MA31894B1 - Composes organiques - Google Patents
Composes organiquesInfo
- Publication number
- MA31894B1 MA31894B1 MA32874A MA32874A MA31894B1 MA 31894 B1 MA31894 B1 MA 31894B1 MA 32874 A MA32874 A MA 32874A MA 32874 A MA32874 A MA 32874A MA 31894 B1 MA31894 B1 MA 31894B1
- Authority
- MA
- Morocco
- Prior art keywords
- compounds
- organic compositions
- relates
- compound
- respond
- Prior art date
Links
- 239000000203 mixture Substances 0.000 title 1
- 150000001875 compounds Chemical class 0.000 abstract 4
- 102000003837 Epithelial Sodium Channels Human genes 0.000 abstract 1
- 108090000140 Epithelial Sodium Channels Proteins 0.000 abstract 1
- 230000000903 blocking effect Effects 0.000 abstract 1
- 201000010099 disease Diseases 0.000 abstract 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 abstract 1
- 238000000034 method Methods 0.000 abstract 1
- 239000008194 pharmaceutical composition Substances 0.000 abstract 1
- 150000003839 salts Chemical group 0.000 abstract 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D519/00—Heterocyclic compounds containing more than one system of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring system not provided for in groups C07D453/00 or C07D455/00
-
- 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
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/4965—Non-condensed pyrazines
- A61K31/497—Non-condensed pyrazines containing further heterocyclic rings
-
- 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
- A61P1/02—Stomatological preparations, e.g. drugs for caries, aphtae, periodontitis
-
- 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
- A61P11/00—Drugs for disorders of the respiratory system
- A61P11/06—Antiasthmatics
-
- 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
- A61P11/08—Bronchodilators
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P27/00—Drugs for disorders of the senses
- A61P27/02—Ophthalmic agents
-
- 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
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/08—Antiallergic agents
-
- 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
-
- 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
- C07D403/12—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 chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/10—Spiro-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/12—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains three hetero rings
- C07D471/20—Spiro-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D473/00—Heterocyclic compounds containing purine ring systems
- C07D473/26—Heterocyclic compounds containing purine ring systems with an oxygen, sulphur, or nitrogen atom directly attached in position 2 or 6, but not in both
- C07D473/32—Nitrogen atom
- C07D473/34—Nitrogen atom attached in position 6, e.g. adenine
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/04—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/10—Spiro-condensed systems
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Pulmonology (AREA)
- Epidemiology (AREA)
- Immunology (AREA)
- Rheumatology (AREA)
- Communicable Diseases (AREA)
- Oncology (AREA)
- Ophthalmology & Optometry (AREA)
- Pain & Pain Management (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Plural Heterocyclic Compounds (AREA)
- Hydrogenated Pyridines (AREA)
- Pyridine Compounds (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
- Processing Or Creating Images (AREA)
- Image Analysis (AREA)
- Image Processing (AREA)
Abstract
L'INVENTION CONCERNE UN COMPOSÉ DE FORMULE (I) SOUS FORME LIBRE, SALINE OU SOLVATÉE, DANS LAQUELLE R1, R2, R3, R4, R5, R6, R7, R8, R9, R10 ET R11 ONT LES SIGNIFICATIONS INDIQUÉES DANS LA DESCRIPTION. LE COMPOSÉ SELON L'INVENTION EST UTILE POUR LE TRAITEMENT DE MALADIES QUI RÉPONDENT AU BLOCAGE DU CANAL SODIQUE ÉPITHÉLIAL. L'INVENTION CONCERNE ÉGALEMENT DES COMPOSITIONS PHARMACEUTIQUES QUI CONTIENNENT LES COMPOSÉS ET DES PROCÉDÉS DE PRÉPARATION DES COMPOSÉS.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP07122739 | 2007-12-10 | ||
| PCT/EP2008/067110 WO2009074575A2 (fr) | 2007-12-10 | 2008-12-09 | Composés organiques |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| MA31894B1 true MA31894B1 (fr) | 2010-12-01 |
Family
ID=39322745
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| MA32874A MA31894B1 (fr) | 2007-12-10 | 2010-05-31 | Composes organiques |
Country Status (30)
| Country | Link |
|---|---|
| US (5) | US8039472B2 (fr) |
| EP (3) | EP2231280B1 (fr) |
| JP (1) | JP5455922B2 (fr) |
| KR (1) | KR101578235B1 (fr) |
| CN (1) | CN101939054B (fr) |
| AR (1) | AR069637A1 (fr) |
| AU (1) | AU2008334629B2 (fr) |
| BR (1) | BRPI0820669A2 (fr) |
| CA (1) | CA2707857C (fr) |
| CL (1) | CL2008003651A1 (fr) |
| CO (1) | CO6310968A2 (fr) |
| CR (1) | CR11470A (fr) |
| CU (1) | CU23967B1 (fr) |
| EA (1) | EA017919B1 (fr) |
| EC (1) | ECSP10010242A (fr) |
| ES (2) | ES2602331T3 (fr) |
| HN (1) | HN2010001165A (fr) |
| IL (1) | IL206165A0 (fr) |
| MA (1) | MA31894B1 (fr) |
| MX (1) | MX2010006421A (fr) |
| MY (1) | MY152955A (fr) |
| NZ (1) | NZ585789A (fr) |
| PE (1) | PE20091096A1 (fr) |
| PL (1) | PL2444120T3 (fr) |
| PT (1) | PT2444120T (fr) |
| TN (1) | TN2010000256A1 (fr) |
| TW (1) | TWI439462B (fr) |
| UA (1) | UA104997C2 (fr) |
| WO (1) | WO2009074575A2 (fr) |
| ZA (1) | ZA201003837B (fr) |
Families Citing this family (90)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6858615B2 (en) | 2002-02-19 | 2005-02-22 | Parion Sciences, Inc. | Phenyl guanidine sodium channel blockers |
| US8354427B2 (en) | 2004-06-24 | 2013-01-15 | Vertex Pharmaceutical Incorporated | Modulators of ATP-binding cassette transporters |
| KR101578235B1 (ko) * | 2007-12-10 | 2015-12-16 | 노파르티스 아게 | 유기 화합물 |
| TWI432198B (zh) | 2008-02-26 | 2014-04-01 | Parion Sciences Inc | 多芳香族鈉通道阻斷劑 |
| UA103198C2 (en) | 2008-08-04 | 2013-09-25 | Новартис Аг | Squaramide derivatives as cxcr2 antagonists |
| US8664237B2 (en) * | 2008-10-02 | 2014-03-04 | The Johns Hopkins University | Spiperone derivatives and methods of treating disorders |
| UA104601C2 (uk) | 2008-10-23 | 2014-02-25 | Вертекс Фармасьютікалз, Інкорпорейтед | Модулятори регулятора трансмембранної провідності при муковісцидозі |
| PT2433940E (pt) | 2009-04-28 | 2014-12-12 | Chugai Pharmaceutical Co Ltd | Derivado de espiroimidazolona |
| US9549967B2 (en) | 2009-05-29 | 2017-01-24 | The University Of North Carolina At Chapel Hill | Regulation of sodium channels by PLUNC proteins |
| AU2010310449A1 (en) * | 2009-10-22 | 2012-05-03 | Vertex Pharmaceuticals Incorporated | Compositions for treatment of cystic fibrosis and other chronic diseases |
| BR112012009584A2 (pt) | 2009-10-23 | 2019-09-24 | Vertex Pharma | formas sólidas de n-(4-(7-azabiciclo[2.2.1]heptan-7-il)-2-(trifluorometil)fenil)-4-oxo-5-(trifluorometil)-1,4-di-hidroquinolina-3-carboxamida |
| RU2553989C2 (ru) | 2009-10-23 | 2015-06-20 | Вертекс Фармасьютикалз Инкорпорейтед | Способ получения модуляторов регулятора трансмембранной проводимости кистозного фиброза |
| AR081920A1 (es) | 2010-05-20 | 2012-10-31 | Vertex Pharma | Procesos de produccion de moduladores del regulador de conductancia transmembrana de fibrosis quistica |
| US8372845B2 (en) * | 2010-09-17 | 2013-02-12 | Novartis Ag | Pyrazine derivatives as enac blockers |
| US9050339B2 (en) | 2010-09-17 | 2015-06-09 | Novartis Ag | Pyrazine derivatives as ENaC blockers |
| AR086745A1 (es) | 2011-06-27 | 2014-01-22 | Parion Sciences Inc | 3,5-diamino-6-cloro-n-(n-(4-(4-(2-(hexil(2,3,4,5,6-pentahidroxihexil)amino)etoxi)fenil)butil)carbamimidoil)pirazina-2-carboxamida |
| EP2760821B1 (fr) | 2011-09-02 | 2017-10-11 | Novartis AG | Sel de choline d'un composé anti-inflammatoire à base de cyclobutènedione substitué |
| WO2013064451A1 (fr) * | 2011-11-02 | 2013-05-10 | Boehringer Ingelheim International Gmbh | Nouveau procédé pour la préparation d'acylguanidines et d'acylthiourées |
| KR102006612B1 (ko) | 2011-11-02 | 2019-08-02 | 베링거 인겔하임 인터내셔날 게엠베하 | 헤테로사이클릭 화합물, 상기 화합물을 포함하는 약제, 이의 용도, 및 이의 제조 방법 |
| US8809340B2 (en) * | 2012-03-19 | 2014-08-19 | Novartis Ag | Crystalline form |
| WO2013155406A1 (fr) * | 2012-04-12 | 2013-10-17 | The Chinese University Of Hong Kong | Contragestion et traitement d'une inflammation par la modulation de l'activité d'un canal sodique dans l'épithélium |
| WO2013158121A1 (fr) | 2012-04-20 | 2013-10-24 | Vertex Pharmaceuticals Incorporated | Formes solides de n-[2,4-bis(1,1-diméthyléthyle)-5-hydroxyphényle]-1,4-dihydro-4-oxoquinoline-3-carboxamide |
| EP2897940B1 (fr) * | 2012-09-24 | 2019-05-01 | Boehringer Ingelheim International GmbH | Composés hétérocycliques, médicaments contenant ces composés, leur utilisation et procédés de leur préparation |
| SMT202500078T1 (it) | 2012-11-02 | 2025-03-12 | Vertex Pharma | Composizioni farmaceutiche per il trattamento di malattie mediate da cftr |
| CN104854106B (zh) | 2012-12-10 | 2017-07-04 | 中外制药株式会社 | 乙内酰脲衍生物 |
| WO2014099673A1 (fr) | 2012-12-17 | 2014-06-26 | Parion Sciences, Inc. | Composés 3,5-diamino -6-chloro-n-(n- (4-phénylbutyl)carbamimidoyl) pyrazine-2-carboxamide |
| ES2674665T3 (es) * | 2012-12-17 | 2018-07-03 | Parion Sciences, Inc. | Compuestos de 3,5-diamino-6-cloro-N-(N-(4-fenilbutilo)carbamimidoilo)-pirazina-2-carboxamida |
| US9593084B2 (en) | 2012-12-17 | 2017-03-14 | Parion Sciences, Inc. | Chloro-pyrazine carboxamide derivatives with epithelial sodium channel blocking activity |
| CN105189478B (zh) | 2013-01-07 | 2019-10-22 | 南加州大学 | 脱氧尿苷三磷酸酶抑制剂 |
| DE202013000888U1 (de) | 2013-01-29 | 2014-05-05 | WKW Erbslöh Automotive GmbH | Vorrichtung zur Abdeckung eines in Längsrichtung eines Kraftfahrzeuges verlaufenden Dachkanals |
| EP2970468B1 (fr) | 2013-03-13 | 2021-07-07 | Novartis AG | Molécules de liaison à notch2 pour le traitement de maladies respiratoires |
| WO2014177469A1 (fr) * | 2013-04-30 | 2014-11-06 | Boehringer Ingelheim International Gmbh,M | Composés de diaminopyrazine, médicaments contenant lesdits composés, leur utilisation et leurs procédés de préparation |
| EP2815749A1 (fr) | 2013-06-20 | 2014-12-24 | IP Gesellschaft für Management mbH | Forme solide de 4-amino-2-(2,6-dioxopiperidine-3-yl)isoindoline-1,3-dione ayant un réseau de diffraction de rayons X spécifique |
| AU2014284268A1 (en) | 2013-07-02 | 2016-01-07 | The California Institute For Biomedical Research | Compounds for treatment of cystic fibrosis |
| US9102633B2 (en) | 2013-12-13 | 2015-08-11 | Parion Sciences, Inc. | Arylalkyl- and aryloxyalkyl-substituted epithelial sodium channel blocking compounds |
| US9790214B2 (en) | 2014-01-03 | 2017-10-17 | University Of Southern California | Heteroatom containing deoxyuridine triphosphatase inhibitors |
| UY36034A (es) | 2014-03-18 | 2015-09-30 | Astrazeneca Ab | Derivados de 3,5-diamino-6-cloro-pirazina-2-carboxamida y sales farmaceuticamente aceptables de estos |
| EP2932966A1 (fr) | 2014-04-16 | 2015-10-21 | Novartis AG | Inhibiteurs de la gamma sécrétase pour traiter des maladies respiratoires |
| EP3153166B1 (fr) | 2014-06-09 | 2022-08-03 | Chugai Seiyaku Kabushiki Kaisha | Composition pharmaceutique contenant un dérivé d'hydantoïne |
| BR112017007224A2 (pt) | 2014-10-08 | 2018-03-06 | Spyryx Biosciences Inc | inibidores de canais de sódio, de peptídeo, aperfeiçoados |
| MX2017005663A (es) | 2014-10-31 | 2018-03-01 | Abbvie Sarl | Tetrahidropiranos sustituidos y metodo de uso. |
| WO2016113170A1 (fr) * | 2015-01-12 | 2016-07-21 | Boehringer Ingelheim International Gmbh | Composés substitués de benzimidazolium utiles dans le traitement de maladies respiratoires |
| US20180002312A1 (en) * | 2015-01-12 | 2018-01-04 | Boehringer Ingelheim International Gmbh | Tetra- and pentasubstituted benzimidazolium compounds useful in the treatment of respiratory diseases |
| WO2016113167A1 (fr) * | 2015-01-12 | 2016-07-21 | Boehringer Ingelheim International Gmbh | Composés subtitués à base de benzimidazolium utilisables dans le traitement de maladies respiratoires |
| BR112017026132A2 (pt) | 2015-06-02 | 2018-08-28 | AbbVie S.à.r.l. | piridinas substituídas e métodos de uso |
| FR3038605B1 (fr) * | 2015-07-06 | 2018-08-24 | Universite Amiens Picardie Jules Verne | Diamines primaires vicinales associees a des motifs chelateurs de metaux et/ou de radicaux libres, actives contre les stress carbonyle et oxydant et leur utilisation |
| WO2017006270A1 (fr) | 2015-07-08 | 2017-01-12 | University Of Southern California | Inhibiteurs de la désoxyuridine triphosphatase |
| US10544105B2 (en) | 2015-07-08 | 2020-01-28 | Cv6 Therapeutics (Ni) Limited | Deoxyuridine triphosphatase inhibitors containing cyclopropano linkage |
| US10570100B2 (en) | 2015-07-08 | 2020-02-25 | University Of Southern California | Deoxyuridine triphosphatase inhibitors containing amino sulfonyl linkage |
| US10570098B2 (en) | 2015-07-08 | 2020-02-25 | Cv6 Therapeutics (Ni) Limited | Hydantoin containing deoxyuridine triphosphatase inhibitors |
| US9840513B2 (en) | 2015-07-16 | 2017-12-12 | Abbvie S.Á.R.L. | Substituted tricyclics and method of use |
| US10130622B2 (en) | 2015-10-09 | 2018-11-20 | Abbvie S.Á.R.L. | Compounds for treatment of cystic fibrosis |
| WO2017060874A1 (fr) | 2015-10-09 | 2017-04-13 | Abbvie S.Á.R.L | Pyrazolo[3,4-b]pyridin-6-carboxamides n-sulfonylés et leur procédé d'utilisation |
| EP3359539A1 (fr) | 2015-10-09 | 2018-08-15 | AbbVie S.À.R.L. | Acides pyrazolo[3,4-b]pyridin-6-carboxyliques substitués et leur utilisation |
| US10402062B2 (en) * | 2016-04-16 | 2019-09-03 | Apple Inc. | Organized timeline |
| EP3448842A1 (fr) | 2016-04-26 | 2019-03-06 | AbbVie S.À.R.L. | Modulateurs de protéine régulatrice de conductance transmembranaire de la fibrose kystique |
| US10138227B2 (en) | 2016-06-03 | 2018-11-27 | Abbvie S.Á.R.L. | Heteroaryl substituted pyridines and methods of use |
| GB201610854D0 (en) | 2016-06-21 | 2016-08-03 | Entpr Therapeutics Ltd | Compounds |
| US10399940B2 (en) | 2016-10-07 | 2019-09-03 | Abbvie S.Á.R.L. | Substituted pyrrolidines and methods of use |
| US9981910B2 (en) | 2016-10-07 | 2018-05-29 | Abbvie S.Á.R.L. | Substituted pyrrolidines and methods of use |
| GB201619694D0 (en) | 2016-11-22 | 2017-01-04 | Entpr Therapeutics Ltd | Compounds |
| WO2018098209A1 (fr) | 2016-11-23 | 2018-05-31 | Cv6 Therapeutics (Ni) Limited | Composés aminosulfonyle |
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| JP2008538107A (ja) | 2005-03-18 | 2008-10-09 | ザ リージェンツ オブ ザ ユニバーシティ オブ カリフォルニア | 変異型cftrプロセシングの修正において活性を有する化合物及びその用途 |
| ATE533749T1 (de) | 2005-05-24 | 2011-12-15 | Vertex Pharma | Modulatoren von atp-bindenden kassettentransportern |
| EP1912983B1 (fr) | 2005-08-11 | 2011-06-08 | Vertex Pharmaceuticals, Inc. | Modulateurs du regulateur de la conductance transmembranaire de la fibrose kystique |
| NL2000284C2 (nl) | 2005-11-04 | 2007-09-28 | Pfizer Ltd | Pyrazine-derivaten. |
| GB0526240D0 (en) * | 2005-12-22 | 2006-02-01 | Novartis Ag | Organic compounds |
| GB0526244D0 (en) | 2005-12-22 | 2006-02-01 | Novartis Ag | Organic compounds |
| EP1976528A2 (fr) | 2005-12-29 | 2008-10-08 | Janssen Pharmaceutica, N.V. | Antagonistes du recepteur de la prokineticine 2 |
| MX2009006472A (es) | 2006-12-14 | 2009-06-26 | Janssen Pharmaceutica Nv | Procedimiento para la preparacion de derivados benzamida piperacinilo y diazepanilo. |
| US8450348B2 (en) | 2007-02-21 | 2013-05-28 | Forma Tm, Llc | Derivatives of squaric acid with anti-proliferative activity |
| WO2009074333A1 (fr) | 2007-12-10 | 2009-06-18 | Synthon B.V. | Synthèse de palipéridone |
| KR101578235B1 (ko) | 2007-12-10 | 2015-12-16 | 노파르티스 아게 | 유기 화합물 |
| EP2341052A4 (fr) | 2008-09-05 | 2011-10-12 | Shionogi & Co | Derive de morpholine à cycles condensés ayant une activite inhibitrice de pi3k |
| WO2011059839A1 (fr) | 2009-10-29 | 2011-05-19 | Sirtris Pharmaceuticals, Inc. | Pyridines bicycliques et analogues en tant que modulateurs de la sirtuine |
| TR201810944T4 (tr) | 2013-10-25 | 2018-08-27 | Novartis Ag | Fgfr4 inhibitörleri olarak halka-füzyonlu bisiklik piridil türevleri. |
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2008
- 2008-12-09 KR KR1020107015184A patent/KR101578235B1/ko not_active Expired - Fee Related
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- 2008-12-09 WO PCT/EP2008/067110 patent/WO2009074575A2/fr not_active Ceased
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- 2008-12-09 UA UAA201007106A patent/UA104997C2/uk unknown
- 2008-12-09 EP EP11184004.7A patent/EP2444120B1/fr active Active
- 2008-12-09 NZ NZ585789A patent/NZ585789A/en not_active IP Right Cessation
- 2008-12-09 EP EP20120173703 patent/EP2520574A1/fr not_active Withdrawn
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- 2008-12-09 ES ES11184004.7T patent/ES2654395T3/es active Active
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- 2008-12-09 CA CA2707857A patent/CA2707857C/fr not_active Expired - Fee Related
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- 2010-06-03 IL IL206165A patent/IL206165A0/en unknown
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