JP2005521741A5 - - Google Patents
Download PDFInfo
- Publication number
- JP2005521741A5 JP2005521741A5 JP2003582115A JP2003582115A JP2005521741A5 JP 2005521741 A5 JP2005521741 A5 JP 2005521741A5 JP 2003582115 A JP2003582115 A JP 2003582115A JP 2003582115 A JP2003582115 A JP 2003582115A JP 2005521741 A5 JP2005521741 A5 JP 2005521741A5
- Authority
- JP
- Japan
- Prior art keywords
- alkyl
- aryl
- hydrogen
- acetic acid
- methoxy
- 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.)
- Granted
Links
- 125000000217 alkyl group Chemical group 0.000 claims 41
- 125000003118 aryl group Chemical group 0.000 claims 24
- 229910052739 hydrogen Inorganic materials 0.000 claims 23
- 239000001257 hydrogen Substances 0.000 claims 23
- 150000002431 hydrogen Chemical class 0.000 claims 18
- 150000001875 compounds Chemical class 0.000 claims 15
- 125000003545 alkoxy group Chemical group 0.000 claims 12
- 229910052736 halogen Inorganic materials 0.000 claims 10
- 150000002367 halogens Chemical class 0.000 claims 10
- 125000003342 alkenyl group Chemical group 0.000 claims 9
- 125000000304 alkynyl group Chemical group 0.000 claims 9
- 125000004093 cyano group Chemical group *C#N 0.000 claims 9
- 125000001188 haloalkyl group Chemical group 0.000 claims 9
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims 9
- 125000004429 atom Chemical group 0.000 claims 6
- 125000005842 heteroatom Chemical group 0.000 claims 6
- 239000008194 pharmaceutical composition Substances 0.000 claims 6
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 5
- 241000124008 Mammalia Species 0.000 claims 5
- 125000000753 cycloalkyl group Chemical group 0.000 claims 5
- 239000000203 mixture Substances 0.000 claims 5
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 4
- 150000003839 salts Chemical class 0.000 claims 4
- ZMZDMBWJUHKJPS-UHFFFAOYSA-M Thiocyanate anion Chemical compound [S-]C#N ZMZDMBWJUHKJPS-UHFFFAOYSA-M 0.000 claims 3
- 125000001183 hydrocarbyl group Chemical group 0.000 claims 3
- 238000004519 manufacturing process Methods 0.000 claims 3
- 229910052760 oxygen Inorganic materials 0.000 claims 3
- 229920006395 saturated elastomer Polymers 0.000 claims 3
- 125000003107 substituted aryl group Chemical group 0.000 claims 3
- 229910052717 sulfur Inorganic materials 0.000 claims 3
- 125000001054 5 membered carbocyclic group Chemical group 0.000 claims 2
- -1 5-trifluoromethyl - pyridin-2-yl Chemical group 0.000 claims 2
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Natural products CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 claims 2
- 239000004215 Carbon black (E152) Substances 0.000 claims 2
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 claims 2
- 230000002152 alkylating effect Effects 0.000 claims 2
- 125000004432 carbon atom Chemical group C* 0.000 claims 2
- 125000001072 heteroaryl group Chemical group 0.000 claims 2
- 229930195733 hydrocarbon Natural products 0.000 claims 2
- 150000002430 hydrocarbons Chemical class 0.000 claims 2
- ZMZDMBWJUHKJPS-UHFFFAOYSA-N hydrogen thiocyanate Natural products SC#N ZMZDMBWJUHKJPS-UHFFFAOYSA-N 0.000 claims 2
- 150000003573 thiols Chemical class 0.000 claims 2
- VFQRJNOXLNYYTE-UHFFFAOYSA-N 2-[3-methoxy-4-[[4-[4-(trifluoromethyl)phenyl]phenyl]methylsulfanyl]phenoxy]acetic acid Chemical compound COC1=CC(OCC(O)=O)=CC=C1SCC1=CC=C(C=2C=CC(=CC=2)C(F)(F)F)C=C1 VFQRJNOXLNYYTE-UHFFFAOYSA-N 0.000 claims 1
- QZCOZWYSOAUBJR-UHFFFAOYSA-N 2-[4-[[4-(2,4-dichlorophenyl)phenyl]methylsulfanyl]-5-methoxy-2-methylphenoxy]acetic acid Chemical compound COC1=CC(OCC(O)=O)=C(C)C=C1SCC1=CC=C(C=2C(=CC(Cl)=CC=2)Cl)C=C1 QZCOZWYSOAUBJR-UHFFFAOYSA-N 0.000 claims 1
- UXBLXTMVLIEOGI-UHFFFAOYSA-N 2-[4-[[4-(4-fluorophenyl)phenyl]methylsulfanyl]-5-methoxy-2-methylphenoxy]acetic acid Chemical compound COC1=CC(OCC(O)=O)=C(C)C=C1SCC1=CC=C(C=2C=CC(F)=CC=2)C=C1 UXBLXTMVLIEOGI-UHFFFAOYSA-N 0.000 claims 1
- QPQVDUHBPMLTTD-UHFFFAOYSA-N 2-[4-[[4-[2-(3-fluorophenyl)ethenyl]phenyl]methylsulfanyl]-5-methoxy-2-methylphenoxy]acetic acid Chemical compound COC1=CC(OCC(O)=O)=C(C)C=C1SCC(C=C1)=CC=C1C=CC1=CC=CC(F)=C1 QPQVDUHBPMLTTD-UHFFFAOYSA-N 0.000 claims 1
- JLQGDIDQGNXZJJ-UHFFFAOYSA-N 2-[4-[[5-(4-chlorophenyl)-1,2-oxazol-3-yl]methylsulfanyl]-5-methoxy-2-methylphenoxy]acetic acid Chemical compound COC1=CC(OCC(O)=O)=C(C)C=C1SCC1=NOC(C=2C=CC(Cl)=CC=2)=C1 JLQGDIDQGNXZJJ-UHFFFAOYSA-N 0.000 claims 1
- COOMMSHFMOKEKM-UHFFFAOYSA-N 2-[5-methoxy-2-methyl-4-[(4-phenylphenyl)methylsulfanyl]phenoxy]acetic acid Chemical compound COC1=CC(OCC(O)=O)=C(C)C=C1SCC1=CC=C(C=2C=CC=CC=2)C=C1 COOMMSHFMOKEKM-UHFFFAOYSA-N 0.000 claims 1
- AJQNSRYZFLLBOI-UHFFFAOYSA-N 2-[5-methoxy-2-methyl-4-[2-[4-[4-(trifluoromethyl)phenyl]phenyl]ethylsulfanyl]phenoxy]acetic acid Chemical compound COC1=CC(OCC(O)=O)=C(C)C=C1SCCC1=CC=C(C=2C=CC(=CC=2)C(F)(F)F)C=C1 AJQNSRYZFLLBOI-UHFFFAOYSA-N 0.000 claims 1
- HXCKESKWJSVFAR-UHFFFAOYSA-N 2-[5-methoxy-2-methyl-4-[[2-methyl-4-[4-(trifluoromethyl)phenyl]phenyl]methylsulfanyl]phenoxy]acetic acid Chemical compound COC1=CC(OCC(O)=O)=C(C)C=C1SCC1=CC=C(C=2C=CC(=CC=2)C(F)(F)F)C=C1C HXCKESKWJSVFAR-UHFFFAOYSA-N 0.000 claims 1
- VVUWGDAIOYKXPE-UHFFFAOYSA-N 2-[5-methoxy-2-methyl-4-[[3-[3-(trifluoromethoxy)phenyl]phenyl]methylsulfanyl]phenoxy]acetic acid Chemical compound COC1=CC(OCC(O)=O)=C(C)C=C1SCC1=CC=CC(C=2C=C(OC(F)(F)F)C=CC=2)=C1 VVUWGDAIOYKXPE-UHFFFAOYSA-N 0.000 claims 1
- GSPKTIOMMLSIHT-UHFFFAOYSA-N 2-[5-methoxy-2-methyl-4-[[3-[4-(trifluoromethyl)phenyl]-1,2-oxazol-5-yl]methylsulfanyl]phenoxy]acetic acid Chemical compound COC1=CC(OCC(O)=O)=C(C)C=C1SCC1=CC(C=2C=CC(=CC=2)C(F)(F)F)=NO1 GSPKTIOMMLSIHT-UHFFFAOYSA-N 0.000 claims 1
- MANTXHYUNLPBHE-UHFFFAOYSA-N 2-[5-methoxy-2-methyl-4-[[3-[4-(trifluoromethyl)phenyl]phenyl]methylsulfanyl]phenoxy]acetic acid Chemical compound COC1=CC(OCC(O)=O)=C(C)C=C1SCC1=CC=CC(C=2C=CC(=CC=2)C(F)(F)F)=C1 MANTXHYUNLPBHE-UHFFFAOYSA-N 0.000 claims 1
- WPLMYOVJSNXPMK-UHFFFAOYSA-N 2-[5-methoxy-2-methyl-4-[[4-[3-(trifluoromethyl)phenyl]phenyl]methylsulfanyl]phenoxy]acetic acid Chemical compound COC1=CC(OCC(O)=O)=C(C)C=C1SCC1=CC=C(C=2C=C(C=CC=2)C(F)(F)F)C=C1 WPLMYOVJSNXPMK-UHFFFAOYSA-N 0.000 claims 1
- YBYRUZQLTYRCRF-UHFFFAOYSA-N 2-[5-methoxy-2-methyl-4-[[4-[4-(trifluoromethyl)phenyl]phenyl]methylsulfanyl]phenoxy]acetic acid Chemical compound COC1=CC(OCC(O)=O)=C(C)C=C1SCC1=CC=C(C=2C=CC(=CC=2)C(F)(F)F)C=C1 YBYRUZQLTYRCRF-UHFFFAOYSA-N 0.000 claims 1
- NWEHHVVXCHVPFQ-UHFFFAOYSA-N 2-[5-methoxy-2-methyl-4-[[4-[5-(trifluoromethyl)pyridin-2-yl]phenyl]methylsulfanyl]phenoxy]acetic acid Chemical compound COC1=CC(OCC(O)=O)=C(C)C=C1SCC1=CC=C(C=2N=CC(=CC=2)C(F)(F)F)C=C1 NWEHHVVXCHVPFQ-UHFFFAOYSA-N 0.000 claims 1
- ONKOHQZZVMTPOM-UHFFFAOYSA-N 2-[5-methoxy-2-methyl-4-[[4-[[4-(trifluoromethyl)phenyl]methoxy]phenyl]methylsulfanyl]phenoxy]acetic acid Chemical compound COC1=CC(OCC(O)=O)=C(C)C=C1SCC(C=C1)=CC=C1OCC1=CC=C(C(F)(F)F)C=C1 ONKOHQZZVMTPOM-UHFFFAOYSA-N 0.000 claims 1
- WIOTZGHDAYUCBC-UHFFFAOYSA-N 2-[5-methoxy-2-methyl-4-[[5-[4-(trifluoromethyl)phenyl]-1,2-oxazol-3-yl]methylsulfanyl]phenoxy]acetic acid Chemical compound COC1=CC(OCC(O)=O)=C(C)C=C1SCC1=NOC(C=2C=CC(=CC=2)C(F)(F)F)=C1 WIOTZGHDAYUCBC-UHFFFAOYSA-N 0.000 claims 1
- HEMOEZGWSUFMTR-UHFFFAOYSA-N 2-[5-methoxy-2-methyl-4-[[6-[4-(trifluoromethyl)phenyl]pyridin-3-yl]methylsulfanyl]phenoxy]acetic acid Chemical compound COC1=CC(OCC(O)=O)=C(C)C=C1SCC1=CC=C(C=2C=CC(=CC=2)C(F)(F)F)N=C1 HEMOEZGWSUFMTR-UHFFFAOYSA-N 0.000 claims 1
- UUBMLUGVHDOXPD-UHFFFAOYSA-N 2-[[7-[[4-[4-(trifluoromethyl)phenyl]phenyl]methylsulfanyl]-2,3-dihydro-1h-inden-4-yl]oxy]acetic acid Chemical compound C1=2CCCC=2C(OCC(=O)O)=CC=C1SCC(C=C1)=CC=C1C1=CC=C(C(F)(F)F)C=C1 UUBMLUGVHDOXPD-UHFFFAOYSA-N 0.000 claims 1
- IVINVXPMKZERSK-UHFFFAOYSA-N 2-[[7-[[4-[[4-(trifluoromethyl)phenyl]methoxy]phenyl]methylsulfanyl]-2,3-dihydro-1h-inden-4-yl]oxy]acetic acid Chemical compound C1=2CCCC=2C(OCC(=O)O)=CC=C1SCC(C=C1)=CC=C1OCC1=CC=C(C(F)(F)F)C=C1 IVINVXPMKZERSK-UHFFFAOYSA-N 0.000 claims 1
- 125000004199 4-trifluoromethylphenyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1*)C(F)(F)F 0.000 claims 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 claims 1
- 208000032928 Dyslipidaemia Diseases 0.000 claims 1
- 208000035150 Hypercholesterolemia Diseases 0.000 claims 1
- 102000016267 Leptin Human genes 0.000 claims 1
- 108010092277 Leptin Proteins 0.000 claims 1
- 208000017170 Lipid metabolism disease Diseases 0.000 claims 1
- 208000008589 Obesity Diseases 0.000 claims 1
- 229910052799 carbon Inorganic materials 0.000 claims 1
- 125000000392 cycloalkenyl group Chemical group 0.000 claims 1
- 239000003085 diluting agent Substances 0.000 claims 1
- 150000002148 esters Chemical group 0.000 claims 1
- NRYBAZVQPHGZNS-ZSOCWYAHSA-N leptin Chemical compound O=C([C@H](CO)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CC=1C2=CC=CC=C2NC=1)NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CO)NC(=O)CNC(=O)[C@H](CCC(N)=O)NC(=O)[C@@H](N)CC(C)C)CCSC)N1CCC[C@H]1C(=O)NCC(=O)N[C@@H](CS)C(O)=O NRYBAZVQPHGZNS-ZSOCWYAHSA-N 0.000 claims 1
- 229940039781 leptin Drugs 0.000 claims 1
- 238000000034 method Methods 0.000 claims 1
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 1
- 235000020824 obesity Nutrition 0.000 claims 1
- 125000002971 oxazolyl group Chemical group 0.000 claims 1
- 239000000546 pharmaceutical excipient Substances 0.000 claims 1
- 230000002265 prevention Effects 0.000 claims 1
- 125000004076 pyridyl group Chemical group 0.000 claims 1
- 229930195734 saturated hydrocarbon Natural products 0.000 claims 1
- 125000000335 thiazolyl group Chemical group 0.000 claims 1
- 208000001072 type 2 diabetes mellitus Diseases 0.000 claims 1
- 229930195735 unsaturated hydrocarbon Natural products 0.000 claims 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US37050802P | 2002-04-05 | 2002-04-05 | |
| US38602602P | 2002-06-05 | 2002-06-05 | |
| PCT/IB2003/001121 WO2003084916A2 (en) | 2002-04-05 | 2003-03-24 | Compounds that modulate ppar activity and methods for their preparation |
Related Child Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2005360431A Division JP2006151985A (ja) | 2002-04-05 | 2005-12-14 | Ｐｐａｒ活性を調節する化合物、及び該化合物の製造方法 |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2005521741A JP2005521741A (ja) | 2005-07-21 |
| JP2005521741A5 true JP2005521741A5 (https=) | 2005-12-22 |
| JP3816922B2 JP3816922B2 (ja) | 2006-08-30 |
Family
ID=28794388
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2003582115A Expired - Fee Related JP3816922B2 (ja) | 2002-04-05 | 2003-03-24 | Ｐｐａｒ活性を調節する化合物、及び該化合物の製造方法 |
| JP2005360431A Withdrawn JP2006151985A (ja) | 2002-04-05 | 2005-12-14 | Ｐｐａｒ活性を調節する化合物、及び該化合物の製造方法 |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2005360431A Withdrawn JP2006151985A (ja) | 2002-04-05 | 2005-12-14 | Ｐｐａｒ活性を調節する化合物、及び該化合物の製造方法 |
Country Status (35)
| Country | Link |
|---|---|
| US (4) | US6875780B2 (https=) |
| EP (1) | EP1494989A2 (https=) |
| JP (2) | JP3816922B2 (https=) |
| KR (1) | KR100687166B1 (https=) |
| CN (1) | CN1649820A (https=) |
| AP (1) | AP1772A (https=) |
| AR (1) | AR039239A1 (https=) |
| AU (1) | AU2003212578A1 (https=) |
| BR (1) | BR0309169A (https=) |
| CA (1) | CA2481246C (https=) |
| CO (1) | CO5640080A2 (https=) |
| DO (1) | DOP2003000620A (https=) |
| EA (2) | EA200700969A1 (https=) |
| GE (1) | GEP20074244B (https=) |
| GT (3) | GT200300075A (https=) |
| HN (1) | HN2003000113A (https=) |
| HR (1) | HRP20040916A2 (https=) |
| IL (1) | IL164015A0 (https=) |
| IS (1) | IS7429A (https=) |
| MA (1) | MA27189A1 (https=) |
| MX (1) | MXPA04009727A (https=) |
| MY (1) | MY134199A (https=) |
| NI (1) | NI200300042A (https=) |
| NO (1) | NO20044795L (https=) |
| NZ (1) | NZ554477A (https=) |
| OA (1) | OA12859A (https=) |
| PA (1) | PA8570701A1 (https=) |
| PE (1) | PE20040307A1 (https=) |
| PL (1) | PL373651A1 (https=) |
| RS (1) | RS82904A (https=) |
| TN (1) | TNSN04191A1 (https=) |
| TW (1) | TWI249522B (https=) |
| UA (1) | UA76838C2 (https=) |
| UY (1) | UY27749A1 (https=) |
| WO (1) | WO2003084916A2 (https=) |
Families Citing this family (86)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7517884B2 (en) * | 1998-03-30 | 2009-04-14 | Kalypsys Inc. | Sulfonyl-substituted bicyclic compounds as modulators of PPAR |
| GB0029974D0 (en) * | 2000-12-08 | 2001-01-24 | Glaxo Group Ltd | Chemical compounds |
| BR0212512A (pt) | 2001-09-14 | 2004-10-26 | Tularik Inc | Composto, composição farmacêutica e métodos para tratar um distúrbio, condição ou doença, elevar os nìveis do colesterol hdl, reduzir os nìveis de triglicerìdeo, tratar diabete, diminuir a resistência à insulina ou diminuir a pressão arterial e modular a ppardelta |
| US6833380B2 (en) | 2002-03-07 | 2004-12-21 | Warner-Lambert Company, Llc | Compounds that modulate PPAR activity and methods of preparation |
| SG147301A1 (en) * | 2002-06-24 | 2008-11-28 | Sugatsune Kogyo | Umbrella retaining lock |
| US7396850B2 (en) * | 2003-01-06 | 2008-07-08 | Eli Lilly And Company | Pyrazole derivative as PPAR modulator |
| US7244763B2 (en) * | 2003-04-17 | 2007-07-17 | Warner Lambert Company Llc | Compounds that modulate PPAR activity and methods of preparation |
| EP1630152A4 (en) * | 2003-05-30 | 2009-09-23 | Takeda Pharmaceutical | CONDENSED CYCLIC COMPOUND |
| WO2005042478A2 (en) | 2003-09-19 | 2005-05-12 | Janssen Pharmaceutica, N.V. | 4-((phenoxyalkyl)thio)-phenoxyacetic acids and analogs |
| MXPA06003019A (es) * | 2003-10-28 | 2006-06-23 | Reddys Lab Ltd Dr | Nuevos compuestos y su uso en medicina: proceso para su preparacion y composiciones farmaceuticas que los contienen. |
| JP2007527416A (ja) | 2003-10-31 | 2007-09-27 | 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 | ペルオキシソーム増殖因子活性化受容体（ｐｐａｒ）二重作動薬として有用なフェノキシ酢酸誘導体 |
| AU2004291262C1 (en) * | 2003-11-05 | 2011-08-11 | F. Hoffmann-La Roche Ag | Phenyl derivatives as PPAR agonists |
| KR100849352B1 (ko) * | 2003-11-05 | 2008-07-29 | 에프. 호프만-라 로슈 아게 | Ｐｐａｒ 활성화제로서 벤조-융합된 화합물 |
| AU2004291259A1 (en) * | 2003-11-05 | 2005-06-02 | F. Hoffmann-La Roche Ag | Heteroaryl derivatives as PPAR activators |
| US20070054902A1 (en) * | 2003-12-02 | 2007-03-08 | Shionogi & Co., Ltd. | Isoxazole derivatives as peroxisome proliferator-activated receptors agonists |
| CA2549385A1 (en) | 2003-12-22 | 2005-07-21 | Eli Lilly And Company | Triazole, oxadiazole and thiadiazole derivative as ppar modulators for the treatment of diabetes |
| WO2005066136A1 (en) * | 2003-12-22 | 2005-07-21 | Eli Lilly And Company | Bicyclic derivatives as ppar modulators |
| AU2004309271A1 (en) | 2003-12-25 | 2005-07-14 | Takeda Pharmaceutical Company Limited | 3-(4-benzyloxyphenyl)propanoic acid derivatives |
| GB0403148D0 (en) * | 2004-02-12 | 2004-03-17 | Smithkline Beecham Corp | Chemical compounds |
| CA2558585C (en) * | 2004-02-27 | 2010-10-12 | Amgen Inc. | Compounds, pharmaceutical compositions and methods for use in treating metabolic disorders |
| WO2005085235A1 (en) * | 2004-03-09 | 2005-09-15 | F. Hoffmann-La Roche Ag | Pyrazolyl indolyl derivatives as ppar activators |
| US7119214B2 (en) * | 2004-04-13 | 2006-10-10 | Cephalon France | Thio-substituted tricyclic and bicyclic aromatic methanesulfinyl derivatives |
| WO2005105736A1 (en) * | 2004-05-05 | 2005-11-10 | Novo Nordisk A/S | Novel compounds, their preparation and use |
| ES2352085T3 (es) * | 2004-05-05 | 2011-02-15 | High Point Pharmaceuticals, Llc | Nuevos compuestos, su preparación y uso. |
| ATE475642T1 (de) * | 2004-05-05 | 2010-08-15 | High Point Pharmaceuticals Llc | Phenoxyessigsäurederivate als ppar-agonisten |
| CA2564365A1 (en) * | 2004-05-14 | 2005-12-01 | Irm Llc | Compounds and compositions as ppar modulators |
| WO2005113519A1 (en) * | 2004-05-14 | 2005-12-01 | Irm Llc | Compounds and compositions as ppar modulators |
| WO2005115384A2 (en) * | 2004-05-25 | 2005-12-08 | Metabolex, Inc. | Bicyclic, substituted triazoles as modulators of ppar and methods of their preparation |
| CA2568009A1 (en) * | 2004-05-25 | 2005-12-08 | Pfizer Products Inc. | Use of ppar agonists to treat ruminants |
| CN1997633A (zh) * | 2004-05-25 | 2007-07-11 | 麦它波莱克斯股份有限公司 | 作为ppar调节剂的取代的三唑及其制备方法 |
| BRPI0512951A (pt) | 2004-07-01 | 2008-04-15 | Hoffmann La Roche | compostos, processo para sua fabricação, composições farmacêuticas contendo os mesmos, uso e método para tratamento e/ou prevenção de doenças que são moduladas pelos agonistas de ppar(delta) e/ou ppar(alpha) |
| US7622491B2 (en) * | 2004-08-13 | 2009-11-24 | Metabolex Inc. | Modulators of PPAR and methods of their preparation |
| MY145712A (en) * | 2004-09-15 | 2012-03-30 | Janssen Pharmaceutica Nv | 4-((phenoxyalkyl)thio)-phenoxyacetic acids and analogs |
| CA2585172C (en) * | 2004-10-29 | 2014-08-12 | Kalypsys, Inc. | Sulfonyl-substituted bicyclic compounds as modulators of ppar |
| US20070190079A1 (en) * | 2004-10-29 | 2007-08-16 | Kalypsys, Inc. | Methods for the selective modulation of ppar |
| AP2007003979A0 (en) * | 2004-11-23 | 2007-06-30 | Warner Lambert Co | 7-(2h-pyrazol-3-yl)-3,5-dihyroxy-heptanoic acid derivatives as hmg co-a reductase inhibitors for thetreatment of lipidemia |
| US7465804B2 (en) * | 2005-05-20 | 2008-12-16 | Amgen Inc. | Compounds, pharmaceutical compositions and methods for their use in treating metabolic disorders |
| ATE529404T1 (de) * | 2005-06-30 | 2011-11-15 | High Point Pharmaceuticals Llc | Phenoxyessigsäuren als ppar-delta-aktivatoren |
| BRPI0615948A2 (pt) * | 2005-09-07 | 2011-05-31 | Plexxikon Inc | composto ativo de ppar, sua composição, seu kit e seu uso |
| JO3006B1 (ar) * | 2005-09-14 | 2016-09-05 | Janssen Pharmaceutica Nv | املاح ليسين مبتكرة من مشتقات حامض 4-((فينوكسي الكيل)ثيو) فينوكسي الخليك |
| EP1924546A1 (en) * | 2005-09-14 | 2008-05-28 | Amgen, Inc | Conformationally constrained 3- (4-hydroxy-phenyl) - substituted-propanoic acids useful for treating metabolic disorders |
| US7741317B2 (en) | 2005-10-21 | 2010-06-22 | Bristol-Myers Squibb Company | LXR modulators |
| HUE040020T2 (hu) * | 2005-10-25 | 2019-02-28 | Kalypsys Inc | PPAR modulátorok sói és eljárások metabolikus betegségek kezelésére |
| US7888376B2 (en) | 2005-11-23 | 2011-02-15 | Bristol-Myers Squibb Company | Heterocyclic CETP inhibitors |
| BRPI0620468A2 (pt) | 2005-12-22 | 2011-11-08 | Transtech Pharma, Inc. | ácidos fenóxi acéticos como ativadores de ppar delta |
| CN101007798B (zh) * | 2006-01-24 | 2011-01-26 | 中国人民解放军军事医学科学院毒物药物研究所 | 苯并间二氧杂环戊烯衍生物及其制备方法和医药用途 |
| WO2007101864A2 (en) * | 2006-03-09 | 2007-09-13 | High Point Pharmaceuticals, Llc | Compounds that modulate ppar activity, their preparation and use |
| US8383660B2 (en) | 2006-03-10 | 2013-02-26 | Pfizer Inc. | Dibenzyl amine compounds and derivatives |
| MX2008011615A (es) * | 2006-03-14 | 2008-09-22 | Amgen Inc | Derivados de acidos carboxilicos biciclicos utiles para tratar trastornos metabolicos. |
| PE20080188A1 (es) * | 2006-04-18 | 2008-03-10 | Janssen Pharmaceutica Nv | Derivados del acido benzoazepin-oxi-acetico como agonistas de ppar-delta usados para aumentar hdl-c, reducir ldl-c y reducir colesterol |
| US20070249519A1 (en) * | 2006-04-20 | 2007-10-25 | Kalypsys, Inc. | Methods for the upregulation of glut4 via modulation of ppar delta in adipose tissue and for the treatment of disease |
| AR060937A1 (es) * | 2006-05-16 | 2008-07-23 | Kalypsys Inc | Compuestos biciclicos sustituidos con sulfonilo como moduladores de ppar |
| EP2064193A1 (en) * | 2006-09-07 | 2009-06-03 | Amgen, Inc | Heterocyclic gpr40 modulators |
| CA2662242C (en) * | 2006-09-07 | 2012-06-12 | Amgen Inc. | Benzo-fused compounds for use in treating metabolic disorders |
| CN101663262B (zh) | 2006-12-01 | 2014-03-26 | 百时美施贵宝公司 | 用于治疗动脉粥样硬化和心血管疾病的作为cetp抑制剂的n-(3-苄基)-2,2-(二苯基)-丙-1胺衍生物 |
| CN101595089A (zh) * | 2006-12-02 | 2009-12-02 | 财团法人首尔大学校产学协力财团 | 作为ppar配体的芳基化合物及其用途 |
| WO2008091863A1 (en) * | 2007-01-23 | 2008-07-31 | Kalypsys, Inc. | Sulfonyl-substituted bicyclic compounds as ppar modulators for the treatment of non-alcoholic steatohepatitis |
| EA200970793A1 (ru) * | 2007-02-23 | 2010-02-26 | Эли Лилли Энд Компани | Модуляторы рецепторов, активируемых пролифераторами пероксисом |
| WO2008112217A1 (en) * | 2007-03-13 | 2008-09-18 | Merck & Co., Inc. | Inhibitors of janus kinases and/or 3-phosphoinositide-dependent protein kinase-1 |
| AU2008241490B2 (en) * | 2007-04-16 | 2011-07-21 | Amgen Inc. | Substituted biphenyl phenoxy-, thiophenyl- and aminophenylpropanoic acid GPR40 modulators |
| WO2009012650A1 (en) * | 2007-07-25 | 2009-01-29 | Institute Of Pharmacology And Toxicology Academy Of Military Medical Sciences P.L.A. | Aryl pyrimidine derivatives, preparation methods and pharmaceutical uses thereof |
| US8030354B2 (en) | 2007-10-10 | 2011-10-04 | Amgen Inc. | Substituted biphenyl GPR40 modulators |
| AU2008338963A1 (en) * | 2007-12-13 | 2009-06-25 | Sri International | PPAR-delta ligands and methods of their use |
| WO2009111056A1 (en) * | 2008-03-06 | 2009-09-11 | Amgen Inc. | Conformationally constrained carboxylic acid derivatives useful for treating metabolic disorders |
| US8461183B2 (en) | 2008-05-26 | 2013-06-11 | Genfit | PPAR agonist compounds, preparation and uses |
| WO2010018547A1 (en) * | 2008-08-13 | 2010-02-18 | Pfizer Inc. | Aminoquinoline compounds |
| AU2009303475B2 (en) * | 2008-10-15 | 2012-09-13 | Amgen Inc. | Spirocyclic GPR40 modulators |
| WO2012178142A1 (en) * | 2011-06-23 | 2012-12-27 | Metabolic Solutions Development Company, Llc | Ppar-sparing compounds and combinations fort the treatment of diabetes and other metabolic diseases |
| EP2870219B1 (en) * | 2012-07-06 | 2016-05-25 | Merck Patent GmbH | Bimesogenic compounds and mesogenic media |
| EP2986599A1 (en) | 2013-04-17 | 2016-02-24 | Pfizer Inc. | N-piperidin-3-ylbenzamide derivatives for treating cardiovascular diseases |
| WO2015035171A1 (en) | 2013-09-09 | 2015-03-12 | High Point Pharmaceuticals, Llc | Use of a ppar-delta agonist for treating muscle atrophy |
| WO2016055901A1 (en) | 2014-10-08 | 2016-04-14 | Pfizer Inc. | Substituted amide compounds |
| CN106831437B (zh) * | 2016-02-03 | 2019-06-21 | 华中师范大学 | 含硝基乙烯基的酯类化合物及其制备方法和应用 |
| AU2018300150A1 (en) | 2017-07-11 | 2020-01-30 | Vertex Pharmaceuticals Incorporated | Carboxamides as modulators of sodium channels |
| RU2764243C2 (ru) | 2017-09-22 | 2022-01-14 | ДЖУБИЛАНТ ЭПИПЭД ЭлЭлСи | Гетероциклические соединения в качестве ингибиторов PAD |
| AU2018352142B2 (en) | 2017-10-18 | 2022-08-25 | Jubilant Epipad LLC | Imidazo-pyridine compounds as PAD inhibitors |
| US11629135B2 (en) | 2017-11-06 | 2023-04-18 | Jubilant Prodell Llc | Pyrimidine derivatives as inhibitors of PD1/PD-L1 activation |
| PT3704120T (pt) | 2017-11-24 | 2024-07-03 | Jubilant Episcribe Llc | Compostos heterocíclicos como inibidores de prmt5 |
| MX2020009517A (es) | 2018-03-13 | 2021-01-20 | Jubilant Prodel LLC | Compuestos biciclicos como inhibidores de la interaccion/activacio n de pdl/pd-l1. |
| WO2020146682A1 (en) | 2019-01-10 | 2020-07-16 | Vertex Pharmaceuticals Incorporated | Carboxamides as modulators of sodium channels |
| US12440481B2 (en) | 2019-01-10 | 2025-10-14 | Vertex Pharmaceuticals Incorporated | Esters and carbamates as modulators of sodium channels |
| BR112021013807A2 (pt) | 2019-01-18 | 2021-11-30 | Astrazeneca Ab | Inibidores de pcsk9 e seus métodos de uso |
| CA3145378A1 (en) * | 2019-06-28 | 2020-12-30 | Sumitomo Chemical Company, Limited | Acrylate derivative, use and production intermediate compound of the same |
| CN112824394B (zh) * | 2019-11-21 | 2024-08-13 | 中国科学院上海药物研究所 | PPARs-FXR多靶点小分子激动剂及其制备方法和用途 |
| US11267795B2 (en) | 2020-07-22 | 2022-03-08 | Reneo Pharmaceuticals, Inc. | Crystalline PPAR-delta agonist |
| WO2023147309A1 (en) | 2022-01-25 | 2023-08-03 | Reneo Pharmaceuticals, Inc. | Use of ppar-delta agonists in the treatment of disease |
Family Cites Families (21)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE3526235A1 (de) | 1984-11-16 | 1986-05-22 | Bayer Ag, 5090 Leverkusen | Fluessigkristallzusammensetzungen |
| DE4002374C2 (de) | 1990-01-27 | 1999-04-15 | Merck Patent Gmbh | Partiell fluorierte Verbindungen und deren Verwendung als Komponente flüssig kristalliner Medien |
| DE4222565A1 (de) * | 1992-07-09 | 1994-01-13 | Hoechst Ag | Meta-substituierte Sechsringaromaten zur Verwendung in Flüssigkristallmischungen |
| JP3187611B2 (ja) | 1993-05-17 | 2001-07-11 | キヤノン株式会社 | 液晶性化合物、これを含む液晶組成物、それを有する液晶素子、それらを用いた表示方法および表示装置 |
| DE69505490T2 (de) | 1994-08-04 | 1999-06-24 | Sumitomo Chemical Co., Ltd., Osaka | Dihalopropenverbindungen, sie enthaltende insektizide/akarizide mittel, und zwischenprodukte |
| JPH09194418A (ja) | 1996-01-18 | 1997-07-29 | Sumitomo Chem Co Ltd | ジハロプロペン化合物、その用途およびその製造中間体 |
| WO1997028149A1 (en) | 1996-02-02 | 1997-08-07 | Merck & Co., Inc. | Method for raising hdl cholesterol levels |
| WO1997028137A1 (en) | 1996-02-02 | 1997-08-07 | Merck & Co., Inc. | Heterocyclic derivatives as antidiabetic and antiobesity agents |
| CN1233241A (zh) | 1996-08-19 | 1999-10-27 | 日本烟草产业株式会社 | 丙酸衍生物及其用途 |
| ATE451346T1 (de) | 1998-03-10 | 2009-12-15 | Ono Pharmaceutical Co | Carbonsäurederivate und medikamente die diese als aktiven wirkstoff enthalten |
| GB9914977D0 (en) | 1999-06-25 | 1999-08-25 | Glaxo Group Ltd | Chemical compounds |
| US6417212B1 (en) | 1999-08-27 | 2002-07-09 | Eli Lilly & Company | Modulators of peroxisome proliferator activated receptors |
| WO2001032621A1 (en) * | 1999-10-29 | 2001-05-10 | Wakunaga Pharmaceutical Co., Ltd. | Novel indole derivatives and drugs containing the same as the active ingredient |
| GB0031107D0 (en) | 2000-12-20 | 2001-01-31 | Glaxo Group Ltd | Chemical compounds |
| GB0031109D0 (en) | 2000-12-20 | 2001-01-31 | Glaxo Group Ltd | Chemical compounds |
| GB0111523D0 (en) | 2001-05-11 | 2001-07-04 | Glaxo Group Ltd | Chemical compounds |
| HRP20031002A2 (en) | 2001-06-07 | 2004-06-30 | Lilly Co Eli | Modulators of peroxisome proliferator activated receptors (ppar) |
| BR0212512A (pt) | 2001-09-14 | 2004-10-26 | Tularik Inc | Composto, composição farmacêutica e métodos para tratar um distúrbio, condição ou doença, elevar os nìveis do colesterol hdl, reduzir os nìveis de triglicerìdeo, tratar diabete, diminuir a resistência à insulina ou diminuir a pressão arterial e modular a ppardelta |
| US20030207924A1 (en) * | 2002-03-07 | 2003-11-06 | Xue-Min Cheng | Compounds that modulate PPAR activity and methods of preparation |
| US6833380B2 (en) * | 2002-03-07 | 2004-12-21 | Warner-Lambert Company, Llc | Compounds that modulate PPAR activity and methods of preparation |
| US6867224B2 (en) * | 2002-03-07 | 2005-03-15 | Warner-Lambert Company | Compounds that modulate PPAR activity and methods of preparation |
-
2003
- 2003-01-22 US US10/347,749 patent/US6875780B2/en not_active Expired - Fee Related
- 2003-03-06 NI NI200300042A patent/NI200300042A/es unknown
- 2003-03-24 AP APAP/P/2004/003135A patent/AP1772A/en active
- 2003-03-24 DO DO2003000620A patent/DOP2003000620A/es unknown
- 2003-03-24 OA OA1200400261A patent/OA12859A/en unknown
- 2003-03-24 HR HRP20040916 patent/HRP20040916A2/hr not_active Application Discontinuation
- 2003-03-24 GE GEAP8431A patent/GEP20074244B/en unknown
- 2003-03-24 IL IL16401503A patent/IL164015A0/xx unknown
- 2003-03-24 BR BR0309169-4A patent/BR0309169A/pt not_active IP Right Cessation
- 2003-03-24 WO PCT/IB2003/001121 patent/WO2003084916A2/en not_active Ceased
- 2003-03-24 MX MXPA04009727A patent/MXPA04009727A/es active IP Right Grant
- 2003-03-24 EA EA200700969A patent/EA200700969A1/ru unknown
- 2003-03-24 AU AU2003212578A patent/AU2003212578A1/en not_active Abandoned
- 2003-03-24 CA CA002481246A patent/CA2481246C/en not_active Expired - Fee Related
- 2003-03-24 EA EA200401153A patent/EA009518B1/ru not_active IP Right Cessation
- 2003-03-24 JP JP2003582115A patent/JP3816922B2/ja not_active Expired - Fee Related
- 2003-03-24 NZ NZ554477A patent/NZ554477A/en unknown
- 2003-03-24 PL PL03373651A patent/PL373651A1/xx unknown
- 2003-03-24 EP EP03708403A patent/EP1494989A2/en not_active Withdrawn
- 2003-03-24 RS YUP-829/04A patent/RS82904A/sr unknown
- 2003-03-24 UA UA20041008021A patent/UA76838C2/uk unknown
- 2003-03-24 KR KR1020047015763A patent/KR100687166B1/ko not_active Expired - Fee Related
- 2003-03-24 CN CNA038097915A patent/CN1649820A/zh active Pending
- 2003-04-01 GT GT200300075A patent/GT200300075A/es unknown
- 2003-04-01 GT GT200300075AK patent/GT200300075AA/es unknown
- 2003-04-01 PE PE2003000327A patent/PE20040307A1/es not_active Application Discontinuation
- 2003-04-01 GT GT200300075BL patent/GT200300075BA/es unknown
- 2003-04-02 MY MYPI20031235A patent/MY134199A/en unknown
- 2003-04-03 AR ARP030101164A patent/AR039239A1/es unknown
- 2003-04-03 UY UY27749A patent/UY27749A1/es not_active Application Discontinuation
- 2003-04-04 TW TW092107732A patent/TWI249522B/zh not_active IP Right Cessation
- 2003-04-04 HN HN2003000113A patent/HN2003000113A/es unknown
- 2003-04-04 PA PA20038570701A patent/PA8570701A1/es unknown
-
2004
- 2004-08-30 IS IS7429A patent/IS7429A/is unknown
- 2004-09-17 CO CO04092873A patent/CO5640080A2/es not_active Application Discontinuation
- 2004-09-28 MA MA27877A patent/MA27189A1/fr unknown
- 2004-10-04 TN TNP2004000191A patent/TNSN04191A1/fr unknown
- 2004-11-02 US US10/979,617 patent/US6939875B2/en not_active Ceased
- 2004-11-02 US US10/979,629 patent/US6964983B2/en not_active Expired - Fee Related
- 2004-11-04 NO NO20044795A patent/NO20044795L/no not_active Application Discontinuation
-
2005
- 2005-11-28 US US11/288,022 patent/USRE39916E1/en not_active Expired - Fee Related
- 2005-12-14 JP JP2005360431A patent/JP2006151985A/ja not_active Withdrawn
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| JP2005521741A5 (https=) | ||
| JP3490704B2 (ja) | チアゾールおよびオキサゾール誘導体ならびにそれらの医薬的使用 | |
| JP4222450B2 (ja) | Ｃ−グリコシド誘導体又はその塩 | |
| RU2312106C2 (ru) | Замещенные 4-алкоксиоксазолпроизводные в качестве агонистов ppar | |
| ES2240558T3 (es) | Derivados de tiazol y oxazol como activadores de receptores activados por el proliferador de peroxisoma humano. | |
| KR910004430B1 (ko) | 5-피리딜-1,3-티아졸 유도체의 제조방법 | |
| JP2007502806A5 (https=) | ||
| RU2007101236A (ru) | Новые гидантоиновые производные для лечения обструктивных заболеваний дыхательных путей | |
| JP2010506918A5 (https=) | ||
| JPWO2002072145A1 (ja) | Ｅｐ１アンタゴニストを有効成分として含有するうつ病の治療剤 | |
| JP2005509024A5 (https=) | ||
| CA2643272A1 (en) | Gent for treating or preventing digestive ulcer | |
| RU2004117887A (ru) | Ариланилиновые агонисты бета2 адренергических рецепторов | |
| JP2005509632A5 (https=) | ||
| JP2004534035A5 (https=) | ||
| KR20090024820A (ko) | 인간 단백질 티로신 포스파타아제 억제제 및 이용 방법 | |
| CA2683738A1 (en) | Indanone derivatives that inhibit prolyl hydroxylase | |
| KR20110027657A (ko) | 카르복실산 화합물 | |
| NZ587056A (en) | Method for modulating calcium ion-release-activated calcium ion channels | |
| KR20040091694A (ko) | Ｐｐａｒ 활성을 조절하는 티아졸 및 옥사졸 유도체 | |
| RU2006107653A (ru) | Связующее вспомогательное вещество и приготовленная на его основе таблетка в форме капли | |
| JP2005528348A5 (https=) | ||
| JP2006516251A5 (https=) | ||
| JP2005526696A5 (https=) | ||
| CA2432211A1 (en) | Dihydronaphthalene derivative compounds and agent comprising the derivative as active ingredient |