JP2009525340A5 - - Google Patents
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- Publication number
- JP2009525340A5 JP2009525340A5 JP2008553332A JP2008553332A JP2009525340A5 JP 2009525340 A5 JP2009525340 A5 JP 2009525340A5 JP 2008553332 A JP2008553332 A JP 2008553332A JP 2008553332 A JP2008553332 A JP 2008553332A JP 2009525340 A5 JP2009525340 A5 JP 2009525340A5
- Authority
- JP
- Japan
- Prior art keywords
- phenyl
- imidazol
- biphenyl
- dioxide
- ylmethyl
- 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
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- -1 1-propyl-butyl Chemical group 0.000 claims 27
- 125000000217 alkyl group Chemical group 0.000 claims 22
- 150000001875 compounds Chemical class 0.000 claims 16
- 150000003839 salts Chemical class 0.000 claims 13
- 229910052739 hydrogen Inorganic materials 0.000 claims 11
- 239000001257 hydrogen Substances 0.000 claims 11
- 239000008194 pharmaceutical composition Substances 0.000 claims 6
- 239000011734 sodium Substances 0.000 claims 6
- 125000004201 2,4-dichlorophenyl group Chemical group [H]C1=C([H])C(*)=C(Cl)C([H])=C1Cl 0.000 claims 5
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 claims 5
- 150000002431 hydrogen Chemical class 0.000 claims 5
- 229910052708 sodium Inorganic materials 0.000 claims 5
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 4
- 239000003085 diluting agent Substances 0.000 claims 4
- 239000003814 drug Substances 0.000 claims 4
- 239000003937 drug carrier Substances 0.000 claims 4
- 239000000203 mixture Substances 0.000 claims 4
- 239000000546 pharmaceutical excipient Substances 0.000 claims 4
- ROPVMNGPSLXSCA-UHFFFAOYSA-N 5-[3-[2-[[4-(4-cyclohexylphenyl)phenyl]methyl]-4-(2,4-dichlorophenyl)imidazol-1-yl]phenyl]-1,1-dioxo-1,2,5-thiadiazolidin-3-one Chemical compound ClC1=CC(Cl)=CC=C1C1=CN(C=2C=C(C=CC=2)N2S(NC(=O)C2)(=O)=O)C(CC=2C=CC(=CC=2)C=2C=CC(=CC=2)C2CCCCC2)=N1 ROPVMNGPSLXSCA-UHFFFAOYSA-N 0.000 claims 3
- 201000010099 disease Diseases 0.000 claims 3
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims 3
- XAEFZNCEHLXOMS-UHFFFAOYSA-M potassium benzoate Chemical compound [K+].[O-]C(=O)C1=CC=CC=C1 XAEFZNCEHLXOMS-UHFFFAOYSA-M 0.000 claims 3
- 102000018997 Growth Hormone Human genes 0.000 claims 2
- 108010051696 Growth Hormone Proteins 0.000 claims 2
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 claims 2
- 125000002947 alkylene group Chemical group 0.000 claims 2
- 125000001309 chloro group Chemical group Cl* 0.000 claims 2
- 125000001153 fluoro group Chemical group F* 0.000 claims 2
- 239000000122 growth hormone Substances 0.000 claims 2
- 125000001188 haloalkyl group Chemical group 0.000 claims 2
- 229910052736 halogen Inorganic materials 0.000 claims 2
- 208000026278 immune system disease Diseases 0.000 claims 2
- 150000002500 ions Chemical class 0.000 claims 2
- 238000004519 manufacturing process Methods 0.000 claims 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 2
- 229910052700 potassium Inorganic materials 0.000 claims 2
- 239000011591 potassium Substances 0.000 claims 2
- 125000000008 (C1-C10) alkyl group Chemical group 0.000 claims 1
- OQTHCHRSZIOATC-UHFFFAOYSA-N 5-[3-[2-[[4-(4-cyclohexylphenyl)phenyl]methyl]-4-(2,6-dichlorophenyl)imidazol-1-yl]phenyl]-1,1-dioxo-1,2,5-thiadiazolidin-3-one Chemical compound ClC1=CC=CC(Cl)=C1C1=CN(C=2C=C(C=CC=2)N2S(NC(=O)C2)(=O)=O)C(CC=2C=CC(=CC=2)C=2C=CC(=CC=2)C2CCCCC2)=N1 OQTHCHRSZIOATC-UHFFFAOYSA-N 0.000 claims 1
- LGRJRZLTNCHYCZ-UHFFFAOYSA-N 5-[3-[2-[[4-(4-tert-butylphenyl)phenyl]methyl]-4-(2,4-dichlorophenyl)imidazol-1-yl]phenyl]-1,1-dioxo-1,2,5-thiadiazolidin-3-one Chemical compound C1=CC(C(C)(C)C)=CC=C1C(C=C1)=CC=C1CC1=NC(C=2C(=CC(Cl)=CC=2)Cl)=CN1C1=CC=CC(N2S(NC(=O)C2)(=O)=O)=C1 LGRJRZLTNCHYCZ-UHFFFAOYSA-N 0.000 claims 1
- VBLWWOMBXNGELX-UHFFFAOYSA-N 5-[3-[2-[[4-[3-(2-cyclohexylethyl)phenyl]phenyl]methyl]-4-(2,4-dichlorophenyl)imidazol-1-yl]phenyl]-1,1-dioxo-1,2,5-thiadiazolidin-3-one Chemical compound ClC1=CC(Cl)=CC=C1C1=CN(C=2C=C(C=CC=2)N2S(NC(=O)C2)(=O)=O)C(CC=2C=CC(=CC=2)C=2C=C(CCC3CCCCC3)C=CC=2)=N1 VBLWWOMBXNGELX-UHFFFAOYSA-N 0.000 claims 1
- TXYJDNWZUTXIEW-UHFFFAOYSA-N 5-[3-[2-[[4-[3-(2-cyclohexylethylsulfanyl)phenyl]phenyl]methyl]-4-(2,4-dichlorophenyl)imidazol-1-yl]phenyl]-1,1-dioxo-1,2,5-thiadiazolidin-3-one Chemical compound ClC1=CC(Cl)=CC=C1C1=CN(C=2C=C(C=CC=2)N2S(NC(=O)C2)(=O)=O)C(CC=2C=CC(=CC=2)C=2C=C(SCCC3CCCCC3)C=CC=2)=N1 TXYJDNWZUTXIEW-UHFFFAOYSA-N 0.000 claims 1
- BIIHQKKOUVZRBW-UHFFFAOYSA-N 5-[3-[2-[[4-[3-(2-cyclohexylethylsulfonyl)phenyl]phenyl]methyl]-4-(2,4-dichlorophenyl)imidazol-1-yl]phenyl]-1,1-dioxo-1,2,5-thiadiazolidin-3-one Chemical compound ClC1=CC(Cl)=CC=C1C1=CN(C=2C=C(C=CC=2)N2S(NC(=O)C2)(=O)=O)C(CC=2C=CC(=CC=2)C=2C=C(C=CC=2)S(=O)(=O)CCC2CCCCC2)=N1 BIIHQKKOUVZRBW-UHFFFAOYSA-N 0.000 claims 1
- UKRPUOPDTNRJGU-UHFFFAOYSA-N 5-[3-[2-[[4-[3-(cyclohexylmethoxy)phenyl]phenyl]methyl]-4-(2,4-dichlorophenyl)imidazol-1-yl]phenyl]-1,1-dioxo-1,2,5-thiadiazolidin-3-one Chemical compound ClC1=CC(Cl)=CC=C1C1=CN(C=2C=C(C=CC=2)N2S(NC(=O)C2)(=O)=O)C(CC=2C=CC(=CC=2)C=2C=C(OCC3CCCCC3)C=CC=2)=N1 UKRPUOPDTNRJGU-UHFFFAOYSA-N 0.000 claims 1
- VZWHFHHFCFNSAG-UHFFFAOYSA-N 5-[3-[2-[[4-[3-(cyclohexylmethoxy)phenyl]phenyl]methyl]-4-(2,6-dichlorophenyl)imidazol-1-yl]phenyl]-1,1-dioxo-1,2,5-thiadiazolidin-3-one Chemical compound ClC1=CC=CC(Cl)=C1C1=CN(C=2C=C(C=CC=2)N2S(NC(=O)C2)(=O)=O)C(CC=2C=CC(=CC=2)C=2C=C(OCC3CCCCC3)C=CC=2)=N1 VZWHFHHFCFNSAG-UHFFFAOYSA-N 0.000 claims 1
- UFYGBSOSGMSRFG-UHFFFAOYSA-N 5-[3-[2-[[4-[3-(cyclohexylmethylsulfanyl)phenyl]phenyl]methyl]-4-(2,4-dichlorophenyl)imidazol-1-yl]phenyl]-1,1-dioxo-1,2,5-thiadiazolidin-3-one Chemical compound ClC1=CC(Cl)=CC=C1C1=CN(C=2C=C(C=CC=2)N2S(NC(=O)C2)(=O)=O)C(CC=2C=CC(=CC=2)C=2C=C(SCC3CCCCC3)C=CC=2)=N1 UFYGBSOSGMSRFG-UHFFFAOYSA-N 0.000 claims 1
- RNLJJRIMAAXDKB-UHFFFAOYSA-N 5-[3-[2-[[4-[3-(cyclohexylmethylsulfonyl)phenyl]phenyl]methyl]-4-(2,4-dichlorophenyl)imidazol-1-yl]phenyl]-1,1-dioxo-1,2,5-thiadiazolidin-3-one Chemical compound ClC1=CC(Cl)=CC=C1C1=CN(C=2C=C(C=CC=2)N2S(NC(=O)C2)(=O)=O)C(CC=2C=CC(=CC=2)C=2C=C(C=CC=2)S(=O)(=O)CC2CCCCC2)=N1 RNLJJRIMAAXDKB-UHFFFAOYSA-N 0.000 claims 1
- CLICTJKGRVHEPA-UHFFFAOYSA-N 5-[3-[2-[[4-[4-(cyclohexylmethoxy)phenyl]phenyl]methyl]-4-(2,4-dichlorophenyl)imidazol-1-yl]phenyl]-1,1-dioxo-1,2,5-thiadiazolidin-3-one Chemical compound ClC1=CC(Cl)=CC=C1C1=CN(C=2C=C(C=CC=2)N2S(NC(=O)C2)(=O)=O)C(CC=2C=CC(=CC=2)C=2C=CC(OCC3CCCCC3)=CC=2)=N1 CLICTJKGRVHEPA-UHFFFAOYSA-N 0.000 claims 1
- BHLLGPUOHKTNMM-UHFFFAOYSA-N 5-[3-[2-[[4-[4-(cyclohexylmethylsulfanyl)phenyl]phenyl]methyl]-4-(2,4-dichlorophenyl)imidazol-1-yl]phenyl]-1,1-dioxo-1,2,5-thiadiazolidin-3-one Chemical compound ClC1=CC(Cl)=CC=C1C1=CN(C=2C=C(C=CC=2)N2S(NC(=O)C2)(=O)=O)C(CC=2C=CC(=CC=2)C=2C=CC(SCC3CCCCC3)=CC=2)=N1 BHLLGPUOHKTNMM-UHFFFAOYSA-N 0.000 claims 1
- LNIFSZOACJPILF-UHFFFAOYSA-N 5-[3-[2-[[4-[4-(cyclohexylmethylsulfonyl)phenyl]phenyl]methyl]-4-(2,4-dichlorophenyl)imidazol-1-yl]phenyl]-1,1-dioxo-1,2,5-thiadiazolidin-3-one Chemical compound ClC1=CC(Cl)=CC=C1C1=CN(C=2C=C(C=CC=2)N2S(NC(=O)C2)(=O)=O)C(CC=2C=CC(=CC=2)C=2C=CC(=CC=2)S(=O)(=O)CC2CCCCC2)=N1 LNIFSZOACJPILF-UHFFFAOYSA-N 0.000 claims 1
- CENWRJLRKOPSID-UHFFFAOYSA-N 5-[3-[4-(2,4-dichlorophenyl)-2-[[4-[3-(3,3-dimethylbutoxy)phenyl]phenyl]methyl]imidazol-1-yl]phenyl]-1,1-dioxo-1,2,5-thiadiazolidin-3-one Chemical compound CC(C)(C)CCOC1=CC=CC(C=2C=CC(CC=3N(C=C(N=3)C=3C(=CC(Cl)=CC=3)Cl)C=3C=C(C=CC=3)N3S(NC(=O)C3)(=O)=O)=CC=2)=C1 CENWRJLRKOPSID-UHFFFAOYSA-N 0.000 claims 1
- BHRVRCUAQMSZBF-UHFFFAOYSA-N 5-[3-[4-(2,4-dichlorophenyl)-2-[[4-[3-(3,3-dimethylbutylsulfonyl)phenyl]phenyl]methyl]imidazol-1-yl]phenyl]-1,1-dioxo-1,2,5-thiadiazolidin-3-one Chemical compound CC(C)(C)CCS(=O)(=O)C1=CC=CC(C=2C=CC(CC=3N(C=C(N=3)C=3C(=CC(Cl)=CC=3)Cl)C=3C=C(C=CC=3)N3S(NC(=O)C3)(=O)=O)=CC=2)=C1 BHRVRCUAQMSZBF-UHFFFAOYSA-N 0.000 claims 1
- QVNJMALMSISSON-UHFFFAOYSA-N 5-[3-[4-(2,4-dichlorophenyl)-2-[[4-[4-(3,3-dimethylbutoxy)phenyl]phenyl]methyl]imidazol-1-yl]phenyl]-1,1-dioxo-1,2,5-thiadiazolidin-3-one Chemical compound C1=CC(OCCC(C)(C)C)=CC=C1C(C=C1)=CC=C1CC1=NC(C=2C(=CC(Cl)=CC=2)Cl)=CN1C1=CC=CC(N2S(NC(=O)C2)(=O)=O)=C1 QVNJMALMSISSON-UHFFFAOYSA-N 0.000 claims 1
- JVKJRJRAQPIGEN-UHFFFAOYSA-N 5-[3-[4-(2,4-dichlorophenyl)-2-[[4-[4-(4,4-dimethylpent-1-enyl)phenyl]phenyl]methyl]imidazol-1-yl]phenyl]-1,1-dioxo-1,2,5-thiadiazolidin-3-one Chemical compound C1=CC(C=CCC(C)(C)C)=CC=C1C(C=C1)=CC=C1CC1=NC(C=2C(=CC(Cl)=CC=2)Cl)=CN1C1=CC=CC(N2S(NC(=O)C2)(=O)=O)=C1 JVKJRJRAQPIGEN-UHFFFAOYSA-N 0.000 claims 1
- AUIVFJGHRNVUJX-UHFFFAOYSA-N 5-[3-[4-(2,4-difluorophenyl)-2-[[4-[3-(3,3-dimethylbutylsulfanyl)phenyl]phenyl]methyl]imidazol-1-yl]phenyl]-1,1-dioxo-1,2,5-thiadiazolidin-3-one Chemical compound CC(C)(C)CCSC1=CC=CC(C=2C=CC(CC=3N(C=C(N=3)C=3C(=CC(F)=CC=3)F)C=3C=C(C=CC=3)N3S(NC(=O)C3)(=O)=O)=CC=2)=C1 AUIVFJGHRNVUJX-UHFFFAOYSA-N 0.000 claims 1
- WQCYRBPCQQVFHZ-UHFFFAOYSA-N 5-[3-[4-(2,4-difluorophenyl)-2-[[4-[3-(3,3-dimethylbutylsulfonyl)phenyl]phenyl]methyl]imidazol-1-yl]phenyl]-1,1-dioxo-1,2,5-thiadiazolidin-3-one Chemical compound CC(C)(C)CCS(=O)(=O)C1=CC=CC(C=2C=CC(CC=3N(C=C(N=3)C=3C(=CC(F)=CC=3)F)C=3C=C(C=CC=3)N3S(NC(=O)C3)(=O)=O)=CC=2)=C1 WQCYRBPCQQVFHZ-UHFFFAOYSA-N 0.000 claims 1
- DDJIWAOSGFQYIE-UHFFFAOYSA-N 5-[3-[4-(2,6-dichlorophenyl)-2-[[4-[3-(3,3-dimethylbutoxy)phenyl]phenyl]methyl]imidazol-1-yl]phenyl]-1,1-dioxo-1,2,5-thiadiazolidin-3-one Chemical compound CC(C)(C)CCOC1=CC=CC(C=2C=CC(CC=3N(C=C(N=3)C=3C(=CC=CC=3Cl)Cl)C=3C=C(C=CC=3)N3S(NC(=O)C3)(=O)=O)=CC=2)=C1 DDJIWAOSGFQYIE-UHFFFAOYSA-N 0.000 claims 1
- YXBVPYFFVRAQCP-UHFFFAOYSA-N 5-[5-[2-[[4-(4-cyclohexylphenyl)phenyl]methyl]-4-(2,4-dichlorophenyl)imidazol-1-yl]-2-methoxyphenyl]-1,1-dioxo-1,2,5-thiadiazolidin-3-one Chemical compound COC1=CC=C(N2C(=NC(=C2)C=2C(=CC(Cl)=CC=2)Cl)CC=2C=CC(=CC=2)C=2C=CC(=CC=2)C2CCCCC2)C=C1N1CC(=O)NS1(=O)=O YXBVPYFFVRAQCP-UHFFFAOYSA-N 0.000 claims 1
- 208000030507 AIDS Diseases 0.000 claims 1
- 208000024827 Alzheimer disease Diseases 0.000 claims 1
- 208000023275 Autoimmune disease Diseases 0.000 claims 1
- 208000035473 Communicable disease Diseases 0.000 claims 1
- 102000004127 Cytokines Human genes 0.000 claims 1
- 108090000695 Cytokines Proteins 0.000 claims 1
- 208000002705 Glucose Intolerance Diseases 0.000 claims 1
- 206010018429 Glucose tolerance impaired Diseases 0.000 claims 1
- 206010028980 Neoplasm Diseases 0.000 claims 1
- 206010067584 Type 1 diabetes mellitus Diseases 0.000 claims 1
- 125000003342 alkenyl group Chemical group 0.000 claims 1
- 125000005275 alkylenearyl group Chemical group 0.000 claims 1
- 208000026935 allergic disease Diseases 0.000 claims 1
- 125000003118 aryl group Chemical group 0.000 claims 1
- 230000015572 biosynthetic process Effects 0.000 claims 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims 1
- 201000011510 cancer Diseases 0.000 claims 1
- 125000000753 cycloalkyl group Chemical group 0.000 claims 1
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 claims 1
- 125000004210 cyclohexylmethyl group Chemical group [H]C([H])(*)C1([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C1([H])[H] 0.000 claims 1
- 125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 claims 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 1
- 239000003102 growth factor Substances 0.000 claims 1
- 125000001072 heteroaryl group Chemical group 0.000 claims 1
- 125000000623 heterocyclic group Chemical group 0.000 claims 1
- 125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims 1
- 208000027866 inflammatory disease Diseases 0.000 claims 1
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 claims 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims 1
- 238000000034 method Methods 0.000 claims 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 1
- 125000003538 pentan-3-yl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])C([H])([H])[H] 0.000 claims 1
- 125000001147 pentyl group Chemical group C(CCCC)* 0.000 claims 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 claims 1
- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims 1
- 125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 claims 1
- 208000024891 symptom Diseases 0.000 claims 1
- 238000003786 synthesis reaction Methods 0.000 claims 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 claims 1
- 125000000876 trifluoromethoxy group Chemical group FC(F)(F)O* 0.000 claims 1
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims 1
- 208000001072 type 2 diabetes mellitus Diseases 0.000 claims 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US76325606P | 2006-01-30 | 2006-01-30 | |
| US60/763,256 | 2006-01-30 | ||
| PCT/US2007/002675 WO2007089857A2 (en) | 2006-01-30 | 2007-01-30 | Substituted imidazole derivatives and their use as ptpase inhibitors |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2009525340A JP2009525340A (ja) | 2009-07-09 |
| JP2009525340A5 true JP2009525340A5 (enExample) | 2010-03-18 |
| JP5180099B2 JP5180099B2 (ja) | 2013-04-10 |
Family
ID=38042619
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2008553332A Expired - Fee Related JP5180099B2 (ja) | 2006-01-30 | 2007-01-30 | 置換イミダゾール誘導体、組成物ならびにｐｔｐアーゼ阻害剤としての使用方法 |
Country Status (13)
| Country | Link |
|---|---|
| US (3) | US7723369B2 (enExample) |
| EP (1) | EP1991544B1 (enExample) |
| JP (1) | JP5180099B2 (enExample) |
| KR (1) | KR20080094806A (enExample) |
| CN (1) | CN101374835B (enExample) |
| AU (1) | AU2007211319B9 (enExample) |
| BR (1) | BRPI0707338A2 (enExample) |
| CA (1) | CA2637024C (enExample) |
| EA (1) | EA019385B1 (enExample) |
| IL (1) | IL192557A (enExample) |
| NZ (1) | NZ569329A (enExample) |
| WO (1) | WO2007089857A2 (enExample) |
| ZA (1) | ZA200805648B (enExample) |
Families Citing this family (23)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AU2005214349B2 (en) * | 2004-02-12 | 2011-11-03 | Transtech Pharma, Inc. | Substituted azole derivatives, compositions, and methods of use |
| BRPI0707338A2 (pt) * | 2006-01-30 | 2011-05-03 | Transtech Pharma Inc | derivados de imidazol, composições, e métodos substituìdos de uso como inibidores de ptpase |
| JP2012529432A (ja) | 2009-06-05 | 2012-11-22 | リンク・メディスン・コーポレーション | アミノピロリジノン誘導体及びその使用 |
| JPWO2011007819A1 (ja) | 2009-07-17 | 2012-12-27 | 塩野義製薬株式会社 | ラクタムまたはベンゼンスルホンアミド化合物を含有する医薬 |
| JP5398076B2 (ja) * | 2009-12-10 | 2014-01-29 | 四国化成工業株式会社 | ２−（ブロモベンジル）−４−（ブロモフェニル）−５−メチルイミダゾール化合物 |
| JP5398075B2 (ja) * | 2010-01-13 | 2014-01-29 | 四国化成工業株式会社 | ４−（ジクロロフェニル）−２−（４−フルオロベンジル）−５−メチルイミダゾール化合物 |
| KR101898610B1 (ko) | 2010-08-31 | 2018-09-14 | 서울대학교산학협력단 | ＰＰＡＲδ 활성물질의 태자 재프로그래밍 용도 |
| US9040525B2 (en) | 2010-10-08 | 2015-05-26 | Mochida Pharmaceutical Co., Ltd. | Cyclic amide derivative |
| WO2012094580A2 (en) | 2011-01-07 | 2012-07-12 | High Point Pharmaceuticals, Llc | Compounds that modulate oxidative stress |
| WO2012147516A1 (ja) | 2011-04-28 | 2012-11-01 | 持田製薬株式会社 | 環状アミド誘導体 |
| US10696642B2 (en) | 2015-09-23 | 2020-06-30 | The General Hospital Corporation | TEAD transcription factor autopalmitoylation inhibitors |
| MA52648A (fr) | 2015-10-07 | 2021-10-13 | Mitobridge Inc | Agonistes de ppar, composés, compositions pharmaceutiques et leurs procédés d'utilisation |
| JP6925367B2 (ja) * | 2016-04-13 | 2021-08-25 | ミトブリッジ，インコーポレーテッド | Ｐｐａｒアゴニスト、化合物、医薬組成物、及びその使用方法 |
| HUE057838T2 (hu) | 2016-06-07 | 2022-06-28 | Jacobio Pharmaceuticals Co Ltd | SHP2 inhibitorokként hasznos új heterociklusos származékok |
| TWI664175B (zh) | 2017-03-23 | 2019-07-01 | 大陸商北京加科思新藥研發有限公司 | 用於作為shp2抑制劑之新穎雜環衍生物 |
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