JP2010505794A5 - - Google Patents

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Publication number
JP2010505794A5
JP2010505794A5 JP2009530875A JP2009530875A JP2010505794A5 JP 2010505794 A5 JP2010505794 A5 JP 2010505794A5 JP 2009530875 A JP2009530875 A JP 2009530875A JP 2009530875 A JP2009530875 A JP 2009530875A JP 2010505794 A5 JP2010505794 A5 JP 2010505794A5
Authority
JP
Japan
Prior art keywords
alkyl
amino
cycloalkyl
indazol
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.)
Abandoned
Application number
JP2009530875A
Other languages
English (en)
Japanese (ja)
Other versions
JP2010505794A (ja
Filing date
Publication date
Application filed filed Critical
Priority claimed from PCT/EP2007/060493 external-priority patent/WO2008040753A1/en
Publication of JP2010505794A publication Critical patent/JP2010505794A/ja
Publication of JP2010505794A5 publication Critical patent/JP2010505794A5/ja
Abandoned legal-status Critical Current

Links

JP2009530875A 2006-10-03 2007-10-03 カリウムチャネル調節剤として有用なインダゾリル誘導体 Abandoned JP2010505794A (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US82794006P 2006-10-03 2006-10-03
DKPA200601280 2006-10-03
PCT/EP2007/060493 WO2008040753A1 (en) 2006-10-03 2007-10-03 Indazolyl derivatives useful as potassium channel modulating agents

Publications (2)

Publication Number Publication Date
JP2010505794A JP2010505794A (ja) 2010-02-25
JP2010505794A5 true JP2010505794A5 (cg-RX-API-DMAC7.html) 2010-11-11

Family

ID=38959688

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2009530875A Abandoned JP2010505794A (ja) 2006-10-03 2007-10-03 カリウムチャネル調節剤として有用なインダゾリル誘導体

Country Status (7)

Country Link
US (1) US8222262B2 (cg-RX-API-DMAC7.html)
EP (1) EP2074113A1 (cg-RX-API-DMAC7.html)
JP (1) JP2010505794A (cg-RX-API-DMAC7.html)
AU (1) AU2007304195A1 (cg-RX-API-DMAC7.html)
CA (1) CA2665398A1 (cg-RX-API-DMAC7.html)
MX (1) MX2009003142A (cg-RX-API-DMAC7.html)
WO (1) WO2008040753A1 (cg-RX-API-DMAC7.html)

Families Citing this family (28)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
LT4193B (en) 1994-04-01 1997-07-25 Microcide Pharmaceuticals Inc Cephalosporin antibiotics
WO2008028935A2 (en) * 2006-09-07 2008-03-13 Neurosearch A/S Pyridinyl-pyrimidine derivatives useful as potassium channel modulating agents
JP2010517970A (ja) * 2007-02-02 2010-05-27 ノイロサーチ アクティーゼルスカブ ピリジニル−ピラゾール誘導体及びカリウムチャネル調節剤としてのそれらの使用
WO2008116910A1 (en) 2007-03-28 2008-10-02 Neurosearch A/S Purinyl derivatives and their use as potassium channel modulators
WO2009037247A1 (en) 2007-09-17 2009-03-26 Neurosearch A/S Pyrazine derivatives and their use as potassium channel modulators
RU2011105810A (ru) 2008-07-17 2012-08-27 Асахи Касеи Фарма Корпорейшн (Jp) Азотсодержащие бициклические гетероциклические соединения
WO2010026087A1 (en) * 2008-09-02 2010-03-11 Neurosearch A/S Pyrazolyl-pyrimidine derivatives and their use as potassium channel modulators
WO2010034706A1 (en) * 2008-09-26 2010-04-01 Neurosearch A/S Substituted purinyl-pyrazol derivatives and their use as potassium channel modulators
WO2010034707A1 (en) 2008-09-26 2010-04-01 Neurosearch A/S Substituted purinyl-pyrazol derivatives and their use as potassium channel modulators
AU2009322836B2 (en) * 2008-11-25 2013-04-04 Merck Sharp & Dohme Corp. Soluble guanylate cyclase activators
EP2549875B1 (en) 2010-03-25 2015-05-13 Merck Sharp & Dohme Corp. Soluble guanylate cyclase activators
CA2800541C (en) 2010-05-27 2016-03-22 Merck Sharp & Dohme Corp. Soluble guanylate cyclase activators
US8895583B2 (en) 2010-10-28 2014-11-25 Merck Sharp & Dohme Corp. Soluble guanylate cyclase activators
CN104411703A (zh) 2012-06-26 2015-03-11 萨尼奥纳有限责任公司 苯基三唑衍生物及其调节gabaa受体复合体的用途
TWI623531B (zh) 2012-11-21 2018-05-11 Ptc治療公司 經取代反向嘧啶bmi-1抑制劑
US9802904B2 (en) 2012-12-28 2017-10-31 The United States Of America, As Represented By The Secretary, Department Of Health And Human Services Inhibitors of the USP1/UAF1 deubiquitinase complex and uses thereof
JP6524094B2 (ja) 2013-08-30 2019-06-05 ピーティーシー セラピューティクス, インコーポレイテッド 置換ピリミジンBmi−1阻害剤
EP3071553A4 (en) 2013-11-21 2017-08-02 PTC Therapeutics, Inc. Substituted pyridine and pyrazine bmi-1 inhibitors
EP3080101A1 (en) 2013-12-10 2016-10-19 Cleave Biosciences, Inc. Monocyclic pyrimidine/pyridine compounds as inhibitors of p97 complex
MX374379B (es) 2014-01-20 2025-03-06 Cleave Biosciences Inc PIRIMIDINAS FUSIONADAS QUE TIENEN UN ANILLO HETEROCÍCLICO 5:6 COMO INHIBIDORES DEL COMPLEJO p97 Y EL USO DE LAS MISMAS EN EL TRATAMIENTO DE AFECCIONES NEOPLÁSICAS.
WO2017133664A1 (en) * 2016-02-05 2017-08-10 Savira Pharmaceuticals Gmbh Bicyclic pyridine and pyrimidine derivatives and their use in the treatment, amelioration or prevention of influenza
WO2017148995A1 (en) 2016-03-04 2017-09-08 Bayer Pharma Aktiengesellschaft 1-(pyrimidin-2-yl)-1h-indazoles having bub1 kinase inhibiting activity
WO2017210545A1 (en) 2016-06-02 2017-12-07 Cadent Therapeutics, Inc. Potassium channel modulators
PL3571193T3 (pl) 2017-01-23 2022-04-25 Cadent Therapeutics, Inc. Modulatory kanału potasowego
US11161854B2 (en) 2017-10-11 2021-11-02 Merck Sharp & Dohme Corp. Indazolyl-spiro[2.2]pentane-carbonitrile derivatives as LRRK2 inhibitors, pharmaceutical compositions, and uses thereof
EP3694331B1 (en) * 2017-10-11 2022-11-16 Merck Sharp & Dohme LLC Indazolyl-spiro[2.3]hexane-carbonitrile derivatives as lrrk2 inhibitors, pharmaceutical compositions, and uses thereof
AU2019340402B2 (en) 2018-08-17 2025-04-03 Ptc Therapeutics, Inc. Method for treating pancreatic cancer
BR112021007552A2 (pt) 2018-10-22 2021-07-27 Cadent Therapeutics, Inc. formas cristalinas de moduladores de canal de potássio

Family Cites Families (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
BR0207975A (pt) * 2001-03-15 2004-06-15 Basf Ag Composto, processo para preparar 5 fenilpiridinas, produto intermediário, agente adequado para combater fungos nocivos fitopatogênicos, e, processo para combater fungos nocivos fitopatogênicos
CL2004000409A1 (es) * 2003-03-03 2005-01-07 Vertex Pharma Compuestos derivados de 2-(cilo sustituido)-1-(amino u oxi sustituido)-quinazolina, inhibidores de canales ionicos de sodio y calcio dependientes de voltaje; composicion farmaceutica; y uso del compuesto en el tratamiento de dolor agudo, cronico, neu
PT1689739T (pt) * 2003-12-03 2016-07-13 Ym Biosciences Australia Pty Inibidores de cinases baseados em azol
US8252806B2 (en) 2005-03-14 2012-08-28 Neurosearch A/S Potassium channel modulating agents and their medical use
JP2008534472A (ja) 2005-03-22 2008-08-28 ノイロサーチ アクティーゼルスカブ カリウムチャンネル調節剤としてのピラゾリル−ピリミジン及びその医学的使用
US20090124645A1 (en) 2005-10-14 2009-05-14 Neurosearch A/S Novel Pyrimidine-2,4-Diamine Derivatives and their Use as Modulators of Small-Conductance Calcium-Activated Potassium Channels
JP2009519995A (ja) * 2005-12-20 2009-05-21 ノイロサーチ アクティーゼルスカブ 呼吸器疾患の治療のためのカリウムチャンネル調節剤としての2−ピリジン−2−イル−キナゾリン誘導体

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