JP2002531552A5 - - Google Patents

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Publication number
JP2002531552A5
JP2002531552A5 JP2000586696A JP2000586696A JP2002531552A5 JP 2002531552 A5 JP2002531552 A5 JP 2002531552A5 JP 2000586696 A JP2000586696 A JP 2000586696A JP 2000586696 A JP2000586696 A JP 2000586696A JP 2002531552 A5 JP2002531552 A5 JP 2002531552A5
Authority
JP
Japan
Prior art keywords
disease
cycloalkyl
pharmaceutically acceptable
alkyl
ischemia
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.)
Pending
Application number
JP2000586696A
Other languages
English (en)
Japanese (ja)
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JP2002531552A (ja
Filing date
Publication date
Application filed filed Critical
Priority claimed from PCT/DK1999/000681 external-priority patent/WO2000034248A1/en
Publication of JP2002531552A publication Critical patent/JP2002531552A/ja
Publication of JP2002531552A5 publication Critical patent/JP2002531552A5/ja
Pending legal-status Critical Current

Links

JP2000586696A 1998-12-04 1999-12-03 イオンチャネル調節剤としての新規ベンズイミダゾロン−、ベンズオキサゾロン−又はベンゾチアゾロン−誘導体 Pending JP2002531552A (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
DK199801610 1998-12-04
DKPA199801610 1998-12-04
PCT/DK1999/000681 WO2000034248A1 (en) 1998-12-04 1999-12-03 New benzimidazolone-, benzoxazolone-, or benzothiazolone derivatives as ion channel modulating agents

Publications (2)

Publication Number Publication Date
JP2002531552A JP2002531552A (ja) 2002-09-24
JP2002531552A5 true JP2002531552A5 (https=) 2007-02-01

Family

ID=8106528

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2000586696A Pending JP2002531552A (ja) 1998-12-04 1999-12-03 イオンチャネル調節剤としての新規ベンズイミダゾロン−、ベンズオキサゾロン−又はベンゾチアゾロン−誘導体

Country Status (8)

Country Link
US (2) US6624186B2 (https=)
EP (1) EP1144387A1 (https=)
JP (1) JP2002531552A (https=)
CN (1) CN1177831C (https=)
AU (1) AU760250B2 (https=)
CA (1) CA2349616A1 (https=)
NZ (1) NZ511334A (https=)
WO (1) WO2000034248A1 (https=)

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HUP0400063A2 (hu) * 2001-02-20 2004-04-28 Bristol-Myers Squibb Company Fluor-oxo-indolszármazékok mint KCNQ káliumcsatorna modulátorok, alkalmazásuk és ezeket tartalmazó gyógyszerkészítmények
US7541443B2 (en) * 2001-06-14 2009-06-02 Tolerrx, Inc. Anti-CD4 antibodies
US7022480B1 (en) 2001-10-11 2006-04-04 The Regents Of The University Of California Exons of the hSKCa3/KCNN3 gene
DE10231105A1 (de) 2002-07-10 2004-01-22 Clariant Gmbh Neue Diketopyrrolopyrrolpigmente
US7632866B2 (en) 2002-10-21 2009-12-15 Ramot At Tel Aviv University Derivatives of N-phenylanthranilic acid and 2-benzimidazolone as potassium channel and/or neuron activity modulators
KR20050074493A (ko) * 2002-10-21 2005-07-18 라모트 앳 텔-아비브 유니버시티 리미티드 칼륨 채널 및/또는 피질 뉴우런 작용 조절제로서 유용한n-페닐안트라닐산 및/또는 2-벤즈이미다졸론의 유도체
AU2005201685B2 (en) * 2002-10-21 2008-10-09 Ramot At Tel Aviv University Ltd. Derivatives of N-Phenylanthranilic Acid and 2-Benzimidazolon as Potassium Channel and/or Cortical Neuron Activity Modulators
DE10250870A1 (de) * 2002-10-31 2004-05-13 Switch Biotech Ag Zusammensetzung enthaltend Aktivatoren von IK-Kaliumkanälen und Calcineurin-Antagonisten und deren Verwendung
WO2004064835A1 (en) * 2003-01-17 2004-08-05 Neurosearch A/S Use of ion channel modulating agents for treating pain
US7176214B2 (en) 2003-05-21 2007-02-13 Bristol-Myers Squibb Company Imidazo-fused oxazolo[4,5-β]pyridine and imidazo-fused thiazolo[4,5-β]pyridine based tricyclic compounds and pharmaceutical compositions comprising same
WO2006115509A2 (en) 2004-06-24 2006-11-02 Novartis Vaccines And Diagnostics Inc. Small molecule immunopotentiators and assays for their detection
EP1958947A1 (en) 2007-02-15 2008-08-20 Ranbaxy Laboratories Limited Inhibitors of phosphodiesterase type 4
US8765815B2 (en) 2007-09-20 2014-07-01 Ramot At Tel-Aviv University Ltd. N-phenyl anthranilic acid derivatives and uses thereof
JO3192B1 (ar) 2011-09-06 2018-03-08 Novartis Ag مركب بنزوثيازولون
JP2014532660A (ja) * 2011-10-28 2014-12-08 メルク・シャープ・アンド・ドーム・コーポレーションMerck Sharp & Dohme Corp. 電位作動型ナトリウムチャネルにおける選択活性を有するベンゾオキサゾリノン化合物
MX2015002399A (es) * 2012-10-29 2015-06-10 Hoffmann La Roche Derivados de oxazolidinona 3,4-disustituidos y su uso como inhibidores del canal de potasio activado con calcio.
US9765039B2 (en) 2012-11-21 2017-09-19 Zenith Epigenetics Ltd. Biaryl derivatives as bromodomain inhibitors
US9073878B2 (en) 2012-11-21 2015-07-07 Zenith Epigenetics Corp. Cyclic amines as bromodomain inhibitors
AU2013365926B9 (en) 2012-12-21 2019-01-17 Zenith Epigenetics Ltd. Novel heterocyclic compounds as bromodomain inhibitors
EP3010918B1 (en) * 2013-06-21 2018-08-15 Zenith Epigenetics Ltd. Novel substituted bicyclic compounds as bromodomain inhibitors
CA2915838C (en) 2013-06-21 2023-04-18 Zenith Epigenetics Corp. Bicyclic bromodomain inhibitors
JP6542212B2 (ja) 2013-07-31 2019-07-10 ゼニス・エピジェネティクス・リミテッドZenith Epigenetics Ltd. ブロモドメイン阻害剤としての新規キナゾリノン
HK1246273B (en) 2014-12-01 2019-12-06 恒翼生物医药(上海)股份有限公司 Substituted pyridines as bromodomain inhibitors
EP3227281A4 (en) 2014-12-01 2018-05-30 Zenith Epigenetics Ltd. Substituted pyridinones as bromodomain inhibitors
EP3230277B1 (en) 2014-12-11 2019-09-18 Zenith Epigenetics Ltd. Substituted heterocycles as bromodomain inhibitors
HK1245247A1 (zh) 2014-12-17 2018-08-24 恒翼生物医药科技(上海)有限公司 溴结构域的抑制剂
CN105294591B (zh) * 2015-11-17 2017-05-10 河南大学 一种高立体和高对映选择性噁唑啉二酮类化合物、制备方法及其应用
KR101751486B1 (ko) 2016-03-02 2017-06-28 광주과학기술원 BKCa 채널 활성화용 조성물
ES3060268T3 (en) 2018-04-13 2026-03-25 Cancer Research Tech Ltd Bcl6 inhibitors
CN109701024B (zh) * 2019-03-04 2020-12-11 复旦大学 Bk通道开放剂的新用途
GB201914860D0 (en) 2019-10-14 2019-11-27 Cancer Research Tech Ltd Inhibitor compounds
EP4074707A4 (en) * 2019-12-10 2024-01-03 Shanghai Zhimeng Biopharma, Inc. COMPOUND WITH NEUROPROTECTIVE EFFECT, PREPARATION METHOD AND USE THEREOF
EP4466253A4 (en) * 2022-01-17 2025-07-02 Univ Ramot SK4 POTASSIUM CHANNEL MODULATORS AND THEIR USES

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IT1050681B (it) * 1974-08-31 1981-03-20 Agfa Gevaert Ag Materiale fotografico a colori e copulante giallo per esso
IT1106962B (it) * 1977-01-17 1985-11-18 Sumitomo Chemical Co Composit derivati del benzossa tiazolone utilizzabili particolarmente come fungicidi
US4420486A (en) * 1981-01-22 1983-12-13 Hokko Chemical Industry Co., Ltd. Benzoxazolone derivatives, processes for preparation thereof and compositions containing them
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FI930860A7 (fi) * 1990-08-29 1993-02-25 Upjohn Co Tropolonijohdoksia ja niiden farmaseuttisia koostumuksia iskeemisten s airauksien ehkäisemiseen ja hoitamiseen
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US5314903A (en) * 1991-12-03 1994-05-24 Neurosearch A/S Benzimidazole compounds useful as calcium channel blockers
DK40192D0 (da) * 1992-03-26 1992-03-26 Neurosearch As Imidazolforbindelser, deres fremstilling og anvendelse
WO1997012613A1 (en) 1995-10-05 1997-04-10 Warner-Lambert Company Method for treating and preventing inflammation and atherosclerosis
DE19539114C1 (de) 1995-10-20 1997-04-17 Hoechst Ag Verfahren zur Aufarbeitung von Benzimidazolone enthaltenden Reaktionsgemischen
RU2227458C2 (ru) 1998-06-18 2004-04-27 Новартис Аг Применение бензазольных соединений в качестве репеллента, композиция их содержащая и способ получения композиции
GB0008939D0 (en) 2000-04-11 2000-05-31 Glaxo Group Ltd Process for preparing substituted benzimidazole compounds

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