CN1902181A - 可用作离子通道调控剂的苯并咪唑 - Google Patents

可用作离子通道调控剂的苯并咪唑 Download PDF

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Publication number
CN1902181A
CN1902181A CNA2004800392479A CN200480039247A CN1902181A CN 1902181 A CN1902181 A CN 1902181A CN A2004800392479 A CNA2004800392479 A CN A2004800392479A CN 200480039247 A CN200480039247 A CN 200480039247A CN 1902181 A CN1902181 A CN 1902181A
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pain
ring
independently selected
formula
group
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Chinese (zh)
Inventor
D·M·威尔森
A·P·特敏
J·E·冈萨雷斯三世
N·奇默曼
张玉莲
L·T·D·范宁
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Vertex Pharmaceuticals Inc
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Vertex Pharmaceuticals Inc
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Publication of CN1902181A publication Critical patent/CN1902181A/zh
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  • Cardiology (AREA)
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  • Hematology (AREA)
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CNA2004800392479A 2003-10-28 2004-10-28 可用作离子通道调控剂的苯并咪唑 Pending CN1902181A (zh)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US51508803P 2003-10-28 2003-10-28
US60/515,088 2003-10-28

Publications (1)

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CN1902181A true CN1902181A (zh) 2007-01-24

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US (2) US7309716B2 (https=)
EP (1) EP1678145A2 (https=)
JP (1) JP2007521325A (https=)
KR (1) KR20060115396A (https=)
CN (1) CN1902181A (https=)
AU (1) AU2004285053B2 (https=)
CA (1) CA2543918A1 (https=)
IL (1) IL175252A0 (https=)
NO (1) NO20062426L (https=)
NZ (1) NZ547109A (https=)
RU (1) RU2006118312A (https=)
WO (1) WO2005042497A2 (https=)
ZA (1) ZA200603864B (https=)

Cited By (6)

* Cited by examiner, † Cited by third party
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CN104926745A (zh) * 2015-07-14 2015-09-23 佛山市赛维斯医药科技有限公司 含苯并异恶唑和末端卤代苄基类结构的化合物及其用途
CN104974103A (zh) * 2015-07-14 2015-10-14 佛山市赛维斯医药科技有限公司 一类含苯并异恶唑和烷氧苯基类结构的化合物及其用途
CN107922350A (zh) * 2015-09-11 2018-04-17 大日本住友制药株式会社 新的苯并咪唑化合物及其医药用途
CN113692276A (zh) * 2019-02-19 2021-11-23 加利福尼亚大学董事会 Nurr1受体调节剂
CN117730074A (zh) * 2021-05-12 2024-03-19 菲斯欧洲地中海大学 作为mpro蛋白酶和sars-cov-2复制的抑制剂的利尿酸衍生物
WO2025067475A1 (zh) * 2023-09-28 2025-04-03 四川大学华西医院 一类镇痛的化合物及其制备方法和用途

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KR101143246B1 (ko) 2007-06-29 2012-05-18 화이자 인코포레이티드 벤즈이미다졸 유도체
CN101883760A (zh) 2007-10-11 2010-11-10 沃泰克斯药物股份有限公司 用作电压-门控钠通道抑制剂的杂芳基酰胺类
WO2009061744A2 (en) * 2007-11-06 2009-05-14 Edison Pharmaceuticals, Inc. 4- (p-quinonyl)-2-hydroxybutanamide derivatives for treatment of mitochondrial diseases
RU2379294C1 (ru) * 2008-05-19 2010-01-20 Государственное образовательное учреждение высшего профессионального образования "Российский химико-технологический университет им. Д.И. Менделеева" (РХТУ им. Д.И. Менделеева) [2-(азол-1-ил)алкилбензимидазол-1-ил]алкановые кислоты и их эфиры, способ их получения (варианты) и рострегуляторная композиция на их основе
KR20110123253A (ko) 2009-03-05 2011-11-14 다이이찌 산쿄 가부시키가이샤 피리딘 유도체
JP2013530180A (ja) 2010-06-16 2013-07-25 パーデュー、ファーマ、リミテッド、パートナーシップ アリール置換インドールおよびその使用
RU2443690C1 (ru) * 2010-12-13 2012-02-27 Российская Федерация, От Имени Которой Выступает Министерство Образования И Науки Российской Федерации 2-(9-антрилметил)амино-1-[3-(диметиламино)пропил]бензимидазол, обладающий свойствами флуоресцентного хемосенсора на катионы h+
EP2681200A4 (en) * 2011-03-03 2015-05-27 Zalicus Pharmaceuticals Ltd INHIBITORS OF BENZIMIDAZOLE TYPE OF SODIUM CHANNEL
EP2758376A4 (en) 2011-09-19 2015-04-29 Vitas Pharma Res Private Ltd HETEROCYCLIC COMPOUNDS AS INHIBITORS OF FATTY ACID BIOSYNTHESIS FOR BACTERIAL INFECTIONS
WO2013101911A2 (en) 2011-12-28 2013-07-04 Allergan, Inc. Benzimidazole derivatives as selective blockers of persistent sodium current
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US9828348B2 (en) * 2013-11-08 2017-11-28 Purdue Pharma L.P. Benzimidazole derivatives and use thereof
US20150203812A1 (en) * 2014-01-20 2015-07-23 Francesco Tombola Inhibitors of Voltage Gated Ion Channels
WO2016029146A1 (en) * 2014-08-22 2016-02-25 University Of Washington Specific inhibitors of methionyl-trna synthetase
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