JP2007521325A5 - - Google Patents
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- Publication number
- JP2007521325A5 JP2007521325A5 JP2006538402A JP2006538402A JP2007521325A5 JP 2007521325 A5 JP2007521325 A5 JP 2007521325A5 JP 2006538402 A JP2006538402 A JP 2006538402A JP 2006538402 A JP2006538402 A JP 2006538402A JP 2007521325 A5 JP2007521325 A5 JP 2007521325A5
- Authority
- JP
- Japan
- Prior art keywords
- aliphatic
- compound
- formula
- pharmaceutically acceptable
- independently selected
- 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
Links
- 150000001875 compounds Chemical class 0.000 claims description 9
- 125000000623 heterocyclic group Chemical group 0.000 claims description 7
- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 5
- 125000005842 heteroatom Chemical group 0.000 claims description 4
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 3
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 3
- 229910052757 nitrogen Inorganic materials 0.000 claims description 3
- 229910052760 oxygen Inorganic materials 0.000 claims description 3
- 239000001301 oxygen Chemical group 0.000 claims description 3
- 229910052717 sulfur Chemical group 0.000 claims description 3
- 239000011593 sulfur Chemical group 0.000 claims description 3
- 125000003118 aryl group Chemical group 0.000 claims description 2
- 125000001931 aliphatic group Chemical group 0.000 claims 3
- 229910052736 halogen Inorganic materials 0.000 claims 2
- 150000002367 halogens Chemical group 0.000 claims 2
- 229910052739 hydrogen Inorganic materials 0.000 claims 2
- 239000001257 hydrogen Substances 0.000 claims 2
- 150000003839 salts Chemical class 0.000 claims 2
- -1 1,2-methylenedioxy Chemical group 0.000 claims 1
- 125000001313 C5-C10 heteroaryl group Chemical group 0.000 claims 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 1
- 239000002671 adjuvant Substances 0.000 claims 1
- 125000002723 alicyclic group Chemical group 0.000 claims 1
- 230000001548 androgenic effect Effects 0.000 claims 1
- 239000003937 drug carrier Substances 0.000 claims 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims 1
- 125000000896 monocarboxylic acid group Chemical group 0.000 claims 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 claims 1
- 239000008194 pharmaceutical composition Substances 0.000 claims 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims 1
- 125000006239 protecting group Chemical group 0.000 claims 1
- 125000001424 substituent group Chemical group 0.000 claims 1
- 239000003981 vehicle Substances 0.000 claims 1
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 1
- 102000016913 Voltage-Gated Sodium Channels Human genes 0.000 description 1
- 108010053752 Voltage-Gated Sodium Channels Proteins 0.000 description 1
- 125000002619 bicyclic group Chemical group 0.000 description 1
- 125000004122 cyclic group Chemical group 0.000 description 1
- 125000002950 monocyclic group Chemical group 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 239000011574 phosphorus Substances 0.000 description 1
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US51508803P | 2003-10-28 | 2003-10-28 | |
| PCT/US2004/036297 WO2005042497A2 (en) | 2003-10-28 | 2004-10-28 | Benzimidazoles useful as modulators of ion channels |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2007521325A JP2007521325A (ja) | 2007-08-02 |
| JP2007521325A5 true JP2007521325A5 (https=) | 2011-07-28 |
Family
ID=34549374
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2006538402A Pending JP2007521325A (ja) | 2003-10-28 | 2004-10-28 | イオンチャネルのモジュレーターとして有用なベンズイミダゾール |
Country Status (13)
| Country | Link |
|---|---|
| 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=) |
Families Citing this family (42)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP4564713B2 (ja) | 2000-11-01 | 2010-10-20 | ミレニアム・ファーマシューティカルズ・インコーポレイテッド | 窒素性複素環式化合物、ならびに窒素性複素環式化合物およびその中間体を作製するための方法 |
| FR2880889B1 (fr) * | 2005-01-14 | 2007-04-06 | Merck Sante Soc Par Actions Si | Derives de l'acide 1h-indole-3-carboxylique, procedes pour leur preparation, compositions pharmaceutiques les contenant et applications en therapeutique |
| GB0514018D0 (en) * | 2005-07-07 | 2005-08-17 | Ionix Pharmaceuticals Ltd | Chemical compounds |
| BRPI0613229A2 (pt) * | 2005-07-12 | 2011-01-04 | Bayer Cropscience Sa | compostos, processo para a preparação de composto, composição fungicida e método para o combate curativo ou preventivo de fungo fitopatogênico |
| AR057455A1 (es) * | 2005-07-22 | 2007-12-05 | Merck & Co Inc | Inhibidores de la transcriptasa reversa de vih y composicion farmaceutica |
| KR20080035700A (ko) * | 2005-08-15 | 2008-04-23 | 아이알엠 엘엘씨 | Ｔｐｏ 모방체로서의 화합물 및 조성물 |
| ES2691411T3 (es) | 2006-03-27 | 2018-11-27 | Wex Medical Limited | Uso de bloqueadores de los canales de sodio para el tratamiento del dolor neuropático que se desarrolla como consecuencia de la quimioterapia |
| US7951829B2 (en) * | 2006-05-03 | 2011-05-31 | Janssen Pharmaceutica Nv | Benzimidazole modulators of VR1 |
| GEP20125702B (en) | 2007-06-29 | 2012-12-10 | Pfizer | Benzimidazole derivatives |
| AU2008310660A1 (en) * | 2007-10-11 | 2009-04-16 | Vertex Pharmaceuticals Incorporated | Heteroaryl amides useful as inhibitors of voltage-gated sodium channels |
| EA038941B1 (ru) | 2007-11-06 | 2021-11-12 | ПиТиСи ТЕРАПЬЮТИКС, ИНК. | ПРОИЗВОДНЫЕ 4-(п-ХИНОНИЛ)-2-ГИДРОКСИБУТАНАМИДА ДЛЯ ЛЕЧЕНИЯ МИТОХОНДРИАЛЬНЫХ ЗАБОЛЕВАНИЙ |
| 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 |
| CA2754446A1 (en) * | 2009-03-05 | 2010-09-10 | Daiichi Sankyo Company, Limited | Pyridine derivative |
| EP2582666B1 (en) | 2010-06-16 | 2014-08-13 | Purdue Pharma L.P. | Aryl substituted indoles and their use as blockers of sodium channels |
| 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+ |
| CA2828456C (en) * | 2011-03-03 | 2021-05-04 | Zalicus Pharmaceuticals Ltd. | N-benzl-amino-carboxamide inhibitors of the sodium channel |
| CA2849057C (en) * | 2011-09-19 | 2021-05-11 | Vitas Pharma Research Pvt Ltd | Heterocyclic compounds as inhibitors of fatty acid biosynthesis for bacterial infections |
| EP2809656A2 (en) | 2011-12-28 | 2014-12-10 | Allergan, Inc. | Benzimidazole derivatives as selective blockers of persistent sodium current |
| US20130172342A1 (en) | 2011-12-28 | 2013-07-04 | Allergan, Inc. | Benzimidazole derivatives as selective blockers of persistent sodium current |
| 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 |
| US10913736B2 (en) * | 2014-08-22 | 2021-02-09 | University Of Washington | Specific inhibitors of methionyl-tRNA synthetase |
| 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 |
| BR112018002115A2 (pt) * | 2015-08-20 | 2018-09-18 | Boehringer Ingelheim Int | benzamidas aneladas |
| SI3348547T1 (sl) * | 2015-09-11 | 2020-10-30 | Sumitomo Dainippon Pharma Co., Ltd. | Derivati benzimidazola kot zaviralci NAV 1.7 (natrijevi kanalčki, napetostno odvisni, tip IX, podenota alfa (SCN9A)) za zdravljenje bolečine, disurije in multiple skleroze |
| GB201619694D0 (en) * | 2016-11-22 | 2017-01-04 | Entpr Therapeutics Ltd | Compounds |
| US11447471B2 (en) | 2017-06-23 | 2022-09-20 | Kyowa Kirin Co., Ltd. | α,β-unsaturated amide compound |
| KR101938982B1 (ko) | 2017-07-17 | 2019-01-15 | 연세대학교 산학협력단 | 자가포식 조절제를 포함하는 대사성 질환 치료용 약학 조성물 |
| KR102070882B1 (ko) * | 2017-10-17 | 2020-01-29 | 성균관대학교산학협력단 | Bietpc를 유효성분으로 포함하는 암 예방 또는 치료용 약학적 조성물 |
| AU2019302534B2 (en) | 2018-07-09 | 2024-10-03 | Lieber Institute, Inc. | Pyridazine compounds for inhibiting NaV1.8 |
| CA3105657A1 (en) | 2018-07-09 | 2020-01-16 | Lieber Institute, Inc. | Pyridine carboxamide compounds for inhibiting nav1.8 |
| CN120097859A (zh) * | 2019-02-19 | 2025-06-06 | 加利福尼亚大学董事会 | Nurr1受体调节剂 |
| MA53521B1 (fr) * | 2021-05-12 | 2023-03-31 | Univ Ibn Tofail | Nouveaux composés inhibiteurs de la protéase mpro et de la réplication du sars-cov2, leurs formulations et applications |
| US20240300939A1 (en) | 2021-06-14 | 2024-09-12 | Scorpion Therapeutics, Inc. | Urea derivatives which can be used to treat cancer |
| EP4408941A1 (en) * | 2021-09-30 | 2024-08-07 | Universidade Do Porto | Antifouling compound, method and uses thereof |
| US12084453B2 (en) | 2021-12-10 | 2024-09-10 | Incyte Corporation | Bicyclic amines as CDK12 inhibitors |
| US11478464B1 (en) | 2022-02-06 | 2022-10-25 | King Faisal University | Method for treating inflammation |
| US11786535B1 (en) | 2023-02-22 | 2023-10-17 | King Faisal University | Methods of inhibiting cyclooxygenase |
| 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 |
| WO2026015548A1 (en) * | 2024-07-08 | 2026-01-15 | Convelo Therapeutics, Inc. | Cyp51 inhibitors and method of using same |
| GB202412414D0 (en) * | 2024-08-23 | 2024-10-09 | Univ Bradford | Methods for treating cancer |
Family Cites Families (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| NL280954A (https=) * | 1961-07-14 | |||
| US4088768A (en) | 1975-05-06 | 1978-05-09 | Eli Lilly And Company | N-heterocyclic ureas as immune regulants |
| DK40192D0 (da) * | 1992-03-26 | 1992-03-26 | Neurosearch As | Imidazolforbindelser, deres fremstilling og anvendelse |
| AU4055300A (en) | 1999-04-02 | 2000-10-23 | Neurogen Corporation | Aryl and heteroaryl fused aminoalkyl-imidazole derivatives: selective modulators of Bradykinin B2 receptors |
| IL146403A0 (en) * | 1999-06-22 | 2002-07-25 | Neurosearch As | Novel benzimidazole derivatives and pharmaceutical compositions comprising these compounds |
| US6316474B1 (en) * | 1999-10-29 | 2001-11-13 | Merck & Co., Inc. | 2-benzyl and 2-heteroaryl benzimidazole NMDA/NR2B antagonists |
| JP2004503527A (ja) * | 2000-06-13 | 2004-02-05 | イーライ・リリー・アンド・カンパニー | スルホンアミド誘導体 |
| US20050113283A1 (en) * | 2002-01-18 | 2005-05-26 | David Solow-Cordero | Methods of treating conditions associated with an EDG-4 receptor |
| CA2473740A1 (en) | 2002-01-18 | 2003-07-31 | David Solow-Cordero | Methods of treating conditions associated with an edg receptor |
-
2004
- 2004-10-28 AU AU2004285053A patent/AU2004285053B2/en not_active Ceased
- 2004-10-28 EP EP04796881A patent/EP1678145A2/en not_active Withdrawn
- 2004-10-28 JP JP2006538402A patent/JP2007521325A/ja active Pending
- 2004-10-28 KR KR1020067010407A patent/KR20060115396A/ko not_active Withdrawn
- 2004-10-28 ZA ZA200603864A patent/ZA200603864B/en unknown
- 2004-10-28 NZ NZ547109A patent/NZ547109A/en not_active IP Right Cessation
- 2004-10-28 WO PCT/US2004/036297 patent/WO2005042497A2/en not_active Ceased
- 2004-10-28 RU RU2006118312/04A patent/RU2006118312A/ru not_active Application Discontinuation
- 2004-10-28 CA CA002543918A patent/CA2543918A1/en not_active Abandoned
- 2004-10-28 US US10/977,609 patent/US7309716B2/en not_active Expired - Fee Related
- 2004-10-28 CN CNA2004800392479A patent/CN1902181A/zh active Pending
-
2006
- 2006-04-27 IL IL175252A patent/IL175252A0/en unknown
- 2006-05-29 NO NO20062426A patent/NO20062426L/no not_active Application Discontinuation
-
2007
- 2007-11-01 US US11/933,724 patent/US7705031B2/en not_active Expired - Lifetime
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