000001072 heteroaryl group Chemical group 0.000 claims description 54
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 50
- 125000003118 aryl group Chemical group 0.000 claims description 48
- 125000000623 heterocyclic group Chemical group 0.000 claims description 46
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 44
- 229910052799 carbon Inorganic materials 0.000 claims description 43
- 125000005102 carbonylalkoxy group Chemical group 0.000 claims description 40
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 40
- 125000004442 acylamino group Chemical group 0.000 claims description 36
- OKTJSMMVPCPJKN-UHFFFAOYSA-N carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 36
- 150000001875 compounds Chemical class 0.000 claims description 36
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 34
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 32
- 125000001570 methylene group Chemical group [H]C([H])([*:1])[*:2] 0.000 claims description 30
- 125000000266 alpha-aminoacyl group Chemical group 0.000 claims description 26
- 150000003839 salts Chemical class 0.000 claims description 25
- 239000011780 sodium chloride Substances 0.000 claims description 25
- 125000005243 carbonyl alkyl group Chemical group 0.000 claims description 23
- 125000004423 acyloxy group Chemical group 0.000 claims description 22
- 125000000392 cycloalkenyl group Chemical group 0.000 claims description 22
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 22
- 125000000304 alkynyl group Chemical group 0.000 claims description 18
- 125000002252 acyl group Chemical group 0.000 claims description 16
- 125000003710 aryl alkyl group Chemical group 0.000 claims description 16
- 125000004104 aryloxy group Chemical group 0.000 claims description 16
- 125000005589 carbonylalkylenealkoxy group Chemical group 0.000 claims description 16
- 125000004001 thioalkyl group Chemical group 0.000 claims description 16
- 125000005121 aminocarbonylalkoxy group Chemical group 0.000 claims description 12
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims description 11
- 125000004432 carbon atoms Chemical group C* 0.000 claims description 10
- 150000003573 thiols Chemical class 0.000 claims description 10
- 206010057668 Cognitive disease Diseases 0.000 claims description 8
- 206010061920 Psychotic disease Diseases 0.000 claims description 8
- 201000010099 disease Diseases 0.000 claims description 8
- 230000001404 mediated Effects 0.000 claims description 8
- 239000002858 neurotransmitter agent Substances 0.000 claims description 8
- 208000009025 Nervous System Disease Diseases 0.000 claims description 6
- 206010029305 Neurological disorder Diseases 0.000 claims description 6
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims description 4
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 4
- 125000000547 substituted alkyl 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
- 125000004214 1-pyrrolidinyl group Chemical group [H]C1([H])N(*)C([H])([H])C([H])([H])C1([H])[H] 0.000 claims description 2
- 125000002393 azetidinyl group Chemical group 0.000 claims description 2
- 125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 claims description 2
- 125000002147 dimethylamino group Chemical group [H]C([H])([H])N(*)C([H])([H])[H] 0.000 claims description 2
- 125000005931 tert-butyloxycarbonyl group Chemical group [H]C([H])([H])C(OC(*)=O)(C([H])([H])[H])C([H])([H])[H] 0.000 claims description 2
- 125000006552 (C3-C8) cycloalkyl group Chemical group 0.000 claims 16
- 125000004648 C2-C8 alkenyl group Chemical group 0.000 claims 15
- 125000004649 C2-C8 alkynyl group Chemical group 0.000 claims 8
- 239000000203 mixture Substances 0.000 claims 4
- 125000001769 aryl amino group Chemical group 0.000 claims 1
- 125000003342 alkenyl group Chemical group 0.000 description 15
- 125000004656 alkyl sulfonylamino group Chemical group 0.000 description 5
- 206010029331 Neuropathy peripheral Diseases 0.000 description 2
- 201000001119 neuropathy Diseases 0.000 description 2
- 125000003277 amino group Chemical group 0.000 description 1
- 125000006312 cyclopentyl amino group Chemical group [H]N(*)C1([H])C([H])([H])C([H])([H])C([H])([H])C1([H])[H] 0.000 description 1
- 239000000546 pharmaceutic aid Substances 0.000 description 1
Applications Claiming Priority (5)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US24514709P | 2009-09-23 | 2009-09-23 | |
US24526009P | 2009-09-23 | 2009-09-23 | |
US61/245,260 | 2009-09-23 | ||
US61/245,147 | 2009-09-23 | ||
PCT/US2010/050080 WO2011038163A1 (en) | 2009-09-23 | 2010-09-23 | Pyrido[3,4-b]indoles and methods of use |
Publications (3)
Publication Number | Publication Date |
---|---|
JP2013505947A JP2013505947A (ja) | 2013-02-21 |
JP2013505947A5 true JP2013505947A5 (US07794700-20100914-C00152.png) | 2013-11-07 |
JP5791612B2 JP5791612B2 (ja) | 2015-10-07 |
Family
ID=43796211
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2012531044A Expired - Fee Related JP5791612B2 (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 (9)
Families Citing this family (37)
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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 |
CN102083830B (zh) | 2008-03-24 | 2014-11-12 | 梅迪维新技术公司 | 吡啶并[3,4-b]吲哚和应用方法 |
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JP5551708B2 (ja) * | 2008-10-31 | 2014-07-16 | 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 | アゼピノ[4,5−b]インドール化合物およびその使用方法 |
JP5588991B2 (ja) | 2008-10-31 | 2014-09-10 | 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 | 剛性の部分を有するピリド[4,3−b]インドール |
AU2010282990B2 (en) | 2009-04-29 | 2015-11-05 | Medivation Technologies, Inc. | Pyrido [4, 3-b] indoles and methods of use |
BRPI1006602A2 (pt) | 2009-04-29 | 2019-01-15 | Medivation Technologies Inc | composto, método para modular um receptor de histamina em um indivíduo, composição farmacêutica, kit e método para tratar um distúrbio cognitivo ou um distúrbio induzido por pelo menos um sintoma associado com a alteração da cognição |
CN102724875B (zh) | 2009-09-23 | 2015-05-27 | 梅迪维新技术公司 | 吡啶并[3,4-b]吲哚化合物及其使用方法 |
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CN110372631B (zh) * | 2019-07-24 | 2021-03-02 | 东南大学成贤学院 | 一种氨噻肟酰胺乙醛的制备方法 |
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2010
- 2010-09-23 CN CN201080047262.3A patent/CN102724875B/zh not_active Expired - Fee Related
- 2010-09-23 EP EP10819492.9A patent/EP2480080A4/en not_active Withdrawn
- 2010-09-23 CA CA2775133A patent/CA2775133A1/en not_active Abandoned
- 2010-09-23 WO PCT/US2010/050080 patent/WO2011038163A1/en active Application Filing
- 2010-09-23 JP JP2012531044A patent/JP5791612B2/ja not_active Expired - Fee Related
- 2010-09-23 AU AU2010298168A patent/AU2010298168B2/en not_active Ceased
- 2010-09-23 BR BR112012006646A patent/BR112012006646A2/pt not_active IP Right Cessation
- 2010-09-23 US US12/889,323 patent/US9079904B2/en not_active Expired - Fee Related
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2013
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- 2013-04-02 HK HK13104014.9A patent/HK1176813A1/xx not_active IP Right Cessation
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2015
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