KR101061599B1 - 비정상 세포 성장 질환의 치료를 위한 단백질 키나아제 저해제인 신규 인다졸 유도체, 이의 약학적으로 허용가능한염 및 이를 유효성분으로 함유하는 약학적 조성물 - Google Patents
비정상 세포 성장 질환의 치료를 위한 단백질 키나아제 저해제인 신규 인다졸 유도체, 이의 약학적으로 허용가능한염 및 이를 유효성분으로 함유하는 약학적 조성물 Download PDFInfo
- Publication number
- KR101061599B1 KR101061599B1 KR1020080122999A KR20080122999A KR101061599B1 KR 101061599 B1 KR101061599 B1 KR 101061599B1 KR 1020080122999 A KR1020080122999 A KR 1020080122999A KR 20080122999 A KR20080122999 A KR 20080122999A KR 101061599 B1 KR101061599 B1 KR 101061599B1
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- South Korea
- Prior art keywords
- phenyl
- indazole
- trifluoromethyl
- carboxylate
- ethyl
- 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.)
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- ULSQYLNKQIQSKO-UHFFFAOYSA-N CCOC(c1n[nH]c2c1ccc(-c(cc1)ccc1NC(Nc(cc1Cl)ccc1Cl)=O)c2)=O Chemical compound CCOC(c1n[nH]c2c1ccc(-c(cc1)ccc1NC(Nc(cc1Cl)ccc1Cl)=O)c2)=O ULSQYLNKQIQSKO-UHFFFAOYSA-N 0.000 description 1
- HQVOYPOPVRAPQK-UHFFFAOYSA-N CCOC(c1n[nH]c2c1ccc(-c(cc1)ccc1NC(c1c[s]c(-c3ccncc3)n1)=O)c2)=O Chemical compound CCOC(c1n[nH]c2c1ccc(-c(cc1)ccc1NC(c1c[s]c(-c3ccncc3)n1)=O)c2)=O HQVOYPOPVRAPQK-UHFFFAOYSA-N 0.000 description 1
- IMXGEBMCSJVJTP-UHFFFAOYSA-N CCOC(c1n[nH]c2cc(-c(cc3)ccc3NC(Cc(cc3OC)ccc3OC)=O)ccc12)=O Chemical compound CCOC(c1n[nH]c2cc(-c(cc3)ccc3NC(Cc(cc3OC)ccc3OC)=O)ccc12)=O IMXGEBMCSJVJTP-UHFFFAOYSA-N 0.000 description 1
- YNTBLLCQFVAEQL-UHFFFAOYSA-N CCOC(c1n[nH]c2cc(-c(cc3)ccc3NC(c([s]3)ccc3Br)=O)ccc12)=O Chemical compound CCOC(c1n[nH]c2cc(-c(cc3)ccc3NC(c([s]3)ccc3Br)=O)ccc12)=O YNTBLLCQFVAEQL-UHFFFAOYSA-N 0.000 description 1
- LGJQYLJXCJRMOC-UHFFFAOYSA-N CN(CC1)CCN1c(cc1)c(C(F)(F)F)cc1NC(Nc1cc(-c2ccc3c(C(OC)=O)n[nH]c3c2)ccc1)=O Chemical compound CN(CC1)CCN1c(cc1)c(C(F)(F)F)cc1NC(Nc1cc(-c2ccc3c(C(OC)=O)n[nH]c3c2)ccc1)=O LGJQYLJXCJRMOC-UHFFFAOYSA-N 0.000 description 1
- QHUKQYYYWSJIHT-UHFFFAOYSA-N CNC(c1n[nH]c2c1ccc(-c(cc1)ccc1NC(c([s]1)ccc1Br)=O)c2)=O Chemical compound CNC(c1n[nH]c2c1ccc(-c(cc1)ccc1NC(c([s]1)ccc1Br)=O)c2)=O QHUKQYYYWSJIHT-UHFFFAOYSA-N 0.000 description 1
- XVELBMAMXSQCPR-UHFFFAOYSA-N CNC(c1n[nH]c2cc(-c(cc3)ccc3NC(Nc3cc(C(F)(F)F)cc(C(F)(F)F)c3)=O)ccc12)=O Chemical compound CNC(c1n[nH]c2cc(-c(cc3)ccc3NC(Nc3cc(C(F)(F)F)cc(C(F)(F)F)c3)=O)ccc12)=O XVELBMAMXSQCPR-UHFFFAOYSA-N 0.000 description 1
- FXSREKNLDCDZGM-UHFFFAOYSA-N COC(c1n[nH]c(cc2)c1cc2-c(cc1)ccc1N)=O Chemical compound COC(c1n[nH]c(cc2)c1cc2-c(cc1)ccc1N)=O FXSREKNLDCDZGM-UHFFFAOYSA-N 0.000 description 1
- CJGGDOZUHHIFCT-UHFFFAOYSA-N O=C(c([s]1)ccc1Br)Nc(cc1)ccc1-c(cc1)cc2c1c(C(NCCN1CCOCC1)=O)n[nH]2 Chemical compound O=C(c([s]1)ccc1Br)Nc(cc1)ccc1-c(cc1)cc2c1c(C(NCCN1CCOCC1)=O)n[nH]2 CJGGDOZUHHIFCT-UHFFFAOYSA-N 0.000 description 1
- YDNTYGXBKXCYEP-UHFFFAOYSA-N O=C(c1n[nH]c2c1ccc(-c(cc1)ccc1NC(Nc(cc1Cl)ccc1Cl)=O)c2)NCCN1CCOCC1 Chemical compound O=C(c1n[nH]c2c1ccc(-c(cc1)ccc1NC(Nc(cc1Cl)ccc1Cl)=O)c2)NCCN1CCOCC1 YDNTYGXBKXCYEP-UHFFFAOYSA-N 0.000 description 1
- RPFYMEMCWURYDR-UHFFFAOYSA-N [O-][N+](c(cc1)ccc1-c1ccc2c(C(O)=O)n[nH]c2c1)=O Chemical compound [O-][N+](c(cc1)ccc1-c1ccc2c(C(O)=O)n[nH]c2c1)=O RPFYMEMCWURYDR-UHFFFAOYSA-N 0.000 description 1
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero rings
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
- A61P17/06—Antipsoriatics
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
- A61P35/02—Antineoplastic agents specific for leukemia
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D231/00—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
- C07D231/54—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings condensed with carbocyclic rings or ring systems
- C07D231/56—Benzopyrazoles; Hydrogenated benzopyrazoles
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
- C07D405/12—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a chain containing hetero atoms as chain links
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D407/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen atoms as the only ring hetero atoms, not provided for by group C07D405/00
- C07D407/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen atoms as the only ring hetero atoms, not provided for by group C07D405/00 containing two hetero rings
- C07D407/04—Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen atoms as the only ring hetero atoms, not provided for by group C07D405/00 containing two hetero rings directly linked by a ring-member-to-ring-member bond
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
- C07D409/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
- C07D409/04—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings directly linked by a ring-member-to-ring-member bond
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
- C07D409/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
- C07D409/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
- C07D417/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing three or more hetero rings
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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
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- Life Sciences & Earth Sciences (AREA)
- Public Health (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Pharmacology & Pharmacy (AREA)
- Veterinary Medicine (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Hematology (AREA)
- Oncology (AREA)
- Dermatology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
Priority Applications (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| KR1020080122999A KR101061599B1 (ko) | 2008-12-05 | 2008-12-05 | 비정상 세포 성장 질환의 치료를 위한 단백질 키나아제 저해제인 신규 인다졸 유도체, 이의 약학적으로 허용가능한염 및 이를 유효성분으로 함유하는 약학적 조성물 |
| CN2009801489968A CN102239150A (zh) | 2008-12-05 | 2009-12-04 | 作为用于增殖性疾病治疗的蛋白激酶抑制剂的新型吲唑衍生物或其药学上可接受的盐以及含有其作为活性成分的药物组合物 |
| US13/132,772 US8754209B2 (en) | 2008-12-05 | 2009-12-04 | Indazole derivatives or pharmaceutically acceptable salts thereof as protein kinase inhibitors for proliferative diseases treatment, and a pharmaceutical composition containing the same as an active ingredient |
| PCT/KR2009/007247 WO2010064875A2 (en) | 2008-12-05 | 2009-12-04 | Novel indazole derivatives or pharmaceutically acceptable salts thereof as protein kinase inhibitors for proliferative diseases treatment, and a pharmaceutical composition containing the same as an active ingredient |
| JP2011539453A JP5537561B2 (ja) | 2008-12-05 | 2009-12-04 | 異常細胞増殖疾患の治療のための蛋白質キナーゼの阻害剤である新規インダゾール誘導体、これの薬学的に許容可能な塩及びこれを有効成分として含有する薬学的組成物 |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| KR1020080122999A KR101061599B1 (ko) | 2008-12-05 | 2008-12-05 | 비정상 세포 성장 질환의 치료를 위한 단백질 키나아제 저해제인 신규 인다졸 유도체, 이의 약학적으로 허용가능한염 및 이를 유효성분으로 함유하는 약학적 조성물 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| KR20100064520A KR20100064520A (ko) | 2010-06-15 |
| KR101061599B1 true KR101061599B1 (ko) | 2011-09-02 |
Family
ID=42233759
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| KR1020080122999A Expired - Fee Related KR101061599B1 (ko) | 2008-12-05 | 2008-12-05 | 비정상 세포 성장 질환의 치료를 위한 단백질 키나아제 저해제인 신규 인다졸 유도체, 이의 약학적으로 허용가능한염 및 이를 유효성분으로 함유하는 약학적 조성물 |
Country Status (5)
| Country | Link |
|---|---|
| US (1) | US8754209B2 (https=) |
| JP (1) | JP5537561B2 (https=) |
| KR (1) | KR101061599B1 (https=) |
| CN (1) | CN102239150A (https=) |
| WO (1) | WO2010064875A2 (https=) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2013100672A1 (ko) * | 2011-12-29 | 2013-07-04 | 제이더블유중외제약㈜ | 단백질 키나아제 저해활성을 가지는 3,6-이치환된 인다졸 유도체 |
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| JP2011513332A (ja) * | 2008-02-29 | 2011-04-28 | アレイ バイオファーマ、インコーポレイテッド | 癌の治療のためのraf阻害剤としてのn−(6−アミノピリジン−3−イル)−3−(スルホンアミド)ベンズアミド誘導体 |
| PE20091561A1 (es) * | 2008-02-29 | 2009-10-30 | Array Biopharma Inc | Compuestos inhibidores de raf y metodos para su uso |
| ES2392482T3 (es) * | 2008-02-29 | 2012-12-11 | Array Biopharma, Inc. | Derivados de imidazo[4,5-b] piridina usados como inhibidores de RAF |
| JP2011513331A (ja) * | 2008-02-29 | 2011-04-28 | アレイ バイオファーマ、インコーポレイテッド | ピラゾール[3,4−b]ピリジンRAF阻害剤 |
| EP2515655B1 (en) | 2009-12-21 | 2015-08-05 | Samumed, LLC | 1h-pyrazolo[3,4-beta]pyridines and therapeutic uses thereof |
| NZ604708A (en) | 2010-05-20 | 2015-05-29 | Array Biopharma Inc | Macrocyclic compounds as trk kinase inhibitors |
| US8754114B2 (en) | 2010-12-22 | 2014-06-17 | Incyte Corporation | Substituted imidazopyridazines and benzimidazoles as inhibitors of FGFR3 |
| EP3473099A1 (en) | 2011-09-14 | 2019-04-24 | Samumed, LLC | Indazole-3-carboxamides and their use as wnt/b-catenin signaling pathway inhibitors |
| CA2862163A1 (en) * | 2012-01-25 | 2013-08-01 | Bayer Pharma Aktiengesellschaft | Substituted phenylimidazopyrazoles and use thereof |
| PH12017500997A1 (en) | 2012-04-04 | 2018-02-19 | Samumed Llc | Indazole inhibitors of the wnt signal pathway and therapeutic uses thereof |
| US8889730B2 (en) * | 2012-04-10 | 2014-11-18 | Pfizer Inc. | Indole and indazole compounds that activate AMPK |
| EP2770994B1 (en) | 2012-05-04 | 2019-08-21 | Samumed, LLC | 1h-pyrazolo[3,4-b]pyridines and therapeutic uses thereof |
| ES2704744T3 (es) | 2012-06-13 | 2019-03-19 | Incyte Holdings Corp | Compuestos tricíclicos sustituidos como inhibidores de FGFR |
| US9388185B2 (en) | 2012-08-10 | 2016-07-12 | Incyte Holdings Corporation | Substituted pyrrolo[2,3-b]pyrazines as FGFR inhibitors |
| US9266892B2 (en) | 2012-12-19 | 2016-02-23 | Incyte Holdings Corporation | Fused pyrazoles as FGFR inhibitors |
| WO2014110086A2 (en) | 2013-01-08 | 2014-07-17 | Samumed, Llc | 3-(benzoimidazol-2-yl)-indazole inhibitors of the wnt signaling pathway and therapeutic uses thereof |
| JP6064062B2 (ja) * | 2013-03-15 | 2017-01-18 | ファイザー・インク | Ampkを活性化させるインダゾール化合物 |
| WO2014172639A1 (en) * | 2013-04-19 | 2014-10-23 | Ruga Corporation | Raf kinase inhibitors |
| EA035095B1 (ru) | 2013-04-19 | 2020-04-27 | Инсайт Холдингс Корпорейшн | Бициклические гетероциклы в качестве ингибиторов fgfr |
| US10017823B2 (en) * | 2013-04-25 | 2018-07-10 | Cbs Bioscience, Co., Ltd | Analytical method for increasing susceptibility of molecular targeted therapy in hepatocellular carcinoma |
| CN103739550B (zh) * | 2014-01-02 | 2016-06-01 | 中国药科大学 | 2,3-二甲基-6-脲-2h-吲唑类化合物及其制备方法与应用 |
| WO2016040184A1 (en) | 2014-09-08 | 2016-03-17 | Samumed, Llc | 3-(3h-imidazo[4,5-b]pyridin-2-yl)-1h-pyrazolo[3,4-c]pyridine and therapeutic uses thereof |
| WO2016040180A1 (en) | 2014-09-08 | 2016-03-17 | Samumed, Llc | 3-(1h-benzo[d]imidazol-2-yl)-1h-pyrazolo[3,4-c]pyridine and therapeutic uses thereof |
| WO2016040185A1 (en) | 2014-09-08 | 2016-03-17 | Samumed, Llc | 2-(1h-indazol-3-yl)-3h-imidazo[4,5-b]pyridine and therapeutic uses thereof |
| WO2016040190A1 (en) | 2014-09-08 | 2016-03-17 | Samumed, Llc | 3-(3h-imidazo[4,5-b]pyridin-2-yl)-1h-pyrazolo[3,4-b]pyridine and therapeutic uses thereof |
| WO2016040181A1 (en) | 2014-09-08 | 2016-03-17 | Samumed, Llc | 3-(1h-imidazo[4,5-c]pyridin-2-yl)-1h-pyrazolo[3,4-c]pyridine and therapeutic uses thereof |
| WO2016040188A1 (en) | 2014-09-08 | 2016-03-17 | Samumed, Llc | 3-(3h-imidazo[4,5-c]pyridin-2-yl)-1h-pyrazolo[3,4-c]pyridine and therapeutic uses thereof |
| WO2016040182A1 (en) | 2014-09-08 | 2016-03-17 | Samumed, Llc | 2-(1h-indazol-3-yl)-1h-imidazo[4,5-c]pyridine and therapeutic uses thereof |
| WO2016040193A1 (en) | 2014-09-08 | 2016-03-17 | Samumed, Llc | 3-(1h-imidazo[4,5-c]pyridin-2-yl)-1h-pyrazolo[3,4-b]pyridine and therapeutic uses thereof |
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| US10336707B2 (en) | 2014-12-16 | 2019-07-02 | Eudendron S.R.L. | Heterocyclic derivatives modulating activity of certain protein kinases |
| MX373169B (es) | 2015-02-20 | 2020-04-24 | Incyte Holdings Corp | Heterociclos bicíclicos como inhibidores de receptores del factor de crecimiento fibroblástico (fgfr). |
| WO2016134294A1 (en) | 2015-02-20 | 2016-08-25 | Incyte Corporation | Bicyclic heterocycles as fgfr4 inhibitors |
| MA41551A (fr) | 2015-02-20 | 2017-12-26 | Incyte Corp | Hétérocycles bicycliques utilisés en tant qu'inhibiteurs de fgfr4 |
| BR112018000808A2 (pt) | 2015-07-16 | 2018-09-04 | Array Biopharma Inc | compostos de pirazolo[1,5-a]piridina substituída como inibidores de ret cinase |
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| FR2871158A1 (fr) | 2004-06-04 | 2005-12-09 | Aventis Pharma Sa | Indazoles substitues, compositions les contenant, procede de fabrication et utilisation |
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Cited By (1)
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| WO2013100672A1 (ko) * | 2011-12-29 | 2013-07-04 | 제이더블유중외제약㈜ | 단백질 키나아제 저해활성을 가지는 3,6-이치환된 인다졸 유도체 |
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| CN102239150A (zh) | 2011-11-09 |
| JP5537561B2 (ja) | 2014-07-02 |
| JP2012510989A (ja) | 2012-05-17 |
| US8754209B2 (en) | 2014-06-17 |
| WO2010064875A3 (en) | 2010-09-10 |
| WO2010064875A2 (en) | 2010-06-10 |
| KR20100064520A (ko) | 2010-06-15 |
| US20120130069A1 (en) | 2012-05-24 |
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