JP2013529196A - キナーゼlrrk2の阻害剤としてのピラゾロピリジン - Google Patents
キナーゼlrrk2の阻害剤としてのピラゾロピリジン Download PDFInfo
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- JP2013529196A JP2013529196A JP2013509631A JP2013509631A JP2013529196A JP 2013529196 A JP2013529196 A JP 2013529196A JP 2013509631 A JP2013509631 A JP 2013509631A JP 2013509631 A JP2013509631 A JP 2013509631A JP 2013529196 A JP2013529196 A JP 2013529196A
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- Prior art keywords
- alkyl
- heterocycloalkyl
- aryl
- heteroaryl
- compound
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- 108010020246 Leucine-Rich Repeat Serine-Threonine Protein Kinase-2 Proteins 0.000 title claims description 65
- 102000009784 Leucine-Rich Repeat Serine-Threonine Protein Kinase-2 Human genes 0.000 title claims description 5
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- 125000001072 heteroaryl group Chemical group 0.000 claims abstract description 103
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- -1 substituted Chemical class 0.000 claims abstract description 63
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- 125000004076 pyridyl group Chemical group 0.000 claims description 15
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Classifications
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- 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
- C07D401/04—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 directly linked by a ring-member-to-ring-member bond
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- A61K31/4353—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems
- A61K31/437—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system containing a five-membered ring having nitrogen as a ring hetero atom, e.g. indolizine, beta-carboline
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- 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
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| PCT/GB2011/050937 WO2011141756A1 (en) | 2010-05-14 | 2011-05-16 | Pyrazolopyridines as inhibitors of the kinase lrrk2 |
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|---|---|---|---|---|
| JP2016516791A (ja) * | 2013-04-18 | 2016-06-09 | ハー・ルンドベック・アクチエゼルスカベット | Lrrk2阻害剤としてのアリールピロロピリジン誘導化合物 |
| JP2016540794A (ja) * | 2013-12-17 | 2016-12-28 | ファイザー・インク | LRRK2阻害薬としての新規の3,4−二置換−1H−ピロロ[2,3−b]ピリジンおよび4,5−二置換−7H−ピロロ[2,3−c]ピリダジン |
| JP2018524390A (ja) * | 2015-07-23 | 2018-08-30 | グラクソスミスクライン、インテレクチュアル、プロパティー、ディベロップメント、リミテッドGlaxosmithkline Intellectual Property Development Limited | 化合物 |
| KR20190067795A (ko) * | 2016-09-09 | 2019-06-17 | 인사이트 코포레이션 | Hpk1 조절제로서의 피라졸로피리딘 유도체 및 암을 치료하기 위한 이의 용도 |
| JP2020519667A (ja) * | 2017-05-15 | 2020-07-02 | ザ・リージェンツ・オブ・ザ・ユニバーシティ・オブ・ミシガンThe Regents Of The University Of Michigan | LSD−1インヒビターとしてのピロロ〔2,3−c〕ピリジン及び関連類似体 |
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| WO2012088266A2 (en) | 2010-12-22 | 2012-06-28 | Incyte Corporation | Substituted imidazopyridazines and benzimidazoles as inhibitors of fgfr3 |
| US8791112B2 (en) | 2011-03-30 | 2014-07-29 | Arrien Pharmaceuticals Llc | Substituted 5-(pyrazin-2-yl)-1H-pyrazolo [3, 4-B] pyridine and pyrazolo [3, 4-B] pyridine derivatives as protein kinase inhibitors |
| GB201204985D0 (en) | 2012-03-21 | 2012-05-02 | Genentech Inc | Compounds |
| WO2013166276A1 (en) | 2012-05-02 | 2013-11-07 | Southern Research Institute | Triazolopyridazine compounds, use as inhibitors of the kinase lrrk2, and methods for preparation thereof |
| CN102675310B (zh) * | 2012-05-09 | 2014-12-24 | 林辉 | 制备吡唑并芳杂环化合物的方法 |
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| US9388185B2 (en) | 2012-08-10 | 2016-07-12 | Incyte Holdings Corporation | Substituted pyrrolo[2,3-b]pyrazines as FGFR inhibitors |
| ES2652514T3 (es) | 2012-11-08 | 2018-02-02 | Pfizer Inc. | Compuestos heteroaromáticos como ligandos de dopamina D1 |
| WO2017156493A1 (en) * | 2016-03-11 | 2017-09-14 | Denali Therapeutics Inc. | Compounds, compositions, and methods |
| US9266892B2 (en) | 2012-12-19 | 2016-02-23 | Incyte Holdings Corporation | Fused pyrazoles as FGFR inhibitors |
| WO2014134772A1 (en) | 2013-03-04 | 2014-09-12 | Merck Sharp & Dohme Corp. | Compounds inhibiting leucine-rich repeat kinase enzyme activity |
| WO2014134776A1 (en) | 2013-03-04 | 2014-09-12 | Merck Sharp & Dohme Corp. | Compounds inhibiting leucine-rich repeat kinase enzyme activity |
| US9440952B2 (en) | 2013-03-04 | 2016-09-13 | Merck Sharp & Dohme Corp. | Compounds inhibiting leucine-rich repeat kinase enzyme activity |
| WO2014134774A1 (en) | 2013-03-04 | 2014-09-12 | Merck Sharp & Dohme Corp. | Compounds inhibiting leucine-rich repeat kinase enzyme activity |
| EP2970333B1 (en) * | 2013-03-15 | 2017-05-03 | Ipsen Pharma S.A.S. | Macrocyclic lrrk2 kinase inhibitors |
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| CN103819396B (zh) * | 2014-02-26 | 2016-06-15 | 四川大学 | 一种手性的1-(3,5-二氯吡啶-4-基)-乙醇的合成方法 |
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| UA111579C2 (uk) * | 2009-08-17 | 2016-05-25 | Інтеллікіне Ллк | ГЕТЕРОЦИКЛІЧНІ ПОХІДНІ 2-АМІНОБЕНЗО[d]ОКСАЗОЛУ, ФАРМАЦЕВТИЧНА КОМПОЗИЦІЯ НА ЇХ ОСНОВІ ТА ЇХ ЗАСТОСУВАННЯ ДЛЯ ЛІКУВАННЯ ЗАХВОРЮВАННЯ, ПОВ'АНОГО З РІ3-КІНАЗОЮ |
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- 2011-05-16 EP EP11720847A patent/EP2569293A1/en not_active Withdrawn
- 2011-05-16 JP JP2013509631A patent/JP2013529196A/ja not_active Withdrawn
- 2011-05-16 US US13/697,878 patent/US20130267513A1/en not_active Abandoned
- 2011-05-16 CN CN201180033483XA patent/CN102971306A/zh active Pending
- 2011-05-16 CA CA2798222A patent/CA2798222A1/en not_active Abandoned
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| JP2016516791A (ja) * | 2013-04-18 | 2016-06-09 | ハー・ルンドベック・アクチエゼルスカベット | Lrrk2阻害剤としてのアリールピロロピリジン誘導化合物 |
| JP2016540794A (ja) * | 2013-12-17 | 2016-12-28 | ファイザー・インク | LRRK2阻害薬としての新規の3,4−二置換−1H−ピロロ[2,3−b]ピリジンおよび4,5−二置換−7H−ピロロ[2,3−c]ピリダジン |
| JP2018524390A (ja) * | 2015-07-23 | 2018-08-30 | グラクソスミスクライン、インテレクチュアル、プロパティー、ディベロップメント、リミテッドGlaxosmithkline Intellectual Property Development Limited | 化合物 |
| KR20190067795A (ko) * | 2016-09-09 | 2019-06-17 | 인사이트 코포레이션 | Hpk1 조절제로서의 피라졸로피리딘 유도체 및 암을 치료하기 위한 이의 용도 |
| JP2019530670A (ja) * | 2016-09-09 | 2019-10-24 | インサイト・コーポレイションIncyte Corporation | Hpk1調節薬としてのピラゾロピリジン誘導体及びがんの治療のためのその用法 |
| JP7076432B2 (ja) | 2016-09-09 | 2022-05-27 | インサイト・コーポレイション | Hpk1調節薬としてのピラゾロピリジン誘導体及びがんの治療のためのその用法 |
| KR102507967B1 (ko) | 2016-09-09 | 2023-03-09 | 인사이트 코포레이션 | Hpk1 조절제로서의 피라졸로피리딘 유도체 및 암을 치료하기 위한 이의 용도 |
| JP2020519667A (ja) * | 2017-05-15 | 2020-07-02 | ザ・リージェンツ・オブ・ザ・ユニバーシティ・オブ・ミシガンThe Regents Of The University Of Michigan | LSD−1インヒビターとしてのピロロ〔2,3−c〕ピリジン及び関連類似体 |
| JP7352284B2 (ja) | 2017-05-15 | 2023-09-28 | ザ・リージェンツ・オブ・ザ・ユニバーシティ・オブ・ミシガン | LSD-1インヒビターとしてのピロロ〔2,3-c〕ピリジン及び関連類似体 |
Also Published As
| Publication number | Publication date |
|---|---|
| AU2011251733A1 (en) | 2012-12-20 |
| US20130267513A1 (en) | 2013-10-10 |
| EP2569293A1 (en) | 2013-03-20 |
| GB201008134D0 (en) | 2010-06-30 |
| WO2011141756A1 (en) | 2011-11-17 |
| CA2798222A1 (en) | 2011-11-17 |
| CN102971306A (zh) | 2013-03-13 |
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