CA2812258C - Method of inhibiting mutant c-kit - Google Patents
Method of inhibiting mutant c-kit Download PDFInfo
- Publication number
- CA2812258C CA2812258C CA2812258A CA2812258A CA2812258C CA 2812258 C CA2812258 C CA 2812258C CA 2812258 A CA2812258 A CA 2812258A CA 2812258 A CA2812258 A CA 2812258A CA 2812258 C CA2812258 C CA 2812258C
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- Prior art keywords
- crenolanib
- kit
- proliferative disease
- compound
- patient
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Classifications
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- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—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
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- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/4164—1,3-Diazoles
- A61K31/4184—1,3-Diazoles condensed with carbocyclic rings, e.g. benzimidazoles
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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
- A61K31/4375—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 six-membered ring having nitrogen as a ring heteroatom, e.g. quinolizines, naphthyridines, berberine, vincamine
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Landscapes
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- Bioinformatics & Cheminformatics (AREA)
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Applications Claiming Priority (2)
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| KR101738063B1 (ko) | 2012-09-21 | 2017-05-19 | 아로그 파마슈티칼스, 인코퍼레이티드 | 구조적으로 활성인 인산화된 ｆｌｔ３ 키나제의 억제 방법 |
| US11642340B2 (en) | 2012-09-26 | 2023-05-09 | Arog Pharmaceuticals, Inc. | Method of inhibiting mutant C-KIT |
| US10835525B2 (en) | 2012-09-26 | 2020-11-17 | Arog Pharmaceuticals, Inc. | Method of inhibiting mutant C-KIT |
| JP6042157B2 (ja) | 2012-09-26 | 2016-12-14 | アログ・ファーマシューティカルズ・リミテッド・ライアビリティ・カンパニーＡｒｏｇ Ｐｈａｒｍａｃｅｕｔｉｃａｌｓ，ＬＬＣ | 変異型ｃ−ｋｉｔの阻害方法 |
| BR112015016282A2 (en) | 2013-01-07 | 2017-07-11 | Arog Pharmaceuticals, Inc. | crenolanib for treatment of mutated flt3 proliferative disorders |
| MX381228B (es) | 2016-06-10 | 2025-03-12 | Vitae Pharmaceuticals Llc | Inhibidores de la interacción de menina-leucemia de linaje mixto. |
| WO2018014519A1 (zh) * | 2016-07-18 | 2018-01-25 | 北京雅康博生物科技有限公司 | 用于检测c-kit基因突变的引物、探针及试剂盒 |
| JP2019532011A (ja) | 2016-11-02 | 2019-11-07 | アログ・ファーマシューティカルズ・インコーポレイテッドＡｒｏｇ Ｐｈａｒｍａｃｅｕｔｉｃａｌｓ，Ｉｎｃ． | Ｆｌｔ３突然変異増殖性疾患および関連する突然変異を治療するためのクレノラニブ |
| CN107382983B (zh) * | 2017-08-24 | 2020-08-07 | 扬州市三药制药有限公司 | 一种治疗白血病药物的合成方法 |
| DE102019204219A1 (de) * | 2019-03-27 | 2020-10-01 | Robert Bosch Gmbh | Verfahren zur Diagnose von Abgassensoren |
| US11471451B2 (en) * | 2019-08-19 | 2022-10-18 | Arog Pharmaceuticals, Inc. | Uses of crenolanib |
| WO2021238957A1 (zh) * | 2020-05-26 | 2021-12-02 | 江苏恒瑞医药股份有限公司 | 法米替尼在制备用于治疗c-KIT或PDGFRA突变的肿瘤的药物中的用途 |
| US11713310B2 (en) | 2020-07-20 | 2023-08-01 | Arog Pharmaceuticals, Inc. | Crystal forms of crenolanib and methods of use thereof |
| JP2023536068A (ja) * | 2020-07-20 | 2023-08-23 | アログ・ファーマシューティカルズ・インコーポレイテッド | クレノラニブの結晶形態およびそれを用いる方法 |
| US11969420B2 (en) | 2020-10-30 | 2024-04-30 | Arog Pharmaceuticals, Inc. | Combination therapy of crenolanib and apoptosis pathway agents for the treatment of proliferative disorders |
| WO2022090547A1 (en) | 2020-10-30 | 2022-05-05 | Dsm Ip Assets B.V. | Production of carotenoids by fermentation |
| CA3207794A1 (en) * | 2021-02-09 | 2022-08-18 | Jasper Therapeutics, Inc. | Modified stem cell compositions and methods for use |
| CN113683594B (zh) * | 2021-09-07 | 2022-12-27 | 曲靖师范学院 | 一种喹啉-苯并咪唑盐类化合物及其合成方法和应用 |
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| US5990146A (en) | 1997-08-20 | 1999-11-23 | Warner-Lambert Company | Benzimidazoles for inhibiting protein tyrosine kinase mediated cellular proliferation |
| JP2001518470A (ja) | 1997-09-26 | 2001-10-16 | メルク エンド カムパニー インコーポレーテッド | 新規な血管形成阻害剤 |
| UA75055C2 (uk) | 1999-11-30 | 2006-03-15 | Пфайзер Продактс Інк. | Похідні бензоімідазолу, що використовуються як антипроліферативний засіб, фармацевтична композиція на їх основі |
| PA8580301A1 (es) * | 2002-08-28 | 2005-05-24 | Pfizer Prod Inc | Nuevos derivados de benzoimidazol utiles como agentes antiproliferativos |
| MXPA05014203A (es) | 2003-06-24 | 2006-02-24 | Pfizer Prod Inc | Procedimientos para la preparacion de derivados de benzoimidazol. |
| US20130230511A1 (en) * | 2012-02-03 | 2013-09-05 | Board Of Regents, The University Of Texas System | Biomarkers for response to tyrosine kinase pathway inhibitors in cancer |
| KR101738063B1 (ko) | 2012-09-21 | 2017-05-19 | 아로그 파마슈티칼스, 인코퍼레이티드 | 구조적으로 활성인 인산화된 ｆｌｔ３ 키나제의 억제 방법 |
| JP6042157B2 (ja) | 2012-09-26 | 2016-12-14 | アログ・ファーマシューティカルズ・リミテッド・ライアビリティ・カンパニーＡｒｏｇ Ｐｈａｒｍａｃｅｕｔｉｃａｌｓ，ＬＬＣ | 変異型ｃ−ｋｉｔの阻害方法 |
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| US9480683B2 (en) | 2016-11-01 |
| CN109010340A (zh) | 2018-12-18 |
| CA2812258A1 (en) | 2014-03-26 |
| CN103655563A (zh) | 2014-03-26 |
| KR20140040594A (ko) | 2014-04-03 |
| US20160367545A1 (en) | 2016-12-22 |
| KR101886006B1 (ko) | 2018-08-06 |
| JP6042157B2 (ja) | 2016-12-14 |
| AU2013204841B2 (en) | 2016-04-28 |
| MX368707B (es) | 2019-10-11 |
| MX2013010840A (es) | 2015-04-27 |
| US20140088147A1 (en) | 2014-03-27 |
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