JP2013525490A5 - - Google Patents

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Publication number
JP2013525490A5
JP2013525490A5 JP2013509201A JP2013509201A JP2013525490A5 JP 2013525490 A5 JP2013525490 A5 JP 2013525490A5 JP 2013509201 A JP2013509201 A JP 2013509201A JP 2013509201 A JP2013509201 A JP 2013509201A JP 2013525490 A5 JP2013525490 A5 JP 2013525490A5
Authority
JP
Japan
Prior art keywords
alkyl
hydroxyl
optionally substituted
halo
het
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
JP2013509201A
Other languages
English (en)
Japanese (ja)
Other versions
JP2013525490A (ja
Filing date
Publication date
Application filed filed Critical
Priority claimed from PCT/US2011/035091 external-priority patent/WO2011140164A1/en
Publication of JP2013525490A publication Critical patent/JP2013525490A/ja
Publication of JP2013525490A5 publication Critical patent/JP2013525490A5/ja
Pending legal-status Critical Current

Links

JP2013509201A 2010-05-06 2011-05-04 Faahのモジュレータとして有用なアザインドール誘導体 Pending JP2013525490A (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US33197410P 2010-05-06 2010-05-06
US61/331,974 2010-05-06
PCT/US2011/035091 WO2011140164A1 (en) 2010-05-06 2011-05-04 Aza-indole derivatives useful as modulators of faah

Publications (2)

Publication Number Publication Date
JP2013525490A JP2013525490A (ja) 2013-06-20
JP2013525490A5 true JP2013525490A5 (enExample) 2014-06-05

Family

ID=44904047

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2013509201A Pending JP2013525490A (ja) 2010-05-06 2011-05-04 Faahのモジュレータとして有用なアザインドール誘導体

Country Status (8)

Country Link
US (1) US20130059850A1 (enExample)
EP (1) EP2566481A4 (enExample)
JP (1) JP2013525490A (enExample)
CN (1) CN102917707A (enExample)
AU (1) AU2011248175A1 (enExample)
BR (1) BR112012028055A2 (enExample)
CA (1) CA2797281A1 (enExample)
WO (1) WO2011140164A1 (enExample)

Families Citing this family (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB201411236D0 (en) 2014-06-25 2014-08-06 Takeda Pharmaceutical Novel compounds
EP3362449B1 (en) * 2015-10-13 2021-06-16 Institut National de la Santé et de la Recherche Médicale (INSERM) Sibiriline derivatives for use for preventing and/or treating disorders associated with cellular necroptosis
AU2017327309A1 (en) * 2016-09-16 2019-04-04 Sumitomo Chemical Company, Limited Heterocyclic compound, and harmful-arthropod-controlling agent containing same
CN109589325B (zh) * 2019-02-19 2019-11-26 牡丹江医学院 一种用于治疗肠炎的药物组合物及其制备方法
JP7631235B2 (ja) * 2019-06-17 2025-02-18 ウーツェーベー ファルマ ゲーエムベーハー 多発性硬化症のようなcns障害を治療するためのgpr17モジュレーターとしてのn‐(フェニル)‐インドール‐3‐スルホンアミド誘導体及び関連化合物
CN111743864B (zh) * 2020-08-05 2022-04-01 牡丹江医学院 一种体育外伤喷雾剂及其制备方法
CN112159423A (zh) * 2020-11-03 2021-01-01 凯美克(上海)医药科技有限公司 1H-吡咯并[2,3-b]吡啶-2-硼酸频哪醇酯的合成方法
CA3205853A1 (en) * 2021-01-25 2022-07-28 Stephane Bach Use of indole, 6- and 7-azaindole derivatives as inhibitors of ferroptosis regulated cell death

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CH574441A5 (enExample) * 1973-06-14 1976-04-15 Ciba Geigy Ag
JPS5239672A (en) * 1975-09-26 1977-03-28 Sankyo Co Ltd Process for preparing indole-2-allyl-3- thioeter compounds
NZ222878A (en) * 1986-12-17 1991-02-26 Merck Frosst Canada Inc 3-hetero-substituted-n-benzyl-indole derivatives, and pharmaceutical compositions
US5095031A (en) * 1990-08-20 1992-03-10 Abbott Laboratories Indole derivatives which inhibit leukotriene biosynthesis
US5527819A (en) * 1991-09-06 1996-06-18 Merck & Co., Inc. Inhibitors of HIV reverse transcriptase
BR9405737A (pt) * 1993-02-24 1995-12-05 Merck & Co Inc Composto processo de inibição de transcriptase reserva de HIV, processo de prevenção contra a infecção pelo HIV ou de tratamento da infecção pelo HIV, composição farmacêutica útil para a inibição da transcriptase reserva de HIV, e, útil para a prevenção ou tratamento de infecção pelo HIV ou para o tratamento da AIDS ou ARC
FR2705346B1 (fr) * 1993-05-18 1995-08-11 Union Pharma Scient Appl Nouveaux dérivés de pipéridinyl thio indole, leurs procédés de préparation, compositions pharmaceutiques les contenant, utiles notamment comme antalgiques .
KR100656037B1 (ko) * 2002-02-01 2006-12-11 에프. 호프만-라 로슈 아게 알파-1 작용제인 치환된 인돌
UA78999C2 (en) * 2002-06-04 2007-05-10 Wyeth Corp 1-(aminoalkyl)-3-sulfonylazaindoles as ligands of 5-hydroxytryptamine-6
TW200403243A (en) * 2002-07-18 2004-03-01 Wyeth Corp 1-Heterocyclylalkyl-3-sulfonylazaindole or-azaindazole derivatives as 5-hydroxytryptamine-6 ligands
US6800655B2 (en) * 2002-08-20 2004-10-05 Sri International Analogs of indole-3-carbinol metabolites as chemotherapeutic and chemopreventive agents
CN100482662C (zh) * 2003-02-14 2009-04-29 惠氏公司 作为5-羟基色胺-6配体的杂环基-3-磺酰基氮杂吲哚或-氮杂吲唑衍生物
KR20070053237A (ko) * 2004-07-27 2007-05-23 에스지엑스 파마슈티컬스, 인코포레이티드 피롤로-피리딘 키나제 조절제
PT1791537E (pt) * 2004-08-19 2010-01-19 Aventis Pharma Inc Derivados de 3-ariltioindole-2-carboxamida e seus análogos como inibidores da cinase da caseína i
GB2422831A (en) * 2005-02-04 2006-08-09 Oxagen Ltd Pyrrolopyridines and their use in the treatment of diseases mediated by PGD2 at the CRTH2 receptor
PT1893612E (pt) * 2005-06-22 2011-11-21 Plexxikon Inc Derivados de pirrolo [2,3-b]piridina como inibidores de proteína quinase
US7960544B2 (en) * 2005-12-16 2011-06-14 Ironwood Pharmaceuticals, Inc. Useful indole compounds
US20090118503A1 (en) * 2007-06-20 2009-05-07 Kevin Sprott Faah inhibitors
JP2011513234A (ja) * 2008-02-22 2011-04-28 アイアールエム・リミテッド・ライアビリティ・カンパニー Gpr119活性モジュレーターとしての化合物および組成物
CN102066323B (zh) * 2008-04-16 2015-05-13 卡罗生物股份公司 新的雌激素受体配体

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