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)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Epidemiology (AREA)
- Biomedical Technology (AREA)
- Cardiology (AREA)
- Heart & Thoracic Surgery (AREA)
- Neurosurgery (AREA)
- Neurology (AREA)
- Urology & Nephrology (AREA)
- Ophthalmology & Optometry (AREA)
- Hematology (AREA)
- Hospice & Palliative Care (AREA)
- Vascular Medicine (AREA)
- Diabetes (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" |
| CN2008801133696A CN101842093B (zh) | 2007-10-23 | 2008-10-23 | Pai-1产生抑制剂 |
| AU2008314979A AU2008314979A1 (en) | 2007-10-23 | 2008-10-23 | Inhibitor of PAI-1 production |
| JP2009538246A JP5470046B2 (ja) | 2007-10-23 | 2008-10-23 | Pai−1産生抑制剤 |
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2007-275557 | 2007-10-23 | ||
| JP2007275557 | 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 |
|---|---|---|---|---|
| EP3391902B1 (en) | 2015-12-18 | 2023-10-18 | Talengen International Limited | Plasminogen for use in the treatment of diabetic angiocardiopathy |
| US11400142B2 (en) | 2015-12-18 | 2022-08-02 | Talengen International Limited | Treatment of diabetic nerve injury comprising administering plasminogen |
| US11090372B2 (en) | 2015-12-18 | 2021-08-17 | Talengen International Limited | Method of treating diabetic nephropathy comprising administering plasminogen |
| DK3395360T3 (da) | 2015-12-18 | 2025-09-15 | Talengen Int Ltd | Plasminogen til forebyggelse eller behandling af diabetisk retinopati |
| WO2018108161A1 (zh) | 2016-12-15 | 2018-06-21 | 深圳瑞健生命科学研究院有限公司 | 一种预防和治疗肥胖症的方法和药物 |
| TW201822803A (zh) | 2016-12-15 | 2018-07-01 | 深圳瑞健生命科學硏究院有限公司 | 一種抑制胰島β細胞凋亡的方法 |
| CN108210904A (zh) * | 2016-12-15 | 2018-06-29 | 深圳瑞健生命科学研究院有限公司 | 治疗动脉粥样硬化及其并发症的药物及其用途 |
| EP3556387A4 (en) | 2016-12-15 | 2020-09-09 | Talengen International Limited | METHOD FOR PREVENTION AND TREATMENT OF LIPID METABOLISM DISORDERS AND RELATED DISEASES |
| 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) |
| 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) |
| WO2003000253A1 (en) | 2001-06-20 | 2003-01-03 | Wyeth | Substituted indole acid derivatives as inhibitors of plasminogen activator inhibitor-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 |
| WO2005030715A1 (en) | 2003-09-25 | 2005-04-07 | Wyeth | Substituted sulfonamide-indole-2-carboxylic acid derivatives as pai-1 inhibitors |
| WO2005030756A1 (en) | 2003-09-25 | 2005-04-07 | Wyeth | Substituted pyrrole-indoles as inhibitors of pai-1 |
| 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 |
| 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)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB1493375A (en) * | 1974-09-20 | 1977-11-30 | Ici Ltd | Salicylanilide derivatives |
| EA008769B1 (ru) * | 2002-06-05 | 2007-08-31 | Инститьют Оф Медисинал Молекьюлар Дизайн. Инк. | Лекарственное средство для лечения диабета |
| EP1535610A4 (en) * | 2002-06-10 | 2008-12-31 | Inst Med Molecular Design Inc | THERAPEUTIC CANCER |
| EP1817287B1 (en) * | 2004-11-24 | 2010-02-10 | Eli Lilly And Company | Aromatic ether derivatives useful as thrombin inhibitors |
-
2008
- 2008-10-23 EP EP08842108A patent/EP2201946A4/en not_active Withdrawn
- 2008-10-23 BR BRPI0816560-2A patent/BRPI0816560A2/pt not_active IP Right Cessation
- 2008-10-23 CA CA2703494A patent/CA2703494A1/en not_active Abandoned
- 2008-10-23 AU AU2008314979A patent/AU2008314979A1/en not_active Abandoned
- 2008-10-23 CN CN2008801133696A patent/CN101842093B/zh not_active Expired - Fee Related
- 2008-10-23 CN CN2012102320448A patent/CN102872020A/zh active Pending
- 2008-10-23 RU RU2010120675/04A patent/RU2010120675A/ru not_active Application Discontinuation
- 2008-10-23 JP JP2009538246A patent/JP5470046B2/ja not_active Expired - Fee Related
- 2008-10-23 WO PCT/JP2008/069207 patent/WO2009054439A1/ja not_active Ceased
- 2008-10-23 KR KR1020107010934A patent/KR20100097113A/ko not_active Ceased
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) |
| 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) |
| WO2003000253A1 (en) | 2001-06-20 | 2003-01-03 | Wyeth | Substituted indole acid derivatives as inhibitors of plasminogen activator inhibitor-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 |
| 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 |
| WO2005030756A1 (en) | 2003-09-25 | 2005-04-07 | Wyeth | Substituted pyrrole-indoles as inhibitors of pai-1 |
| 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 |
| WO2005030715A1 (en) | 2003-09-25 | 2005-04-07 | Wyeth | Substituted sulfonamide-indole-2-carboxylic acid derivatives as pai-1 inhibitors |
| 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 |
Non-Patent Citations (15)
| Title |
|---|
| BIOCHEM. BIOPHYS. RES. COMMUN., vol. 294, no. 5, 2002, pages 1155 - 1160 |
| BIOCHEMISTRY, vol. 37, no. 5, 1998, pages 1227 - 1234 |
| COMP. HEPATOL., vol. 6, 2 May 2007 (2007-05-02), pages 5 |
| FASEB J., vol. 15, no. 10, 2001, pages 1840 - 1842 |
| GEN. DIAGN. PATHOL., vol. 141, no. 1, 1995, pages 41 - 48 |
| J. IMMUNOL., vol. 165, 2000, pages 3154 - 3161 |
| J. IMMUNOL., vol. 165, no. 6, 2000, pages 3154 - 3161 |
| J. MED CHEM., vol. 47, no. 14, 2004, pages 3491 - 3494 |
| MOL. MED., vol. 2, no. 5, 1996, pages 568 - 582 |
| NAT. MED., vol. 4, no. 8, 1998, pages 923 - 928 |
| NATURE, vol. 346, no. 6279, 1990, pages 74 - 76 |
| PATHOBIOLOGY, vol. 71, 2004, pages 295 - 301 |
| PROC. NATL. ACAD. SCI. U. S. A., vol. 89, no. 15, 1992, pages 6998 - 7002 |
| See also references of EP2201946A4 * |
| SPENCER J. R., BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, vol. 12, 2002, pages 2023 - 2026, XP008131173 * |
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 |
| CA2703494A1 (en) | 2009-04-30 |
| EP2201946A1 (en) | 2010-06-30 |
| CN101842093B (zh) | 2012-08-22 |
| AU2008314979A1 (en) | 2009-04-30 |
| JP5470046B2 (ja) | 2014-04-16 |
| BRPI0816560A2 (pt) | 2015-09-01 |
| RU2010120675A (ru) | 2011-11-27 |
| JPWO2009054439A1 (ja) | 2011-03-03 |
| EP2201946A4 (en) | 2012-01-25 |
| CN101842093A (zh) | 2010-09-22 |
| CN102872020A (zh) | 2013-01-16 |
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