NO20062561L - Kinoliner nyttige for behandling av kardiovaskulaere sykdommer - Google Patents
Kinoliner nyttige for behandling av kardiovaskulaere sykdommerInfo
- Publication number
- NO20062561L NO20062561L NO20062561A NO20062561A NO20062561L NO 20062561 L NO20062561 L NO 20062561L NO 20062561 A NO20062561 A NO 20062561A NO 20062561 A NO20062561 A NO 20062561A NO 20062561 L NO20062561 L NO 20062561L
- Authority
- NO
- Norway
- Prior art keywords
- treatment
- cardiovascular diseases
- useful
- quinolines useful
- quinolines
- Prior art date
Links
- 208000024172 Cardiovascular disease Diseases 0.000 title 1
- 229940111121 antirheumatic drug quinolines Drugs 0.000 title 1
- 150000003248 quinolines Chemical class 0.000 title 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- 201000010099 disease Diseases 0.000 abstract 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 abstract 1
- 230000005764 inhibitory process Effects 0.000 abstract 1
- 230000001404 mediated effect Effects 0.000 abstract 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- 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
-
- 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
- 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
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/04—Antibacterial 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P5/00—Drugs for disorders of the endocrine system
- A61P5/14—Drugs for disorders of the endocrine system of the thyroid hormones, e.g. T3, T4
-
- 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
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D215/00—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems
- C07D215/02—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom
- C07D215/12—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom with substituted hydrocarbon radicals attached to ring carbon atoms
- C07D215/14—Radicals substituted by oxygen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D215/00—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems
- C07D215/02—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom
- C07D215/16—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom 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
- C07D215/48—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen
- C07D215/54—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen attached in position 3
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/06—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
- C07D405/04—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
- C07D405/06—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
- C07D405/12—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- 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
- C07D409/04—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 directly linked by a ring-member-to-ring-member bond
-
- 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
-
- 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
- C07D409/12—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 chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/04—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/06—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
- C07D417/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Veterinary Medicine (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Public Health (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Diabetes (AREA)
- Obesity (AREA)
- Communicable Diseases (AREA)
- Vascular Medicine (AREA)
- Cardiology (AREA)
- Heart & Thoracic Surgery (AREA)
- Hematology (AREA)
- Endocrinology (AREA)
- Urology & Nephrology (AREA)
- Oncology (AREA)
- Pain & Pain Management (AREA)
- Rheumatology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Quinoline Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US52900903P | 2003-12-12 | 2003-12-12 | |
US60029604P | 2004-08-10 | 2004-08-10 | |
PCT/US2004/041399 WO2005058834A2 (fr) | 2003-12-12 | 2004-12-10 | Quinolines convenant pour le traitement de maladies cardio-vasculaires |
Publications (1)
Publication Number | Publication Date |
---|---|
NO20062561L true NO20062561L (no) | 2006-09-08 |
Family
ID=34704262
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
NO20062561A NO20062561L (no) | 2003-12-12 | 2006-06-02 | Kinoliner nyttige for behandling av kardiovaskulaere sykdommer |
Country Status (18)
Country | Link |
---|---|
US (1) | US7576215B2 (fr) |
EP (2) | EP2284157A1 (fr) |
JP (1) | JP2007516258A (fr) |
KR (1) | KR20070001922A (fr) |
AR (1) | AR047329A1 (fr) |
AU (1) | AU2004298486A1 (fr) |
BR (1) | BRPI0417543A (fr) |
CA (1) | CA2547518A1 (fr) |
CR (1) | CR8410A (fr) |
EC (1) | ECSP066635A (fr) |
IL (1) | IL175892A0 (fr) |
NO (1) | NO20062561L (fr) |
PA (1) | PA8619901A1 (fr) |
PE (1) | PE20050676A1 (fr) |
RU (1) | RU2006124843A (fr) |
SV (1) | SV2005001973A (fr) |
TW (1) | TW200529845A (fr) |
WO (1) | WO2005058834A2 (fr) |
Families Citing this family (78)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP1490047B1 (fr) * | 2002-03-27 | 2009-12-30 | SmithKline Beecham Corporation | Certains heterocycles aminoalkyles pharmaceutiquement utiles |
JP2005521721A (ja) * | 2002-03-27 | 2005-07-21 | スミスクライン・ビーチャム・コーポレイション | 酸およびエステル化合物ならびにその使用方法 |
US7247748B2 (en) * | 2002-03-27 | 2007-07-24 | Smithkline Corporation | Amide compounds and methods of using the same |
AU2003226094A1 (en) * | 2002-03-27 | 2003-10-13 | Smithkline Beecham Corporation | Compounds and methods |
US7786165B2 (en) | 2004-03-15 | 2010-08-31 | Takeda Pharmaceutical Company Limited | Aminophenylpropanoic acid derivative |
JP4859665B2 (ja) | 2004-03-30 | 2012-01-25 | 武田薬品工業株式会社 | アルコキシフェニルプロパン酸誘導体 |
EP2172222A3 (fr) * | 2004-04-26 | 2010-06-23 | Ono Pharmaceutical Co., Ltd. | Nouvelle maladie à médiation BLT2, agent de liaison BLT2 et composé |
US20070299092A1 (en) * | 2004-05-20 | 2007-12-27 | Wyeth | Quinone Substituted Quinazoline and Quinoline Kinase Inhibitors |
JP4936476B2 (ja) | 2005-06-28 | 2012-05-23 | 第一三共株式会社 | Lxrリガンドの試験方法 |
GB0521083D0 (en) * | 2005-10-17 | 2005-11-23 | Novartis Ag | Organic compounds |
WO2007050271A2 (fr) * | 2005-10-25 | 2007-05-03 | Wyeth | Modulateurs de 5-lipoxygenase |
US7939545B2 (en) | 2006-05-16 | 2011-05-10 | Boehringer Ingelheim International Gmbh | Inhibitors of human immunodeficiency virus replication |
AU2007297721A1 (en) * | 2006-09-19 | 2008-03-27 | Wyeth | Use of LXR agonists for the treatment of osteoarthritis |
WO2008036238A2 (fr) * | 2006-09-19 | 2008-03-27 | Wyeth | Utilisation de modulateurs lxr dans la prévention et le traitement du vieillissement cutané |
TW200825054A (en) * | 2006-10-18 | 2008-06-16 | Wyeth Corp | Quinoline compounds |
EP2099444A4 (fr) * | 2006-12-14 | 2012-11-07 | Nps Pharma Inc | Utilisation de dérivés de la d-sérine pour le traitement de troubles de l'anxiété |
US20090069373A1 (en) * | 2007-02-28 | 2009-03-12 | Wyeth | Quinoline Acids |
ES2320955B1 (es) * | 2007-03-02 | 2010-03-16 | Laboratorios Almirall S.A. | Nuevos derivados de 3-((1,2,4)triazolo(4,3-a)piridin-7-il)benzamida. |
RU2009137190A (ru) * | 2007-03-08 | 2011-04-20 | Плексксикон, Инк. (Us) | Соединения, обладающие активностью в отношении ppar |
ES2329639B1 (es) * | 2007-04-26 | 2010-09-23 | Laboratorios Almirall S.A. | Nuevos derivados de 4,8-difenilpoliazanaftaleno. |
BRPI0812816B8 (pt) * | 2007-06-18 | 2021-05-25 | Richter Gedeon Nyrt | compostos derivados de sulfonil-quinolina, ligantes com preferência para subtipo de receptor mglur1 e mglur5, processos para a preparação dos referidos compostos, formulação farmacêutica compreendedo os referidos compostos e uso dos mesmos |
US8063220B2 (en) | 2007-06-22 | 2011-11-22 | Richter Gedeon Nyrt. | Sulfonyl-quinoline derivatives |
CA2705318C (fr) | 2007-11-15 | 2013-12-31 | Boehringer Ingelheim International Gmbh | Inhibiteurs de la replication du virus de l'immunodeficience humaine |
JP5285709B2 (ja) | 2007-11-16 | 2013-09-11 | ギリアード サイエンシス インコーポレーテッド | ヒト免疫不全ウイルスの複製阻害薬 |
AU2008345696A1 (en) * | 2007-12-21 | 2009-07-09 | Wyeth Llc | Benzimidazole compounds |
WO2009102789A2 (fr) * | 2008-02-15 | 2009-08-20 | Wyeth | Utilisation d'agonistes de rxr pour le traitement de l'arthrose |
EP2108641A1 (fr) | 2008-04-11 | 2009-10-14 | Laboratorios Almirall, S.A. | Nouveaux dérivés substitués de spiro[cycloalkyl-1,3'-indo]-2'(1'H)-one et leur utilisation comme ihibiteurs de p38 mitogen-activated kinase |
EP2113503A1 (fr) * | 2008-04-28 | 2009-11-04 | Laboratorios Almirall, S.A. | Nouveaux dérivés d'indolin-2-one substitués et leur utilisation comme inhibiteurs de p38 mitogen-activated kinase |
WO2009133692A1 (fr) | 2008-04-30 | 2009-11-05 | 興和株式会社 | Composé quinoline |
US8153634B2 (en) | 2008-05-29 | 2012-04-10 | Kowa Company, Ltd. | Carbinol derivatives having cyclic linker |
US9029408B2 (en) | 2008-06-16 | 2015-05-12 | Gtx, Inc. | Compounds for treatment of cancer |
US8822513B2 (en) | 2010-03-01 | 2014-09-02 | Gtx, Inc. | Compounds for treatment of cancer |
US9447049B2 (en) | 2010-03-01 | 2016-09-20 | University Of Tennessee Research Foundation | Compounds for treatment of cancer |
RU2514427C2 (ru) * | 2008-06-16 | 2014-04-27 | Юниверсити Оф Теннесси Рисёч Фаундейшн | Соединения для лечения рака |
WO2010012650A1 (fr) * | 2008-07-28 | 2010-02-04 | Syddansk Universitet | Composés destinés au traitement de troubles métaboliques |
JP5281647B2 (ja) * | 2008-09-08 | 2013-09-04 | 日本曹達株式会社 | 含窒素ヘテロ環化合物およびその塩並びに農園芸用殺菌剤 |
CA2741537A1 (fr) * | 2008-11-07 | 2010-05-14 | Wyeth Llc | Modulateurs de lxr a base de quinoxaline |
RU2404971C2 (ru) * | 2008-12-02 | 2010-11-27 | ЗАО "Фарм-Синтез" | Новые производные хинолина, способ их получения, их применение для лечения микобактериальных инфекций, фармацевтическая композиция на их основе |
US8598354B2 (en) | 2008-12-05 | 2013-12-03 | University Of South Florida | Compounds having antiparasitic or anti-infectious activity |
AU2009322170A1 (en) * | 2008-12-05 | 2011-07-14 | Medicines For Malaria Venture | Compounds having antiparasitic or anti-infectious activity |
KR101671046B1 (ko) | 2009-04-29 | 2016-10-31 | 코와 가부시키가이샤 | 헤테로환 링커를 갖는 카르비놀 화합물 |
CA2759083A1 (fr) | 2009-04-30 | 2010-11-04 | Novartis Ag | Derives d'imidazole et leur utilisation comme modulateurs des kinases dependantes des cyclines |
CA2765819A1 (fr) * | 2009-06-25 | 2010-12-29 | Amgen Inc. | Composes heterocycliques et leurs utilisations en tant qu'inhibiteurs de l'activite p13 k |
AU2010347233B2 (en) | 2010-03-01 | 2015-06-18 | Oncternal Therapeutics, Inc. | Compounds for treatment of cancer |
CN103097355A (zh) * | 2010-07-08 | 2013-05-08 | 惠氏有限责任公司 | 用于治疗皮肤病的新的喹啉酯 |
CN103517908A (zh) | 2010-09-07 | 2014-01-15 | Seoul大学校产学协力财团 | 二倍半萜化合物及其用途 |
ES2379242B1 (es) * | 2010-09-28 | 2013-03-04 | Consejo Superior De Investigaciones Científicas (Csic) | Derivados de cromeno. |
ES2941477T3 (es) | 2012-08-13 | 2023-05-23 | Univ Rockefeller | Agonista de LXRbeta para el tratamiento de cáncer |
KR20150070348A (ko) | 2012-10-16 | 2015-06-24 | 얀센 파마슈티카 엔.브이. | RoRγt의 헤테로아릴 결합 퀴놀리닐 조절제 |
BR112015008308A2 (pt) | 2012-10-16 | 2017-12-05 | Janssen Pharmaceutica Nv | moduladores de quinolinila ligados por metileno do ror-gama-t |
SG11201502935VA (en) | 2012-10-16 | 2015-09-29 | Janssen Pharmaceutica Nv | Phenyl linked quinolinyl modulators of ror-gamma-t |
CN103965105A (zh) * | 2013-01-29 | 2014-08-06 | 中山大学 | 苯乙烯基喹啉衍生物及其在治疗阿尔茨海默病症中的应用 |
WO2014123203A1 (fr) * | 2013-02-06 | 2014-08-14 | 京都薬品工業株式会社 | Agent thérapeutique destiné à traiter le diabète |
RU2708247C2 (ru) | 2013-03-05 | 2019-12-05 | Юниверсити Оф Теннесси Рисерч Фаундейшн | Соединение для лечения рака |
US9328095B2 (en) | 2013-10-15 | 2016-05-03 | Janssen Pharmaceutica Nv | Heteroaryl linked quinolinyl modulators of RORgammat |
US10555941B2 (en) | 2013-10-15 | 2020-02-11 | Janssen Pharmaceutica Nv | Alkyl linked quinolinyl modulators of RORγt |
BR112016008257A2 (pt) | 2013-10-15 | 2017-09-26 | Janssen Pharmaceutica Nv | moduladores de roryt de álcool quinolínico secundário |
KR20160068956A (ko) | 2013-10-15 | 2016-06-15 | 얀센 파마슈티카 엔.브이. | RORyT의 퀴놀리닐 조절제 |
JP6423423B2 (ja) | 2013-10-15 | 2018-11-14 | ヤンセン ファーマシューティカ エヌ.ベー. | Rorγtのアルキル結合キノリニルモジュレーター |
US9284308B2 (en) | 2013-10-15 | 2016-03-15 | Janssen Pharmaceutica Nv | Methylene linked quinolinyl modulators of RORγt |
US9403816B2 (en) | 2013-10-15 | 2016-08-02 | Janssen Pharmaceutica Nv | Phenyl linked quinolinyl modulators of RORγt |
US9221804B2 (en) | 2013-10-15 | 2015-12-29 | Janssen Pharmaceutica Nv | Secondary alcohol quinolinyl modulators of RORγt |
WO2015106164A1 (fr) | 2014-01-10 | 2015-07-16 | Rgenix, Inc. | Agonistes du récepteur x du foie et leurs utilisations |
CN104036909B (zh) * | 2014-06-25 | 2016-09-28 | 桂林理工大学 | 磁性材料[Cu3(N3)6(DMF)2]n及合成方法 |
WO2016057454A1 (fr) | 2014-10-06 | 2016-04-14 | The Johns Hopkins University | Ciblage de récepteurs nucléaires de foie comme traitement pour la maladie de wilson |
EP3402477A4 (fr) | 2016-01-11 | 2019-08-21 | The Rockefeller University | Méthodes pour le traitement de troubles associés à des cellules suppressives dérivées de cellules myéloïdes |
EP3246028A1 (fr) * | 2016-05-18 | 2017-11-22 | Max-Planck-Gesellschaft zur Förderung der Wissenschaften e.V. | Composés de quinoléine pour augmenter la libération d'insuline |
TW201815787A (zh) | 2016-09-23 | 2018-05-01 | 美商基利科學股份有限公司 | 磷脂醯肌醇3-激酶抑制劑 |
TW201825465A (zh) | 2016-09-23 | 2018-07-16 | 美商基利科學股份有限公司 | 磷脂醯肌醇3-激酶抑制劑 |
TW201813963A (zh) | 2016-09-23 | 2018-04-16 | 美商基利科學股份有限公司 | 磷脂醯肌醇3-激酶抑制劑 |
US11084781B2 (en) * | 2017-05-12 | 2021-08-10 | Research Triangle Institute | Diarylureas as CB1 allosteric modulators |
WO2019074241A1 (fr) * | 2017-10-11 | 2019-04-18 | 정원혁 | Inhibiteur de l'interaction entre pd-1 et pd-l1, comprenant un dérivé de phénylacétylène |
EP4155300A1 (fr) | 2017-10-30 | 2023-03-29 | The U.S.A. as represented by the Secretary, Department of Health and Human Services | Analogues de quinoléine substitués utilisés en tant qu'inhibiteurs d'aldéhyde déshydrogénase 1a1 (aldh1a1) |
WO2019104062A1 (fr) | 2017-11-21 | 2019-05-31 | Rgenix, Inc. | Polymorphes et leurs utilisations |
CN113302206A (zh) | 2018-11-26 | 2021-08-24 | 戴纳立制药公司 | 治疗脂质代谢失调的方法 |
US11884647B2 (en) | 2019-10-18 | 2024-01-30 | The Regents Of The University Of California | Compounds and methods for targeting pathogenic blood vessels |
WO2021096589A1 (fr) * | 2019-11-15 | 2021-05-20 | Georgia State University Research Foundation, Inc. | Inhibiteurs de polymérase à petites molécules |
ES2982346T3 (es) | 2019-12-13 | 2024-10-15 | Inspirna Inc | Sales metálicas y usos de las mismas |
Family Cites Families (101)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE2962658D1 (en) | 1978-01-28 | 1982-06-24 | Croda Synthetic Chem Ltd | Process for the preparation of aromatic (b)-fused pyridines and novel thieno(b)pyridines |
US4407803A (en) | 1981-08-17 | 1983-10-04 | Abbott Laboratories | Antiinflammatory 1-(quinolinyl)-2-pyrazoline derivatives |
DE3413078A1 (de) | 1984-04-06 | 1985-10-24 | Miles Laboratories, Inc., Elkhart, Ind. | Chromogene aminosaeure- und peptidester, verfahren zu deren herstellung, verwendung dieser verbindungen in analysenverfahren sowie mittel zum nachweis esterolytischer und/oder proteolytischer enzyme |
CA1336714C (fr) | 1987-08-20 | 1995-08-15 | Yoshihiro Fujikawa | Mevalonolactone de type quinoleine utilisee comme inhibiteurs de la biosynthese du cholesterol |
US4761419A (en) | 1987-12-07 | 1988-08-02 | Warner-Lambert Company | 6-(((substituted)quinolinyl)ethyl)-and ethenyl)tetrahydro-4-hydroxypyran-2-one inhibitors of cholesterol biosynthesis |
NZ231631A (en) | 1988-12-08 | 1992-07-28 | Duphar Int Res | Heterocyclically-substituted piperazine and diazepine derivatives and anxiolytic compositions |
DE3905908A1 (de) | 1989-02-25 | 1990-09-06 | Bayer Ag | Substituierte chinoline, verfahren zu ihrer herstellung und ihre verwendung in arzneimitteln |
US5753675A (en) | 1989-03-03 | 1998-05-19 | Novartis Pharmaceuticals Corporation | Quinoline analogs of mevalonolactone and derivatives thereof |
DE3908298A1 (de) | 1989-03-14 | 1990-09-20 | Bayer Ag | Substituierte (chinolin-2-yl-methoxy)phenyl-n,n'-sulfonylharnstoffe, verfahren zu ihrer herstellung und ihre verwendung in arzneimitteln |
DE3916663A1 (de) | 1989-05-23 | 1990-11-29 | Bayer Ag | Substituierte (chinolin-2-yl-methoxy)phenyl-acyl-sulfonamide und -cyanamide, verfahren zu ihrer herstellung und ihre verwendung in arzneimitteln |
DE3927369A1 (de) | 1989-08-19 | 1991-02-21 | Bayer Ag | Substituierte n-(chinolin-2-yl-methoxy)benzyl-sulfonyl-harnstoffe |
DE3927931A1 (de) | 1989-08-24 | 1991-02-28 | Bayer Ag | Disubstituierte (chinolin-2-yl-methoxy)phenylessigsaeure-derivate |
DE3927930A1 (de) | 1989-08-24 | 1991-02-28 | Bayer Ag | Cyclisch substituierte (chinolin-2-yl-methoxy)phenyl-essig-saeure-derivate |
MX22406A (es) | 1989-09-15 | 1994-01-31 | Pfizer | Nuevos derivados de n-aril y n-heteroarilamidas y urea como inhibidores de acil coenzima a: acil transferasa del colesterol (acat). |
DE3935139A1 (de) | 1989-10-21 | 1991-04-25 | Bayer Ag | Substituierte (chinolin-2-yl-methoxy)phenyl-thioharnstoffe |
DE3935491A1 (de) | 1989-10-25 | 1991-05-02 | Bayer Ag | Substituierte (chinolin-2-yl-methoxy)phenyl-carbonylharnstoffe |
JPH03181465A (ja) * | 1989-12-11 | 1991-08-07 | Takeda Chem Ind Ltd | キノリン誘導体 |
GB9113137D0 (en) | 1990-07-13 | 1991-08-07 | Ici Plc | Thioxo heterocycles |
JPH04182469A (ja) | 1990-11-16 | 1992-06-30 | Terumo Corp | 新規なチオエステル化合物 |
JP2696150B2 (ja) | 1991-02-05 | 1998-01-14 | 株式会社大塚製薬工場 | キノリン誘導体 |
MX9200299A (es) | 1991-02-07 | 1992-12-01 | Roussel Uclaf | Nuevos derivados biciclicos nitrogenados, su procedimiento de preparacion los nuevos compuestos intermedios obtenidos su aplicacion como medicamentos y las composiciones farmaceuticas que los contienen. |
US6004979A (en) | 1991-02-07 | 1999-12-21 | Hoechst Marion Roussel | Nitrogenous bicycles |
DE4139751A1 (de) | 1991-12-03 | 1993-06-09 | Bayer Ag, 5090 Leverkusen, De | Thiazolyl substituierte chinolylmethoxyphenylessigsaeurederivate |
DE4105551A1 (de) | 1991-02-22 | 1992-08-27 | Bayer Ag | 2-substituierte chinoline, verfahren zu ihrer herstellung sowie ihre verwendung in arzneimitteln |
DE4112533A1 (de) | 1991-04-17 | 1992-10-22 | Bayer Ag | Verfahren zur herstellung von enantiomerenreinen substituierten (chinolin-2-yl-methoxy)phenyl-essigsaeuren |
EP0590094A1 (fr) * | 1991-04-26 | 1994-04-06 | Pfizer Inc. | Derives de 4-aryle-3-(heteroarylureido)quinoline |
US5366987A (en) * | 1991-08-22 | 1994-11-22 | Warner-Lambert Company | Isoxazolyl-substituted alkyl amide ACAT inhibitors |
DE4128681A1 (de) | 1991-08-29 | 1993-03-04 | Bayer Ag | Substituierte mandelsaeurederivate, verfahren zu ihrer herstellung sowie ihre verwendung in arzneimitteln |
PT100905A (pt) | 1991-09-30 | 1994-02-28 | Eisai Co Ltd | Compostos heterociclicos azotados biciclicos contendo aneis de benzeno, ciclo-hexano ou piridina e de pirimidina, piridina ou imidazol substituidos e composicoes farmaceuticas que os contem |
JP3130342B2 (ja) | 1991-10-04 | 2001-01-31 | 日産化学工業株式会社 | 動脈硬化性血管内膜肥厚抑制薬 |
JPH05128327A (ja) | 1991-11-01 | 1993-05-25 | Mitsubishi Electric Corp | Icカード |
JPH05130897A (ja) | 1991-11-11 | 1993-05-28 | Terumo Corp | チオール化合物測定用試薬組成物 |
DE4139749A1 (de) | 1991-12-03 | 1993-06-09 | Bayer Ag, 5090 Leverkusen, De | Chinolylmethoxyphenyl-essigsaeureamide |
DE4139750A1 (de) | 1991-12-03 | 1993-06-09 | Bayer Ag, 5090 Leverkusen, De | Chinolylmethoxyphenylessigsaeure-acylamide und -harnstoffe |
IL104369A0 (en) * | 1992-01-13 | 1993-05-13 | Smithkline Beecham Corp | Novel compounds and compositions |
US5183825A (en) | 1992-04-07 | 1993-02-02 | American Home Products Corporation | 4-arylmethyl-5-alkyl-3H-pyrazol-3-ones and hypoglycemic use |
EP0570112A1 (fr) | 1992-04-23 | 1993-11-18 | Zeneca Limited | Dérivés de cycloalcanes |
DE4226519A1 (de) | 1992-08-11 | 1994-02-17 | Bayer Ag | 3-Substituierte Chinolylmethoxy-phenylessigsäurederivate |
JPH0692939A (ja) | 1992-09-16 | 1994-04-05 | Kyowa Hakko Kogyo Co Ltd | イミダゾール誘導体 |
DE4243279A1 (de) | 1992-12-21 | 1994-06-23 | Bayer Ag | Substituierte Triole |
ES2114654T3 (es) * | 1993-06-08 | 1998-06-01 | Vertex Pharma | Piridazinas como inhibidores de la enzima de conversion de la interleuquina-1beta. |
JPH0710870A (ja) | 1993-06-23 | 1995-01-13 | Asahi Glass Co Ltd | 新規アミノピリジン誘導体およびその塩 |
US5593992A (en) * | 1993-07-16 | 1997-01-14 | Smithkline Beecham Corporation | Compounds |
DK0724588T3 (da) * | 1993-09-17 | 2000-05-15 | Smithkline Beecham Corp | Lægemiddelbindende protein |
JPH0789957A (ja) | 1993-09-22 | 1995-04-04 | Nissan Chem Ind Ltd | ビフェニルメチルアミン誘導体 |
US5453509A (en) | 1993-10-08 | 1995-09-26 | Synaptic Pharmaceutical Corporation | Functionalization of acyl pyridinium salts |
DE4411657A1 (de) | 1994-04-02 | 1995-10-05 | Basf Ag | Verfahren zur Herstellung von 6-Hydroxymethylchinolinen |
FR2722198B1 (fr) | 1994-07-08 | 1996-10-04 | Pf Medicament | 1derives de silylmethyl-anilines, le2fabrication, et leur utilisation co |
US5521213A (en) | 1994-08-29 | 1996-05-28 | Merck Frosst Canada, Inc. | Diaryl bicyclic heterocycles as inhibitors of cyclooxygenase-2 |
DE19500120A1 (de) | 1995-01-04 | 1996-07-11 | Bayer Ag | Neue acylierte Pseudopeptide mit trifluormethyl-subsstituiertem 2-Azabicyclooctan |
DE19500122A1 (de) | 1995-01-04 | 1996-07-11 | Bayer Ag | Neue Pseudopeptide mit trifluormethyl-substituierten 2-Azabicyclooctan |
US5650415A (en) * | 1995-06-07 | 1997-07-22 | Sugen, Inc. | Quinoline compounds |
US5837719A (en) * | 1995-08-10 | 1998-11-17 | Merck & Co., Inc. | 2,5-substituted aryl pyrroles, compositions containing such compounds and methods of use |
DE19532714A1 (de) | 1995-09-05 | 1997-03-06 | Bayer Ag | Kombination von 5-Lipoxygenase- und Leukotriensynthese Inhibitoren mit Glucocorticosteroiden |
JPH1067658A (ja) | 1995-09-13 | 1998-03-10 | Takeda Chem Ind Ltd | 免疫抑制剤 |
AR006520A1 (es) | 1996-03-20 | 1999-09-08 | Astra Pharma Prod | Derivados de 2-arilpirazolisoquinolina y cinolinona y procedimiento para su preparacion. |
CZ296163B6 (cs) | 1996-05-20 | 2006-01-11 | Karboxyamidy chinolinu jako inhibitory TNF a inhibitory PDE-IV | |
EP0808627A2 (fr) | 1996-05-22 | 1997-11-26 | Hoechst Aktiengesellschaft | Utilisation des antagonistes de la bradykinine non-peptidiques pour le traitement et la prévention des maladies de foie fibrotiques chroniques, des maladies de foie aigues et complications |
JPH101471A (ja) | 1996-06-13 | 1998-01-06 | Green Cross Corp:The | N−[(キノリン−2−イル)フェニル]スルホンアミド類の結晶およびその製造方法 |
WO1998014430A1 (fr) | 1996-10-02 | 1998-04-09 | Sumitomo Pharmaceuticals Co., Ltd. | Derives de pyrimidine |
JP2001503756A (ja) | 1996-11-06 | 2001-03-21 | ダーウィン・ディスカバリー・リミテッド | キノリン類およびこれらの治療的使用 |
AU8191998A (en) | 1997-02-04 | 1998-08-25 | Trega Biosciences, Inc. | 4-substituted-quinoline derivatives and 4-substitute-quinoline combinatorial libraries |
DE19709125A1 (de) | 1997-03-06 | 1998-09-10 | Bayer Ag | Substituierte Chinoline |
US6514977B1 (en) | 1997-05-22 | 2003-02-04 | G.D. Searle & Company | Substituted pyrazoles as p38 kinase inhibitors |
EP0991623A2 (fr) | 1997-06-19 | 2000-04-12 | Sepracor, Inc. | Agents antimicrobiens quinoleine-indole, utilisations et compositions associees |
AR016294A1 (es) | 1997-07-02 | 2001-07-04 | Smithkline Beecham Corp | Compuesto de imidazol sustituido, composicion farmaceutica que la contiene, su uso en la fabricacion de un medicamento y procedimiento para supreparacion |
US6538022B1 (en) | 1997-09-24 | 2003-03-25 | Orion Corporation | Compounds for deactivating phospholamban function on Ca-ATPase (phopholamban inhibitors) |
JP2002508366A (ja) | 1997-12-12 | 2002-03-19 | スミスクライン・ビーチャム・パブリック・リミテッド・カンパニー | キノリンピペラジンおよびキノリンピペリジン誘導体、それらの製造方法、ならびに複合的5−ht1a、5−ht1bおよび5−ht1d受容体アンタゴニストとしてのそれらの用途 |
US6184226B1 (en) | 1998-08-28 | 2001-02-06 | Scios Inc. | Quinazoline derivatives as inhibitors of P-38 α |
GB9819384D0 (en) | 1998-09-04 | 1998-10-28 | Cerebrus Ltd | Chemical compounds II |
GB9819382D0 (en) | 1998-09-04 | 1998-10-28 | Cerebrus Ltd | Chemical compounds I |
JP2002534512A (ja) | 1999-01-15 | 2002-10-15 | ノボ ノルディスク アクティーゼルスカブ | 非ペプチドglp−1アゴニスト |
US6316503B1 (en) * | 1999-03-15 | 2001-11-13 | Tularik Inc. | LXR modulators |
DE60008206T2 (de) | 1999-11-30 | 2004-12-02 | Pfizer Products Inc., Groton | Chinolinderivate verwendbar zur Hemmung der Farnesyl-Protein Transferase |
CA2392568A1 (fr) * | 1999-12-13 | 2001-06-14 | Merck & Co., Inc. | Procede de prevention et/ou de traitement de l'atherosclerose |
GB0002032D0 (en) | 2000-01-28 | 2000-03-22 | Zeneca Ltd | Chemical compounds |
CA2396865C (fr) | 2000-02-04 | 2009-04-14 | Janssen Pharmaceutica N.V. | Inhibiteurs de la farnesyl proteine transferase pour le traitement du cancer du sein |
ATE375794T1 (de) | 2000-02-24 | 2007-11-15 | Janssen Pharmaceutica Nv | Dosierschema enthaldend farnesyl protein transferase inhibitoren für die behandlung von krebs |
EP1261348A2 (fr) | 2000-02-29 | 2002-12-04 | Janssen Pharmaceutica N.V. | Combinaisons d'inhibiteur de farnesyl proteine transferase et d'agents d'alkylation antitumoraux |
EP1261342A2 (fr) | 2000-02-29 | 2002-12-04 | Janssen Pharmaceutica N.V. | Combinaisons d'inhibiteur de farnesyl-proteine transferase |
CA2397253A1 (fr) | 2000-02-29 | 2001-09-07 | Janssen Pharmaceutica N.V. | Combinaisons d'inhibiteurs de farnesyl proteine transferase et de derives antitumoraux d'anthracycline |
JP2003525255A (ja) | 2000-02-29 | 2003-08-26 | ジヤンセン・フアーマシユーチカ・ナームローゼ・フエンノートシヤツプ | ファルネシルタンパク質トランスフェラーゼ阻害剤とさらなる抗癌剤との組み合わせ剤 |
WO2001064199A2 (fr) | 2000-02-29 | 2001-09-07 | Janssen Pharmaceutica N.V. | Combinaisons d'inhibiteur de farnesyl-proteine transferase avec compose a base de taxane |
US20030022918A1 (en) | 2000-02-29 | 2003-01-30 | Horak Ivan David | Farnesyl protein transferase inhibitor combinations with an her2 antibody |
US20030027808A1 (en) | 2000-02-29 | 2003-02-06 | Palmer Peter Albert | Farnesyl protein transferase inhibitor combinations with platinum compounds |
WO2001070227A1 (fr) | 2000-03-17 | 2001-09-27 | Merck & Co., Inc. | Antagonistes de l'hormone de liberation de la gonadotropine |
AU4742101A (en) | 2000-03-17 | 2001-10-03 | Merck & Co., Inc. | Antagonists of gonadotropin releasing hormone |
JP2001261654A (ja) | 2000-03-21 | 2001-09-26 | Mitsui Chemicals Inc | キノリン誘導体およびそれを有効成分として含有する核内レセプター作動薬 |
US6495562B1 (en) | 2000-04-25 | 2002-12-17 | Abbott Laboratories | Naphthamidine urokinase inhibitors |
AU2001262984A1 (en) * | 2000-05-03 | 2001-11-12 | Tularik, Inc. | Treatment of hypertriglyceridemia and other conditions using lxr modulators |
US6949656B2 (en) | 2000-08-08 | 2005-09-27 | Shionogi & Co., Ltd. | Cyclic amine derivatives and use thereof |
GB0023918D0 (en) | 2000-09-29 | 2000-11-15 | King S College London | Antiparasitic compounds |
US6919351B2 (en) | 2000-10-12 | 2005-07-19 | Merck & Co., Inc. | Aza-and polyaza-naphthalenyl-carboxamides useful as HIV integrase inhibitors |
US7226945B2 (en) | 2000-10-13 | 2007-06-05 | Astrazeneca Ab | Estrogen receptor-β ligands |
WO2002090375A2 (fr) | 2001-05-03 | 2002-11-14 | The University Of Chicago | Agonistes du recepteur x hepatique |
JP2002371078A (ja) | 2001-06-12 | 2002-12-26 | Sankyo Co Ltd | キノリン誘導体及びキノロン誘導体 |
EP1270535A3 (fr) | 2001-06-20 | 2004-02-18 | Clariant GmbH | Méthode de préparation de composés aromatiques substitués |
FR2827599A1 (fr) | 2001-07-20 | 2003-01-24 | Neuro3D | Composes derives de quinoleine et quinoxaline,preparation et utilisations |
EP2168576A3 (fr) * | 2001-09-14 | 2010-05-26 | Shionogi & Co., Ltd. | Composés tricycliques dans le traitement de la dyslipidémie et des maladies artériosclérotiques |
AU2002336433A1 (en) * | 2001-10-08 | 2003-04-22 | Eli Lilly And Company | Tricyclic compounds useful for modulating lxr |
JP2005533007A (ja) * | 2002-03-27 | 2005-11-04 | スミスクライン・ビーチャム・コーポレイション | Lxr調節因子を用いる治療方法 |
-
2004
- 2004-12-10 BR BRPI0417543-3A patent/BRPI0417543A/pt not_active IP Right Cessation
- 2004-12-10 AU AU2004298486A patent/AU2004298486A1/en not_active Abandoned
- 2004-12-10 JP JP2006544016A patent/JP2007516258A/ja active Pending
- 2004-12-10 EP EP10181673A patent/EP2284157A1/fr not_active Withdrawn
- 2004-12-10 CA CA002547518A patent/CA2547518A1/fr not_active Abandoned
- 2004-12-10 WO PCT/US2004/041399 patent/WO2005058834A2/fr active Application Filing
- 2004-12-10 TW TW093138244A patent/TW200529845A/zh unknown
- 2004-12-10 EP EP04813688A patent/EP1692111A2/fr not_active Withdrawn
- 2004-12-10 SV SV2004001973A patent/SV2005001973A/es not_active Application Discontinuation
- 2004-12-10 AR ARP040104624A patent/AR047329A1/es not_active Application Discontinuation
- 2004-12-10 US US11/010,236 patent/US7576215B2/en not_active Expired - Fee Related
- 2004-12-10 KR KR1020067014042A patent/KR20070001922A/ko not_active Application Discontinuation
- 2004-12-10 PE PE2004001236A patent/PE20050676A1/es not_active Application Discontinuation
- 2004-12-10 RU RU2006124843/04A patent/RU2006124843A/ru not_active Application Discontinuation
- 2004-12-10 PA PA20048619901A patent/PA8619901A1/es unknown
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- 2006-05-24 IL IL175892A patent/IL175892A0/en unknown
- 2006-06-02 NO NO20062561A patent/NO20062561L/no not_active Application Discontinuation
- 2006-06-12 EC EC2006006635A patent/ECSP066635A/es unknown
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EP1692111A2 (fr) | 2006-08-23 |
IL175892A0 (en) | 2006-10-05 |
ECSP066635A (es) | 2006-10-25 |
SV2005001973A (es) | 2005-11-04 |
CR8410A (es) | 2006-10-04 |
JP2007516258A (ja) | 2007-06-21 |
CA2547518A1 (fr) | 2005-06-30 |
TW200529845A (en) | 2005-09-16 |
KR20070001922A (ko) | 2007-01-04 |
BRPI0417543A (pt) | 2007-03-27 |
PA8619901A1 (es) | 2005-11-25 |
AU2004298486A1 (en) | 2005-06-30 |
WO2005058834A2 (fr) | 2005-06-30 |
AR047329A1 (es) | 2006-01-18 |
PE20050676A1 (es) | 2005-11-02 |
WO2005058834A3 (fr) | 2005-11-17 |
RU2006124843A (ru) | 2008-01-20 |
US20050131014A1 (en) | 2005-06-16 |
US7576215B2 (en) | 2009-08-18 |
EP2284157A1 (fr) | 2011-02-16 |
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