ECSP045234A - PROCEDIMIENTO PARA LA FABRICACION DE DERIVADOS DE ACIDO MEVALONICO INHIBIDORES DE ß-HIDROXI-ß-METILGLUTARILO-CO-ENZIMA-A REDUCTASA - Google Patents
PROCEDIMIENTO PARA LA FABRICACION DE DERIVADOS DE ACIDO MEVALONICO INHIBIDORES DE ß-HIDROXI-ß-METILGLUTARILO-CO-ENZIMA-A REDUCTASAInfo
- Publication number
- ECSP045234A ECSP045234A EC2004005234A ECSP045234A ECSP045234A EC SP045234 A ECSP045234 A EC SP045234A EC 2004005234 A EC2004005234 A EC 2004005234A EC SP045234 A ECSP045234 A EC SP045234A EC SP045234 A ECSP045234 A EC SP045234A
- Authority
- EC
- Ecuador
- Prior art keywords
- manufacture
- glutarilo
- enzima
- reductasa
- hidroxi
- Prior art date
Links
- 238000004519 manufacturing process Methods 0.000 title abstract 2
- 238000000034 method Methods 0.000 title abstract 2
- KJTLQQUUPVSXIM-ZCFIWIBFSA-N (R)-mevalonic acid Chemical class OCC[C@](O)(C)CC(O)=O KJTLQQUUPVSXIM-ZCFIWIBFSA-N 0.000 title 1
- 230000002401 inhibitory effect Effects 0.000 title 1
- 150000003839 salts Chemical class 0.000 abstract 2
- 150000001875 compounds Chemical class 0.000 abstract 1
- 150000002596 lactones Chemical class 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/28—Phosphorus compounds with one or more P—C bonds
- C07F9/535—Organo-phosphoranes
- C07F9/5352—Phosphoranes containing the structure P=C-
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/06—Antihyperlipidemics
-
- 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
- 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
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C51/00—Preparation of carboxylic acids or their salts, halides or anhydrides
- C07C51/09—Preparation of carboxylic acids or their salts, halides or anhydrides from carboxylic acid esters or lactones
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C59/00—Compounds having carboxyl groups bound to acyclic carbon atoms and containing any of the groups OH, O—metal, —CHO, keto, ether, groups, groups, or groups
- C07C59/40—Unsaturated compounds
- C07C59/42—Unsaturated compounds containing hydroxy or O-metal groups
-
- 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
- C07D213/24—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 substituted hydrocarbon radicals attached to ring carbon atoms
- C07D213/26—Radicals substituted by halogen atoms or nitro radicals
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D309/00—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings
- C07D309/16—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member
- C07D309/28—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member 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
- C07D309/30—Oxygen atoms, e.g. delta-lactones
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F15/00—Compounds containing elements of Groups 8, 9, 10 or 18 of the Periodic Table
- C07F15/0006—Compounds containing elements of Groups 8, 9, 10 or 18 of the Periodic Table compounds of the platinum group
- C07F15/0033—Iridium compounds
- C07F15/004—Iridium compounds without a metal-carbon linkage
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F15/00—Compounds containing elements of Groups 8, 9, 10 or 18 of the Periodic Table
- C07F15/0006—Compounds containing elements of Groups 8, 9, 10 or 18 of the Periodic Table compounds of the platinum group
- C07F15/0046—Ruthenium compounds
- C07F15/0053—Ruthenium compounds without a metal-carbon linkage
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F15/00—Compounds containing elements of Groups 8, 9, 10 or 18 of the Periodic Table
- C07F15/0006—Compounds containing elements of Groups 8, 9, 10 or 18 of the Periodic Table compounds of the platinum group
- C07F15/0073—Rhodium compounds
- C07F15/008—Rhodium compounds without a metal-carbon linkage
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F15/00—Compounds containing elements of Groups 8, 9, 10 or 18 of the Periodic Table
- C07F15/02—Iron compounds
- C07F15/025—Iron compounds without a metal-carbon linkage
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F15/00—Compounds containing elements of Groups 8, 9, 10 or 18 of the Periodic Table
- C07F15/04—Nickel compounds
- C07F15/045—Nickel compounds without a metal-carbon linkage
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F15/00—Compounds containing elements of Groups 8, 9, 10 or 18 of the Periodic Table
- C07F15/06—Cobalt compounds
- C07F15/065—Cobalt compounds without a metal-carbon linkage
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- General Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Veterinary Medicine (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Pharmacology & Pharmacy (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- General Chemical & Material Sciences (AREA)
- Public Health (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Molecular Biology (AREA)
- Biochemistry (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Vascular Medicine (AREA)
- Hematology (AREA)
- Cardiology (AREA)
- Heart & Thoracic Surgery (AREA)
- Urology & Nephrology (AREA)
- Diabetes (AREA)
- Obesity (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
- Preparation Of Compounds By Using Micro-Organisms (AREA)
- Quinoline Compounds (AREA)
- Indole Compounds (AREA)
Abstract
La invención se refiere a un procedimiento para la fabricación de un compuesto de la fórmula (I); o una sal, especialmente una sal farmacéuticamente aceptable con una base del mismo, o una lactona del mismo, en donde el elemento (a) representa -CH2-CH2- o -CH=CH, y R representa un radical cíclico.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GBGB0204129.1A GB0204129D0 (en) | 2002-02-21 | 2002-02-21 | Process for the manufacture of organic compounds |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ECSP045234A true ECSP045234A (es) | 2004-09-28 |
Family
ID=9931523
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| EC2004005234A ECSP045234A (es) | 2002-02-21 | 2004-08-16 | PROCEDIMIENTO PARA LA FABRICACION DE DERIVADOS DE ACIDO MEVALONICO INHIBIDORES DE ß-HIDROXI-ß-METILGLUTARILO-CO-ENZIMA-A REDUCTASA |
Country Status (18)
| Country | Link |
|---|---|
| US (3) | US7208623B2 (es) |
| EP (1) | EP1478640A1 (es) |
| JP (1) | JP2005520818A (es) |
| KR (1) | KR100978970B1 (es) |
| CN (1) | CN1318412C (es) |
| AU (1) | AU2003218994B2 (es) |
| BR (1) | BR0307801A (es) |
| CA (1) | CA2473075A1 (es) |
| EC (1) | ECSP045234A (es) |
| GB (1) | GB0204129D0 (es) |
| IL (1) | IL163279A (es) |
| MX (1) | MXPA04008110A (es) |
| NO (1) | NO20043919L (es) |
| NZ (1) | NZ534394A (es) |
| PL (1) | PL370596A1 (es) |
| RU (1) | RU2335500C2 (es) |
| WO (1) | WO2003070717A1 (es) |
| ZA (1) | ZA200405436B (es) |
Families Citing this family (21)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB0204129D0 (en) | 2002-02-21 | 2002-04-10 | Novartis Ag | Process for the manufacture of organic compounds |
| CN101219992B (zh) | 2003-02-12 | 2011-08-31 | 日产化学工业株式会社 | 匹伐他汀钙的晶形 |
| GB0324791D0 (en) | 2003-10-24 | 2003-11-26 | Astrazeneca Ab | Chemical process |
| US20070179166A1 (en) * | 2003-12-24 | 2007-08-02 | Valerie Niddam-Hildesheim | Process for preparation of statins with high syn to anti ratio |
| US7851624B2 (en) * | 2003-12-24 | 2010-12-14 | Teva Pharamaceutical Industries Ltd. | Triol form of rosuvastatin and synthesis of rosuvastatin |
| EP1634870A1 (en) * | 2004-08-27 | 2006-03-15 | Zhejiang Hisun Pharmaceutical Co. Ltd. | Process and intermediates for the selective synthesis of Fluvastatin |
| EP1817027A2 (en) * | 2004-09-27 | 2007-08-15 | Ranbaxy Laboratories Limited | Process for preparating enantiomerically pure fluvastatin sodium and a novel polymorphic form thereof |
| US8354530B2 (en) | 2005-07-28 | 2013-01-15 | Lek Pharmaceuticals d. d | Process for the synthesis of rosuvastatin calcium |
| US8455640B2 (en) | 2006-05-03 | 2013-06-04 | Msn Laboratories Limited | Process for statins and its pharmaceutically acceptable salts thereof |
| US8404841B2 (en) | 2006-10-09 | 2013-03-26 | Msn Laboratories Limited | Process for the preparation of statins and their pharmaceutically acceptable salts thereof |
| WO2008053334A2 (en) * | 2006-10-31 | 2008-05-08 | Aurobindo Pharma Limited | An improved process for preparing rosuvastatin calcium |
| EP2125754B1 (en) * | 2007-02-08 | 2012-04-11 | Aurobindo Pharma Limited | Process for preparation of rosuvastatin calcium |
| KR20090033183A (ko) * | 2007-04-18 | 2009-04-01 | 테바 파마슈티컬 인더스트리즈 리미티드 | 로수바스타틴 중간체 및 로수바스타틴의 제조 방법 |
| US20090069563A1 (en) * | 2007-07-12 | 2009-03-12 | Valerie Niddam-Hildesheim | Rosuvastatin intermediates and their preparation |
| KR101063146B1 (ko) * | 2008-11-10 | 2011-09-07 | 미래파인켐 주식회사 | 피타바스타틴 중간체의 제조방법 및 이를 이용한 피타바스타틴 헤미 칼슘염의 제조방법 |
| EP2387561A4 (en) | 2009-01-19 | 2012-07-25 | Msn Lab Ltd | IMPROVED PROCESS FOR THE PREPARATION OF HIGH-PURITY (3R, 5S) -7-β-CYCLOPROPYL-4- (4-FLUOROPHENYL) QUINOLIN-3-YL-3,5-DIHYDROXY-6 (E) -HEPTENOIC ACID, INCLUDING ITS PHARMACEUTICALLY ACCEPTABLE SALTS |
| EP2526099B1 (en) | 2010-01-18 | 2016-03-30 | MSN Laboratories Limited | Improved process for the preparation of amide intermediates and their use thereof |
| EP2638013A4 (en) * | 2010-11-12 | 2014-03-26 | Hetero Research Foundation | NEW POLYMORPHS OF CALCIUM PIVASTATIN |
| FR2970178B1 (fr) | 2011-01-07 | 2014-06-20 | Liliane Therese Jacquot | Promedicaments pour une delivrance specifique au niveau du foie et une meilleure tolerance |
| CN103058925B (zh) * | 2011-11-02 | 2015-09-02 | 石药集团中奇制药技术(石家庄)有限公司 | 一种匹伐他汀钙的制备方法 |
| TWI516520B (zh) | 2014-10-31 | 2016-01-11 | 財團法人工業技術研究院 | 波長轉換聚合物、其製法及包含其之波長轉換裝置 |
Family Cites Families (21)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4851427A (en) | 1985-10-25 | 1989-07-25 | Sandoz Pharm. Corp. | Pyrrole analogs of mevalonolactone, derivatives thereof and pharmaceutical use |
| CA1336714C (en) | 1987-08-20 | 1995-08-15 | Yoshihiro Fujikawa | Quinoline type mevalonolactone inhibitors of cholesterol biosynthesis |
| FI94339C (fi) * | 1989-07-21 | 1995-08-25 | Warner Lambert Co | Menetelmä farmaseuttisesti käyttökelpoisen /R-(R*,R*)/-2-(4-fluorifenyyli)- , -dihydroksi-5-(1-metyylietyyli)-3-fenyyli-4-/(fenyyliamino)karbonyyli/-1H-pyrroli-1-heptaanihapon ja sen farmaseuttisesti hyväksyttävien suolojen valmistamiseksi |
| DK0577040T3 (da) | 1992-07-02 | 1998-02-02 | Hoechst Ag | Fremgangsmåde til fremstilling af (3R,5S)6-hydroxy-3,,5-O-isopropyliden-3,5-dihydroxyhexansyre-tert.-butylester |
| US5763688A (en) | 1994-12-07 | 1998-06-09 | Research Development Corporation Of Japan | Method for producing an alcohol |
| EP0916637B1 (en) | 1995-12-06 | 2005-04-20 | Japan Science and Technology Agency | Process for preparating optically active compounds |
| JP3159661B2 (ja) * | 1997-02-21 | 2001-04-23 | 科学技術振興事業団 | 光学活性アルコール類の製造方法 |
| US6187961B1 (en) * | 1997-11-06 | 2001-02-13 | Roche Vitamins Inc. | Process for the preparation of trans-(R,R)-actinol |
| JPH11322649A (ja) * | 1998-03-16 | 1999-11-24 | Mitsubishi Chemical Corp | 光学活性アルコールの製造方法 |
| JPH11335385A (ja) * | 1998-05-20 | 1999-12-07 | Takasago Internatl Corp | 遷移金属錯体および該錯体を用いた光学活性アルコールの製造方法 |
| JP2000212110A (ja) * | 1999-01-27 | 2000-08-02 | Mitsubishi Chemicals Corp | 光学活性α―アルキルベンジルアルコ―ル類の製造方法 |
| JP3630002B2 (ja) * | 1999-03-03 | 2005-03-16 | 三菱化学株式会社 | 光学活性1,2−ジオール類の製造方法 |
| JP2000327659A (ja) * | 1999-03-15 | 2000-11-28 | Mitsubishi Chemicals Corp | 光学活性ピリジルアルコール類の製造方法 |
| US6211412B1 (en) * | 1999-03-29 | 2001-04-03 | The University Of Kansas | Synthesis of epothilones |
| US6603015B2 (en) * | 1999-03-29 | 2003-08-05 | University Of Kansas | Synthesis of epothilones |
| JP2001104795A (ja) * | 1999-10-13 | 2001-04-17 | Mitsubishi Chemicals Corp | ルテニウム触媒組成物 |
| JP3720235B2 (ja) * | 2000-03-14 | 2005-11-24 | 高砂香料工業株式会社 | 光学活性ルテニウムホスフィン錯体の製造方法及び該錯体を用いた光学活性アルコールの製造方法 |
| DK1136475T3 (da) * | 2000-03-22 | 2004-12-27 | Hoffmann La Roche | Piperidin- og piperazinderivater til anvendelse i behandlingen af Alzheimer |
| AU2001274049A1 (en) * | 2000-05-26 | 2001-12-11 | Ciba Specialty Chemicals Holding Inc. | Process for the preparation of indole derivatives and intermediates of the process |
| WO2002008169A1 (en) * | 2000-07-24 | 2002-01-31 | Chirotech Technology Limited | Ruthenium complexes and their use in asymmetric hydrogenation |
| GB0204129D0 (en) | 2002-02-21 | 2002-04-10 | Novartis Ag | Process for the manufacture of organic compounds |
-
2002
- 2002-02-21 GB GBGB0204129.1A patent/GB0204129D0/en not_active Ceased
-
2003
- 2003-02-20 BR BR0307801-9A patent/BR0307801A/pt not_active IP Right Cessation
- 2003-02-20 KR KR1020047013033A patent/KR100978970B1/ko not_active Expired - Fee Related
- 2003-02-20 NZ NZ534394A patent/NZ534394A/en not_active IP Right Cessation
- 2003-02-20 JP JP2003569624A patent/JP2005520818A/ja active Pending
- 2003-02-20 CA CA002473075A patent/CA2473075A1/en not_active Abandoned
- 2003-02-20 AU AU2003218994A patent/AU2003218994B2/en not_active Ceased
- 2003-02-20 CN CNB038042886A patent/CN1318412C/zh not_active Expired - Fee Related
- 2003-02-20 PL PL03370596A patent/PL370596A1/xx not_active Application Discontinuation
- 2003-02-20 RU RU2004128256/04A patent/RU2335500C2/ru not_active IP Right Cessation
- 2003-02-20 EP EP03714750A patent/EP1478640A1/en not_active Withdrawn
- 2003-02-20 MX MXPA04008110A patent/MXPA04008110A/es active IP Right Grant
- 2003-02-20 WO PCT/EP2003/001738 patent/WO2003070717A1/en not_active Ceased
- 2003-02-20 US US10/504,655 patent/US7208623B2/en not_active Expired - Fee Related
-
2004
- 2004-07-08 ZA ZA200405436A patent/ZA200405436B/en unknown
- 2004-07-29 IL IL163279A patent/IL163279A/en not_active IP Right Cessation
- 2004-08-16 EC EC2004005234A patent/ECSP045234A/es unknown
- 2004-09-20 NO NO20043919A patent/NO20043919L/no not_active Application Discontinuation
-
2007
- 2007-03-09 US US11/684,134 patent/US20070155970A1/en not_active Abandoned
-
2008
- 2008-07-23 US US12/220,259 patent/US20080312462A1/en not_active Abandoned
Also Published As
| Publication number | Publication date |
|---|---|
| US7208623B2 (en) | 2007-04-24 |
| GB0204129D0 (en) | 2002-04-10 |
| CN1636004A (zh) | 2005-07-06 |
| KR20040111360A (ko) | 2004-12-31 |
| ZA200405436B (en) | 2005-06-17 |
| PL370596A1 (en) | 2005-05-30 |
| AU2003218994B2 (en) | 2007-08-09 |
| US20050159480A1 (en) | 2005-07-21 |
| BR0307801A (pt) | 2004-12-21 |
| MXPA04008110A (es) | 2004-11-26 |
| AU2003218994A1 (en) | 2003-09-09 |
| CN1318412C (zh) | 2007-05-30 |
| CA2473075A1 (en) | 2003-08-23 |
| US20080312462A1 (en) | 2008-12-18 |
| RU2335500C2 (ru) | 2008-10-10 |
| US20070155970A1 (en) | 2007-07-05 |
| KR100978970B1 (ko) | 2010-08-30 |
| JP2005520818A (ja) | 2005-07-14 |
| NO20043919L (no) | 2004-09-20 |
| RU2004128256A (ru) | 2005-06-27 |
| IL163279A (en) | 2010-06-30 |
| NZ534394A (en) | 2006-10-27 |
| WO2003070717A1 (en) | 2003-08-28 |
| EP1478640A1 (en) | 2004-11-24 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| ECSP045234A (es) | PROCEDIMIENTO PARA LA FABRICACION DE DERIVADOS DE ACIDO MEVALONICO INHIBIDORES DE ß-HIDROXI-ß-METILGLUTARILO-CO-ENZIMA-A REDUCTASA | |
| AR051778A2 (es) | Derivados del acido dimetilaminocrotonico y procesos para supreparacion | |
| NO20060870L (no) | Fluorsubstituert omega-karboksyaryldifenylurea for behandling og profylakse av sykdommer og tilstander | |
| EA200870117A1 (ru) | Азаиндоловые ингибиторы аурора-киназ | |
| DE60225671D1 (de) | Pharmazeutisch wirksame piperidinderivate | |
| EA200500203A1 (ru) | Новый способ синтеза и новая кристаллическая форма агомелатина и фармацевтические композиции, которые её содержат | |
| UA96565C2 (ru) | Пиридильные ингибиторы хеджхоговской передачи сигнала | |
| NO20091858L (no) | Hydrobenzamid derivater som inhibitorer av HSP90 | |
| EA200700096A1 (ru) | Производные 2-карбамид-4-фенилтиазола, способ их получения и их применение в терапии | |
| DK1613304T3 (da) | DPP-IV-inhibitorer | |
| NO20064077L (no) | Kemokinreseptorantagonister | |
| AR066972A1 (es) | Derivados azapeptidicos | |
| SE0400284D0 (sv) | Novel compounds | |
| EA200600621A1 (ru) | Производные тетрагидронафталина, способ их получения и их применение в качестве противовоспалительных средств | |
| CY1111327T1 (el) | Υποκατεστημενα παραγωγα κυκλοεξυλοξεικου οξεος | |
| AR050518A1 (es) | Proceso de amonolisis para la preparacion de intermedarios para inhibidores de dpp iv | |
| NO20065719L (no) | I det vesentlige rene 2-{[2-(2-metylamino-pyrimidin-4-yl)-1H-indol-5-karbonyl]-amlno}-3-(fenylpyridin-2-yl-amino)-propionsyre som en IkB kinaseinhibitor. | |
| DE602005016297D1 (de) | Antithrombotische diamide | |
| CY1109569T1 (el) | Υποκατεστημενα παραγωγα κυκλοεξανο-1,4-διαμινης | |
| SA523451905B1 (ar) | Cdk2 مركبات بيريميدينيل-بيرازول بها استبدال كمثبطات | |
| DK1670778T3 (da) | Omlejrede pentanoler, en fremgangsmåde til fremstilling heraf og anvendelse heraf som betændelsehæmmende | |
| UY27577A1 (es) | Inhibidores de la integrasa del vih | |
| ATE441630T1 (de) | Substituierte cyclopenten-verbindungen | |
| ATE553077T1 (de) | Peptidaseinhibitoren | |
| UA97348C2 (en) | HETEROCYCLIC NF-kB INHIBITORS |