ES2572980T3 - Combinación de inhibidores de la proteasa del VHC con un tensioactivo - Google Patents
Combinación de inhibidores de la proteasa del VHC con un tensioactivo Download PDFInfo
- Publication number
- ES2572980T3 ES2572980T3 ES06760571.7T ES06760571T ES2572980T3 ES 2572980 T3 ES2572980 T3 ES 2572980T3 ES 06760571 T ES06760571 T ES 06760571T ES 2572980 T3 ES2572980 T3 ES 2572980T3
- Authority
- ES
- Spain
- Prior art keywords
- surfactant
- combination
- protease inhibitors
- hcv protease
- hydrochloride salt
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K38/00—Medicinal preparations containing peptides
- A61K38/04—Peptides having up to 20 amino acids in a fully defined sequence; Derivatives thereof
- A61K38/12—Cyclic peptides, e.g. bacitracins; Polymyxins; Gramicidins S, C; Tyrocidins A, B or C
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- 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
- A61K31/445—Non condensed piperidines, e.g. piperocaine
- A61K31/4523—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems
- A61K31/454—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. pimozide, domperidone
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- 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
- A61K31/47—Quinolines; Isoquinolines
- A61K31/4709—Non-condensed quinolines and containing further heterocyclic rings
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- A61K38/05—Dipeptides
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- A61K38/04—Peptides having up to 20 amino acids in a fully defined sequence; Derivatives thereof
- A61K38/06—Tripeptides
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- A61K38/04—Peptides having up to 20 amino acids in a fully defined sequence; Derivatives thereof
- A61K38/08—Peptides having 5 to 11 amino acids
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- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
- A61K47/06—Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite
- A61K47/08—Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite containing oxygen, e.g. ethers, acetals, ketones, quinones, aldehydes, peroxides
- A61K47/10—Alcohols; Phenols; Salts thereof, e.g. glycerol; Polyethylene glycols [PEG]; Poloxamers; PEG/POE alkyl ethers
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- A—HUMAN NECESSITIES
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- A61P1/04—Drugs for disorders of the alimentary tract or the digestive system for ulcers, gastritis or reflux esophagitis, e.g. antacids, inhibitors of acid secretion, mucosal protectants
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- A—HUMAN NECESSITIES
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- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K2300/00—Mixtures or combinations of active ingredients, wherein at least one active ingredient is fully defined in groups A61K31/00 - A61K41/00
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- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Veterinary Medicine (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Organic Chemistry (AREA)
- Epidemiology (AREA)
- Immunology (AREA)
- Gastroenterology & Hepatology (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Biomedical Technology (AREA)
- Neurology (AREA)
- Neurosurgery (AREA)
- Pulmonology (AREA)
- Rheumatology (AREA)
- Physical Education & Sports Medicine (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Dermatology (AREA)
- Diabetes (AREA)
- Communicable Diseases (AREA)
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- Transplantation (AREA)
- Hematology (AREA)
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- Ophthalmology & Optometry (AREA)
- Molecular Biology (AREA)
- Obesity (AREA)
Abstract
Una formulacion farmaceutica que comprende: (a) al menos un tensioactivo, en donde dicho al menos un tensioactivo es lauril sulfato de sodio, y (b) al menos un compuesto seleccionado entre el grupo que consiste en el compuesto de Formula Ia:**Fórmula** y sales o solvatos farmaceuticamente aceptables de la misma.
Description
Método D
En otra variación más, la sal de clorhidrato 1.13 se convirtió en el carbamato de 4-nitrofenilo 1.15 mediante la reacción con cloroformiato de 4-nitrofenilo. El tratamiento posterior con una amina (o sal de clorhidrato de amina) de elección proporcionó el compuesto objetivo 1.14.
10 Método E
En otra variación más, la sal de clorhidrato dipeptídica 1.04 se convirtió en el carbamato de 4-nitrofenilo como se ha descrito anteriormente. El tratamiento con una amina (o sal de clorhidrato de amina) de elección proporcionó el
15 derivado de urea 1.05. La hidrólisis y la elaboración adicional como se ha descrito en los Métodos A/B proporcionaron los compuestos objetivo 1.14.
15
Claims (1)
-
imagen1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US68694505P | 2005-06-02 | 2005-06-02 | |
| US686945P | 2005-06-02 | ||
| PCT/US2006/021003 WO2006130628A2 (en) | 2005-06-02 | 2006-05-31 | Combination of hcv protease inhibitors with a surfactant |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ES2572980T3 true ES2572980T3 (es) | 2016-06-03 |
Family
ID=37482240
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ES06760571.7T Expired - Lifetime ES2572980T3 (es) | 2005-06-02 | 2006-05-31 | Combinación de inhibidores de la proteasa del VHC con un tensioactivo |
Country Status (17)
| Country | Link |
|---|---|
| US (1) | US7772178B2 (es) |
| EP (1) | EP1919478B1 (es) |
| JP (2) | JP5160415B2 (es) |
| KR (1) | KR20080021634A (es) |
| CN (1) | CN101212970B (es) |
| AR (1) | AR055198A1 (es) |
| AU (1) | AU2006252553B2 (es) |
| BR (1) | BRPI0610737A2 (es) |
| CA (1) | CA2611155A1 (es) |
| ES (1) | ES2572980T3 (es) |
| MX (1) | MX2007015270A (es) |
| NO (1) | NO20076613L (es) |
| NZ (1) | NZ563365A (es) |
| PE (1) | PE20070011A1 (es) |
| TW (1) | TWI428138B (es) |
| WO (1) | WO2006130628A2 (es) |
| ZA (1) | ZA200709987B (es) |
Families Citing this family (56)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| MY140680A (en) | 2002-05-20 | 2010-01-15 | Bristol Myers Squibb Co | Hepatitis c virus inhibitors |
| US7816326B2 (en) * | 2004-02-27 | 2010-10-19 | Schering Corporation | Sulfur compounds as inhibitors of hepatitis C virus NS3 serine protease |
| RU2428428C9 (ru) | 2004-02-27 | 2012-03-10 | Шеринг Корпорейшн | Серусодержащие соединения, действующие как ингибиторы сериновой протеазы ns3 вируса гепатита с |
| US8119602B2 (en) * | 2005-06-02 | 2012-02-21 | Schering Corporation | Administration of HCV protease inhibitors in combination with food to improve bioavailability |
| EP2305696A3 (en) * | 2005-07-25 | 2011-10-12 | Intermune, Inc. | Macrocyclic inhibitors of Hepatitis C virus replication |
| EA200801050A1 (ru) | 2005-10-11 | 2008-12-30 | Интермьюн, Инк. | Соединения и способы ингибирования репликации вирусного гепатита с |
| WO2007120595A2 (en) * | 2006-04-11 | 2007-10-25 | Novartis Ag | Amines for the treatment of hcv |
| US8420122B2 (en) | 2006-04-28 | 2013-04-16 | Merck Sharp & Dohme Corp. | Process for the precipitation and isolation of 6,6-dimethyl-3-aza-bicyclo [3.1.0] hexane-amide compounds by controlled precipitation and pharmaceutical formulations containing same |
| WO2008008776A2 (en) | 2006-07-11 | 2008-01-17 | Bristol-Myers Squibb Company | Hepatitis c virus inhibitors |
| US8343477B2 (en) | 2006-11-01 | 2013-01-01 | Bristol-Myers Squibb Company | Inhibitors of hepatitis C virus |
| US7772180B2 (en) | 2006-11-09 | 2010-08-10 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
| US7763584B2 (en) | 2006-11-16 | 2010-07-27 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
| US8003604B2 (en) | 2006-11-16 | 2011-08-23 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
| US7888464B2 (en) | 2006-11-16 | 2011-02-15 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
| CA2686546A1 (en) | 2007-05-10 | 2008-11-20 | Intermune, Inc. | Novel peptide inhibitors of hepatitis c virus replication |
| US8309685B2 (en) * | 2007-12-21 | 2012-11-13 | Celgene Avilomics Research, Inc. | HCV protease inhibitors and uses thereof |
| WO2009082697A1 (en) | 2007-12-21 | 2009-07-02 | Avila Therapeutics, Inc. | Hcv protease inhibitors and uses thereof |
| AR069799A1 (es) * | 2007-12-21 | 2010-02-17 | Novartis Ag | Composicion farmaceutica |
| US8202996B2 (en) | 2007-12-21 | 2012-06-19 | Bristol-Myers Squibb Company | Crystalline forms of N-(tert-butoxycarbonyl)-3-methyl-L-valyl-(4R)-4-((7-chloro-4-methoxy-1-isoquinolinyl)oxy)-N- ((1R,2S)-1-((cyclopropylsulfonyl)carbamoyl)-2-vinylcyclopropyl)-L-prolinamide |
| CN104557880A (zh) * | 2007-12-21 | 2015-04-29 | 阿维拉制药公司 | Hcv蛋白酶抑制剂和其用途 |
| US8293705B2 (en) | 2007-12-21 | 2012-10-23 | Avila Therapeutics, Inc. | HCV protease inhibitors and uses thereof |
| US8163921B2 (en) | 2008-04-16 | 2012-04-24 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
| CN102046648A (zh) | 2008-05-29 | 2011-05-04 | 百时美施贵宝公司 | 丙型肝炎病毒抑制剂 |
| US7964560B2 (en) | 2008-05-29 | 2011-06-21 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
| EP2323631A1 (en) * | 2008-08-07 | 2011-05-25 | Schering Corporation | Pharmaceutical formulations of an hcv protease inhibitor in a solid molecular dispersion |
| US8188137B2 (en) | 2008-08-15 | 2012-05-29 | Avila Therapeutics, Inc. | HCV protease inhibitors and uses thereof |
| US8207341B2 (en) | 2008-09-04 | 2012-06-26 | Bristol-Myers Squibb Company | Process or synthesizing substituted isoquinolines |
| UY32099A (es) | 2008-09-11 | 2010-04-30 | Enanta Pharm Inc | Inhibidores macrocíclicos de serina proteasas de hepatitis c |
| US8044087B2 (en) | 2008-09-29 | 2011-10-25 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
| US8563505B2 (en) | 2008-09-29 | 2013-10-22 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
| US8283310B2 (en) | 2008-12-15 | 2012-10-09 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
| WO2010138889A1 (en) | 2009-05-28 | 2010-12-02 | Concert Pharmaceuticals, Inc. | Peptides for the treatment of hcv infections |
| US8232246B2 (en) * | 2009-06-30 | 2012-07-31 | Abbott Laboratories | Anti-viral compounds |
| CN103534256B (zh) | 2010-12-30 | 2016-08-10 | 益安药业 | 大环丙型肝炎丝氨酸蛋白酶抑制剂 |
| KR20140003521A (ko) | 2010-12-30 | 2014-01-09 | 이난타 파마슈티칼스, 인코포레이티드 | 페난트리딘 매크로사이클릭 c형 간염 세린 프로테아제 억제제 |
| US8957203B2 (en) | 2011-05-05 | 2015-02-17 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
| US10201584B1 (en) | 2011-05-17 | 2019-02-12 | Abbvie Inc. | Compositions and methods for treating HCV |
| US8691757B2 (en) | 2011-06-15 | 2014-04-08 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
| DE112012003510T5 (de) | 2011-10-21 | 2015-03-19 | Abbvie Inc. | Verfahren zur Behandlung von HCV umfassend mindestens zwei direkt wirkende antivirale Wirkstoffe, Ribavirin aber nicht Interferon |
| US8466159B2 (en) | 2011-10-21 | 2013-06-18 | Abbvie Inc. | Methods for treating HCV |
| CN104023726A (zh) | 2011-10-21 | 2014-09-03 | 艾伯维公司 | 用于治疗hcv的一种或多种daa的联合治疗(例如,与abt-072或abt-333) |
| US8492386B2 (en) | 2011-10-21 | 2013-07-23 | Abbvie Inc. | Methods for treating HCV |
| WO2013072327A1 (en) | 2011-11-14 | 2013-05-23 | Sanofi | Use of boceprevir and related compounds in atherosclerosis, heart failure, renal diseases, liver diseases or inflammatory diseases |
| WO2014053533A1 (en) | 2012-10-05 | 2014-04-10 | Sanofi | Use of substituted 3-heteroaroylamino-propionic acid derivatives as pharmaceuticals for prevention/treatment of atrial fibrillation |
| JP6154474B2 (ja) | 2012-10-19 | 2017-06-28 | ブリストル−マイヤーズ スクイブ カンパニーBristol−Myers Squibb Company | C型肝炎ウイルス阻害剤 |
| EP2914613B1 (en) | 2012-11-02 | 2017-11-22 | Bristol-Myers Squibb Company | Hepatitis c virus inhibitors |
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-
2006
- 2006-05-31 US US11/444,078 patent/US7772178B2/en not_active Expired - Fee Related
- 2006-05-31 WO PCT/US2006/021003 patent/WO2006130628A2/en not_active Ceased
- 2006-05-31 EP EP06760571.7A patent/EP1919478B1/en not_active Expired - Lifetime
- 2006-05-31 CA CA002611155A patent/CA2611155A1/en not_active Abandoned
- 2006-05-31 CN CN2006800195249A patent/CN101212970B/zh not_active Expired - Fee Related
- 2006-05-31 AR ARP060102260A patent/AR055198A1/es unknown
- 2006-05-31 JP JP2008514785A patent/JP5160415B2/ja not_active Expired - Fee Related
- 2006-05-31 NZ NZ563365A patent/NZ563365A/en not_active IP Right Cessation
- 2006-05-31 KR KR1020077028243A patent/KR20080021634A/ko not_active Ceased
- 2006-05-31 PE PE2006000582A patent/PE20070011A1/es not_active Application Discontinuation
- 2006-05-31 BR BRPI0610737-0A patent/BRPI0610737A2/pt not_active IP Right Cessation
- 2006-05-31 MX MX2007015270A patent/MX2007015270A/es active IP Right Grant
- 2006-05-31 ES ES06760571.7T patent/ES2572980T3/es not_active Expired - Lifetime
- 2006-05-31 AU AU2006252553A patent/AU2006252553B2/en not_active Ceased
- 2006-06-01 TW TW095119307A patent/TWI428138B/zh not_active IP Right Cessation
-
2007
- 2007-11-19 ZA ZA200709987A patent/ZA200709987B/xx unknown
- 2007-12-21 NO NO20076613A patent/NO20076613L/no not_active Application Discontinuation
-
2012
- 2012-09-19 JP JP2012205626A patent/JP2012250996A/ja active Pending
Also Published As
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| MX2007015270A (es) | 2008-02-21 |
| CN101212970B (zh) | 2010-07-21 |
| WO2006130628A2 (en) | 2006-12-07 |
| US7772178B2 (en) | 2010-08-10 |
| JP2008542383A (ja) | 2008-11-27 |
| KR20080021634A (ko) | 2008-03-07 |
| WO2006130628A3 (en) | 2007-09-13 |
| US20070010431A1 (en) | 2007-01-11 |
| CN101212970A (zh) | 2008-07-02 |
| ZA200709987B (en) | 2008-11-26 |
| CA2611155A1 (en) | 2006-12-07 |
| EP1919478A2 (en) | 2008-05-14 |
| NZ563365A (en) | 2011-02-25 |
| AU2006252553A1 (en) | 2006-12-07 |
| JP2012250996A (ja) | 2012-12-20 |
| PE20070011A1 (es) | 2007-03-08 |
| AR055198A1 (es) | 2007-08-08 |
| TW200716157A (en) | 2007-05-01 |
| NO20076613L (no) | 2008-03-03 |
| EP1919478B1 (en) | 2016-03-23 |
| BRPI0610737A2 (pt) | 2010-07-20 |
| TWI428138B (zh) | 2014-03-01 |
| JP5160415B2 (ja) | 2013-03-13 |
| AU2006252553B2 (en) | 2012-03-29 |
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