JP2016534059A5 - - Google Patents
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- JP2016534059A5 JP2016534059A5 JP2016525063A JP2016525063A JP2016534059A5 JP 2016534059 A5 JP2016534059 A5 JP 2016534059A5 JP 2016525063 A JP2016525063 A JP 2016525063A JP 2016525063 A JP2016525063 A JP 2016525063A JP 2016534059 A5 JP2016534059 A5 JP 2016534059A5
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- KFLQYBLSEZRKTN-MOPGFXCFSA-N CC(N(CC[C@H]1NC(C=C)=O)C[C@@H]1Nc1nc(ccc(-c(c(Cl)c(cc2OC)OC)c2Cl)c2)c2cn1)=O Chemical compound CC(N(CC[C@H]1NC(C=C)=O)C[C@@H]1Nc1nc(ccc(-c(c(Cl)c(cc2OC)OC)c2Cl)c2)c2cn1)=O KFLQYBLSEZRKTN-MOPGFXCFSA-N 0.000 description 1
- 0 CCN(C1O)c2cc(N[C@](CCCC3)[C@]3NC(C#C)=O)ncc2C=C1c(c(Cl)c(*)cc1OC)c1Cl Chemical compound CCN(C1O)c2cc(N[C@](CCCC3)[C@]3NC(C#C)=O)ncc2C=C1c(c(Cl)c(*)cc1OC)c1Cl 0.000 description 1
- ZAOOOJFIXJSQSK-QWHCGFSZSA-N CCN(c(nc(N[C@H](CCC1)[C@H]1NC(C=C)=O)nc1)c1N=C1c(c(Cl)c(cc2OC)OC)c2Cl)C1=O Chemical compound CCN(c(nc(N[C@H](CCC1)[C@H]1NC(C=C)=O)nc1)c1N=C1c(c(Cl)c(cc2OC)OC)c2Cl)C1=O ZAOOOJFIXJSQSK-QWHCGFSZSA-N 0.000 description 1
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- JHMGYDVAEUYQHL-UHFFFAOYSA-N COc(cc(c(Cl)c1-c(cc2)cc3c2nc(NC2CCCCC2)nc3)OC)c1Cl Chemical compound COc(cc(c(Cl)c1-c(cc2)cc3c2nc(NC2CCCCC2)nc3)OC)c1Cl JHMGYDVAEUYQHL-UHFFFAOYSA-N 0.000 description 1
- WEYGASMDUSXWOC-MSOLQXFVSA-N COc(cc(c(Cl)c1-c(cc2)cc3c2nc(N[C@@H](CCCC2)[C@@H]2NC(C=C)=O)nc3)OC)c1Cl Chemical compound COc(cc(c(Cl)c1-c(cc2)cc3c2nc(N[C@@H](CCCC2)[C@@H]2NC(C=C)=O)nc3)OC)c1Cl WEYGASMDUSXWOC-MSOLQXFVSA-N 0.000 description 1
- NCKDVUYBTAQHDX-COYJEINXSA-N COc(cc(c(Cl)c1-c(cc2)cc3c2nc(N[C@@H](CCCC2)[C@H]2NC(/C=C\COc(c(Cl)c2-c4ccc5nc(N[C@@H](CNCC6)[C@@H]6NC(C=C)=O)ncc5c4)cc(OC)c2Cl)=O)nc3)OC)c1Cl Chemical compound COc(cc(c(Cl)c1-c(cc2)cc3c2nc(N[C@@H](CCCC2)[C@H]2NC(/C=C\COc(c(Cl)c2-c4ccc5nc(N[C@@H](CNCC6)[C@@H]6NC(C=C)=O)ncc5c4)cc(OC)c2Cl)=O)nc3)OC)c1Cl NCKDVUYBTAQHDX-COYJEINXSA-N 0.000 description 1
- BVDNESAVRVJTNC-CCLHPLFOSA-N COc(cc(c(Cl)c1-c(cc2)cc3c2nc(N[C@@H]([C@H](C2)NC(C#C)=O)c4c2cccc4)nc3)OC)c1Cl Chemical compound COc(cc(c(Cl)c1-c(cc2)cc3c2nc(N[C@@H]([C@H](C2)NC(C#C)=O)c4c2cccc4)nc3)OC)c1Cl BVDNESAVRVJTNC-CCLHPLFOSA-N 0.000 description 1
- WEYGASMDUSXWOC-QZTJIDSGSA-N COc(cc(c(Cl)c1-c(cc2)cc3c2nc(N[C@H](CCCC2)[C@@H]2NC(C=C)=O)nc3)OC)c1Cl Chemical compound COc(cc(c(Cl)c1-c(cc2)cc3c2nc(N[C@H](CCCC2)[C@@H]2NC(C=C)=O)nc3)OC)c1Cl WEYGASMDUSXWOC-QZTJIDSGSA-N 0.000 description 1
- WEYGASMDUSXWOC-ZWKOTPCHSA-N COc(cc(c(Cl)c1-c(cc2)cc3c2nc(N[C@H](CCCC2)[C@H]2NC(C=C)=O)nc3)OC)c1Cl Chemical compound COc(cc(c(Cl)c1-c(cc2)cc3c2nc(N[C@H](CCCC2)[C@H]2NC(C=C)=O)nc3)OC)c1Cl WEYGASMDUSXWOC-ZWKOTPCHSA-N 0.000 description 1
- GKQWMHRQOVMSIE-SJORKVTESA-N COc(cc(c(Cl)c1-c(cc2)cc3c2nc(N[C@H](CCOC2)[C@H]2NC(C=C)=O)nc3)OC)c1Cl Chemical compound COc(cc(c(Cl)c1-c(cc2)cc3c2nc(N[C@H](CCOC2)[C@H]2NC(C=C)=O)nc3)OC)c1Cl GKQWMHRQOVMSIE-SJORKVTESA-N 0.000 description 1
- JPCIRONPDKKKBK-DLBZAZTESA-N COc(cc(c(Cl)c1-c(cc2)cc3c2nc(N[C@H](CNCC2)[C@H]2NC(C=C)=O)nc3)OC)c1Cl Chemical compound COc(cc(c(Cl)c1-c(cc2)cc3c2nc(N[C@H](CNCC2)[C@H]2NC(C=C)=O)nc3)OC)c1Cl JPCIRONPDKKKBK-DLBZAZTESA-N 0.000 description 1
- MGZKYOAQVGSSGC-DLBZAZTESA-N COc(cc(c(Cl)c1-c(cc2)cc3c2nc(N[C@H](COCC2)[C@H]2NC(C=C)=O)nc3)OC)c1Cl Chemical compound COc(cc(c(Cl)c1-c(cc2)cc3c2nc(N[C@H](COCC2)[C@H]2NC(C=C)=O)nc3)OC)c1Cl MGZKYOAQVGSSGC-DLBZAZTESA-N 0.000 description 1
- FRVZTFULMVCLRE-HYVNUMGLSA-N COc(cc(c(Cl)c1-c(cc2)cc3c2nc(N[C@H](C[C@@H](C2)O)[C@H]2NC(C=C)=O)nc3)OC)c1Cl Chemical compound COc(cc(c(Cl)c1-c(cc2)cc3c2nc(N[C@H](C[C@@H](C2)O)[C@H]2NC(C=C)=O)nc3)OC)c1Cl FRVZTFULMVCLRE-HYVNUMGLSA-N 0.000 description 1
- AWQOOPSJCUIVQO-JKSUJKDBSA-N COc(cc(c(Cl)c1-c(cc2Cl)cc3c2nc(N[C@H](COCC2)[C@H]2NC(C=C)=O)nc3)OC)c1Cl Chemical compound COc(cc(c(Cl)c1-c(cc2Cl)cc3c2nc(N[C@H](COCC2)[C@H]2NC(C=C)=O)nc3)OC)c1Cl AWQOOPSJCUIVQO-JKSUJKDBSA-N 0.000 description 1
Applications Claiming Priority (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201361895472P | 2013-10-25 | 2013-10-25 | |
| US61/895,472 | 2013-10-25 | ||
| US201461927782P | 2014-01-15 | 2014-01-15 | |
| US61/927,782 | 2014-01-15 | ||
| PCT/US2014/061974 WO2015061572A1 (en) | 2013-10-25 | 2014-10-23 | Inhibitors of the fibroblast growth factor receptor |
Related Child Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2018186710A Division JP2019019131A (ja) | 2013-10-25 | 2018-10-01 | 繊維芽細胞成長因子受容体の阻害剤 |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2016534059A JP2016534059A (ja) | 2016-11-04 |
| JP2016534059A5 true JP2016534059A5 (https=) | 2017-11-30 |
| JP6458023B2 JP6458023B2 (ja) | 2019-01-23 |
Family
ID=51947473
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2016525063A Active JP6458023B2 (ja) | 2013-10-25 | 2014-10-23 | 繊維芽細胞成長因子受容体の阻害剤 |
| JP2018186710A Pending JP2019019131A (ja) | 2013-10-25 | 2018-10-01 | 繊維芽細胞成長因子受容体の阻害剤 |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2018186710A Pending JP2019019131A (ja) | 2013-10-25 | 2018-10-01 | 繊維芽細胞成長因子受容体の阻害剤 |
Country Status (27)
| Country | Link |
|---|---|
| US (4) | US9434700B2 (https=) |
| EP (2) | EP3395814B1 (https=) |
| JP (2) | JP6458023B2 (https=) |
| KR (1) | KR102405452B1 (https=) |
| CN (2) | CN105658642B (https=) |
| AU (1) | AU2014339972B9 (https=) |
| BR (1) | BR112016008849B8 (https=) |
| CA (1) | CA2928042C (https=) |
| CY (1) | CY1125393T1 (https=) |
| DK (1) | DK3395814T3 (https=) |
| ES (1) | ES2924111T3 (https=) |
| HR (1) | HRP20220840T1 (https=) |
| HU (1) | HUE059037T2 (https=) |
| IL (1) | IL244738B (https=) |
| LT (1) | LT3395814T (https=) |
| MX (1) | MX2016005297A (https=) |
| PH (1) | PH12016500739B1 (https=) |
| PL (1) | PL3395814T3 (https=) |
| PT (1) | PT3395814T (https=) |
| RS (1) | RS63405B1 (https=) |
| RU (1) | RU2704112C2 (https=) |
| SI (1) | SI3395814T1 (https=) |
| SM (1) | SMT202200292T1 (https=) |
| TW (1) | TWI675828B (https=) |
| UY (1) | UY35798A (https=) |
| WO (1) | WO2015061572A1 (https=) |
| ZA (1) | ZA201601971B (https=) |
Families Citing this family (110)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AR077468A1 (es) | 2009-07-09 | 2011-08-31 | Array Biopharma Inc | Compuestos de pirazolo (1,5 -a) pirimidina sustituidos como inhibidores de trk- quinasa |
| US8754114B2 (en) | 2010-12-22 | 2014-06-17 | Incyte Corporation | Substituted imidazopyridazines and benzimidazoles as inhibitors of FGFR3 |
| RS58514B1 (sr) | 2012-06-13 | 2019-04-30 | Incyte Holdings Corp | Supstituisana triciklična jedinjenja kao inhibitori fgfr |
| SG11201500125QA (en) * | 2012-07-11 | 2015-02-27 | Blueprint Medicines Corp | Inhibitors of the fibroblast growth factor receptor |
| US9388185B2 (en) | 2012-08-10 | 2016-07-12 | Incyte Holdings Corporation | Substituted pyrrolo[2,3-b]pyrazines as FGFR inhibitors |
| WO2014160521A1 (en) | 2013-03-15 | 2014-10-02 | Blueprint Medicines Corporation | Piperazine derivatives and their use as kit modulators |
| EP3943087A1 (en) | 2013-03-15 | 2022-01-26 | Celgene CAR LLC | Heteroaryl compounds and uses thereof |
| CN105307657B (zh) | 2013-03-15 | 2020-07-10 | 西建卡尔有限责任公司 | 杂芳基化合物和其用途 |
| US9321786B2 (en) | 2013-03-15 | 2016-04-26 | Celgene Avilomics Research, Inc. | Heteroaryl compounds and uses thereof |
| PH12015502383B1 (en) | 2013-04-19 | 2023-02-03 | Incyte Holdings Corp | Bicyclic heterocycles as fgfr inhibitors |
| SI3057969T1 (sl) | 2013-10-17 | 2018-10-30 | Blueprint Medicines Corporation | Sestavki, uporabni za zdravljenje motenj, povezanih s KIT |
| PH12016500676B1 (en) | 2013-10-18 | 2022-07-20 | Eisai R&D Man Co Ltd | Pyrimidine fgfr4 inhibitors |
| RS63405B1 (sr) | 2013-10-25 | 2022-08-31 | Blueprint Medicines Corp | Inhibitori receptora faktora rasta fibroblasta |
| TN2016000115A1 (en) | 2013-10-25 | 2017-07-05 | Novartis Ag | Ring-fused bicyclic pyridyl derivatives as fgfr4 inhibitors. |
| US9695165B2 (en) | 2014-01-15 | 2017-07-04 | Blueprint Medicines Corporation | Inhibitors of the fibroblast growth factor receptor |
| CN105294682B (zh) | 2014-07-26 | 2017-07-07 | 广东东阳光药业有限公司 | Cdk类小分子抑制剂的化合物及其用途 |
| 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 |
| US10851105B2 (en) | 2014-10-22 | 2020-12-01 | Incyte Corporation | Bicyclic heterocycles as FGFR4 inhibitors |
| WO2016127074A1 (en) | 2015-02-06 | 2016-08-11 | Blueprint Medicines Corporation | 2-(pyridin-3-yl)-pyrimidine derivatives as ret inhibitors |
| MA41551A (fr) | 2015-02-20 | 2017-12-26 | Incyte Corp | Hétérocycles bicycliques utilisés en tant qu'inhibiteurs de fgfr4 |
| TWI712601B (zh) | 2015-02-20 | 2020-12-11 | 美商英塞特公司 | 作為fgfr抑制劑之雙環雜環 |
| US9580423B2 (en) | 2015-02-20 | 2017-02-28 | Incyte Corporation | Bicyclic heterocycles as FGFR4 inhibitors |
| 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 |
| KR102548229B1 (ko) | 2015-04-14 | 2023-06-27 | 에자이 알앤드디 매니지먼트 가부시키가이샤 | 결정질 fgfr4 억제제 화합물 및 그의 용도 |
| BR112018000808A2 (pt) | 2015-07-16 | 2018-09-04 | Array Biopharma Inc | compostos de pirazolo[1,5-a]piridina substituída como inibidores de ret cinase |
| CN108026102A (zh) | 2015-07-24 | 2018-05-11 | 蓝印药品公司 | 可用于治疗与kit和pdgfr相关的病症的化合物 |
| BR112018003588A2 (pt) | 2015-08-26 | 2018-09-25 | Blueprint Medicines Corp | compostos e composições úteis para tratamento de distúrbios relacionados ao ntrk |
| EP3368039A1 (en) | 2015-10-26 | 2018-09-05 | The Regents of The University of Colorado, A Body Corporate | Point mutations in trk inhibitor-resistant cancer and methods relating to the same |
| SI3371171T1 (sl) | 2015-11-02 | 2024-03-29 | Blueprint Medicines Corporation | Inhibitorji ret |
| SG10201912607SA (en) | 2015-11-19 | 2020-02-27 | Blueprint Medicines Corp | Compounds and compositions useful for treating disorders related to ntrk |
| US10183928B2 (en) | 2016-03-17 | 2019-01-22 | Blueprint Medicines Corporation | Inhibitors of RET |
| FI3439662T3 (fi) | 2016-04-04 | 2024-09-04 | Loxo Oncology Inc | (s)-n-(5-((r)-2-(2,5-difluorifenyyli)pyrrolidin-1-yyli)pyratsolo[1,5-a]pyrimidin-3-yyli)-3-hydroksipyrrolidiini-1-karboksamidin nesteformulaatioita |
| US10045991B2 (en) | 2016-04-04 | 2018-08-14 | Loxo Oncology, Inc. | Methods of treating pediatric cancers |
| AU2017246547B2 (en) | 2016-04-04 | 2023-02-23 | Loxo Oncology, Inc. | Methods of treating pediatric cancers |
| CN109311889B (zh) | 2016-04-15 | 2021-11-16 | 缆图药品公司 | 激活素受体样激酶抑制剂 |
| JP7372740B2 (ja) | 2016-05-10 | 2023-11-01 | エーザイ・アール・アンド・ディー・マネジメント株式会社 | 細胞生存性及び／又は細胞増殖を低減するための薬物の組み合わせ |
| EP3458456B1 (en) | 2016-05-18 | 2020-11-25 | Loxo Oncology Inc. | Preparation of (s)-n-(5-((r)-2-(2,5-difluorophenyl)pyrrolidin-1-yl)pyrazolo[1,5-a]pyrimidin-3-yl)-3-hydroxypyrrolidine-1-carboxamide |
| US10227329B2 (en) | 2016-07-22 | 2019-03-12 | Blueprint Medicines Corporation | Compounds useful for treating disorders related to RET |
| WO2018022761A1 (en) | 2016-07-27 | 2018-02-01 | Blueprint Medicines Corporation | Substituted cyclopentane-amides for treating disorders related to ret |
| CN107793395B (zh) * | 2016-09-01 | 2021-01-05 | 南京药捷安康生物科技有限公司 | 成纤维细胞生长因子受体抑制剂及其用途 |
| WO2018049233A1 (en) | 2016-09-08 | 2018-03-15 | Nicolas Stransky | Inhibitors of the fibroblast growth factor receptor in combination with cyclin-dependent kinase inhibitors |
| TWI752098B (zh) | 2016-10-10 | 2022-01-11 | 美商亞雷生物製藥股份有限公司 | 作為ret激酶抑制劑之經取代吡唑并[1,5-a]吡啶化合物 |
| TWI704148B (zh) | 2016-10-10 | 2020-09-11 | 美商亞雷生物製藥股份有限公司 | 作為ｒｅｔ激酶抑制劑之經取代吡唑并[1,5-a]吡啶化合物 |
| JOP20190092A1 (ar) | 2016-10-26 | 2019-04-25 | Array Biopharma Inc | عملية لتحضير مركبات بيرازولو[1، 5-a]بيريميدين وأملاح منها |
| CN106986809B (zh) * | 2016-12-02 | 2020-03-24 | 广东省微生物研究所（广东省微生物分析检测中心） | 一种5-溴-6-氯-3-吲哚辛酯的合成方法 |
| AU2017378943B2 (en) * | 2016-12-19 | 2020-06-18 | Abbisko Therapeutics Co., Ltd. | FGFR4 inhibitor, preparation method therefor and pharmaceutical use thereof |
| CN108264511B (zh) * | 2017-01-03 | 2021-04-13 | 浙江海正药业股份有限公司 | 杂环类衍生物及其制备方法和其在医药上的用途 |
| WO2018136663A1 (en) | 2017-01-18 | 2018-07-26 | Array Biopharma, Inc. | Ret inhibitors |
| WO2018136661A1 (en) | 2017-01-18 | 2018-07-26 | Andrews Steven W | SUBSTITUTED PYRAZOLO[1,5-a]PYRAZINE COMPOUNDS AS RET KINASE INHIBITORS |
| CN108503593B (zh) * | 2017-02-28 | 2021-04-27 | 暨南大学 | 2-氨基嘧啶类化合物及其应用 |
| KR102583737B1 (ko) * | 2017-03-03 | 2023-09-26 | 오클랜드 유니서비시즈 리미티드 | Fgfr 키나제 저해제 및 약학적 용도 |
| JOP20190213A1 (ar) | 2017-03-16 | 2019-09-16 | Array Biopharma Inc | مركبات حلقية ضخمة كمثبطات لكيناز ros1 |
| US11040979B2 (en) | 2017-03-31 | 2021-06-22 | Blueprint Medicines Corporation | Substituted pyrrolo[1,2-b]pyridazines for treating disorders related to KIT and PDGFR |
| CN108689878B (zh) * | 2017-04-10 | 2023-05-09 | 浙江九洲药业股份有限公司 | 光学活性二氨基衍生物的制备方法 |
| AR111960A1 (es) | 2017-05-26 | 2019-09-04 | Incyte Corp | Formas cristalinas de un inhibidor de fgfr y procesos para su preparación |
| CA3074885A1 (en) * | 2017-09-05 | 2019-03-14 | Bioardis Llc | Aromatic derivative, preparation method for same, and medical applications thereof |
| TWI876442B (zh) | 2017-10-10 | 2025-03-11 | 美商絡速藥業公司 | 6-(2-羥基-2-甲基丙氧基)-4-(6-(6-((6-甲氧基吡啶-3-基)甲基)-3,6-二氮雜雙環[3.1.1]庚-3-基)吡啶-3-基)吡唑并[1,5-a]吡啶-3-甲腈之調配物 |
| TWI791053B (zh) | 2017-10-10 | 2023-02-01 | 美商亞雷生物製藥股份有限公司 | 6-(2-羥基-2-甲基丙氧基)-4-(6-(6-((6-甲氧基吡啶-3-基)甲基)-3,6-二氮雜雙環[3.1.1]庚-3-基)吡啶-3-基)吡唑并[1,5-a]吡啶-3-甲腈之結晶形式及其醫藥組合物 |
| EP3697786B1 (en) | 2017-10-18 | 2022-08-31 | Blueprint Medicines Corporation | Substituted pyrrolopyridines as inhibitors of activin receptor-like kinase |
| AU2018361264B2 (en) | 2017-11-01 | 2021-04-01 | Guangdong Xianqiang Pharmaceutical Co., Ltd | Salt form and crystal form of compound as FGFR4 inhibitor and preparation method thereof |
| CN109745325B (zh) * | 2017-11-08 | 2022-02-15 | 上海翰森生物医药科技有限公司 | Fgfr4抑制剂、其制备方法和用途 |
| US11472802B2 (en) | 2018-01-18 | 2022-10-18 | Array Biopharma Inc. | Substituted pyrazolyl[4,3-c]pyridine compounds as RET kinase inhibitors |
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