AR068947A1 - Inhibidor de la proteina activadora de la 5- lipoxigenasa (flap), composiciones farmaceuticas, sales y solvatos - Google Patents
Inhibidor de la proteina activadora de la 5- lipoxigenasa (flap), composiciones farmaceuticas, sales y solvatosInfo
- Publication number
- AR068947A1 AR068947A1 ARP080104583A ARP080104583A AR068947A1 AR 068947 A1 AR068947 A1 AR 068947A1 AR P080104583 A ARP080104583 A AR P080104583A AR P080104583 A ARP080104583 A AR P080104583A AR 068947 A1 AR068947 A1 AR 068947A1
- Authority
- AR
- Argentina
- Prior art keywords
- pharmaceutically acceptable
- pharmaceutical composition
- pharmaceutical
- methoxypyridin
- ylmethoxy
- Prior art date
Links
- 239000008194 pharmaceutical composition Substances 0.000 title abstract 9
- 239000012453 solvate Substances 0.000 title abstract 5
- 102000001381 Arachidonate 5-Lipoxygenase Human genes 0.000 title 1
- 108010093579 Arachidonate 5-lipoxygenase Proteins 0.000 title 1
- 230000003213 activating effect Effects 0.000 title 1
- 239000003112 inhibitor Substances 0.000 title 1
- 102000004169 proteins and genes Human genes 0.000 title 1
- 108090000623 proteins and genes Proteins 0.000 title 1
- -1 pyridin-2-ylmethoxy Chemical group 0.000 abstract 10
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 abstract 4
- GUBGYTABKSRVRQ-UHFFFAOYSA-N 2-(hydroxymethyl)-6-[4,5,6-trihydroxy-2-(hydroxymethyl)oxan-3-yl]oxyoxane-3,4,5-triol Chemical compound OCC1OC(OC2C(O)C(O)C(O)OC2CO)C(O)C(O)C1O GUBGYTABKSRVRQ-UHFFFAOYSA-N 0.000 abstract 2
- IWTFOFMTUOBLHG-UHFFFAOYSA-N 2-methoxypyridine Chemical compound COC1=CC=CC=N1 IWTFOFMTUOBLHG-UHFFFAOYSA-N 0.000 abstract 2
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 abstract 2
- 239000002253 acid Substances 0.000 abstract 2
- 150000002617 leukotrienes Chemical class 0.000 abstract 2
- HQKMJHAJHXVSDF-UHFFFAOYSA-L magnesium stearate Chemical compound [Mg+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O HQKMJHAJHXVSDF-UHFFFAOYSA-L 0.000 abstract 2
- 150000003839 salts Chemical class 0.000 abstract 2
- FBPFZTCFMRRESA-KVTDHHQDSA-N D-Mannitol Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-KVTDHHQDSA-N 0.000 abstract 1
- 241000124008 Mammalia Species 0.000 abstract 1
- 229930195725 Mannitol Natural products 0.000 abstract 1
- WHNWPMSKXPGLAX-UHFFFAOYSA-N N-Vinyl-2-pyrrolidone Chemical compound C=CN1CCCC1=O WHNWPMSKXPGLAX-UHFFFAOYSA-N 0.000 abstract 1
- 239000004480 active ingredient Substances 0.000 abstract 1
- 229940125715 antihistaminic agent Drugs 0.000 abstract 1
- 239000000739 antihistaminic agent Substances 0.000 abstract 1
- 229940125388 beta agonist Drugs 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- 229960000913 crospovidone Drugs 0.000 abstract 1
- 201000010099 disease Diseases 0.000 abstract 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 abstract 1
- 239000005414 inactive ingredient Substances 0.000 abstract 1
- 239000004615 ingredient Substances 0.000 abstract 1
- 229940125369 inhaled corticosteroids Drugs 0.000 abstract 1
- 229940125389 long-acting beta agonist Drugs 0.000 abstract 1
- 235000019359 magnesium stearate Nutrition 0.000 abstract 1
- 239000000594 mannitol Substances 0.000 abstract 1
- 235000010355 mannitol Nutrition 0.000 abstract 1
- 239000000203 mixture Substances 0.000 abstract 1
- 239000008203 oral pharmaceutical composition Substances 0.000 abstract 1
- 239000008184 oral solid dosage form Substances 0.000 abstract 1
- 229910052763 palladium Inorganic materials 0.000 abstract 1
- 239000008177 pharmaceutical agent Substances 0.000 abstract 1
- 235000013809 polyvinylpolypyrrolidone Nutrition 0.000 abstract 1
- 229920000523 polyvinylpolypyrrolidone Polymers 0.000 abstract 1
- 208000023504 respiratory system disease Diseases 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/10—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a carbon chain containing aromatic rings
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/04—Drugs for disorders of the alimentary tract or the digestive system for ulcers, gastritis or reflux esophagitis, e.g. antacids, inhibitors of acid secretion, mucosal protectants
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
- A61P11/02—Nasal agents, e.g. decongestants
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
- A61P11/06—Antiasthmatics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
- A61P11/08—Bronchodilators
-
- 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
- A61P25/04—Centrally acting analgesics, e.g. opioids
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
-
- 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
- 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
- A61P9/12—Antihypertensives
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing three or more hetero rings
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Public Health (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Pulmonology (AREA)
- Cardiology (AREA)
- Pain & Pain Management (AREA)
- Heart & Thoracic Surgery (AREA)
- Biomedical Technology (AREA)
- Neurology (AREA)
- Neurosurgery (AREA)
- Rheumatology (AREA)
- Otolaryngology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Medicinal Preparation (AREA)
- Plural Heterocyclic Compounds (AREA)
Abstract
Composiciones farmacéuticas adecuadas para administracion oral a un mamífero, así como métodos de uso de tales composiciones farmacéuticas orales para el tratamiento de enfermedades o condiciones respiratorias, así como otras enfermedades o condiciones que dependen del leucotrieno o en las cuales interviene el leucotrieno. Reivindicacion 1: Se reivindica una composicion farmacéutica que comprende: a) un ácido 3-[5-(piridin-2-ilmetoxi)-3-(2-metil-2-propiltio)-1-[4-(2-metoxipiridin-5-il)bencil]-indol-2-il]-2,2-dimetil-propionico, o un solvato farmacéuticamente aceptable de éste, o una sal farmacéuticamente aceptable de ácido 3-[5-(piridin-2-ilmetoxi)-3-(2-metil-2-propiltio)-1-[4-(2-metoxipiridin-5-il)bencil]-indol-2-il]j-2,2-dimetil-propionico o solvato farmacéuticamente aceptable de éste, como el principio activo en la composicion farmacéutica; y b) al menos un ingrediente inactivo farmacéuticamente aceptable. Reivindicacion 2: La composicion farmacéutica de la reivindicacion 1 en donde: un ácido 3-[5-(piridin-2-ilmetoxi)-3-(2-metil-2-propiltio)-1-[4-(2-metoxipiridin-5-il)bencil]-indol-2-il]-2,2-dimetil-propionico, o un solvato farmacéuticamente aceptable de éste, o una sal farmacéuticamente aceptable de ácido 3-[5-(piridin-2-ilmetoxi)-3-(2-metil-2-propiltio)-1-[4-(2-metoxipiridin-5-il)bencil]-indol-2-il]-2,2-dimetil-propionico o solvato farmacéuticamente aceptable de éste, está en fase amorfa, es una forma parcialmente cristalina o una forma cristalina. Reivindicacion 13: La composicion farmacéutica de la reivindicacion 9, en donde la composicion farmacéutica comprende una cantidad detectable de paladio menor de alrededor de 20ppm. Reivindicacion 27: La composicion farmacéutica de la reivindicacion 14, en donde la composicion farmacéutica comprende una cantidad detectable de un compuesto seleccionado del grupo de formulas (2). Reivindicacion 66: La composicion farmacéutica de forma de dosificacion solida oral de la reivindicacion 64, en donde: los ingredientes farmacéuticos inactivos incluyen celulosa microcristalina silicificada (SMCC), manitol, crospovidona y estearato de magnesio. Reivindicacion 88: El método de una cualquiera de las reivindicaciones 84-86, en donde el método además comprende la administracion de al menos otro agente farmacéutico seleccionado de corticoesteroides inhalados, agonistas beta de corta duracion, agonistas beta de accion prolongada y antihistaminas.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US98312407P | 2007-10-26 | 2007-10-26 | |
| US98311907P | 2007-10-26 | 2007-10-26 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AR068947A1 true AR068947A1 (es) | 2009-12-16 |
Family
ID=40580422
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ARP080104583A AR068947A1 (es) | 2007-10-26 | 2008-10-21 | Inhibidor de la proteina activadora de la 5- lipoxigenasa (flap), composiciones farmaceuticas, sales y solvatos |
Country Status (17)
| Country | Link |
|---|---|
| US (1) | US8697730B2 (es) |
| EP (1) | EP2212312A4 (es) |
| JP (1) | JP2011500846A (es) |
| KR (1) | KR20100080561A (es) |
| CN (1) | CN101910154A (es) |
| AR (1) | AR068947A1 (es) |
| AU (1) | AU2008316615A1 (es) |
| BR (1) | BRPI0818831A2 (es) |
| CA (1) | CA2702798A1 (es) |
| CL (1) | CL2008003181A1 (es) |
| EA (1) | EA201000486A1 (es) |
| MX (1) | MX2010004501A (es) |
| PE (1) | PE20090948A1 (es) |
| TW (1) | TW200920369A (es) |
| UY (1) | UY31431A1 (es) |
| WO (1) | WO2009055721A2 (es) |
| ZA (1) | ZA201002692B (es) |
Families Citing this family (17)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB2431927B (en) | 2005-11-04 | 2010-03-17 | Amira Pharmaceuticals Inc | 5-Lipoxygenase-activating protein (FLAP) inhibitors |
| US7977359B2 (en) | 2005-11-04 | 2011-07-12 | Amira Pharmaceuticals, Inc. | 5-lipdxygenase-activating protein (FLAP) inhibitors |
| US8399666B2 (en) | 2005-11-04 | 2013-03-19 | Panmira Pharmaceuticals, Llc | 5-lipoxygenase-activating protein (FLAP) inhibitors |
| EP2086531A4 (en) * | 2006-11-30 | 2009-09-30 | Amira Pharmaceuticals Inc | COMPOSITIONS AND TREATMENTS COMPRISING 5-LIPOXYGENASE-ACTIVATING PROTEIN INHIBITORS AND NITRIC OXIDE MODULATORS |
| SG190667A1 (en) | 2008-05-23 | 2013-06-28 | Panmira Pharmaceuticals Llc | 5-lipoxygenase-activating protein inhibitor |
| CA2793742C (en) * | 2010-03-23 | 2015-06-23 | Scinopharm Taiwan Ltd. | Process and intermediates for preparing lapatinib |
| KR101137929B1 (ko) * | 2010-05-31 | 2012-05-09 | 에스케이하이닉스 주식회사 | 비휘발성 메모리 장치 및 그 제조 방법 |
| WO2014031586A2 (en) * | 2012-08-20 | 2014-02-27 | Tallikut Pharmaceuticals, Inc. | Methods for treating cardiovascular diseases |
| WO2014204511A2 (en) | 2013-06-18 | 2014-12-24 | Isonea Limited | Compliance monitoring for asthma inhalers |
| US9802920B2 (en) | 2013-12-13 | 2017-10-31 | Hoffman-La Roche Inc. | Inhibitors of bruton's tyrosine kinase |
| JP6219523B2 (ja) | 2013-12-13 | 2017-10-25 | エフ.ホフマン−ラ ロシュ アーゲーF. Hoffmann−La Roche Aktiengesellschaft | ブルトンチロシンキナーゼの阻害剤 |
| CA2929747C (en) | 2013-12-13 | 2018-01-23 | F. Hoffmann-La Roche Ag | Inhibitors of bruton's tyrosine kinase |
| US10080748B2 (en) | 2014-02-04 | 2018-09-25 | Bioscience Pharma Partners, Llc | Use of flap inhibitors to reduce neuroinflammation mediated injury in the central nervous system |
| WO2017100212A1 (en) * | 2015-12-08 | 2017-06-15 | Biomatrica, Inc. | Reduction of erythrocyte sedimentation rate |
| CN112126986B (zh) * | 2020-04-30 | 2023-07-18 | 苏州京脉生物科技有限公司 | 一种定量miRNA的测序文库制备和分析方法 |
| CN115267002A (zh) * | 2022-08-08 | 2022-11-01 | 江苏慧聚药业股份有限公司 | Gc-ms/ms联用测定醰露替尼中游离肼的方法 |
| CN117665187B (zh) * | 2023-11-23 | 2024-08-16 | 宁波大红鹰药业股份有限公司 | 一种舒林酸中间体杂质的测定方法 |
Family Cites Families (126)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2431491A1 (fr) | 1978-07-18 | 1980-02-15 | Delalande Sa | Nouveaux derives aminoalkoxy-5 benzofurannes et indoles, leur procede de preparation et leur application en therapeutique |
| DK151884C (da) * | 1979-03-07 | 1988-06-13 | Pfizer | Analogifremgangsmaade til fremstilling af 3-(1-imidazolylalkyl)indolderivater eller farmaceutisk acceptable syreadditionssalte deraf |
| JPS60123485A (ja) * | 1983-12-08 | 1985-07-02 | Yoshitomi Pharmaceut Ind Ltd | インド−ル−3−カルボキサミド誘導体 |
| US5109009A (en) * | 1985-03-08 | 1992-04-28 | Leo Pharmaceutical Products Ltd. | Quinoline and pyridine compounds and inhibition of 5-lipoxygenases therewith |
| IE58870B1 (en) * | 1985-03-08 | 1993-11-17 | Leo Pharm Prod Ltd | Pyridine derivatives |
| US5081138A (en) * | 1986-12-17 | 1992-01-14 | Merck Frosst Canada, Inc. | 3-hetero-substituted-n-benzyl-indoles and prevention of leucotriene synthesis therewith |
| US5225421A (en) * | 1986-12-17 | 1993-07-06 | Merck Frosst Canada, Inc. | 3-hetero-substituted-N-benzyl-indoles and medical methods of use therefor |
| US5232916A (en) * | 1988-06-27 | 1993-08-03 | Merck Frosst Canada, Inc. | Quinoline ether alkanoic acids |
| CA1337427C (en) | 1989-08-22 | 1995-10-24 | Merck Frosst Canada Incorporated | (quinolin-2-ylmethoxy)indoles as inhibitors of the biosynthesis of leukotrienes |
| US5272145A (en) * | 1989-08-22 | 1993-12-21 | Merck Frosst Canada, Inc. | (Quinolin-2-ylmethoxy)indoles as inhibitors of the biosynthesis of leukotrienes |
| US5204344A (en) * | 1989-08-22 | 1993-04-20 | Merck Frosst Canada, Inc. | (Quinolin-2-ylmethoxy)indoles as inhibitors of the biosynthesis of leukotrienes |
| NZ234883A (en) | 1989-08-22 | 1995-01-27 | Merck Frosst Canada Inc | Quinolin-2-ylmethoxy indole derivatives, preparation and pharmaceutical compositions thereof |
| US5252585A (en) * | 1992-02-03 | 1993-10-12 | Merck Frosst Canada, Inc. | Fluorinated quinoline indoles as inhibitors of the biosynthesis of leukotrienes |
| US5420289A (en) * | 1989-10-27 | 1995-05-30 | American Home Products Corporation | Substituted indole-, indene-, pyranoindole- and tetrahydrocarbazole-alkanoic acid derivatives as inhibitors of PLA2 and lipoxygenase |
| US5229516A (en) * | 1989-10-27 | 1993-07-20 | American Home Products Corporation | Substituted indole-, indene-, pyranoindole- and tetrahydrocarbazole-alkanoic acid derivatives as inhibitors of PLA2 and lipoxygenase |
| CA2032253C (en) | 1989-12-15 | 2000-11-28 | John W. Gillard | 5-lipoxygenase activating protein |
| US5093356A (en) * | 1990-01-16 | 1992-03-03 | Merck Frosst Canada, Inc. | Indenyl hydroxamic acids and hydroxy ureas as inhibitors of 5-lipoxygenase |
| US5081145A (en) * | 1990-02-01 | 1992-01-14 | Merck Frosst Canada, Inc. | Indole-2-alkanoic acids compositions of and anti allergic use thereof |
| US5095031A (en) * | 1990-08-20 | 1992-03-10 | Abbott Laboratories | Indole derivatives which inhibit leukotriene biosynthesis |
| JPH0764841B2 (ja) * | 1990-10-03 | 1995-07-12 | ファイザー製薬株式会社 | インドール誘導体およびその用途 |
| US5182367A (en) * | 1990-11-30 | 1993-01-26 | Merck & Co., Inc. | 5-lipoxygenase activating protein |
| GB9108811D0 (en) | 1991-04-24 | 1991-06-12 | Erba Carlo Spa | N-imidazolyl derivatives of substituted indole |
| US5202321A (en) * | 1991-06-13 | 1993-04-13 | Merck Frosst Canada, Inc. | Thiopyrano[2,3,4-c,d]indoles as inhibitors of leukotriene biosynthesis |
| JPH06100551A (ja) | 1991-09-06 | 1994-04-12 | Dainippon Ink & Chem Inc | 光学活性な2,5置換テトラヒドロフラン誘導体、その製造方法、その誘導体を含む液晶組成物及び液晶表示素子 |
| US5190968A (en) * | 1991-09-30 | 1993-03-02 | Merck Frosst Canada, Inc. | (Polycyclic-arylmethoxy) indoles as inhibitors of leukotriene biosynthesis |
| US5389650A (en) * | 1991-09-30 | 1995-02-14 | Merck Frosst Canada, Inc. | (Azaarylmethoxy)indoles as inhibitors of leukotriene biosynthesis |
| CA2079374C (en) | 1991-09-30 | 2003-08-05 | Merck Frosst Canada Incorporated | (bicyclic-azaarylmethoxy)indoles as inhibitors of leukotriene biosynthesis |
| US5290798A (en) * | 1991-09-30 | 1994-03-01 | Merck Frosst Canada, Inc. | (hetero-arylmethoxy)indoles as inhibitors of leukotriene biosynthesis |
| US5273980A (en) * | 1991-09-30 | 1993-12-28 | Merck Frosst Canada Inc. | Bicyclic-azaarylmethoxy) indoles as inhibitors of leukotriene biosynthesis |
| US5308850A (en) * | 1991-09-30 | 1994-05-03 | Merck Frosst Canada, Inc. | (Bicyclic-hetero-arylmethoxy)indoles as inhibitors of leukotriene biosynthesis |
| ZA928276B (en) | 1991-10-31 | 1993-05-06 | Daiichi Seiyaku Co | Aromatic amidine derivates and salts thereof. |
| US5254567A (en) * | 1991-11-15 | 1993-10-19 | Merck Frosst Canada, Inc. | Amorphous (quinolin-2-ylmethoxy)indole compounds which have useful pharmaceutical utility |
| CH683522A5 (de) | 1992-03-13 | 1994-03-31 | Hoffmann La Roche | Verfahren zur Herstellung von Diarylen. |
| EP0597112A4 (en) | 1992-03-27 | 1994-06-22 | Kyoto Pharma Ind | Novel imidazole derivative, pharmaceutical use thereof, and intermediate therefor. |
| SK279958B6 (sk) * | 1992-04-02 | 1999-06-11 | Smithkline Beecham Corporation | Zlúčeniny s protialergickým a protizápalovým účink |
| JPH0658881A (ja) | 1992-06-12 | 1994-03-04 | Mitsubishi Rayon Co Ltd | 光学活性化合物の絶対配置判定法、絶対配置判定用試薬及び絶対配置判定装置 |
| US5334719A (en) * | 1992-06-17 | 1994-08-02 | Merck Frosst Canada, Inc. | Bicyclic(azaaromatic)indoles as inhibitors of leukotriene bisynthesis |
| US5314898A (en) * | 1992-06-29 | 1994-05-24 | Merck & Co., Inc. | Aryl thiopyrano[4,3,2-cd]indoles as inhibitors of leukotriene biosynthesis |
| US5288743A (en) * | 1992-11-20 | 1994-02-22 | Abbott Laboratories | Indole carboxylate derivatives which inhibit leukotriene biosynthesis |
| JP3457694B2 (ja) | 1993-02-04 | 2003-10-20 | 第一製薬株式会社 | インフルエンザ感染予防・治療薬 |
| US5374635A (en) * | 1993-03-29 | 1994-12-20 | Merck Frosst Canada, Inc. | Furo[3,2-b]pyridines and thieno[3,2-b]pyridines as inhibitors of leukotriene biosynthesis |
| JPH075651A (ja) | 1993-06-14 | 1995-01-10 | Fuji Photo Film Co Ltd | ハロゲン化銀カラー写真感光材料の処理方法 |
| DE4338770A1 (de) | 1993-11-12 | 1995-05-18 | Matthias Dr Lehr | Indol-2-alkansäuren und ihre Derivate als Hemmstoffe der Phospholipase A¶2¶ |
| US5399699A (en) * | 1994-01-24 | 1995-03-21 | Abbott Laboratories | Indole iminooxy derivatives which inhibit leukotriene biosynthesis |
| US5420282A (en) * | 1994-02-15 | 1995-05-30 | Abbott Laboratories | Thiopyrano(2,3,4-c,d) indolyloxime ether alkylcarboxylates |
| US5696076A (en) * | 1994-06-22 | 1997-12-09 | Human Genome Sciences, Inc. | 5-lipoxygenase-activating protein II |
| FR2721610B1 (fr) * | 1994-06-28 | 1996-08-23 | Adir | Nouveaux dérivés (thia)cycloalkyl [b] indoles, leur procédé de préparation et les compositions pharmaceutiques qui les contiennent. |
| JPH0820532A (ja) | 1994-07-05 | 1996-01-23 | Dai Ichi Seiyaku Co Ltd | 抗膵炎剤 |
| TW396200B (en) * | 1994-10-19 | 2000-07-01 | Sumitomo Chemical Co | Liquid crystal composition and liquid crystal element containing such composition |
| US5702637A (en) * | 1995-04-19 | 1997-12-30 | Minnesota Mining And Manufacturing Company | Liquid crystal compounds having a chiral fluorinated terminal portion |
| JPH092977A (ja) | 1995-06-21 | 1997-01-07 | Dai Ichi Seiyaku Co Ltd | 経口投与用医薬組成物 |
| US5750558A (en) * | 1996-06-06 | 1998-05-12 | Abbott Laboratories | Oxime derivatives of indole and indene compounds as inhibitors of prostaglandin biosynthesis |
| US5877329A (en) * | 1996-08-13 | 1999-03-02 | Merck & Co., Inc. | Palladium catalyzed indolization |
| JPH1180032A (ja) | 1997-09-12 | 1999-03-23 | Dai Ichi Seiyaku Co Ltd | 複合体 |
| JPH11189531A (ja) | 1997-12-26 | 1999-07-13 | Dai Ichi Seiyaku Co Ltd | 経粘膜投与用医薬組成物 |
| JPH11193265A (ja) | 1997-12-26 | 1999-07-21 | Dai Ichi Seiyaku Co Ltd | 3−(7−アミジノ−2−ナフチル)−2−フェニルプロピオン酸誘導体の塩 |
| CA2260499A1 (en) | 1998-01-29 | 1999-07-29 | Sumitomo Pharmaceuticals Company Limited | Pharmaceutical compositions for the treatment of ischemic brain damage |
| US6500853B1 (en) * | 1998-02-28 | 2002-12-31 | Genetics Institute, Llc | Inhibitors of phospholipase enzymes |
| ES2272061T5 (es) * | 1998-04-15 | 2012-02-24 | Merck Serono Biodevelopment | Secuencia genómica de la proteína activadora de 5-lipoxigenasa (flap), marcadores polimórficos de la misma y métodos para la detección de asma. |
| US6867209B1 (en) * | 1998-05-22 | 2005-03-15 | Scios, Inc. | Indole-type derivatives as inhibitors of p38 kinase |
| JP2000007590A (ja) | 1998-06-23 | 2000-01-11 | Daicel Chem Ind Ltd | 置換芳香族化合物の製造方法 |
| JP2000302671A (ja) | 1999-04-27 | 2000-10-31 | Hitoshi Sezaki | 経口投与用医薬組成物 |
| DE19948417A1 (de) * | 1999-10-07 | 2001-04-19 | Morphochem Ag | Imidazol-Derivate und ihre Verwendung als Arzneimittel |
| JP2001139462A (ja) | 1999-11-10 | 2001-05-22 | Dai Ichi Seiyaku Co Ltd | 新規製剤 |
| US20010039037A1 (en) * | 2000-04-05 | 2001-11-08 | Lee Harland | Novel polypeptide |
| WO2001096336A2 (en) * | 2000-06-14 | 2001-12-20 | Warner-Lambert Company | 6,5-fused bicyclic heterocycles |
| JP2002226429A (ja) | 2001-02-06 | 2002-08-14 | Fuji Photo Film Co Ltd | アクリル酸エステル化合物の製造方法 |
| US6627646B2 (en) * | 2001-07-17 | 2003-09-30 | Sepracor Inc. | Norastemizole polymorphs |
| EP1314733A1 (en) | 2001-11-22 | 2003-05-28 | Aventis Pharma Deutschland GmbH | Indole-2-carboxamides as factor Xa inhibitors |
| USH2153H1 (en) * | 2002-04-24 | 2006-04-04 | Smithkline Beecham Corp. | Association of asthma with polymorphisms in the cysteinyl leukotriene 2 receptor |
| JPWO2004000795A1 (ja) | 2002-06-20 | 2005-10-20 | 協和醗酵工業株式会社 | ビニルパーフルオロアルカンスルホン酸エステル誘導体の製造法 |
| HRP20050181A2 (en) | 2002-08-29 | 2006-03-31 | Merck & Co. Inc. | Indoles having anti-diabetic activity |
| AU2003292508A1 (en) | 2002-11-28 | 2004-06-18 | Suven Life Sciences Limited | N-arylalkyl-3-aminoalkoxyindoles and their use as 5-ht ligands |
| US20040198800A1 (en) * | 2002-12-19 | 2004-10-07 | Geoffrey Allan | Lipoxygenase inhibitors as hypolipidemic and anti-hypertensive agents |
| GB0301350D0 (en) | 2003-01-21 | 2003-02-19 | Merck Sharp & Dohme | Therapeutic agents |
| JP4513351B2 (ja) | 2003-02-12 | 2010-07-28 | チッソ株式会社 | 結合基にフッ素化されたアルキル基を有する液晶性化合物、液晶組成物および液晶表示素子 |
| WO2004078719A1 (ja) | 2003-03-06 | 2004-09-16 | Ono Pharmaceutical Co., Ltd. | インドール誘導体化合物およびその化合物を有効成分とする薬剤 |
| EP1479677A1 (en) | 2003-05-19 | 2004-11-24 | Aventis Pharma Deutschland GmbH | New indole derivatives as factor xa inhibitors |
| WO2004108671A1 (en) | 2003-06-06 | 2004-12-16 | Suven Life Sciences Limited | Substituted indoles with serotonin receptor affinity, process for their preparation and pharmaceutical compositions containing them |
| JP2006528630A (ja) * | 2003-07-24 | 2006-12-21 | メルク エンド カムパニー インコーポレーテッド | ジフェニル置換シクロアルカン類、そのような化合物を含む組成物、ならびに使用方法 |
| WO2005019381A1 (en) | 2003-08-25 | 2005-03-03 | Merck Patent Gmbh | Liquid crystalline medium |
| AU2004270187A1 (en) | 2003-09-04 | 2005-03-17 | Aventis Pharmaceuticals Inc. | Substituted indoles as inhibitors of poly (ADP-ribose) polymerase (PARP) |
| JP4363133B2 (ja) | 2003-09-09 | 2009-11-11 | 東洋インキ製造株式会社 | 有機エレクトロルミネッセンス用素子材料およびそれを用いた有機エレクトロルミネッセンス素子 |
| US7268159B2 (en) | 2003-09-25 | 2007-09-11 | Wyeth | Substituted indoles |
| JP2005170939A (ja) | 2003-11-20 | 2005-06-30 | Takeda Chem Ind Ltd | 糖尿病の予防・治療剤 |
| WO2005054176A1 (en) | 2003-11-25 | 2005-06-16 | Eli Lilly And Company | Peroxisome proliferator activated receptor modulators |
| US20070054902A1 (en) | 2003-12-02 | 2007-03-08 | Shionogi & Co., Ltd. | Isoxazole derivatives as peroxisome proliferator-activated receptors agonists |
| EP1708997B1 (en) | 2003-12-03 | 2009-10-21 | Merck and Co., Inc. | 1-alkyl-3-thio-substituted indole-2-alkynoic acids useful for the treatment for alzheimer's disease and related conditions |
| JP5142450B2 (ja) | 2003-12-25 | 2013-02-13 | 徹也 西尾 | ジアミノ化合物、ビニル化合物、高分子化合物、配向膜、該配向膜を用いた有機半導体装置、導電性高分子、該導電性高分子を使用したエレクトロルミネッセンス素子、液晶配向膜、及び該液晶配向膜を用いた光学素子 |
| WO2005066157A1 (en) | 2004-01-02 | 2005-07-21 | Suven Life Sciences | 3-(pyrolidin-3-l) indoles as 5-ht6 receptor modulators |
| JP2005194250A (ja) | 2004-01-09 | 2005-07-21 | Sumitomo Chemical Takeda Agro Co Ltd | トリアゾール化合物、その製造法および用途 |
| WO2005082346A1 (en) | 2004-02-26 | 2005-09-09 | Merck & Co, Inc. | Use of cysteinyl leukotriene 2 receptor antagonists |
| CA2564563C (en) * | 2004-05-03 | 2011-07-05 | F. Hoffmann-La Roche Ag | Indolyl derivatives as liver-x-receptor modulators |
| JP2008502670A (ja) | 2004-06-18 | 2008-01-31 | バイオリポックス エービー | 炎症の治療に有用なインドール類 |
| WO2006014262A2 (en) | 2004-07-02 | 2006-02-09 | Merck & Co., Inc. | Indoles having anti-diabetic activity |
| GB0420719D0 (en) | 2004-09-17 | 2004-10-20 | Addex Pharmaceuticals Sa | Novel allosteric modulators |
| WO2006041961A1 (en) | 2004-10-05 | 2006-04-20 | GOVERNMENT OF THE UNITED STATES OF AMERICA, as represented by THE SECRETARY, DEPARTMENT OF HEALTHAND HUMAN SERVICES | Arylthioindole tubulin polymerization inhibitors and methods of treating or preventing cancer using same |
| US7947694B2 (en) | 2005-01-14 | 2011-05-24 | Janssen Pharmaceutica Nv | Substituted pyrazolo[3,4-D]pyrimidines as cell cycle kinase inhibitors |
| US20080249091A1 (en) | 2005-01-19 | 2008-10-09 | Benjamin Pelcman | Indoles Useful in the Treatment of Inflammation |
| US20100197687A1 (en) | 2005-01-19 | 2010-08-05 | Benjamin Pelcman | Indoles Useful in the Treatment of Inflammation |
| EP1838669A1 (en) | 2005-01-19 | 2007-10-03 | Biolipox AB | Indoles useful in the treatment of inflammation |
| KR20070114123A (ko) | 2005-01-19 | 2007-11-29 | 바이올리폭스 에이비 | 염증 치료에 유용한 인돌 |
| CA2600860A1 (en) | 2005-03-09 | 2006-09-21 | Merck & Co., Inc. | Diphenyl substituted cycloalkanes, compositions containing such compounds and methods of use |
| RU2453540C2 (ru) | 2005-04-21 | 2012-06-20 | Лаборатуар Сероно С.А. | 2,3-замещенные пиразинсульфонамиды в качестве ингибиторов crth2 |
| GB0516156D0 (en) | 2005-08-05 | 2005-09-14 | Eisai London Res Lab Ltd | JNK inhibitors |
| US7405302B2 (en) * | 2005-10-11 | 2008-07-29 | Amira Pharmaceuticals, Inc. | 5-lipoxygenase-activating protein (FLAP) inhibitors |
| CN101360731B (zh) | 2005-10-11 | 2013-01-30 | 联邦高等教育系统-匹兹堡大学 | 作为淀粉样发生蛋白成像剂的同位素标记苯并呋喃化合物 |
| GB2431927B (en) | 2005-11-04 | 2010-03-17 | Amira Pharmaceuticals Inc | 5-Lipoxygenase-activating protein (FLAP) inhibitors |
| US20070225285A1 (en) | 2005-11-04 | 2007-09-27 | Amira Pharmaceuticals, Inc. | 5-lipoxygenase-activating protein (flap) inhibitors |
| US8399666B2 (en) * | 2005-11-04 | 2013-03-19 | Panmira Pharmaceuticals, Llc | 5-lipoxygenase-activating protein (FLAP) inhibitors |
| US20070244128A1 (en) * | 2005-11-04 | 2007-10-18 | Amira Pharmaceuticals, Inc. | 5-lipoxygenase-activating protein (flap) inhibitors |
| UY29896A1 (es) | 2005-11-04 | 2007-06-29 | Astrazeneca Ab | Nuevos derivados de cromano, composiciones farmacéuticas conteniéndolos, procesos de preparación y aplicaciones |
| US20070219206A1 (en) * | 2005-11-04 | 2007-09-20 | Amira Pharmaceuticals, Inc. | 5-lipoxygenase-activating protein (flap) inhibitors |
| UY29892A1 (es) | 2005-11-04 | 2007-06-29 | Astrazeneca Ab | Nuevos derivados de cromano, composiciones farmaceuticas conteniendolos, procesos de preparacion y aplicaciones |
| US7977359B2 (en) | 2005-11-04 | 2011-07-12 | Amira Pharmaceuticals, Inc. | 5-lipdxygenase-activating protein (FLAP) inhibitors |
| TW200815377A (en) | 2006-04-24 | 2008-04-01 | Astellas Pharma Inc | Oxadiazolidinedione compound |
| CA2656564C (en) | 2006-06-29 | 2015-06-16 | Kinex Pharmaceuticals, Llc | Biaryl compositions and methods for modulating a kinase cascade |
| JP2009023986A (ja) | 2006-11-08 | 2009-02-05 | Pharma Ip | 抗癌剤としてのビアリール誘導体 |
| EP3048099A3 (en) | 2006-11-15 | 2016-09-21 | YM BioSciences Australia Pty Ltd | Inhibitors of kinase activity |
| EP2086531A4 (en) | 2006-11-30 | 2009-09-30 | Amira Pharmaceuticals Inc | COMPOSITIONS AND TREATMENTS COMPRISING 5-LIPOXYGENASE-ACTIVATING PROTEIN INHIBITORS AND NITRIC OXIDE MODULATORS |
| JP2010518025A (ja) | 2007-02-05 | 2010-05-27 | アミラ ファーマシューティカルス,インコーポレーテッド | 5−リポキシゲナーゼ活性化タンパク質(flap)インヒビターとしての逆インドール |
| US8039505B2 (en) * | 2007-04-11 | 2011-10-18 | University Of Utah Research Foundation | Compounds for modulating T-cells |
| WO2009002746A1 (en) | 2007-06-22 | 2008-12-31 | Decode Genetics Ehf. | Dosing schedules of leukotriene synthesis inhibitors for human therapy |
| SG190667A1 (en) | 2008-05-23 | 2013-06-28 | Panmira Pharmaceuticals Llc | 5-lipoxygenase-activating protein inhibitor |
| US8546431B2 (en) * | 2008-10-01 | 2013-10-01 | Panmira Pharmaceuticals, Llc | 5-lipoxygenase-activating protein (FLAP) inhibitors |
| CA2779786A1 (en) * | 2009-11-03 | 2011-05-12 | Claire Frances Crawford | Novel processes |
-
2008
- 2008-10-09 TW TW097139061A patent/TW200920369A/zh unknown
- 2008-10-21 AR ARP080104583A patent/AR068947A1/es not_active Application Discontinuation
- 2008-10-23 PE PE2008001818A patent/PE20090948A1/es not_active Application Discontinuation
- 2008-10-24 MX MX2010004501A patent/MX2010004501A/es unknown
- 2008-10-24 EA EA201000486A patent/EA201000486A1/ru unknown
- 2008-10-24 CN CN2008801235755A patent/CN101910154A/zh active Pending
- 2008-10-24 KR KR1020107011485A patent/KR20100080561A/ko not_active Withdrawn
- 2008-10-24 WO PCT/US2008/081190 patent/WO2009055721A2/en not_active Ceased
- 2008-10-24 EP EP08842178A patent/EP2212312A4/en not_active Withdrawn
- 2008-10-24 CA CA2702798A patent/CA2702798A1/en not_active Abandoned
- 2008-10-24 JP JP2010531287A patent/JP2011500846A/ja active Pending
- 2008-10-24 AU AU2008316615A patent/AU2008316615A1/en not_active Abandoned
- 2008-10-24 US US12/257,876 patent/US8697730B2/en not_active Expired - Fee Related
- 2008-10-24 UY UY31431A patent/UY31431A1/es unknown
- 2008-10-24 BR BRPI0818831 patent/BRPI0818831A2/pt not_active Application Discontinuation
- 2008-10-24 CL CL2008003181A patent/CL2008003181A1/es unknown
-
2010
- 2010-04-16 ZA ZA2010/02692A patent/ZA201002692B/en unknown
Also Published As
| Publication number | Publication date |
|---|---|
| TW200920369A (en) | 2009-05-16 |
| WO2009055721A3 (en) | 2009-08-20 |
| EP2212312A2 (en) | 2010-08-04 |
| CN101910154A (zh) | 2010-12-08 |
| CL2008003181A1 (es) | 2009-03-06 |
| KR20100080561A (ko) | 2010-07-08 |
| MX2010004501A (es) | 2010-05-13 |
| US20100075934A1 (en) | 2010-03-25 |
| EP2212312A4 (en) | 2011-10-05 |
| UY31431A1 (es) | 2009-05-29 |
| EA201000486A1 (ru) | 2010-12-30 |
| CA2702798A1 (en) | 2009-04-30 |
| BRPI0818831A2 (pt) | 2015-04-22 |
| PE20090948A1 (es) | 2009-07-27 |
| AU2008316615A1 (en) | 2009-04-30 |
| WO2009055721A2 (en) | 2009-04-30 |
| US8697730B2 (en) | 2014-04-15 |
| JP2011500846A (ja) | 2011-01-06 |
| ZA201002692B (en) | 2011-06-29 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| AR068947A1 (es) | Inhibidor de la proteina activadora de la 5- lipoxigenasa (flap), composiciones farmaceuticas, sales y solvatos | |
| RU2485131C2 (ru) | Производные пиридина, замещенные гетероциклическим кольцом и фосфоноксиметильной группой и содержащие их противогрибковые средства | |
| AR070299A1 (es) | Derivados de pirazolopirimidinas como inhibidores de quinasas dependientes de ciclinas, usos y composiciones farmaceuticas | |
| WO2016179566A1 (en) | Methods of treating a neurodegenerative disease | |
| AR075735A1 (es) | Composiciones farmaceuticas de liberacion inmediata que comprenden oxicodona y naloxona. uso | |
| JP2007533686A5 (es) | ||
| KR102059027B1 (ko) | Hdac6 억제제를 유효성분으로 포함하는 가려움증 예방 또는 치료용 약제학적 조성물 | |
| KR20160100976A (ko) | 제약 조합물 | |
| EP4523748A2 (en) | Treatment of pain and vasoconstriction | |
| MX386033B (es) | Agente terapéutico para enfermedades hepáticas. | |
| NZ587202A (en) | Methods for measuring a patient response upon administration of a drug and compositions thereof | |
| US20080234236A1 (en) | Reduction of adverse events after percutaneous intervention by use of a thrombin receptor antagonist | |
| AR061166A1 (es) | Composiciones farmaceuticas para la liberacion sostenida de fenilferina | |
| WO2010098600A3 (en) | Substituted azole derivatives, pharmaceutical composition containing the derivatives, and method for treating parkinson's disease using the same | |
| JP2012502047A5 (es) | ||
| JP2005505539A (ja) | パーキンソン病の治療のためのcb1受容体アンタゴニストと、脳のドーパミン作用性神経伝達を活性化する製品を含む組成物 | |
| MA46268A (fr) | Dérivés de 5-[2-(pyridin-2-ylamino)-1,3-thiazol-5-yl]-2,3-dihydro-1h-isoindol-1-one et leur utilisation en tant qu'inhibiteurs doubles de phosphatidylinositol 3-kinase delta & gamma | |
| NO20092764L (no) | Isosorbid mononitrat derivater for behandling av okular hypertensjon | |
| HRP20130892T1 (hr) | Farmaceutske formulacije i njihove upotrebe u lijeäśenju ženske seksualne disfunkcije | |
| MA33563B1 (fr) | 5-(3,4-dichloro-phényl)-n-(2-hydroxy-cyclohexyl)-6-(2,2,2-trifluoro-éthoxy)-nicotinamide et ses sels utilisés comme agents augmentant le cholestérol hdl | |
| ES2358931T3 (es) | Uso de un inhibidor de quinasa p38 para el tratamiento de trastornos psiquiatricos. | |
| AR045330A1 (es) | Forma de dosificacion oral, procedimiento para su preparacion y uso del compuesto 5-(4-(2-(n-metil-n- (2-piridil)amino)etoxi )bencil) tiazolidin-2,4-diona o una sal o solvato farmaceuticamente aceptable del mismo para prepararla | |
| MX2022016497A (es) | Derivados heterociclicos, composiciones farmaceuticas y su uso en el tratamiento, mejora o prevencion de la enfermedad fibrotica. | |
| RU2009127776A (ru) | Профилактическое или терапевтическое средство от алопеции | |
| ES2232128T3 (es) | Nuevas combinaciones de farmacos de un inhibidor de la recaptacion de noradrenalina (n.a.r.i.), preferentemente reboxetina y pindolol. |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| FA | Abandonment or withdrawal |