JP2004537557A5 - - Google Patents
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- JP2004537557A5 JP2004537557A5 JP2003513981A JP2003513981A JP2004537557A5 JP 2004537557 A5 JP2004537557 A5 JP 2004537557A5 JP 2003513981 A JP2003513981 A JP 2003513981A JP 2003513981 A JP2003513981 A JP 2003513981A JP 2004537557 A5 JP2004537557 A5 JP 2004537557A5
- Authority
- JP
- Japan
- Prior art keywords
- methyl
- methoxy
- carboxamide
- pyrimidine
- dimethyl
- 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.)
- Pending
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- 150000001875 compounds Chemical class 0.000 claims description 36
- 150000003839 salts Chemical class 0.000 claims description 21
- -1 hydroxy, amino Chemical group 0.000 claims description 16
- 239000008194 pharmaceutical composition Substances 0.000 claims description 2
- 125000000217 alkyl group Chemical group 0.000 claims 15
- 125000004356 hydroxy functional group Chemical group O* 0.000 claims 8
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 claims 7
- 238000000034 method Methods 0.000 claims 7
- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims 7
- 229910052757 nitrogen Inorganic materials 0.000 claims 6
- 125000003545 alkoxy group Chemical group 0.000 claims 4
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 claims 4
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims 4
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 4
- 229910052760 oxygen Inorganic materials 0.000 claims 4
- 229910052717 sulfur Inorganic materials 0.000 claims 4
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims 3
- 125000003118 aryl group Chemical group 0.000 claims 3
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims 3
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims 3
- 125000005842 heteroatom Chemical group 0.000 claims 3
- 230000000414 obstructive effect Effects 0.000 claims 3
- 239000001301 oxygen Chemical group 0.000 claims 3
- 208000023504 respiratory system disease Diseases 0.000 claims 3
- 230000002441 reversible effect Effects 0.000 claims 3
- 125000001424 substituent group Chemical group 0.000 claims 3
- 239000011593 sulfur Chemical group 0.000 claims 3
- 125000002861 (C1-C4) alkanoyl group Chemical group 0.000 claims 2
- 125000004769 (C1-C4) alkylsulfonyl group Chemical group 0.000 claims 2
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 claims 2
- TYONQVMMGHFCBR-UHFFFAOYSA-N 1-(cyclopropylmethyl)-n-methoxy-n,3-dimethyl-2,4-dioxo-6-(quinolin-4-ylmethyl)thieno[2,3-d]pyrimidine-5-carboxamide Chemical compound O=C1N(C)C(=O)C=2C(C(=O)N(C)OC)=C(CC=3C4=CC=CC=C4N=CC=3)SC=2N1CC1CC1 TYONQVMMGHFCBR-UHFFFAOYSA-N 0.000 claims 2
- GXAYTGQJFGCPQE-UHFFFAOYSA-N 1-ethyl-n-methoxy-n,3-dimethyl-2,4-dioxo-6-(quinolin-4-ylmethyl)thieno[2,3-d]pyrimidine-5-carboxamide Chemical compound C1=CC=C2C(CC=3SC=4N(C(N(C)C(=O)C=4C=3C(=O)N(C)OC)=O)CC)=CC=NC2=C1 GXAYTGQJFGCPQE-UHFFFAOYSA-N 0.000 claims 2
- 230000006052 T cell proliferation Effects 0.000 claims 2
- 125000005115 alkyl carbamoyl group Chemical group 0.000 claims 2
- 125000004414 alkyl thio group Chemical group 0.000 claims 2
- 125000001589 carboacyl group Chemical group 0.000 claims 2
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims 2
- 125000004093 cyano group Chemical group *C#N 0.000 claims 2
- 125000004122 cyclic group Chemical group 0.000 claims 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 2
- 125000000524 functional group Chemical group 0.000 claims 2
- 229910052736 halogen Inorganic materials 0.000 claims 2
- 125000005843 halogen group Chemical group 0.000 claims 2
- 150000002367 halogens Chemical class 0.000 claims 2
- 125000000623 heterocyclic group Chemical group 0.000 claims 2
- 230000002401 inhibitory effect Effects 0.000 claims 2
- 238000004519 manufacturing process Methods 0.000 claims 2
- 125000000325 methylidene group Chemical group [H]C([H])=* 0.000 claims 2
- BZGPCILIRUKTSL-UHFFFAOYSA-N n-methoxy-n,3-dimethyl-6-[(2-methyl-1h-indol-3-yl)methyl]-1-(2-methylpropyl)-2,4-dioxothieno[2,3-d]pyrimidine-5-carboxamide Chemical compound CC(C)CN1C(=O)N(C)C(=O)C2=C1SC(CC=1C3=CC=CC=C3NC=1C)=C2C(=O)N(C)OC BZGPCILIRUKTSL-UHFFFAOYSA-N 0.000 claims 2
- 125000004433 nitrogen atom Chemical group N* 0.000 claims 2
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 claims 2
- 125000004043 oxo group Chemical group O=* 0.000 claims 2
- 239000000651 prodrug Substances 0.000 claims 2
- 229940002612 prodrug Drugs 0.000 claims 2
- 125000000464 thioxo group Chemical group S=* 0.000 claims 2
- 125000004385 trihaloalkyl group Chemical group 0.000 claims 2
- NAWXUBYGYWOOIX-SFHVURJKSA-N (2s)-2-[[4-[2-(2,4-diaminoquinazolin-6-yl)ethyl]benzoyl]amino]-4-methylidenepentanedioic acid Chemical compound C1=CC2=NC(N)=NC(N)=C2C=C1CCC1=CC=C(C(=O)N[C@@H](CC(=C)C(O)=O)C(O)=O)C=C1 NAWXUBYGYWOOIX-SFHVURJKSA-N 0.000 claims 1
- 125000004768 (C1-C4) alkylsulfinyl group Chemical group 0.000 claims 1
- 125000004890 (C1-C6) alkylamino group Chemical group 0.000 claims 1
- HNGUIAIZYGMWAI-UHFFFAOYSA-N 1-(2,2-dimethylpropyl)-n-methoxy-n,3-dimethyl-2,4-dioxo-6-(quinolin-4-ylmethyl)thieno[2,3-d]pyrimidine-5-carboxamide Chemical compound CC(C)(C)CN1C(=O)N(C)C(=O)C2=C1SC(CC=1C3=CC=CC=C3N=CC=1)=C2C(=O)N(C)OC HNGUIAIZYGMWAI-UHFFFAOYSA-N 0.000 claims 1
- 125000004206 2,2,2-trifluoroethyl group Chemical group [H]C([H])(*)C(F)(F)F 0.000 claims 1
- KKZUMAMOMRDVKA-UHFFFAOYSA-N 2-chloropropane Chemical group [CH2]C(C)Cl KKZUMAMOMRDVKA-UHFFFAOYSA-N 0.000 claims 1
- LBBGSBPIRZEZSY-UHFFFAOYSA-N 6-(1h-indol-3-ylmethyl)-n-methoxy-n,3-dimethyl-1-(2-methylpropyl)-2,4-dioxothieno[2,3-d]pyrimidine-5-carboxamide Chemical compound CC(C)CN1C(=O)N(C)C(=O)C2=C1SC(CC=1C3=CC=CC=C3NC=1)=C2C(=O)N(C)OC LBBGSBPIRZEZSY-UHFFFAOYSA-N 0.000 claims 1
- SFXOTKPNEUNUFM-UHFFFAOYSA-N 6-(1h-indole-3-carbonyl)-n-methoxy-n,3-dimethyl-1-(2-methylpropyl)-2,4-dioxothieno[2,3-d]pyrimidine-5-carboxamide Chemical compound C1=CC=C2C(C(=O)C3=C(C=4C(=O)N(C)C(=O)N(CC(C)C)C=4S3)C(=O)N(C)OC)=CNC2=C1 SFXOTKPNEUNUFM-UHFFFAOYSA-N 0.000 claims 1
- JWJLXCMYIXOEKN-UHFFFAOYSA-N 6-(2h-indazol-3-ylmethyl)-n-methoxy-n,3-dimethyl-1-(2-methylpropyl)-2,4-dioxothieno[2,3-d]pyrimidine-5-carboxamide Chemical compound CC(C)CN1C(=O)N(C)C(=O)C2=C1SC(CC=1C3=CC=CC=C3NN=1)=C2C(=O)N(C)OC JWJLXCMYIXOEKN-UHFFFAOYSA-N 0.000 claims 1
- SLMBPMJXKUQBMS-UHFFFAOYSA-N 6-[(1-acetylindol-3-yl)methyl]-n-methoxy-n,3-dimethyl-1-(2-methylpropyl)-2,4-dioxothieno[2,3-d]pyrimidine-5-carboxamide Chemical compound CC(C)CN1C(=O)N(C)C(=O)C2=C1SC(CC=1C3=CC=CC=C3N(C(C)=O)C=1)=C2C(=O)N(C)OC SLMBPMJXKUQBMS-UHFFFAOYSA-N 0.000 claims 1
- CBYGQTUGONAURO-UHFFFAOYSA-N 6-[(2-chloroimidazol-1-yl)methyl]-n-methoxy-n,3-dimethyl-1-(2-methylpropyl)-2,4-dioxothieno[2,3-d]pyrimidine-5-carboxamide Chemical compound S1C=2N(CC(C)C)C(=O)N(C)C(=O)C=2C(C(=O)N(C)OC)=C1CN1C=CN=C1Cl CBYGQTUGONAURO-UHFFFAOYSA-N 0.000 claims 1
- SQEPUNKKDKMSHT-UHFFFAOYSA-N 6-[(3-chloroquinolin-4-yl)methyl]-n-methoxy-n,3-dimethyl-1-(2-methylpropyl)-2,4-dioxothieno[2,3-d]pyrimidine-5-carboxamide Chemical compound CC(C)CN1C(=O)N(C)C(=O)C2=C1SC(CC=1C3=CC=CC=C3N=CC=1Cl)=C2C(=O)N(C)OC SQEPUNKKDKMSHT-UHFFFAOYSA-N 0.000 claims 1
- YHKNTGMCONSUEO-UHFFFAOYSA-N 6-[(4,5-dichloro-2-methylimidazol-1-yl)methyl]-n-(2-hydroxyethoxy)-n,3-dimethyl-1-(2-methylpropyl)-2,4-dioxothieno[2,3-d]pyrimidine-5-carboxamide Chemical compound OCCON(C)C(=O)C=1C=2C(=O)N(C)C(=O)N(CC(C)C)C=2SC=1CN1C(C)=NC(Cl)=C1Cl YHKNTGMCONSUEO-UHFFFAOYSA-N 0.000 claims 1
- COWXFPKRNKUORL-UHFFFAOYSA-N 6-[(4,5-dichloro-2-methylimidazol-1-yl)methyl]-n-(2-hydroxyethyl)-n-methoxy-3-methyl-1-(2-methylpropyl)-2,4-dioxothieno[2,3-d]pyrimidine-5-carboxamide Chemical compound S1C=2N(CC(C)C)C(=O)N(C)C(=O)C=2C(C(=O)N(CCO)OC)=C1CN1C(C)=NC(Cl)=C1Cl COWXFPKRNKUORL-UHFFFAOYSA-N 0.000 claims 1
- VIDVFTXECDAGAM-UHFFFAOYSA-N 6-[(4,5-dichloro-2-methylimidazol-1-yl)methyl]-n-ethyl-n-methoxy-3-methyl-1-(2-methylpropyl)-2,4-dioxothieno[2,3-d]pyrimidine-5-carboxamide Chemical compound S1C=2N(CC(C)C)C(=O)N(C)C(=O)C=2C(C(=O)N(OC)CC)=C1CN1C(C)=NC(Cl)=C1Cl VIDVFTXECDAGAM-UHFFFAOYSA-N 0.000 claims 1
- CMLJYPLKIKPWDF-UHFFFAOYSA-N 6-[(4,5-dichloro-2-methylimidazol-1-yl)methyl]-n-methoxy-n,3-dimethyl-1-(2-methylpropyl)-2,4-dioxothieno[2,3-d]pyrimidine-5-carboxamide Chemical compound S1C=2N(CC(C)C)C(=O)N(C)C(=O)C=2C(C(=O)N(C)OC)=C1CN1C(C)=NC(Cl)=C1Cl CMLJYPLKIKPWDF-UHFFFAOYSA-N 0.000 claims 1
- LQRASRFLUDKWAX-UHFFFAOYSA-N 6-[(4,5-dichloro-2-methylimidazol-1-yl)methyl]-n-methoxy-n,3-dimethyl-2,4-dioxo-1-propan-2-ylthieno[2,3-d]pyrimidine-5-carboxamide Chemical compound S1C=2N(C(C)C)C(=O)N(C)C(=O)C=2C(C(=O)N(C)OC)=C1CN1C(C)=NC(Cl)=C1Cl LQRASRFLUDKWAX-UHFFFAOYSA-N 0.000 claims 1
- YIYNBXNJBFLKQE-UHFFFAOYSA-N 6-[(4,5-dichloro-2-methylimidazol-1-yl)methyl]-n-methoxy-n,3-dimethyl-2,4-dioxo-1-propylthieno[2,3-d]pyrimidine-5-carboxamide Chemical compound CON(C)C(=O)C=1C=2C(=O)N(C)C(=O)N(CCC)C=2SC=1CN1C(C)=NC(Cl)=C1Cl YIYNBXNJBFLKQE-UHFFFAOYSA-N 0.000 claims 1
- VZMVSPBAUSGBBT-UHFFFAOYSA-N 6-[[4,5-dichloro-2-(hydroxymethyl)imidazol-1-yl]methyl]-n-methoxy-n,3-dimethyl-1-(2-methylpropyl)-2,4-dioxothieno[2,3-d]pyrimidine-5-carboxamide Chemical compound S1C=2N(CC(C)C)C(=O)N(C)C(=O)C=2C(C(=O)N(C)OC)=C1CN1C(CO)=NC(Cl)=C1Cl VZMVSPBAUSGBBT-UHFFFAOYSA-N 0.000 claims 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 1
- 206010062016 Immunosuppression Diseases 0.000 claims 1
- 239000002671 adjuvant Substances 0.000 claims 1
- 125000003342 alkenyl group Chemical group 0.000 claims 1
- 125000004453 alkoxycarbonyl group Chemical group 0.000 claims 1
- 125000003785 benzimidazolyl group Chemical group N1=C(NC2=C1C=CC=C2)* 0.000 claims 1
- 125000003354 benzotriazolyl group Chemical group N1N=NC2=C1C=CC=C2* 0.000 claims 1
- 125000002603 chloroethyl group Chemical group [H]C([*])([H])C([H])([H])Cl 0.000 claims 1
- 125000004186 cyclopropylmethyl group Chemical group [H]C([H])(*)C1([H])C([H])([H])C1([H])[H] 0.000 claims 1
- 125000004982 dihaloalkyl group Chemical group 0.000 claims 1
- 239000003085 diluting agent Substances 0.000 claims 1
- 239000003814 drug Substances 0.000 claims 1
- WCDWBPCFGJXFJZ-UHFFFAOYSA-N etanidazole Chemical group OCCNC(=O)CN1C=CN=C1[N+]([O-])=O WCDWBPCFGJXFJZ-UHFFFAOYSA-N 0.000 claims 1
- 125000001188 haloalkyl group Chemical group 0.000 claims 1
- 229910052739 hydrogen Inorganic materials 0.000 claims 1
- 239000001257 hydrogen Substances 0.000 claims 1
- 125000005946 imidazo[1,2-a]pyridyl group Chemical group 0.000 claims 1
- 125000002883 imidazolyl group Chemical group 0.000 claims 1
- 230000001506 immunosuppresive effect Effects 0.000 claims 1
- 125000003453 indazolyl group Chemical group N1N=C(C2=C1C=CC=C2)* 0.000 claims 1
- 125000001041 indolyl group Chemical group 0.000 claims 1
- 230000001939 inductive effect Effects 0.000 claims 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims 1
- 125000000842 isoxazolyl group Chemical group 0.000 claims 1
- HWQFWHOXXCWOJM-UHFFFAOYSA-N n-(2-hydroxyethyl)-n-methoxy-3-methyl-1-(2-methylpropyl)-6-[(2-methylsulfanylimidazol-1-yl)methyl]-2,4-dioxothieno[2,3-d]pyrimidine-5-carboxamide Chemical compound S1C=2N(CC(C)C)C(=O)N(C)C(=O)C=2C(C(=O)N(CCO)OC)=C1CN1C=CN=C1SC HWQFWHOXXCWOJM-UHFFFAOYSA-N 0.000 claims 1
- OZGWACQETOIWCE-UHFFFAOYSA-N n-methoxy-n,3-dimethyl-1-(2-methylpropyl)-2,4-dioxo-6-(1h-pyrrolo[2,3-b]pyridin-3-ylmethyl)thieno[2,3-d]pyrimidine-5-carboxamide Chemical compound CC(C)CN1C(=O)N(C)C(=O)C2=C1SC(CC=1C3=CC=CN=C3NC=1)=C2C(=O)N(C)OC OZGWACQETOIWCE-UHFFFAOYSA-N 0.000 claims 1
- CWEFUJMDBUNBKZ-UHFFFAOYSA-N n-methoxy-n,3-dimethyl-1-(2-methylpropyl)-2,4-dioxo-6-[(2,4,5-trichloroimidazol-1-yl)methyl]thieno[2,3-d]pyrimidine-5-carboxamide Chemical compound S1C=2N(CC(C)C)C(=O)N(C)C(=O)C=2C(C(=O)N(C)OC)=C1CN1C(Cl)=NC(Cl)=C1Cl CWEFUJMDBUNBKZ-UHFFFAOYSA-N 0.000 claims 1
- FQXRBDBNEITFPH-UHFFFAOYSA-N n-methoxy-n,3-dimethyl-1-(2-methylpropyl)-2,4-dioxo-6-[(2-oxo-1,3-benzothiazol-3-yl)methyl]thieno[2,3-d]pyrimidine-5-carboxamide Chemical compound CC(C)CN1C(=O)N(C)C(=O)C2=C1SC(CN1C(SC3=CC=CC=C31)=O)=C2C(=O)N(C)OC FQXRBDBNEITFPH-UHFFFAOYSA-N 0.000 claims 1
- AYZHIPAPDNBZJQ-UHFFFAOYSA-N n-methoxy-n,3-dimethyl-1-(2-methylpropyl)-2,4-dioxo-6-[(2-propan-2-ylimidazol-1-yl)methyl]thieno[2,3-d]pyrimidine-5-carboxamide Chemical compound S1C=2N(CC(C)C)C(=O)N(C)C(=O)C=2C(C(=O)N(C)OC)=C1CN1C=CN=C1C(C)C AYZHIPAPDNBZJQ-UHFFFAOYSA-N 0.000 claims 1
- BLZGLDJQMDPSMB-UHFFFAOYSA-N n-methoxy-n,3-dimethyl-1-(2-methylpropyl)-2,4-dioxo-6-[(2-propylbenzimidazol-1-yl)methyl]thieno[2,3-d]pyrimidine-5-carboxamide Chemical compound CC(C)CN1C(=O)N(C)C(=O)C2=C1SC(CN1C3=CC=CC=C3N=C1CCC)=C2C(=O)N(C)OC BLZGLDJQMDPSMB-UHFFFAOYSA-N 0.000 claims 1
- JLTFCEWEQXCIRD-UHFFFAOYSA-N n-methoxy-n,3-dimethyl-1-(2-methylpropyl)-6-(2-methylsulfanylbenzimidazol-1-yl)-2,4-dioxothieno[2,3-d]pyrimidine-5-carboxamide Chemical compound CSC1=NC2=CC=CC=C2N1C1=C(C(=O)N(C)OC)C(C(=O)N(C)C(=O)N2CC(C)C)=C2S1 JLTFCEWEQXCIRD-UHFFFAOYSA-N 0.000 claims 1
- ROPZMWZSGVUPET-UHFFFAOYSA-N n-methoxy-n,3-dimethyl-1-(2-methylpropyl)-6-[(2-methyl-1h-pyrrolo[2,3-b]pyridin-3-yl)methyl]-2,4-dioxothieno[2,3-d]pyrimidine-5-carboxamide Chemical compound CC(C)CN1C(=O)N(C)C(=O)C2=C1SC(CC=1C3=CC=CN=C3NC=1C)=C2C(=O)N(C)OC ROPZMWZSGVUPET-UHFFFAOYSA-N 0.000 claims 1
- GQLKYTHLQYPEBI-UHFFFAOYSA-N n-methoxy-n,3-dimethyl-1-(2-methylpropyl)-6-[(2-methylsulfanylimidazol-1-yl)methyl]-2,4-dioxothieno[2,3-d]pyrimidine-5-carboxamide Chemical compound S1C=2N(CC(C)C)C(=O)N(C)C(=O)C=2C(C(=O)N(C)OC)=C1CN1C=CN=C1SC GQLKYTHLQYPEBI-UHFFFAOYSA-N 0.000 claims 1
- PXROSKUMGPMFKF-UHFFFAOYSA-N n-methoxy-n,3-dimethyl-2,4-dioxo-1-propyl-6-(quinolin-4-ylmethyl)thieno[2,3-d]pyrimidine-5-carboxamide Chemical compound C1=CC=C2C(CC=3SC=4N(C(N(C)C(=O)C=4C=3C(=O)N(C)OC)=O)CCC)=CC=NC2=C1 PXROSKUMGPMFKF-UHFFFAOYSA-N 0.000 claims 1
- BZKSHTJFQWYDQL-UHFFFAOYSA-N n-methoxy-n,3-dimethyl-6-[(2-methyl-1h-pyrrolo[2,3-b]pyridin-3-yl)methyl]-2,4-dioxo-1-propan-2-ylthieno[2,3-d]pyrimidine-5-carboxamide Chemical compound CC(C)N1C(=O)N(C)C(=O)C2=C1SC(CC=1C3=CC=CN=C3NC=1C)=C2C(=O)N(C)OC BZKSHTJFQWYDQL-UHFFFAOYSA-N 0.000 claims 1
- CPMMQUAFPDUCCF-UHFFFAOYSA-N n-methoxy-n,3-dimethyl-6-[(2-methyl-1h-pyrrolo[2,3-b]pyridin-3-yl)methyl]-2,4-dioxo-1-propylthieno[2,3-d]pyrimidine-5-carboxamide Chemical compound C1=CC=C2C(CC=3SC=4N(C(N(C)C(=O)C=4C=3C(=O)N(C)OC)=O)CCC)=C(C)NC2=N1 CPMMQUAFPDUCCF-UHFFFAOYSA-N 0.000 claims 1
- ZAEYEOOWSNCQAZ-UHFFFAOYSA-N n-methoxy-n,3-dimethyl-6-[(3-methyl-2-oxobenzimidazol-1-yl)methyl]-1-(2-methylpropyl)-2,4-dioxothieno[2,3-d]pyrimidine-5-carboxamide Chemical compound CC(C)CN1C(=O)N(C)C(=O)C2=C1SC(CN1C(N(C)C3=CC=CC=C31)=O)=C2C(=O)N(C)OC ZAEYEOOWSNCQAZ-UHFFFAOYSA-N 0.000 claims 1
- QXICFGCADMCHQD-UHFFFAOYSA-N n-methoxy-n,3-dimethyl-6-[[2-(methylamino)benzimidazol-1-yl]methyl]-1-(2-methylpropyl)-2,4-dioxothieno[2,3-d]pyrimidine-5-carboxamide Chemical compound CC(C)CN1C(=O)N(C)C(=O)C2=C1SC(CN1C3=CC=CC=C3N=C1NC)=C2C(=O)N(C)OC QXICFGCADMCHQD-UHFFFAOYSA-N 0.000 claims 1
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 claims 1
- 125000001971 neopentyl group Chemical group [H]C([*])([H])C(C([H])([H])[H])(C([H])([H])[H])C([H])([H])[H] 0.000 claims 1
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims 1
- 125000003226 pyrazolyl group Chemical group 0.000 claims 1
- 125000004943 pyrimidin-6-yl group Chemical group N1=CN=CC=C1* 0.000 claims 1
- QDXGKRWDQCEABB-UHFFFAOYSA-N pyrimidine-5-carboxamide Chemical compound NC(=O)C1=CN=CN=C1 QDXGKRWDQCEABB-UHFFFAOYSA-N 0.000 claims 1
- 125000000168 pyrrolyl group Chemical group 0.000 claims 1
- 125000005493 quinolyl group Chemical group 0.000 claims 1
- 125000006413 ring segment Chemical group 0.000 claims 1
- 230000002194 synthesizing effect Effects 0.000 claims 1
- 238000002560 therapeutic procedure Methods 0.000 claims 1
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 3
- 239000002253 acid Substances 0.000 description 3
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 3
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 3
- ROSDSFDQCJNGOL-UHFFFAOYSA-N Dimethylamine Chemical compound CNC ROSDSFDQCJNGOL-UHFFFAOYSA-N 0.000 description 2
- BAVYZALUXZFZLV-UHFFFAOYSA-N Methylamine Chemical compound NC BAVYZALUXZFZLV-UHFFFAOYSA-N 0.000 description 2
- YNAVUWVOSKDBBP-UHFFFAOYSA-N Morpholine Chemical compound C1COCCN1 YNAVUWVOSKDBBP-UHFFFAOYSA-N 0.000 description 2
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| WO (1) | WO2003008422A1 (enExample) |
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| SE9801399D0 (sv) | 1998-04-21 | 1998-04-21 | Astra Pharma Prod | Method and apparatus for filling containers |
| GB0117583D0 (en) * | 2001-07-19 | 2001-09-12 | Astrazeneca Ab | Novel compounds |
| GB0118479D0 (en) * | 2001-07-28 | 2001-09-19 | Astrazeneca Ab | Novel compounds |
| WO2004065395A1 (en) * | 2003-01-17 | 2004-08-05 | Astrazeneca Ab | Thienopyridazinones and their use in modulation of autoimmune disease |
| SE0300119D0 (sv) * | 2003-01-17 | 2003-01-17 | Astrazeneca Ab | Novel compounds |
| SE0300120D0 (sv) * | 2003-01-17 | 2003-01-17 | Astrazeneca Ab | Novel compounds |
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| AU2006202209B2 (en) | 2005-05-27 | 2011-04-14 | Lifescan, Inc. | Amniotic fluid derived cells |
| WO2006133052A2 (en) * | 2005-06-08 | 2006-12-14 | Centocor, Inc. | A cellular therapy for ocular degeneration |
| DK2395004T3 (en) | 2005-06-22 | 2016-03-21 | Plexxikon Inc | Pyrrolo [2,3-b] pyridine derivatives as protein kinase inhibitors |
| US20070122448A1 (en) * | 2005-11-28 | 2007-05-31 | Alireza Rezania | Compositions and methods to create a vascularized environment for cellular transplantation |
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| US8741643B2 (en) * | 2006-04-28 | 2014-06-03 | Lifescan, Inc. | Differentiation of pluripotent stem cells to definitive endoderm lineage |
| WO2008063888A2 (en) | 2006-11-22 | 2008-05-29 | Plexxikon, Inc. | Compounds modulating c-fms and/or c-kit activity and uses therefor |
| KR20090115142A (ko) * | 2007-01-30 | 2009-11-04 | 유니버시티 오브 조지아 리서치 파운데이션, 인코포레이티드 | 초기 중배엽 세포，내배엽 및 중배엽 계통의 생성에 유용한 중내배엽 세포의 안정한 집단 및 다능성 유주 세포（ｍｍｃ） |
| US9080145B2 (en) * | 2007-07-01 | 2015-07-14 | Lifescan Corporation | Single pluripotent stem cell culture |
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| KR101597731B1 (ko) | 2008-02-21 | 2016-02-26 | 센토코 오르토 바이오테크 인코포레이티드 | 세포 부착, 배양 및 탈리를 위한 방법, 표면 개질 플레이트 및 조성물 |
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| US8623648B2 (en) * | 2008-04-24 | 2014-01-07 | Janssen Biotech, Inc. | Treatment of pluripotent cells |
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| BRPI0919885A2 (pt) * | 2008-10-31 | 2015-08-11 | Centocor Ortho Biotech Inc | Diferenciação de células-tronco embrionárias humanas para a linhagem endócrina pancreática |
| KR102025158B1 (ko) * | 2008-10-31 | 2019-09-25 | 얀센 바이오테크 인코포레이티드 | 인간 배아 줄기 세포의 췌장 내분비 계통으로의 분화 |
| PL2366022T3 (pl) * | 2008-11-20 | 2016-11-30 | Sposoby i kompozycje do przyłączania i hodowli komórek na podłożach planarnych | |
| JP2012509085A (ja) | 2008-11-20 | 2012-04-19 | ヤンセン バイオテツク，インコーポレーテツド | マイクロキャリア上での多能性幹細胞の培養 |
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| CN103952372B (zh) | 2009-07-20 | 2016-10-05 | 詹森生物科技公司 | 人胚胎干细胞的分化 |
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| KR101841271B1 (ko) * | 2009-12-23 | 2018-03-22 | 얀센 바이오테크 인코포레이티드 | 인간 배아 줄기 세포의 분화 |
| EP4410991A3 (en) | 2009-12-23 | 2024-10-09 | Janssen Biotech, Inc. | Differentiation of human embryonic stem cells |
| KR20130025375A (ko) * | 2010-03-01 | 2013-03-11 | 얀센 바이오테크 인코포레이티드 | 만능 줄기 세포로부터 유래된 세포의 정제 방법 |
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| WO2012030538A2 (en) | 2010-08-31 | 2012-03-08 | Janssen Biotech, Inc. | Differentiation of human embryonic stem cells |
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| JP6557147B2 (ja) | 2012-12-31 | 2019-08-07 | ヤンセン バイオテツク，インコーポレーテツド | Ｈｂ９調節物を用いたヒト胚性幹細胞の膵臓内分泌細胞への分化 |
| US10370644B2 (en) | 2012-12-31 | 2019-08-06 | Janssen Biotech, Inc. | Method for making human pluripotent suspension cultures and cells derived therefrom |
| EP2938722B1 (en) | 2012-12-31 | 2021-12-08 | Janssen Biotech, Inc. | Suspension and clustering of human pluripotent cells for differentiation into pancreatic endocrine cells |
| SG10201709338RA (en) | 2012-12-31 | 2017-12-28 | Janssen Biotech Inc | Culturing of human embryonic stem cells at the air-liquid interface for differentiation into pancreatic endocrine cells |
| WO2014159662A1 (en) | 2013-03-13 | 2014-10-02 | University Of Miami | Method for isolation and purification of microvesicles from cell culture supernatants and biological fluids |
| CN117821369A (zh) | 2014-05-16 | 2024-04-05 | 詹森生物科技公司 | 小分子增强胰腺内分泌细胞中的mafa表达的用途 |
| EP4231015B1 (en) | 2015-11-30 | 2024-10-30 | Kadimastem Ltd. | Methods for differentiating and purifying pancreatic endocrine cells |
| MA45479A (fr) | 2016-04-14 | 2019-02-20 | Janssen Biotech Inc | Différenciation de cellules souches pluripotentes en cellules de l'endoderme de l'intestin moyen |
| AU2021327376A1 (en) | 2020-08-21 | 2023-04-20 | University Of Miami | Compositions and methods of treatment using microvesicles from bone marrow-derived mesenchymal stem cells |
| EP4511045A1 (en) | 2022-04-19 | 2025-02-26 | University of Miami | Compositions comprising microvesicles for use in the prevention and treatment of graft versus host disease |
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|---|---|---|---|---|
| US6469014B1 (en) * | 1997-05-28 | 2002-10-22 | Astrazeneca Ab | Thieno[2,3-d] pyrimidinediones, their preparation and use in therapy |
| SE9702001D0 (sv) | 1997-05-28 | 1997-05-28 | Astra Pharma Prod | Novel compounds |
| DE19738855C2 (de) * | 1997-09-05 | 2001-01-04 | Lohmann Therapie Syst Lts | Transdermales therapeutisches System mit haftklebender Reservoirschicht und unidirektional elastischer Rückschicht |
| EP1036076B1 (en) | 1997-12-05 | 2002-09-04 | AstraZeneca UK Limited | Novel compounds |
| US6232320B1 (en) | 1998-06-04 | 2001-05-15 | Abbott Laboratories | Cell adhesion-inhibiting antiinflammatory compounds |
| WO2000012514A1 (en) | 1998-08-28 | 2000-03-09 | Astrazeneca Ab | Novel compounds |
| GB0117583D0 (en) * | 2001-07-19 | 2001-09-12 | Astrazeneca Ab | Novel compounds |
| GB0118479D0 (en) | 2001-07-28 | 2001-09-19 | Astrazeneca Ab | Novel compounds |
| SE0300119D0 (sv) | 2003-01-17 | 2003-01-17 | Astrazeneca Ab | Novel compounds |
| SE0300120D0 (sv) * | 2003-01-17 | 2003-01-17 | Astrazeneca Ab | Novel compounds |
| WO2004065395A1 (en) | 2003-01-17 | 2004-08-05 | Astrazeneca Ab | Thienopyridazinones and their use in modulation of autoimmune disease |
-
2001
- 2001-07-19 GB GBGB0117583.5A patent/GB0117583D0/en not_active Ceased
-
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- 2002-07-16 EP EP02745634A patent/EP1412362B1/en not_active Expired - Lifetime
- 2002-07-16 JP JP2003513981A patent/JP2004537557A/ja active Pending
- 2002-07-16 ES ES02745634T patent/ES2268059T3/es not_active Expired - Lifetime
- 2002-07-16 WO PCT/GB2002/003250 patent/WO2003008422A1/en not_active Ceased
- 2002-07-16 AT AT02745634T patent/ATE334988T1/de not_active IP Right Cessation
- 2002-07-16 DE DE60213609T patent/DE60213609T2/de not_active Expired - Fee Related
- 2002-07-16 US US10/483,161 patent/US7361660B2/en not_active Expired - Fee Related
-
2008
- 2008-02-28 US US12/039,204 patent/US20080153855A1/en not_active Abandoned
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