JP2008543915A - 2−(フェニルアミノ)ベンズイミダゾール誘導体及び低コンダクタンスカルシウム依存性カリウムチャネルのモジュレーターとしてのそれらの使用 - Google Patents

2−(フェニルアミノ)ベンズイミダゾール誘導体及び低コンダクタンスカルシウム依存性カリウムチャネルのモジュレーターとしてのそれらの使用 Download PDF

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JP2008543915A
JP2008543915A JP2008517496A JP2008517496A JP2008543915A JP 2008543915 A JP2008543915 A JP 2008543915A JP 2008517496 A JP2008517496 A JP 2008517496A JP 2008517496 A JP2008517496 A JP 2008517496A JP 2008543915 A JP2008543915 A JP 2008543915A
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benzimidazol
trifluoromethyl
aniline
disease
alkyl
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JP2008543915A5 (cg-RX-API-DMAC7.html
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セーレンセン、ウルリック、スバネ
トイバー、レーネ
ペーターズ、ダン
ストレベク、ドルテ
ヨハンセン、ティナ、ホルム
ニールセン、カリン、サンダガー
クリストファーセン、パレ
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ノイロサーチ アクティーゼルスカブ
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Publication of JP2008543915A5 publication Critical patent/JP2008543915A5/ja
Abandoned legal-status Critical Current

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    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D235/00Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings
    • C07D235/02Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings condensed with carbocyclic rings or ring systems
    • C07D235/04Benzimidazoles; Hydrogenated benzimidazoles
    • C07D235/24Benzimidazoles; Hydrogenated benzimidazoles with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached in position 2
    • C07D235/30Nitrogen atoms not forming part of a nitro radical
    • AHUMAN NECESSITIES
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JP2008517496A 2005-06-21 2006-06-21 2−(フェニルアミノ)ベンズイミダゾール誘導体及び低コンダクタンスカルシウム依存性カリウムチャネルのモジュレーターとしてのそれらの使用 Abandoned JP2008543915A (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US69225205P 2005-06-21 2005-06-21
DKPA200500910 2005-06-21
PCT/EP2006/063405 WO2006136580A2 (en) 2005-06-21 2006-06-21 2-(phenylamino)benzimidazole derivatives and their use as modulators of small-conductance calcium-activated potassium channels

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Publication Number Publication Date
JP2008543915A true JP2008543915A (ja) 2008-12-04
JP2008543915A5 JP2008543915A5 (cg-RX-API-DMAC7.html) 2009-07-23

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JP2008517496A Abandoned JP2008543915A (ja) 2005-06-21 2006-06-21 2−(フェニルアミノ)ベンズイミダゾール誘導体及び低コンダクタンスカルシウム依存性カリウムチャネルのモジュレーターとしてのそれらの使用

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Country Link
US (1) US7960561B2 (cg-RX-API-DMAC7.html)
EP (1) EP1896427A2 (cg-RX-API-DMAC7.html)
JP (1) JP2008543915A (cg-RX-API-DMAC7.html)
CA (1) CA2612922A1 (cg-RX-API-DMAC7.html)
MX (1) MX2007015689A (cg-RX-API-DMAC7.html)
WO (1) WO2006136580A2 (cg-RX-API-DMAC7.html)

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Publication number Priority date Publication date Assignee Title
GB0715103D0 (en) * 2007-08-03 2007-09-12 Lectus Therapeutics Ltd Calcium ion channel modulators and uses thereof
CA3207643A1 (en) 2015-09-23 2017-03-30 XWPharma Ltd. Prodrugs of gamma-hydroxybutyric acid, compositions and uses thereof
EP3419973B1 (en) * 2016-02-24 2020-04-08 Acesion Pharma ApS Novel potassium channel inhibitors
WO2017160922A1 (en) * 2016-03-16 2017-09-21 Kalyra Pharmaceuticals, Inc. Analgesic compounds
BR112019020464A2 (pt) 2017-03-30 2020-04-28 Xw Laboratories Inc. compostos derivados de heteroarila bicíclica, composição farmacêutica compreendendo os ditos compostos, adesivo transdérmico compreendendo a dita composição e uso terapêutico dos compostos e composição
US11168074B2 (en) * 2017-08-23 2021-11-09 Acesion Pharma Aps Potassium channel inhibitors
ES2947089T3 (es) 2018-09-30 2023-08-01 Xwpharma Ltd Compuestos como antagonistas del receptor histamínico 3 neuronal y usos de los mismos
WO2021127461A1 (en) 2019-12-20 2021-06-24 Xw Laboratories Limited Methods of synthesizing 4-valyloxybutyric acid
KR20230008190A (ko) 2020-06-18 2023-01-13 엑스더블유파마 리미티드 수용성 원료의약품의 약학적 과립화제
AU2021292406B2 (en) 2020-06-18 2024-03-14 XWPharma Ltd. Controlled release granulations of water-soluble active pharmaceutical ingredients
WO2022020621A1 (en) 2020-07-24 2022-01-27 XWPharma Ltd. Pharmaceutical compositions and pharmacokinetics of a gamma-hydroxybutyric acid derivative
AU2021357705B2 (en) 2020-10-05 2024-09-26 XWPharma Ltd. Modified release compositions of a gamma-hydroxybutyric acid derivative
EP4308086B1 (en) 2021-03-19 2025-10-15 XWPharma Ltd. Pharmacokinetics of combined release formulations of a gamma-hydroxybutyric acid derivative

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BE632578A (cg-RX-API-DMAC7.html) * 1963-05-22
GB1171904A (en) * 1965-10-21 1969-11-26 Unilever Ltd Anilinobenzimidazoles having Antibacterial Properties
JP2869561B2 (ja) 1989-05-22 1999-03-10 大塚製薬株式会社 血小板粘着抑制剤
WO1998040381A1 (en) * 1997-03-14 1998-09-17 Vertex Pharmaceuticals Incorporated Inhibitors of impdh enzyme
WO2001021160A2 (en) 1999-09-23 2001-03-29 Axxima Pharmaceuticals Aktiengesellschaft Carboxymide and aniline derivatives as selective inhibitors of pathogens
DE10060292A1 (de) * 2000-12-05 2002-06-20 Aventis Pharma Gmbh Verwendung substituierter Benzimidazole zur Herstellung eines Medikaments zur Behandlung von Krankheiten, welche durch Inhibierung des Na+/H+-Austauschers beeinflusst werden können und sie enthaltendes Medikament
WO2003043345A1 (fr) 2001-11-16 2003-05-22 Ntt Docomo, Inc. Procede de codage d'image, procede de decodage d'image, codeur et decodeur d'image, programme, signal de donnees informatiques et systeme d'emission d'image
DE10304294A1 (de) * 2003-02-04 2004-08-12 Aventis Pharma Deutschland Gmbh N-Substituierte(Benzoimidazol-2-yl)-phenyl, Verfahren zu ihrer Herstellung , ihre Verwendung als Medikament oder Diagnostikum sowie sie enthaltendes Medikament
US20050054705A1 (en) 2003-02-04 2005-03-10 Aventis Pharma Deutschland Gmbh N-substituted (benzoimidazol-2-yl) phenylamines, process for their preparation, their use as medicament or diagnostic aid, and medicament comprising them
WO2004098494A2 (en) 2003-04-30 2004-11-18 Cytokinetics, Inc. Compounds, compositions, and methods
EP1677791A4 (en) 2003-10-31 2007-08-15 Takeda Pharmaceutical NITROGENIC CONDENSED HETEROCYCLIC COMPOUNDS

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WO2006136580A3 (en) 2007-04-12
CA2612922A1 (en) 2006-12-28
US7960561B2 (en) 2011-06-14
WO2006136580A2 (en) 2006-12-28
MX2007015689A (es) 2008-02-21
US20090076106A1 (en) 2009-03-19
EP1896427A2 (en) 2008-03-12

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