JP2007525516A5 - - Google Patents
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- Publication number
- JP2007525516A5 JP2007525516A5 JP2007500959A JP2007500959A JP2007525516A5 JP 2007525516 A5 JP2007525516 A5 JP 2007525516A5 JP 2007500959 A JP2007500959 A JP 2007500959A JP 2007500959 A JP2007500959 A JP 2007500959A JP 2007525516 A5 JP2007525516 A5 JP 2007525516A5
- Authority
- JP
- Japan
- Prior art keywords
- alkyl
- phenyl
- alkylene
- heteroaryl
- aryl
- 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
- 150000001875 compounds Chemical class 0.000 claims 24
- 125000001072 heteroaryl group Chemical group 0.000 claims 20
- 125000003118 aryl group Chemical group 0.000 claims 19
- 125000004209 (C1-C8) alkyl group Chemical group 0.000 claims 10
- 229910052739 hydrogen Inorganic materials 0.000 claims 9
- 239000001257 hydrogen Substances 0.000 claims 9
- 125000004648 C2-C8 alkenyl group Chemical group 0.000 claims 8
- 125000004649 C2-C8 alkynyl group Chemical group 0.000 claims 8
- 125000002947 alkylene group Chemical group 0.000 claims 8
- 125000004093 cyano group Chemical group *C#N 0.000 claims 7
- 229910052760 oxygen Inorganic materials 0.000 claims 7
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 5
- 125000000217 alkyl group Chemical group 0.000 claims 5
- 125000004404 heteroalkyl group Chemical group 0.000 claims 5
- 125000004474 heteroalkylene group Chemical group 0.000 claims 5
- -1 thiazolidinedione-yl Chemical group 0.000 claims 5
- 150000002431 hydrogen Chemical group 0.000 claims 4
- UHOVQNZJYSORNB-UHFFFAOYSA-N monobenzene Natural products C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 claims 4
- 125000006833 (C1-C5) alkylene group Chemical group 0.000 claims 3
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims 3
- 125000006552 (C3-C8) cycloalkyl group Chemical group 0.000 claims 3
- 201000010099 disease Diseases 0.000 claims 3
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims 3
- 239000003814 drug Substances 0.000 claims 3
- 125000005842 heteroatom Chemical group 0.000 claims 3
- 229910052757 nitrogen Inorganic materials 0.000 claims 3
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 3
- 229910052717 sulfur Inorganic materials 0.000 claims 3
- 208000001072 type 2 diabetes mellitus Diseases 0.000 claims 3
- VJYBBKPKVPQHSX-UHFFFAOYSA-N 3-[4-[(4-methoxyphenyl)methoxy]phenyl]pent-4-ynoic acid Chemical compound C1=CC(OC)=CC=C1COC1=CC=C(C(CC(O)=O)C#C)C=C1 VJYBBKPKVPQHSX-UHFFFAOYSA-N 0.000 claims 2
- 208000031226 Hyperlipidaemia Diseases 0.000 claims 2
- 125000004450 alkenylene group Chemical group 0.000 claims 2
- 125000002993 cycloalkylene group Chemical group 0.000 claims 2
- 125000000592 heterocycloalkyl group Chemical group 0.000 claims 2
- 125000006588 heterocycloalkylene group Chemical group 0.000 claims 2
- NOESYZHRGYRDHS-UHFFFAOYSA-N insulin Chemical compound N1C(=O)C(NC(=O)C(CCC(N)=O)NC(=O)C(CCC(O)=O)NC(=O)C(C(C)C)NC(=O)C(NC(=O)CN)C(C)CC)CSSCC(C(NC(CO)C(=O)NC(CC(C)C)C(=O)NC(CC=2C=CC(O)=CC=2)C(=O)NC(CCC(N)=O)C(=O)NC(CC(C)C)C(=O)NC(CCC(O)=O)C(=O)NC(CC(N)=O)C(=O)NC(CC=2C=CC(O)=CC=2)C(=O)NC(CSSCC(NC(=O)C(C(C)C)NC(=O)C(CC(C)C)NC(=O)C(CC=2C=CC(O)=CC=2)NC(=O)C(CC(C)C)NC(=O)C(C)NC(=O)C(CCC(O)=O)NC(=O)C(C(C)C)NC(=O)C(CC(C)C)NC(=O)C(CC=2NC=NC=2)NC(=O)C(CO)NC(=O)CNC2=O)C(=O)NCC(=O)NC(CCC(O)=O)C(=O)NC(CCCNC(N)=N)C(=O)NCC(=O)NC(CC=3C=CC=CC=3)C(=O)NC(CC=3C=CC=CC=3)C(=O)NC(CC=3C=CC(O)=CC=3)C(=O)NC(C(C)O)C(=O)N3C(CCC3)C(=O)NC(CCCCN)C(=O)NC(C)C(O)=O)C(=O)NC(CC(N)=O)C(O)=O)=O)NC(=O)C(C(C)CC)NC(=O)C(CO)NC(=O)C(C(C)O)NC(=O)C1CSSCC2NC(=O)C(CC(C)C)NC(=O)C(NC(=O)C(CCC(N)=O)NC(=O)C(CC(N)=O)NC(=O)C(NC(=O)C(N)CC=1C=CC=CC=1)C(C)C)CC1=CN=CN1 NOESYZHRGYRDHS-UHFFFAOYSA-N 0.000 claims 2
- 208000017169 kidney disease Diseases 0.000 claims 2
- 238000004519 manufacturing process Methods 0.000 claims 2
- 239000000203 mixture Substances 0.000 claims 2
- 125000004433 nitrogen atom Chemical group N* 0.000 claims 2
- 125000005704 oxymethylene group Chemical group [H]C([H])([*:2])O[*:1] 0.000 claims 2
- 150000003839 salts Chemical class 0.000 claims 2
- JEXFYYALLIJTNH-GOSISDBHSA-N (2r)-3-[(2-methylpropan-2-yl)oxy]-3-oxo-2-[(4-phenylmethoxyphenyl)methyl]propanoic acid Chemical compound C1=CC(C[C@@H](C(=O)OC(C)(C)C)C(O)=O)=CC=C1OCC1=CC=CC=C1 JEXFYYALLIJTNH-GOSISDBHSA-N 0.000 claims 1
- 125000003161 (C1-C6) alkylene group Chemical group 0.000 claims 1
- RCECATFPGPUPHW-UHFFFAOYSA-N 2-(n-(4-benzamidophenyl)anilino)acetic acid Chemical compound C=1C=C(NC(=O)C=2C=CC=CC=2)C=CC=1N(CC(=O)O)C1=CC=CC=C1 RCECATFPGPUPHW-UHFFFAOYSA-N 0.000 claims 1
- CVBJWCJYJMMHGC-UHFFFAOYSA-N 2-[4-[2-[[5-(4-chlorophenyl)furan-2-carbonyl]amino]ethyl]phenoxy]-2-methylpropanoic acid Chemical compound C1=CC(OC(C)(C)C(O)=O)=CC=C1CCNC(=O)C1=CC=C(C=2C=CC(Cl)=CC=2)O1 CVBJWCJYJMMHGC-UHFFFAOYSA-N 0.000 claims 1
- AQAMBIJONMEPPJ-UHFFFAOYSA-N 2-[[2-[3-(3,4-dihydro-2h-1,5-benzodioxepin-7-yl)-2-methyl-4-oxochromen-7-yl]oxyacetyl]amino]acetic acid Chemical compound O1CCCOC2=CC(C=3C(=O)C4=CC=C(OCC(=O)NCC(O)=O)C=C4OC=3C)=CC=C21 AQAMBIJONMEPPJ-UHFFFAOYSA-N 0.000 claims 1
- ITCRVQYXNASVEK-UHFFFAOYSA-N 3-(3,4-dimethoxyphenyl)-3-(furan-2-carbonylamino)propanoic acid Chemical compound C1=C(OC)C(OC)=CC=C1C(CC(O)=O)NC(=O)C1=CC=CO1 ITCRVQYXNASVEK-UHFFFAOYSA-N 0.000 claims 1
- MIOAEEYDTLXLIO-UHFFFAOYSA-N 3-(4-chlorophenyl)-3-(furan-2-carbonylamino)propanoic acid Chemical compound C=1C=C(Cl)C=CC=1C(CC(=O)O)NC(=O)C1=CC=CO1 MIOAEEYDTLXLIO-UHFFFAOYSA-N 0.000 claims 1
- NSEKSGAGVILKPQ-UHFFFAOYSA-N 3-(4-phenylmethoxyphenyl)pent-4-enoic acid Chemical compound C1=CC(C(C=C)CC(=O)O)=CC=C1OCC1=CC=CC=C1 NSEKSGAGVILKPQ-UHFFFAOYSA-N 0.000 claims 1
- SAXJVFTTWMMNML-UHFFFAOYSA-N 3-[(4-chlorobenzoyl)amino]-3-[4-(dimethylamino)phenyl]propanoic acid Chemical compound C1=CC(N(C)C)=CC=C1C(CC(O)=O)NC(=O)C1=CC=C(Cl)C=C1 SAXJVFTTWMMNML-UHFFFAOYSA-N 0.000 claims 1
- QWQOJGSHENBCAF-UHFFFAOYSA-N 3-[2-[2-(3,4-dimethylphenoxy)ethylsulfanyl]benzimidazol-1-yl]propanoic acid Chemical compound C1=C(C)C(C)=CC=C1OCCSC1=NC2=CC=CC=C2N1CCC(O)=O QWQOJGSHENBCAF-UHFFFAOYSA-N 0.000 claims 1
- KVEYFKWVTVCKMX-UHFFFAOYSA-N 3-[3-[2-chloro-4-(trifluoromethyl)phenoxy]phenyl]propanoic acid Chemical compound OC(=O)CCC1=CC=CC(OC=2C(=CC(=CC=2)C(F)(F)F)Cl)=C1 KVEYFKWVTVCKMX-UHFFFAOYSA-N 0.000 claims 1
- PPJHTJXGKHYVCG-UHFFFAOYSA-N 3-[4-(4-bromophenyl)phenyl]-3-phenylsulfanylpropanoic acid Chemical compound C=1C=C(C=2C=CC(Br)=CC=2)C=CC=1C(CC(=O)O)SC1=CC=CC=C1 PPJHTJXGKHYVCG-UHFFFAOYSA-N 0.000 claims 1
- DHQNEDXCTOTLHE-UHFFFAOYSA-N 3-[4-(4-bromophenyl)phenyl]-4-phenylbutanoic acid Chemical compound C=1C=C(C=2C=CC(Br)=CC=2)C=CC=1C(CC(=O)O)CC1=CC=CC=C1 DHQNEDXCTOTLHE-UHFFFAOYSA-N 0.000 claims 1
- CJWSPUJYICTNJU-UHFFFAOYSA-N 3-[5-[2-chloro-6-fluoro-4-(trifluoromethyl)phenoxy]-2,4-dinitrophenyl]propanoic acid Chemical compound C1=C([N+]([O-])=O)C(CCC(=O)O)=CC(OC=2C(=CC(=CC=2F)C(F)(F)F)Cl)=C1[N+]([O-])=O CJWSPUJYICTNJU-UHFFFAOYSA-N 0.000 claims 1
- IGJHXBXWVKYBQR-UHFFFAOYSA-N 3-amino-3-[4-[(4-bromo-2-methyl-5-oxo-1-phenylpyrazol-3-yl)methoxy]-3-methoxyphenyl]propanoic acid Chemical compound COC1=CC(C(N)CC(O)=O)=CC=C1OCC(N1C)=C(Br)C(=O)N1C1=CC=CC=C1 IGJHXBXWVKYBQR-UHFFFAOYSA-N 0.000 claims 1
- 201000001320 Atherosclerosis Diseases 0.000 claims 1
- AANBGNWGPUCJNQ-UHFFFAOYSA-N BrC1=C(OCC(O)=O)C(OCC)=CC(C(=NN)C=2C=C(Cl)C(Cl)=CC=2)=C1 Chemical compound BrC1=C(OCC(O)=O)C(OCC)=CC(C(=NN)C=2C=C(Cl)C(Cl)=CC=2)=C1 AANBGNWGPUCJNQ-UHFFFAOYSA-N 0.000 claims 1
- 208000024172 Cardiovascular disease Diseases 0.000 claims 1
- 206010048768 Dermatosis Diseases 0.000 claims 1
- 208000007342 Diabetic Nephropathies Diseases 0.000 claims 1
- 206010012689 Diabetic retinopathy Diseases 0.000 claims 1
- 208000032928 Dyslipidaemia Diseases 0.000 claims 1
- 102100026148 Free fatty acid receptor 1 Human genes 0.000 claims 1
- 208000002705 Glucose Intolerance Diseases 0.000 claims 1
- 206010018429 Glucose tolerance impaired Diseases 0.000 claims 1
- 101000912510 Homo sapiens Free fatty acid receptor 1 Proteins 0.000 claims 1
- 208000035150 Hypercholesterolemia Diseases 0.000 claims 1
- 206010060378 Hyperinsulinaemia Diseases 0.000 claims 1
- 206010020772 Hypertension Diseases 0.000 claims 1
- 102000004877 Insulin Human genes 0.000 claims 1
- 108090001061 Insulin Proteins 0.000 claims 1
- 206010022489 Insulin Resistance Diseases 0.000 claims 1
- 206010023379 Ketoacidosis Diseases 0.000 claims 1
- 208000007976 Ketosis Diseases 0.000 claims 1
- 208000017170 Lipid metabolism disease Diseases 0.000 claims 1
- 208000001145 Metabolic Syndrome Diseases 0.000 claims 1
- 206010028980 Neoplasm Diseases 0.000 claims 1
- 208000008589 Obesity Diseases 0.000 claims 1
- 206010030113 Oedema Diseases 0.000 claims 1
- 201000001880 Sexual dysfunction Diseases 0.000 claims 1
- 208000007536 Thrombosis Diseases 0.000 claims 1
- 201000000690 abdominal obesity-metabolic syndrome Diseases 0.000 claims 1
- 125000003342 alkenyl group Chemical group 0.000 claims 1
- 125000000304 alkynyl group Chemical group 0.000 claims 1
- 201000011510 cancer Diseases 0.000 claims 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims 1
- 208000033679 diabetic kidney disease Diseases 0.000 claims 1
- 239000003085 diluting agent Substances 0.000 claims 1
- 239000003937 drug carrier Substances 0.000 claims 1
- 201000006549 dyspepsia Diseases 0.000 claims 1
- 238000009472 formulation Methods 0.000 claims 1
- 125000004464 hydroxyphenyl group Chemical group 0.000 claims 1
- 201000001421 hyperglycemia Diseases 0.000 claims 1
- 230000003451 hyperinsulinaemic effect Effects 0.000 claims 1
- 201000008980 hyperinsulinism Diseases 0.000 claims 1
- 208000020346 hyperlipoproteinemia Diseases 0.000 claims 1
- 208000006575 hypertriglyceridemia Diseases 0.000 claims 1
- 229940125396 insulin Drugs 0.000 claims 1
- 230000001404 mediated effect Effects 0.000 claims 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 1
- 125000000325 methylidene group Chemical group [H]C([H])=* 0.000 claims 1
- 235000020824 obesity Nutrition 0.000 claims 1
- MLBYLEUJXUBIJJ-UHFFFAOYSA-N pent-4-ynoic acid Chemical compound OC(=O)CCC#C MLBYLEUJXUBIJJ-UHFFFAOYSA-N 0.000 claims 1
- 239000008194 pharmaceutical composition Substances 0.000 claims 1
- 239000000546 pharmaceutical excipient Substances 0.000 claims 1
- 239000000651 prodrug Substances 0.000 claims 1
- 229940002612 prodrug Drugs 0.000 claims 1
- 125000004076 pyridyl group Chemical group 0.000 claims 1
- 231100000872 sexual dysfunction Toxicity 0.000 claims 1
- 208000017520 skin disease Diseases 0.000 claims 1
- 239000012453 solvate Substances 0.000 claims 1
- 125000000446 sulfanediyl group Chemical group *S* 0.000 claims 1
- 208000011580 syndromic disease Diseases 0.000 claims 1
- 125000004299 tetrazol-5-yl group Chemical group [H]N1N=NC(*)=N1 0.000 claims 1
- 229940124597 therapeutic agent Drugs 0.000 claims 1
- 230000001225 therapeutic effect Effects 0.000 claims 1
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims 1
Applications Claiming Priority (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US54874104P | 2004-02-27 | 2004-02-27 | |
| US60/548,741 | 2004-02-27 | ||
| US60157904P | 2004-08-12 | 2004-08-12 | |
| US60/601,579 | 2004-08-12 | ||
| PCT/US2005/005815 WO2005086661A2 (en) | 2004-02-27 | 2005-02-24 | Compounds, pharmaceutical compositions and methods for use in treating metabolic disorders |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2007525516A JP2007525516A (ja) | 2007-09-06 |
| JP2007525516A5 true JP2007525516A5 (https=) | 2008-03-27 |
| JP5299810B2 JP5299810B2 (ja) | 2013-09-25 |
Family
ID=34976072
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2007500959A Expired - Fee Related JP5299810B2 (ja) | 2004-02-27 | 2005-02-24 | 代謝疾患の治療に使用するための、化合物、薬学的組成物及び方法 |
Country Status (19)
| Country | Link |
|---|---|
| US (2) | US7816367B2 (https=) |
| EP (1) | EP1737809B1 (https=) |
| JP (1) | JP5299810B2 (https=) |
| KR (1) | KR20070004769A (https=) |
| CN (1) | CN1946666A (https=) |
| AR (1) | AR048306A1 (https=) |
| AU (1) | AU2005220728B2 (https=) |
| BR (1) | BRPI0508098A (https=) |
| CA (1) | CA2558585C (https=) |
| CR (1) | CR8642A (https=) |
| EA (1) | EA011010B1 (https=) |
| EC (1) | ECSP066887A (https=) |
| ES (1) | ES2433466T3 (https=) |
| IL (1) | IL177717A0 (https=) |
| IS (1) | IS8542A (https=) |
| MA (1) | MA28466B1 (https=) |
| NO (1) | NO20064362L (https=) |
| TW (1) | TW200539854A (https=) |
| WO (1) | WO2005086661A2 (https=) |
Families Citing this family (114)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB0319069D0 (en) * | 2003-08-14 | 2003-09-17 | Glaxo Group Ltd | Therapeutically useful compounds |
| CA2558585C (en) * | 2004-02-27 | 2010-10-12 | Amgen Inc. | Compounds, pharmaceutical compositions and methods for use in treating metabolic disorders |
| US7262318B2 (en) * | 2004-03-10 | 2007-08-28 | Pfizer, Inc. | Substituted heteroaryl- and phenylsulfamoyl compounds |
| US7517910B2 (en) * | 2004-03-30 | 2009-04-14 | Takeda Pharmaceutical Company Limited | Alkoxyphenylpropanoic acid derivatives |
| US20050288340A1 (en) * | 2004-06-29 | 2005-12-29 | Pfizer Inc | Substituted heteroaryl- and phenylsulfamoyl compounds |
| KR20140018997A (ko) | 2005-01-07 | 2014-02-13 | 신타 파마슈티칼스 코프. | 염증 및 면역 관련 용도를 위한 화합물 |
| GB0505437D0 (en) * | 2005-03-17 | 2005-04-20 | Merck Sharp & Dohme | Therapeutic agents |
| US7465804B2 (en) * | 2005-05-20 | 2008-12-16 | Amgen Inc. | Compounds, pharmaceutical compositions and methods for their use in treating metabolic disorders |
| US8097610B2 (en) | 2005-08-26 | 2012-01-17 | Shionogi & Co., Ltd. | Derivative having PPAR agonistic activity |
| EP1924546A1 (en) * | 2005-09-14 | 2008-05-28 | Amgen, Inc | Conformationally constrained 3- (4-hydroxy-phenyl) - substituted-propanoic acids useful for treating metabolic disorders |
| EP1940786B1 (en) | 2005-09-16 | 2010-08-18 | Arrow Therapeutics Limited | Biphenyl derivatives and their use in treating hepatitis c |
| KR100968705B1 (ko) * | 2005-10-27 | 2010-07-06 | 주식회사유한양행 | 신규의 2-페닐피리미딘 유도체 및 그의 제조방법 |
| UA95613C2 (ru) | 2005-11-09 | 2011-08-25 | Уеллстат Терепьютикс Корпорейшн | Соединения для лечения расстройсв метаболизма |
| US20090176885A1 (en) * | 2006-02-02 | 2009-07-09 | Wellstat Therapeutics Corporation | Compounds for the treatment of metabolic disorders |
| MX2008011615A (es) * | 2006-03-14 | 2008-09-22 | Amgen Inc | Derivados de acidos carboxilicos biciclicos utiles para tratar trastornos metabolicos. |
| TW200815377A (en) | 2006-04-24 | 2008-04-01 | Astellas Pharma Inc | Oxadiazolidinedione compound |
| 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 |
| US7750048B2 (en) * | 2006-11-15 | 2010-07-06 | Janssen Pharmaceutica Nv | GPR40 agonists |
| TW200838526A (en) | 2006-12-01 | 2008-10-01 | Astellas Pharma Inc | Carboxylic acid derivatives |
| JP5175866B2 (ja) * | 2007-02-22 | 2013-04-03 | アイアールエム・リミテッド・ライアビリティ・カンパニー | Ｇタンパク質共役受容体を調節するための化合物および方法 |
| AU2008241490B2 (en) * | 2007-04-16 | 2011-07-21 | Amgen Inc. | Substituted biphenyl phenoxy-, thiophenyl- and aminophenylpropanoic acid GPR40 modulators |
| US8030354B2 (en) | 2007-10-10 | 2011-10-04 | Amgen Inc. | Substituted biphenyl GPR40 modulators |
| BRPI0818687A2 (pt) * | 2007-10-26 | 2017-05-02 | Japan Tobacco Inc | composto espiro, o sal deste farmaceuticamente aceitavél ou o solvato deste, composição farmacêutica, medicamento agonista de gpr40, agente promotor da secreção de insulina ou um agente hipoglicêmico, uso do composto espíro, o sal deste farmaceuticamente aceitavél ou o solvato deste, e, métodos para a ativação de gpr40, para promover secreção de insulina ou diminuir o nível de glicose sanguínea, e para tratar ou prevenir uma doença. |
| WO2009055932A1 (en) * | 2007-11-02 | 2009-05-07 | Prometic Biosciences Inc. | Substituted phenylpropionic acids as stimulators of hematopoiesis and erythropoiesis |
| JP2011504505A (ja) | 2007-11-21 | 2011-02-10 | デコード ジェネティクス イーエイチエフ | 肺および心血管障害を治療するためのビアリールｐｄｅ４抑制剤 |
| WO2009111056A1 (en) * | 2008-03-06 | 2009-09-11 | Amgen Inc. | Conformationally constrained carboxylic acid derivatives useful for treating metabolic disorders |
| US8633245B2 (en) * | 2008-04-11 | 2014-01-21 | Institute Of Medicinal Molecular Design, Inc. | PAI-1 inhibitor |
| EP2272817A4 (en) * | 2008-04-11 | 2011-12-14 | Inst Med Molecular Design Inc | PAI-1 INHIBITORS |
| KR20110027657A (ko) * | 2008-06-25 | 2011-03-16 | 다이이찌 산쿄 가부시키가이샤 | 카르복실산 화합물 |
| JP2012503595A (ja) | 2008-07-28 | 2012-02-09 | シダンスク ユニバーシティ | 代謝病の治療用の化合物 |
| AU2009303475B2 (en) | 2008-10-15 | 2012-09-13 | Amgen Inc. | Spirocyclic GPR40 modulators |
| EA022417B1 (ru) * | 2008-10-21 | 2015-12-30 | Саймабэй Терапевтикс, Инк. | Арильные агонисты рецептора gpr120 и их применение |
| AR074760A1 (es) | 2008-12-18 | 2011-02-09 | Metabolex Inc | Agonistas del receptor gpr120 y usos de los mismos en medicamentos para el tratamiento de diabetes y el sindrome metabolico. |
| JP2012136438A (ja) * | 2009-04-22 | 2012-07-19 | Astellas Pharma Inc | テトラゾール化合物 |
| AR078522A1 (es) | 2009-10-15 | 2011-11-16 | Lilly Co Eli | Compuesto de espiropiperidina, composicion farmaceutica que lo comprende, su uso para preparar un medicamento util para tratar diabetes y compuesto intermediario para su sintesis |
| DE102009046115A1 (de) | 2009-10-28 | 2011-09-08 | Bayer Schering Pharma Aktiengesellschaft | Substituierte 3-Phenylpropansäuren und ihre Verwendung |
| AU2010312365A1 (en) | 2009-10-30 | 2012-06-07 | Mochida Pharmaceutical Co.,Ltd. | Novel 3-hydroxy-5-arylisoxazole derivative |
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| EP2332427A1 (en) | 2009-12-07 | 2011-06-15 | Nestec S.A. | low caloric fat replacers |
| CN104710381A (zh) | 2009-12-25 | 2015-06-17 | 持田制药株式会社 | 新的3-羟基-5-芳基异噻唑衍生物 |
| US8299117B2 (en) | 2010-06-16 | 2012-10-30 | Metabolex Inc. | GPR120 receptor agonists and uses thereof |
| 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 |
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- 2006-08-27 IL IL177717A patent/IL177717A0/en unknown
- 2006-09-13 MA MA29319A patent/MA28466B1/fr unknown
- 2006-09-20 CR CR8642A patent/CR8642A/es not_active Application Discontinuation
- 2006-09-26 NO NO20064362A patent/NO20064362L/no not_active Application Discontinuation
- 2006-09-27 EC EC2006006887A patent/ECSP066887A/es unknown
- 2006-09-27 IS IS8542A patent/IS8542A/is unknown
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