MA27987A1 - Derives nitro-oxy de losartan, valsatan, candesartan, telmisartan, eprosartan et olmesartan comme bloqueurs des recepteurs de l'angiontensine-ii pour le traitement des maladies cardiovasculaires. - Google Patents
Derives nitro-oxy de losartan, valsatan, candesartan, telmisartan, eprosartan et olmesartan comme bloqueurs des recepteurs de l'angiontensine-ii pour le traitement des maladies cardiovasculaires.Info
- Publication number
- MA27987A1 MA27987A1 MA28789A MA28789A MA27987A1 MA 27987 A1 MA27987 A1 MA 27987A1 MA 28789 A MA28789 A MA 28789A MA 28789 A MA28789 A MA 28789A MA 27987 A1 MA27987 A1 MA 27987A1
- Authority
- MA
- Morocco
- Prior art keywords
- valsatan
- olmesartan
- eprosartan
- telmisartan
- candesartan
- Prior art date
Links
- RMMXLENWKUUMAY-UHFFFAOYSA-N telmisartan Chemical class CCCC1=NC2=C(C)C=C(C=3N(C4=CC=CC=C4N=3)C)C=C2N1CC(C=C1)=CC=C1C1=CC=CC=C1C(O)=O RMMXLENWKUUMAY-UHFFFAOYSA-N 0.000 title abstract 4
- -1 VALSATAN Chemical class 0.000 title abstract 3
- 239000002083 C09CA01 - Losartan Substances 0.000 title abstract 2
- 239000002080 C09CA02 - Eprosartan Chemical class 0.000 title abstract 2
- 239000002053 C09CA06 - Candesartan Substances 0.000 title abstract 2
- 239000005537 C09CA07 - Telmisartan Chemical class 0.000 title abstract 2
- 239000005480 Olmesartan Substances 0.000 title abstract 2
- 229960000932 candesartan Drugs 0.000 title abstract 2
- SGZAIDDFHDDFJU-UHFFFAOYSA-N candesartan Chemical class CCOC1=NC2=CC=CC(C(O)=O)=C2N1CC(C=C1)=CC=C1C1=CC=CC=C1C1=NN=N[N]1 SGZAIDDFHDDFJU-UHFFFAOYSA-N 0.000 title abstract 2
- 229960004563 eprosartan Drugs 0.000 title abstract 2
- OROAFUQRIXKEMV-LDADJPATSA-N eprosartan Chemical class C=1C=C(C(O)=O)C=CC=1CN1C(CCCC)=NC=C1\C=C(C(O)=O)/CC1=CC=CS1 OROAFUQRIXKEMV-LDADJPATSA-N 0.000 title abstract 2
- 229960004773 losartan Drugs 0.000 title abstract 2
- KJJZZJSZUJXYEA-UHFFFAOYSA-N losartan Chemical class CCCCC1=NC(Cl)=C(CO)N1CC1=CC=C(C=2C(=CC=CC=2)C=2[N]N=NN=2)C=C1 KJJZZJSZUJXYEA-UHFFFAOYSA-N 0.000 title abstract 2
- 229960005117 olmesartan Drugs 0.000 title abstract 2
- 229960005187 telmisartan Drugs 0.000 title abstract 2
- 208000024172 Cardiovascular disease Diseases 0.000 title 1
- 102000008873 Angiotensin II receptor Human genes 0.000 abstract 1
- 108050000824 Angiotensin II receptor Proteins 0.000 abstract 1
- 229910004679 ONO2 Inorganic materials 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- 125000001893 nitrooxy group Chemical group [O-][N+](=O)O* 0.000 abstract 1
- VTRAEEWXHOVJFV-UHFFFAOYSA-N olmesartan Chemical compound CCCC1=NC(C(C)(C)O)=C(C(O)=O)N1CC1=CC=C(C=2C(=CC=CC=2)C=2NN=NN=2)C=C1 VTRAEEWXHOVJFV-UHFFFAOYSA-N 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D257/00—Heterocyclic compounds containing rings having four nitrogen atoms as the only ring hetero atoms
- C07D257/02—Heterocyclic compounds containing rings having four nitrogen atoms as the only ring hetero atoms not condensed with other rings
- C07D257/04—Five-membered rings
-
- 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
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/4164—1,3-Diazoles
- A61K31/4178—1,3-Diazoles not condensed 1,3-diazoles and containing further heterocyclic rings, e.g. pilocarpine, nitrofurantoin
-
- 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
- A61P13/00—Drugs for disorders of the urinary system
- A61P13/12—Drugs for disorders of the urinary system of the kidneys
-
- 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
- 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
- A61P9/04—Inotropic agents, i.e. stimulants of cardiac contraction; Drugs for heart failure
-
- 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
-
- 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
- C07D235/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings
- C07D235/02—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings condensed with carbocyclic rings or ring systems
- C07D235/04—Benzimidazoles; Hydrogenated benzimidazoles
- C07D235/20—Two benzimidazolyl-2 radicals linked together directly or via a hydrocarbon or substituted hydrocarbon radical
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/10—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a carbon chain containing aromatic rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
- C07D409/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
- C07D409/06—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Cardiology (AREA)
- Heart & Thoracic Surgery (AREA)
- Urology & Nephrology (AREA)
- Vascular Medicine (AREA)
- Hospice & Palliative Care (AREA)
- Diabetes (AREA)
- Hematology (AREA)
- Pain & Pain Management (AREA)
- Rheumatology (AREA)
- Gastroenterology & Hepatology (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Plural Heterocyclic Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Abstract
Dérivés nitrooxy des bloqueurs des récepteurs pour l'angiotensine II losartan, valsatan, candésartan, telmisartan, éprosartan et olmésartan et les composés y relatifs de formule (I) : R-(Y-ONO2)8 dans laquelle R est de formule (II) ou (III) : R0 est ex. : et R1 est : (IIa), (IIb), (IIc), (IId) ou (IIe).
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP03102379 | 2003-07-31 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| MA27987A1 true MA27987A1 (fr) | 2006-07-03 |
Family
ID=34112476
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| MA28789A MA27987A1 (fr) | 2003-07-31 | 2006-02-13 | Derives nitro-oxy de losartan, valsatan, candesartan, telmisartan, eprosartan et olmesartan comme bloqueurs des recepteurs de l'angiontensine-ii pour le traitement des maladies cardiovasculaires. |
Country Status (29)
| Country | Link |
|---|---|
| US (1) | US20060276523A1 (fr) |
| EP (1) | EP1653950B1 (fr) |
| JP (1) | JP2007500684A (fr) |
| KR (1) | KR20060056352A (fr) |
| CN (1) | CN100496490C (fr) |
| AR (1) | AR045145A1 (fr) |
| AT (1) | ATE383155T1 (fr) |
| AU (1) | AU2004260830B2 (fr) |
| BR (1) | BRPI0413028A (fr) |
| CA (1) | CA2534451A1 (fr) |
| CY (1) | CY1110447T1 (fr) |
| DE (1) | DE602004011230T2 (fr) |
| DK (1) | DK1653950T3 (fr) |
| EC (1) | ECSP066334A (fr) |
| ES (1) | ES2299861T3 (fr) |
| HR (1) | HRP20060084A2 (fr) |
| IL (1) | IL172703A0 (fr) |
| IS (1) | IS2534B (fr) |
| MA (1) | MA27987A1 (fr) |
| MX (1) | MXPA06001263A (fr) |
| NO (1) | NO20060900L (fr) |
| NZ (1) | NZ544463A (fr) |
| PL (2) | PL1653950T3 (fr) |
| PT (1) | PT1653950E (fr) |
| RU (1) | RU2374240C2 (fr) |
| SI (1) | SI1653950T1 (fr) |
| UA (1) | UA87983C2 (fr) |
| WO (1) | WO2005011646A2 (fr) |
| ZA (1) | ZA200600856B (fr) |
Families Citing this family (38)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2006008196A1 (fr) * | 2004-07-20 | 2006-01-26 | Nicox S.A. | Procede destine a la preparation d'esters nitro-oxy, de thioesters nitro-oxy, de carbonates nitro-oxy et de thiocarbonates nitro-oxy, produits intermediaires utiles dans ce procede et leur preparation |
| WO2006079610A1 (fr) * | 2005-01-31 | 2006-08-03 | Nicox S.A. | Derives de sartane nitrooxy en tant que bloqueurs d'un recepteur d'angiotensine ii pour le traitement de maladies cardio-vasculaires et inflammatoires |
| RU2306930C1 (ru) * | 2005-12-28 | 2007-09-27 | Михаил Владимирович Покровский | Способ коррекции эндотелиальной дисфункции комбинацией лозартана и l-аргинина при l-name-индуцированном дефиците оксида азота |
| CN101024643A (zh) * | 2006-02-20 | 2007-08-29 | 上海艾力斯医药科技有限公司 | 咪唑－5－羧酸类衍生物、制备方法及其应用 |
| TW200821303A (en) * | 2006-08-08 | 2008-05-16 | Speedel Experimenta Ag | Organic compounds |
| WO2008058402A1 (fr) | 2006-11-17 | 2008-05-22 | Queen's University At Kingston | Composés et procédés pour traiter des troubles de repliement de protéine |
| AU2006351517B8 (en) | 2006-12-06 | 2012-01-19 | Shenzhen Salubris Pharmaceuticals Co., Ltd. | The salts of imidazol-5-carboxylic acid derivatives, preparation methods and use thereof |
| EP2121664B1 (fr) * | 2006-12-13 | 2013-10-16 | Merck Sharp & Dohme Corp. | Dérivés dinitrate comme antagonistes des récepteurs de l'angiotensine ii |
| TW200831079A (en) * | 2006-12-13 | 2008-08-01 | Merck & Co Inc | Angiotensin II receptor antagonists |
| CN101214242A (zh) * | 2007-01-05 | 2008-07-09 | 上海艾力斯医药科技有限公司 | 新的药用组合物 |
| EP1980559A1 (fr) * | 2007-04-10 | 2008-10-15 | CTG Pharma S.r.l. | Agents cardiovasculaires |
| CN101317842A (zh) | 2007-06-07 | 2008-12-10 | 上海艾力斯医药科技有限公司 | 一种咪唑-5-羧酸衍生物的治疗用途 |
| CN101407511B (zh) * | 2007-10-11 | 2013-01-09 | 上海艾力斯生物医药有限公司 | 一种结晶型的咪唑-5-羧酸衍生物 |
| AR069340A1 (es) * | 2007-11-26 | 2010-01-13 | Merck & Co Inc | Antagonistas del receptor de angiotensina ii |
| PT2230934E (pt) | 2007-12-14 | 2012-11-20 | Aerodesigns Inc | Distribuir produtos alimentares aerossolizáveis |
| JP2011510082A (ja) * | 2008-01-24 | 2011-03-31 | メルク・シャープ・エンド・ドーム・コーポレイション | アンジオテンシンｉｉ受容体拮抗薬 |
| AU2009210484A1 (en) | 2008-02-08 | 2009-08-13 | Merck Sharp & Dohme Corp. | Angiotensin II receptor antagonists |
| US20100311800A1 (en) * | 2008-02-26 | 2010-12-09 | Nicoletta Almirante | Angiotensin ii receptor antagonists |
| JP2011513269A (ja) * | 2008-02-26 | 2011-04-28 | ニコックス エス エイ | 新規アンジオテンシンｉｉレセプターブロッカー誘導体 |
| EP2291076A4 (fr) * | 2008-05-15 | 2012-03-21 | Merck Sharp & Dohme | Antagonistes du récepteur de l'angiotensine ll |
| CN101596189A (zh) * | 2008-06-05 | 2009-12-09 | 上海艾力斯生物医药有限公司 | 含有咪唑-5-羧酸类衍生物的药用组合物 |
| US20110077279A1 (en) * | 2008-06-09 | 2011-03-31 | Nicoletta Almirante | Angiotensin ii receptor antagonists |
| AR073259A1 (es) * | 2008-07-29 | 2010-10-28 | Merck & Co Inc | Derivados de furosemida utiles como diureticos |
| WO2010015447A1 (fr) * | 2008-08-08 | 2010-02-11 | Nicox S.A. | Antagonistes des récepteurs de l'angiotensine ii |
| EP2194048A1 (fr) | 2008-12-02 | 2010-06-09 | Dirk Sartor | Esters de nitrate pour le traitement de maladies vasculaires et métaboliques |
| JP2012511002A (ja) * | 2008-12-05 | 2012-05-17 | メルク・シャープ・エンド・ドーム・コーポレイション | アンジオテンシンｉｉ受容体アンタゴニストとしてのニトロオキシ誘導体 |
| WO2010085014A1 (fr) | 2009-01-23 | 2010-07-29 | Hanmi Pharm. Co., Ltd. | Composition pharmaceutique solide comprenant de l'amlodipine et du losartan et son procédé de fabrication |
| CA2796710A1 (fr) | 2010-04-19 | 2011-10-27 | Cardiolynx Ag | Derives de valsartan portant des donneurs d'oxyde d'azote dans le traitement de maladies vasculaires et metaboliques |
| EP2560634A1 (fr) * | 2010-04-23 | 2013-02-27 | Piramal Enterprises Limited | Promédicaments d'agents thérapeutiques libérant de l'oxyde nitrique |
| WO2011160974A2 (fr) | 2010-06-21 | 2011-12-29 | Nicox S.A. | Dérivés de statines |
| JO3350B1 (ar) | 2011-03-07 | 2019-03-13 | Merck Sharp & Dohme | مشتقات حلقية غير متجانسة محتوية على مجموعات أمينو أولية ومركبات داي أزينيومديولات |
| US9844599B2 (en) | 2013-01-21 | 2017-12-19 | Apparao Satyam | Nitric oxide releasing produgs of therapeutic agents |
| CN103275074B (zh) * | 2013-06-21 | 2016-08-10 | 黄冈鲁班药业股份有限公司 | 一种奥美沙坦衍生物及其制备方法 |
| CN105820125B (zh) * | 2015-01-09 | 2018-12-07 | 北京中医药大学 | 一种用于治疗高血压的化合物及其制备方法和用途 |
| CN108349911B (zh) | 2015-09-07 | 2022-05-13 | 浙江华海药业股份有限公司 | 可释放一氧化氮的前药分子 |
| CN106800537B (zh) | 2017-01-18 | 2019-02-01 | 广东隆赋药业股份有限公司 | 丁苯酞-替米沙坦杂合物及其制备方法和用途 |
| CN108892624B (zh) * | 2018-06-20 | 2020-12-15 | 重庆威鹏药业有限公司 | 沙库巴曲硝基氧衍生物及其制备方法和应用 |
| CN114105881B (zh) * | 2020-08-31 | 2024-01-26 | 沈阳海诺威医药科技有限公司 | 血小板聚集抑制剂及其制备方法和用途 |
Family Cites Families (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CA1338238C (fr) * | 1988-01-07 | 1996-04-09 | David John Carini | Imidazoles bloquant les recepteurs de l'angiotensine ii et combinaisons de ces imidazoles avec des diuretiques et des anti-inflammatoires non steroidiens |
| ATE190051T1 (de) * | 1989-06-14 | 2000-03-15 | Smithkline Beecham Corp | Imidazoalkensäure |
| WO1991000277A1 (fr) * | 1989-06-30 | 1991-01-10 | E.I. Du Pont De Nemours And Company | Imidazoles substitues |
| RU2067581C1 (ru) * | 1989-06-30 | 1996-10-10 | Е.И.Дюпон Де Немур Энд Компани | Аралкилзамещенные имидазолы, обладающие противогипертоническим действием, способ их получения и фармацевтический состав, обладающий ингибирующей активностью в отношении ангиотензина ii |
| AT398202B (de) * | 1991-10-04 | 1994-10-25 | Chem Pharm Forsch Gmbh | Neue imidazolderivate, verfahren zu ihrer herstellung und ihre verwendung |
| FR2725987B1 (fr) * | 1994-10-19 | 1997-01-10 | Sanofi Sa | Procede pour la preparation d'un derive de tetrazole sous deux formes cristallines et nouvelle forme cristalline de ce derive |
| IT1311924B1 (it) * | 1999-04-13 | 2002-03-20 | Nicox Sa | Composti farmaceutici. |
| EP1312379A4 (fr) * | 2000-08-25 | 2004-08-25 | Takeda Chemical Industries Ltd | Agents de reduction du fibrinogene |
| ITMI20011744A1 (it) * | 2001-08-09 | 2003-02-09 | Nicox Sa | Farmaci per le vasculopatie |
-
2004
- 2004-07-20 KR KR1020067001893A patent/KR20060056352A/ko not_active Ceased
- 2004-07-20 CN CNB200480022483XA patent/CN100496490C/zh not_active Expired - Fee Related
- 2004-07-20 US US10/566,292 patent/US20060276523A1/en not_active Abandoned
- 2004-07-20 PT PT04766269T patent/PT1653950E/pt unknown
- 2004-07-20 BR BRPI0413028-6A patent/BRPI0413028A/pt not_active IP Right Cessation
- 2004-07-20 PL PL04766269T patent/PL1653950T3/pl unknown
- 2004-07-20 HR HR20060084A patent/HRP20060084A2/hr not_active Application Discontinuation
- 2004-07-20 ES ES04766269T patent/ES2299861T3/es not_active Expired - Lifetime
- 2004-07-20 MX MXPA06001263A patent/MXPA06001263A/es active IP Right Grant
- 2004-07-20 PL PL379420A patent/PL379420A1/pl not_active Application Discontinuation
- 2004-07-20 AT AT04766269T patent/ATE383155T1/de not_active IP Right Cessation
- 2004-07-20 WO PCT/EP2004/051550 patent/WO2005011646A2/fr not_active Ceased
- 2004-07-20 UA UAA200600273A patent/UA87983C2/ru unknown
- 2004-07-20 CA CA002534451A patent/CA2534451A1/fr not_active Abandoned
- 2004-07-20 RU RU2006105804/04A patent/RU2374240C2/ru not_active IP Right Cessation
- 2004-07-20 AU AU2004260830A patent/AU2004260830B2/en not_active Ceased
- 2004-07-20 EP EP04766269A patent/EP1653950B1/fr not_active Expired - Lifetime
- 2004-07-20 SI SI200430655T patent/SI1653950T1/sl unknown
- 2004-07-20 NZ NZ544463A patent/NZ544463A/en unknown
- 2004-07-20 DE DE602004011230T patent/DE602004011230T2/de not_active Expired - Lifetime
- 2004-07-20 JP JP2006521571A patent/JP2007500684A/ja active Pending
- 2004-07-20 DK DK04766269T patent/DK1653950T3/da active
- 2004-07-28 AR ARP040102685A patent/AR045145A1/es unknown
-
2005
- 2005-12-20 IL IL172703A patent/IL172703A0/en not_active IP Right Cessation
-
2006
- 2006-01-30 EC EC2006006334A patent/ECSP066334A/es unknown
- 2006-01-30 ZA ZA200600856A patent/ZA200600856B/en unknown
- 2006-02-13 MA MA28789A patent/MA27987A1/fr unknown
- 2006-02-24 NO NO20060900A patent/NO20060900L/no not_active Application Discontinuation
- 2006-02-27 IS IS8332A patent/IS2534B/is unknown
-
2008
- 2008-04-07 CY CY20081100385T patent/CY1110447T1/el unknown
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| Publication | Publication Date | Title |
|---|---|---|
| MA27987A1 (fr) | Derives nitro-oxy de losartan, valsatan, candesartan, telmisartan, eprosartan et olmesartan comme bloqueurs des recepteurs de l'angiontensine-ii pour le traitement des maladies cardiovasculaires. | |
| MA27771A1 (fr) | 5,7-diaminopyrazolo[4,3-d]pyrimidines utiles dans le traitement de l'hypertension | |
| EA200501504A1 (ru) | Лиганды каннабиноидных рецепторов и их применение | |
| EA200301213A1 (ru) | Лиганды рецепторов 5-ht и их применение | |
| DE60027420D1 (de) | Tri-aryl-säurederivate als ppar rezeptor liganden | |
| EA200700047A1 (ru) | Новые алкильные производные в качестве метаботропных рецепторов глутамата | |
| MA31894B1 (fr) | Composes organiques | |
| TNSN07275A1 (fr) | Derives de triazole substitues, servant d'antagonistes d'ocytocine | |
| MA27728A1 (fr) | Antagonistes des recepteurs de cgrp | |
| MA31574B1 (fr) | Dérivés de pyrazole et leur utilisation comme inhibiteurs de raf | |
| IL215026A (en) | 1r7zb antagonist, methods and compounds @ which include @ the same | |
| MA30427B1 (fr) | Derives bicycliques utilises comme inhibiteurs de cetp | |
| NO20044475L (no) | 2-(2,6-diklorfenyl)-diarulimidazoler | |
| EA200501771A1 (ru) | Лиганды каннабиноидных рецепторов и их применения | |
| MA29772B1 (fr) | Benzimidazoles substitues et procedes de preparation | |
| MA30394B1 (fr) | Synthese d'acylaminoalcenylene-amides pouvant etre employes en tant qu'antagonistes de la substance p | |
| TNSN02014A1 (fr) | Composes nouveaux agonistes de ppar et compositions les contenant | |
| ATE304533T1 (de) | Tetrahydrochinolinderivate als muscarinische agonisten | |
| MA28681B1 (fr) | 3-aminocyclopentanecarboxamides utiles comme modulateurs de récepteurs de chimiokines | |
| MA29839B1 (fr) | Derives de carboxamides servant d'antagonistes des recepteurs muscariniques | |
| ATE365730T1 (de) | Neuartige verbindungen | |
| EA200300716A1 (ru) | Гетероциклилалкилиндольные или -азаиндольные соединения в качестве лиганд 5-гидрокситриптамина-6 | |
| NO20055632L (no) | Aromatiske oksyfenyl- og aromatiske sulfanylfenylderivater | |
| BR0305708A (pt) | Derivados de benzimidazol para o tratamento de disfunção sexual | |
| MA27549A1 (fr) | N-sulfonyl-4-methylene-amino-3-hydroxy-2-pyridones |