CO5790167A1 - Nueva asociacion de un inhibidor de la corriente sinusal if y de un inhibidor calcico y las composiciones farmaceuticas que las contienen - Google Patents
Nueva asociacion de un inhibidor de la corriente sinusal if y de un inhibidor calcico y las composiciones farmaceuticas que las contienenInfo
- Publication number
- CO5790167A1 CO5790167A1 CO06127373A CO06127373A CO5790167A1 CO 5790167 A1 CO5790167 A1 CO 5790167A1 CO 06127373 A CO06127373 A CO 06127373A CO 06127373 A CO06127373 A CO 06127373A CO 5790167 A1 CO5790167 A1 CO 5790167A1
- Authority
- CO
- Colombia
- Prior art keywords
- inhibitor
- hydrates
- calcium
- association according
- crystalline forms
- Prior art date
Links
- 239000000480 calcium channel blocker Substances 0.000 title abstract 5
- 239000003112 inhibitor Substances 0.000 title abstract 4
- 239000008194 pharmaceutical composition Substances 0.000 title 1
- 150000004677 hydrates Chemical class 0.000 abstract 6
- 239000002253 acid Substances 0.000 abstract 4
- 150000003839 salts Chemical class 0.000 abstract 4
- ZPBWCRDSRKPIDG-UHFFFAOYSA-N amlodipine benzenesulfonate Chemical compound OS(=O)(=O)C1=CC=CC=C1.CCOC(=O)C1=C(COCCN)NC(C)=C(C(=O)OC)C1C1=CC=CC=C1Cl ZPBWCRDSRKPIDG-UHFFFAOYSA-N 0.000 abstract 3
- HLUKNZUABFFNQS-ZMBIFBSDSA-N ivabradine hydrochloride Chemical compound Cl.C1CC2=CC(OC)=C(OC)C=C2CC(=O)N1CCCN(C)C[C@H]1CC2=C1C=C(OC)C(OC)=C2 HLUKNZUABFFNQS-ZMBIFBSDSA-N 0.000 abstract 3
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 abstract 3
- SYIUPRKONIOYIL-UHFFFAOYSA-N 1-benzazepin-3-one Chemical compound N1=CC(=O)C=CC2=CC=CC=C21 SYIUPRKONIOYIL-UHFFFAOYSA-N 0.000 abstract 2
- 229960000528 amlodipine Drugs 0.000 abstract 2
- 229960003825 ivabradine Drugs 0.000 abstract 2
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 abstract 2
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 abstract 2
- 229960004005 amlodipine besylate Drugs 0.000 abstract 1
- 125000004925 dihydropyridyl group Chemical class N1(CC=CC=C1)* 0.000 abstract 1
- 229960000504 ivabradine hydrochloride Drugs 0.000 abstract 1
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K45/00—Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
- A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
-
- 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
- A61K31/4422—1,4-Dihydropyridines, e.g. nifedipine, nicardipine
-
- 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
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/55—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole
-
- 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
-
- 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
- A61P9/06—Antiarrhythmics
-
- 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
Landscapes
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- Epidemiology (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Organic Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Heart & Thoracic Surgery (AREA)
- Cardiology (AREA)
- Neurology (AREA)
- Urology & Nephrology (AREA)
- Vascular Medicine (AREA)
- Neurosurgery (AREA)
- Biomedical Technology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
Abstract
? Asociación de un inhibidor selectivo y específico de la corriente sinusal lf y de un inhibidor cálcico. La asociación según la reivindicación 1, en la que el inhibidor selectivo y específico de la corriente sinusal If es la ivabradina o 3-{3-[{[(7S)-3,4-dimetoxibicicIo[4.2.0] octa-1,3,5-trien-7-il]metil}(metil)amino]propil}-7,8-dimetoxi-1,3,4,5-tetrahidro-2H-3-benzazepin-2-ona o uno de sus hidratos, formas cristalinas o sales de adición de un ácido farmacéuticamente aceptable. La asociación según la reivindicación 1, en la que el inhibidor selectivo y específico de la corriente sinusal If es el hidrocloruro de ivabradina o 3-{3-[{[(7S)-3,4-dimetoxibiciclo[4.2.0]octa-1,3,5-trien-7-ilmetil}(metil)amino]propil}-7,8-dimetoxi-1,3,4,5-tetrahidro-2H-3-benzazepin-2-ona, o uno de sus hidratos o formas cristalinas. La asociación según la reivindicación 1, en la que el inhibidor cálcico pertenece a la clase de las dihidropiridinas. La asociación según la reivindicación 1, en la que el inhibidor cálcico es el amlodipino o uno de sus hidratos, formas cristalinas o sales de adición de un ácido farmacéuticamente aceptable. La asociación según la reivindicación 1, en la que el inhibidor cálcico es el besilato de amlodipino, o uno de sus hidratos o formas cristalinas. La asociación según la reivindicación 1, que contiene la ivabradina o uno de sus hidratos, formas cristalinas o sales de adición de un ácido farmacéuticamcnte aceptable, y el amlodipino o uno de sus hidratos, formas cristalinas o sales de adición de un ácido farmacéuticamente aceptable. <EMI FILE="06127373_1" ID="1" IMF=JPEG HE=50 WI=50 >
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR0513008A FR2894826B1 (fr) | 2005-12-21 | 2005-12-21 | Nouvelle association d'un inhibiteur du courant if sinusal et d'un inhibiteur calcique et les compositions pharmaceutiques qui la contiennent |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CO5790167A1 true CO5790167A1 (es) | 2007-08-31 |
Family
ID=37075950
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CO06127373A CO5790167A1 (es) | 2005-12-21 | 2006-12-20 | Nueva asociacion de un inhibidor de la corriente sinusal if y de un inhibidor calcico y las composiciones farmaceuticas que las contienen |
Country Status (41)
| Country | Link |
|---|---|
| US (3) | US20070142356A1 (es) |
| EP (1) | EP1800683B1 (es) |
| JP (2) | JP4783275B2 (es) |
| KR (1) | KR100907584B1 (es) |
| CN (1) | CN101015556B (es) |
| AP (1) | AP2208A (es) |
| AR (1) | AR058575A1 (es) |
| AT (1) | ATE488239T1 (es) |
| AU (1) | AU2006252211B2 (es) |
| BR (1) | BRPI0605516A (es) |
| CA (1) | CA2571649C (es) |
| CO (1) | CO5790167A1 (es) |
| CR (1) | CR8813A (es) |
| CY (1) | CY1111007T1 (es) |
| DE (1) | DE602006018247D1 (es) |
| DK (1) | DK1800683T3 (es) |
| EA (1) | EA013536B1 (es) |
| ES (1) | ES2356660T3 (es) |
| FR (1) | FR2894826B1 (es) |
| GE (1) | GEP20094603B (es) |
| GT (1) | GT200600523A (es) |
| HK (1) | HK1106442A1 (es) |
| HR (1) | HRP20110028T1 (es) |
| IL (1) | IL180209A (es) |
| JO (1) | JO2675B1 (es) |
| MA (1) | MA28724B1 (es) |
| MX (1) | MXPA06014884A (es) |
| MY (1) | MY143563A (es) |
| NO (1) | NO337509B1 (es) |
| NZ (1) | NZ552222A (es) |
| PE (1) | PE20071133A1 (es) |
| PL (1) | PL1800683T3 (es) |
| PT (1) | PT1800683E (es) |
| RS (1) | RS51534B (es) |
| SA (1) | SA06270482B1 (es) |
| SG (1) | SG133546A1 (es) |
| SI (1) | SI1800683T1 (es) |
| TW (1) | TWI373344B (es) |
| UA (1) | UA91507C2 (es) |
| WO (1) | WO2007077329A2 (es) |
| ZA (1) | ZA200610822B (es) |
Families Citing this family (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2894826B1 (fr) * | 2005-12-21 | 2010-10-22 | Servier Lab | Nouvelle association d'un inhibiteur du courant if sinusal et d'un inhibiteur calcique et les compositions pharmaceutiques qui la contiennent |
| FR2920773B1 (fr) | 2007-09-11 | 2009-10-23 | Servier Lab | Derives de 1,2,4,5-tetrahydro-3h-benzazepines, leur procede de preparation et les compositions pharmaceutiques qui les contiennent |
| FR2927538B1 (fr) * | 2008-02-14 | 2010-02-19 | Servier Lab | Association d'un inhibiteur du courant if sinusal et d'un beta-bloquant. |
| CN101564394B (zh) * | 2008-04-21 | 2010-12-15 | 鲁南制药集团股份有限公司 | 含有伊伐布雷定和曲美他嗪的药物组合物 |
| WO2009158005A1 (en) * | 2008-06-27 | 2009-12-30 | Concert Pharmaceuticals, Inc. | Benzazepinone compounds |
| FR2938194B1 (fr) * | 2008-11-07 | 2012-08-31 | Servier Lab | Utilisation de l'ivabradine comme agent de diagnostic dans la methode d'angiographie coronaire par tomodensitometrie multicoupe |
Family Cites Families (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB8608335D0 (en) * | 1986-04-04 | 1986-05-08 | Pfizer Ltd | Pharmaceutically acceptable salts |
| FR2681862B1 (fr) * | 1991-09-27 | 1993-11-12 | Adir Cie | Nouvelles (benzocycloalkyl)alkylamines, leur procede de preparation, et les compositions pharmaceutiques qui les contiennent. |
| US20030092745A1 (en) * | 2000-02-25 | 2003-05-15 | Pfizer Inc. | Combination therapy |
| WO2003024457A1 (fr) * | 2001-09-11 | 2003-03-27 | Asahi Kasei Kabushiki Kaisha | Composition medicinale pour la prevention ou le traitement des troubles vasculaires cerebraux et de la cardiopathie |
| AR037565A1 (es) * | 2001-11-21 | 2004-11-17 | Synthon Bv | Formas de sales de amlodipina y procedimientos para prepararlas. |
| FR2868777B1 (fr) * | 2004-04-13 | 2006-05-26 | Servier Lab | Nouveau procede de synthese de l'ivabradine et de ses sels d'addition a un acide pharmaceutiquement acceptable |
| FR2894826B1 (fr) * | 2005-12-21 | 2010-10-22 | Servier Lab | Nouvelle association d'un inhibiteur du courant if sinusal et d'un inhibiteur calcique et les compositions pharmaceutiques qui la contiennent |
-
2005
- 2005-12-21 FR FR0513008A patent/FR2894826B1/fr not_active Expired - Fee Related
-
2006
- 2006-12-14 CR CR8813A patent/CR8813A/es not_active Application Discontinuation
- 2006-12-15 MA MA29539A patent/MA28724B1/fr unknown
- 2006-12-18 AP AP2006003858A patent/AP2208A/xx active
- 2006-12-18 PE PE2006001618A patent/PE20071133A1/es active IP Right Grant
- 2006-12-18 SG SG200608806-6A patent/SG133546A1/en unknown
- 2006-12-18 MX MXPA06014884A patent/MXPA06014884A/es active IP Right Grant
- 2006-12-19 NO NO20065903A patent/NO337509B1/no not_active IP Right Cessation
- 2006-12-20 IL IL180209A patent/IL180209A/en active IP Right Grant
- 2006-12-20 WO PCT/FR2006/002805 patent/WO2007077329A2/fr active Application Filing
- 2006-12-20 TW TW095148015A patent/TWI373344B/zh not_active IP Right Cessation
- 2006-12-20 GT GT200600523A patent/GT200600523A/es unknown
- 2006-12-20 AR ARP060105640A patent/AR058575A1/es not_active Application Discontinuation
- 2006-12-20 GE GEAP20069773A patent/GEP20094603B/en unknown
- 2006-12-20 PL PL06291991T patent/PL1800683T3/pl unknown
- 2006-12-20 DE DE602006018247T patent/DE602006018247D1/de active Active
- 2006-12-20 EA EA200602156A patent/EA013536B1/ru unknown
- 2006-12-20 MY MYPI20064723A patent/MY143563A/en unknown
- 2006-12-20 UA UAA200613551A patent/UA91507C2/ru unknown
- 2006-12-20 SI SI200630854T patent/SI1800683T1/sl unknown
- 2006-12-20 EP EP06291991A patent/EP1800683B1/fr active Active
- 2006-12-20 PT PT06291991T patent/PT1800683E/pt unknown
- 2006-12-20 CO CO06127373A patent/CO5790167A1/es not_active Application Discontinuation
- 2006-12-20 SA SA06270482A patent/SA06270482B1/ar unknown
- 2006-12-20 NZ NZ552222A patent/NZ552222A/en not_active IP Right Cessation
- 2006-12-20 RS RSP-2010/0554A patent/RS51534B/en unknown
- 2006-12-20 ES ES06291991T patent/ES2356660T3/es active Active
- 2006-12-20 DK DK06291991.5T patent/DK1800683T3/da active
- 2006-12-20 AT AT06291991T patent/ATE488239T1/de active
- 2006-12-21 JP JP2006343824A patent/JP4783275B2/ja active Active
- 2006-12-21 CA CA2571649A patent/CA2571649C/fr active Active
- 2006-12-21 US US11/643,046 patent/US20070142356A1/en not_active Abandoned
- 2006-12-21 ZA ZA200610822A patent/ZA200610822B/xx unknown
- 2006-12-21 JO JO2006490A patent/JO2675B1/en active
- 2006-12-21 AU AU2006252211A patent/AU2006252211B2/en not_active Ceased
- 2006-12-21 CN CN2006100643177A patent/CN101015556B/zh not_active Expired - Fee Related
- 2006-12-21 BR BRPI0605516-8A patent/BRPI0605516A/pt not_active Application Discontinuation
- 2006-12-21 KR KR1020060131725A patent/KR100907584B1/ko not_active Expired - Fee Related
-
2007
- 2007-11-05 HK HK07111993.7A patent/HK1106442A1/xx not_active IP Right Cessation
-
2009
- 2009-04-22 US US12/386,687 patent/US20090215745A1/en not_active Abandoned
-
2010
- 2010-11-26 JP JP2010263499A patent/JP2011068661A/ja active Pending
- 2010-11-29 CY CY20101101086T patent/CY1111007T1/el unknown
-
2011
- 2011-01-17 HR HR20110028T patent/HRP20110028T1/hr unknown
- 2011-05-13 US US13/068,551 patent/US20110230466A1/en not_active Abandoned
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Legal Events
| Date | Code | Title | Description |
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| FC | Application refused |