JP2006519846A - 複素環式キナーゼインヒビター:使用および合成の方法 - Google Patents
複素環式キナーゼインヒビター:使用および合成の方法 Download PDFInfo
- Publication number
- JP2006519846A JP2006519846A JP2006507031A JP2006507031A JP2006519846A JP 2006519846 A JP2006519846 A JP 2006519846A JP 2006507031 A JP2006507031 A JP 2006507031A JP 2006507031 A JP2006507031 A JP 2006507031A JP 2006519846 A JP2006519846 A JP 2006519846A
- Authority
- JP
- Japan
- Prior art keywords
- alkyl
- independently
- heterocyclyl
- heteroaryl
- halo
- 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
Links
- 0 *c(cc1*)cc(C(*)=C2)c1NC2Cl Chemical compound *c(cc1*)cc(C(*)=C2)c1NC2Cl 0.000 description 5
- JSMRMEYFZHIPJV-UHFFFAOYSA-N C1C2CCC1C2 Chemical compound C1C2CCC1C2 JSMRMEYFZHIPJV-UHFFFAOYSA-N 0.000 description 1
- XNGGOZMQVSCJTK-UHFFFAOYSA-N CC(C)C(C1)NCCN1c1ccc(C)cn1 Chemical compound CC(C)C(C1)NCCN1c1ccc(C)cn1 XNGGOZMQVSCJTK-UHFFFAOYSA-N 0.000 description 1
- PMLNNFPSPHSEIY-UHFFFAOYSA-N CC(C)C(C1)NCCN1c1nccc(C)c1 Chemical compound CC(C)C(C1)NCCN1c1nccc(C)c1 PMLNNFPSPHSEIY-UHFFFAOYSA-N 0.000 description 1
- IJVBPPXPSQZWCL-UHFFFAOYSA-N CC(C1)C=CC=C1C(CCN(C)C1)C1O Chemical compound CC(C1)C=CC=C1C(CCN(C)C1)C1O IJVBPPXPSQZWCL-UHFFFAOYSA-N 0.000 description 1
- QZLNNYLAJWKONP-UHFFFAOYSA-N CC(C1)NCCN1c1ccc(C)cn1 Chemical compound CC(C1)NCCN1c1ccc(C)cn1 QZLNNYLAJWKONP-UHFFFAOYSA-N 0.000 description 1
- XDOKYYDCEMWKRK-UHFFFAOYSA-N CC(C1)NCCN1c1nccc(C)c1 Chemical compound CC(C1)NCCN1c1nccc(C)c1 XDOKYYDCEMWKRK-UHFFFAOYSA-N 0.000 description 1
- IXNSBMOYARYVOK-UMEJXRAUSA-N CC/C=C\C=C(/C)\C1CCNCC1 Chemical compound CC/C=C\C=C(/C)\C1CCNCC1 IXNSBMOYARYVOK-UMEJXRAUSA-N 0.000 description 1
- DKDAWOLEAYIHDA-ONVRAGQBSA-N CC/C=C\C=C(/CC)\N1CCN(C)CC1 Chemical compound CC/C=C\C=C(/CC)\N1CCN(C)CC1 DKDAWOLEAYIHDA-ONVRAGQBSA-N 0.000 description 1
- DMJQVHYYBCILSQ-UHFFFAOYSA-N CCC(C1)NCCN1c1ccc(CC)cn1 Chemical compound CCC(C1)NCCN1c1ccc(CC)cn1 DMJQVHYYBCILSQ-UHFFFAOYSA-N 0.000 description 1
- HAULHQCTDBENHS-UHFFFAOYSA-N CCCNCCN(CC)c1cc(C)ccn1 Chemical compound CCCNCCN(CC)c1cc(C)ccn1 HAULHQCTDBENHS-UHFFFAOYSA-N 0.000 description 1
- ZOBKIUOQZMGNKB-UHFFFAOYSA-N Cc1cc(C2CCN(C)CC2)ccc1 Chemical compound Cc1cc(C2CCN(C)CC2)ccc1 ZOBKIUOQZMGNKB-UHFFFAOYSA-N 0.000 description 1
- AATIJVIDRPDSLK-UHFFFAOYSA-N Cc1cc(C2CCNCC2)ncc1 Chemical compound Cc1cc(C2CCNCC2)ncc1 AATIJVIDRPDSLK-UHFFFAOYSA-N 0.000 description 1
- ZVDSNSHPCVKFOJ-UHFFFAOYSA-N Cc1cc(N2CCN(C)CC2)ncc1 Chemical compound Cc1cc(N2CCN(C)CC2)ncc1 ZVDSNSHPCVKFOJ-UHFFFAOYSA-N 0.000 description 1
- ZFBRKSGGMODDHD-UHFFFAOYSA-N Cc1cc(N2CCNCC2)ncc1 Chemical compound Cc1cc(N2CCNCC2)ncc1 ZFBRKSGGMODDHD-UHFFFAOYSA-N 0.000 description 1
- UYULZXPEIOSEAP-UHFFFAOYSA-N Cc1ccc(C(CCN(C)C2)C2O)cc1 Chemical compound Cc1ccc(C(CCN(C)C2)C2O)cc1 UYULZXPEIOSEAP-UHFFFAOYSA-N 0.000 description 1
- LVSCTTDQRVNYDZ-UHFFFAOYSA-N Cc1ccc(C2CCNCC2)nc1 Chemical compound Cc1ccc(C2CCNCC2)nc1 LVSCTTDQRVNYDZ-UHFFFAOYSA-N 0.000 description 1
- CATAGJZATFZGMJ-UHFFFAOYSA-N Cc1ccc(N2CCN(C)CC2)nc1 Chemical compound Cc1ccc(N2CCN(C)CC2)nc1 CATAGJZATFZGMJ-UHFFFAOYSA-N 0.000 description 1
- QDRKPHJFMGUXPN-UHFFFAOYSA-N Cc1ccc(N2CCNCC2)nc1 Chemical compound Cc1ccc(N2CCNCC2)nc1 QDRKPHJFMGUXPN-UHFFFAOYSA-N 0.000 description 1
- JIWHIRLNKIUYSM-UHFFFAOYSA-N Cc1cccc(N2CCNCC2)c1 Chemical compound Cc1cccc(N2CCNCC2)c1 JIWHIRLNKIUYSM-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- 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
- C07D401/06—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 carbon chain containing only aliphatic carbon atoms
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
-
- 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P19/00—Drugs for skeletal disorders
- A61P19/02—Drugs for skeletal disorders for joint disorders, e.g. arthritis, arthrosis
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/02—Immunomodulators
-
- 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
- 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
- C07D405/14—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 three or more hetero rings
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- 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)
- Immunology (AREA)
- Rheumatology (AREA)
- Pain & Pain Management (AREA)
- Dermatology (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Physical Education & Sports Medicine (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
Applications Claiming Priority (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US45345703P | 2003-03-10 | 2003-03-10 | |
| US46091003P | 2003-04-07 | 2003-04-07 | |
| US46302503P | 2003-04-15 | 2003-04-15 | |
| US50271003P | 2003-09-12 | 2003-09-12 | |
| PCT/US2004/007286 WO2004080463A1 (en) | 2003-03-10 | 2004-03-10 | Heterocyclic kinase inhibitors: methods of use and synthesis |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2006519846A true JP2006519846A (ja) | 2006-08-31 |
| JP2006519846A5 JP2006519846A5 (enExample) | 2008-02-21 |
Family
ID=32996376
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2006507031A Pending JP2006519846A (ja) | 2003-03-10 | 2004-03-10 | 複素環式キナーゼインヒビター:使用および合成の方法 |
Country Status (5)
| Country | Link |
|---|---|
| EP (1) | EP1601357A4 (enExample) |
| JP (1) | JP2006519846A (enExample) |
| CA (1) | CA2518398A1 (enExample) |
| MX (1) | MXPA05009722A (enExample) |
| WO (1) | WO2004080463A1 (enExample) |
Cited By (16)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2010528027A (ja) * | 2007-05-18 | 2010-08-19 | グラクソスミスクライン・リミテッド・ライアビリティ・カンパニー | Pi3キナーゼ阻害物質としてのキノリン誘導体 |
| JP2010536872A (ja) * | 2007-08-22 | 2010-12-02 | アラーガン、インコーポレイテッド | 治療用キノリンおよびナフタレン誘導体 |
| JP2010540483A (ja) * | 2007-09-27 | 2010-12-24 | エフ.ホフマン−ラ ロシュ アーゲー | 5−ht5a受容体アンタゴニストとしてのキノリン誘導体 |
| JP2011513350A (ja) * | 2008-03-05 | 2011-04-28 | エフ.ホフマン−ラ ロシュ アーゲー | 2−アミノキノリン類 |
| JP2013514358A (ja) * | 2009-12-17 | 2013-04-25 | メルク・シャープ・エンド・ドーム・コーポレイション | キノリンアミド化合物m1受容体陽性アロステリックモデュレータ |
| JP2013536211A (ja) * | 2010-08-27 | 2013-09-19 | グリュネンタール・ゲゼルシャフト・ミト・ベシュレンクテル・ハフツング | Kcnq2/3調節因子としての置換2−アミノ−キノリン−3−カルボキサミド |
| JP2017538673A (ja) * | 2014-10-31 | 2017-12-28 | ジェノシアンス ファルマ | 新規抗癌剤としての置換2,4ジアミノキノリン |
| JP2019514951A (ja) * | 2016-05-04 | 2019-06-06 | ジェノシアンス ファルマ | 増殖性疾患の治療に使用される置換2,4−ジアミノ−キノリン誘導体 |
| JP2020045342A (ja) * | 2009-06-12 | 2020-03-26 | アビバックス | Aidsを治療する為に有用な化合物 |
| JP2020523328A (ja) * | 2017-06-14 | 2020-08-06 | チア タイ ティエンチン ファーマシューティカル グループ カンパニー リミテッドChia Tai Tianqing Pharmaceutical Group Co., Ltd. | Syk阻害薬及びその使用方法 |
| US10975063B2 (en) | 2009-06-12 | 2021-04-13 | Abivax | Compound, and production method thereof, and methods of treatment using the compound |
| JP2021535179A (ja) * | 2018-09-05 | 2021-12-16 | ジェノシアンス ファルマ | 線維症、オートファジー、並びにカテプシンb(ctsb)、l(ctsl)及びd(ctsd)関連疾患のための新しい薬剤としての置換2,4ジアミノキノリン |
| JP2022513844A (ja) * | 2018-12-14 | 2022-02-09 | チア タイ ティエンチン ファーマシューティカル グループ カンパニー リミテッド | Syk阻害剤の塩及びその結晶形 |
| US11441181B2 (en) | 2013-01-17 | 2022-09-13 | Abivax | miRNA-124 as a biomarker |
| US11649211B2 (en) | 2014-07-17 | 2023-05-16 | Abivax | Use of quinoline derivatives for the treatment of inflammatory diseases |
| US11992499B2 (en) | 2018-12-20 | 2024-05-28 | Abivax | Quinoline derivatives for use in the treatment of inflammation diseases |
Families Citing this family (59)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| TWI328009B (en) | 2003-05-21 | 2010-08-01 | Glaxo Group Ltd | Quinoline derivatives as phosphodiesterase inhibitors |
| MY179032A (en) | 2004-10-25 | 2020-10-26 | Cancer Research Tech Ltd | Ortho-condensed pyridine and pyrimidine derivatives (e.g.purines) as protein kinase inhibitors |
| KR20080000665A (ko) | 2005-04-22 | 2008-01-02 | 알란토스 파마슈티컬즈 홀딩, 인코포레이티드 | 디펩티딜 펩티다아제-ⅳ 억제제 |
| JP4976394B2 (ja) * | 2005-08-17 | 2012-07-18 | シェーリング コーポレイション | 新規な高親和性のキノリンベースのキナーゼリガンド |
| EP3719018B1 (en) | 2006-04-25 | 2025-08-27 | Astex Therapeutics Ltd | Purine and deazapurine derivatives as pharmaceutical compounds |
| US7511063B2 (en) * | 2006-08-16 | 2009-03-31 | Schering Corporation | High affinity quinoline-based kinase ligands |
| WO2008059370A2 (en) | 2006-11-17 | 2008-05-22 | Pfizer Japan Inc. | Substituted bicyclocarboxyamide compounds |
| DE602007008469D1 (de) | 2006-12-07 | 2010-09-23 | Hoffmann La Roche | 2-aminochinoline als 5-ht(5a)-rezeptorantagonisten |
| JP5671236B2 (ja) | 2007-03-14 | 2015-02-18 | ランバクシー ラボラトリーズ リミテッド | ホスホジエステラーゼ阻害剤としてのピラゾロ(3,4−b)ピリジン誘導体 |
| WO2008150364A1 (en) * | 2007-05-23 | 2008-12-11 | Merck & Co., Inc. | Cyclopropyl pyrrolidine orexin receptor antagonists |
| NZ585261A (en) | 2007-10-11 | 2011-10-28 | Astrazeneca Ab | Pyrrolo [2, 3 -d] pyrimidin derivatives as protein kinase b inhibitors |
| WO2009051112A1 (ja) | 2007-10-15 | 2009-04-23 | Takeda Pharmaceutical Company Limited | アミド化合物およびその用途 |
| EP2215089B1 (en) | 2007-11-02 | 2012-06-27 | Vertex Pharmaceuticals Incorporated | [1h- pyrazolo [3, 4-b]pyridine-4-yl]-phenyle or -pyridin-2-yle derivatives as protein kinase c-theta |
| WO2009095752A1 (en) * | 2008-01-29 | 2009-08-06 | Glenmark Pharmaceuticals, S.A. | Fused pyrazole derivatives as cannabinoid receptor modulators |
| BRPI0909824A2 (pt) * | 2008-03-07 | 2019-03-06 | F. Hoffmann-La Roche Ag | 2-aminoquinolinas |
| AU2009221389A1 (en) * | 2008-03-07 | 2009-09-11 | F. Hoffmann-La Roche Ag | 2-Aminoquinoline derivatives |
| WO2009112395A1 (en) | 2008-03-12 | 2009-09-17 | F. Hoffmann-La Roche Ag | 2-aminoquinolines as 5-ht5a receptor antagonists |
| GB0812969D0 (en) | 2008-07-15 | 2008-08-20 | Sentinel Oncology Ltd | Pharmaceutical compounds |
| PL2401267T3 (pl) | 2009-02-27 | 2014-06-30 | Ambit Biosciences Corp | Pochodne chinazoliny modulujące kinazę JAK i ich zastosowanie w metodach |
| WO2010101949A1 (en) * | 2009-03-02 | 2010-09-10 | Sirtris Pharmaceuticals, Inc. | 8-substituted quinolines and related analogs as sirtuin modulators |
| BR112012018865A2 (pt) | 2010-01-29 | 2016-04-12 | Boehringer Ingelheim Int | naftiridinas substituídas e seu uso como inibidores de quinase syk |
| US8815902B2 (en) | 2010-06-15 | 2014-08-26 | Merck Sharp & Dohme Corp. | Tetrahydroquinoline amide M1 receptor positive allosteric modulators |
| CN103298805A (zh) | 2010-09-01 | 2013-09-11 | 埃姆比特生物科学公司 | 喹唑啉化合物及其使用方法 |
| EP2489663A1 (en) | 2011-02-16 | 2012-08-22 | Almirall, S.A. | Compounds as syk kinase inhibitors |
| WO2012122370A2 (en) | 2011-03-08 | 2012-09-13 | Eutropics Pharmaceuticals, Inc. | Compositions and methods useful for treating diseases |
| ME03589B (me) | 2011-04-01 | 2020-07-20 | Astrazeneca Ab | Terapeutski tretman |
| MX2013013090A (es) | 2011-05-10 | 2013-12-16 | Merck Sharp & Dohme | Aminopirimidinas como inhibidores de tirosina cinaza del bazo. |
| JP2014513687A (ja) | 2011-05-10 | 2014-06-05 | メルク・シャープ・アンド・ドーム・コーポレーション | Syk阻害薬としてのピリジルアミノピリジン |
| EP2706852B1 (en) | 2011-05-10 | 2018-08-22 | Merck Sharp & Dohme Corp. | Bipyridylaminopyridines as syk inhibitors |
| JP5860960B2 (ja) | 2011-07-26 | 2016-02-16 | 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 | 置換キノリン類及び医薬としてのそれらの使用 |
| EP2763976B1 (en) | 2011-10-05 | 2016-05-18 | Merck Sharp & Dohme Corp. | 2-pyridyl carboxamide-containing spleen tyrosine kinase (syk) inhibitors |
| EP2763974B1 (en) | 2011-10-05 | 2016-09-14 | Merck Sharp & Dohme Corp. | Phenyl carboxamide-containing spleen tyrosine kinase (syk) inhibitors |
| WO2013052393A1 (en) | 2011-10-05 | 2013-04-11 | Merck Sharp & Dohme Corp. | 3-PYRIDYL CARBOXAMIDE-CONTAINING SPLEEN TYROSINE KINASE (Syk) INHIBITORS |
| PT2785349T (pt) | 2011-11-30 | 2019-12-11 | Astrazeneca Ab | Tratamento combinado de cancro |
| AU2013204533B2 (en) | 2012-04-17 | 2017-02-02 | Astrazeneca Ab | Crystalline forms |
| WO2013192128A1 (en) | 2012-06-20 | 2013-12-27 | Merck Sharp & Dohme Corp. | Imidazolyl analogs as syk inhibitors |
| WO2013192423A2 (en) | 2012-06-20 | 2013-12-27 | Eutropics Pharmaceuticals, Inc. | Methods and compositions useful for treating diseases involving bcl-2 family proteins with quinoline derivatives |
| WO2013192125A1 (en) | 2012-06-20 | 2013-12-27 | Merck Sharp & Dohme Corp. | Pyrazolyl derivatives as syk inhibitors |
| EP2863916B1 (en) | 2012-06-22 | 2018-07-18 | Merck Sharp & Dohme Corp. | Substituted pyridine spleen tyrosine kinase (syk) inhibitors |
| US9416111B2 (en) | 2012-06-22 | 2016-08-16 | Merck Sharp & Dohme Corp. | Substituted diazine and triazine spleen tyrosine kinease (Syk) inhibitors |
| WO2014031438A2 (en) | 2012-08-20 | 2014-02-27 | Merck Sharp & Dohme Corp. | SUBSTITUTED PHENYL SPLEEN TYROSINE KINASE (Syk) INHIBITORS |
| EP2900665B1 (en) | 2012-09-28 | 2018-01-03 | Merck Sharp & Dohme Corp. | Triazolyl derivatives as syk inhibitors |
| EP2922544B1 (en) | 2012-11-21 | 2018-08-01 | Eutropics Pharmaceuticals, Inc. | Methods and compositions useful for treating diseases involving bcl-2 family proteins with quinoline derivatives |
| US10732182B2 (en) | 2013-08-01 | 2020-08-04 | Eutropics Pharmaceuticals, Inc. | Method for predicting cancer sensitivity |
| EP3063302B1 (en) | 2013-10-30 | 2019-12-04 | Eutropics Pharmaceuticals, Inc. | Methods for determining chemosensitivity and chemotoxicity |
| EP3083559B1 (en) | 2013-12-20 | 2021-03-10 | Merck Sharp & Dohme Corp. | Thiazole-substituted aminoheteroaryls as spleen tyrosine kinase inhibitors |
| US9783531B2 (en) | 2013-12-20 | 2017-10-10 | Merck Sharp & Dohme Corp. | Thiazole-substituted aminoheteroaryls as spleen tyrosine kinase inhibitors |
| EP3083560B1 (en) | 2013-12-20 | 2021-10-27 | Merck Sharp & Dohme Corp. | Thiazole-substituted aminoheteroaryls as spleen tyrosine kinase inhibitors |
| EP3116506B1 (en) | 2014-03-13 | 2019-04-17 | Merck Sharp & Dohme Corp. | 2-pyrazine carboxamides as spleen tyrosine kinase inhibitors |
| WO2019023278A1 (en) * | 2017-07-25 | 2019-01-31 | Crinetics Pharmaceuticals, Inc. | MODULATORS OF SOMATOSTATIN AND USES THEREOF |
| US11691971B2 (en) | 2020-06-19 | 2023-07-04 | Incyte Corporation | Naphthyridinone compounds as JAK2 V617F inhibitors |
| US11753413B2 (en) | 2020-06-19 | 2023-09-12 | Incyte Corporation | Substituted pyrrolo[2,1-f][1,2,4]triazine compounds as JAK2 V617F inhibitors |
| US11767323B2 (en) | 2020-07-02 | 2023-09-26 | Incyte Corporation | Tricyclic pyridone compounds as JAK2 V617F inhibitors |
| SI4175719T1 (sl) | 2020-07-02 | 2025-07-31 | Incyte Corporation | Triciklične sečninske spojine kot zaviralci jak2 v617f |
| US11661422B2 (en) | 2020-08-27 | 2023-05-30 | Incyte Corporation | Tricyclic urea compounds as JAK2 V617F inhibitors |
| WO2022140231A1 (en) | 2020-12-21 | 2022-06-30 | Incyte Corporation | Deazaguaine compounds as jak2 v617f inhibitors |
| US11958861B2 (en) | 2021-02-25 | 2024-04-16 | Incyte Corporation | Spirocyclic lactams as JAK2 V617F inhibitors |
| JP2024543981A (ja) * | 2021-12-01 | 2024-11-26 | アンスティチュ ナショナル ドゥ ラ サンテ エ ドゥ ラ ルシェルシュ メディカル | 炎症性疾患の処置に使用するためのirapアミノペプチダーゼ阻害剤の使用 |
| US12084430B2 (en) | 2022-03-17 | 2024-09-10 | Incyte Corporation | Tricyclic urea compounds as JAK2 V617F inhibitors |
Citations (16)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE537104C (de) * | 1926-05-04 | 1933-03-17 | Chem Ind Basel | Verfahren zur Darstellung von substituierten Chinolincarbonsaeureamiden |
| US2472066A (en) * | 1949-06-07 | Z-arylamino-x-halogenoqtjinolines | ||
| DE858698C (de) * | 1951-02-09 | 1952-12-08 | Basf Ag | Verfahren zur Herstellung von Pyridin- und Chinolinderivaten |
| GB811957A (en) * | 1956-03-01 | 1959-04-15 | Geigy Ag J R | Improvements relating to 2-hydroxy-4-arylamino-quinolines |
| US3479360A (en) * | 1967-02-22 | 1969-11-18 | Roussel Uclaf | 2-methyl or phenyl-7- or 8-chloroquinolines |
| US3755332A (en) * | 1971-07-01 | 1973-08-28 | Ciba Geigy Corp | Substituted 4 indazolaminoquinolines |
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| GB9622363D0 (en) * | 1996-10-28 | 1997-01-08 | Celltech Therapeutics Ltd | Chemical compounds |
| US6197788B1 (en) * | 1997-11-26 | 2001-03-06 | Vernalis Research Limited | (−)-mefloquine to block puringergic receptors and to treat movement or neurodegenerative disorders |
| GB0206215D0 (en) * | 2002-03-15 | 2002-05-01 | Novartis Ag | Organic compounds |
| MXPA05000081A (es) * | 2002-06-27 | 2005-04-11 | Schering Ag | Quinolinas sustituidas antagonistas del receptor ccr5. |
| EP1631810A4 (en) * | 2003-03-10 | 2008-11-05 | Schering Corp | Ligand ANALYSIS |
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- 2004-03-10 WO PCT/US2004/007286 patent/WO2004080463A1/en not_active Ceased
- 2004-03-10 EP EP04719237A patent/EP1601357A4/en not_active Withdrawn
- 2004-03-10 CA CA002518398A patent/CA2518398A1/en not_active Abandoned
- 2004-03-10 JP JP2006507031A patent/JP2006519846A/ja active Pending
- 2004-03-10 MX MXPA05009722A patent/MXPA05009722A/es not_active Application Discontinuation
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| GB811957A (en) * | 1956-03-01 | 1959-04-15 | Geigy Ag J R | Improvements relating to 2-hydroxy-4-arylamino-quinolines |
| US3479360A (en) * | 1967-02-22 | 1969-11-18 | Roussel Uclaf | 2-methyl or phenyl-7- or 8-chloroquinolines |
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| WO2000076982A1 (en) * | 1999-06-16 | 2000-12-21 | University Of Iowa Research Foundation | Antagonism of immunostimulatory cpg-oligonucleotides by 4-aminoquinolines and other weak bases |
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| JP2010528027A (ja) * | 2007-05-18 | 2010-08-19 | グラクソスミスクライン・リミテッド・ライアビリティ・カンパニー | Pi3キナーゼ阻害物質としてのキノリン誘導体 |
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Also Published As
| Publication number | Publication date |
|---|---|
| WO2004080463A1 (en) | 2004-09-23 |
| CA2518398A1 (en) | 2004-09-23 |
| MXPA05009722A (es) | 2006-03-09 |
| EP1601357A4 (en) | 2007-10-03 |
| EP1601357A1 (en) | 2005-12-07 |
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