KR20060129069A - 카스파제 억제제 및 이의 용도 - Google Patents
카스파제 억제제 및 이의 용도 Download PDFInfo
- Publication number
- KR20060129069A KR20060129069A KR1020067019903A KR20067019903A KR20060129069A KR 20060129069 A KR20060129069 A KR 20060129069A KR 1020067019903 A KR1020067019903 A KR 1020067019903A KR 20067019903 A KR20067019903 A KR 20067019903A KR 20060129069 A KR20060129069 A KR 20060129069A
- Authority
- KR
- South Korea
- Prior art keywords
- formula
- compound
- aliphatic
- carboxylic acid
- oxo
- 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.)
- Ceased
Links
- 0 *[C@@](C(N(CCCCCC1)[C@@]1C(NC(C1)[C@@](O*)OC1=O)=O)=O)N* Chemical compound *[C@@](C(N(CCCCCC1)[C@@]1C(NC(C1)[C@@](O*)OC1=O)=O)=O)N* 0.000 description 18
- IJBGNKFVYKZBNU-XAYKYTGQSA-N CC(C)(C)[C@@H](C(N(CCC1)[C@@H]1C(N[C@@H](CC(O)=O)C=O)=O)=O)NC(c(cccc1O)c1Cl)=O Chemical compound CC(C)(C)[C@@H](C(N(CCC1)[C@@H]1C(N[C@@H](CC(O)=O)C=O)=O)=O)NC(c(cccc1O)c1Cl)=O IJBGNKFVYKZBNU-XAYKYTGQSA-N 0.000 description 1
- RXQDMVCJFZOPKS-JQBYSNGBSA-N CC(C)(C)[C@@H](C(N(CCC1)[C@@H]1C(N[C@@H](CC(O)=O)C=O)=O)=O)NC(c(cccc1OCC2CC2)c1Cl)O Chemical compound CC(C)(C)[C@@H](C(N(CCC1)[C@@H]1C(N[C@@H](CC(O)=O)C=O)=O)=O)NC(c(cccc1OCC2CC2)c1Cl)O RXQDMVCJFZOPKS-JQBYSNGBSA-N 0.000 description 1
- UQCHETQJZPBTAV-UHFFFAOYSA-N CC(C)C(C(N(C1CC2CC1)C2C(NC(CC(O)=O)C=O)=O)=O)NC(c(cccc1OC)c1F)=O Chemical compound CC(C)C(C(N(C1CC2CC1)C2C(NC(CC(O)=O)C=O)=O)=O)NC(c(cccc1OC)c1F)=O UQCHETQJZPBTAV-UHFFFAOYSA-N 0.000 description 1
- RKDIJDUANHCPKR-LIDKGGFZSA-N CC(C)[C@@H](C(N(CCC1)[C@@H]1C(NC(CCO)C=O)O)=O)NC(c(c(N)ccc1)c1Cl)O Chemical compound CC(C)[C@@H](C(N(CCC1)[C@@H]1C(NC(CCO)C=O)O)=O)NC(c(c(N)ccc1)c1Cl)O RKDIJDUANHCPKR-LIDKGGFZSA-N 0.000 description 1
- AXZKGXZIJJFLBC-FTRWYGJKSA-N CC(C)[C@@H](C(N(CCC1)[C@@H]1C(N[C@@H](CC(O)=O)C=O)=O)=O)NCc(cccc1OC)c1Cl Chemical compound CC(C)[C@@H](C(N(CCC1)[C@@H]1C(N[C@@H](CC(O)=O)C=O)=O)=O)NCc(cccc1OC)c1Cl AXZKGXZIJJFLBC-FTRWYGJKSA-N 0.000 description 1
- GMYQMTNSRPVICT-ZKHUHEIGSA-N CC(C1C)C1(C(N(CCC1)[C@@H]1C(N[C@](C1)([C@@H]1C(O)=O)C=O)=O)=O)NC(c(cccc1Cl)c1Cl)=O Chemical compound CC(C1C)C1(C(N(CCC1)[C@@H]1C(N[C@](C1)([C@@H]1C(O)=O)C=O)=O)=O)NC(c(cccc1Cl)c1Cl)=O GMYQMTNSRPVICT-ZKHUHEIGSA-N 0.000 description 1
- QXCMXMYCUJDKJJ-UHFFFAOYSA-N CCN1C(C2)=CCC2C1N Chemical compound CCN1C(C2)=CCC2C1N QXCMXMYCUJDKJJ-UHFFFAOYSA-N 0.000 description 1
- PHQLSRCISUSWAU-JMZAEGDUSA-N CCO[C@@H](C(C1)NC([C@H]([C@@H](CC2)C[C@H]2C2)N2C([C@H](C(C)(C)C)NC(c2c(C)c(OC)ccc2)=O)=O)=O)OC1=O Chemical compound CCO[C@@H](C(C1)NC([C@H]([C@@H](CC2)C[C@H]2C2)N2C([C@H](C(C)(C)C)NC(c2c(C)c(OC)ccc2)=O)=O)=O)OC1=O PHQLSRCISUSWAU-JMZAEGDUSA-N 0.000 description 1
- LMMVTUNILVIEFV-QFXJDEEGSA-N CCO[C@@H]([C@H](C1)NC([C@H](CCC2)N2C([C@H](C(C)(C)C)NC(c2c(C)c(NC(C)=O)ccc2)=O)=O)=O)OC1O Chemical compound CCO[C@@H]([C@H](C1)NC([C@H](CCC2)N2C([C@H](C(C)(C)C)NC(c2c(C)c(NC(C)=O)ccc2)=O)=O)=O)OC1O LMMVTUNILVIEFV-QFXJDEEGSA-N 0.000 description 1
- MHMMBJSXNVSHBJ-LZTCXMBHSA-N CCO[C@@H]([C@H](C1)NC([C@H](CCC2)N2C([C@H](C(C)(C)C/[O]=C/c2c(C)c(NC(C)=O)ccc2)N)=O)=O)OC1=O Chemical compound CCO[C@@H]([C@H](C1)NC([C@H](CCC2)N2C([C@H](C(C)(C)C/[O]=C/c2c(C)c(NC(C)=O)ccc2)N)=O)=O)OC1=O MHMMBJSXNVSHBJ-LZTCXMBHSA-N 0.000 description 1
- SBEJBAHVKUYWHD-ZXVLUALBSA-N CCO[C@@H]([C@H](C1)NC([C@H](CCC2)N2C([C@H](C(C)C)NC(c(c(Cl)cnc2)c2Cl)=O)=O)=O)OC1O Chemical compound CCO[C@@H]([C@H](C1)NC([C@H](CCC2)N2C([C@H](C(C)C)NC(c(c(Cl)cnc2)c2Cl)=O)=O)=O)OC1O SBEJBAHVKUYWHD-ZXVLUALBSA-N 0.000 description 1
- STEFLYJOMUVBNF-OTCCDFFUSA-N CCO[C@H](C(C1)NC(C(C2CC3CC2)N3C(C(C(C)(C)C)NC(c(cccc2)c2Cl)=O)=O)=O)OC1=O Chemical compound CCO[C@H](C(C1)NC(C(C2CC3CC2)N3C(C(C(C)(C)C)NC(c(cccc2)c2Cl)=O)=O)=O)OC1=O STEFLYJOMUVBNF-OTCCDFFUSA-N 0.000 description 1
Classifications
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- 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
- C07D405/02—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
- C07D405/12—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 linked by a chain containing hetero atoms as chain links
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- A61K38/06—Tripeptides
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| PE20011350A1 (es) | 2000-05-19 | 2002-01-15 | Vertex Pharma | PROFARMACO DE UN INHIBIDOR DE ENZIMA CONVERTIDORA DE INTERLEUCINA-1ß (ICE) |
| CA2559303C (en) * | 2004-03-12 | 2013-09-10 | Vertex Pharmaceuticals Incorporated | Processes and intermediates for the preparation of aspartic acetal caspase inhibitors |
| CN102362867A (zh) * | 2004-05-15 | 2012-02-29 | 沃泰克斯药物股份有限公司 | 使用ice抑制剂治疗癫痫发作 |
| EP1778221A2 (en) * | 2004-05-27 | 2007-05-02 | Vertex Pharmaceuticals Incorporated | Ice inhibitors for the treatment of autoinflammatory diseases |
| WO2011094426A1 (en) * | 2010-01-29 | 2011-08-04 | The United State Of America, As Represented By The Secretary, Department Of Health & Human Services | Caspase inhibitors |
| US9956260B1 (en) | 2011-07-22 | 2018-05-01 | The J. David Gladstone Institutes | Treatment of HIV-1 infection and AIDS |
| WO2015175381A1 (en) | 2014-05-12 | 2015-11-19 | Conatus Pharmaceuticals, Inc. | Treatment of the complications of chronic liver disease with caspase inhibitors |
| WO2017079566A1 (en) | 2015-11-05 | 2017-05-11 | Conatus Pharmaceuticals, Inc. | Caspase inhibitors for use in the treatment of liver cancer |
| JP2019500397A (ja) | 2015-12-31 | 2019-01-10 | クオナトウス ファーマシューティカルズ,インコーポレイテッド | カスパーゼ阻害剤を肝疾患の治療に使用する方法 |
| CN105853408B (zh) * | 2016-04-15 | 2018-12-04 | 浙江大学 | 苯酰胺衍生物在制备Caspase-1抑制剂中的应用 |
| RU2019113150A (ru) | 2016-10-05 | 2020-11-06 | Новартис Аг | Комбинация композиций, содержащих агонисты fxr, предназначенная для лечения или предупреждения фиброзирующего, цирротического заболевания или нарушения |
| WO2022123062A1 (en) | 2020-12-11 | 2022-06-16 | INSERM (Institut National de la Santé et de la Recherche Médicale) | Blocking caspase and/or fasl for preventing fatal outcome in covid-19 patients |
| WO2024044098A2 (en) * | 2022-08-23 | 2024-02-29 | Alexion Pharmaceuticals, Inc. | Pharmaceutical compounds for the treatment of complement mediated disorders |
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| GB9005014D0 (en) * | 1990-03-06 | 1990-05-02 | Janssen Pharmaceutica Nv | N.(4.piperidinyl)(dihydrobenzofuran or dihydro.2h.benzopyran)carboxamide derivatives |
| US5716929A (en) * | 1994-06-17 | 1998-02-10 | Vertex Pharmaceuticals, Inc. | Inhibitors of interleukin-1β converting enzyme |
| DE59508773D1 (de) * | 1994-07-22 | 2000-11-09 | Byk Gulden Lomberg Chem Fab | Dihydrobenzofurane |
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| AU739321B2 (en) * | 1996-09-12 | 2001-10-11 | Idun Pharmaceuticals, Incorporated | C-terminal modified (N-substituted)-2-indolyl dipeptides as inhibitors of the ICE/ced-3 family of cysteine proteases |
| FR2766188B1 (fr) | 1997-07-15 | 2000-02-11 | Hoechst Marion Roussel Inc | Nouveau procede de preparation de derives amines d'alkyloxy furanone, composes issus de ce procede et utilisation de ces composes |
| TR200103406T2 (tr) * | 1998-03-19 | 2002-06-21 | Vertex Pharmaceuticals Incorporated | Kaspaz inhibitörleri. |
| US7053056B2 (en) | 1998-07-02 | 2006-05-30 | Idun Pharmaceuticals, Inc. | C-terminal modified oxamyl dipeptides as inhibitors of the ICE/ced-3 family of cysteine proteases |
| CA2360689A1 (en) | 1999-01-29 | 2000-08-03 | Senju Pharmaceutical Co., Ltd. | Anti-inflammatory agents and inhibitors against increase in ocular tension caused by irradiation with lasers, containing 1,4-dihydropyridine derivatives |
| ES2347133T3 (es) | 2000-04-24 | 2010-10-26 | Vertex Pharmaceuticals Incorporated | Procedimiento e intermedios para preparar acetales de acido aspartico sustituidos. |
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| US6645994B1 (en) | 2001-06-01 | 2003-11-11 | Alcon, Inc. | Method of treating dry eye disorders |
| AU2003211052A1 (en) | 2002-02-11 | 2003-09-04 | Vertex Pharmaceuticals Incorporated | Phospholipids as caspase inhibitor prodrugs |
| CA2559303C (en) * | 2004-03-12 | 2013-09-10 | Vertex Pharmaceuticals Incorporated | Processes and intermediates for the preparation of aspartic acetal caspase inhibitors |
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| AU2005219861A1 (en) | 2005-09-15 |
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| CN102161656A (zh) | 2011-08-24 |
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| CA2557645A1 (en) | 2005-09-15 |
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