JP2012520249A5 - - Google Patents

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JP2012520249A5
JP2012520249A5 JP2011553352A JP2011553352A JP2012520249A5 JP 2012520249 A5 JP2012520249 A5 JP 2012520249A5 JP 2011553352 A JP2011553352 A JP 2011553352A JP 2011553352 A JP2011553352 A JP 2011553352A JP 2012520249 A5 JP2012520249 A5 JP 2012520249A5
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Japan
Prior art keywords
pain
urinary incontinence
epilepsy
mania
migraine
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JP2011553352A
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JP2012520249A (ja
JP5727946B2 (ja
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Priority claimed from PCT/EP2010/001509 external-priority patent/WO2010102811A1/de
Publication of JP2012520249A publication Critical patent/JP2012520249A/ja
Publication of JP2012520249A5 publication Critical patent/JP2012520249A5/ja
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Expired - Fee Related legal-status Critical Current
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さらに、KCNQ2/3Kチャンネルは、多数の他の疾患、例えば偏頭痛(米国特許第2002/0128277号明細書)、認識疾患(Gribkoff著, Expert Opin Ther Targets 2003; 7(6): 737−748)、不安状態(Korsgaard et al.著, J Pharmacol Exp Ther. 2005, 14(1): 282−92)、てんかん(Wickenden et al.著, Expert Opin Ther Pat 2004, 14(4): 457−469; Gribkoff著, Expert Opin Ther Targets 2008, 12(5): 565−81; Miceli et al.著, Curr Opin Pharmacol 2008, 8(1): 65−74)、尿失禁(Streng et al.著, J Urol 2004;172: 2054−2058)、依存症(Hansen et al.著, Eur J Pharmacol 2007, 570(1−3): 77−88)、躁病/双極性障害(Dencker et al.著, Epilepsy Behav 2008, 12(1): 49−53)、筋失調に関連する運動障害(Richter et al.著, Br J Pharmacol 2006, 149(6): 747−53)の治療のための適当な対象である。
有利に、本発明による医薬は、痛み、有利に急性痛、慢性痛、神経障害性痛、筋肉性痛及び炎症性痛からなる群から選択される痛み;てんかん、尿失禁、不安状態、依存症、躁病、双極性障害、偏頭痛、認識疾患、筋失調と関連する運動障害及び/又は尿失禁からなる群から選択される1種又は数種の疾患の治療のために適している。
痛み、有利に急性痛、慢性痛、神経障害性痛、筋肉性痛及び炎症性痛から選択される痛み;てんかん、尿失禁、不安状態、依存症、躁病、双極性障害、偏頭痛、認識障害、筋失調と関連する運動障害及び/又は尿失禁を治療するための医薬を製造するための、少なくとも1種の本発明による置換された2−メルカプトキノリン−3−カルボキサミド並びに場合により1種若しくは数種の製剤学的に許容された助剤の使用が有利である。
本発明の他の主題は、痛み、有利に急性痛、慢性痛、神経障害性痛、筋肉性痛及び炎症性痛から選択される痛み;てんかん、尿失禁、不安状態、依存症、躁病、双極性障害、偏頭痛、認識障害、筋失調と関連する運動障害及び/又は尿失禁を治療するための、少なくとも1種の本発明による置換された2−メルカプトキノリン−3−カルボキサミド並びに場合により1種若しくは数種の製剤学的に許容された助剤である。

Claims (1)

  1. 痛み、てんかん、尿失禁、不安状態、依存症、躁病、双極性障害、偏頭痛、認識障害、筋失調と関連する運動障害及び/又は尿失禁の治療のための医薬を製造するための、それぞれ個々の立体異性体又はその混合物、遊離化合物及び/又はその生理学的に許容される塩の形態での請求項1から13のいずれか一項に記載の少なくとも1種の置換されたカルボキサミド又はN−ベンジル−2−(3−クロロ−2−ヒドロキシプロピルチオ)−4−(2,4−ジクロロフェニル)キノリン−3−カルボキサミドの化合物の使用。
JP2011553352A 2009-03-12 2010-03-11 Kcnq2/3モジュレータとしての置換された2−メルカプトキノリン−3−カルボキサミド Expired - Fee Related JP5727946B2 (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
EP09003597 2009-03-12
EP09003597.3 2009-03-12
PCT/EP2010/001509 WO2010102811A1 (de) 2009-03-12 2010-03-11 Substituierte 2-mercaptochinolin-3-carboxamide als kcnq2/3 modulatoren

Publications (3)

Publication Number Publication Date
JP2012520249A JP2012520249A (ja) 2012-09-06
JP2012520249A5 true JP2012520249A5 (ja) 2014-10-16
JP5727946B2 JP5727946B2 (ja) 2015-06-03

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JP2011553352A Expired - Fee Related JP5727946B2 (ja) 2009-03-12 2010-03-11 Kcnq2/3モジュレータとしての置換された2−メルカプトキノリン−3−カルボキサミド

Country Status (20)

Country Link
US (2) US20100234372A1 (ja)
EP (1) EP2406229A1 (ja)
JP (1) JP5727946B2 (ja)
KR (1) KR20110132590A (ja)
CN (1) CN102348692A (ja)
AR (1) AR075824A1 (ja)
AU (1) AU2010223513B2 (ja)
BR (1) BRPI1008939A2 (ja)
CA (1) CA2755004A1 (ja)
CL (1) CL2011002209A1 (ja)
CO (1) CO6410292A2 (ja)
EC (1) ECSP11011348A (ja)
IL (1) IL214945A0 (ja)
MX (1) MX2011009369A (ja)
NZ (1) NZ595625A (ja)
PE (1) PE20120790A1 (ja)
RU (1) RU2011141188A (ja)
TW (1) TWI461197B (ja)
WO (1) WO2010102811A1 (ja)
ZA (1) ZA201107444B (ja)

Families Citing this family (27)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP3178067B2 (ja) 1991-02-26 2001-06-18 ぺんてる株式会社 スズ−ニッケル二元合金電気めっき液組成物
WO2010102778A2 (de) * 2009-03-10 2010-09-16 Grünenthal GmbH Substituierte 3-aminoisoxazolopyridine als kcnq2/3 modulatoren
TWI504395B (zh) * 2009-03-10 2015-10-21 Substituted 3-amino-2-mercaptoquinoline as a KCNQ2 / 3 modifier
TW201038565A (en) 2009-03-12 2010-11-01 Gruenenthal Gmbh Substituted 2-mercapto-3-aminopyridines as KCNQ2/3 modulators
TWI475020B (zh) 2009-03-12 2015-03-01 The substituted nicotine amide as a KCNQ2 / 3 modifier
AR082732A1 (es) 2010-08-27 2012-12-26 Gruenenthal Gmbh 2-oxiquinolina-3-carboxamidas sustituidas como moduladores de kcnq2/3
WO2012025239A1 (en) 2010-08-27 2012-03-01 Grünenthal GmbH Substituted 2-oxo- and 2-thioxo-dihydroquinoline-3-carboxamides as kcnq2/3 modulators
CA2807886A1 (en) 2010-09-01 2012-03-08 Gruenenthal Gmbh Substituted 1-oxo-dihydroisoquinoline-3-carboxamides as kcnq2/3 modulators
AU2013329832A1 (en) 2012-10-11 2015-05-28 Grunenthal Gmbh Treatment and/or prophylaxis of TSPO mediated diseases and/or disorders
MX2015006689A (es) 2012-11-28 2015-08-20 Grünenthal GmbH Carboxamidas especificas como moduladores de kcnq2/3.
US9248122B2 (en) 2012-11-28 2016-02-02 Grünenthal GmbH Heteroquinoline-3-carboxamides as KCNQ2/3 modulators
CA2892652A1 (en) 2012-11-28 2014-06-05 Grunenthal Gmbh Heteroquinoline-3-carboxamides as kcnq2/3 modulators
NZ710111A (en) 2013-01-31 2020-08-28 Vertex Pharma Quinoline and quinoxaline amides as modulators of sodium channels
JP2016511237A (ja) 2013-02-01 2016-04-14 アセチロン ファーマシューティカルズ インコーポレイテッドAcetylon Pharmaceuticals,Inc. 選択的hdac3阻害剤
US9139583B2 (en) 2013-02-01 2015-09-22 Acetylon Pharmaceuticals, Inc. Selective HDAC3 inhibitors
HK1217092A1 (zh) 2013-02-15 2016-12-23 Kala Pharmaceuticals, Inc. 治疗性化合物及其用途
US9688688B2 (en) 2013-02-20 2017-06-27 Kala Pharmaceuticals, Inc. Crystalline forms of 4-((4-((4-fluoro-2-methyl-1H-indol-5-yl)oxy)-6-methoxyquinazolin-7-yl)oxy)-1-(2-oxa-7-azaspiro[3.5]nonan-7-yl)butan-1-one and uses thereof
BR112015020139A2 (pt) 2013-02-20 2017-07-18 Kala Pharmaceuticals Inc compostos terapêuticos e usos dos mesmos
KR20160099084A (ko) 2013-11-01 2016-08-19 칼라 파마슈티컬스, 인크. 치료 화합물의 결정질 형태 및 그의 용도
US9890173B2 (en) 2013-11-01 2018-02-13 Kala Pharmaceuticals, Inc. Crystalline forms of therapeutic compounds and uses thereof
PH12015000236B1 (en) * 2015-07-06 2024-01-10 Samsung Electronics Co Ltd Electronic device for providing a calibrated keyboard configuration
CA3036065A1 (en) 2016-09-08 2018-03-15 Kala Pharmaceuticals, Inc. Crystalline forms of therapeutic compounds and uses thereof
CA3036336A1 (en) 2016-09-08 2018-03-15 Kala Pharmaceuticals, Inc. Crystalline forms of therapeutic compounds and uses thereof
EP3509423A4 (en) 2016-09-08 2020-05-13 Kala Pharmaceuticals, Inc. CRYSTALLINE FORMS OF THERAPEUTIC COMPOUNDS AND USES THEREOF
JP7120549B2 (ja) * 2016-12-15 2022-08-17 小野薬品工業株式会社 Trek(twik関連kチャネル)チャネルのアクチベータ
DE102018212006B3 (de) * 2018-07-18 2019-10-31 Universität Greifswald Thioether als Modulatoren von Kv7.2/Kv7.3-Kanälen
EP4580618A2 (en) * 2022-08-30 2025-07-09 Pannex Therapeutics Inc. Pannexin-1 modulators and methods of treating disorders in which pannexin-1 is implicated

Family Cites Families (38)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE2706977A1 (de) 1977-02-18 1978-08-24 Hoechst Ag Benzoesaeuren und deren derivate sowie verfahren zu ihrer herstellung
FR2532939A1 (fr) * 1982-09-13 1984-03-16 Roussel Uclaf Nouveaux derives de l'acide 4-hydroxy 3-quinoleine carboxylique substitues en 2, leur preparation, leur application comme medicament, les compositions les renfermant et les nouveaux intermediaires obtenus
DE4032147A1 (de) 1990-10-10 1992-04-16 Bayer Ag Verwendung von substituierten 2-mercaptonicotinsaeurederivaten zur bekaempfung von endoparasiten, neue substituierte 2-mercaptonicotinsaeurederivate und verfahren zu ihrer herstellung
EP0716077A1 (de) 1994-12-08 1996-06-12 Ciba-Geigy Ag Aromatisch substituierte Omega-Aminoalkansäureamide und Alkansäurediamide und ihre Verwendung als Renininhibitoren
WO1996026925A1 (en) 1995-03-01 1996-09-06 Banyu Pharmaceutical Co., Ltd. Arylthioacetamide derivatives
DE19738616A1 (de) 1997-09-04 1999-03-11 Clariant Gmbh 4-Hydroxychinolin-3-carbonsäure-Derivate als Lichtschutzmittel
DE19738615A1 (de) * 1997-09-04 1999-03-11 Clariant Gmbh Neue Lichtschutzmittel auf Basis von sterisch gehinderten Aminen
WO2000042026A1 (en) * 1999-01-15 2000-07-20 Novo Nordisk A/S Non-peptide glp-1 agonists
EP1208085B1 (en) 1999-08-04 2007-12-05 Icagen, Inc. Benzanilides as potassium channel openers
BR0012934A (pt) 1999-08-04 2003-07-29 Icagen Inc Processos para a redução de dor e de ansiedade
IL157313A0 (en) * 2001-02-20 2004-02-19 Bristol Myers Squibb Co Modulators of kcnq potassium channels and uses thereof
HUP0303841A2 (hu) 2001-02-20 2004-03-01 Bristol-Myers Squibb Company 2,4-Diszubsztituált-5-pirimidinkarboxamid-származékok mint KCNQ káliumcsatorna modulátorok és ezeket tartalmazó gyógyszerkészítmények és előállításuk
US6593349B2 (en) 2001-03-19 2003-07-15 Icagen, Inc. Bisarylamines as potassium channel openers
JP2004526756A (ja) * 2001-04-06 2004-09-02 スミスクライン ビーチャム コーポレーション hYAK1及びhYAK3キナーゼのキノリン阻害剤
JP2005539081A (ja) 2002-09-17 2005-12-22 ファルマシア コーポレイション 芳香族肝臓x受容体モジュレーター
AU2003303484C1 (en) 2002-12-23 2012-06-14 Icagen, Inc. Quinazolinones as potassium channel modulators
EP1449841A1 (en) 2003-02-19 2004-08-25 Bayer CropScience SA New fungicidal compounds
AU2004279855A1 (en) 2003-10-08 2005-04-21 Vertex Pharmaceuticals Incorporated Modulators of ATP-binding cassette transporters containing cycloalkyl or pyranyl groups
CN1950334A (zh) 2004-05-04 2007-04-18 辉瑞有限公司 邻位取代的芳基或杂芳基酰胺化合物
MX341797B (es) * 2004-06-24 2016-09-02 Vertex Pharmaceuticals Incorporated * Moduladores de transportadores con casete de union con atp.
CA2585490A1 (en) 2004-11-12 2006-05-18 Galapagos Nv Nitrogen heteroaromatic compounds which bind to the active site of protein kinase enzymes
WO2006092143A1 (en) 2005-03-03 2006-09-08 H. Lundbeck A/S Substituted pyridine derivatives
DE102005038947A1 (de) 2005-05-18 2006-11-30 Grünenthal GmbH Substituierte Benzo[d]isoxazol-3-yl-amin-Verbindungen und deren Verwendung in Arzneimitteln
US8133907B2 (en) 2005-07-20 2012-03-13 Eli Lilly And Company Pyridine derivatives as dipeptedyl peptidase inhibitors
US7915410B2 (en) 2005-09-09 2011-03-29 Bristol-Myers Squibb Company Acyclic IKur inhibitors
WO2007057447A1 (en) 2005-11-18 2007-05-24 Neurosearch A/S Novel quinazoline derivatives and their medical use
WO2008011080A2 (en) 2006-07-20 2008-01-24 Amgen Inc. Benzo(d) isoxazole derivatives as c-kit tyrosine kinase inhibitors for the treatment of disorders associated with the over production of histamine
CA2658190C (en) 2006-07-20 2013-01-29 Amgen Inc. Di-amino-substituted heterocyclic compounds and methods of use
US20100022589A1 (en) 2006-07-27 2010-01-28 Mccoull William Pyridine-3-carboxamide compounds and their use for inhibiting 11-beta-hydroxysteroid dehydrogenase
DE102006049452A1 (de) 2006-10-17 2008-05-08 Grünenthal GmbH Substituierte Tetrahydropyrolopiperazin-Verbindungen und deren Verwendung in Arzneimitteln
WO2008066900A1 (en) * 2006-11-28 2008-06-05 Valeant Pharmaceuticals International 1,4 diamino bicyclic retigabine analogues as potassium channel modulators
US8563566B2 (en) 2007-08-01 2013-10-22 Valeant Pharmaceuticals International Naphthyridine derivatives as potassium channel modulators
BRPI0814758A2 (pt) 2007-08-03 2015-03-03 Hoffmann La Roche Piridinacarboxamida e derivados de benzamida como ligantes taar1
CA2702469A1 (en) 2007-10-19 2009-04-23 Boehringer Ingelheim International Gmbh Ccr10 antagonists
TWI504395B (zh) * 2009-03-10 2015-10-21 Substituted 3-amino-2-mercaptoquinoline as a KCNQ2 / 3 modifier
WO2010102778A2 (de) * 2009-03-10 2010-09-16 Grünenthal GmbH Substituierte 3-aminoisoxazolopyridine als kcnq2/3 modulatoren
TWI475020B (zh) * 2009-03-12 2015-03-01 The substituted nicotine amide as a KCNQ2 / 3 modifier
TW201038565A (en) * 2009-03-12 2010-11-01 Gruenenthal Gmbh Substituted 2-mercapto-3-aminopyridines as KCNQ2/3 modulators

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