WO2006087630A3 - OXYPYRAZOLE HMG Co-A REDUCTASE INHIBITORS - Google Patents
OXYPYRAZOLE HMG Co-A REDUCTASE INHIBITORS Download PDFInfo
- Publication number
- WO2006087630A3 WO2006087630A3 PCT/IB2006/000334 IB2006000334W WO2006087630A3 WO 2006087630 A3 WO2006087630 A3 WO 2006087630A3 IB 2006000334 W IB2006000334 W IB 2006000334W WO 2006087630 A3 WO2006087630 A3 WO 2006087630A3
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- hmg
- oxypyrazole
- reductase inhibitors
- reductase
- compounds
- Prior art date
Links
Classifications
-
- 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
- C07D231/00—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
- C07D231/02—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
- C07D231/10—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D231/14—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members 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
- C07D231/18—One oxygen or sulfur atom
- C07D231/20—One oxygen atom attached in position 3 or 5
- C07D231/22—One oxygen atom attached in position 3 or 5 with aryl radicals attached to ring nitrogen 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
- C07D405/06—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
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Abstract
Novel compounds and pharmaceutical compositions useful as hypocholesterolemic and hypolipidemic agents are described. More specifically, potent inhibitors of the enzyme 3-hydroxy-3-methylglutaryl-coenzyme A reductase (“HMG CoA reductase”) are described. Method of using such compounds and compositions to treat subjects, including humans, suffering from hyperlipidemia, hypercholesterolemia, hypertriglyceridemia, atherosclerosis, Alzheimer’s Disease, benign prostatic hypertrophy (BPH), diabetes and osteoporosis are also described.
Applications Claiming Priority (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US65346905P | 2005-02-16 | 2005-02-16 | |
US60/653,469 | 2005-02-16 | ||
US74869805P | 2005-12-08 | 2005-12-08 | |
US60/748,698 | 2005-12-08 |
Publications (2)
Publication Number | Publication Date |
---|---|
WO2006087630A2 WO2006087630A2 (en) | 2006-08-24 |
WO2006087630A3 true WO2006087630A3 (en) | 2006-10-05 |
Family
ID=36739908
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/IB2006/000334 WO2006087630A2 (en) | 2005-02-16 | 2006-02-07 | OXYPYRAZOLE HMG Co-A REDUCTASE INHIBITORS |
Country Status (1)
Country | Link |
---|---|
WO (1) | WO2006087630A2 (en) |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2013510163A (en) | 2009-11-06 | 2013-03-21 | チェルシー・セラピューティクス,インコーポレイテッド | Enzyme inhibitory compounds |
BR112013004882A2 (en) | 2010-08-31 | 2016-05-03 | Snu R&Db Foundation | use of fetal reprogramming of ppar delta agonist |
Citations (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1986000307A2 (en) * | 1984-06-22 | 1986-01-16 | Sandoz Ag | Pyrazole analogs of mevalonolactone and derivatives thereof, processes for their production and their use |
WO1986007054A1 (en) * | 1985-05-22 | 1986-12-04 | Sandoz Ag | Imidazole analogs of mevalonolactone and derivatives thereof |
EP0252476A2 (en) * | 1986-07-07 | 1988-01-13 | Warner-Lambert Company | Trans-6-[2-(N-heteroaryl-3,5-disubstituted) pyrazol-4-yl)-ethyl]- or ethenyl] tetrahydro-4-hydroxypyran-2-one-derivatives a process for their preparation and the use thereof |
EP0433842A2 (en) * | 1989-12-21 | 1991-06-26 | ZAMBON GROUP S.p.A. | 1,2,3-Triazole derivatives active as inhibitors of the enzyme HMG-COA reductase and pharmaceutical compositions containing them |
WO2004005250A1 (en) * | 2002-07-08 | 2004-01-15 | Ranbaxy Laboratories Limited | Hmg-coa reductase inhibitors |
WO2004105752A1 (en) * | 2003-05-30 | 2004-12-09 | Ranbaxy Laboratories Limited | Substituted pyrrole derivatives as hmg-coa reductase inhibitors |
WO2006056845A1 (en) * | 2004-11-23 | 2006-06-01 | Warner-Lambert Company Llc | 7-(2h-pyrazol-3-yl)-3, 5-dihyroxy-heptanoic acid derivatives as hmg co-a reductase inhibitors for the treatment of lipidemia |
-
2006
- 2006-02-07 WO PCT/IB2006/000334 patent/WO2006087630A2/en active Application Filing
Patent Citations (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1986000307A2 (en) * | 1984-06-22 | 1986-01-16 | Sandoz Ag | Pyrazole analogs of mevalonolactone and derivatives thereof, processes for their production and their use |
WO1986007054A1 (en) * | 1985-05-22 | 1986-12-04 | Sandoz Ag | Imidazole analogs of mevalonolactone and derivatives thereof |
EP0252476A2 (en) * | 1986-07-07 | 1988-01-13 | Warner-Lambert Company | Trans-6-[2-(N-heteroaryl-3,5-disubstituted) pyrazol-4-yl)-ethyl]- or ethenyl] tetrahydro-4-hydroxypyran-2-one-derivatives a process for their preparation and the use thereof |
EP0433842A2 (en) * | 1989-12-21 | 1991-06-26 | ZAMBON GROUP S.p.A. | 1,2,3-Triazole derivatives active as inhibitors of the enzyme HMG-COA reductase and pharmaceutical compositions containing them |
WO2004005250A1 (en) * | 2002-07-08 | 2004-01-15 | Ranbaxy Laboratories Limited | Hmg-coa reductase inhibitors |
WO2004105752A1 (en) * | 2003-05-30 | 2004-12-09 | Ranbaxy Laboratories Limited | Substituted pyrrole derivatives as hmg-coa reductase inhibitors |
WO2006056845A1 (en) * | 2004-11-23 | 2006-06-01 | Warner-Lambert Company Llc | 7-(2h-pyrazol-3-yl)-3, 5-dihyroxy-heptanoic acid derivatives as hmg co-a reductase inhibitors for the treatment of lipidemia |
Also Published As
Publication number | Publication date |
---|---|
WO2006087630A2 (en) | 2006-08-24 |
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