JP2017530154A5 - - Google Patents

Download PDF

Info

Publication number
JP2017530154A5
JP2017530154A5 JP2017517705A JP2017517705A JP2017530154A5 JP 2017530154 A5 JP2017530154 A5 JP 2017530154A5 JP 2017517705 A JP2017517705 A JP 2017517705A JP 2017517705 A JP2017517705 A JP 2017517705A JP 2017530154 A5 JP2017530154 A5 JP 2017530154A5
Authority
JP
Japan
Prior art keywords
alkyl
alkoxy
ring
hydroxy
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
JP2017517705A
Other languages
English (en)
Japanese (ja)
Other versions
JP6585167B2 (ja
JP2017530154A (ja
Filing date
Publication date
Application filed filed Critical
Priority claimed from PCT/US2015/053677 external-priority patent/WO2016054483A1/en
Publication of JP2017530154A publication Critical patent/JP2017530154A/ja
Publication of JP2017530154A5 publication Critical patent/JP2017530154A5/ja
Application granted granted Critical
Publication of JP6585167B2 publication Critical patent/JP6585167B2/ja
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

JP2017517705A 2014-10-03 2015-10-02 Fgfr4阻害剤としての縮環二環式ピリジル誘導体の使用 Active JP6585167B2 (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
CN2014088094 2014-10-03
CNPCT/CN2014/088094 2014-10-03
PCT/US2015/053677 WO2016054483A1 (en) 2014-10-03 2015-10-02 Use of ring-fused bicyclic pyridyl derivatives as fgfr4 inhibitors

Related Child Applications (1)

Application Number Title Priority Date Filing Date
JP2019161051A Division JP6794514B2 (ja) 2014-10-03 2019-09-04 Fgfr4阻害剤としての縮環二環式ピリジル誘導体の使用

Publications (3)

Publication Number Publication Date
JP2017530154A JP2017530154A (ja) 2017-10-12
JP2017530154A5 true JP2017530154A5 (cg-RX-API-DMAC7.html) 2018-11-15
JP6585167B2 JP6585167B2 (ja) 2019-10-02

Family

ID=54330059

Family Applications (2)

Application Number Title Priority Date Filing Date
JP2017517705A Active JP6585167B2 (ja) 2014-10-03 2015-10-02 Fgfr4阻害剤としての縮環二環式ピリジル誘導体の使用
JP2019161051A Active JP6794514B2 (ja) 2014-10-03 2019-09-04 Fgfr4阻害剤としての縮環二環式ピリジル誘導体の使用

Family Applications After (1)

Application Number Title Priority Date Filing Date
JP2019161051A Active JP6794514B2 (ja) 2014-10-03 2019-09-04 Fgfr4阻害剤としての縮環二環式ピリジル誘導体の使用

Country Status (6)

Country Link
US (3) US20180185341A1 (cg-RX-API-DMAC7.html)
EP (1) EP3200786B1 (cg-RX-API-DMAC7.html)
JP (2) JP6585167B2 (cg-RX-API-DMAC7.html)
ES (1) ES2756748T3 (cg-RX-API-DMAC7.html)
PL (1) PL3200786T3 (cg-RX-API-DMAC7.html)
WO (1) WO2016054483A1 (cg-RX-API-DMAC7.html)

Families Citing this family (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP6585167B2 (ja) * 2014-10-03 2019-10-02 ノバルティス アーゲー Fgfr4阻害剤としての縮環二環式ピリジル誘導体の使用
JP7103952B2 (ja) * 2016-05-20 2022-07-20 江▲蘇▼豪森▲薬▼▲業▼集▲団▼有限公司 Fgfr4阻害剤、その製造方法及び応用
WO2018055503A1 (en) 2016-09-20 2018-03-29 Novartis Ag Combination comprising a pd-1 antagonist and an fgfr4 inhibitor
ES2934341T3 (es) * 2016-11-02 2023-02-21 Novartis Ag Combinaciones de inhibidores de FGFR4 y secuestrantes de ácidos biliares
TWI723480B (zh) * 2018-07-27 2021-04-01 大陸商北京加科思新藥研發有限公司 用作fgfr4抑制劑的稠環衍生物
CN114364798A (zh) 2019-03-21 2022-04-15 欧恩科斯欧公司 用于治疗癌症的Dbait分子与激酶抑制剂的组合
US20220401436A1 (en) 2019-11-08 2022-12-22 INSERM (Institute National de la Santé et de la Recherche Médicale) Methods for the treatment of cancers that have acquired resistance to kinase inhibitors
WO2021148581A1 (en) 2020-01-22 2021-07-29 Onxeo Novel dbait molecule and its use

Family Cites Families (65)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5424186A (en) 1989-06-07 1995-06-13 Affymax Technologies N.V. Very large scale immobilized polymer synthesis
US5143854A (en) 1989-06-07 1992-09-01 Affymax Technologies N.V. Large scale photolithographic solid phase synthesis of polypeptides and receptor binding screening thereof
GB9420999D0 (en) 1994-10-18 1994-12-07 Smithkline Beecham Plc Novel compounds
CA2261633A1 (en) 1996-07-29 1998-02-05 Banyu Pharmaceutical Co., Ltd. Chemokine receptor antagonists
US6048861A (en) 1997-12-17 2000-04-11 Merck & Co., Inc. Integrin receptor antagonists
CO4980854A1 (es) 1998-02-10 2000-11-27 Novartis Ag Inhibidores de celulas b particularmente amidas, proceso par su produccion y composiciones farmaceuticas que los contiene
CA2386474A1 (en) 1999-09-20 2001-03-29 Takeda Chemical Industries, Ltd. Melanin concentrating hormone antagonist
WO2001034602A2 (en) * 1999-11-08 2001-05-17 Merck & Co., Inc. Process and intermediates for the preparation of imidazolidinone alpha v integrin antagonists
US6407241B1 (en) 1999-11-08 2002-06-18 Merck & Co., Inc. Process and intermediates for the preparation of imidazolidinone αv integrin antagonists
JPWO2003068753A1 (ja) 2002-02-14 2005-06-02 小野薬品工業株式会社 N−カルバモイル窒素含有縮合環化合物およびその化合物を有効成分として含有する薬剤
JPWO2004007472A1 (ja) 2002-07-10 2005-11-17 小野薬品工業株式会社 Ccr4アンタゴニストおよびその医薬用途
BR0313871A (pt) * 2002-08-30 2005-07-19 Eisai Co Ltd Derivados aromáticos contendo nitrogênio
US7098332B2 (en) * 2002-12-20 2006-08-29 Hoffmann-La Roche Inc. 5,8-Dihydro-6H-pyrido[2,3-d]pyrimidin-7-ones
MXPA05006742A (es) 2002-12-20 2005-09-08 Warner Lambert Co Benzoxazinas y derivados de las mismas como inhibidores de fosfoinositido-3-quinasas.
JP2007524596A (ja) 2003-02-28 2007-08-30 トランスフォーム・ファーマシューティカルズ・インコーポレイテッド 共結晶医薬組成物
TW201018661A (en) 2003-03-14 2010-05-16 Ono Pharmaceutical Co Heterocyclic rinf having nitrogen atom derivatives and medicament containing the derivatives as active ingredient
AU2004229404B2 (en) 2003-04-11 2008-01-10 Taigen Biotechnology Aminoquinoline compounds
JP4895811B2 (ja) 2003-09-11 2012-03-14 ケミア,インコーポレイテッド サイトカイン阻害剤
BRPI0613045A2 (pt) 2005-07-15 2010-12-14 Hoffmann La Roche aminas cÍclicas fundidas a heteroarila
EP1963320A1 (en) * 2005-12-07 2008-09-03 OSI Pharmaceuticals, Inc. Pyrrolopyridine kinase inhibiting compounds
CN101336237B (zh) 2005-12-21 2015-09-30 诺华股份有限公司 作为fgf抑制剂的嘧啶基芳基脲衍生物
CN101405002A (zh) 2005-12-29 2009-04-08 詹森药业有限公司 激肽原2受体拮抗剂
AU2007254005B2 (en) 2006-02-10 2012-11-29 Genentech, Inc. Anti-FGF19 antibodies and methods using same
JPWO2007105637A1 (ja) 2006-03-10 2009-07-30 小野薬品工業株式会社 含窒素複素環誘導体およびそれらを有効成分とする薬剤
EP2049490A1 (en) * 2006-06-09 2009-04-22 Astra Zeneca AB N-(benzoyl)-o- [2- (pyridin- 2 -ylamino) ethyl]-l-tyrosine derivatives and related compounds as a5b1 antagonists for the treatment of solid tumors
WO2007146230A2 (en) 2006-06-14 2007-12-21 Merck & Co., Inc. Non-nucleoside reverse transcriptase inhibitors
EP1918376A1 (en) 2006-11-03 2008-05-07 Max-Planck-Gesellschaft zur Förderung der Wissenschaften e.V. FGFR4 promotes cancer cell resistance in response to chemotherapeutic drugs
WO2008112509A1 (en) 2007-03-09 2008-09-18 Novartis Ag Treatment of melanoma
NO2550972T3 (cg-RX-API-DMAC7.html) 2007-04-02 2018-07-21
JP2011507848A (ja) 2007-12-21 2011-03-10 ザ スクリプス リサーチ インスティチュート Rhoキナーゼインヒビターとしてのベンゾピランおよびアナログ
FR2933702A1 (fr) 2008-07-08 2010-01-15 Sanofi Aventis Antagonistes specifiques du recepteur fgf-r4
CN102224170A (zh) 2008-09-03 2011-10-19 利琴蒂亚有限公司 抑制与fgfr4相关的癌细胞侵袭的材料和方法
EP2341052A4 (en) 2008-09-05 2011-10-12 Shionogi & Co RING-CONDENSED MORPHOLINE DERIVATIVITY WITH PI3K-INHIBITING EFFECT
WO2010080478A1 (en) 2008-12-19 2010-07-15 Genentech, Inc. Compounds and methods of use
GB0906472D0 (en) 2009-04-15 2009-05-20 Astex Therapeutics Ltd New compounds
GB0906470D0 (en) * 2009-04-15 2009-05-20 Astex Therapeutics Ltd New compounds
SG175877A1 (en) 2009-05-04 2011-12-29 Plexxikon Inc Compounds and methods for inhibition of renin, and indications therefor
MX2012004995A (es) 2009-10-29 2012-10-03 Sirtris Pharmaceuticals Inc Piridinas biciclicas y analogos como moduladores de sirtuina.
CN102596916B (zh) 2009-10-30 2015-06-17 诺瓦提斯公司 3-(2,6-二氯-3,5-二甲氧基-苯基)-1-{6-[4-(4-乙基-哌嗪-1-基)-苯基氨基]-嘧啶-4-基}-1-甲基-脲的n-氧化物
JPWO2011093501A1 (ja) 2010-02-01 2013-06-06 日本ケミファ株式会社 Gpr119作動薬
WO2011111880A1 (ko) 2010-03-08 2011-09-15 주식회사 메디젠텍 세포핵에서 세포질로의 gsk3의 이동을 억제하는 화합물을 함유하는 세포핵에서 세포질로의 gsk3 이동에 의해 발생되는 질환의 치료 또는 예방용 약학적 조성물
ES2823350T3 (es) 2010-07-29 2021-05-06 Rigel Pharmaceuticals Inc Compuestos heterocíclicos que activan AMPK y métodos de uso de los mismos
WO2012061337A1 (en) * 2010-11-02 2012-05-10 Exelixis, Inc. Fgfr2 modulators
JP5620417B2 (ja) * 2011-02-07 2014-11-05 中外製薬株式会社 アミノピラゾール誘導体を含む医薬
KR20140051846A (ko) 2011-03-18 2014-05-02 루핀 리미티드 칼슘 감지 수용체 조절자로서의 벤조[b][1,4]옥사진 유도체
EP2694551A1 (en) 2011-04-07 2014-02-12 Genentech, Inc. Anti-fgfr4 antibodies and methods of use
GB201118656D0 (en) * 2011-10-28 2011-12-07 Astex Therapeutics Ltd New compounds
BR112015000653A2 (pt) 2012-07-11 2019-11-05 Blueprint Medicines Corp compostos inibidores do receptor de fator de crescimento de fibroblasto, sua composição farmacêutica e seus usos
US9403774B2 (en) 2012-10-12 2016-08-02 Bristol-Myers Squibb Company Guanidine and amine substituted tetrahydroisoquinoline compounds as factor xia inhibitors
WO2014059202A1 (en) 2012-10-12 2014-04-17 Bristol-Myers Squibb Company Guanidine substituted tetrahydroisoquinoline compounds as factor xia inhibitors
WO2014079709A1 (en) 2012-11-23 2014-05-30 Ab Science Use of small molecule inhibitors/activators in combination with (deoxy)nucleoside or (deoxy)nucleotide analogs for treatment of cancer and hematological malignancies or viral infections
EA036160B1 (ru) 2013-03-15 2020-10-08 Селджен Кар Ллс Гетероарильные соединения и их применение
AR095464A1 (es) 2013-03-15 2015-10-21 Celgene Avilomics Res Inc Compuestos de heteroarilo y usos de los mismos
DK2986610T5 (en) 2013-04-19 2018-12-10 Incyte Holdings Corp BICYCLIC HETEROCYCLES AS FGFR INHIBITORS
GB201307577D0 (en) 2013-04-26 2013-06-12 Astex Therapeutics Ltd New compounds
US9783504B2 (en) 2013-07-09 2017-10-10 Dana-Farber Cancer Institute, Inc. Kinase inhibitors for the treatment of disease
AR097455A1 (es) 2013-08-28 2016-03-16 Astellas Pharma Inc Composición farmacéutica que contiene compuesto de pirimidina como un ingrediente activo
SG11201602069WA (en) 2013-10-18 2016-04-28 Eisai R&D Man Co Ltd Pyrimidine fgfr4 inhibitors
PH12016500739B1 (en) 2013-10-25 2022-04-29 Blueprint Medicines Corp Inhibitors of the fibrolast growth factor receptor
CN105683188B (zh) 2013-10-25 2018-02-09 诺华股份有限公司 作为fgfr4抑制剂的稠环二环吡啶基衍生物
WO2015195509A2 (en) 2014-06-16 2015-12-23 Ngm Biopharmaceuticals, Inc. Methods and uses for modulating bile acid homeostasis and treatment of bile acid disorders and diseases
JP6585167B2 (ja) * 2014-10-03 2019-10-02 ノバルティス アーゲー Fgfr4阻害剤としての縮環二環式ピリジル誘導体の使用
JP2018509448A (ja) * 2015-03-25 2018-04-05 ノバルティス アーゲー 組合せ医薬
US9802917B2 (en) * 2015-03-25 2017-10-31 Novartis Ag Particles of N-(5-cyano-4-((2-methoxyethyl)amino)pyridin-2-yl)-7-formyl-6-((4-methyl-2-oxopiperazin-1-yl)methyl)-3,4-dihydro-1,8-naphthyridine-1(2H)-carboxamide
ES2934341T3 (es) 2016-11-02 2023-02-21 Novartis Ag Combinaciones de inhibidores de FGFR4 y secuestrantes de ácidos biliares

Similar Documents

Publication Publication Date Title
JP2017530154A5 (cg-RX-API-DMAC7.html)
JP6823095B2 (ja) 噴霧乾燥製剤
JP6664385B2 (ja) Bub1阻害薬としてのベンジル置換インダゾール類
RU2686323C2 (ru) Новые соединения и композиции для ингибирования fasn
TWI875756B (zh) Cdk抑制劑
JP7215687B2 (ja) キナーゼ阻害活性を有する化合物、その製造方法及び用途
ES2985987T3 (es) Derivado de N-(aza-aril)ciclolactam-1-carboxamida, método de preparación correspondiente y uso del mismo
KR101312122B1 (ko) Smo 억제제로서의 피리다진 유도체
JP6952695B2 (ja) インフルエンザウイルス複製の阻害剤、その適用方法および使用
JP6021805B2 (ja) 腫瘍治療剤
JP2010528026A5 (cg-RX-API-DMAC7.html)
CN107922431A (zh) Hpk1抑制剂及其使用方法
RU2013109143A (ru) Бензимидазол- и азабензимидазолсодержащие соединения, которые ингибируют киназу анапластической лимфомы
AU2014337154A1 (en) Co-crystals of (s)-N-methyl-8-(1-((2'-methyl-[4,5'-bipyrimidin]-6-yl)amino)propan-2-yl)quinoline-4-carboxamide and deuterated derivatives thereof as DNA-PK inhibitors
WO2015058067A1 (en) Co-crystals of (s)-n-methyl-8-(1-((2'-methyl-[4,5'-bipyrimidin]-6-yl)amino)propan-2-yl)quinoline-4-carboxamide and deuterated derivatives thereof as dna-pk inhibitors
JP2016525076A5 (cg-RX-API-DMAC7.html)
CN105308036A (zh) 用于激酶调节的化合物和方法及其适应症
JP2016526540A5 (cg-RX-API-DMAC7.html)
TW201028393A (en) Kinase inhibitors and methods of their use
JP2013527175A5 (cg-RX-API-DMAC7.html)
JP2016506418A (ja) 非選択的キナーゼ阻害剤
RU2014154009A (ru) Комбинация ингибитора 17-альфа-гидроксилазы (с17,20-лиазы) и специфического ингибитора pi-3k для лечения онкологического заболевания
JP2017527586A (ja) 癌の治療に有用な縮合二環式(ヘテロ)芳香族化合物
JP2013173787A (ja) 薬剤耐性癌の処置方法
TW201731841A (zh) 6‐芳基或6‐異芳基‐4‐嗎啉‐4‐芳基‐吡啶‐2‐酮化合物