JP2010535804A - Pi3キナーゼ阻害薬としてのキノキサリン誘導体 - Google Patents
Pi3キナーゼ阻害薬としてのキノキサリン誘導体 Download PDFInfo
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- JP2010535804A JP2010535804A JP2010520295A JP2010520295A JP2010535804A JP 2010535804 A JP2010535804 A JP 2010535804A JP 2010520295 A JP2010520295 A JP 2010520295A JP 2010520295 A JP2010520295 A JP 2010520295A JP 2010535804 A JP2010535804 A JP 2010535804A
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- substituted
- cancer
- amino
- alkyl
- heterocycloalkyl
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- 0 CC(C)[*@](C*)(C=CC(C)N)C=N* Chemical compound CC(C)[*@](C*)(C=CC(C)N)C=N* 0.000 description 5
- YQPUONDOWMMGGF-UHFFFAOYSA-N Brc(cc1)cc2c1ncc(N1CCOCC1)n2 Chemical compound Brc(cc1)cc2c1ncc(N1CCOCC1)n2 YQPUONDOWMMGGF-UHFFFAOYSA-N 0.000 description 1
- DLCATYORGKSQMY-IPXBKODISA-N C/C=N\C/C(/C)=N\N Chemical compound C/C=N\C/C(/C)=N\N DLCATYORGKSQMY-IPXBKODISA-N 0.000 description 1
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- C—CHEMISTRY; METALLURGY
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- 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
- C07D405/04—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 directly linked by a ring-member-to-ring-member bond
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- C07D401/14—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 three or more hetero rings
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- 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
- C07D403/04—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 directly linked by a ring-member-to-ring-member bond
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- C07D403/14—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 three or more hetero rings
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- 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
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- 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
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- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—Ortho-condensed systems
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- C07D495/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms
- C07D495/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
- C07D495/04—Ortho-condensed systems
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- 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)
- Cardiology (AREA)
- Neurology (AREA)
- Biomedical Technology (AREA)
- Pulmonology (AREA)
- Neurosurgery (AREA)
- Heart & Thoracic Surgery (AREA)
- Oncology (AREA)
- Urology & Nephrology (AREA)
- Reproductive Health (AREA)
- Hospice & Palliative Care (AREA)
- Hematology (AREA)
- Dermatology (AREA)
- Rheumatology (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Pregnancy & Childbirth (AREA)
- Communicable Diseases (AREA)
- Psychiatry (AREA)
- Psychology (AREA)
- Vascular Medicine (AREA)
- Physical Education & Sports Medicine (AREA)
- Pain & Pain Management (AREA)
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- Diabetes (AREA)
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Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US95484507P | 2007-08-09 | 2007-08-09 | |
PCT/US2008/072401 WO2009021083A1 (en) | 2007-08-09 | 2008-08-07 | Quinoxaline derivatives as pi3 kinase inhibitors |
Publications (1)
Publication Number | Publication Date |
---|---|
JP2010535804A true JP2010535804A (ja) | 2010-11-25 |
Family
ID=40341726
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2010520295A Withdrawn JP2010535804A (ja) | 2007-08-09 | 2008-08-07 | Pi3キナーゼ阻害薬としてのキノキサリン誘導体 |
Country Status (3)
Country | Link |
---|---|
EP (1) | EP2173354A4 (de) |
JP (1) | JP2010535804A (de) |
WO (1) | WO2009021083A1 (de) |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2013543883A (ja) * | 2010-11-29 | 2013-12-09 | アステックス、セラピューティックス、リミテッド | 癌疾患の治療のためのfgfrキナーゼ阻害剤としての置換ベンゾピラジン誘導体 |
JP2015524843A (ja) * | 2012-08-13 | 2015-08-27 | エンヴォイ セラピューティクス インコーポレイテッド | Gpr6モジュレーターとしてのキノキサリン誘導体 |
JP2016536302A (ja) * | 2013-10-23 | 2016-11-24 | バイエル・クロップサイエンス・アクチェンゲゼルシャフト | 有害生物防除剤としての置換されているキノキサリン誘導体 |
JP2018535199A (ja) * | 2015-10-09 | 2018-11-29 | ヤンセン ファーマシューティカ エヌ.ベー. | PI3Kβ阻害剤としてのキノキサリンおよびピリドピラジン誘導体 |
JP2020512352A (ja) * | 2017-03-29 | 2020-04-23 | ヤンセン ファーマシューティカ エヌ.ベー. | PI3Kβ阻害剤としてのキノキサリン及びピリドピラジン誘導体 |
Families Citing this family (46)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB0908905D0 (en) | 2009-05-26 | 2009-07-01 | Sentinel Oncology Ltd | Pharmaceutical compounds |
JP5728683B2 (ja) * | 2009-09-04 | 2015-06-03 | バイエル・インテレクチュアル・プロパティ・ゲゼルシャフト・ミット・ベシュレンクテル・ハフツングBayer Intellectual Property GmbH | チロシンスレオニンキナーゼ阻害剤としての置換アミノキノキサリン |
GB201007286D0 (en) | 2010-04-30 | 2010-06-16 | Astex Therapeutics Ltd | New compounds |
WO2012088266A2 (en) | 2010-12-22 | 2012-06-28 | Incyte Corporation | Substituted imidazopyridazines and benzimidazoles as inhibitors of fgfr3 |
GB201118652D0 (en) | 2011-10-28 | 2011-12-07 | Astex Therapeutics Ltd | New compounds |
GB201118675D0 (en) | 2011-10-28 | 2011-12-14 | Astex Therapeutics Ltd | New compounds |
GB201118656D0 (en) | 2011-10-28 | 2011-12-07 | Astex Therapeutics Ltd | New compounds |
GB201118654D0 (en) | 2011-10-28 | 2011-12-07 | Astex Therapeutics Ltd | New compounds |
US9512126B2 (en) | 2012-03-14 | 2016-12-06 | Bayer Intellectual Property Gmbh | Substituted imidazopyridazines |
GB201209609D0 (en) | 2012-05-30 | 2012-07-11 | Astex Therapeutics Ltd | New compounds |
GB201209613D0 (en) | 2012-05-30 | 2012-07-11 | Astex Therapeutics Ltd | New compounds |
WO2014007951A2 (en) | 2012-06-13 | 2014-01-09 | Incyte Corporation | Substituted tricyclic compounds as fgfr inhibitors |
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 |
CN104995182A (zh) | 2013-02-07 | 2015-10-21 | 默克专利股份公司 | 被取代的喹喔啉衍生物及其作为mGluR4的正变构调节剂的用途 |
KR102469849B1 (ko) | 2013-04-19 | 2022-11-23 | 인사이트 홀딩스 코포레이션 | Fgfr 저해제로서 이환식 헤테로사이클 |
GB201307577D0 (en) | 2013-04-26 | 2013-06-12 | Astex Therapeutics Ltd | New compounds |
PE20160156A1 (es) | 2013-06-11 | 2016-04-20 | Bayer Pharma AG | Derivados de prodroga de triazolpiridinas sustituidas |
US10179783B2 (en) | 2014-02-14 | 2019-01-15 | Taketa Pharmaceutical Company Limited | Tetrahydropyridopyrazines as modulators of GPR6 |
JO3512B1 (ar) | 2014-03-26 | 2020-07-05 | Astex Therapeutics Ltd | مشتقات كينوكسالين مفيدة كمعدلات لإنزيم fgfr كيناز |
JP6752715B2 (ja) | 2014-03-26 | 2020-09-09 | アステックス、セラピューティックス、リミテッドAstex Therapeutics Limited | 組合せ |
CN106456648B (zh) | 2014-03-26 | 2021-11-02 | 阿斯特克斯治疗有限公司 | Fgfr抑制剂和igf1r抑制剂的组合 |
US10851105B2 (en) | 2014-10-22 | 2020-12-01 | Incyte Corporation | Bicyclic heterocycles as FGFR4 inhibitors |
JOP20200201A1 (ar) | 2015-02-10 | 2017-06-16 | Astex Therapeutics Ltd | تركيبات صيدلانية تشتمل على n-(3.5- ثنائي ميثوكسي فينيل)-n'-(1-ميثيل إيثيل)-n-[3-(ميثيل-1h-بيرازول-4-يل) كينوكسالين-6-يل]إيثان-1.2-ثنائي الأمين |
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 |
EA038045B1 (ru) | 2015-02-20 | 2021-06-28 | Инсайт Корпорейшн | Бициклические гетероциклы в качестве ингибиторов fgfr |
US10478494B2 (en) | 2015-04-03 | 2019-11-19 | Astex Therapeutics Ltd | FGFR/PD-1 combination therapy for the treatment of cancer |
WO2017019828A1 (en) * | 2015-07-30 | 2017-02-02 | Bristol-Myers Squibb Company | Aryl substituted bicyclic heteroaryl compounds |
RU2747644C2 (ru) | 2015-09-23 | 2021-05-11 | Янссен Фармацевтика Нв | Бигетероарил-замещенные 1,4-бензодиазепины и пути их применения для лечения рака |
EP3353177B1 (de) | 2015-09-23 | 2020-06-03 | Janssen Pharmaceutica NV | Trizyklische heterozyklen zur behandlung von krebs |
MX2018015709A (es) | 2016-06-16 | 2019-03-21 | Janssen Pharmaceutica Nv | Derivados de azabencimidazol como inhibidores de pi3k beta. |
EP3472160B1 (de) | 2016-06-16 | 2021-02-24 | Janssen Pharmaceutica NV | Bicyclische pyridin-, pyrazin- und pyrimidinderivate als pi3k-beta-hemmer |
AR111960A1 (es) | 2017-05-26 | 2019-09-04 | Incyte Corp | Formas cristalinas de un inhibidor de fgfr y procesos para su preparación |
MX2020011718A (es) | 2018-05-04 | 2021-02-15 | Incyte Corp | Formas solidas de un inhibidor de receptores del factor de crecimiento de fibroblastos (fgfr) y procesos para prepararlas. |
PE20210919A1 (es) | 2018-05-04 | 2021-05-19 | Incyte Corp | Sales de un inhibidor de fgfr |
WO2020185532A1 (en) | 2019-03-08 | 2020-09-17 | Incyte Corporation | Methods of treating cancer with an fgfr inhibitor |
WO2021007269A1 (en) | 2019-07-09 | 2021-01-14 | Incyte Corporation | Bicyclic heterocycles as fgfr inhibitors |
IL291901A (en) | 2019-10-14 | 2022-06-01 | Incyte Corp | Bicyclyl heterocycles as fgr suppressors |
US11566028B2 (en) | 2019-10-16 | 2023-01-31 | Incyte Corporation | Bicyclic heterocycles as FGFR inhibitors |
JP2023505257A (ja) | 2019-12-04 | 2023-02-08 | インサイト・コーポレイション | Fgfr阻害剤の誘導体 |
EP4069696A1 (de) | 2019-12-04 | 2022-10-12 | Incyte Corporation | Tricyclische heterocyclen als fgfr-inhibitoren |
CN112979613B (zh) * | 2019-12-16 | 2022-04-26 | 四川大学华西医院 | 2-(1h-吡唑-3-基)吡啶衍生物及其制备方法和用途 |
WO2021146424A1 (en) | 2020-01-15 | 2021-07-22 | Incyte Corporation | Bicyclic heterocycles as fgfr inhibitors |
JP2024522189A (ja) | 2021-06-09 | 2024-06-11 | インサイト・コーポレイション | Fgfr阻害剤としての三環式ヘテロ環 |
CN114605391B (zh) * | 2022-02-21 | 2024-01-26 | 广州六顺生物科技股份有限公司 | 喹喔啉类衍生物及其制备方法和应用 |
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US7148237B2 (en) * | 2001-03-01 | 2006-12-12 | Shionogi & Co., Ltd. | Nitrogen-containing heteroaryl compounds having HIV integrase inhibitory activity |
US20040102360A1 (en) * | 2002-10-30 | 2004-05-27 | Barnett Stanley F. | Combination therapy |
AU2003290734A1 (en) * | 2002-11-27 | 2004-06-23 | Eli Lilly And Company | Novel compounds as pharmaceutical agents |
CN103819416A (zh) * | 2005-10-07 | 2014-05-28 | 埃克塞里艾克西斯公司 | N-(3-氨基-喹喔啉-2-基)-磺酰胺衍生物及其作为磷脂酰肌醇3-激酶抑制剂的用途 |
CL2008001356A1 (es) * | 2007-05-10 | 2008-11-14 | Smithkline Beecham Corp | Compuestos derivados de quinoxalina, inhibidores de la pi3 quinasa _(p13ka, pi3ko, pi3b y/o pi3ky); composicion farmaceutica; uso para tratar un trastorno autoinmune, enfermedad inflamatoria, cardiovascular, neurodegerativa, alergia, asma, enfermedad renal, cancer, rechazo de transplante, lesiones pulmonares. |
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2008
- 2008-08-07 EP EP08797323A patent/EP2173354A4/de not_active Withdrawn
- 2008-08-07 WO PCT/US2008/072401 patent/WO2009021083A1/en active Application Filing
- 2008-08-07 JP JP2010520295A patent/JP2010535804A/ja not_active Withdrawn
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JP2013543883A (ja) * | 2010-11-29 | 2013-12-09 | アステックス、セラピューティックス、リミテッド | 癌疾患の治療のためのfgfrキナーゼ阻害剤としての置換ベンゾピラジン誘導体 |
JP2015524843A (ja) * | 2012-08-13 | 2015-08-27 | エンヴォイ セラピューティクス インコーポレイテッド | Gpr6モジュレーターとしてのキノキサリン誘導体 |
JP2018008999A (ja) * | 2012-08-13 | 2018-01-18 | 武田薬品工業株式会社 | Gpr6モジュレーターとしてのキノキサリン誘導体 |
JP2016536302A (ja) * | 2013-10-23 | 2016-11-24 | バイエル・クロップサイエンス・アクチェンゲゼルシャフト | 有害生物防除剤としての置換されているキノキサリン誘導体 |
JP2018535199A (ja) * | 2015-10-09 | 2018-11-29 | ヤンセン ファーマシューティカ エヌ.ベー. | PI3Kβ阻害剤としてのキノキサリンおよびピリドピラジン誘導体 |
JP2020512352A (ja) * | 2017-03-29 | 2020-04-23 | ヤンセン ファーマシューティカ エヌ.ベー. | PI3Kβ阻害剤としてのキノキサリン及びピリドピラジン誘導体 |
JP7053654B2 (ja) | 2017-03-29 | 2022-04-12 | ヤンセン ファーマシューティカ エヌ.ベー. | PI3Kβ阻害剤としてのキノキサリン及びピリドピラジン誘導体 |
Also Published As
Publication number | Publication date |
---|---|
EP2173354A1 (de) | 2010-04-14 |
WO2009021083A1 (en) | 2009-02-12 |
WO2009021083A8 (en) | 2009-04-09 |
EP2173354A4 (de) | 2011-10-05 |
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