JP2010531344A5 - - Google Patents

Download PDF

Info

Publication number
JP2010531344A5
JP2010531344A5 JP2010514135A JP2010514135A JP2010531344A5 JP 2010531344 A5 JP2010531344 A5 JP 2010531344A5 JP 2010514135 A JP2010514135 A JP 2010514135A JP 2010514135 A JP2010514135 A JP 2010514135A JP 2010531344 A5 JP2010531344 A5 JP 2010531344A5
Authority
JP
Japan
Prior art keywords
carbonyl
cyclohexanecarboxamide
tetrahydro
pyrido
cyanocyclopropyl
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
JP2010514135A
Other languages
English (en)
Japanese (ja)
Other versions
JP2010531344A (ja
Filing date
Publication date
Application filed filed Critical
Priority claimed from PCT/GB2008/050486 external-priority patent/WO2009001129A1/en
Publication of JP2010531344A publication Critical patent/JP2010531344A/ja
Publication of JP2010531344A5 publication Critical patent/JP2010531344A5/ja
Pending legal-status Critical Current

Links

JP2010514135A 2007-06-26 2008-06-24 カテプシンk阻害剤としての1−シアノシクロプロピル誘導体 Pending JP2010531344A (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US94617807P 2007-06-26 2007-06-26
US4284008P 2008-04-07 2008-04-07
PCT/GB2008/050486 WO2009001129A1 (en) 2007-06-26 2008-06-24 1-cyanocyclopropyl-derivatives as cathepsin k inhibitors

Publications (2)

Publication Number Publication Date
JP2010531344A JP2010531344A (ja) 2010-09-24
JP2010531344A5 true JP2010531344A5 (enExample) 2011-02-17

Family

ID=39761131

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2010514135A Pending JP2010531344A (ja) 2007-06-26 2008-06-24 カテプシンk阻害剤としての1−シアノシクロプロピル誘導体

Country Status (19)

Country Link
US (1) US8008279B2 (enExample)
EP (1) EP2170879B1 (enExample)
JP (1) JP2010531344A (enExample)
KR (1) KR20100039862A (enExample)
CN (1) CN101687864A (enExample)
AR (1) AR067156A1 (enExample)
AU (1) AU2008269513B2 (enExample)
BR (1) BRPI0813306A2 (enExample)
CA (1) CA2689945A1 (enExample)
CL (1) CL2008001899A1 (enExample)
CO (1) CO6251264A2 (enExample)
EC (1) ECSP109882A (enExample)
IL (1) IL202519A0 (enExample)
NZ (1) NZ581719A (enExample)
PE (1) PE20090841A1 (enExample)
RU (1) RU2470023C2 (enExample)
TW (1) TW200911806A (enExample)
UY (1) UY31180A1 (enExample)
WO (1) WO2009001129A1 (enExample)

Families Citing this family (26)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CA2727055C (en) 2008-01-11 2016-12-20 Albany Molecular Research, Inc. (1-azinone) -substituted pyridoindoles as mch antagonists
JP5666036B2 (ja) * 2008-01-25 2015-02-04 メディベイション テクノロジーズ, インコーポレイテッド 新規2,3,4,5−テトラヒドロ−1H−ピリド[4,3−b]インドール化合物およびその使用方法
RU2544856C2 (ru) * 2008-01-25 2015-03-20 Сергей Олегович Бачурин НОВЫЕ ПРОИЗВОДНЫЕ 2,3,4,5-ТЕТРАГИДРО-1-ПИРИДО[4,3-b]ИНДОЛА И СПОСОБЫ ИХ ПРИМЕНЕНИЯ
TW201018694A (en) 2008-09-29 2010-05-16 Abbott Lab Indole and indoline derivatives and methods of use thereof
US9625475B2 (en) 2008-09-29 2017-04-18 Abbvie Inc. Indole and indoline derivatives and methods of use thereof
US8853391B2 (en) 2008-12-18 2014-10-07 Merck Patent Gmbh Tricyclic azaindoles
US7893099B2 (en) * 2009-06-11 2011-02-22 Hoffman-La Roche Inc. Cyclopentane derivatives
WO2011003005A1 (en) * 2009-07-01 2011-01-06 Albany Molecular Research, Inc. Azinone-substituted azepino[b]indole and pyrido-pyrrolo-azepine mch-1 antagonists, methods of making, and use thereof
US8629158B2 (en) * 2009-07-01 2014-01-14 Albany Molecular Research, Inc. Azabicycloalkane-indole and azabicycloalkane-pyrrolo-pyridine MCH-1 antagonists, methods of making, and use thereof
WO2011003021A1 (en) * 2009-07-01 2011-01-06 Albany Molecular Research, Inc. Azinone-substituted azabicycloalkane-indole and azabicycloalkane-pyrrolo-pyridine mch-1 antagonists, methods of making, and use thereof
WO2011003012A1 (en) * 2009-07-01 2011-01-06 Albany Molecular Research, Inc. Azinone-substituted azapolycycle mch-1 antagonists, methods of making, and use thereof
AP2012006204A0 (en) * 2009-10-21 2012-04-30 Boehringer Ingelheim Int Indazole and pyrazolopyridine compounds as CCR1 receptor antagonists.
JP5542214B2 (ja) 2009-10-27 2014-07-09 ベーリンガー インゲルハイム インターナショナル ゲゼルシャフト ミット ベシュレンクテル ハフツング Ccr1受容体アンタゴニストとしての複素環化合物
WO2011075487A1 (en) 2009-12-17 2011-06-23 Abbott Laboratories Bridgehead amine ring -fused indoles and indolines useful to treat neurodegenerative and neuropsychiatry disorders
WO2011084433A2 (en) 2009-12-17 2011-07-14 Abbott Laboratories Aza-bridged ring-fused indoles and indolines
US8871786B2 (en) 2010-04-30 2014-10-28 Boehringer Ingelheim International Gmbh Azaindazole amide compounds as CCR1 receptor antagonists
US8697700B2 (en) 2010-12-21 2014-04-15 Albany Molecular Research, Inc. Piperazinone-substituted tetrahydro-carboline MCH-1 antagonists, methods of making, and uses thereof
WO2012088124A2 (en) 2010-12-21 2012-06-28 Albany Molecular Research, Inc. Tetrahydro-azacarboline mch-1 antagonists, methods of making, and uses thereof
CA2829045A1 (en) 2011-02-18 2012-08-23 Medivation Technologies, Inc. Compounds and methods for treatment of hypertension
RU2625796C2 (ru) * 2012-01-11 2017-07-19 Ф. Хоффманн-Ля Рош Аг Макроциклические амиды в качестве ингибиторов протеазы
CN103086923B (zh) * 2013-01-21 2014-04-23 吉林大学 肼腈类组织蛋白酶k抑制剂及其在治疗骨质疏松症方面的应用
RU2692799C2 (ru) * 2013-10-08 2019-06-27 Мерк Шарп И Доум Корп. Ингибиторы цистеинпротеаз катепсинов
WO2016027285A2 (en) * 2014-08-22 2016-02-25 Alkem Laboratories Ltd. Bicyclic heteroaryl amides as cathepsin cysteine protease inhibitors
CN105837479B (zh) * 2016-04-05 2017-10-27 吉林大学 肼腈类组织蛋白酶k抑制剂及其在制备治疗骨关节炎药物中的应用
AU2018244449B2 (en) 2017-03-29 2024-07-11 Minerva Biotechnologies Corporation Agents for differentiating stem cells and treating cancer
EP4467544A4 (en) * 2022-01-21 2026-04-15 Shandong New Time Pharmaceutical Co Ltd CATHEPSIN K INHIBITOR, ITS PREPARATION PROCESS AND ITS USE

Family Cites Families (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE60028045T2 (de) * 1999-07-30 2007-02-15 Boehringer Ingelheim Pharmaceuticals, Inc., Ridgefield Neue bernsteinsäure derivative als cysteine-protease-inhibitoren
DE60132975T2 (de) * 2000-01-06 2009-02-26 Merck Frosst Canada Inc., Kirkland Neue substanzen und verbindungen als protease-inhibitoren
WO2001068645A2 (en) 2000-03-15 2001-09-20 Axys Pharmaceuticals, Inc. N-cyanomethylcarboxamides and their use as protease inhibitors
DE60229114D1 (en) * 2001-03-02 2008-11-13 Axys Pharm Inc Cathepsincystein-proteasehemmer
RU2278863C2 (ru) * 2001-08-10 2006-06-27 Орто-Макнейл Фармасьютикал, Инк. Замещенные пиразолы, фармацевтическая композиция и способ ингибирования активности катепсина s
PL370766A1 (en) * 2001-12-04 2005-05-30 F.Hoffmann-La Roche Ag Substituted 2-amino-cycloalkanecarboxamides and their use as cysteine protease inhibitors
SE0201977D0 (sv) * 2002-06-24 2002-06-24 Astrazeneca Ab Novel compounds
SE0203712D0 (sv) 2002-12-13 2002-12-13 Astrazeneca Ab Novel compounds
WO2004056324A2 (en) 2002-12-19 2004-07-08 Bristol-Myers Squibb Company Substituted tricyclic gamma-carbolines as serotonin receptor agonists and antagonists

Similar Documents

Publication Publication Date Title
RU2470023C2 (ru) 1-цианоциклопропильные производные в качестве ингибиторов катепсина к
AU2017283769B2 (en) Compounds and compositions for inhibiting the activity of SHP2
JP7149276B2 (ja) Pd-l1内在化誘導物質としてのテトラヒドロイミダゾ[4,5-c]ピリジン誘導体
JP7853532B2 (ja) 医学的障害を治療するためのサイクリン依存性キナーゼ阻害化合物
JP2019070030A (ja) 二環式複素環化合物および治療におけるそれらの使用
WO2023049831A1 (en) Treatment of human papillomavirus-associated cancers by pd-l1 inhibitors
HUP0003386A2 (hu) CRF antagonisták alkalmazása depresszió, kardiovaszkuláris betegségek kezelésére szolgáló gyógyszerkészítmények előállítására
WO2005023771A1 (ja) ケモカインレセプターアンタゴニストおよびその医薬用途
KR102646470B1 (ko) 헤테로시클릭 화합물
JP6235001B2 (ja) 置換ベンゾチエノピリミジン
TW200538128A (en) Therapeutic combinations of atypical antipsychotics with corticotropin releasing factor antagonists
WO2012118850A1 (en) Serine/threonine kinase inhibitors
AU2016298962B2 (en) Compounds and pharmaceutical composition associated with ubiquitination-proteasome system
JP2020524148A (ja) 置換5−シアノインドール化合物及びその使用
ES2800173T3 (es) Compuestos de atropisómeros tricíclicos
JP2015518842A (ja) 置換ピロロピリミジン
KR20160030239A (ko) 치환된 피라졸로-피리딘아민
AU2017208119A1 (en) 6,7,8,9-tetrahydro-5H-pyrido[2,3-d]azepine dopamine D3 ligands
JP6200996B2 (ja) (−)−フペルジンaの関連組成物
ES2795368T3 (es) Compuesto heterocíclico novedoso
JP7667742B2 (ja) Atp競合性akt阻害剤gdc-0068とe3リガーゼリガンドとの結合によるaktの分解および使用方法
CN121002031A (zh) 作为毒蕈碱型乙酰胆碱受体m4的正向别构调节剂的吡咯并吡啶衍生物
CN120936610A (zh) 可用于治疗神经障碍和精神障碍的作为毒蕈碱型乙酰胆碱受体m4正向别构调节剂的1,6-萘啶衍生物
JP2025540907A (ja) Ret-lddタンパク質分解誘導剤
RU2808435C2 (ru) Гетероциклическое соединение