NO993738L - 2-amino-substituted pyridines which can be used in the treatment of arteriosclerosis and hyper-lipoproteinemia - Google Patents
2-amino-substituted pyridines which can be used in the treatment of arteriosclerosis and hyper-lipoproteinemiaInfo
- Publication number
- NO993738L NO993738L NO993738A NO993738A NO993738L NO 993738 L NO993738 L NO 993738L NO 993738 A NO993738 A NO 993738A NO 993738 A NO993738 A NO 993738A NO 993738 L NO993738 L NO 993738L
- Authority
- NO
- Norway
- Prior art keywords
- amino
- substituted pyridines
- arteriosclerosis
- treatment
- lipoproteinemia
- Prior art date
Links
- -1 2-amino-substituted pyridines Chemical class 0.000 title abstract 4
- 206010003210 Arteriosclerosis Diseases 0.000 title abstract 2
- 208000011775 arteriosclerosis disease Diseases 0.000 title abstract 2
- 208000031226 Hyperlipidaemia Diseases 0.000 title 1
- 208000020346 hyperlipoproteinemia Diseases 0.000 title 1
- 150000001875 compounds Chemical class 0.000 abstract 2
- 150000004679 hydroxides Chemical class 0.000 abstract 2
- 239000004480 active ingredient Substances 0.000 abstract 1
- 239000003814 drug Substances 0.000 abstract 1
- 229940079593 drug Drugs 0.000 abstract 1
- 150000002894 organic compounds Chemical class 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen 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
- C07D213/72—Nitrogen atoms
- C07D213/74—Amino or imino radicals substituted by hydrocarbon or substituted hydrocarbon radicals
-
- 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
- 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
-
- 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
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Obesity (AREA)
- Diabetes (AREA)
- Hematology (AREA)
- Urology & Nephrology (AREA)
- Vascular Medicine (AREA)
- Cardiology (AREA)
- Heart & Thoracic Surgery (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Pyridine Compounds (AREA)
Abstract
Det beskrives nye 2-amino-substituerte pyridiner med formel (I). Disse fremstilles ved først å omdanne tilsvarende pyridinaldehyder til tilsvarende hydroksyder ved hjelp av metallorganiske forbindelser som Grignard-forbindelser og så å redusere hydroksydene til en deshydroksyforbindelse. De nye 2-amino-substituerte pyridiner er egnet for anvendelse som aktive bestanddeler i medikamenter og særlig slike som benyttes ved behandling av arteriosklerose.New 2-amino-substituted pyridines of formula (I) are disclosed. These are prepared by first converting corresponding pyridinal aldehydes to corresponding hydroxides by means of metallic organic compounds such as Grignard compounds and then reducing the hydroxides to a dehydroxy compound. The new 2-amino-substituted pyridines are suitable for use as active ingredients in drugs and especially those used in the treatment of arteriosclerosis.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19704243A DE19704243A1 (en) | 1997-02-05 | 1997-02-05 | New 2-amino-substituted pyridines |
| PCT/EP1998/000362 WO1998034920A1 (en) | 1997-02-05 | 1998-01-23 | 2-amino substituted pyridines for use in the treatment of arteriosclerosis and hyperlipoproteinaemia |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| NO993738D0 NO993738D0 (en) | 1999-08-02 |
| NO993738L true NO993738L (en) | 1999-09-17 |
Family
ID=7819326
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NO993738A NO993738L (en) | 1997-02-05 | 1999-08-02 | 2-amino-substituted pyridines which can be used in the treatment of arteriosclerosis and hyper-lipoproteinemia |
Country Status (19)
| Country | Link |
|---|---|
| EP (1) | EP0973744A1 (en) |
| JP (1) | JP2001510478A (en) |
| KR (1) | KR20000070756A (en) |
| CN (1) | CN1252057A (en) |
| AU (1) | AU730109B2 (en) |
| BG (1) | BG103631A (en) |
| BR (1) | BR9807181A (en) |
| CA (1) | CA2279636A1 (en) |
| CZ (1) | CZ279299A3 (en) |
| DE (1) | DE19704243A1 (en) |
| HU (1) | HUP0001022A2 (en) |
| ID (1) | ID24208A (en) |
| IL (1) | IL131127A0 (en) |
| NO (1) | NO993738L (en) |
| NZ (1) | NZ337011A (en) |
| PL (1) | PL334899A1 (en) |
| SK (1) | SK104099A3 (en) |
| TR (1) | TR199901857T2 (en) |
| WO (1) | WO1998034920A1 (en) |
Families Citing this family (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE19845402B4 (en) * | 1998-10-02 | 2005-04-07 | Aventis Pharma Deutschland Gmbh | Heterocyclic substituted propanolamine derivatives, process for their preparation, pharmaceutical compositions containing them and their use |
| JP4547148B2 (en) | 2001-06-22 | 2010-09-22 | ベンド・リサーチ・インコーポレーテッド | Pharmaceutical composition of adsorbate of amorphous drug |
| MXPA03011784A (en) | 2001-06-22 | 2004-04-02 | Pfizer Prod Inc | Pharmaceutical compositions of dispersions of drugs and neutral polymers. |
| WO2003063833A1 (en) | 2002-02-01 | 2003-08-07 | Pfizer Products Inc. | Pharmaceutical compositions of amorphous dispersions of drugs and lipophilic microphase-forming materials |
| AU2004222436A1 (en) | 2003-03-17 | 2004-09-30 | Japan Tobacco Inc. | Method for increasing the oral bioavailability of S-(2-(((1- (2-ethylbutyl) cyclohexyl)carbonyl) amino) phenyl)-2-methylpropanethioate |
| CL2004001884A1 (en) | 2003-08-04 | 2005-06-03 | Pfizer Prod Inc | DRYING PROCEDURE FOR SPRAYING FOR THE FORMATION OF SOLID DISPERSIONS AMORPHES OF A PHARMACO AND POLYMERS. |
| MXPA06001417A (en) | 2003-08-04 | 2006-05-15 | Pfizer Prod Inc | Pharmaceutical compositions of adsorbates of amorphous drugs and lipophilic microphase-forming materials. |
| RU2330682C2 (en) | 2003-09-26 | 2008-08-10 | Джапан Тобакко Инк. | Method of residual lipoproteins producing inhibition |
| DOP2005000123A (en) * | 2004-07-02 | 2011-07-15 | Merck Sharp & Dohme | CETP INHIBITORS |
| WO2006032987A1 (en) * | 2004-09-23 | 2006-03-30 | Pfizer Products Inc. | Indoline compounds and their use in the treatment of arteriosclerosis |
| EP2548894A1 (en) | 2005-02-03 | 2013-01-23 | Bend Research, Inc. | Pharmaceutical compositions with enhanced performance |
| US20100113473A1 (en) | 2008-10-30 | 2010-05-06 | Player Mark R | Aryl amide compound as an acetyl coenzyme a carboxylase inhibitor |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5169857A (en) * | 1988-01-20 | 1992-12-08 | Bayer Aktiengesellschaft | 7-(polysubstituted pyridyl)-hept-6-endates useful for treating hyperproteinaemia, lipoproteinaemia or arteriosclerosis |
-
1997
- 1997-02-05 DE DE19704243A patent/DE19704243A1/en not_active Withdrawn
-
1998
- 1998-01-23 SK SK1040-99A patent/SK104099A3/en unknown
- 1998-01-23 WO PCT/EP1998/000362 patent/WO1998034920A1/en not_active Ceased
- 1998-01-23 CZ CZ992792A patent/CZ279299A3/en unknown
- 1998-01-23 KR KR1019997007015A patent/KR20000070756A/en not_active Withdrawn
- 1998-01-23 CA CA002279636A patent/CA2279636A1/en not_active Abandoned
- 1998-01-23 HU HU0001022A patent/HUP0001022A2/en unknown
- 1998-01-23 TR TR1999/01857T patent/TR199901857T2/en unknown
- 1998-01-23 IL IL13112798A patent/IL131127A0/en unknown
- 1998-01-23 ID IDW990821D patent/ID24208A/en unknown
- 1998-01-23 BR BR9807181-5A patent/BR9807181A/en not_active IP Right Cessation
- 1998-01-23 AU AU62123/98A patent/AU730109B2/en not_active Ceased
- 1998-01-23 JP JP53369198A patent/JP2001510478A/en active Pending
- 1998-01-23 EP EP98904126A patent/EP0973744A1/en not_active Ceased
- 1998-01-23 NZ NZ337011A patent/NZ337011A/en unknown
- 1998-01-23 CN CN98803916A patent/CN1252057A/en active Pending
- 1998-01-23 PL PL98334899A patent/PL334899A1/en unknown
-
1999
- 1999-08-02 NO NO993738A patent/NO993738L/en not_active Application Discontinuation
- 1999-08-03 BG BG103631A patent/BG103631A/en unknown
Also Published As
| Publication number | Publication date |
|---|---|
| TR199901857T2 (en) | 1999-10-21 |
| JP2001510478A (en) | 2001-07-31 |
| KR20000070756A (en) | 2000-11-25 |
| NO993738D0 (en) | 1999-08-02 |
| ID24208A (en) | 2000-07-13 |
| AU730109B2 (en) | 2001-02-22 |
| NZ337011A (en) | 2001-04-27 |
| AU6212398A (en) | 1998-08-26 |
| CN1252057A (en) | 2000-05-03 |
| EP0973744A1 (en) | 2000-01-26 |
| WO1998034920A1 (en) | 1998-08-13 |
| CA2279636A1 (en) | 1998-08-13 |
| DE19704243A1 (en) | 1998-08-06 |
| PL334899A1 (en) | 2000-03-27 |
| HUP0001022A2 (en) | 2000-09-28 |
| SK104099A3 (en) | 2000-01-18 |
| BR9807181A (en) | 2000-01-25 |
| CZ279299A3 (en) | 1999-11-17 |
| IL131127A0 (en) | 2001-01-28 |
| BG103631A (en) | 2000-11-30 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| GEP20012578B (en) | (54) Heteroaryl Succinamides, Pharmaceutical Compositions Containing the Same and Methods for Treatment of the Diseases Caused by Metalloproteinase Activity | |
| GEP20032922B (en) | Benzoheterocycles and Their Use as MEK Inhibitors | |
| NO20074773L (en) | Caspase Inhibitors and Their Use | |
| NO983003L (en) | Vitronectin receptor antagonists | |
| DE69919334D1 (en) | PHENYLALANINE DERIVATIVES AS INHIBITORS OF ALPHA4 INTEGRINES | |
| ATE191218T1 (en) | RAPAMYCIN DERIVATIVES AS IMMUNOSUPPRESSORS | |
| NO20030301L (en) | New heteroaryl derivatives and their use as pharmaceuticals | |
| DE60030741D1 (en) | CHINAZOLINE COMPOUNDS AS A REMEDY | |
| ATE260910T1 (en) | 4-HETEROARYL-TETRAHYDROCINOLINES AND THEIR USE AS CHOLESTEROL ESTER TRANSFER PROTEIN (CTEP) INHIBITORS | |
| RU94036758A (en) | Use of 2-phenyl-3-aroylbenzothiophenes for peri-menopause syndrome | |
| WO1998042659A3 (en) | Aryl- or heteroarylsulfonamide substituted hydroxamic acid derivates, process for their preparation and their use as pharmaceuticals | |
| CA2015838A1 (en) | Method of topically treating acne vulgaris | |
| RU94044453A (en) | Use of 2-phenyl-3-aroylbenzothiophenes for seborrhea and acne inhibition | |
| WO1992019617A3 (en) | Substituted dibenzoxazepine compounds, pharmaceutical compositions and methods of use | |
| EP1695711A3 (en) | Parenteral formulations comprising boronic acid species for selective thrombin inhibition | |
| GEP20002187B (en) | Carboxamide Derivatives of Pyrrolidine, Piperidine and Hexahydroazepine, Composition for the Treatment of Thrombosis Disorders Induced by Thrombocytes, Intermediate Compounds and Method for Their Preparation | |
| ATE267187T1 (en) | DIHYDROBENZOFURANES AND RELATED COMPOUNDS USEFUL AS ANTI-INFLAMMATORY AGENTS | |
| ATE233252T1 (en) | SUBSTITUTED DIHYDROBENZOFURANES AS PDE INHIBITORS | |
| DE60205899D1 (en) | 1-biaryl-1,8-naphthyridin-4-one als phosphodieseterase-inhibitoren | |
| ATE365535T1 (en) | METHOD FOR TREATING THE SKIN BY ELECTROSTATIC SPRAYING AN EMULSION CONTAINING AN INSULATING EXTERNAL AND A CONDUCTIVE INNER PHASE | |
| TR199901857T2 (en) | New 2-amino-substituted pyridines | |
| DK1083887T3 (en) | Pharmaceutical preparation for the treatment of ulcers | |
| NO970123L (en) | New chemical compound, its preparation and use as a drug | |
| DE69736945D1 (en) | BIPHENYL COMPOUNDS AND ITS APPLICATION AS ESTROGENIC AGENTS | |
| ATE115949T1 (en) | SUBSTITUTED MANDELIC ACID DERIVATIVES, AS 5-LIPOXYGENASE INHIBITORS. |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| FC2A | Withdrawal, rejection or dismissal of laid open patent application |