JP2012528828A5 - - Google Patents

Download PDF

Info

Publication number
JP2012528828A5
JP2012528828A5 JP2012513613A JP2012513613A JP2012528828A5 JP 2012528828 A5 JP2012528828 A5 JP 2012528828A5 JP 2012513613 A JP2012513613 A JP 2012513613A JP 2012513613 A JP2012513613 A JP 2012513613A JP 2012528828 A5 JP2012528828 A5 JP 2012528828A5
Authority
JP
Japan
Prior art keywords
pyrid
pharmaceutical composition
benign
methyl
substituted
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.)
Granted
Application number
JP2012513613A
Other languages
English (en)
Japanese (ja)
Other versions
JP5596137B2 (ja
JP2012528828A (ja
Filing date
Publication date
Application filed filed Critical
Priority claimed from PCT/EP2010/057719 external-priority patent/WO2010139731A1/en
Publication of JP2012528828A publication Critical patent/JP2012528828A/ja
Publication of JP2012528828A5 publication Critical patent/JP2012528828A5/ja
Application granted granted Critical
Publication of JP5596137B2 publication Critical patent/JP5596137B2/ja
Expired - Fee Related legal-status Critical Current
Anticipated expiration legal-status Critical

Links

JP2012513613A 2009-06-04 2010-06-02 1H−イミダゾ[4,5−c]キノリノン誘導体 Expired - Fee Related JP5596137B2 (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US18414109P 2009-06-04 2009-06-04
US61/184,141 2009-06-04
PCT/EP2010/057719 WO2010139731A1 (en) 2009-06-04 2010-06-02 1H-IMIDAZO[4,5-c]QUINOLINONE DERIVATIVES

Publications (3)

Publication Number Publication Date
JP2012528828A JP2012528828A (ja) 2012-11-15
JP2012528828A5 true JP2012528828A5 (enExample) 2014-07-03
JP5596137B2 JP5596137B2 (ja) 2014-09-24

Family

ID=42697442

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2012513613A Expired - Fee Related JP5596137B2 (ja) 2009-06-04 2010-06-02 1H−イミダゾ[4,5−c]キノリノン誘導体

Country Status (30)

Country Link
US (2) US8476294B2 (enExample)
EP (1) EP2438064A1 (enExample)
JP (1) JP5596137B2 (enExample)
KR (1) KR101445458B1 (enExample)
CN (1) CN102574845B (enExample)
AR (1) AR076949A1 (enExample)
AU (1) AU2010255727B2 (enExample)
BR (1) BRPI1010621A2 (enExample)
CA (1) CA2763821A1 (enExample)
CL (1) CL2011003052A1 (enExample)
CO (1) CO6470887A2 (enExample)
CR (1) CR20110608A (enExample)
CU (1) CU24064B1 (enExample)
DO (1) DOP2011000373A (enExample)
EA (1) EA020715B1 (enExample)
EC (1) ECSP11011500A (enExample)
GE (1) GEP20156267B (enExample)
IL (1) IL216452A0 (enExample)
MA (1) MA33332B1 (enExample)
MX (1) MX2011012943A (enExample)
NI (1) NI201100209A (enExample)
NZ (1) NZ596487A (enExample)
PE (1) PE20120224A1 (enExample)
SG (1) SG176572A1 (enExample)
TN (1) TN2011000626A1 (enExample)
TW (1) TWI464168B (enExample)
UA (1) UA106074C2 (enExample)
UY (1) UY32682A (enExample)
WO (1) WO2010139731A1 (enExample)
ZA (1) ZA201108439B (enExample)

Families Citing this family (27)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE102010035744A1 (de) 2010-08-28 2012-03-01 Merck Patent Gmbh Imidazolonylchinoline
KR20140014104A (ko) * 2010-12-06 2014-02-05 피라말 엔터프라이지즈 리미티드 치환된 이미다조퀴놀린 유도체
JO3003B1 (ar) 2011-01-14 2016-09-05 Lilly Co Eli مركب أيميدازو [4، 5 -c ] كينولين-2- واحد واستخدامه كمثبط كيناز PI3/mtor
JP5820080B2 (ja) * 2011-11-17 2015-11-24 山▲東▼▲軒▼竹医▲葯▼科技有限公司 三環系PI3K及び/又はmTOR抑制剤
WO2014141118A1 (en) * 2013-03-14 2014-09-18 Piramal Enterprises Limited Imidazo[4,5-c]quinoline derivatives and uses thereof
BR112015025686B1 (pt) 2013-04-15 2020-10-27 Fmc Corporation composto, composições fungicidas e método para o controle das doenças dos vegetais
JP6576929B2 (ja) * 2013-09-11 2019-09-18 メルク パテント ゲーエムベーハー ヘテロ環化合物
JP6441910B2 (ja) 2013-09-30 2018-12-19 シャンハイ インリ ファーマシューティカル カンパニー リミティド 縮合ピリミジン化合物、中間体、その調製方法、組成物及び使用
US10989719B2 (en) * 2013-10-11 2021-04-27 National University Corporation Tokyo Medical And Dental University Methods for treating spinocerebellar ataxia type I using RPA1
CA2931147C (en) * 2013-11-20 2018-05-29 Beijing Forelandpharma Co. Ltd. Imidazolone derivatives, pharmceutical compositions and uses thereof
NO2714752T3 (enExample) 2014-05-08 2018-04-21
JP6195684B2 (ja) 2014-06-03 2017-09-13 アクテリオン ファーマシューティカルズ リミテッドActelion Pharmaceuticals Ltd ピラゾール化合物及びt型カルシウムチャンネルブロッカーとしてのそれらの使用
DK3560924T3 (da) * 2015-04-02 2021-06-28 Merck Patent Gmbh Imidazolonylquinoliner og deres anvendelse som atm-kinase-inhibitorer
GB201516504D0 (en) 2015-09-17 2015-11-04 Astrazeneca Ab Imadazo(4,5-c)quinolin-2-one Compounds and their use in treating cancer
GB201519568D0 (en) * 2015-11-05 2015-12-23 Astrazeneca Ab Imidazo[4,5-c]quinolin-2-one compounds and their use in treating cancer
US10988472B2 (en) 2016-10-13 2021-04-27 The United States Of America, As Represented By The Secretary, Department Of Health And Human Services Compounds and method for blocking transmission of malarial parasite
LT3554490T (lt) 2016-12-16 2022-04-25 Idorsia Pharmaceuticals Ltd Farmacinis derinys, apimantis t tipo kalcio kanalo blokatorių
CA3050348A1 (en) 2017-02-06 2018-08-09 Idorsia Pharmaceuticals Ltd A novel process for the synthesis of 1-aryl-1-trifluoromethylcyclopropanes
JOP20190209A1 (ar) * 2017-03-16 2019-09-12 Astrazeneca Ab مركبات إيميدازو [ 4، 5-c ] كينولين-2-أون ديوترومية واستخدامها في علاج السرطان
EP3728228A1 (en) 2017-12-22 2020-10-28 Ravenna Pharmaceuticals, Inc. Aminopyridine derivatives as phosphatidylinositol phosphate kinase inhibitors
TW202112767A (zh) 2019-06-17 2021-04-01 美商佩特拉製藥公司 作為磷脂酸肌醇磷酸激酶抑制劑之胺基吡啶衍生物
CN116574099A (zh) * 2019-09-23 2023-08-11 南京征祥医药有限公司 磷酸二酯酶抑制剂及用途
EP4142710B1 (en) 2020-09-21 2024-01-31 Wei Zhong Substituted 1-(3,3-difluoropiperidin-4-yl)-imidazo[4,5-c] quinolin-2-one compounds with blood-brain barrier penetrable capability
US20230380203A1 (en) * 2021-01-26 2023-11-23 Boe Technology Group Co., Ltd. Quantum dot light-emitting device, display apparatus and manufacturing method
JP2024534187A (ja) * 2021-08-31 2024-09-18 インサイト・コーポレイション Krasの阻害剤としてのナフチリジン化合物
CN116768928A (zh) * 2023-06-15 2023-09-19 上海毕臣生化科技有限公司 一种3-叔丁基-5-硼酸酯基吡啶的合成方法
CN117384154A (zh) * 2023-09-04 2024-01-12 广州医科大学 一种吡咯并喹啉酮化合物、合成方法及其应用

Family Cites Families (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB0211649D0 (en) * 2002-05-21 2002-07-03 Novartis Ag Organic compounds
JP2007511575A (ja) 2003-11-21 2007-05-10 ノバルティス アクチエンゲゼルシャフト タンパク質キナーゼ阻害剤としての1h−イミダゾキノリン誘導体
AR046845A1 (es) * 2003-11-21 2005-12-28 Novartis Ag Derivados de 1h-imidazo[4,5-c]quinolina para tratamiento de enfermedades dependientes de las proteino-quinasas
CN101056877B (zh) 2004-09-14 2010-06-09 诺华疫苗和诊断公司 咪唑并喹啉化合物
GB0510390D0 (en) * 2005-05-20 2005-06-29 Novartis Ag Organic compounds
WO2007056112A2 (en) 2005-11-04 2007-05-18 Coley Pharmaceutical Group, Inc. Hydroxy and alkoxy substituted 1h-imidazoquinolines and methods
KR20090080530A (ko) 2006-11-20 2009-07-24 노파르티스 아게 2-메틸-2-[4-(3-메틸-2-옥소-8-퀴놀린-3-일-2,3-디히드로-이미다조[4,5-c]퀴놀린-1-일)-페닐]-프로피오니트릴의 염 및 결정 형태
RU2478387C2 (ru) * 2007-02-20 2013-04-10 Новартис Аг ИМИДАЗОХИНОЛИНЫ В КАЧЕСТВЕ ДВОЙНЫХ ИНГИБИТОРОВ ЛИПИДКИНАЗЫ И mTOR
PL2182948T3 (pl) * 2007-07-24 2013-07-31 Novartis Ag Zastosowanie imidazochinolin do leczenia chorób EGFR-zależnych albo chorób wykazujących nabytą oporność wobec środków ukierunkowanych na członków rodziny EGFR
US20090082387A1 (en) * 2007-09-26 2009-03-26 Protia, Llc Deuterium-enriched nvp-bez234
EP2474323A3 (en) 2008-03-26 2012-10-10 Novartis AG Imidazoquinolines and pyrimidine derivatives as potent modulators of vegf-driven angiogenic processes
EP2303890A4 (en) 2008-06-19 2012-04-11 Progenics Pharm Inc INHIBITORS OF PHOSPHATIDYLINOSITE-3-KINASE
WO2010038165A1 (en) 2008-09-30 2010-04-08 Pfizer Inc. Imidazo[1,5]naphthyridine compounds, their pharmaceutical use and compositions

Similar Documents

Publication Publication Date Title
AU2020250211B2 (en) Bicyclic heterocycles as fgfr inhibitors
KR101466412B1 (ko) 피롤로피리미딘 화합물 및 그의 용도
KR101445458B1 (ko) 1H-이미다조[4,5-c]퀴놀리논 유도체
US8188113B2 (en) Dihydropyridopyrimidinyl, dihydronaphthyidinyl and related compounds useful as kinase inhibitors for the treatment of proliferative diseases
ES2682493T3 (es) Compuestos derivados de piridilo bicíclicos fusionados a anillo como inhibidores de FGFR4
IL303451A (en) Prmts inhibitors
AU2010269674B2 (en) Azabicyclo compound and salt thereof
US20220348573A1 (en) Fgfr4 inhibitor, preparation method therefor and pharmaceutical use thereof
EA032416B1 (ru) Соединения триазолопиримидина и их применения
MX2015004151A (es) Inhibidores del factor de diferenciacion de crecimiento-8 (gdf-8).
CN111683950B (zh) AhR调节剂
RS55863B1 (sr) Inhibitori kinaze pirazolil hinoksalina
CN105777756A (zh) 杂芳化合物及其在药物中的应用
AU2012299899A1 (en) Bicyclic heteroaromatic compounds
JP2024023699A (ja) 環式化合物およびその使用方法
ES2586527T9 (es) Compuestos heterocíclicos y uso de los mismos como moduladores del receptor de tirosina quinasas de tipo III
WO2010000364A1 (de) Pyrrolopyridinyl-pyrimidin-2-yl-amin-derivate
KR102590854B1 (ko) Crhr2 길항제로서의 축합 환상 요소 유도체
ES2598830T3 (es) Compuestos bicíclicos o sales de los mismos para el uso en el tratamiento del cáncer
JP2022539208A (ja) チロシンキナーゼ非受容体1(tnk1)阻害剤およびその使用
JP7860103B2 (ja) 複素環式スピロ化合物及びその使用方法
EA052528B1 (ru) Циклические соединения и способы их применения
CN117897159A (zh) 杂环化合物及使用方法
BR112017017418B1 (pt) Heterociclos bicíclicos como inibidores de fgfr, seu uso e composição farmacêutica que os compreende