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

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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
DKPA199801610 1998-12-04
DK199801610 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 (enExample) 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 (enExample)
EP (1) EP1144387A1 (enExample)
JP (1) JP2002531552A (enExample)
CN (1) CN1177831C (enExample)
AU (1) AU760250B2 (enExample)
CA (1) CA2349616A1 (enExample)
NZ (1) NZ511334A (enExample)
WO (1) WO2000034248A1 (enExample)

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GB0021487D0 (en) * 2000-09-01 2000-10-18 Pfizer Ltd Pharmaceutical
EP1345618B1 (de) * 2000-12-28 2005-03-23 Switch Biotech Aktiengesellschaft Chlorzoxazon zur behandlung von psoriasis
CA2438805A1 (en) * 2001-02-20 2002-08-29 Bristol-Myers Squibb Company Fluoro oxindole derivatives as modulators of kcnq potassium channels
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
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
AU2003272068A1 (en) * 2002-10-21 2004-05-04 Ramot At Tel Aviv University Ltd. Derivatives of n-phenylanthranilic acid and 2-benzimidazolon as potassium channel and/or cortical neuron activity modulators
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
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
CA2571710A1 (en) 2004-06-24 2006-11-02 Nicholas Valiante Small molecule immunopotentiators and assays for their detection
EP1958947A1 (en) 2007-02-15 2008-08-20 Ranbaxy Laboratories Limited Inhibitors of phosphodiesterase type 4
CN101868443A (zh) 2007-09-20 2010-10-20 特拉维夫大学拉莫特有限公司 N-苯基邻氨基苯甲酸衍生物及其用途
JO3192B1 (ar) 2011-09-06 2018-03-08 Novartis Ag مركب بنزوثيازولون
KR20140095067A (ko) 2011-10-28 2014-07-31 머크 샤프 앤드 돔 코포레이션 전압-게이팅 나트륨 채널에서의 선택적 활성을 갖는 벤족사졸리논 화합물
SG11201500585XA (en) * 2012-10-29 2015-04-29 Hoffmann La Roche 3,4-disubstituted oxazolidinone derivatives and their use as inhibitors of the calcium activated potassium channel
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
CA2895905A1 (en) 2012-12-21 2014-06-26 Zenith Epigenetics Corp. Novel heterocyclic compounds as bromodomain inhibitors
WO2015004533A2 (en) * 2013-06-21 2015-01-15 Zenith Epigenetics Corp. Novel substituted bicyclic compounds as bromodomain inhibitors
PL3010503T3 (pl) 2013-06-21 2020-08-24 Zenith Epigenetics Ltd. Nowe bicykliczne inhibitory bromodomen
EP3027604B1 (en) 2013-07-31 2019-02-20 Zenith Epigenetics Ltd. Novel quinazolinones as bromodomain inhibitors
US10710992B2 (en) 2014-12-01 2020-07-14 Zenith Epigenetics Ltd. Substituted pyridinones as bromodomain inhibitors
EP3227280B1 (en) 2014-12-01 2019-04-24 Zenith Epigenetics Ltd. Substituted pyridines as bromodomain inhibitors
CN107207474B (zh) 2014-12-11 2021-05-07 恒翼生物医药科技(上海)有限公司 被取代的杂环作为溴结构域抑制剂
US10231953B2 (en) 2014-12-17 2019-03-19 Zenith Epigenetics Ltd. Inhibitors of bromodomains
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
JP7493454B2 (ja) 2018-04-13 2024-05-31 キャンサー・リサーチ・テクノロジー・リミテッド Bcl6阻害剤
CN109701024B (zh) * 2019-03-04 2020-12-11 复旦大学 Bk通道开放剂的新用途
NZ789439A (en) * 2019-12-10 2025-07-25 Shanghai Zhimeng Biopharma Inc Compound having neuroprotective effect, preparation method therefor and use thereof
EP4466253A4 (en) * 2022-01-17 2025-07-02 Univ Ramot SK4 POTASSIUM CHANNEL MODULATORS AND THEIR USES

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US2927116A (en) * 1960-03-01 Chlorobenzimidazolone compounds
GB1363735A (en) * 1970-10-23 1974-08-14 Hoechst Ag Process for the manufacture of benzimidazolones
CA1058191A (en) * 1974-08-31 1979-07-10 Karl Kuffner Color photographic material containing new 2-equivalent yellow couplers
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
DE3839743A1 (de) 1988-11-25 1990-05-31 Hoechst Ag Verfahren zur herstellung von benzimidazolonen
EP0401582B1 (de) * 1989-06-01 1994-07-20 BASF Aktiengesellschaft Fünfring-heterocyclisch anellierte Chinolinderivate
ATE159251T1 (de) * 1990-08-29 1997-11-15 Upjohn Co Tropolonderivate und pharmazeutische zubereitungen davon zur vorbeugung und behandlung von ischämischen krankheiten
NZ239540A (en) * 1990-09-24 1993-11-25 Neurosearch As 1-phenyl benzimidazole derivatives and medicaments
US5296493A (en) * 1991-05-23 1994-03-22 Neurosearch A/S 1-substituted-2-(N-phenyl-N-(phenylmethyl)methanamine)-4,5-dihydro-imidazoles and related compounds and their use in treating calcium overload in brain cells
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
AU6966696A (en) 1995-10-05 1997-04-28 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
AR019678A1 (es) 1998-06-18 2002-03-13 Novartis Ag Compuestos organicos
GB0008939D0 (en) 2000-04-11 2000-05-31 Glaxo Group Ltd Process for preparing substituted benzimidazole compounds

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