WO2009054439A1 - Pai-1産生抑制剤 - Google Patents
Pai-1産生抑制剤 Download PDFInfo
- Publication number
- WO2009054439A1 WO2009054439A1 PCT/JP2008/069207 JP2008069207W WO2009054439A1 WO 2009054439 A1 WO2009054439 A1 WO 2009054439A1 JP 2008069207 W JP2008069207 W JP 2008069207W WO 2009054439 A1 WO2009054439 A1 WO 2009054439A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- pai
- group
- production inhibitor
- benzene ring
- alkyl group
- 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
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
- A61K31/535—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
- A61K31/5375—1,4-Oxazines, e.g. morpholine
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D295/00—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms
- C07D295/16—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms acylated on ring nitrogen atoms
- C07D295/20—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms acylated on ring nitrogen atoms by radicals derived from carbonic acid, or sulfur or nitrogen analogues thereof
-
- 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
- A61K31/16—Amides, e.g. hydroxamic acids
- A61K31/165—Amides, e.g. hydroxamic acids having aromatic rings, e.g. colchicine, atenolol, progabide
- A61K31/166—Amides, e.g. hydroxamic acids having aromatic rings, e.g. colchicine, atenolol, progabide having the carbon of a carboxamide group directly attached to the aromatic ring, e.g. procainamide, procarbazine, metoclopramide, labetalol
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/28—Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P27/00—Drugs for disorders of the senses
- A61P27/02—Ophthalmic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P7/00—Drugs for disorders of the blood or the extracellular fluid
- A61P7/02—Antithrombotic agents; Anticoagulants; Platelet aggregation inhibitors
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Medicinal Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Neurology (AREA)
- Epidemiology (AREA)
- Cardiology (AREA)
- Heart & Thoracic Surgery (AREA)
- Neurosurgery (AREA)
- Biomedical Technology (AREA)
- Urology & Nephrology (AREA)
- Ophthalmology & Optometry (AREA)
- Vascular Medicine (AREA)
- Hospice & Palliative Care (AREA)
- Diabetes (AREA)
- Hematology (AREA)
- Psychiatry (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Abstract
Priority Applications (6)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CA2703494A CA2703494A1 (en) | 2007-10-23 | 2008-10-23 | Inhibitor of pai-1 production |
| EP08842108A EP2201946A4 (en) | 2007-10-23 | 2008-10-23 | HAMMER OF PAI-1 PRODUCTION |
| BRPI0816560-2A BRPI0816560A2 (pt) | 2007-10-23 | 2008-10-23 | Método de inibição de produção de pai-1 método para prevenção ou melhora de uma doença causada por uma super-produção de pai-1" |
| JP2009538246A JP5470046B2 (ja) | 2007-10-23 | 2008-10-23 | Pai−1産生抑制剤 |
| AU2008314979A AU2008314979A1 (en) | 2007-10-23 | 2008-10-23 | Inhibitor of PAI-1 production |
| CN2008801133696A CN101842093B (zh) | 2007-10-23 | 2008-10-23 | Pai-1产生抑制剂 |
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2007275557 | 2007-10-23 | ||
| JP2007-275557 | 2007-10-23 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| WO2009054439A1 true WO2009054439A1 (ja) | 2009-04-30 |
Family
ID=40579541
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PCT/JP2008/069207 Ceased WO2009054439A1 (ja) | 2007-10-23 | 2008-10-23 | Pai-1産生抑制剤 |
Country Status (9)
| Country | Link |
|---|---|
| EP (1) | EP2201946A4 (ja) |
| JP (1) | JP5470046B2 (ja) |
| KR (1) | KR20100097113A (ja) |
| CN (2) | CN101842093B (ja) |
| AU (1) | AU2008314979A1 (ja) |
| BR (1) | BRPI0816560A2 (ja) |
| CA (1) | CA2703494A1 (ja) |
| RU (1) | RU2010120675A (ja) |
| WO (1) | WO2009054439A1 (ja) |
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2013501737A (ja) * | 2009-08-14 | 2013-01-17 | バイエル・クロップサイエンス・アーゲー | 殺虫性カルボキサミド類 |
| CN107207417A (zh) * | 2014-11-13 | 2017-09-26 | 埃罗米克斯公司 | 新方法 |
| US9827253B2 (en) | 2013-11-06 | 2017-11-28 | Aeromics, Inc. | Prodrug salts |
| US9994514B2 (en) | 2012-05-08 | 2018-06-12 | Aeromics, Inc. | Methods of treating cerebral edema and spinal cord edema |
| WO2024172001A1 (ja) * | 2023-02-13 | 2024-08-22 | 本岡 知子 | 抗トリパノソーマ薬 |
Families Citing this family (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| TWI725092B (zh) | 2015-12-18 | 2021-04-21 | 大陸商深圳瑞健生命科學硏究院有限公司 | 纖溶酶原在製備預防或治療糖尿病腎病或其相關病症之藥劑上的用途 |
| WO2017101870A1 (zh) | 2015-12-18 | 2017-06-22 | 深圳瑞健生命科学研究院有限公司 | 一种预防或治疗糖尿病性视网膜病变的方法 |
| TWI624268B (zh) | 2015-12-18 | 2018-05-21 | Talengen Institute Of Life Sciences Co Ltd | 纖溶酶原在製備藥劑上的用途及包括纖溶酶原之藥劑 |
| WO2017101867A1 (zh) | 2015-12-18 | 2017-06-22 | 深圳瑞健生命科学研究院有限公司 | 一种预防或治疗糖尿病性神经损伤及其相关病症的方法 |
| WO2018107688A1 (zh) | 2016-12-15 | 2018-06-21 | 深圳瑞健生命科学研究院有限公司 | 一种预防和治疗脂肪肝的方法 |
| JP7175270B2 (ja) | 2016-12-15 | 2022-11-18 | タレンゲン インターナショナル リミテッド | グルカゴン、インスリンを正常なバランスに戻らせる方法 |
| US11207387B2 (en) | 2016-12-15 | 2021-12-28 | Talengen International Limited | Method and drug for preventing and treating obesity |
| CN108210896A (zh) * | 2016-12-15 | 2018-06-29 | 深圳瑞健生命科学研究院有限公司 | 预防和治疗高脂血症的药物及其用途 |
| CN115504940A (zh) * | 2021-06-23 | 2022-12-23 | 中国科学院上海药物研究所 | 一种酰胺类化合物、其制备方法和制药用途 |
| CN113519544A (zh) * | 2021-08-27 | 2021-10-22 | 皖南医学院 | 一种植物源杀螨剂及其制备方法和应用 |
Citations (25)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS62501703A (ja) * | 1984-11-29 | 1987-07-09 | イタルファルマコ・エッセ・ピ・ア | アミノ−サリチル酸誘導体、その塩、それらの製法およびそれらを含有する医薬組成物 |
| WO1995021832A1 (en) | 1994-02-14 | 1995-08-17 | Xenova Limited | Pharmaceutical piperazine compounds |
| WO1995032190A2 (en) | 1994-05-24 | 1995-11-30 | Xenova Limited | Pharmaceutical diketopiperazine compounds |
| WO1999065449A2 (en) | 1998-06-19 | 1999-12-23 | Smithkline Beecham Corporation | INHIBITORS OF TRANSCRIPTION FACTOR NF-λB |
| WO2002049632A1 (en) | 2000-12-18 | 2002-06-27 | Institute Of Medicinal Molecular Design. Inc. | Inhibitors against the production and release of inflammatory cytokines |
| GB2372740A (en) | 2001-01-17 | 2002-09-04 | Xenova Ltd | Diketopiperazines |
| WO2003000671A1 (en) | 2001-06-20 | 2003-01-03 | Wyeth | Naphthyl benzofuran derivatives as inhibitors of plasminogen activator inhibitor-1 (pai-1) |
| WO2003000253A1 (en) | 2001-06-20 | 2003-01-03 | Wyeth | Substituted indole acid derivatives as inhibitors of plasminogen activator inhibitor-1 (pai-1) |
| WO2003000258A1 (en) | 2001-06-20 | 2003-01-03 | Wyeth | Aryloxy-acetic acid compounds useful as inhibitors of plasminogen activator inhibitor-1 (pai-1) |
| WO2003000684A1 (en) | 2001-06-20 | 2003-01-03 | Wyeth | Substituted naphthyl indole derivatives as inhibitors of plasminogen activator inhibitor type-1 (pai-1) |
| WO2003100064A1 (en) | 2002-05-29 | 2003-12-04 | Kyowa Hakko Kogyo Co., Ltd. | Novel ubiquitin ligase |
| WO2003103654A1 (ja) | 2002-06-10 | 2003-12-18 | 株式会社医薬分子設計研究所 | NF−κB活性化阻害剤 |
| WO2003103658A1 (ja) | 2002-06-05 | 2003-12-18 | 株式会社医薬分子設計研究所 | 免疫関連プロテインキナーゼ阻害剤 |
| WO2004052856A1 (en) | 2002-12-10 | 2004-06-24 | Wyeth | Substituted indole oxo-acetyl amino acetic acid derivatives as inhibitors of plasminogen activator inhibitor-1 (pai-1) |
| WO2004052893A2 (en) | 2002-12-10 | 2004-06-24 | Wyeth | Substituted dihydropyrano indole-3,4-dione derivatives and 3-oxoacetic acid substituted 2-hydroxymethylindole derivatives as inhibitors of plasminogen activator inhibitor-1 (pai-1) |
| WO2005026127A1 (ja) * | 2003-09-11 | 2005-03-24 | Institute Of Medicinal Molecular Design. Inc. | プラスミノゲンアクチベータインヒビター-1阻害剤 |
| WO2005030756A1 (en) | 2003-09-25 | 2005-04-07 | Wyeth | Substituted pyrrole-indoles as inhibitors of pai-1 |
| WO2005030204A1 (en) | 2003-09-25 | 2005-04-07 | Wyeth | Substituted oxadiazolidinediones as pai-1 inhibitors |
| WO2005030192A1 (en) | 2003-09-25 | 2005-04-07 | Wyeth | 4- (1h-indol-3-yl-methylideneaminoxy-propoxy) -benzioc acid derivatives and related compounds as pai-1 inhibitors for the treatment of impairment of the fibrinolytic system and of thrombisis |
| WO2005030715A1 (en) | 2003-09-25 | 2005-04-07 | Wyeth | Substituted sulfonamide-indole-2-carboxylic acid derivatives as pai-1 inhibitors |
| WO2005030716A1 (en) | 2003-09-25 | 2005-04-07 | Wyeth | Heterocyclic- or aryloxy, -thio or -amino substituted indoles-2-carboxylic acids or esters as pai-1 |
| US20050124664A1 (en) | 2003-10-30 | 2005-06-09 | Eric Sartori | Urea thiadiazole inhibitors of plasminogen activator inhibior-1 |
| US20050124667A1 (en) | 2003-10-30 | 2005-06-09 | Eric Sartori | Oxamide inhibitors of plasminogen activator inhibitor-1 |
| US20050143384A1 (en) | 2003-10-30 | 2005-06-30 | Eric Sartori | Amide thiadiazole inhibitors of plasminogen activator inhibitor-1 |
| WO2006095713A1 (ja) * | 2005-03-08 | 2006-09-14 | Institute Of Medicinal Molecular Design. Inc. | プラスミノゲンアクチベータインヒビター-1阻害剤 |
Family Cites Families (4)
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| GB1493375A (en) * | 1974-09-20 | 1977-11-30 | Ici Ltd | Salicylanilide derivatives |
| WO2003103648A1 (ja) * | 2002-06-05 | 2003-12-18 | 株式会社医薬分子設計研究所 | 糖尿病治療薬 |
| EA010835B1 (ru) * | 2002-06-10 | 2008-12-30 | Инститьют Оф Медисинал Молекьюлар Дизайн. Инк. | Лекарственное средство для лечения рака |
| ES2339138T3 (es) * | 2004-11-24 | 2010-05-17 | Eli Lilly And Company | Derivados de eteres aromaticos utiles como inhibidores de la trombina. |
-
2008
- 2008-10-23 CN CN2008801133696A patent/CN101842093B/zh not_active Expired - Fee Related
- 2008-10-23 RU RU2010120675/04A patent/RU2010120675A/ru not_active Application Discontinuation
- 2008-10-23 WO PCT/JP2008/069207 patent/WO2009054439A1/ja not_active Ceased
- 2008-10-23 CN CN2012102320448A patent/CN102872020A/zh active Pending
- 2008-10-23 EP EP08842108A patent/EP2201946A4/en not_active Withdrawn
- 2008-10-23 CA CA2703494A patent/CA2703494A1/en not_active Abandoned
- 2008-10-23 KR KR1020107010934A patent/KR20100097113A/ko not_active Ceased
- 2008-10-23 JP JP2009538246A patent/JP5470046B2/ja not_active Expired - Fee Related
- 2008-10-23 AU AU2008314979A patent/AU2008314979A1/en not_active Abandoned
- 2008-10-23 BR BRPI0816560-2A patent/BRPI0816560A2/pt not_active IP Right Cessation
Patent Citations (26)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS62501703A (ja) * | 1984-11-29 | 1987-07-09 | イタルファルマコ・エッセ・ピ・ア | アミノ−サリチル酸誘導体、その塩、それらの製法およびそれらを含有する医薬組成物 |
| WO1995021832A1 (en) | 1994-02-14 | 1995-08-17 | Xenova Limited | Pharmaceutical piperazine compounds |
| WO1995032190A2 (en) | 1994-05-24 | 1995-11-30 | Xenova Limited | Pharmaceutical diketopiperazine compounds |
| WO1999065449A2 (en) | 1998-06-19 | 1999-12-23 | Smithkline Beecham Corporation | INHIBITORS OF TRANSCRIPTION FACTOR NF-λB |
| WO2002049632A1 (en) | 2000-12-18 | 2002-06-27 | Institute Of Medicinal Molecular Design. Inc. | Inhibitors against the production and release of inflammatory cytokines |
| GB2372740A (en) | 2001-01-17 | 2002-09-04 | Xenova Ltd | Diketopiperazines |
| WO2003000671A1 (en) | 2001-06-20 | 2003-01-03 | Wyeth | Naphthyl benzofuran derivatives as inhibitors of plasminogen activator inhibitor-1 (pai-1) |
| WO2003000253A1 (en) | 2001-06-20 | 2003-01-03 | Wyeth | Substituted indole acid derivatives as inhibitors of plasminogen activator inhibitor-1 (pai-1) |
| WO2003000258A1 (en) | 2001-06-20 | 2003-01-03 | Wyeth | Aryloxy-acetic acid compounds useful as inhibitors of plasminogen activator inhibitor-1 (pai-1) |
| WO2003000684A1 (en) | 2001-06-20 | 2003-01-03 | Wyeth | Substituted naphthyl indole derivatives as inhibitors of plasminogen activator inhibitor type-1 (pai-1) |
| WO2003100064A1 (en) | 2002-05-29 | 2003-12-04 | Kyowa Hakko Kogyo Co., Ltd. | Novel ubiquitin ligase |
| WO2003103658A1 (ja) | 2002-06-05 | 2003-12-18 | 株式会社医薬分子設計研究所 | 免疫関連プロテインキナーゼ阻害剤 |
| WO2003103654A1 (ja) | 2002-06-10 | 2003-12-18 | 株式会社医薬分子設計研究所 | NF−κB活性化阻害剤 |
| WO2004052856A1 (en) | 2002-12-10 | 2004-06-24 | Wyeth | Substituted indole oxo-acetyl amino acetic acid derivatives as inhibitors of plasminogen activator inhibitor-1 (pai-1) |
| WO2004052893A2 (en) | 2002-12-10 | 2004-06-24 | Wyeth | Substituted dihydropyrano indole-3,4-dione derivatives and 3-oxoacetic acid substituted 2-hydroxymethylindole derivatives as inhibitors of plasminogen activator inhibitor-1 (pai-1) |
| WO2005026127A1 (ja) * | 2003-09-11 | 2005-03-24 | Institute Of Medicinal Molecular Design. Inc. | プラスミノゲンアクチベータインヒビター-1阻害剤 |
| EP1666469A1 (en) | 2003-09-11 | 2006-06-07 | Institute of Medicinal Molecular Design, Inc. | Plasminogen activator inhibitor-1 inhibitor |
| WO2005030192A1 (en) | 2003-09-25 | 2005-04-07 | Wyeth | 4- (1h-indol-3-yl-methylideneaminoxy-propoxy) -benzioc acid derivatives and related compounds as pai-1 inhibitors for the treatment of impairment of the fibrinolytic system and of thrombisis |
| WO2005030204A1 (en) | 2003-09-25 | 2005-04-07 | Wyeth | Substituted oxadiazolidinediones as pai-1 inhibitors |
| WO2005030715A1 (en) | 2003-09-25 | 2005-04-07 | Wyeth | Substituted sulfonamide-indole-2-carboxylic acid derivatives as pai-1 inhibitors |
| WO2005030716A1 (en) | 2003-09-25 | 2005-04-07 | Wyeth | Heterocyclic- or aryloxy, -thio or -amino substituted indoles-2-carboxylic acids or esters as pai-1 |
| WO2005030756A1 (en) | 2003-09-25 | 2005-04-07 | Wyeth | Substituted pyrrole-indoles as inhibitors of pai-1 |
| US20050124664A1 (en) | 2003-10-30 | 2005-06-09 | Eric Sartori | Urea thiadiazole inhibitors of plasminogen activator inhibior-1 |
| US20050124667A1 (en) | 2003-10-30 | 2005-06-09 | Eric Sartori | Oxamide inhibitors of plasminogen activator inhibitor-1 |
| US20050143384A1 (en) | 2003-10-30 | 2005-06-30 | Eric Sartori | Amide thiadiazole inhibitors of plasminogen activator inhibitor-1 |
| WO2006095713A1 (ja) * | 2005-03-08 | 2006-09-14 | Institute Of Medicinal Molecular Design. Inc. | プラスミノゲンアクチベータインヒビター-1阻害剤 |
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| See also references of EP2201946A4 * |
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Cited By (15)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2013501737A (ja) * | 2009-08-14 | 2013-01-17 | バイエル・クロップサイエンス・アーゲー | 殺虫性カルボキサミド類 |
| US9227923B2 (en) | 2009-08-14 | 2016-01-05 | Bayer Intellectual Property Gmbh | Pesticidal carboxamides |
| US12503425B2 (en) | 2012-05-08 | 2025-12-23 | Aeromics, Inc. | Methods of treating or controlling cytotoxic cerebral edema |
| US11873266B2 (en) | 2012-05-08 | 2024-01-16 | Aeromics, Inc. | Methods of treating or controlling cytotoxic cerebral edema consequent to an ischemic stroke |
| US9994514B2 (en) | 2012-05-08 | 2018-06-12 | Aeromics, Inc. | Methods of treating cerebral edema and spinal cord edema |
| US11084778B2 (en) | 2012-05-08 | 2021-08-10 | Aeromics, Inc. | Methods of treating cardiac edema, neuromyelitis optica, and hyponatremia |
| US10894055B2 (en) | 2013-11-06 | 2021-01-19 | Aeromics, Inc. | Pharmaceutical compositions, methods of making pharmaceutical compositions, and kits comprising 2-{[3,5-bis(trifluoromethyl)phenyl]carbamoyl}4-chlorophenyl dihydrogen phosphate |
| US11071744B2 (en) | 2013-11-06 | 2021-07-27 | Aeromics, Inc. | Prodrug salts |
| US10258636B2 (en) | 2013-11-06 | 2019-04-16 | Aeromics, Inc. | Prodrug salts |
| US11801254B2 (en) | 2013-11-06 | 2023-10-31 | Aeromics, Inc. | Pharmaceutical compositions and methods of making pharmaceutical compositions comprising 2-{[3,5-bis(trifluoromethyl)phenyl]carbamoyl}-4-chlorophenyl dihydrogen phosphate |
| US9827253B2 (en) | 2013-11-06 | 2017-11-28 | Aeromics, Inc. | Prodrug salts |
| US12213987B2 (en) | 2013-11-06 | 2025-02-04 | Aeromics, Inc. | Prodrug salts |
| US12496308B2 (en) | 2013-11-06 | 2025-12-16 | Aeromics, Inc. | Methods of administering a pharmaceutically acceptable salt of 2-{[3,5-bis(trifluoromethyl)phenyl]carbamoyl}-4-chlorophenyl dihydrogen phosphate |
| CN107207417A (zh) * | 2014-11-13 | 2017-09-26 | 埃罗米克斯公司 | 新方法 |
| WO2024172001A1 (ja) * | 2023-02-13 | 2024-08-22 | 本岡 知子 | 抗トリパノソーマ薬 |
Also Published As
| Publication number | Publication date |
|---|---|
| KR20100097113A (ko) | 2010-09-02 |
| EP2201946A1 (en) | 2010-06-30 |
| CA2703494A1 (en) | 2009-04-30 |
| RU2010120675A (ru) | 2011-11-27 |
| EP2201946A4 (en) | 2012-01-25 |
| BRPI0816560A2 (pt) | 2015-09-01 |
| JPWO2009054439A1 (ja) | 2011-03-03 |
| CN101842093A (zh) | 2010-09-22 |
| JP5470046B2 (ja) | 2014-04-16 |
| CN101842093B (zh) | 2012-08-22 |
| CN102872020A (zh) | 2013-01-16 |
| AU2008314979A1 (en) | 2009-04-30 |
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