JP2005529077A - ペルオキシソーム増殖因子活性化受容体調節物質 - Google Patents
ペルオキシソーム増殖因子活性化受容体調節物質 Download PDFInfo
- Publication number
- JP2005529077A JP2005529077A JP2003570846A JP2003570846A JP2005529077A JP 2005529077 A JP2005529077 A JP 2005529077A JP 2003570846 A JP2003570846 A JP 2003570846A JP 2003570846 A JP2003570846 A JP 2003570846A JP 2005529077 A JP2005529077 A JP 2005529077A
- Authority
- JP
- Japan
- Prior art keywords
- phenyl
- methyl
- trifluoromethyl
- propionic acid
- thiazol
- 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.)
- Pending
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- 0 CC(COc1cc(N[U])c(CCC(OC)=O)cc1)C(*1)=C(N*)N=C1C(C=C1)=C*C1=C1C=CC=C*1 Chemical compound CC(COc1cc(N[U])c(CCC(OC)=O)cc1)C(*1)=C(N*)N=C1C(C=C1)=C*C1=C1C=CC=C*1 0.000 description 4
- MKHDPFCSSMAGKJ-UHFFFAOYSA-N CC(C)(C(O)=O)Oc(c(C)c1)ccc1O Chemical compound CC(C)(C(O)=O)Oc(c(C)c1)ccc1O MKHDPFCSSMAGKJ-UHFFFAOYSA-N 0.000 description 1
- XWQCYQDOPREOJB-UHFFFAOYSA-N CC(C)c1c(C(C)Oc(cc2)cc(C)c2OCC(O)=O)[s]c(-c2ccc(C(F)(F)F)cc2)n1 Chemical compound CC(C)c1c(C(C)Oc(cc2)cc(C)c2OCC(O)=O)[s]c(-c2ccc(C(F)(F)F)cc2)n1 XWQCYQDOPREOJB-UHFFFAOYSA-N 0.000 description 1
- AXAWPBFUXAXODB-UHFFFAOYSA-N CC(C)c1c(C(C)Oc2ccc(CCC3(CC3)O)c(C)c2)[o]c(-c(cc2)ccc2-c2cccnc2)c1 Chemical compound CC(C)c1c(C(C)Oc2ccc(CCC3(CC3)O)c(C)c2)[o]c(-c(cc2)ccc2-c2cccnc2)c1 AXAWPBFUXAXODB-UHFFFAOYSA-N 0.000 description 1
- WUDIOQAVLMDQOJ-UHFFFAOYSA-N CC(C)c1c(C(C)[O-]c(cc2)cc(C)c2OCC(O)=O)[s]c(-c2ccc(C(F)(F)F)cc2)n1 Chemical compound CC(C)c1c(C(C)[O-]c(cc2)cc(C)c2OCC(O)=O)[s]c(-c2ccc(C(F)(F)F)cc2)n1 WUDIOQAVLMDQOJ-UHFFFAOYSA-N 0.000 description 1
- AFGYQILJWHCLFU-UHFFFAOYSA-N CC(C)c1c(CO)[s]c(-c2ccc(C(F)(F)F)cc2)n1 Chemical compound CC(C)c1c(CO)[s]c(-c2ccc(C(F)(F)F)cc2)n1 AFGYQILJWHCLFU-UHFFFAOYSA-N 0.000 description 1
- ARGNYQNTBIGVIL-OAHLLOKOSA-N CC(C)c1c([C@H](C)COc(cc(CC(O)=O)cc2)c2OC)[o]c(-c2ccc(C(F)(F)F)cc2)n1 Chemical compound CC(C)c1c([C@H](C)COc(cc(CC(O)=O)cc2)c2OC)[o]c(-c2ccc(C(F)(F)F)cc2)n1 ARGNYQNTBIGVIL-OAHLLOKOSA-N 0.000 description 1
- JTNNHMDYVWLQJZ-MRXNPFEDSA-N CC(C)c1c([C@H](C)COc2cc(CCC(O)=O)ccc2)[o]c(-c2ccc(C(F)(F)F)cc2)n1 Chemical compound CC(C)c1c([C@H](C)COc2cc(CCC(O)=O)ccc2)[o]c(-c2ccc(C(F)(F)F)cc2)n1 JTNNHMDYVWLQJZ-MRXNPFEDSA-N 0.000 description 1
- XTHNGEKZASUPOF-UHFFFAOYSA-N CC(COc1cc(C)c(CCC(O)=O)cc1)C1=C(C)O[C](C(C=C2)=CCC2Sc2ccccc2)O1 Chemical compound CC(COc1cc(C)c(CCC(O)=O)cc1)C1=C(C)O[C](C(C=C2)=CCC2Sc2ccccc2)O1 XTHNGEKZASUPOF-UHFFFAOYSA-N 0.000 description 1
- QHILINQCBPBPFD-UHFFFAOYSA-N CC(COc1cc(C)c(CCC(OC)=O)cc1)c1c(C)[o]c(-c(cc2)ccc2Br)n1 Chemical compound CC(COc1cc(C)c(CCC(OC)=O)cc1)c1c(C)[o]c(-c(cc2)ccc2Br)n1 QHILINQCBPBPFD-UHFFFAOYSA-N 0.000 description 1
- LCSKWOMGBBFXDC-UHFFFAOYSA-N CC(COc1cc(CC(O)=O)ccc1)c1c(C)[o]c(-c2ccc(C(C)(F)F)cc2)n1 Chemical compound CC(COc1cc(CC(O)=O)ccc1)c1c(C)[o]c(-c2ccc(C(C)(F)F)cc2)n1 LCSKWOMGBBFXDC-UHFFFAOYSA-N 0.000 description 1
- FOHQZGNUUMPHKD-UHFFFAOYSA-N CC(COc1ccc(CCC(O)=O)c(C)c1)c1c(C)nc(-c(cc2)ccc2-c2ncccn2)[o]1 Chemical compound CC(COc1ccc(CCC(O)=O)c(C)c1)c1c(C)nc(-c(cc2)ccc2-c2ncccn2)[o]1 FOHQZGNUUMPHKD-UHFFFAOYSA-N 0.000 description 1
- YUEIBTWXZDMLKE-UHFFFAOYSA-N CC(COc1ccc(CCC(O)=O)c(C)c1)c1c(C)nc(-c2ccc(C(F)(F)F)cc2)[s]1 Chemical compound CC(COc1ccc(CCC(O)=O)c(C)c1)c1c(C)nc(-c2ccc(C(F)(F)F)cc2)[s]1 YUEIBTWXZDMLKE-UHFFFAOYSA-N 0.000 description 1
- DSFLIHCQIGAEHA-UHFFFAOYSA-N CC(COc1cccc(CC(O)=O)c1)c1c(C)[o]c(-c2ccc(C(F)(F)F)cc2)n1 Chemical compound CC(COc1cccc(CC(O)=O)c1)c1c(C)[o]c(-c2ccc(C(F)(F)F)cc2)n1 DSFLIHCQIGAEHA-UHFFFAOYSA-N 0.000 description 1
- PHYYSRQIIPYQJD-UHFFFAOYSA-N CC(COc1cccc(CC(O)=O)c1)c1c(C)nc(-c2ccc(C(F)(F)F)cc2)[s]1 Chemical compound CC(COc1cccc(CC(O)=O)c1)c1c(C)nc(-c2ccc(C(F)(F)F)cc2)[s]1 PHYYSRQIIPYQJD-UHFFFAOYSA-N 0.000 description 1
- JDVGOQOMIFSRPS-UHFFFAOYSA-N CC(c1c(C(C)(C)C)nc(-c2ccc(C(C=C)(F)F)cc2)[o]1)Oc1ccc(CCC(O)=O)c(C)c1 Chemical compound CC(c1c(C(C)(C)C)nc(-c2ccc(C(C=C)(F)F)cc2)[o]1)Oc1ccc(CCC(O)=O)c(C)c1 JDVGOQOMIFSRPS-UHFFFAOYSA-N 0.000 description 1
- DTPISPGRPCEBGA-UHFFFAOYSA-N CCC(COc1cc(C)c(CCC(O)=C2CC2)cc1)c1c(C)[s]c(-c(cc2)ccc2-c2ncccc2)n1 Chemical compound CCC(COc1cc(C)c(CCC(O)=C2CC2)cc1)c1c(C)[s]c(-c(cc2)ccc2-c2ncccc2)n1 DTPISPGRPCEBGA-UHFFFAOYSA-N 0.000 description 1
- XADNRZCJRFULDG-UHFFFAOYSA-N CCOC(C(C(CCc(c(N)ccc1)c1N)=O)N)=O Chemical compound CCOC(C(C(CCc(c(N)ccc1)c1N)=O)N)=O XADNRZCJRFULDG-UHFFFAOYSA-N 0.000 description 1
- RICCWHIBTQBAMF-UHFFFAOYSA-N CCOC(C(C(CCc1ccccc1)=O)Cl)=O Chemical compound CCOC(C(C(CCc1ccccc1)=O)Cl)=O RICCWHIBTQBAMF-UHFFFAOYSA-N 0.000 description 1
- PRDJGEFZGPKCSG-UHFFFAOYSA-N CCOC(CC(CCc1ccccc1)=O)=O Chemical compound CCOC(CC(CCc1ccccc1)=O)=O PRDJGEFZGPKCSG-UHFFFAOYSA-N 0.000 description 1
- SESNWHGFRVSVQK-UHFFFAOYSA-N CCOC(c1c(CCc2ccccc2)nc(-c2ccc(C(F)(F)F)cc2)[s]1)=O Chemical compound CCOC(c1c(CCc2ccccc2)nc(-c2ccc(C(F)(F)F)cc2)[s]1)=O SESNWHGFRVSVQK-UHFFFAOYSA-N 0.000 description 1
- AATYGGXFIRKDSB-UHFFFAOYSA-N CCc1c(C=O)[o]c(-c2ccc(C(F)(F)F)cc2)n1 Chemical compound CCc1c(C=O)[o]c(-c2ccc(C(F)(F)F)cc2)n1 AATYGGXFIRKDSB-UHFFFAOYSA-N 0.000 description 1
- MUIQJKXZCJYZKP-INIZCTEOSA-N C[C@@H](c1c(C)nc(-c2ccc(C(F)(F)F)cc2)[o]1)[O-]Cc1cc(C)c(CCC(O)=O)cc1 Chemical compound C[C@@H](c1c(C)nc(-c2ccc(C(F)(F)F)cc2)[o]1)[O-]Cc1cc(C)c(CCC(O)=O)cc1 MUIQJKXZCJYZKP-INIZCTEOSA-N 0.000 description 1
- MWNSIVVGQJVEAX-MRVPVSSYSA-N C[C@H](CO)c1c(C)[o]c(-c2ccc(C(F)(F)F)cc2)n1 Chemical compound C[C@H](CO)c1c(C)[o]c(-c2ccc(C(F)(F)F)cc2)n1 MWNSIVVGQJVEAX-MRVPVSSYSA-N 0.000 description 1
- XIDQRQSMCPWFBE-LJQANCHMSA-N C[C@H](c1c(CCc2ccccc2)nc(-c2ccc(C(F)(F)F)cc2)[s]1)Sc(cc1C)ccc1OCC(O)=O Chemical compound C[C@H](c1c(CCc2ccccc2)nc(-c2ccc(C(F)(F)F)cc2)[s]1)Sc(cc1C)ccc1OCC(O)=O XIDQRQSMCPWFBE-LJQANCHMSA-N 0.000 description 1
- QAGVLZPIONQLNN-QGZVFWFLSA-N C[C@H](c1c(COc(c(F)ccc2)c2Cl)nc(-c2ccc(C(F)(F)F)cc2)[s]1)Oc1ccc(CCC(O)=O)c(C)c1 Chemical compound C[C@H](c1c(COc(c(F)ccc2)c2Cl)nc(-c2ccc(C(F)(F)F)cc2)[s]1)Oc1ccc(CCC(O)=O)c(C)c1 QAGVLZPIONQLNN-QGZVFWFLSA-N 0.000 description 1
- WYSFAUFTFUPUGW-UHFFFAOYSA-N Cc1c(C(COc2ccc(CCC(O)=O)c(C)c2)C=C)nc(-c(cc2)ccc2-c2ncccn2)[s]1 Chemical compound Cc1c(C(COc2ccc(CCC(O)=O)c(C)c2)C=C)nc(-c(cc2)ccc2-c2ncccn2)[s]1 WYSFAUFTFUPUGW-UHFFFAOYSA-N 0.000 description 1
- CNGIHPSQMNNAEC-UHFFFAOYSA-N Cc1c(CCOc2cc(C)c(CCC(O)=O)cc2)nc(-c(cc2)ccc2-c2ncccn2)[s]1 Chemical compound Cc1c(CCOc2cc(C)c(CCC(O)=O)cc2)nc(-c(cc2)ccc2-c2ncccn2)[s]1 CNGIHPSQMNNAEC-UHFFFAOYSA-N 0.000 description 1
- SEHCYQHVWYXBGI-UHFFFAOYSA-N Cc1c(CO)[s]c(-c2ccc(C(F)(F)F)cc2)n1 Chemical compound Cc1c(CO)[s]c(-c2ccc(C(F)(F)F)cc2)n1 SEHCYQHVWYXBGI-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D263/00—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings
- C07D263/02—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings
- C07D263/30—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D263/32—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
-
- 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
- A61P3/08—Drugs for disorders of the metabolism for glucose homeostasis
- A61P3/10—Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
-
- 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
- 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
- C07D277/00—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings
- C07D277/02—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings
- C07D277/20—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D277/22—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
- C07D277/24—Radicals substituted by oxygen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D277/00—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings
- C07D277/02—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings
- C07D277/20—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D277/22—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
- C07D277/26—Radicals substituted by sulfur atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D277/00—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings
- C07D277/02—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings
- C07D277/20—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D277/22—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
- C07D277/28—Radicals substituted by nitrogen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D277/00—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings
- C07D277/02—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings
- C07D277/20—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D277/22—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
- C07D277/30—Radicals substituted by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
-
- 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
- C07D403/10—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 carbon chain containing aromatic rings
-
- 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
- C07D413/10—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 aromatic rings
-
- 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
- C07D417/04—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 directly linked by a ring-member-to-ring-member bond
-
- 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
- C07D417/10—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 carbon chain containing aromatic rings
-
- 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
- C07D417/14—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 three or more hetero rings
Landscapes
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Animal Behavior & Ethology (AREA)
- Diabetes (AREA)
- General Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Hematology (AREA)
- Obesity (AREA)
- Endocrinology (AREA)
- Emergency Medicine (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)
- Thiazole And Isothizaole Compounds (AREA)
- Medicinal Preparation (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
- Medicines Containing Material From Animals Or Micro-Organisms (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Electrochromic Elements, Electrophoresis, Or Variable Reflection Or Absorption Elements (AREA)
- Steroid Compounds (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US35980802P | 2002-02-25 | 2002-02-25 | |
| PCT/US2003/002679 WO2003072100A1 (en) | 2002-02-25 | 2003-02-13 | Peroxisome proliferator activated receptor modulators |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2005529077A true JP2005529077A (ja) | 2005-09-29 |
| JP2005529077A5 JP2005529077A5 (enExample) | 2006-01-05 |
Family
ID=27766138
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2003570846A Pending JP2005529077A (ja) | 2002-02-25 | 2003-02-13 | ペルオキシソーム増殖因子活性化受容体調節物質 |
Country Status (8)
| Country | Link |
|---|---|
| US (1) | US7153878B2 (enExample) |
| EP (1) | EP1480640B1 (enExample) |
| JP (1) | JP2005529077A (enExample) |
| AT (1) | ATE369855T1 (enExample) |
| AU (1) | AU2003217274A1 (enExample) |
| DE (1) | DE60315603T2 (enExample) |
| ES (1) | ES2290439T3 (enExample) |
| WO (1) | WO2003072100A1 (enExample) |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2009526867A (ja) * | 2006-02-15 | 2009-07-23 | アボット・ラボラトリーズ | 新規なアセチル−CoAカルボキシラーゼ(ACC)阻害薬およびそれらの糖尿病、肥満および代謝症候群での使用 |
| JP2010511604A (ja) * | 2006-12-02 | 2010-04-15 | ソウル ナショナル ユニバーシティー インダストリー ファンデーション | ペルオキシソーム増殖因子活性化受容体リガンドアリール化合物及びこれらの化合物の用途 |
| JP2010515724A (ja) * | 2007-01-08 | 2010-05-13 | ソウル ナショナル ユニバーシティー インダストリー ファンデーション | ペルオキシソーム増殖因子活性化受容体δリガンドチアゾール化合物及びこれを含有する医薬、化粧品及び健康食品組成物 |
Families Citing this family (46)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20040072838A1 (en) * | 2000-12-20 | 2004-04-15 | Pierette Banker | Thiazole and oxazole derivatives as activators of human peroxisome proliferator activated receptors |
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| KR20000068151A (ko) * | 1996-08-19 | 2000-11-25 | 미즈노 마사루 | 프로피온산 유도체 및 그의 용도 |
| GB9914977D0 (en) | 1999-06-25 | 1999-08-25 | Glaxo Group Ltd | Chemical compounds |
| EP1310494B1 (en) * | 2000-08-11 | 2012-01-25 | Nippon Chemiphar Co., Ltd. | PPAR (delta) ACTIVATORS |
| WO2002018355A1 (en) * | 2000-08-23 | 2002-03-07 | Eli Lilly And Company | Oxazolyl-aryloxyacetic acid derivatives and their use as ppar agonists |
| GB0031107D0 (en) | 2000-12-20 | 2001-01-31 | Glaxo Group Ltd | Chemical compounds |
| JP2005529077A (ja) | 2002-02-25 | 2005-09-29 | イーライ・リリー・アンド・カンパニー | ペルオキシソーム増殖因子活性化受容体調節物質 |
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- 2003-02-13 AT AT03713316T patent/ATE369855T1/de not_active IP Right Cessation
- 2003-02-13 ES ES03713316T patent/ES2290439T3/es not_active Expired - Lifetime
- 2003-02-13 US US10/505,089 patent/US7153878B2/en not_active Expired - Fee Related
- 2003-02-13 AU AU2003217274A patent/AU2003217274A1/en not_active Abandoned
- 2003-02-13 DE DE60315603T patent/DE60315603T2/de not_active Expired - Fee Related
- 2003-02-13 EP EP03713316A patent/EP1480640B1/en not_active Expired - Lifetime
- 2003-02-13 WO PCT/US2003/002679 patent/WO2003072100A1/en not_active Ceased
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2009526867A (ja) * | 2006-02-15 | 2009-07-23 | アボット・ラボラトリーズ | 新規なアセチル−CoAカルボキシラーゼ(ACC)阻害薬およびそれらの糖尿病、肥満および代謝症候群での使用 |
| JP2010511604A (ja) * | 2006-12-02 | 2010-04-15 | ソウル ナショナル ユニバーシティー インダストリー ファンデーション | ペルオキシソーム増殖因子活性化受容体リガンドアリール化合物及びこれらの化合物の用途 |
| JP2010515724A (ja) * | 2007-01-08 | 2010-05-13 | ソウル ナショナル ユニバーシティー インダストリー ファンデーション | ペルオキシソーム増殖因子活性化受容体δリガンドチアゾール化合物及びこれを含有する医薬、化粧品及び健康食品組成物 |
Also Published As
| Publication number | Publication date |
|---|---|
| DE60315603D1 (de) | 2007-09-27 |
| US7153878B2 (en) | 2006-12-26 |
| DE60315603T2 (de) | 2008-05-21 |
| EP1480640B1 (en) | 2007-08-15 |
| US20050107449A1 (en) | 2005-05-19 |
| ES2290439T3 (es) | 2008-02-16 |
| ATE369855T1 (de) | 2007-09-15 |
| EP1480640A1 (en) | 2004-12-01 |
| WO2003072100A1 (en) | 2003-09-04 |
| AU2003217274A1 (en) | 2003-09-09 |
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