JP2021519312A - カルパインモジュレーター及びその治療的使用 - Google Patents
カルパインモジュレーター及びその治療的使用 Download PDFInfo
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- JP2021519312A JP2021519312A JP2020551973A JP2020551973A JP2021519312A JP 2021519312 A JP2021519312 A JP 2021519312A JP 2020551973 A JP2020551973 A JP 2020551973A JP 2020551973 A JP2020551973 A JP 2020551973A JP 2021519312 A JP2021519312 A JP 2021519312A
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Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- 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
- A61K31/415—1,2-Diazoles
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- 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
- A61K31/415—1,2-Diazoles
- A61K31/4155—1,2-Diazoles non condensed and containing further heterocyclic rings
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- 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
- A61K31/42—Oxazoles
- A61K31/421—1,3-Oxazoles, e.g. pemoline, trimethadione
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- 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
- A61K31/42—Oxazoles
- A61K31/422—Oxazoles not condensed and containing further heterocyclic rings
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- 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
- A61K31/433—Thidiazoles
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- 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
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/4427—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
- A61K31/4439—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. omeprazole
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
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| AU2017292646A1 (en) | 2016-07-05 | 2019-02-07 | Blade Therapeutics, Inc. | Calpain modulators and therapeutic uses thereof |
| WO2018064119A1 (en) | 2016-09-28 | 2018-04-05 | Blade Therapeutics, Inc. | Calpain modulators and therapeutic uses thereof |
| BR112020026744A2 (pt) * | 2018-06-28 | 2021-03-30 | Blade Therapeutics, Inc. | Métodos para tratar fibrose hepática com o uso de inibidores de calpaína |
| PH12022553378A1 (en) | 2020-06-10 | 2024-03-25 | Univ Leuven Kath | Anti-viral compounds for treating coronavirus, picornavirus, and norovirus infections |
| AU2022306289A1 (en) | 2021-07-09 | 2024-01-18 | Aligos Therapeutics, Inc. | Anti-viral compounds |
| WO2023043816A1 (en) | 2021-09-17 | 2023-03-23 | Aligos Therapeutics, Inc. | Anti-viral compounds for treating coronavirus, picornavirus, and norovirus infections |
Citations (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2000055124A2 (en) * | 1999-03-15 | 2000-09-21 | Axys Pharmaceuticals, Inc. | Novel compounds and compositions as protease inhibitors |
| JP2001501955A (ja) * | 1996-10-15 | 2001-02-13 | ビーエーエスエフ アクチェンゲゼルシャフト | 新規のピペリジン―ケトカルボン酸誘導体、その製造および使用 |
| JP2001518506A (ja) * | 1997-10-07 | 2001-10-16 | セフアロン・インコーポレーテツド | キノリン−含有α−ケトアミドシステインおよびセリンプロテアーゼインヒビター |
| US20050014816A1 (en) * | 2003-07-03 | 2005-01-20 | Pfizer Inc | Thiophene amino acid derivatives, process for preparing them and pharmaceutical compositions containing them |
| JP2009506078A (ja) * | 2005-08-26 | 2009-02-12 | バーテックス ファーマシューティカルズ インコーポレイテッド | セリンプロテアーゼの阻害剤 |
| JP2010514738A (ja) * | 2006-12-29 | 2010-05-06 | アボット ゲーエムベーハー ウント カンパニー カーゲー | カルボキサミド化合物およびカルパイン阻害剤としてのこれらの使用 |
| JP2013515039A (ja) * | 2009-12-22 | 2013-05-02 | アボット ゲーエムベーハー ウント カンパニー カーゲー | カルボキサミド化合物類およびカラパイン阻害剤としてのその使用 |
| JP2020500207A (ja) * | 2016-09-28 | 2020-01-09 | ブレード・セラピューティクス・インコーポレイテッド | カルパインモジュレーター及びそれらの治療上の使用 |
| JP2021519764A (ja) * | 2018-03-28 | 2021-08-12 | ブレード・セラピューティクス・インコーポレイテッド | 線維性疾患を処置する方法 |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| SE9102462D0 (sv) * | 1991-08-28 | 1991-08-28 | Astra Ab | New isosteric peptides |
| EP0650368A1 (en) * | 1992-06-24 | 1995-05-03 | Cortex Pharmaceuticals, Inc. | Use of calpain inhibitors in the inhibition and treatment of medical conditions associated with increased calpain activity |
| WO2005000793A1 (ja) * | 2003-06-26 | 2005-01-06 | Taisho Pharmaceutical Co., Ltd. | 2位置換シクロアルキルカルボン酸誘導体 |
| US7964624B1 (en) * | 2005-08-26 | 2011-06-21 | Vertex Pharmaceuticals Incorporated | Inhibitors of serine proteases |
| JP2017517475A (ja) * | 2014-02-19 | 2017-06-29 | エーテーハー チューリヒ | 化合物ライブラリーの製造方法 |
| KR102519948B1 (ko) * | 2016-06-29 | 2023-04-11 | 더 리젠츠 오브 더 유니버시티 오브 캘리포니아 | 암 치료용 화합물 및 조성물 |
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Patent Citations (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2001501955A (ja) * | 1996-10-15 | 2001-02-13 | ビーエーエスエフ アクチェンゲゼルシャフト | 新規のピペリジン―ケトカルボン酸誘導体、その製造および使用 |
| JP2001518506A (ja) * | 1997-10-07 | 2001-10-16 | セフアロン・インコーポレーテツド | キノリン−含有α−ケトアミドシステインおよびセリンプロテアーゼインヒビター |
| WO2000055124A2 (en) * | 1999-03-15 | 2000-09-21 | Axys Pharmaceuticals, Inc. | Novel compounds and compositions as protease inhibitors |
| US20050014816A1 (en) * | 2003-07-03 | 2005-01-20 | Pfizer Inc | Thiophene amino acid derivatives, process for preparing them and pharmaceutical compositions containing them |
| JP2009506078A (ja) * | 2005-08-26 | 2009-02-12 | バーテックス ファーマシューティカルズ インコーポレイテッド | セリンプロテアーゼの阻害剤 |
| JP2010514738A (ja) * | 2006-12-29 | 2010-05-06 | アボット ゲーエムベーハー ウント カンパニー カーゲー | カルボキサミド化合物およびカルパイン阻害剤としてのこれらの使用 |
| JP2013515039A (ja) * | 2009-12-22 | 2013-05-02 | アボット ゲーエムベーハー ウント カンパニー カーゲー | カルボキサミド化合物類およびカラパイン阻害剤としてのその使用 |
| JP2020500207A (ja) * | 2016-09-28 | 2020-01-09 | ブレード・セラピューティクス・インコーポレイテッド | カルパインモジュレーター及びそれらの治療上の使用 |
| JP2021519764A (ja) * | 2018-03-28 | 2021-08-12 | ブレード・セラピューティクス・インコーポレイテッド | 線維性疾患を処置する方法 |
Non-Patent Citations (1)
| Title |
|---|
| KLING, A. ET AL.: "Mitigating the Metabolic Liability of Carbonyl Reduction: Novel Calpain Inhibitors with P1' Extentio", ACS MEDICINAL CHEMISTRY LETTERS, vol. 9, JPN7023000951, 2018, pages 221 - 226, ISSN: 0005010744 * |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2021519764A (ja) * | 2018-03-28 | 2021-08-12 | ブレード・セラピューティクス・インコーポレイテッド | 線維性疾患を処置する方法 |
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| AU2019242387A1 (en) | 2020-11-19 |
| EP3774737A4 (en) | 2021-12-22 |
| WO2019190885A1 (en) | 2019-10-03 |
| PE20212111A1 (es) | 2021-11-04 |
| PH12020551555A1 (en) | 2021-07-12 |
| KR20200139702A (ko) | 2020-12-14 |
| RU2020130022A (ru) | 2022-05-04 |
| TW202003472A (zh) | 2020-01-16 |
| MX2020010033A (es) | 2020-10-14 |
| EP3774737A1 (en) | 2021-02-17 |
| IL277548A (en) | 2020-11-30 |
| AR115303A1 (es) | 2020-12-23 |
| US20210009564A1 (en) | 2021-01-14 |
| CA3095164A1 (en) | 2019-10-03 |
| ECSP20068210A (es) | 2020-11-30 |
| CL2020002496A1 (es) | 2021-03-12 |
| CN112204014A (zh) | 2021-01-08 |
| BR112020019560A2 (pt) | 2021-01-05 |
| SG11202008750XA (en) | 2020-10-29 |
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