KR20090038469A - 치환된 이미다졸론 유도체, 그 제조 및 용도 - Google Patents
치환된 이미다졸론 유도체, 그 제조 및 용도 Download PDFInfo
- Publication number
- KR20090038469A KR20090038469A KR1020097003832A KR20097003832A KR20090038469A KR 20090038469 A KR20090038469 A KR 20090038469A KR 1020097003832 A KR1020097003832 A KR 1020097003832A KR 20097003832 A KR20097003832 A KR 20097003832A KR 20090038469 A KR20090038469 A KR 20090038469A
- Authority
- KR
- South Korea
- Prior art keywords
- methyl
- butyl
- oxy
- carboxy
- group
- 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.)
- Withdrawn
Links
- 0 Cc1c(*N(C(*)=NC2(*)*)C2=*)[s]c2nc(-c3c(*)c(*)c(*)c(*)c3*)n[n]12 Chemical compound Cc1c(*N(C(*)=NC2(*)*)C2=*)[s]c2nc(-c3c(*)c(*)c(*)c(*)c3*)n[n]12 0.000 description 2
- HXNYVMIBYDXJRO-UHFFFAOYSA-N CC(C)(C)OC(C(C)(C)Oc(cc1)ccc1Sc1ccc(C)cc1)=O Chemical compound CC(C)(C)OC(C(C)(C)Oc(cc1)ccc1Sc1ccc(C)cc1)=O HXNYVMIBYDXJRO-UHFFFAOYSA-N 0.000 description 1
- PUZMHYOSEFMDHY-UHFFFAOYSA-N CC(C)(C)OC(C(C)(C)Oc1cccc(-c2ccc(CN(C(Cc3c[s]cc3)=NC34CCCC3)C4=O)cc2)c1)=O Chemical compound CC(C)(C)OC(C(C)(C)Oc1cccc(-c2ccc(CN(C(Cc3c[s]cc3)=NC34CCCC3)C4=O)cc2)c1)=O PUZMHYOSEFMDHY-UHFFFAOYSA-N 0.000 description 1
- OEPOIGMABNTJKW-UHFFFAOYSA-N CC(N1)=NC2(CCCC2)C1=O Chemical compound CC(N1)=NC2(CCCC2)C1=O OEPOIGMABNTJKW-UHFFFAOYSA-N 0.000 description 1
- LCASQUYYHKHPMV-UHFFFAOYSA-N CCC(N1Cc(cc2)ccc2-c2cc(OC(C)(C)C(OC(C)(C)C)=O)ccc2)=NC2(CCCC2)C1=O Chemical compound CCC(N1Cc(cc2)ccc2-c2cc(OC(C)(C)C(OC(C)(C)C)=O)ccc2)=NC2(CCCC2)C1=O LCASQUYYHKHPMV-UHFFFAOYSA-N 0.000 description 1
- JHFVSGIMLDFLIC-UHFFFAOYSA-N CCC(c(c(Br)c1)ccc1OC)=O Chemical compound CCC(c(c(Br)c1)ccc1OC)=O JHFVSGIMLDFLIC-UHFFFAOYSA-N 0.000 description 1
- BHCGDEJUEYWMDO-UHFFFAOYSA-N CCC(c(c(OC)c1)ccc1Br)=O Chemical compound CCC(c(c(OC)c1)ccc1Br)=O BHCGDEJUEYWMDO-UHFFFAOYSA-N 0.000 description 1
- IDVXNUXAPPJJTR-UHFFFAOYSA-N CCCC(N1Cc(cc2)ccc2-c2cc(OC(C)(C)C(O)=O)ccc2)=NC2(CCCC2)C1=O Chemical compound CCCC(N1Cc(cc2)ccc2-c2cc(OC(C)(C)C(O)=O)ccc2)=NC2(CCCC2)C1=O IDVXNUXAPPJJTR-UHFFFAOYSA-N 0.000 description 1
- XUDWUUVCXPXBDZ-UHFFFAOYSA-N CCCCC(N1CCc(cc2)ccc2OC(C)(C)C(O)=O)=NC2(CCCC2)C1=O Chemical compound CCCCC(N1CCc(cc2)ccc2OC(C)(C)C(O)=O)=NC2(CCCC2)C1=O XUDWUUVCXPXBDZ-UHFFFAOYSA-N 0.000 description 1
- HPBNEAJLAGYDAH-UHFFFAOYSA-N CCCCC(N1Cc(c(C)c2)ccc2Br)=NC2(CCCC2)C1=O Chemical compound CCCCC(N1Cc(c(C)c2)ccc2Br)=NC2(CCCC2)C1=O HPBNEAJLAGYDAH-UHFFFAOYSA-N 0.000 description 1
- NHWHURLIPBVSRI-UHFFFAOYSA-N CCCCC(N1Cc(cc2)cc(C)c2Br)=NC2(CCCCC2)C1=O Chemical compound CCCCC(N1Cc(cc2)cc(C)c2Br)=NC2(CCCCC2)C1=O NHWHURLIPBVSRI-UHFFFAOYSA-N 0.000 description 1
- JEVZPQLQHPRNJE-UHFFFAOYSA-N CCCCC(N1Cc(cc2)ccc2-c(cc(cc2)OC)c2F)=NC2(CCCCC2)C1=O Chemical compound CCCCC(N1Cc(cc2)ccc2-c(cc(cc2)OC)c2F)=NC2(CCCCC2)C1=O JEVZPQLQHPRNJE-UHFFFAOYSA-N 0.000 description 1
- GRTIVSXMYFPCGX-UHFFFAOYSA-N CCCCC(N1Cc(cc2)ccc2-c(cc2)ccc2OCCCC(C)(C)C(OC)=O)=NC2(CCCCC2)C1=O Chemical compound CCCCC(N1Cc(cc2)ccc2-c(cc2)ccc2OCCCC(C)(C)C(OC)=O)=NC2(CCCCC2)C1=O GRTIVSXMYFPCGX-UHFFFAOYSA-N 0.000 description 1
- DJZYZCCLFGJEPV-UHFFFAOYSA-N CCCCC(N1Cc(cc2)ccc2-c(cc2O)ccc2[N+]([O-])=O)=NC2(CCCC2)C1=O Chemical compound CCCCC(N1Cc(cc2)ccc2-c(cc2O)ccc2[N+]([O-])=O)=NC2(CCCC2)C1=O DJZYZCCLFGJEPV-UHFFFAOYSA-N 0.000 description 1
- OTWIJPRENJUXJB-UHFFFAOYSA-N CCCCC(N1Cc(cc2)ccc2-c(cc2OC(C)(C)C(O)=O)ccc2OC)=NC2(CCCC2)C1=O Chemical compound CCCCC(N1Cc(cc2)ccc2-c(cc2OC(C)(C)C(O)=O)ccc2OC)=NC2(CCCC2)C1=O OTWIJPRENJUXJB-UHFFFAOYSA-N 0.000 description 1
- LMXZZZUUAASKAG-UHFFFAOYSA-N CCCCC(N1Cc(cc2)ccc2-c2c(CCC)ccc(OC(CC)C(OCC)=O)c2)=NC2(CCCC2)C1=O Chemical compound CCCCC(N1Cc(cc2)ccc2-c2c(CCC)ccc(OC(CC)C(OCC)=O)c2)=NC2(CCCC2)C1=O LMXZZZUUAASKAG-UHFFFAOYSA-N 0.000 description 1
- RWHKAYAPQGALNB-UHFFFAOYSA-N CCCCC(N1Cc(cc2)ccc2-c2cc(O)ccc2CC)=NC2(CCCC2)C1=O Chemical compound CCCCC(N1Cc(cc2)ccc2-c2cc(O)ccc2CC)=NC2(CCCC2)C1=O RWHKAYAPQGALNB-UHFFFAOYSA-N 0.000 description 1
- XDBNSFOFHFDPRP-UHFFFAOYSA-N CCCCC(N1Cc(cc2)ccc2-c2cc(OC(C(C)C)C(O)=O)ccc2)=NC2(CCCCC2)C1=O Chemical compound CCCCC(N1Cc(cc2)ccc2-c2cc(OC(C(C)C)C(O)=O)ccc2)=NC2(CCCCC2)C1=O XDBNSFOFHFDPRP-UHFFFAOYSA-N 0.000 description 1
- IKUNSMNCQHNAPQ-UHFFFAOYSA-N CCCCC(N1Cc(cc2)ccc2-c2cc(OC(C(C)C)C(O)=O)ccc2CCC)=NC2(CCCC2)C1=O Chemical compound CCCCC(N1Cc(cc2)ccc2-c2cc(OC(C(C)C)C(O)=O)ccc2CCC)=NC2(CCCC2)C1=O IKUNSMNCQHNAPQ-UHFFFAOYSA-N 0.000 description 1
- HQRGONLIDOUAKK-UHFFFAOYSA-N CCCCC(N1Cc(cc2)ccc2-c2cc(OC(C)(C)C(O)=O)ccc2)=NC2(CCCC2)C1=O Chemical compound CCCCC(N1Cc(cc2)ccc2-c2cc(OC(C)(C)C(O)=O)ccc2)=NC2(CCCC2)C1=O HQRGONLIDOUAKK-UHFFFAOYSA-N 0.000 description 1
- CJNBWFTZPRWHTQ-UHFFFAOYSA-N CCCCC(N1Cc(cc2)ccc2-c2cc(OC(C)C(O)=O)ccc2)=NC2(CCCCC2)C1=O Chemical compound CCCCC(N1Cc(cc2)ccc2-c2cc(OC(C)C(O)=O)ccc2)=NC2(CCCCC2)C1=O CJNBWFTZPRWHTQ-UHFFFAOYSA-N 0.000 description 1
- MSRJPTCMERGCCU-UHFFFAOYSA-N CCCCC(N1Cc(cc2)ccc2-c2cc(OCC#N)ccc2)=NC2(CCCCC2)C1=O Chemical compound CCCCC(N1Cc(cc2)ccc2-c2cc(OCC#N)ccc2)=NC2(CCCCC2)C1=O MSRJPTCMERGCCU-UHFFFAOYSA-N 0.000 description 1
- CKGBUHAZFDSXTO-UHFFFAOYSA-N CCCCC(N1Cc(cc2)ccc2-c2ccc(CC(C)C)c(OC(C)(C)C(O)=O)c2)=NC2(CCCC2)C1=O Chemical compound CCCCC(N1Cc(cc2)ccc2-c2ccc(CC(C)C)c(OC(C)(C)C(O)=O)c2)=NC2(CCCC2)C1=O CKGBUHAZFDSXTO-UHFFFAOYSA-N 0.000 description 1
- BHYHGGPQZMGPRP-UHFFFAOYSA-N CCCCC(N1Cc(cc2)ccc2-c2ccc(CCC)c(O)c2)=NC2(CCCC2)C1=O Chemical compound CCCCC(N1Cc(cc2)ccc2-c2ccc(CCC)c(O)c2)=NC2(CCCC2)C1=O BHYHGGPQZMGPRP-UHFFFAOYSA-N 0.000 description 1
- IAFYTMFOMZQQMU-UHFFFAOYSA-N CCCCC(N1Cc(cc2)ccc2-c2cccc(OC3(CCC3)C(OCC)=O)c2)=NC2(CCCCC2)C1=O Chemical compound CCCCC(N1Cc(cc2)ccc2-c2cccc(OC3(CCC3)C(OCC)=O)c2)=NC2(CCCCC2)C1=O IAFYTMFOMZQQMU-UHFFFAOYSA-N 0.000 description 1
- PYNONTNKCWKCMN-UHFFFAOYSA-N CCCCC(N1Cc(cc2)ccc2C(c2cc(OC(C)(C)C(O)=O)ccc2)=O)=NC(C)(C)C1=O Chemical compound CCCCC(N1Cc(cc2)ccc2C(c2cc(OC(C)(C)C(O)=O)ccc2)=O)=NC(C)(C)C1=O PYNONTNKCWKCMN-UHFFFAOYSA-N 0.000 description 1
- FLHVXUIGONLENR-UHFFFAOYSA-N CCCCC(N1Cc(cc2)ccc2Oc2cccc(OC(C)(C)C(OC(C)(C)C)=O)c2)=NC2(CCCC2)C1=O Chemical compound CCCCC(N1Cc(cc2)ccc2Oc2cccc(OC(C)(C)C(OC(C)(C)C)=O)c2)=NC2(CCCC2)C1=O FLHVXUIGONLENR-UHFFFAOYSA-N 0.000 description 1
- OTTMZVYFBLMCMP-UHFFFAOYSA-N CCCCC(N1Cc(cc2)ccc2Sc2cccc(OC(C)(C)C(O)=O)c2)=NC2(CCCC2)C1=O Chemical compound CCCCC(N1Cc(cc2)ccc2Sc2cccc(OC(C)(C)C(O)=O)c2)=NC2(CCCC2)C1=O OTTMZVYFBLMCMP-UHFFFAOYSA-N 0.000 description 1
- GZTBNFSPMVOYCC-UHFFFAOYSA-N CCCCC(N1Cc2c(C)[n]3nc(-c(cc4)ccc4OC(C)(C)C(O)=O)nc3[s]2)=NC2(CCCC2)C1=O Chemical compound CCCCC(N1Cc2c(C)[n]3nc(-c(cc4)ccc4OC(C)(C)C(O)=O)nc3[s]2)=NC2(CCCC2)C1=O GZTBNFSPMVOYCC-UHFFFAOYSA-N 0.000 description 1
- DKRVMYBLHYMGNV-UHFFFAOYSA-N CCCCC(N1Cc2c(C)[n]3nc(-c4cc(OC(C)(C)C(OCC)=O)ccc4)nc3[s]2)=NC2(CCCC2)C1=O Chemical compound CCCCC(N1Cc2c(C)[n]3nc(-c4cc(OC(C)(C)C(OCC)=O)ccc4)nc3[s]2)=NC2(CCCC2)C1=O DKRVMYBLHYMGNV-UHFFFAOYSA-N 0.000 description 1
- MSUBAXVPYWQPRJ-UHFFFAOYSA-N CCCCC(N1Cc2cccc(-c(cc3)ccc3OC(C)(C)C(OCC)=O)c2)=NC2(CCCC2)C1=O Chemical compound CCCCC(N1Cc2cccc(-c(cc3)ccc3OC(C)(C)C(OCC)=O)c2)=NC2(CCCC2)C1=O MSUBAXVPYWQPRJ-UHFFFAOYSA-N 0.000 description 1
- YKSUEQRNXOAPPK-UHFFFAOYSA-N CCCCC(OCC)=N Chemical compound CCCCC(OCC)=N YKSUEQRNXOAPPK-UHFFFAOYSA-N 0.000 description 1
- FCPMMNRJYVFKBX-YMNIQAILSA-N CCC[C@H](C)C(N1)=NC2(C[IH]CC2)C1=O Chemical compound CCC[C@H](C)C(N1)=NC2(C[IH]CC2)C1=O FCPMMNRJYVFKBX-YMNIQAILSA-N 0.000 description 1
- FOGZQGMFFNTURS-UHFFFAOYSA-N CCOC(C(C)(C)Oc(cccc1)c1Br)=O Chemical compound CCOC(C(C)(C)Oc(cccc1)c1Br)=O FOGZQGMFFNTURS-UHFFFAOYSA-N 0.000 description 1
- ZGNKVLNPAFWDIC-UHFFFAOYSA-N COc1cc(Br)ccc1CBr Chemical compound COc1cc(Br)ccc1CBr ZGNKVLNPAFWDIC-UHFFFAOYSA-N 0.000 description 1
- MVHUQKVDGXYQRW-UHFFFAOYSA-N O=C1NC(Cc2c[s]cc2)=NC11CCCC1 Chemical compound O=C1NC(Cc2c[s]cc2)=NC11CCCC1 MVHUQKVDGXYQRW-UHFFFAOYSA-N 0.000 description 1
Images
Classifications
-
- 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
-
- 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
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/4164—1,3-Diazoles
- A61K31/4166—1,3-Diazoles having oxo groups directly attached to the heterocyclic ring, e.g. phenytoin
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/28—Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
-
- 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
-
- 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
- A61P3/04—Anorexiants; Antiobesity agents
-
- 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
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/08—Drugs for disorders of the metabolism for glucose homeostasis
-
- 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
- A61P35/00—Antineoplastic 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
- A61P7/00—Drugs for disorders of the blood or the extracellular fluid
-
- 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
-
- 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
-
- 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
- A61P9/12—Antihypertensives
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
- C07D233/54—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
- C07D233/66—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two 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
- C07D233/70—One oxygen atom
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D235/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings
- C07D235/02—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings condensed with carbocyclic rings or ring systems
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Medicinal Chemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Diabetes (AREA)
- Hematology (AREA)
- Obesity (AREA)
- Neurosurgery (AREA)
- Biomedical Technology (AREA)
- Cardiology (AREA)
- Heart & Thoracic Surgery (AREA)
- Neurology (AREA)
- Emergency Medicine (AREA)
- Endocrinology (AREA)
- Vascular Medicine (AREA)
- Child & Adolescent Psychology (AREA)
- Urology & Nephrology (AREA)
- Hospice & Palliative Care (AREA)
- Psychiatry (AREA)
- Pain & Pain Management (AREA)
- Rheumatology (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Plural Heterocyclic Compounds (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR0606752A FR2903984B1 (fr) | 2006-07-24 | 2006-07-24 | Derives d'imidazolones substitues, preparation et utilisations |
| FR0606752 | 2006-07-24 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| KR20090038469A true KR20090038469A (ko) | 2009-04-20 |
Family
ID=37843186
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| KR1020097003832A Withdrawn KR20090038469A (ko) | 2006-07-24 | 2007-07-24 | 치환된 이미다졸론 유도체, 그 제조 및 용도 |
Country Status (16)
| Country | Link |
|---|---|
| US (1) | US20100004159A1 (https=) |
| EP (1) | EP2049107A2 (https=) |
| JP (1) | JP2009544675A (https=) |
| KR (1) | KR20090038469A (https=) |
| CN (1) | CN101522192A (https=) |
| AU (1) | AU2007279135A1 (https=) |
| BR (1) | BRPI0715326A2 (https=) |
| CA (1) | CA2658625A1 (https=) |
| EA (1) | EA200900211A1 (https=) |
| FR (1) | FR2903984B1 (https=) |
| IL (1) | IL196671A0 (https=) |
| MX (1) | MX2009000900A (https=) |
| NO (1) | NO20090348L (https=) |
| NZ (1) | NZ575011A (https=) |
| WO (1) | WO2008012470A2 (https=) |
| ZA (1) | ZA200901268B (https=) |
Families Citing this family (20)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP2025674A1 (de) | 2007-08-15 | 2009-02-18 | sanofi-aventis | Substituierte Tetrahydronaphthaline, Verfahren zu ihrer Herstellung und ihre Verwendung als Arzneimittel |
| WO2011107494A1 (de) | 2010-03-03 | 2011-09-09 | Sanofi | Neue aromatische glykosidderivate, diese verbindungen enthaltende arzneimittel und deren verwendung |
| EP2552209A4 (en) * | 2010-03-26 | 2014-01-22 | Merck Sharp & Dohme | NEW SPIROIMIDAZOLON DERIVATIVES AS GLUCAGON RECEPTOR ANTAGONISTS, COMPOSITIONS AND METHOD FOR THEIR USE |
| WO2011157827A1 (de) | 2010-06-18 | 2011-12-22 | Sanofi | Azolopyridin-3-on-derivate als inhibitoren von lipasen und phospholipasen |
| US8530413B2 (en) | 2010-06-21 | 2013-09-10 | Sanofi | Heterocyclically substituted methoxyphenyl derivatives with an oxo group, processes for preparation thereof and use thereof as medicaments |
| TW201215388A (en) | 2010-07-05 | 2012-04-16 | Sanofi Sa | (2-aryloxyacetylamino)phenylpropionic acid derivatives, processes for preparation thereof and use thereof as medicaments |
| TW201221505A (en) | 2010-07-05 | 2012-06-01 | Sanofi Sa | Aryloxyalkylene-substituted hydroxyphenylhexynoic acids, process for preparation thereof and use thereof as a medicament |
| TW201215387A (en) | 2010-07-05 | 2012-04-16 | Sanofi Aventis | Spirocyclically substituted 1,3-propane dioxide derivatives, processes for preparation thereof and use thereof as a medicament |
| US8633231B2 (en) | 2010-07-13 | 2014-01-21 | Merck Sharp & Dohme Corp. | Substituted imidazolones, compositions containing such compounds and methods of use |
| WO2013037390A1 (en) | 2011-09-12 | 2013-03-21 | Sanofi | 6-(4-hydroxy-phenyl)-3-styryl-1h-pyrazolo[3,4-b]pyridine-4-carboxylic acid amide derivatives as kinase inhibitors |
| EP2760862B1 (en) | 2011-09-27 | 2015-10-21 | Sanofi | 6-(4-hydroxy-phenyl)-3-alkyl-1h-pyrazolo[3,4-b]pyridine-4-carboxylic acid amide derivatives as kinase inhibitors |
| WO2014209034A1 (en) * | 2013-06-27 | 2014-12-31 | Lg Life Sciences Ltd. | Biaryl derivatives as gpr120 agonists |
| WO2015095011A1 (en) | 2013-12-17 | 2015-06-25 | Janssen Pharmaceutica Nv | Imidazolin-5-one derivative useful as fasn inhibitors for the treatment of cancer |
| CN105439946B (zh) * | 2014-08-13 | 2018-02-02 | 益方生物科技(上海)有限公司 | 羧酸化合物及其制备方法和用途 |
| CN104177298B (zh) * | 2014-09-18 | 2018-10-02 | 湘潭大学 | 4,4-二取代-4,5-二氢-1h–咪唑-5-酮、衍生物及其合成方法 |
| MX386470B (es) | 2015-07-17 | 2025-03-18 | Pasteur Institut | Agente estimulador del receptor 5-hidroxi triptamina 1b para usarse como un promotor de la autorrenovación y/o diferenciación de células satélite. |
| JP2018526411A (ja) * | 2015-09-11 | 2018-09-13 | ラクオリア創薬株式会社 | Trpm8拮抗剤としてのイミダゾリノン誘導体 |
| EP3795563B1 (en) | 2016-03-31 | 2024-07-17 | Oncternal Therapeutics, Inc. | Indoline analogs and uses thereof |
| BR112019000706A8 (pt) | 2016-07-15 | 2022-12-06 | Pasteur Institut | Agente de estímulo do receptor 1b de 5-hidroxitriptamina para reparo de pele e/ou cabelo |
| CN113121394B (zh) * | 2019-12-30 | 2022-11-08 | 中国药科大学 | 一种苯氧乙酸类衍生物的制备方法 |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7544812B2 (en) * | 2001-11-30 | 2009-06-09 | Eli Lilly And Company | Peroxisome proliferator activated receptor agonists |
| US7232828B2 (en) * | 2002-08-10 | 2007-06-19 | Bethesda Pharmaceuticals, Inc. | PPAR Ligands that do not cause fluid retention, edema or congestive heart failure |
| WO2004082621A2 (en) * | 2003-03-15 | 2004-09-30 | Bethesda Pharmaceuticals, Inc. | Novel ppar agonists, pharmaceutical compositions and uses thereof |
-
2006
- 2006-07-24 FR FR0606752A patent/FR2903984B1/fr not_active Expired - Fee Related
-
2007
- 2007-07-24 EA EA200900211A patent/EA200900211A1/ru unknown
- 2007-07-24 WO PCT/FR2007/051716 patent/WO2008012470A2/fr not_active Ceased
- 2007-07-24 NZ NZ575011A patent/NZ575011A/en not_active IP Right Cessation
- 2007-07-24 US US12/309,642 patent/US20100004159A1/en not_active Abandoned
- 2007-07-24 BR BRPI0715326-0A patent/BRPI0715326A2/pt not_active IP Right Cessation
- 2007-07-24 CA CA002658625A patent/CA2658625A1/fr not_active Abandoned
- 2007-07-24 AU AU2007279135A patent/AU2007279135A1/en not_active Abandoned
- 2007-07-24 KR KR1020097003832A patent/KR20090038469A/ko not_active Withdrawn
- 2007-07-24 JP JP2009521318A patent/JP2009544675A/ja active Pending
- 2007-07-24 MX MX2009000900A patent/MX2009000900A/es active IP Right Grant
- 2007-07-24 EP EP07823633A patent/EP2049107A2/fr not_active Withdrawn
- 2007-07-24 CN CNA2007800352070A patent/CN101522192A/zh active Pending
-
2009
- 2009-01-22 NO NO20090348A patent/NO20090348L/no not_active Application Discontinuation
- 2009-01-22 IL IL196671A patent/IL196671A0/en unknown
- 2009-02-23 ZA ZA200901268A patent/ZA200901268B/xx unknown
Also Published As
| Publication number | Publication date |
|---|---|
| FR2903984A1 (fr) | 2008-01-25 |
| MX2009000900A (es) | 2009-06-18 |
| AU2007279135A1 (en) | 2008-01-31 |
| JP2009544675A (ja) | 2009-12-17 |
| NZ575011A (en) | 2011-12-22 |
| WO2008012470A3 (fr) | 2008-03-20 |
| CN101522192A (zh) | 2009-09-02 |
| NO20090348L (no) | 2009-04-24 |
| WO2008012470A2 (fr) | 2008-01-31 |
| CA2658625A1 (fr) | 2008-01-31 |
| IL196671A0 (en) | 2009-11-18 |
| ZA200901268B (en) | 2010-04-28 |
| BRPI0715326A2 (pt) | 2013-08-13 |
| EA200900211A1 (ru) | 2009-06-30 |
| US20100004159A1 (en) | 2010-01-07 |
| FR2903984B1 (fr) | 2008-10-03 |
| EP2049107A2 (fr) | 2009-04-22 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| KR20090038469A (ko) | 치환된 이미다졸론 유도체, 그 제조 및 용도 | |
| KR101416262B1 (ko) | 치환된 1, 3-디페닐프로판 유도체, 그 제조 및 용도 | |
| ES2423793T3 (es) | Compuestos agonistas de PPAR, preparación y usos para el tratamiento de la diabetes y/o dislipidemias | |
| CN101605775B (zh) | 取代的3-苯基-1-(苯基噻吩基)丙-1-酮类以及3-苯基-1-(苯基呋喃基)丙-1-酮类的衍生物、制备以及用途 | |
| PL176250B1 (pl) | Sposób wytwarzania pochodnych indanu | |
| WO1997017317A1 (en) | 4-phenyl-4-oxo-butanoic acid derivatives with kynurenine-3-hydroxylase inhibiting activity | |
| SK282979B6 (sk) | Benzopyránové deriváty, spôsob ich prípravy a ich použitie | |
| JP5258761B2 (ja) | Cox−2阻害剤としてのフェニル酢酸誘導体 | |
| WO1995032175A1 (en) | Di-tert-butylphenol compounds useful as anti-inflammatory agents | |
| US7491728B2 (en) | Pyrimidinone compounds as calcilytics | |
| Rather et al. | Synthesis and Evaluation of Novel 2‐Substituted‐quinazolin‐4 (3H)‐ones as Potent Analgesic and Anti‐inflammatory Agents | |
| Class et al. | Patent application title: SUBSTITUTED IMIDAZOLONE DERIVATIVES, PREPARATIONS AND USES Inventors: Edith Bouey (Lorgies, FR) Christophe Masson (Lambersart, FR) Karine Bertrand (Frelinghien, FR) Assignees: GENFIT | |
| EP0629604A2 (en) | Alicyclic phospholipase A2 inhibitors | |
| Baccus et al. | Synthesis of fatty acid binding protein inhibitors: a new approach for diabetes treatment |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PA0105 | International application |
Patent event date: 20090224 Patent event code: PA01051R01D Comment text: International Patent Application |
|
| PG1501 | Laying open of application | ||
| PC1203 | Withdrawal of no request for examination | ||
| WITN | Application deemed withdrawn, e.g. because no request for examination was filed or no examination fee was paid |