JP2005526028A5 - - Google Patents
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- Publication number
- JP2005526028A5 JP2005526028A5 JP2003566002A JP2003566002A JP2005526028A5 JP 2005526028 A5 JP2005526028 A5 JP 2005526028A5 JP 2003566002 A JP2003566002 A JP 2003566002A JP 2003566002 A JP2003566002 A JP 2003566002A JP 2005526028 A5 JP2005526028 A5 JP 2005526028A5
- Authority
- JP
- Japan
- Prior art keywords
- aliphatic
- ring
- benzimidazol
- optionally substituted
- halo
- 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
- 125000001931 aliphatic group Chemical group 0.000 claims description 128
- 229910052739 hydrogen Inorganic materials 0.000 claims description 33
- 229910052736 halogen Inorganic materials 0.000 claims description 19
- 150000002367 halogens Chemical class 0.000 claims description 19
- 239000001257 hydrogen Substances 0.000 claims description 19
- 125000001072 heteroaryl group Chemical group 0.000 claims description 13
- 125000000217 alkyl group Chemical group 0.000 claims description 12
- 125000001424 substituent group Chemical group 0.000 claims description 12
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 7
- 125000003118 aryl group Chemical group 0.000 claims description 5
- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims 40
- 229910052757 nitrogen Inorganic materials 0.000 claims 27
- 125000005843 halogen group Chemical group 0.000 claims 26
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims 17
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims 17
- 125000005842 heteroatom Chemical group 0.000 claims 17
- 239000000203 mixture Substances 0.000 claims 17
- 229910052760 oxygen Inorganic materials 0.000 claims 17
- 239000001301 oxygen Chemical group 0.000 claims 17
- 229910052717 sulfur Chemical group 0.000 claims 17
- 239000011593 sulfur Chemical group 0.000 claims 17
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 claims 14
- 150000001875 compounds Chemical class 0.000 claims 13
- 125000000623 heterocyclic group Chemical group 0.000 claims 13
- -1 1,2-methylenedioxy Chemical group 0.000 claims 12
- 125000001118 alkylidene group Chemical group 0.000 claims 12
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 12
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims 7
- 125000000325 methylidene group Chemical group [H]C([H])=* 0.000 claims 6
- 150000003839 salts Chemical class 0.000 claims 6
- 125000006570 (C5-C6) heteroaryl group Chemical group 0.000 claims 5
- 150000002431 hydrogen Chemical class 0.000 claims 5
- CMDJAJYFXCBMBU-UHFFFAOYSA-N 2-[2-(4-amino-1,2,5-oxadiazol-3-yl)benzimidazol-1-yl]-n-(2-fluorophenyl)acetamide Chemical compound NC1=NON=C1C1=NC2=CC=CC=C2N1CC(=O)NC1=CC=CC=C1F CMDJAJYFXCBMBU-UHFFFAOYSA-N 0.000 claims 4
- 125000003341 7 membered heterocyclic group Chemical group 0.000 claims 4
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 claims 4
- 206010012601 diabetes mellitus Diseases 0.000 claims 4
- 229920006395 saturated elastomer Polymers 0.000 claims 4
- 208000024891 symptom Diseases 0.000 claims 3
- GLQIZLCZHSQBLY-UHFFFAOYSA-N 2-(1h-benzimidazol-2-yl)-4-chloroaniline Chemical compound NC1=CC=C(Cl)C=C1C1=NC2=CC=CC=C2N1 GLQIZLCZHSQBLY-UHFFFAOYSA-N 0.000 claims 2
- OIIBRYKPFULYFU-UHFFFAOYSA-N 2-[2-(4-amino-1,2,5-oxadiazol-3-yl)benzimidazol-1-yl]-n-(2,6-dimethylphenyl)acetamide Chemical compound CC1=CC=CC(C)=C1NC(=O)CN1C2=CC=CC=C2N=C1C1=NON=C1N OIIBRYKPFULYFU-UHFFFAOYSA-N 0.000 claims 2
- RKDKILJBYDCMPH-UHFFFAOYSA-N 2-[2-(4-amino-1,2,5-oxadiazol-3-yl)benzimidazol-1-yl]-n-(3,4-difluorophenyl)acetamide Chemical compound NC1=NON=C1C1=NC2=CC=CC=C2N1CC(=O)NC1=CC=C(F)C(F)=C1 RKDKILJBYDCMPH-UHFFFAOYSA-N 0.000 claims 2
- CLAATNFGGLOUTN-UHFFFAOYSA-N 2-[2-(4-amino-1,2,5-oxadiazol-3-yl)benzimidazol-1-yl]-n-(3,4-dimethoxyphenyl)acetamide Chemical compound C1=C(OC)C(OC)=CC=C1NC(=O)CN1C2=CC=CC=C2N=C1C1=NON=C1N CLAATNFGGLOUTN-UHFFFAOYSA-N 0.000 claims 2
- IBQVTCXZQBZBDN-UHFFFAOYSA-N 2-[2-(4-amino-1,2,5-oxadiazol-3-yl)benzimidazol-1-yl]-n-(3-fluorophenyl)acetamide Chemical compound NC1=NON=C1C1=NC2=CC=CC=C2N1CC(=O)NC1=CC=CC(F)=C1 IBQVTCXZQBZBDN-UHFFFAOYSA-N 0.000 claims 2
- MZAJMJXYFARZRU-UHFFFAOYSA-N 2-[2-(4-amino-1,2,5-oxadiazol-3-yl)benzimidazol-1-yl]-n-[2-(trifluoromethyl)phenyl]acetamide Chemical compound NC1=NON=C1C1=NC2=CC=CC=C2N1CC(=O)NC1=CC=CC=C1C(F)(F)F MZAJMJXYFARZRU-UHFFFAOYSA-N 0.000 claims 2
- DLHZNLYFGBAMAP-UHFFFAOYSA-N 2-[2-(4-amino-1,2,5-oxadiazol-3-yl)benzimidazol-1-yl]-n-tert-butylacetamide Chemical compound N=1C2=CC=CC=C2N(CC(=O)NC(C)(C)C)C=1C1=NON=C1N DLHZNLYFGBAMAP-UHFFFAOYSA-N 0.000 claims 2
- WVJHNSPIODGZJK-UHFFFAOYSA-N 2-[2-(4-amino-1,2,5-oxadiazol-3-yl)benzimidazol-1-yl]acetamide Chemical compound N=1C2=CC=CC=C2N(CC(=O)N)C=1C1=NON=C1N WVJHNSPIODGZJK-UHFFFAOYSA-N 0.000 claims 2
- VFLJHDYRDURZEP-UHFFFAOYSA-N 2-[2-(4-amino-1,2,5-oxadiazol-3-yl)benzimidazol-1-yl]acetic acid Chemical compound NC1=NON=C1C1=NC2=CC=CC=C2N1CC(O)=O VFLJHDYRDURZEP-UHFFFAOYSA-N 0.000 claims 2
- RSNMFVBZWSSWKA-UHFFFAOYSA-N 2-[2-(4-amino-1,2,5-oxadiazol-3-yl)benzimidazol-1-yl]acetonitrile Chemical compound NC1=NON=C1C1=NC2=CC=CC=C2N1CC#N RSNMFVBZWSSWKA-UHFFFAOYSA-N 0.000 claims 2
- PZFLXZUSYPMQHT-UHFFFAOYSA-N 2-[[2-(4-amino-1,2,5-oxadiazol-3-yl)benzimidazol-1-yl]methyl]benzonitrile Chemical compound NC1=NON=C1C1=NC2=CC=CC=C2N1CC1=CC=CC=C1C#N PZFLXZUSYPMQHT-UHFFFAOYSA-N 0.000 claims 2
- HCRQPXYLXXLKPT-UHFFFAOYSA-N 4-(1-ethylbenzimidazol-2-yl)-1,2,5-oxadiazol-3-amine Chemical compound N=1C2=CC=CC=C2N(CC)C=1C1=NON=C1N HCRQPXYLXXLKPT-UHFFFAOYSA-N 0.000 claims 2
- ZIHIDNWPEZFEMR-UHFFFAOYSA-N 4-(1-methylbenzimidazol-2-yl)-1,2,5-oxadiazol-3-amine Chemical compound N=1C2=CC=CC=C2N(C)C=1C1=NON=C1N ZIHIDNWPEZFEMR-UHFFFAOYSA-N 0.000 claims 2
- BKGOWPYQEFOGAO-UHFFFAOYSA-N 4-(1-prop-2-ynylbenzimidazol-2-yl)-1,2,5-oxadiazol-3-amine Chemical compound NC1=NON=C1C1=NC2=CC=CC=C2N1CC#C BKGOWPYQEFOGAO-UHFFFAOYSA-N 0.000 claims 2
- OOQLAKYHQPZMKP-UHFFFAOYSA-N 4-(1-propan-2-ylbenzimidazol-2-yl)-1,2,5-oxadiazol-3-amine Chemical compound N=1C2=CC=CC=C2N(C(C)C)C=1C1=NON=C1N OOQLAKYHQPZMKP-UHFFFAOYSA-N 0.000 claims 2
- UZZWGLMVBYGQSK-UHFFFAOYSA-N 4-(1-propylbenzimidazol-2-yl)-1,2,5-oxadiazol-3-amine Chemical compound N=1C2=CC=CC=C2N(CCC)C=1C1=NON=C1N UZZWGLMVBYGQSK-UHFFFAOYSA-N 0.000 claims 2
- PAMMUBFLEAQXAD-UHFFFAOYSA-N 4-(6-methyl-1H-benzimidazol-2-yl)-1,2,5-oxadiazol-3-amine Chemical compound N=1C2=CC(C)=CC=C2NC=1C1=NON=C1N PAMMUBFLEAQXAD-UHFFFAOYSA-N 0.000 claims 2
- KNJOGMJHNSVZCC-UHFFFAOYSA-N 4-[1-(2h-tetrazol-5-ylmethyl)benzimidazol-2-yl]-1,2,5-oxadiazol-3-amine Chemical compound NC1=NON=C1C1=NC2=CC=CC=C2N1CC1=NNN=N1 KNJOGMJHNSVZCC-UHFFFAOYSA-N 0.000 claims 2
- LLDVRUBUBPSOMY-UHFFFAOYSA-N 4-[1-(cyclopropylmethyl)benzimidazol-2-yl]-1,2,5-oxadiazol-3-amine Chemical compound NC1=NON=C1C1=NC2=CC=CC=C2N1CC1CC1 LLDVRUBUBPSOMY-UHFFFAOYSA-N 0.000 claims 2
- ROJIDUVOWRJHNV-UHFFFAOYSA-N 4-[1-[(2,4-dichlorophenyl)methyl]benzimidazol-2-yl]-1,2,5-oxadiazol-3-amine Chemical compound NC1=NON=C1C1=NC2=CC=CC=C2N1CC1=CC=C(Cl)C=C1Cl ROJIDUVOWRJHNV-UHFFFAOYSA-N 0.000 claims 2
- GXKYZANVBKVGOS-UHFFFAOYSA-N 4-[1-[(2,6-dichlorophenyl)methyl]benzimidazol-2-yl]-1,2,5-oxadiazol-3-amine Chemical compound NC1=NON=C1C1=NC2=CC=CC=C2N1CC1=C(Cl)C=CC=C1Cl GXKYZANVBKVGOS-UHFFFAOYSA-N 0.000 claims 2
- CPRADZBJYGDHHF-UHFFFAOYSA-N 4-[1-[(2-chloro-6-fluorophenyl)methyl]benzimidazol-2-yl]-1,2,5-oxadiazol-3-amine Chemical compound NC1=NON=C1C1=NC2=CC=CC=C2N1CC1=C(F)C=CC=C1Cl CPRADZBJYGDHHF-UHFFFAOYSA-N 0.000 claims 2
- HIUITJWNRMJIBF-UHFFFAOYSA-N 4-[1-[(2-methylphenyl)methyl]benzimidazol-2-yl]-1,2,5-oxadiazol-3-amine Chemical compound CC1=CC=CC=C1CN1C2=CC=CC=C2N=C1C1=NON=C1N HIUITJWNRMJIBF-UHFFFAOYSA-N 0.000 claims 2
- VHBPIHGCMKHKLE-UHFFFAOYSA-N 4-[1-[(3,4-dichlorophenyl)methyl]benzimidazol-2-yl]-1,2,5-oxadiazol-3-amine Chemical compound NC1=NON=C1C1=NC2=CC=CC=C2N1CC1=CC=C(Cl)C(Cl)=C1 VHBPIHGCMKHKLE-UHFFFAOYSA-N 0.000 claims 2
- NSIJURZMDSCFBL-UHFFFAOYSA-N 4-[1-[(3-bromophenyl)methyl]benzimidazol-2-yl]-1,2,5-oxadiazol-3-amine Chemical compound NC1=NON=C1C1=NC2=CC=CC=C2N1CC1=CC=CC(Br)=C1 NSIJURZMDSCFBL-UHFFFAOYSA-N 0.000 claims 2
- LAQLCMYZQGUKFA-UHFFFAOYSA-N 4-[1-[(4-chlorophenyl)methyl]benzimidazol-2-yl]-1,2,5-oxadiazol-3-amine Chemical compound NC1=NON=C1C1=NC2=CC=CC=C2N1CC1=CC=C(Cl)C=C1 LAQLCMYZQGUKFA-UHFFFAOYSA-N 0.000 claims 2
- ITWVPIOKFJWICI-UHFFFAOYSA-N 4-[1-[(4-methylphenyl)methyl]benzimidazol-2-yl]-1,2,5-oxadiazol-3-amine Chemical compound C1=CC(C)=CC=C1CN1C2=CC=CC=C2N=C1C1=NON=C1N ITWVPIOKFJWICI-UHFFFAOYSA-N 0.000 claims 2
- PQJCCZPMTJZYDF-UHFFFAOYSA-N 4-[2-(4-amino-1,2,5-oxadiazol-3-yl)benzimidazol-1-yl]butanenitrile Chemical compound NC1=NON=C1C1=NC2=CC=CC=C2N1CCCC#N PQJCCZPMTJZYDF-UHFFFAOYSA-N 0.000 claims 2
- PCNDJXKNXGMECE-UHFFFAOYSA-N Phenazine Natural products C1=CC=CC2=NC3=CC=CC=C3N=C21 PCNDJXKNXGMECE-UHFFFAOYSA-N 0.000 claims 2
- KYQCOXFCLRTKLS-UHFFFAOYSA-N Pyrazine Natural products C1=CN=CC=N1 KYQCOXFCLRTKLS-UHFFFAOYSA-N 0.000 claims 2
- 125000004423 acyloxy group Chemical group 0.000 claims 2
- 125000005605 benzo group Chemical group 0.000 claims 2
- QEPDSNAEMKSMGN-UHFFFAOYSA-N chembl1329127 Chemical compound NC1=NON=C1C1=NC2=CC=CC=C2N1 QEPDSNAEMKSMGN-UHFFFAOYSA-N 0.000 claims 2
- 125000003838 furazanyl group Chemical group 0.000 claims 2
- IKUGCHSAVSKMEA-UHFFFAOYSA-N n-[2-(1h-benzimidazol-2-yl)phenyl]acetamide Chemical compound CC(=O)NC1=CC=CC=C1C1=NC2=CC=CC=C2N1 IKUGCHSAVSKMEA-UHFFFAOYSA-N 0.000 claims 2
- VPCQBVROXHOCLQ-UHFFFAOYSA-N n-[2-(1h-benzimidazol-2-yl)phenyl]propanamide Chemical compound CCC(=O)NC1=CC=CC=C1C1=NC2=CC=CC=C2N1 VPCQBVROXHOCLQ-UHFFFAOYSA-N 0.000 claims 2
- LGXJGCZIHDEMDL-UHFFFAOYSA-N n-[4-(1-ethylbenzimidazol-2-yl)-1,2,5-oxadiazol-3-yl]-2,2,2-trifluoroacetamide Chemical compound N=1C2=CC=CC=C2N(CC)C=1C1=NON=C1NC(=O)C(F)(F)F LGXJGCZIHDEMDL-UHFFFAOYSA-N 0.000 claims 2
- XUYDLORMICPNES-UHFFFAOYSA-N n-[4-[1-(cyanomethyl)benzimidazol-2-yl]-1,2,5-oxadiazol-3-yl]acetamide Chemical compound CC(=O)NC1=NON=C1C1=NC2=CC=CC=C2N1CC#N XUYDLORMICPNES-UHFFFAOYSA-N 0.000 claims 2
- 125000003373 pyrazinyl group Chemical group 0.000 claims 2
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 claims 2
- 125000001544 thienyl group Chemical group 0.000 claims 2
- FAIVIYCNLYZSDO-UHFFFAOYSA-N 4-(1-benzylbenzimidazol-2-yl)-1,2,5-oxadiazol-3-amine Chemical compound NC1=NON=C1C1=NC2=CC=CC=C2N1CC1=CC=CC=C1 FAIVIYCNLYZSDO-UHFFFAOYSA-N 0.000 claims 1
- NYUVVVDGKCTKKF-UHFFFAOYSA-N 4-[1-(2-methylpropyl)benzimidazol-2-yl]-1,2,5-oxadiazol-3-amine Chemical compound N=1C2=CC=CC=C2N(CC(C)C)C=1C1=NON=C1N NYUVVVDGKCTKKF-UHFFFAOYSA-N 0.000 claims 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims 1
- 102000002254 Glycogen Synthase Kinase 3 Human genes 0.000 claims 1
- 108010014905 Glycogen Synthase Kinase 3 Proteins 0.000 claims 1
- 102000036243 Lymphocyte Specific Protein Tyrosine Kinase p56(lck) Human genes 0.000 claims 1
- 108010002481 Lymphocyte Specific Protein Tyrosine Kinase p56(lck) Proteins 0.000 claims 1
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims 1
- 239000012472 biological sample Substances 0.000 claims 1
- 229910052799 carbon Inorganic materials 0.000 claims 1
- 125000004186 cyclopropylmethyl group Chemical group [H]C([H])(*)C1([H])C([H])([H])C1([H])[H] 0.000 claims 1
- 201000010099 disease Diseases 0.000 claims 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims 1
- 239000003937 drug carrier Substances 0.000 claims 1
- MEXYDCGTNFLIOA-UHFFFAOYSA-N ethyl 2-[2-(4-amino-1,2,5-oxadiazol-3-yl)benzimidazol-1-yl]acetate Chemical compound N=1C2=CC=CC=C2N(CC(=O)OCC)C=1C1=NON=C1N MEXYDCGTNFLIOA-UHFFFAOYSA-N 0.000 claims 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 1
- 125000003037 imidazol-2-yl group Chemical group [H]N1C([*])=NC([H])=C1[H] 0.000 claims 1
- 230000002401 inhibitory effect Effects 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
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims 1
- OLGMRMJENRKJRP-UHFFFAOYSA-N n-[2-(1h-benzimidazol-2-yl)phenyl]-2-methylpropanamide Chemical compound CC(C)C(=O)NC1=CC=CC=C1C1=NC2=CC=CC=C2N1 OLGMRMJENRKJRP-UHFFFAOYSA-N 0.000 claims 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 claims 1
- 150000001721 carbon Chemical class 0.000 description 2
- 125000001475 halogen functional group Chemical group 0.000 description 2
- 125000006615 aromatic heterocyclic group Chemical group 0.000 description 1
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US35484302P | 2002-02-06 | 2002-02-06 | |
| PCT/US2003/003655 WO2003066629A2 (en) | 2002-02-06 | 2003-02-06 | Heteroaryl compounds useful as inhibitors of gsk-3 |
Related Child Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2010043557A Division JP2010132697A (ja) | 2002-02-06 | 2010-02-26 | Gsk−3の阻害剤として有用なヘテロアリール化合物 |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2005526028A JP2005526028A (ja) | 2005-09-02 |
| JP2005526028A5 true JP2005526028A5 (enExample) | 2011-01-06 |
| JP4656838B2 JP4656838B2 (ja) | 2011-03-23 |
Family
ID=27734431
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2003566002A Expired - Fee Related JP4656838B2 (ja) | 2002-02-06 | 2003-02-06 | Gsk−3の阻害剤として有用なヘテロアリール化合物 |
| JP2010043557A Pending JP2010132697A (ja) | 2002-02-06 | 2010-02-26 | Gsk−3の阻害剤として有用なヘテロアリール化合物 |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2010043557A Pending JP2010132697A (ja) | 2002-02-06 | 2010-02-26 | Gsk−3の阻害剤として有用なヘテロアリール化合物 |
Country Status (13)
| Country | Link |
|---|---|
| US (2) | US20040034037A1 (enExample) |
| EP (2) | EP2322521B1 (enExample) |
| JP (2) | JP4656838B2 (enExample) |
| KR (1) | KR20040084896A (enExample) |
| AU (1) | AU2003215087B2 (enExample) |
| CA (1) | CA2475633C (enExample) |
| ES (1) | ES2437391T3 (enExample) |
| MX (1) | MXPA04007697A (enExample) |
| NO (1) | NO20043726L (enExample) |
| PL (1) | PL372198A1 (enExample) |
| RU (1) | RU2004126671A (enExample) |
| SG (1) | SG159380A1 (enExample) |
| WO (1) | WO2003066629A2 (enExample) |
Families Citing this family (117)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DK1318997T3 (da) * | 2000-09-15 | 2006-09-25 | Vertex Pharma | Pyrazolforbindelser der er nyttige som proteinkinase-inhibitorer |
| GB0206860D0 (en) * | 2002-03-22 | 2002-05-01 | Glaxo Group Ltd | Compounds |
| GB0206861D0 (en) * | 2002-03-22 | 2002-05-01 | Glaxo Group Ltd | Medicaments |
| US20040002524A1 (en) * | 2002-06-24 | 2004-01-01 | Richard Chesworth | Benzimidazole compounds and their use as estrogen agonists/antagonists |
| WO2004058265A1 (en) * | 2002-12-24 | 2004-07-15 | Biofocus Plc | Compound libraries of 2,3-substituted pyrazine derivatives capable of binding to g-protein coupled receptors |
| JP2006516626A (ja) * | 2003-01-28 | 2006-07-06 | スミスクライン ビーチャム コーポレーション | 化学的化合物 |
| JP2006520794A (ja) * | 2003-03-21 | 2006-09-14 | スミスクライン ビーチャム コーポレーション | 化合物 |
| EP1636215B1 (en) * | 2003-05-23 | 2008-01-23 | Basilea Pharmaceutica AG | Furazanobenzimidazoles |
| TWI372050B (en) | 2003-07-03 | 2012-09-11 | Astex Therapeutics Ltd | (morpholin-4-ylmethyl-1h-benzimidazol-2-yl)-1h-pyrazoles |
| TW200523262A (en) * | 2003-07-29 | 2005-07-16 | Smithkline Beecham Corp | Inhibitors of AKT activity |
| AU2004267094A1 (en) | 2003-08-20 | 2005-03-03 | Vertex Pharmaceuticals Incorporated | (4 -amino -1,2, 5-oxadiazol-4-yl) -hetxiroaromatic compounds useful as protein kinase inhibitors |
| JP2007507549A (ja) * | 2003-10-06 | 2007-03-29 | グラクソ グループ リミテッド | キナーゼ阻害剤としての1,6,7−三置換アザベンゾイミダゾールの調製 |
| DE102004010194A1 (de) * | 2004-03-02 | 2005-10-13 | Aventis Pharma Deutschland Gmbh | 4-Benzimidazol-2-yl-pyridazin-3-on-Derivate, ihre Herstellung und Verwendung in Arzneimitteln |
| DE102004010207A1 (de) | 2004-03-02 | 2005-09-15 | Aventis Pharma S.A. | Neue 4-Benzimidazol-2-yl-pyridazin-3-on-Derivate |
| US7781478B2 (en) | 2004-07-14 | 2010-08-24 | Ptc Therapeutics, Inc. | Methods for treating hepatitis C |
| JP2008506702A (ja) | 2004-07-14 | 2008-03-06 | ピーティーシー セラピューティクス,インコーポレーテッド | C型肝炎を治療するための方法 |
| US7772271B2 (en) | 2004-07-14 | 2010-08-10 | Ptc Therapeutics, Inc. | Methods for treating hepatitis C |
| US7868037B2 (en) | 2004-07-14 | 2011-01-11 | Ptc Therapeutics, Inc. | Methods for treating hepatitis C |
| NZ553329A (en) | 2004-07-22 | 2010-09-30 | Ptc Therapeutics Inc | Thienopyridines for treating hepatitis C |
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2003
- 2003-02-06 KR KR10-2004-7012258A patent/KR20040084896A/ko not_active Withdrawn
- 2003-02-06 ES ES10180554.7T patent/ES2437391T3/es not_active Expired - Lifetime
- 2003-02-06 JP JP2003566002A patent/JP4656838B2/ja not_active Expired - Fee Related
- 2003-02-06 RU RU2004126671/04A patent/RU2004126671A/ru not_active Application Discontinuation
- 2003-02-06 CA CA2475633A patent/CA2475633C/en not_active Expired - Fee Related
- 2003-02-06 EP EP10180554.7A patent/EP2322521B1/en not_active Expired - Lifetime
- 2003-02-06 MX MXPA04007697A patent/MXPA04007697A/es not_active Application Discontinuation
- 2003-02-06 EP EP03710903A patent/EP1472245A2/en not_active Withdrawn
- 2003-02-06 US US10/360,535 patent/US20040034037A1/en not_active Abandoned
- 2003-02-06 PL PL03372198A patent/PL372198A1/xx not_active Application Discontinuation
- 2003-02-06 AU AU2003215087A patent/AU2003215087B2/en not_active Ceased
- 2003-02-06 WO PCT/US2003/003655 patent/WO2003066629A2/en not_active Ceased
- 2003-02-06 SG SG200605228-6A patent/SG159380A1/en unknown
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2004
- 2004-09-06 NO NO20043726A patent/NO20043726L/no unknown
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2007
- 2007-07-12 US US11/776,756 patent/US20070270420A1/en not_active Abandoned
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2010
- 2010-02-26 JP JP2010043557A patent/JP2010132697A/ja active Pending