NO20045137L - Diketohydrazinderivatforbindelser og legemidler inneholdende forbindelser som aktiv ingrediens - Google Patents
Diketohydrazinderivatforbindelser og legemidler inneholdende forbindelser som aktiv ingrediensInfo
- Publication number
- NO20045137L NO20045137L NO20045137A NO20045137A NO20045137L NO 20045137 L NO20045137 L NO 20045137L NO 20045137 A NO20045137 A NO 20045137A NO 20045137 A NO20045137 A NO 20045137A NO 20045137 L NO20045137 L NO 20045137L
- Authority
- NO
- Norway
- Prior art keywords
- compounds
- formula
- active ingredient
- drugs containing
- diketohydrazine
- Prior art date
Links
- 150000001875 compounds Chemical class 0.000 title abstract 4
- 239000004480 active ingredient Substances 0.000 title 1
- 239000003814 drug Substances 0.000 title 1
- 229940079593 drug Drugs 0.000 title 1
- 206010012289 Dementia Diseases 0.000 abstract 2
- 201000010099 disease Diseases 0.000 abstract 2
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 abstract 2
- 230000002401 inhibitory effect Effects 0.000 abstract 2
- 208000020925 Bipolar disease Diseases 0.000 abstract 1
- 208000019838 Blood disease Diseases 0.000 abstract 1
- 102000005927 Cysteine Proteases Human genes 0.000 abstract 1
- 108010005843 Cysteine Proteases Proteins 0.000 abstract 1
- 102000016387 Pancreatic elastase Human genes 0.000 abstract 1
- 108010067372 Pancreatic elastase Proteins 0.000 abstract 1
- 230000001684 chronic effect Effects 0.000 abstract 1
- 208000014951 hematologic disease Diseases 0.000 abstract 1
- 208000018706 hematopoietic system disease Diseases 0.000 abstract 1
- 230000002440 hepatic effect Effects 0.000 abstract 1
- 230000002757 inflammatory effect Effects 0.000 abstract 1
- 230000000302 ischemic effect Effects 0.000 abstract 1
- 208000019423 liver disease Diseases 0.000 abstract 1
- 208000030159 metabolic disease Diseases 0.000 abstract 1
- 230000001537 neural effect Effects 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D209/02—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
- C07D209/44—Iso-indoles; Hydrogenated iso-indoles
- C07D209/48—Iso-indoles; Hydrogenated iso-indoles with oxygen atoms in positions 1 and 3, e.g. phthalimide
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- A61K31/341—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having five-membered rings with one oxygen as the only ring hetero atom, e.g. isosorbide not condensed with another ring, e.g. ranitidine, furosemide, bufetolol, muscarine
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Abstract
Foreliggende oppfinnelse vedrører et diketohydrazinderivat med formel (I) og et farmasøytisk akseptabelt salt derav. (Symbolene i formelen har den sarmne betydning som beskrevet i beskrivelsen). Forbindelsen med formel (I) har en hermnende aktivitet overfor cysteinprotease, og den er nyttig for behandling av inflammatoriske sykdorrmier, irrmiimsykdormner, iskemiske sykdorrmier, respiratoriske sykdonmier, sirkulasjonssykdommer, blodsykdommer, neuronale sykdommer, hepatiske eller bihære sykdonmier, ben- eller leddsykdommer, metaboliske sykdonmier, etc, og forbindelsen har inhiberende aktivitet overfor elastase, og den er også nyttig for behandling av eOPD ("chronic obstacle puhnonary diseases").
Applications Claiming Priority (2)
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JP2002123796 | 2002-04-25 | ||
PCT/JP2003/005252 WO2003091202A1 (fr) | 2002-04-25 | 2003-04-24 | Composes derives de dicetohydrazine et medicaments contenant ces composes comme ingredient actif |
Publications (2)
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UA79749C2 (en) | 1996-10-18 | 2007-07-25 | Vertex Pharma | Inhibitors of serine proteases, particularly hepatitis c virus ns3 protease |
BR0309670A (pt) * | 2002-04-25 | 2005-03-15 | Ono Pharmaceutical Co | Compostos derivados dicetohidrazina e drogas contendo os compostos como o ingrediente ativo |
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 |
MY148123A (en) | 2003-09-05 | 2013-02-28 | Vertex Pharma | Inhibitors of serine proteases, particularly hcv ns3-ns4a protease |
WO2005077969A2 (en) * | 2004-02-04 | 2005-08-25 | Vertex Pharmaceuticals Incorporated | Inhibitors of serine proteases, particularly hcv ns3-ns4a protease |
EP1741441A4 (en) * | 2004-04-26 | 2010-03-03 | Ono Pharmaceutical Co | BONE-ENHANCING AGENT CHARACTERIZED BY USING CATHEPSIN K INHIBITOR WITH PTH |
JP4513517B2 (ja) * | 2004-11-12 | 2010-07-28 | 宇部興産株式会社 | 3−(n−アシルアミノ)−2−アシルオキシ−3−(4−テトラヒドロピラニル)−2−プロペン酸エステル及びその製法 |
WO2006076796A1 (en) * | 2005-01-19 | 2006-07-27 | Merck Frosst Canada Ltd. | Cathepsin k inhibitors and obesity |
JP5034277B2 (ja) * | 2005-03-11 | 2012-09-26 | 宇部興産株式会社 | 3−(n−アシルアミノ)−3−(4−テトラヒドロピラニル)−2−オキソプロパン酸エステル及び3−(n−アシルアミノ)−3−(4−テトラヒドロピラニル)−2−オキソプロパノヒドラジドの製造方法 |
US20100292298A1 (en) * | 2006-02-21 | 2010-11-18 | Agency For Science, Technology And Research | Method and reagents for treating hepatic fibrosis and inflammation |
ES2392675T3 (es) * | 2006-06-01 | 2012-12-12 | Sanofi | Nitrilos espirocíclicos como inhibidores de proteasa |
WO2008149971A1 (ja) | 2007-06-08 | 2008-12-11 | Kyoto University | 脳動脈瘤の治療または予防薬 |
EP2216047A4 (en) | 2007-10-24 | 2011-12-28 | Nat Univ Corp Tokyo Med & Dent | REGULATOR FOR SIGNALING THE TOLL LIKE RECEPTOR WITH A CATHEPSIN INHIBITOR AS AN ACTIVE SUBSTANCE |
CA2631071A1 (en) * | 2008-05-09 | 2009-11-09 | Tong-Jun Lin | Inhibition of calpain reduces allergic inflammation |
WO2011069149A2 (en) * | 2009-12-04 | 2011-06-09 | Dcb-Usa Llc | Cathepsin s inhibitors |
BR112012013861A2 (pt) * | 2009-12-10 | 2017-09-26 | Medivir Uk Ltd | ibidores da cisteína protease |
CN102241627B (zh) * | 2010-05-14 | 2014-07-02 | 中国人民解放军总医院 | 脲类化合物及其医药用途 |
CN102675061B (zh) * | 2011-10-31 | 2016-01-20 | 合肥市济泉医药科技有限公司 | 白藜芦醇的醚衍生物和医疗用途 |
WO2014113068A1 (en) * | 2013-01-18 | 2014-07-24 | Loma Linda University | Compositions and methods for diagnosing and treating sepsis |
EP3009444B1 (en) * | 2013-06-14 | 2017-12-20 | Seikagaku Corporation | Alpha-oxoacyl amino-caprolactam derivative |
KR102007072B1 (ko) | 2013-08-12 | 2019-08-02 | 카티바, 인크. | 인쇄 가능한 유기 발광 다이오드 잉크 배합물을 위한 에스테르계 용매 시스템 |
EP3426674A4 (en) | 2016-03-09 | 2019-08-14 | Blade Therapeutics, Inc. | CYCLIC KETO AMID COMPOUNDS AS CALPAIN MODULATORS AND METHOD FOR THE PRODUCTION AND USE THEREOF |
US11292801B2 (en) | 2016-07-05 | 2022-04-05 | Blade Therapeutics, Inc. | Calpain modulators and therapeutic uses thereof |
US20190175690A1 (en) * | 2016-08-16 | 2019-06-13 | Children's Medical Center Corporation | Compositions and methods for cardiac repair |
JOP20190024A1 (ar) | 2016-08-26 | 2019-02-19 | Gilead Sciences Inc | مركبات بيروليزين بها استبدال واستخداماتها |
AU2017336523B2 (en) | 2016-09-28 | 2022-07-21 | Blade Therapeutics, Inc. | Calpain modulators and therapeutic uses thereof |
CA3091142C (en) | 2018-02-26 | 2023-04-11 | Gilead Sciences, Inc. | Substituted pyrrolizine compounds and uses thereof |
CN113372368B (zh) * | 2020-03-09 | 2022-04-12 | 苏州爱科百发生物医药技术有限公司 | 一种弹性蛋白酶抑制剂前药及其用途 |
IL298324A (en) | 2020-06-10 | 2023-01-01 | Aligos Therapeutics Inc | Antiviral compounds for the treatment of coronavirus, picornavirus and novovirus infections |
WO2022072975A1 (en) * | 2020-10-01 | 2022-04-07 | University Of Georgia Research Foundation, Inc. | Compositions and methods of treatment for sars-cov-2 through papain protease inhibition |
CA3224494A1 (en) | 2021-07-09 | 2023-01-12 | Koen Vandyck | Anti-viral compounds |
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CN115192564B (zh) * | 2022-05-23 | 2023-11-17 | 四川大学华西医院 | 一种苯丙氨酸衍生物、药物组合物及其在肿瘤治疗中的应用 |
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IL110898A0 (en) | 1993-09-10 | 1994-11-28 | Narhex Australia Pty Ltd | Polar-substituted hydrocarbons |
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BR0309670A (pt) * | 2002-04-25 | 2005-03-15 | Ono Pharmaceutical Co | Compostos derivados dicetohidrazina e drogas contendo os compostos como o ingrediente ativo |
EP1741441A4 (en) * | 2004-04-26 | 2010-03-03 | Ono Pharmaceutical Co | BONE-ENHANCING AGENT CHARACTERIZED BY USING CATHEPSIN K INHIBITOR WITH PTH |
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