PE20070717A1 - Sal de maleato y polimorfo de [2-({4-[(dimetilamino)iminometil]fenil}carbonilamino)-5-metoxifenil]-n-(5-cloro-(2-piridil))carboxamida - Google Patents
Sal de maleato y polimorfo de [2-({4-[(dimetilamino)iminometil]fenil}carbonilamino)-5-metoxifenil]-n-(5-cloro-(2-piridil))carboxamidaInfo
- Publication number
- PE20070717A1 PE20070717A1 PE2006001368A PE2006001368A PE20070717A1 PE 20070717 A1 PE20070717 A1 PE 20070717A1 PE 2006001368 A PE2006001368 A PE 2006001368A PE 2006001368 A PE2006001368 A PE 2006001368A PE 20070717 A1 PE20070717 A1 PE 20070717A1
- Authority
- PE
- Peru
- Prior art keywords
- iminometil
- carbonylamine
- polymorph
- dimethylamine
- carboxamide
- Prior art date
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
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives 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
- A61K31/185—Acids; Anhydrides, halides or salts thereof, e.g. sulfur acids, imidic, hydrazonic or hydroximic acids
- A61K31/19—Carboxylic acids, e.g. valproic acid
- A61K31/194—Carboxylic acids, e.g. valproic acid having two or more carboxyl groups, e.g. succinic, maleic or phthalic acid
-
- 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
- A61K31/60—Salicylic acid; Derivatives thereof
- A61K31/612—Salicylic acid; Derivatives thereof having the hydroxy group in position 2 esterified, e.g. salicylsulfuric acid
- A61K31/616—Salicylic acid; Derivatives thereof having the hydroxy group in position 2 esterified, e.g. salicylsulfuric acid by carboxylic acids, e.g. acetylsalicylic acid
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/20—Pills, tablets, discs, rods
-
- 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
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D213/72—Nitrogen atoms
- C07D213/75—Amino or imino radicals, acylated by carboxylic or carbonic acids, or by sulfur or nitrogen analogues thereof, e.g. carbamates
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02A—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE
- Y02A50/00—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE in human health protection, e.g. against extreme weather
- Y02A50/30—Against vector-borne diseases, e.g. mosquito-borne, fly-borne, tick-borne or waterborne diseases whose impact is exacerbated by climate change
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Epidemiology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Cardiology (AREA)
- Heart & Thoracic Surgery (AREA)
- Urology & Nephrology (AREA)
- Vascular Medicine (AREA)
- Hematology (AREA)
- Pulmonology (AREA)
- Diabetes (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Pyridine Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Medicinal Preparation (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
SE REFIERE A UN COMPUESTO DE [2-({4-[(DIMETILAMINO)IMINOMETIL]FENIL}CARBONILAMINO)-5-METOXIFENIL]-N-(5-CLORO-(2-PIRIDIL))CARBOXAMIDA Y UN ACIDO DE PREFERENCIA ACIDO MALEICO, ACIDO PROPIONICO, CARACTERIZADO PORQUE CONTIENE UN PATRON DE DIFRACCION DE RAYOS X EN POLVO DE 4,9; 9,7; 13,8; 14,1; 15,2; 20,8; ENTRE OTROS (GRADO 2 THETA). REFERIDA TAMBIEN A UNA COMPOSICION FARMACEUTICA. DICHO POLIMORFO ES INHIBIDOR DEL FACTOR Xa, UTIL EN EL TRATAMIENTO DE SINDROME CORONARIO AGUDO, INFARTO DE MIOCARDIO, ANGINA INESTABLE, EMBOLIA PULMONAR, ENTRE OTROS
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US73522405P | 2005-11-08 | 2005-11-08 |
Publications (1)
Publication Number | Publication Date |
---|---|
PE20070717A1 true PE20070717A1 (es) | 2007-08-17 |
Family
ID=38023988
Family Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PE2006001368A PE20070717A1 (es) | 2005-11-08 | 2006-11-07 | Sal de maleato y polimorfo de [2-({4-[(dimetilamino)iminometil]fenil}carbonilamino)-5-metoxifenil]-n-(5-cloro-(2-piridil))carboxamida |
PE2010000471A PE20110070A1 (es) | 2005-11-08 | 2006-11-07 | Procedimiento de preparacion del compuesto [2-({4-[(dimetilamino)iminometil]fenil}carbonilamino)-5-metoxifenil]-n-(5-cloro(2-piridil))carboxamida |
Family Applications After (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PE2010000471A PE20110070A1 (es) | 2005-11-08 | 2006-11-07 | Procedimiento de preparacion del compuesto [2-({4-[(dimetilamino)iminometil]fenil}carbonilamino)-5-metoxifenil]-n-(5-cloro(2-piridil))carboxamida |
Country Status (21)
Country | Link |
---|---|
US (7) | US7598276B2 (es) |
EP (2) | EP2431358A1 (es) |
JP (2) | JP5227178B2 (es) |
KR (1) | KR101358574B1 (es) |
CN (2) | CN102336702B (es) |
AR (2) | AR056787A1 (es) |
AT (1) | ATE549317T1 (es) |
AU (1) | AU2006311544B2 (es) |
BR (1) | BRPI0618362A2 (es) |
CA (1) | CA2627086C (es) |
DK (1) | DK1948608T3 (es) |
ES (1) | ES2384116T3 (es) |
HK (1) | HK1115131A1 (es) |
IL (2) | IL190524A (es) |
NZ (2) | NZ592533A (es) |
PE (2) | PE20070717A1 (es) |
PT (1) | PT1948608E (es) |
RU (1) | RU2440986C2 (es) |
TW (1) | TWI443088B (es) |
WO (1) | WO2007056517A2 (es) |
ZA (1) | ZA200803820B (es) |
Families Citing this family (45)
Publication number | Priority date | Publication date | Assignee | Title |
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DK1259485T3 (da) | 2000-02-29 | 2006-04-10 | Millennium Pharm Inc | Benzamider og beslægtede inhibitorer for faktor Xa |
AU2005257999B2 (en) | 2004-06-18 | 2011-12-08 | Millennium Pharmaceuticals, Inc. | Factor Xa inhibitors |
US7696352B2 (en) * | 2004-06-18 | 2010-04-13 | Millennium Pharmaceuticals, Inc. | Factor Xa inhibitors |
PE20070717A1 (es) | 2005-11-08 | 2007-08-17 | Millennium Pharm Inc | Sal de maleato y polimorfo de [2-({4-[(dimetilamino)iminometil]fenil}carbonilamino)-5-metoxifenil]-n-(5-cloro-(2-piridil))carboxamida |
WO2007112367A2 (en) * | 2006-03-27 | 2007-10-04 | Portola Pharmaceuticals, Inc. | Potassium channel modulators and platelet procoagulant activity |
CA2651303A1 (en) | 2006-05-05 | 2007-11-15 | Millennium Pharmaceuticals, Inc. | Factor xa inhibitors |
WO2008057972A1 (en) | 2006-11-02 | 2008-05-15 | Millennium Pharmaceuticals, Inc. | Methods of synthesizing pharmaceutical salts of a factor xa inhibitor |
WO2008073670A2 (en) * | 2006-12-08 | 2008-06-19 | Millennium Pharmaceuticals, Inc. | Unit dose formulations and methods of treating thrombosis with an oral factor xa inhibitor |
US20080293704A1 (en) * | 2007-01-05 | 2008-11-27 | Millennium Pharmaceuticals, Inc. | FACTOR Xa INHIBITORS |
TWI384986B (zh) * | 2007-01-17 | 2013-02-11 | Lg Life Sciences Ltd | 抗病毒劑之順丁烯二酸單鹽以及含有該單鹽之醫藥組成物 |
AU2008239659B2 (en) * | 2007-04-13 | 2013-09-05 | Millennium Pharmaceuticals, Inc. | Combination anticoagulant therapy with a compound that acts as a factor Xa inhibitor |
EP2586439A1 (en) * | 2007-05-02 | 2013-05-01 | Portola Pharmaceuticals, Inc. | Combination therapy with a compound acting as a platelet ADP receptor inhibitor |
EP2915564B1 (en) | 2007-09-28 | 2020-11-04 | Portola Pharmaceuticals, Inc. | Antidotes for factor XA inhibitors and methods of using the same |
UY31531A1 (es) * | 2007-12-17 | 2009-08-03 | Sales derivadas de 8-oxoadenina composiciones farmacéuticas que las contienen y su uso en terapia como moduladores de receptor tipo toll (tlr) | |
EP2364165B1 (en) | 2008-11-14 | 2018-01-03 | Portola Pharmaceuticals, Inc. | Antidotes for factor xa inhibitors and methods of using the same in combination with blood coagulating agents |
EP3604510A1 (en) | 2009-03-30 | 2020-02-05 | Portola Pharmaceuticals, Inc. | Antidotes for factor xa inhibitors and methods of using the same |
JP6163304B2 (ja) * | 2009-07-15 | 2017-07-12 | ポートラ ファーマシューティカルズ, インコーポレイテッド | 第Xa因子インヒビターの解毒剤の単位用量処方物およびその使用方法 |
US8742120B2 (en) * | 2009-12-17 | 2014-06-03 | Millennium Pharmaceuticals, Inc. | Methods of preparing factor xa inhibitors and salts thereof |
CA2784921A1 (en) * | 2009-12-17 | 2011-07-14 | Millennium Pharmaceuticals, Inc. | Salts and crystalline forms of a factor xa inhibitor |
ES2610145T3 (es) | 2009-12-17 | 2017-04-26 | Millennium Pharmaceuticals, Inc. | Procedimientos de síntesis de inhibidores del factor Xa |
EA015918B1 (ru) * | 2010-03-03 | 2011-12-30 | Дмитрий Геннадьевич ТОВБИН | УРЕТАНЫ, МОЧЕВИНЫ, АМИДЫ И РОДСТВЕННЫЕ ИНГИБИТОРЫ ФАКТОРА Xa |
AR082804A1 (es) * | 2010-09-01 | 2013-01-09 | Portola Pharm Inc | Formas cristalinas de un inhibidor del factor xa |
TW201240664A (en) | 2010-09-01 | 2012-10-16 | Portola Pharm Inc | Methods and formulations of treating thrombosis with betrixaban and a P-glycoprotein inhibitor |
CN102952138B (zh) * | 2011-08-17 | 2016-07-06 | 上海特化医药科技有限公司 | 一种吡唑并嘧啶酮化合物的盐、多晶型物及其药物组合物、制备方法和应用 |
US20150224091A1 (en) | 2011-08-31 | 2015-08-13 | Portola Pharmaceuticals, Inc. | Prevention and treatment of thrombosis in medically ill patients |
US9200268B2 (en) * | 2012-12-27 | 2015-12-01 | Portola Pharmaceuticals, Inc. | Compounds and methods for purification of serine proteases |
US20140346397A1 (en) | 2012-12-27 | 2014-11-27 | Portola Pharmaceuticals, Inc. | Compounds and methods for purification of serine proteases |
CN104341343B (zh) * | 2013-07-24 | 2018-09-28 | 四川海思科制药有限公司 | 贝曲西班的晶型及其制备方法和用途 |
CN105085387A (zh) * | 2014-05-20 | 2015-11-25 | 四川海思科制药有限公司 | 贝曲西班盐及其制备方法和用途 |
CN107073082B (zh) | 2014-08-20 | 2021-04-30 | 博尔托拉制药公司 | Xa因子解毒剂的冻干制剂 |
WO2017091757A1 (en) | 2015-11-24 | 2017-06-01 | Portola Pharmaceuticals, Inc. | Isotopically enriched betrixaban |
CN106995405A (zh) * | 2016-01-25 | 2017-08-01 | 重庆医药工业研究院有限责任公司 | 一种贝曲西班马来酸盐无定型物及其制备方法 |
EP3419650B1 (en) | 2016-02-24 | 2021-06-02 | Alexion Pharmaceuticals, Inc. | Lyophilized formulations for factor xa antidote |
EP3463352A4 (en) * | 2016-06-02 | 2019-10-30 | Dr. Reddy S Laboratories Limited | POLYMORPH OF BETRIXABAN AND ITS MALEATE SALT |
EP3254674A1 (en) | 2016-06-08 | 2017-12-13 | Sandoz Ag | Pharmaceutical compositions of betrixaban maleate |
DK3472314T3 (da) | 2016-06-17 | 2021-07-26 | Alexion Pharma Inc | Fremstilling af faktor-xa-derivater |
WO2018042320A1 (en) * | 2016-08-30 | 2018-03-08 | Dr. Reddy’S Laboratories Limited | Salts of betrixaban and processes for preparation thereof |
EP3293174A1 (en) | 2016-09-09 | 2018-03-14 | Sandoz Ag | Crystalline salts of betrixaban |
WO2018069936A1 (en) | 2016-10-13 | 2018-04-19 | Mylan Laboratories Limited | Polymorphs and solid dispersion of betrixaban and methods for the preparation thereof |
CN108017576B (zh) * | 2016-11-01 | 2022-06-21 | 石药集团中奇制药技术(石家庄)有限公司 | 一种贝曲西班及其盐酸盐的制备方法,以及它们的晶型 |
CN108586325A (zh) * | 2017-03-16 | 2018-09-28 | 上海度德医药科技有限公司 | 一种Betrixaban中间体的制备方法 |
WO2018229796A2 (en) | 2017-06-14 | 2018-12-20 | Mylan Laboratories Limited | A process for betrixaban hydrochloride and betrixaban maleate salt |
CN107868039A (zh) * | 2017-11-27 | 2018-04-03 | 中国药科大学 | 一种贝曲沙班中间体n-(5-氯-2-吡啶基)-2-[(4-氰基苯甲酰基)氨基]-5-甲氧基苯甲酰胺的制备方法 |
WO2022211680A1 (ru) * | 2021-03-30 | 2022-10-06 | Общество С Ограниченной Ответственностью "Фармадиол" | Способ получения антикоагулянта n-(5-хлорпиридин-2-ил)-2-({4-[этан-имидоил(метил)амино]бензоил}амино)-5-метилбензамид гидрохлорида |
CN115057854A (zh) * | 2022-04-19 | 2022-09-16 | 河北常山生化药业股份有限公司 | 马来酸阿伐曲泊帕中间体的制备方法 |
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WO1994013693A1 (en) | 1992-12-15 | 1994-06-23 | Corvas International, Inc. | NOVEL INHIBITORS OF FACTOR Xa |
GB9226238D0 (en) | 1992-12-16 | 1993-02-10 | Scherer Ltd R P | Encapsulation apparatus and process |
EP0798295B1 (en) | 1994-12-02 | 2003-02-26 | Yamanouchi Pharmaceutical Co. Ltd. | Novel amidinonaphthyl derivative or salt thereof |
US5849759A (en) | 1995-12-08 | 1998-12-15 | Berlex Laboratories, Inc. | Naphthyl-substituted benzimidazole derivatives as anti-coagulants |
PL334250A1 (en) | 1996-12-23 | 2000-02-14 | Du Pont Pharm Co | Nitrogen containing hetero-aromatic compounds and inhibitors of xa factor |
EP1020434A4 (en) | 1997-08-27 | 2000-11-15 | Kissei Pharmaceutical | 3-AMIDINOANILINE DERIVATIVES, INHIBITORS OF THE ACTIVATED BLOOD COINTENANCE FACTOR X AND INTERMEDIATE PRODUCTS FOR PRODUCING BOTH |
US6140351A (en) | 1997-12-19 | 2000-10-31 | Berlex Laboratories, Inc. | Ortho-anthranilamide derivatives as anti-coagulants |
KR100760434B1 (ko) * | 1999-09-17 | 2007-10-04 | 밀레니엄 파머슈티컬스 인코퍼레이티드 | 벤즈아미드 및 관련된 Xa 인자의 억제제 |
US6844367B1 (en) * | 1999-09-17 | 2005-01-18 | Millennium Pharmaceuticals, Inc. | Benzamides and related inhibitors of factor Xa |
DK1259485T3 (da) * | 2000-02-29 | 2006-04-10 | Millennium Pharm Inc | Benzamider og beslægtede inhibitorer for faktor Xa |
US6627646B2 (en) * | 2001-07-17 | 2003-09-30 | Sepracor Inc. | Norastemizole polymorphs |
PE20070717A1 (es) | 2005-11-08 | 2007-08-17 | Millennium Pharm Inc | Sal de maleato y polimorfo de [2-({4-[(dimetilamino)iminometil]fenil}carbonilamino)-5-metoxifenil]-n-(5-cloro-(2-piridil))carboxamida |
WO2008057972A1 (en) | 2006-11-02 | 2008-05-15 | Millennium Pharmaceuticals, Inc. | Methods of synthesizing pharmaceutical salts of a factor xa inhibitor |
-
2006
- 2006-11-07 PE PE2006001368A patent/PE20070717A1/es active IP Right Grant
- 2006-11-07 KR KR1020087011799A patent/KR101358574B1/ko active IP Right Grant
- 2006-11-07 EP EP11187927A patent/EP2431358A1/en not_active Withdrawn
- 2006-11-07 CA CA2627086A patent/CA2627086C/en not_active Expired - Fee Related
- 2006-11-07 RU RU2008123055/04A patent/RU2440986C2/ru not_active Application Discontinuation
- 2006-11-07 PT PT06837238T patent/PT1948608E/pt unknown
- 2006-11-07 AU AU2006311544A patent/AU2006311544B2/en not_active Ceased
- 2006-11-07 NZ NZ592533A patent/NZ592533A/xx not_active IP Right Cessation
- 2006-11-07 DK DK06837238.2T patent/DK1948608T3/da active
- 2006-11-07 EP EP06837238A patent/EP1948608B1/en active Active
- 2006-11-07 NZ NZ567992A patent/NZ567992A/en not_active IP Right Cessation
- 2006-11-07 US US11/594,280 patent/US7598276B2/en active Active
- 2006-11-07 BR BRPI0618362-0A patent/BRPI0618362A2/pt not_active Application Discontinuation
- 2006-11-07 AT AT06837238T patent/ATE549317T1/de active
- 2006-11-07 CN CN201110197429.0A patent/CN102336702B/zh active Active
- 2006-11-07 PE PE2010000471A patent/PE20110070A1/es not_active Application Discontinuation
- 2006-11-07 WO PCT/US2006/043635 patent/WO2007056517A2/en active Application Filing
- 2006-11-07 ES ES06837238T patent/ES2384116T3/es active Active
- 2006-11-07 JP JP2008540190A patent/JP5227178B2/ja not_active Expired - Fee Related
- 2006-11-07 CN CN2006800415554A patent/CN101304971B/zh active Active
- 2006-11-08 AR ARP060104900A patent/AR056787A1/es not_active Application Discontinuation
- 2006-11-08 TW TW095141382A patent/TWI443088B/zh not_active IP Right Cessation
-
2008
- 2008-03-31 IL IL190524A patent/IL190524A/en active IP Right Grant
- 2008-05-05 ZA ZA200803820A patent/ZA200803820B/xx unknown
- 2008-09-23 HK HK08110550.3A patent/HK1115131A1/xx not_active IP Right Cessation
-
2009
- 2009-08-28 US US12/550,291 patent/US8557852B2/en not_active Expired - Fee Related
-
2011
- 2011-06-12 IL IL213487A patent/IL213487A0/en unknown
-
2012
- 2012-09-12 US US13/612,476 patent/US20130064806A1/en not_active Abandoned
- 2012-09-18 JP JP2012204757A patent/JP5662980B2/ja active Active
-
2014
- 2014-02-17 US US14/182,209 patent/US9061019B2/en not_active Expired - Fee Related
-
2015
- 2015-05-18 US US14/715,507 patent/US9555023B2/en active Active
-
2016
- 2016-12-12 AR ARP160103799A patent/AR106960A2/es unknown
- 2016-12-20 US US15/385,651 patent/US20170326119A1/en not_active Abandoned
-
2018
- 2018-03-08 US US15/915,940 patent/US20190046510A1/en not_active Abandoned
Also Published As
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