RU2008148325A - Полиморфные формы(2s)-(4е)-n-метил-5-(3-изопропоксипиридин)ил) 4-пентен-2амина для лечения расстройств центральной нервной системы - Google Patents
Полиморфные формы(2s)-(4е)-n-метил-5-(3-изопропоксипиридин)ил) 4-пентен-2амина для лечения расстройств центральной нервной системы Download PDFInfo
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Abstract
1. Кристаллический полиморф А (2S)-(4E)-N-метил-5-[3-(5-изопропоксипиридин)ил]-4-пентен-2-амина п-гидроксибензоата, показывающий порошковую рентгенограмму с характеристическими пиками, выраженными в градусах (2-θ°): приблизительно 7,6 и 15,2 и 19,7. ! 2. Кристаллический полиморф В (2S)-(4E)-N-метил-5-[3-(5-изопропоксипиридин)ил]-4-пентен-2-амина п-гидроксибензоата, показывающий порошковую рентгенограмму с характеристическими пиками, выраженными в градусах (2-θ°): приблизительно 8,0, 9,6 и 16,1. ! 3. Смесь полиморфов, содержащая полиморфы А по п.1 и B по п.2 в соотношениях 5:95-95:5. ! 4. Полиморф (2S)-(4E)-N-метил-5-[3-(5-изопропоксипиридин)ил]-4-пентен-2-амина п-гидроксибензоата, где полиморф отделяют перекристаллизацией из этанола, метанола, изопропилового спирта, ацетона, этилацетата и/или ацетонитрила. ! 5. Кристаллический полиморф А, имеющий порошковую рентгенограмму, по существу, такую же, что показана в таблице 1. ! 6. Кристаллический полиморф В, имеющий порошковую рентгенограмму, по существу, такую же, что показана в таблице 2. ! 7. Полиоморф по любому одному из пп.1-6 для применения в терапии. ! 8. Применение полиморфа по любому одному из пп.1-6 в приготовлении лекарственного средства для лечения расстройств центральной нервной системы. ! 9. Способ лечения расстройств центральной нервной системы, включающий введение млекопитающему, нуждающемуся в таком лечении, терапевтически эффективного количества полиморфа по любому одному из пп.1-6. ! 10. Способ по п.9, где расстройство выбирают из группы, включающей возрастное нарушение памяти, умеренные когнитивные нарушения, предстарческое слабоумие (раннее начало болезни Альцгеймера), старческое слабоумие (слабоумие Альцгей
Claims (14)
1. Кристаллический полиморф А (2S)-(4E)-N-метил-5-[3-(5-изопропоксипиридин)ил]-4-пентен-2-амина п-гидроксибензоата, показывающий порошковую рентгенограмму с характеристическими пиками, выраженными в градусах (2-θ°): приблизительно 7,6 и 15,2 и 19,7.
2. Кристаллический полиморф В (2S)-(4E)-N-метил-5-[3-(5-изопропоксипиридин)ил]-4-пентен-2-амина п-гидроксибензоата, показывающий порошковую рентгенограмму с характеристическими пиками, выраженными в градусах (2-θ°): приблизительно 8,0, 9,6 и 16,1.
3. Смесь полиморфов, содержащая полиморфы А по п.1 и B по п.2 в соотношениях 5:95-95:5.
4. Полиморф (2S)-(4E)-N-метил-5-[3-(5-изопропоксипиридин)ил]-4-пентен-2-амина п-гидроксибензоата, где полиморф отделяют перекристаллизацией из этанола, метанола, изопропилового спирта, ацетона, этилацетата и/или ацетонитрила.
5. Кристаллический полиморф А, имеющий порошковую рентгенограмму, по существу, такую же, что показана в таблице 1.
6. Кристаллический полиморф В, имеющий порошковую рентгенограмму, по существу, такую же, что показана в таблице 2.
7. Полиоморф по любому одному из пп.1-6 для применения в терапии.
8. Применение полиморфа по любому одному из пп.1-6 в приготовлении лекарственного средства для лечения расстройств центральной нервной системы.
9. Способ лечения расстройств центральной нервной системы, включающий введение млекопитающему, нуждающемуся в таком лечении, терапевтически эффективного количества полиморфа по любому одному из пп.1-6.
10. Способ по п.9, где расстройство выбирают из группы, включающей возрастное нарушение памяти, умеренные когнитивные нарушения, предстарческое слабоумие (раннее начало болезни Альцгеймера), старческое слабоумие (слабоумие Альцгеймеровского типа), деменцию с тельцами Леви, сосудистую деменцию, болезнь Альцгеймера, удар, комплекс СПИД-деменции, синдром дефицита внимания, синдром дефицита внимания с гиперактивностью, дислексию, шизофрению, шизофреноподобное расстройство и шизоаффективное расстройство.
11. Способ по п.9, где расстройство выбирают из группы, включающей лечение от легкого до среднего слабоумия Альцгеймеровского типа, синдрома дефицита внимания, умеренного когнитивного нарушения и возрастного нарушения памяти.
12. Фармацевтическая композиция, содержащая в качестве активного компонента терапевтически эффективное количество полиморфа по любому одному из пп.1-6 вместе с одним или более фармацевтически пригодными разбавителями, наполнителями и/или инертными носителями.
13. Фармацевтическая композиция по п.12, предназначенная для лечения расстройств центральной нервной системы.
14. Агент для лечения расстройств центральной нервной системы, который содержит в качестве активного компонента полиморф по любому одному из пп.1-6.
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Families Citing this family (14)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US7790757B2 (en) | 1998-06-16 | 2010-09-07 | Targacept, Inc. | Compounds capable of activating cholinergic receptors |
UA88792C2 (ru) * | 2004-11-10 | 2009-11-25 | Таргасепт, Інк. | Гидроксибензоатные соли метаникотиновых соединений |
US7459469B2 (en) | 2004-11-10 | 2008-12-02 | Targacept, Inc. | Hydroxybenzoate salts of metanicotine compounds |
TWI389889B (zh) | 2006-05-09 | 2013-03-21 | Targacept Inc | (2s)-(4e)-n-甲基-5-〔3-(5-異丙氧基吡啶)基〕-4-戊烯-2-胺之新穎多晶型 |
EP2021325A2 (en) * | 2006-05-09 | 2009-02-11 | AstraZeneca AB | Salt forms of (2s)-(4e)-n-methyl-5-[3-(5-isopropoxypyridin)yl]-4-penten-2-amine |
WO2008034041A2 (en) * | 2006-09-15 | 2008-03-20 | Astrazeneca Ab | Therapeutic combinations |
EP2112923A1 (en) * | 2007-01-22 | 2009-11-04 | Targacept Inc. | Intranasal, buccal, and sublingual administration of metanicotine analogs |
CN101772343A (zh) * | 2007-07-31 | 2010-07-07 | 塔格赛普有限公司 | (2s)-(4e)-n-甲基-5-(3-(5-异丙氧基吡啶)基)-4-戊烯-2-胺的经皮给药 |
CN102065845A (zh) * | 2008-06-11 | 2011-05-18 | 阿斯利康(瑞典)有限公司 | 含有(2s)-(4e)-n-甲基-5-(5-异丙氧基吡啶-3-基)-戊-4-烯-2-胺的舌下组合物 |
WO2010080757A2 (en) * | 2009-01-07 | 2010-07-15 | Astrazeneca Ab | Combinations with an alpha-4beta-2 nicotinic agonist |
FR2959107B1 (fr) | 2010-04-23 | 2015-03-27 | Oreal | Unite d'application d'un produit cosmetique |
US8703802B2 (en) * | 2010-05-20 | 2014-04-22 | Targacept, Inc. | Process for the preparation of aryl substituted olefinic amines |
WO2013184732A1 (en) * | 2012-06-06 | 2013-12-12 | Targacept, Inc. | Crystalline (2s)-(4e)-n-methyl-5-[3-(5-isopropoxypyridin)yl]4-penten-2-amine 1,5-naphthalenedisulfonate |
KR101579904B1 (ko) | 2014-09-05 | 2016-01-05 | 동신대학교산학협력단 | 마스카라 |
Family Cites Families (67)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4192946A (en) | 1978-06-29 | 1980-03-11 | Ciba-Geigy Corporation | Process for producing 3-hydroxy-5-halopyridines |
DE3148651A1 (de) | 1981-12-09 | 1983-07-21 | Henkel Kgaa | "haarfaerbemittel, enthaltend 5-halo-2,3-pyridindiole als kupplerkomponente" |
US4582823A (en) | 1984-08-15 | 1986-04-15 | Warner-Lambert Company | Method for treating schizophrenia and medicaments therefor |
WO1989000158A1 (en) | 1987-07-02 | 1989-01-12 | Pfizer Inc. | Bridged-diazabicycloalkyl quinolone carboxylic acids and esters |
IT1226727B (it) | 1988-07-29 | 1991-02-05 | Simes | Farmaci precursori della dopamina. |
US4922901A (en) | 1988-09-08 | 1990-05-08 | R. J. Reynolds Tobacco Company | Drug delivery articles utilizing electrical energy |
ATE118216T1 (de) | 1989-04-20 | 1995-02-15 | Zambon Spa | Dopamin-medikament-vorstufe. |
US5187166A (en) | 1990-07-31 | 1993-02-16 | Nisshin Flour Milling Co., Ltd. | Azabicyclo derivatives and their use as antiemetics |
WO1992012122A1 (en) | 1990-12-27 | 1992-07-23 | Abbott Laboratories | N-protected aminoalkylaldehydes |
DE69213559T2 (de) | 1991-05-30 | 1997-02-27 | Mitsui Toatsu Chemicals | Tetravinylpyrazine-Verbindung, Verfahren zur Herstellung derselben und elektrolumineszentes Element und damit hergesteller nichtlinearer optischer Stoff |
US5212188A (en) | 1992-03-02 | 1993-05-18 | R. J. Reynolds Tabacco Company | Method for treatment of neurodegenerative diseases |
IL107184A (en) | 1992-10-09 | 1997-08-14 | Abbott Lab | Heterocyclic ether compounds that enhance cognitive function |
US5852041A (en) | 1993-04-07 | 1998-12-22 | Sibia Neurosciences, Inc. | Substituted pyridines useful as modulators of acethylcholine receptors |
US5493026A (en) | 1993-10-25 | 1996-02-20 | Organix, Inc. | Substituted 2-carboxyalkyl-3-(fluorophenyl)-8-(3-halopropen-2-yl) nortropanes and their use as imaging for agents for neurodegenerative disorders |
IT1274018B (it) | 1994-02-23 | 1997-07-14 | Riace Ets | Derivati del 3,8-diazabiciclo(3.2.1.)ottano ad attivita' analgesica |
DE69523155T2 (de) | 1994-06-14 | 2002-02-07 | Pfizer Inc., New York | Benzimidazolonderivate mit zentraler dopaminerger aktivität |
GB2295387A (en) | 1994-11-23 | 1996-05-29 | Glaxo Inc | Quinazoline antagonists of alpha 1c adrenergic receptors |
US5616707A (en) | 1995-01-06 | 1997-04-01 | Crooks; Peter A. | Compounds which are useful for prevention and treatment of central nervous system disorders |
US5604231A (en) | 1995-01-06 | 1997-02-18 | Smith; Carr J. | Pharmaceutical compositions for prevention and treatment of ulcerative colitis |
US5597919A (en) | 1995-01-06 | 1997-01-28 | Dull; Gary M. | Pyrimidinyl or Pyridinyl alkenyl amine compounds |
US5585388A (en) | 1995-04-07 | 1996-12-17 | Sibia Neurosciences, Inc. | Substituted pyridines useful as modulators of acetylcholine receptors |
US5583140A (en) | 1995-05-17 | 1996-12-10 | Bencherif; Merouane | Pharmaceutical compositions for the treatment of central nervous system disorders |
IL118279A (en) | 1995-06-07 | 2006-10-05 | Abbott Lab | Compounds 3 - Pyridyloxy (or Thio) Alkyl Heterocyclic Pharmaceutical Compositions Containing Them and Their Uses for Preparing Drugs to Control Synaptic Chemical Transmission |
US5616716A (en) | 1996-01-06 | 1997-04-01 | Dull; Gary M. | (3-(5-ethoxypyridin)yl)-alkenyl 1 amine compounds |
AT403803B (de) | 1996-04-19 | 1998-05-25 | Sanochemia Ltd | Neue benzazepinderivate, diese enthaltende arzneimittel und verwendung derselben zum herstellen von arzneimitteln |
US6979695B2 (en) | 1996-04-23 | 2005-12-27 | Targacept, Inc. | Compounds capable of activating cholinergic receptors |
EP1997806A1 (en) | 1996-04-23 | 2008-12-03 | Targacept, Inc. | Pahrmaceutical compositions for prevention and treatment of central nervous system disorders |
US5663356A (en) | 1996-04-23 | 1997-09-02 | Ruecroft; Graham | Method for preparation of aryl substituted alefinic secondary amino compounds |
US20020052497A1 (en) | 2000-03-09 | 2002-05-02 | Targacept, Inc. | Compounds capable of activating cholinergic receptors |
US5726189A (en) | 1996-05-03 | 1998-03-10 | The United States Of America, Represented By The Secretary, Department Of Health And Human Services | Method for imaging nicotinic acetylcholinergic receptors in the brain using radiolabeled pyridyl-7-azabicyclo 2.2.1!heptanes |
US5861423A (en) | 1997-02-21 | 1999-01-19 | Caldwell; William Scott | Pharmaceutical compositions incorporating aryl substituted olefinic amine compounds |
US5811442A (en) | 1997-02-21 | 1998-09-22 | Bencherif; Merouane | Pharmaceutical compositions for the treatment of conditions associated with decreased blood flow |
ES2172882T3 (es) | 1997-05-08 | 2002-10-01 | Pfizer Prod Inc | Procedimientos y productos intermedios para la preparacion de derivados indazol sustituidos. |
EP1027336B1 (en) | 1997-10-27 | 2004-10-06 | Neurosearch A/S | Heteroaryl diazacycloalkanes as cholinergic ligands at nicotinic acetylcholine receptors |
US6632823B1 (en) | 1997-12-22 | 2003-10-14 | Merck & Co., Inc. | Substituted pyridine compounds useful as modulators of acetylcholine receptors |
EP1086082B9 (en) | 1998-06-16 | 2005-03-02 | Targacept, Inc. | Arylsubstituted olefinic amines and their use as cholinergic receptors agonists |
US6232316B1 (en) | 1998-06-16 | 2001-05-15 | Targacept, Inc. | Methods for treatment of CNS disorders |
US6218383B1 (en) | 1998-08-07 | 2001-04-17 | Targacept, Inc. | Pharmaceutical compositions for the prevention and treatment of central nervous system disorders |
US6337351B1 (en) | 1998-10-22 | 2002-01-08 | Targacept, Inc. | Pharmaceutical compositions and methods for use |
US6953855B2 (en) | 1998-12-11 | 2005-10-11 | Targacept, Inc. | 3-substituted-2(arylalkyl)-1-azabicycloalkanes and methods of use thereof |
FR2788982B1 (fr) | 1999-02-02 | 2002-08-02 | Synthelabo | Compositions pharmaceutiques contenant de la nicotine et leur application dans le sevrage tabagique |
WO2000075110A1 (en) | 1999-06-07 | 2000-12-14 | Targacept, Inc. | Pharmaceutical compositions and methods for use |
GB9922271D0 (en) | 1999-09-21 | 1999-11-17 | Zeneca Ltd | Formulation |
US6506769B2 (en) | 1999-10-06 | 2003-01-14 | Boehringer Ingelheim Pharmaceuticals, Inc. | Heterocyclic compounds useful as inhibitors of tyrosine kinases |
EP1274433A1 (en) | 2000-04-13 | 2003-01-15 | Innovata Biomed Limited | Medicaments for treating respiratory disorders comprising formoterol and fluticasone |
US6432954B1 (en) | 2000-07-14 | 2002-08-13 | Targacept, Inc. | Pharmaceutical compositions and methods for use |
US6743812B1 (en) | 2000-07-14 | 2004-06-01 | Targacept, Inc. | Pharmaceutical compositions and methods for use |
CN1610547A (zh) | 2001-03-29 | 2005-04-27 | 伊莱利利公司 | 用作5-ht6受体拮抗剂的n-(2-芳乙基)苄胺 |
GB2381750A (en) | 2001-10-10 | 2003-05-14 | Inspire Pharmaceuticals Inc | Treatment for enhancing joint lubrication |
BR0214929A (pt) | 2001-12-14 | 2006-05-30 | Targacept Inc | métodos e composições para o tratamento de distúrbios do sistema nervoso central |
EP1575495A4 (en) | 2002-03-27 | 2009-12-02 | Smithkline Beecham Corp | COMPOUNDS AND METHODS |
US20040044023A1 (en) | 2002-08-30 | 2004-03-04 | Marc Cantillon | Compositions and methods for treating or preventing memory impairment |
US20070191815A1 (en) | 2004-09-13 | 2007-08-16 | Chrono Therapeutics, Inc. | Biosynchronous transdermal drug delivery |
US20050203130A1 (en) | 2003-12-02 | 2005-09-15 | Erik Buntinx | Use of D4 and 5-HT2A antagonists, inverse agonists or partial agonists |
CA2549638A1 (en) | 2003-12-23 | 2005-07-14 | Pfizer Products Inc. | Therapeutic combination for cognition enhancement and psychotic disorders |
US20050171088A1 (en) | 2004-01-30 | 2005-08-04 | Astrazeneca Ab | Treatment of psychoses with dibenzothiazepine antipsychotic |
AU2004319105A1 (en) | 2004-03-29 | 2005-11-10 | Mediquest Therapeutics, Inc. | Polyamine analogs that activate antizyme frameshifting |
WO2006015299A2 (en) | 2004-07-30 | 2006-02-09 | Microchips, Inc. | Multi-reservoir device for transdermal drug delivery and sensing |
JP4148199B2 (ja) | 2004-07-30 | 2008-09-10 | 松下電工株式会社 | 電気かみそり |
US7459469B2 (en) * | 2004-11-10 | 2008-12-02 | Targacept, Inc. | Hydroxybenzoate salts of metanicotine compounds |
UA88792C2 (ru) | 2004-11-10 | 2009-11-25 | Таргасепт, Інк. | Гидроксибензоатные соли метаникотиновых соединений |
EP2021325A2 (en) | 2006-05-09 | 2009-02-11 | AstraZeneca AB | Salt forms of (2s)-(4e)-n-methyl-5-[3-(5-isopropoxypyridin)yl]-4-penten-2-amine |
TWI389889B (zh) | 2006-05-09 | 2013-03-21 | Targacept Inc | (2s)-(4e)-n-甲基-5-〔3-(5-異丙氧基吡啶)基〕-4-戊烯-2-胺之新穎多晶型 |
WO2007146319A2 (en) | 2006-06-13 | 2007-12-21 | Symphony Medical, Inc. | Methods and apparatus for using polymer-based beads and hydrogels for cardiac applications |
WO2008034041A2 (en) | 2006-09-15 | 2008-03-20 | Astrazeneca Ab | Therapeutic combinations |
US20080167286A1 (en) | 2006-12-12 | 2008-07-10 | Abbott Laboratories | Pharmaceutical compositions and their methods of use |
EP2112923A1 (en) | 2007-01-22 | 2009-11-04 | Targacept Inc. | Intranasal, buccal, and sublingual administration of metanicotine analogs |
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