CO6251293A2 - Compuestos de piridazina cristalino - Google Patents
Compuestos de piridazina cristalinoInfo
- Publication number
- CO6251293A2 CO6251293A2 CO09144800A CO09144800A CO6251293A2 CO 6251293 A2 CO6251293 A2 CO 6251293A2 CO 09144800 A CO09144800 A CO 09144800A CO 09144800 A CO09144800 A CO 09144800A CO 6251293 A2 CO6251293 A2 CO 6251293A2
- Authority
- CO
- Colombia
- Prior art keywords
- compound
- crystalline compound
- crystalline
- composition
- amorphous
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—Ortho-condensed systems
-
- 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
- A61P1/16—Drugs for disorders of the alimentary tract or the digestive system for liver or gallbladder disorders, e.g. hepatoprotective agents, cholagogues, litholytics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/12—Antivirals
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/12—Antivirals
- A61P31/14—Antivirals for RNA viruses
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/12—Antivirals
- A61P31/14—Antivirals for RNA viruses
- A61P31/16—Antivirals for RNA viruses for influenza or rhinoviruses
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Virology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Animal Behavior & Ethology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Veterinary Medicine (AREA)
- Pharmacology & Pharmacy (AREA)
- Oncology (AREA)
- Communicable Diseases (AREA)
- Molecular Biology (AREA)
- Pulmonology (AREA)
- Gastroenterology & Hepatology (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Medicinal Preparation (AREA)
- Peptides Or Proteins (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Abstract
1.- Un compuesto cristalino de fórmula (1)y sus sales, los cuales están sustancialmente libres de compuesto (1) amorfo. 2.- El compuesto cristalino de la reivindicación 1 que tiene un comienzo endotérmico a alrededor de 235°C en el perfil de calorimetría de barrido diferencial (DSC). 3.- El compuesto cristalino de la reivindicación 2 que tiene un calor de fusión (DHf) de alrededor de 81 J/g (42 KJ/mole). 4.- El compuesto cristalino de la reivindicación 3 que tiene al menos un pico aproximado a un ángulo de difracción 2? (°) de alrededor de 17 medido mediante difractometría de rayos X en polvo. 5.- El compuesto cristalino de la reivindicación 1, el cual es la base libre. 6.- El compuesto cristalino de la reivindicación 1, en la forma de agujas o varillas. 7.- Una composición que comprende el compuesto cristalino de la reivindicación 1 conteniendo menos de alrededor del 40% en peso del compuesto (1) amorfo. 8.- Una composición que comprende el compuesto cristalino de la reivindicación 7, el cual contiene menos de alrededor del 10% en peso del compuesto (1) amorfo. 9.- Una composición que comprende el compuesto cristalino de la reivindicación 8, en donde el compuesto (1) cristalino contiene menos de alrededor de 100 ppm de cloruros. 10.- El compuesto cristalino de la reivindicación 1, el cual ha sido micronizado. 11.- El compuesto cristalino que es la base libre sustancialmente libre del compuesto (1) amorfo y alguna otra forma cristalina del compuesto (1). 12.- El compuesto cristalino de la reivindicación 1, el cual está sustancialmente libre de la sal cloruro del compuesto (1). 13.- Una composición que comprende el compuesto cristalino de la reivindicación 1 y un excipiente farmacéuticamente aceptable.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US95859507P | 2007-07-06 | 2007-07-06 |
Publications (1)
Publication Number | Publication Date |
---|---|
CO6251293A2 true CO6251293A2 (es) | 2011-02-21 |
Family
ID=39790369
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CO09144800A CO6251293A2 (es) | 2007-07-06 | 2009-12-17 | Compuestos de piridazina cristalino |
Country Status (19)
Country | Link |
---|---|
US (2) | US8106054B2 (es) |
EP (1) | EP2170881A1 (es) |
JP (2) | JP5366944B2 (es) |
KR (1) | KR101229528B1 (es) |
CN (1) | CN101778847B (es) |
AP (1) | AP2593A (es) |
AR (1) | AR066158A1 (es) |
AU (1) | AU2008275756B2 (es) |
BR (1) | BRPI0814801A2 (es) |
CA (1) | CA2691917C (es) |
CO (1) | CO6251293A2 (es) |
EA (2) | EA201270275A1 (es) |
EC (1) | ECSP109919A (es) |
IL (1) | IL202694A0 (es) |
MX (1) | MX2009013833A (es) |
TW (1) | TWI447116B (es) |
UA (1) | UA99466C2 (es) |
WO (1) | WO2009009001A1 (es) |
ZA (1) | ZA201000826B (es) |
Families Citing this family (15)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB0215293D0 (en) * | 2002-07-03 | 2002-08-14 | Rega Foundation | Viral inhibitors |
AU2004309390B2 (en) | 2003-12-22 | 2011-06-02 | Gilead Sciences, Inc. | Imidazo[4,5-c]pyridine compounds and methods of antiviral treatment |
JP2008524335A (ja) | 2004-12-21 | 2008-07-10 | ギリアド サイエンシズ, インコーポレイテッド | イミダゾ[4,5−c]ピリジン化合物および抗ウイルス処置法 |
ES2339298T3 (es) | 2006-07-07 | 2010-05-18 | Gilead Sciences, Inc. | Compuesto de piridazina novedoso y uso del mismo. |
DK2094702T3 (en) | 2006-12-14 | 2015-12-07 | Gilead Sciences Inc | viral inhibitors |
UA99466C2 (en) | 2007-07-06 | 2012-08-27 | Гилиад Сайенсиз, Инк. | Crystalline pyridazine compound |
AU2010333656B2 (en) | 2009-12-18 | 2015-08-27 | Boehringer Ingelheim International Gmbh | HCV combination therapy |
EP2571882A1 (en) | 2010-05-21 | 2013-03-27 | Gilead Sciences, Inc. | Heterocyclic flaviviridae virus inhibitors |
NZ613370A (en) | 2010-12-20 | 2015-05-29 | Gilead Sciences Inc | Combinations for treating hcv |
US20120204871A1 (en) * | 2011-02-10 | 2012-08-16 | Julio Cesar Vega | Stable, non-corrosive formulations for pressurized metered dose inhalers |
DE202012013074U1 (de) | 2011-09-16 | 2014-10-29 | Gilead Pharmasset Lcc | Zusammensetzungen zur Behandlung von HCV |
SI2950786T1 (sl) | 2013-01-31 | 2020-03-31 | Gilead Pharmasset Llc | Formulacija kombinacije dveh protivirusnih spojin |
HRP20211456T1 (hr) | 2014-12-26 | 2021-12-24 | Emory University | Protuvirusni derivati n4-hidroksicitidina |
KR102248165B1 (ko) | 2017-12-07 | 2021-05-06 | 에모리 유니버시티 | N4-하이드록시사이티딘 및 유도체 및 이와 관련된 항-바이러스 용도 |
CN114195812A (zh) * | 2021-12-30 | 2022-03-18 | 大连联化化学有限公司 | 一种合成2,4-二三氟甲基苯硼酸的方法 |
Family Cites Families (92)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2191978A (en) | 1935-10-10 | 1940-02-27 | Ig Farbenindustrie Ag | Quaternary nitrogen compounds and process of preparing them |
US2411662A (en) | 1943-05-13 | 1946-11-26 | Geigy Ag J R | Imino-di-fatty acid amide |
US2548863A (en) | 1946-05-29 | 1951-04-17 | Wyeth Corp | Substituted glycinamides |
US2516674A (en) | 1948-10-29 | 1950-07-25 | Wyeth Corp | Substituted glycinamide |
US3985891A (en) | 1973-02-03 | 1976-10-12 | Boehringer Ingelheim Gmbh | 2-Phenyl-imidazo (4,5-b)pyridines and salts thereof |
SU813921A1 (ru) | 1979-10-26 | 1986-12-23 | Институт физико-органической химии и углехимии АН УССР | Стирильные производные имидазо(4,5- @ )пиридиний иодида,обладающие фунгицидной активностью |
SU851940A1 (ru) | 1980-03-20 | 1988-04-30 | Институт физико-органической химии и углехимии АН УССР | Четвертичные соли имидазо @ 4,5-с @ пиридини ,обладающие антимикробной и фунгистатической активностью |
SU860463A1 (ru) | 1980-04-09 | 1998-05-27 | Институт физико-органической химии и углехимии АН Украинской ССР | Производные 4-амино-1,3-диметилимидазо [4,5-с] пиридин-2-она, обладающие акарицидным действием |
SU1048742A1 (ru) | 1981-03-30 | 1986-12-23 | Институт физико-органической химии и углехимии АН УССР | 2,4-Дистирилпроизводные имидазо-(4,5- @ )пиридини ,обладающие бактериостатической и фунгистатической активностью |
US4358387A (en) | 1981-08-10 | 1982-11-09 | Texaco Inc. | Cylinder lubricating oil composition |
CA1183847A (en) | 1981-10-01 | 1985-03-12 | Georges Van Daele | N-(3-hydroxy-4-piperidinyl)benzamide derivatives |
US5137896A (en) | 1981-10-01 | 1992-08-11 | Janssen Pharmaceutica N.V. | N-(3-hydroxy-4-piperidinyl)benzamide derivatives |
FR2527608B1 (fr) | 1982-05-28 | 1986-10-10 | Sandoz Sa | Nouveaux composes heterocycliques, leur preparation et leur utilisation comme medicaments |
US4692443A (en) | 1983-10-17 | 1987-09-08 | Eli Lilly And Company | 3-bicyclicpyridinium-methyl cephalosporins |
EP0138552A3 (en) | 1983-10-17 | 1986-03-19 | Eli Lilly And Company | Improvements on or relating to 3-bicyclicpyridinium-methyl cephalosporins |
GB8501542D0 (en) | 1985-01-22 | 1985-02-20 | Erba Farmitalia | 4 5 6 7-tetrahydro-imidazo(4 5-clpyridine derivatives |
GB8530602D0 (en) | 1985-12-12 | 1986-01-22 | Fujisawa Pharmaceutical Co | Heterocyclic compounds |
DE3781173T2 (de) | 1986-02-03 | 1992-12-17 | Janssen Pharmaceutica Nv | N-heterozyklische-4-piperidinamine enthaltende anti-histaminische zusammensetzungen. |
US4804658A (en) | 1986-09-15 | 1989-02-14 | G. D. Searle & Co. | Imidazopyridine derivatives and pharmaceutical compositions |
NZ225447A (en) | 1987-07-20 | 1991-12-23 | Merck & Co Inc | Piperazinyl derivatives of purine and purine isosteres and pharmaceutical compositions |
US5057517A (en) | 1987-07-20 | 1991-10-15 | Merck & Co., Inc. | Piperazinyl derivatives of purines and isosteres thereof as hypoglycemic agents |
US4914108A (en) | 1988-03-14 | 1990-04-03 | G. D. Searle & Co. | 5-substituted(4,5-c)imidazopyridine compounds which have useful platelet activating factor antagonistic activity |
US5302601A (en) | 1988-03-14 | 1994-04-12 | G. D. Searle & Co. | 5-substituted imidazo[4,5-c]pyridines |
US5227384A (en) | 1988-03-14 | 1993-07-13 | G. D. Searle & Co. | 5-substituted [4,5-c] imidazopyridines and pharmaceutical use thereof |
US5019581A (en) | 1988-03-14 | 1991-05-28 | G. D. Searle & Co. | 5-substituted (4,5-c) imidazopyridine compounds which have useful platelet activating factor antagonistic activity |
US5332744A (en) | 1989-05-30 | 1994-07-26 | Merck & Co., Inc. | Substituted imidazo-fused 6-membered heterocycles as angiotensin II antagonists |
US4990518A (en) | 1989-09-13 | 1991-02-05 | G. D. Searle & Co. | Pharmacologically active heteroaryl substituted imidazo (4,5-c) pyridines |
US4988707A (en) | 1989-09-13 | 1991-01-29 | G. D. Searle & Co. | Pharmacologically active phenylalkanoyl substituted imidazo (4,5-C) pyridines |
FR2663332B1 (fr) | 1990-06-15 | 1997-11-07 | Roussel Uclaf | Nouvelles cephalosporines comportant en position 3 un radical propenyle substitue par un ammonium quaternaire, leur procede de preparation, leur application comme medicaments, les compositions les renfermant et les nouveaux intermediaires obtenus. |
US5011832A (en) | 1990-06-26 | 1991-04-30 | Merck & Co., Inc. | 2-biphenyl-carbapenem antibacterial agents |
JPH04327587A (ja) | 1991-04-26 | 1992-11-17 | Asahi Chem Ind Co Ltd | 6’−c−アルキル−3−デアザネプラノシンa誘導体、その製造法およびその用途 |
DE4122474A1 (de) | 1991-07-06 | 1993-01-07 | Basf Ag | Fungizide mischung |
GB9116056D0 (en) | 1991-07-24 | 1991-09-11 | British Bio Technology | Compounds |
US5587372A (en) | 1991-12-12 | 1996-12-24 | Roussel Uclaf | Cephalosporins |
GB9202792D0 (en) | 1992-02-11 | 1992-03-25 | British Bio Technology | Compounds |
DE4211474A1 (de) | 1992-04-06 | 1993-10-07 | Merck Patent Gmbh | Imidazopyridine |
US20030073159A1 (en) * | 1992-05-11 | 2003-04-17 | Human Genome Sciences, Inc. | Human inhibitor of apoptosis gene 1 |
US5208242A (en) | 1992-08-26 | 1993-05-04 | G. D. Searle & Co. | 5-substituted-4-phenyl-5H-imidazo[4,5-c]pyridine derivatives |
DE4230464A1 (de) | 1992-09-11 | 1994-03-17 | Merck Patent Gmbh | Imidazolderivate |
DE4236026A1 (de) | 1992-10-24 | 1994-04-28 | Merck Patent Gmbh | Imidazopyridine |
JP3115455B2 (ja) | 1992-12-18 | 2000-12-04 | 明治製菓株式会社 | 新規セファロスポリン誘導体 |
US5374638A (en) | 1993-03-19 | 1994-12-20 | Merck & Co., Inc. | Six membered ring fused imidazoles substituted with phenoxyphenylacetic acid derivatives used to treat asthma |
DE4309969A1 (de) | 1993-03-26 | 1994-09-29 | Bayer Ag | Substituierte heteroanellierte Imidazole |
DE4318813A1 (de) | 1993-06-07 | 1994-12-08 | Merck Patent Gmbh | Imidazopyridine |
DE4324580A1 (de) | 1993-07-22 | 1995-01-26 | Thomae Gmbh Dr K | Bicyclische Heterocyclen, diese Verbindungen enthaltende Arzneimittel und Verfahren zu ihrer Herstellung |
US5486525A (en) | 1993-12-16 | 1996-01-23 | Abbott Laboratories | Platelet activating factor antagonists: imidazopyridine indoles |
US5563143A (en) | 1994-09-21 | 1996-10-08 | Pfizer Inc. | Catechol diether compounds as inhibitors of TNF release |
US5585492A (en) | 1994-10-11 | 1996-12-17 | G. D. Searle & Co. | LTA4 Hydrolase inhibitors |
US6506876B1 (en) | 1994-10-11 | 2003-01-14 | G.D. Searle & Co. | LTA4 hydrolase inhibitor pharmaceutical compositions and methods of use |
US6080870A (en) | 1996-04-03 | 2000-06-27 | Merck & Co., Inc. | Biaryl substituted imidazole compounds useful as farnesyl-protein transferase inhibitors |
US5859035A (en) | 1996-04-03 | 1999-01-12 | Merck & Co., Inc. | Arylheteroaryl inhibitors of farnesyl-protein transferase |
US6063930A (en) | 1996-04-03 | 2000-05-16 | Merck & Co., Inc. | Substituted imidazole compounds useful as farnesyl-protein transferase inhibitors |
US5854265A (en) | 1996-04-03 | 1998-12-29 | Merck & Co., Inc. | Biheteroaryl inhibitors of farnesyl-protein transferase |
US5880140A (en) | 1996-04-03 | 1999-03-09 | Merck & Co., Inc. | Biheteroaryl inhibitors of farnesyl-protein transferase |
US5874452A (en) | 1996-04-03 | 1999-02-23 | Merck & Co., Inc. | Biheteroaryl inhibitors of farnesyl-protein transferase |
US5939557A (en) | 1996-04-03 | 1999-08-17 | Merck & Co., Inc. | Inhibitors of farnesyl-protein transferase |
US5872136A (en) | 1996-04-03 | 1999-02-16 | Merck & Co., Inc. | Arylheteroaryl inhibitors of farnesyl-protein transferase |
US5883105A (en) | 1996-04-03 | 1999-03-16 | Merck & Co., Inc. | Inhibitors of farnesyl-protein transferase |
CA2311742C (en) | 1997-11-28 | 2009-06-16 | Sumitomo Pharmaceuticals Co., Ltd. | 6-amino-9-benzyl-8-hydroxypurine derivatives |
DE19845153A1 (de) | 1998-10-01 | 2000-04-06 | Merck Patent Gmbh | Imidazo[4,5]-pyridin-4-on-derivate |
DE19900471A1 (de) | 1999-01-08 | 2000-07-13 | Merck Patent Gmbh | Imidazo[4,5c]-pyridin-4-on-derivate |
JP4055363B2 (ja) | 1999-01-08 | 2008-03-05 | チッソ株式会社 | ボラン誘導体および有機電界発光素子 |
CA2373073A1 (en) | 1999-05-07 | 2000-11-16 | Takeda Chemical Industries, Ltd. | Cyclic compounds and uses thereof |
US6844367B1 (en) | 1999-09-17 | 2005-01-18 | Millennium Pharmaceuticals, Inc. | Benzamides and related inhibitors of factor Xa |
US6770666B2 (en) | 1999-12-27 | 2004-08-03 | Japan Tobacco Inc. | Fused-ring compounds and use thereof as drugs |
ID30204A (id) | 1999-12-27 | 2001-11-15 | Japan Tobacco Inc | Senyawa-senyawa cincin terfusi dan penggunaannya sebagai obat |
DK1259485T3 (da) | 2000-02-29 | 2006-04-10 | Millennium Pharm Inc | Benzamider og beslægtede inhibitorer for faktor Xa |
EP1132381A1 (en) | 2000-03-08 | 2001-09-12 | Cermol S.A. | Ester derivatives of dimethylpropionic acid and pharmaceutical compositions containing them |
US6448281B1 (en) | 2000-07-06 | 2002-09-10 | Boehringer Ingelheim (Canada) Ltd. | Viral polymerase inhibitors |
JP4331944B2 (ja) | 2001-04-17 | 2009-09-16 | 大日本住友製薬株式会社 | 新規アデニン誘導体 |
AR035543A1 (es) | 2001-06-26 | 2004-06-16 | Japan Tobacco Inc | Agente terapeutico para la hepatitis c que comprende un compuesto de anillo condensado, compuesto de anillo condensado, composicion farmaceutica que lo comprende, compuestos de benzimidazol, tiazol y bifenilo utiles como intermediarios para producir dichos compuestos, uso del compuesto de anillo con |
US20030073836A1 (en) | 2001-07-05 | 2003-04-17 | Boehringer Ingelheim Pharma Kg | Heteroarylcarboxylic acid amides, the preparation thereof and their use as pharmaceutical compositions |
US7294457B2 (en) | 2001-08-07 | 2007-11-13 | Boehringer Ingelheim (Canada) Ltd. | Direct binding assay for identifying inhibitors of HCV polymerase |
DE10140246A1 (de) | 2001-08-09 | 2003-03-06 | Forsch Pigmente Und Lacke E V | Verfahren zur Behandlung von Oberflächen von Substraten |
EP1429759A4 (en) | 2001-09-26 | 2004-12-15 | Bristol Myers Squibb Co | COMPOUNDS FOR TREATING HEPATITIS C VIRUS |
JP2005525309A (ja) | 2002-01-10 | 2005-08-25 | ベーリンガー インゲルハイム ファルマ ゲゼルシャフト ミット ベシュレンクテル ハフツング ウント コンパニー コマンディトゲゼルシャフト | 医薬品としての使用のためのMTPインヒビター又はapoB分泌インヒビターとフィブレートの組み合わせ |
GB0215293D0 (en) | 2002-07-03 | 2002-08-14 | Rega Foundation | Viral inhibitors |
CA2496249C (en) | 2002-08-21 | 2012-01-24 | Boehringer Ingelheim Pharma Gmbh & Co. Kg | 8-[3-amino-piperidin-1-yl]-xanthines, the production thereof and the use of the same as medicaments |
EP1539141B1 (en) | 2002-08-29 | 2010-07-14 | Boehringer Ingelheim Pharmaceuticals Inc. | 3-(sulfonamidoethyl)-indole derivatives for use as glucocorticoid mimetics in the treatment of inflammatory, allergic and proliferative diseases |
WO2004054974A2 (en) | 2002-12-13 | 2004-07-01 | Smithkline Beecham Corporation | Piperidine derivatives as ccr5 antagonists |
US7223785B2 (en) | 2003-01-22 | 2007-05-29 | Boehringer Ingelheim International Gmbh | Viral polymerase inhibitors |
US7098231B2 (en) | 2003-01-22 | 2006-08-29 | Boehringer Ingelheim International Gmbh | Viral polymerase inhibitors |
US20040242613A1 (en) | 2003-01-30 | 2004-12-02 | Boehringer Ingelheim Pharmaceuticals, Inc. | Pyrimidine derivatives useful as inhibitors of PKC-theta |
US7566707B2 (en) | 2003-06-18 | 2009-07-28 | Boehringer Ingelheim International Gmbh | Imidazopyridazinone and imidazopyridone derivatives, the preparation thereof and their use as pharmaceutical compositions |
MXPA06004641A (es) | 2003-11-05 | 2006-06-27 | Hoffmann La Roche | Derivados de fenilo como agonistas para. |
AU2004309390B2 (en) | 2003-12-22 | 2011-06-02 | Gilead Sciences, Inc. | Imidazo[4,5-c]pyridine compounds and methods of antiviral treatment |
KR101238430B1 (ko) | 2004-07-27 | 2013-02-28 | 길리애드 사이언시즈, 인코포레이티드 | 이미다조[4,5-d]피리미딘, 그들의 용도 및 제조방법 |
EP1791932A1 (en) | 2004-09-13 | 2007-06-06 | Ciba Specialty Chemicals Holding Inc. | Alkylaminoacetamide lubricant additives |
JP2008524335A (ja) | 2004-12-21 | 2008-07-10 | ギリアド サイエンシズ, インコーポレイテッド | イミダゾ[4,5−c]ピリジン化合物および抗ウイルス処置法 |
WO2007063744A1 (ja) | 2005-11-30 | 2007-06-07 | Fujifilm Corporation | 平版刷版の後露光方法、後露光装置、露光装置、露光用器具、現像方法、及び現像装置 |
ES2339298T3 (es) * | 2006-07-07 | 2010-05-18 | Gilead Sciences, Inc. | Compuesto de piridazina novedoso y uso del mismo. |
UA99466C2 (en) | 2007-07-06 | 2012-08-27 | Гилиад Сайенсиз, Инк. | Crystalline pyridazine compound |
-
2008
- 2008-03-07 UA UAA201000199A patent/UA99466C2/ru unknown
- 2008-07-03 AU AU2008275756A patent/AU2008275756B2/en not_active Ceased
- 2008-07-03 EP EP08826188A patent/EP2170881A1/en not_active Withdrawn
- 2008-07-03 KR KR1020107002588A patent/KR101229528B1/ko not_active IP Right Cessation
- 2008-07-03 AR ARP080102883A patent/AR066158A1/es unknown
- 2008-07-03 EA EA201270275A patent/EA201270275A1/ru unknown
- 2008-07-03 WO PCT/US2008/008259 patent/WO2009009001A1/en active Application Filing
- 2008-07-03 TW TW097125103A patent/TWI447116B/zh not_active IP Right Cessation
- 2008-07-03 CA CA2691917A patent/CA2691917C/en not_active Expired - Fee Related
- 2008-07-03 JP JP2010514874A patent/JP5366944B2/ja not_active Expired - Fee Related
- 2008-07-03 EA EA200971080A patent/EA018173B1/ru not_active IP Right Cessation
- 2008-07-03 AP AP2009005078A patent/AP2593A/xx active
- 2008-07-03 CN CN200880023677XA patent/CN101778847B/zh not_active Expired - Fee Related
- 2008-07-03 BR BRPI0814801A patent/BRPI0814801A2/pt not_active IP Right Cessation
- 2008-07-03 US US12/217,347 patent/US8106054B2/en not_active Expired - Fee Related
- 2008-07-03 MX MX2009013833A patent/MX2009013833A/es active IP Right Grant
-
2009
- 2009-12-13 IL IL202694A patent/IL202694A0/en unknown
- 2009-12-17 CO CO09144800A patent/CO6251293A2/es active IP Right Grant
-
2010
- 2010-01-29 EC EC2010009919A patent/ECSP109919A/es unknown
- 2010-02-04 ZA ZA2010/00826A patent/ZA201000826B/en unknown
-
2011
- 2011-12-23 US US13/336,512 patent/US8569488B2/en not_active Expired - Fee Related
-
2013
- 2013-07-26 JP JP2013155248A patent/JP2013216695A/ja active Pending
Also Published As
Publication number | Publication date |
---|---|
KR20100044201A (ko) | 2010-04-29 |
AR066158A1 (es) | 2009-07-29 |
WO2009009001A1 (en) | 2009-01-15 |
JP2010532757A (ja) | 2010-10-14 |
ZA201000826B (en) | 2010-11-24 |
CA2691917A1 (en) | 2009-01-15 |
AP2009005078A0 (en) | 2009-12-31 |
CN101778847A (zh) | 2010-07-14 |
AU2008275756A1 (en) | 2009-01-15 |
AU2008275756B2 (en) | 2012-01-19 |
US20120108601A1 (en) | 2012-05-03 |
KR101229528B1 (ko) | 2013-02-04 |
TWI447116B (zh) | 2014-08-01 |
AP2593A (en) | 2013-02-07 |
CA2691917C (en) | 2013-12-03 |
EA200971080A1 (ru) | 2010-08-30 |
MX2009013833A (es) | 2010-03-10 |
UA99466C2 (en) | 2012-08-27 |
US8106054B2 (en) | 2012-01-31 |
JP2013216695A (ja) | 2013-10-24 |
US20090036460A1 (en) | 2009-02-05 |
IL202694A0 (en) | 2010-06-30 |
ECSP109919A (es) | 2010-04-30 |
EP2170881A1 (en) | 2010-04-07 |
EA018173B1 (ru) | 2013-06-28 |
WO2009009001A9 (en) | 2010-11-11 |
US8569488B2 (en) | 2013-10-29 |
CN101778847B (zh) | 2013-07-24 |
JP5366944B2 (ja) | 2013-12-11 |
BRPI0814801A2 (pt) | 2017-03-28 |
TW200918531A (en) | 2009-05-01 |
EA201270275A1 (ru) | 2012-09-28 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CO6251293A2 (es) | Compuestos de piridazina cristalino | |
ES2543567T3 (es) | Métodos de utilización de inhibidores de ALK | |
AR062357A1 (es) | Derivados de fenilo, piridina y quinolina, composiciones farmaceuticas y su utilizacion como medicamentos | |
AR121612A2 (es) | Inhibidores de glucosilceramida sintasa | |
PE20180799A1 (es) | Reguladores de nrf2 | |
ES2368691T3 (es) | Derivados de benzotiazepina y su utilización como moduladores de los receptores ampa y nmda. | |
CY1120478T1 (el) | Παραγωγα 2,6-υποκατεστημενης πουρινης και η χρηση αυτων στην αγωγη υπερπλαστικων διαταραχων | |
AR068509A1 (es) | Antagosnistas del receptor de bradiquinina b1 | |
CO5770098A1 (es) | Forma cristalina beta-d del clorhitrato de la ivabradina, su procedimiento de preparacion y las composiciones farmaceuticas que las contienen | |
AR065322A1 (es) | 2-aminooxazolinas comoligandos de taar1 | |
CO5790166A1 (es) | Forma cristalina delta de clorhidrato de ivabradina, su procedimiento de preparacion y composicines farmaceuticas que las contienen | |
CY1114906T1 (el) | Νεα παραγωγα 6-τριαζολοπυριδαζινο-σουλφανυλο βενζοθειαζολης και βενζιμιδαζολης, η διαδικασια της παρασκευης τους, η εφαρμογη τους ως φαρμακα, φαρμακευτικες συνθεσεις και νεα χρηση κυριως ως αναστολεις του μετ | |
CU24099B1 (es) | Derivados de sulfonamida para el tratamiento del dolor | |
ES2968840T3 (es) | Compuestos de aminocarbonilcarbamato y su uso en el tratamiento de trastornos hipercinéticos tales como el TDAH | |
AR075583A1 (es) | Derivados de isoxazol/o-piridina con eslabon etilo o etenilo | |
CY1112011T1 (el) | Παραγωγα αζαδικυκλο (3.1.0) εξανιου χρησιμα ως ρυθμιστες υποδοχεων d3 ντοπαμινης | |
AR074304A1 (es) | Moduladores heterociclicos de gamma- secretasa | |
NZ594597A (en) | Substituted piperidines as ccr3 antagonists | |
AR088061A1 (es) | Compuestos de pirazol-4-il-heterociclil-carboxamida y metodos de uso | |
BRPI0518068A (pt) | composto ou um éster ou sal farmaceuticamente aceitável do mesmo, composição farmacêutica, inibidor seletivo de aurora a, agente anti-tumor, e, preparação combinada | |
JP2013500342A5 (es) | ||
MX2009013335A (es) | Derivados de piperidina/piperazina. | |
NO20072409L (no) | Substituerte n-sulfonylaminobenzyl-2-fenoksy acetamid-forbindelser | |
BR112015010941A2 (pt) | pró-fármacos de gemcitabina e suas utilizações | |
AR079957A1 (es) | Derivados de acidos grasos de salicilatos composiciones farmaceuticas y uso de los mismos |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
FG | Application granted |