JP2010532352A5 - - Google Patents
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- Publication number
- JP2010532352A5 JP2010532352A5 JP2010514802A JP2010514802A JP2010532352A5 JP 2010532352 A5 JP2010532352 A5 JP 2010532352A5 JP 2010514802 A JP2010514802 A JP 2010514802A JP 2010514802 A JP2010514802 A JP 2010514802A JP 2010532352 A5 JP2010532352 A5 JP 2010532352A5
- Authority
- JP
- Japan
- Prior art keywords
- alkyl
- ring
- alkoxy
- optionally substituted
- alkynyl
- 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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- 150000001875 compounds Chemical class 0.000 claims description 185
- -1 carboxy, hydroxy Chemical group 0.000 claims description 159
- 125000000008 (C1-C10) alkyl group Chemical group 0.000 claims description 158
- 125000003342 alkenyl group Chemical group 0.000 claims description 138
- 125000000304 alkynyl group Chemical group 0.000 claims description 138
- 125000000217 alkyl group Chemical group 0.000 claims description 128
- 125000005843 halogen group Chemical group 0.000 claims description 112
- 125000000027 (C1-C10) alkoxy group Chemical group 0.000 claims description 111
- 125000003118 aryl group Chemical group 0.000 claims description 98
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 87
- 125000004453 alkoxycarbonyl group Chemical group 0.000 claims description 81
- 125000001589 carboacyl group Chemical group 0.000 claims description 81
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 80
- 229910052717 sulfur Inorganic materials 0.000 claims description 80
- 125000001072 heteroaryl group Chemical group 0.000 claims description 76
- 125000004423 acyloxy group Chemical group 0.000 claims description 69
- 125000004122 cyclic group Chemical group 0.000 claims description 61
- 125000003545 alkoxy group Chemical group 0.000 claims description 59
- 229910052760 oxygen Inorganic materials 0.000 claims description 59
- 125000000623 heterocyclic group Chemical group 0.000 claims description 56
- 125000004432 carbon atom Chemical group C* 0.000 claims description 52
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 48
- 229910052801 chlorine Inorganic materials 0.000 claims description 40
- 229910052731 fluorine Inorganic materials 0.000 claims description 40
- 229910052794 bromium Inorganic materials 0.000 claims description 38
- 125000001188 haloalkyl group Chemical group 0.000 claims description 38
- 239000000651 prodrug Substances 0.000 claims description 36
- 229940002612 prodrug Drugs 0.000 claims description 36
- 150000003839 salts Chemical class 0.000 claims description 36
- RWRDLPDLKQPQOW-UHFFFAOYSA-N Pyrrolidine Chemical group C1CCNC1 RWRDLPDLKQPQOW-UHFFFAOYSA-N 0.000 claims description 34
- 229910052757 nitrogen Inorganic materials 0.000 claims description 29
- 229910052740 iodine Inorganic materials 0.000 claims description 27
- 229910052736 halogen Inorganic materials 0.000 claims description 24
- 150000002367 halogens Chemical class 0.000 claims description 22
- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 22
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 claims description 22
- 125000004573 morpholin-4-yl group Chemical group N1(CCOCC1)* 0.000 claims description 21
- 125000005505 thiomorpholino group Chemical group 0.000 claims description 20
- GLUUGHFHXGJENI-UHFFFAOYSA-N Piperazine Chemical compound C1CNCCN1 GLUUGHFHXGJENI-UHFFFAOYSA-N 0.000 claims description 18
- 229910052739 hydrogen Inorganic materials 0.000 claims description 18
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 18
- 125000003386 piperidinyl group Chemical group 0.000 claims description 18
- 125000004193 piperazinyl group Chemical group 0.000 claims description 17
- 125000004429 atom Chemical group 0.000 claims description 16
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 claims description 15
- 125000005110 aryl thio group Chemical group 0.000 claims description 14
- 239000008194 pharmaceutical composition Substances 0.000 claims description 14
- 125000004421 aryl sulphonamide group Chemical group 0.000 claims description 13
- 125000004422 alkyl sulphonamide group Chemical group 0.000 claims description 12
- 125000002619 bicyclic group Chemical group 0.000 claims description 12
- 125000004438 haloalkoxy group Chemical group 0.000 claims description 12
- 208000005176 Hepatitis C Diseases 0.000 claims description 10
- 102000014150 Interferons Human genes 0.000 claims description 10
- 108010050904 Interferons Proteins 0.000 claims description 10
- 229940079322 interferon Drugs 0.000 claims description 10
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims description 10
- 125000004778 2,2-difluoroethyl group Chemical group [H]C([H])(*)C([H])(F)F 0.000 claims description 8
- 125000005119 alkyl cycloalkyl group Chemical group 0.000 claims description 8
- 125000003710 aryl alkyl group Chemical group 0.000 claims description 8
- 125000004104 aryloxy group Chemical group 0.000 claims description 8
- 239000003814 drug Substances 0.000 claims description 8
- 125000005842 heteroatom Chemical group 0.000 claims description 8
- 239000002777 nucleoside Substances 0.000 claims description 8
- 229940124597 therapeutic agent Drugs 0.000 claims description 8
- 229910052799 carbon Inorganic materials 0.000 claims description 7
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims description 7
- 125000006432 1-methyl cyclopropyl group Chemical group [H]C([H])([H])C1(*)C([H])([H])C1([H])[H] 0.000 claims description 6
- CKLJMWTZIZZHCS-REOHCLBHSA-N L-aspartic acid Chemical compound OC(=O)[C@@H](N)CC(O)=O CKLJMWTZIZZHCS-REOHCLBHSA-N 0.000 claims description 6
- YNAVUWVOSKDBBP-UHFFFAOYSA-N Morpholine Chemical group C1COCCN1 YNAVUWVOSKDBBP-UHFFFAOYSA-N 0.000 claims description 6
- 102000012479 Serine Proteases Human genes 0.000 claims description 6
- 108010022999 Serine Proteases Proteins 0.000 claims description 6
- 235000003704 aspartic acid Nutrition 0.000 claims description 6
- 125000002393 azetidinyl group Chemical group 0.000 claims description 6
- OQFSQFPPLPISGP-UHFFFAOYSA-N beta-carboxyaspartic acid Natural products OC(=O)C(N)C(C(O)=O)C(O)=O OQFSQFPPLPISGP-UHFFFAOYSA-N 0.000 claims description 6
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 6
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 6
- 125000001971 neopentyl group Chemical group [H]C([*])([H])C(C([H])([H])[H])(C([H])([H])[H])C([H])([H])[H] 0.000 claims description 6
- 150000003833 nucleoside derivatives Chemical class 0.000 claims description 6
- 125000000962 organic group Chemical group 0.000 claims description 6
- 125000001424 substituent group Chemical group 0.000 claims description 6
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 claims description 6
- BRNULMACUQOKMR-UHFFFAOYSA-N thiomorpholine Chemical group C1CSCCN1 BRNULMACUQOKMR-UHFFFAOYSA-N 0.000 claims description 6
- 125000000876 trifluoromethoxy group Chemical group FC(F)(F)O* 0.000 claims description 6
- 239000003112 inhibitor Substances 0.000 claims description 5
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 5
- 125000004182 2-chlorophenyl group Chemical group [H]C1=C([H])C(Cl)=C(*)C([H])=C1[H] 0.000 claims description 4
- 125000001731 2-cyanoethyl group Chemical group [H]C([H])(*)C([H])([H])C#N 0.000 claims description 4
- 125000004777 2-fluoroethyl group Chemical group [H]C([H])(F)C([H])([H])* 0.000 claims description 4
- 125000004198 2-fluorophenyl group Chemical group [H]C1=C([H])C(F)=C(*)C([H])=C1[H] 0.000 claims description 4
- OAKJQQAXSVQMHS-UHFFFAOYSA-N Hydrazine Chemical compound NN OAKJQQAXSVQMHS-UHFFFAOYSA-N 0.000 claims description 4
- IWUCXVSUMQZMFG-AFCXAGJDSA-N Ribavirin Chemical class N1=C(C(=O)N)N=CN1[C@H]1[C@H](O)[C@H](O)[C@@H](CO)O1 IWUCXVSUMQZMFG-AFCXAGJDSA-N 0.000 claims description 4
- 125000005213 alkyl heteroaryl group Chemical group 0.000 claims description 4
- 125000005037 alkyl phenyl group Chemical group 0.000 claims description 4
- 235000001014 amino acid Nutrition 0.000 claims description 4
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 4
- 239000001257 hydrogen Substances 0.000 claims description 4
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 4
- 150000003949 imides Chemical class 0.000 claims description 4
- 125000001841 imino group Chemical group [H]N=* 0.000 claims description 4
- 230000003993 interaction Effects 0.000 claims description 4
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 4
- 125000004433 nitrogen atom Chemical group N* 0.000 claims description 4
- 125000003261 o-tolyl group Chemical group [H]C1=C([H])C(*)=C(C([H])=C1[H])C([H])([H])[H] 0.000 claims description 4
- 125000004430 oxygen atom Chemical group O* 0.000 claims description 4
- 125000003854 p-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1Cl 0.000 claims description 4
- 125000005931 tert-butyloxycarbonyl group Chemical group [H]C([H])([H])C(OC(*)=O)(C([H])([H])[H])C([H])([H])[H] 0.000 claims description 4
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims description 4
- 229920002554 vinyl polymer Polymers 0.000 claims description 4
- CRCTZWNJRMZUIO-UHFFFAOYSA-N 1,1,1,3,3,3-hexafluoropropane Chemical group FC(F)(F)[CH]C(F)(F)F CRCTZWNJRMZUIO-UHFFFAOYSA-N 0.000 claims description 2
- IWUCXVSUMQZMFG-RGDLXGNYSA-N 1-[(2s,3s,4r,5s)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]-1,2,4-triazole-3-carboxamide Chemical compound N1=C(C(=O)N)N=CN1[C@@H]1[C@@H](O)[C@@H](O)[C@H](CO)O1 IWUCXVSUMQZMFG-RGDLXGNYSA-N 0.000 claims description 2
- 125000001637 1-naphthyl group Chemical group [H]C1=C([H])C([H])=C2C(*)=C([H])C([H])=C([H])C2=C1[H] 0.000 claims description 2
- 125000001462 1-pyrrolyl group Chemical group [*]N1C([H])=C([H])C([H])=C1[H] 0.000 claims description 2
- 125000004206 2,2,2-trifluoroethyl group Chemical group [H]C([H])(*)C(F)(F)F 0.000 claims description 2
- 125000004200 2-methoxyethyl group Chemical group [H]C([H])([H])OC([H])([H])C([H])([H])* 0.000 claims description 2
- TZYVRXZQAWPIAB-FCLHUMLKSA-N 5-amino-3-[(2r,3r,4s,5r)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]-4h-[1,3]thiazolo[4,5-d]pyrimidine-2,7-dione Chemical compound O=C1SC=2C(=O)NC(N)=NC=2N1[C@@H]1O[C@H](CO)[C@@H](O)[C@H]1O TZYVRXZQAWPIAB-FCLHUMLKSA-N 0.000 claims description 2
- 101001023866 Arabidopsis thaliana Mannosyl-oligosaccharide glucosidase GCS1 Proteins 0.000 claims description 2
- 239000004475 Arginine Substances 0.000 claims description 2
- OUYCCCASQSFEME-QMMMGPOBSA-N L-tyrosine Chemical compound OC(=O)[C@@H](N)CC1=CC=C(O)C=C1 OUYCCCASQSFEME-QMMMGPOBSA-N 0.000 claims description 2
- KZSNJWFQEVHDMF-BYPYZUCNSA-N L-valine Chemical compound CC(C)[C@H](N)C(O)=O KZSNJWFQEVHDMF-BYPYZUCNSA-N 0.000 claims description 2
- 101800001838 Serine protease/helicase NS3 Proteins 0.000 claims description 2
- KZSNJWFQEVHDMF-UHFFFAOYSA-N Valine Natural products CC(C)C(N)C(O)=O KZSNJWFQEVHDMF-UHFFFAOYSA-N 0.000 claims description 2
- ODKSFYDXXFIFQN-UHFFFAOYSA-N arginine Natural products OC(=O)C(N)CCCNC(N)=N ODKSFYDXXFIFQN-UHFFFAOYSA-N 0.000 claims description 2
- 230000015572 biosynthetic process Effects 0.000 claims description 2
- 125000001995 cyclobutyl group Chemical group [H]C1([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 claims description 2
- 125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 claims description 2
- 239000003937 drug carrier Substances 0.000 claims description 2
- 230000002349 favourable effect Effects 0.000 claims description 2
- HNDVDQJCIGZPNO-UHFFFAOYSA-N histidine Natural products OC(=O)C(N)CC1=CN=CN1 HNDVDQJCIGZPNO-UHFFFAOYSA-N 0.000 claims description 2
- 229950003954 isatoribine Drugs 0.000 claims description 2
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims description 2
- 125000005928 isopropyloxycarbonyl group Chemical group [H]C([H])([H])C([H])(OC(*)=O)C([H])([H])[H] 0.000 claims description 2
- 238000013160 medical therapy Methods 0.000 claims description 2
- 238000000034 method Methods 0.000 claims description 2
- 125000006518 morpholino carbonyl group Chemical group [H]C1([H])OC([H])([H])C([H])([H])N(C(*)=O)C1([H])[H] 0.000 claims description 2
- 239000000137 peptide hydrolase inhibitor Substances 0.000 claims description 2
- 238000002360 preparation method Methods 0.000 claims description 2
- 230000000069 prophylactic effect Effects 0.000 claims description 2
- 229960000329 ribavirin Drugs 0.000 claims description 2
- HZCAHMRRMINHDJ-DBRKOABJSA-N ribavirin Natural products O[C@@H]1[C@H](O)[C@@H](CO)O[C@H]1N1N=CN=C1 HZCAHMRRMINHDJ-DBRKOABJSA-N 0.000 claims description 2
- 238000003786 synthesis reaction Methods 0.000 claims description 2
- NHKZSTHOYNWEEZ-AFCXAGJDSA-N taribavirin Chemical compound N1=C(C(=N)N)N=CN1[C@H]1[C@H](O)[C@H](O)[C@@H](CO)O1 NHKZSTHOYNWEEZ-AFCXAGJDSA-N 0.000 claims description 2
- 229950006081 taribavirin Drugs 0.000 claims description 2
- 125000003718 tetrahydrofuranyl group Chemical group 0.000 claims description 2
- 230000001225 therapeutic effect Effects 0.000 claims description 2
- OUYCCCASQSFEME-UHFFFAOYSA-N tyrosine Natural products OC(=O)C(N)CC1=CC=C(O)C=C1 OUYCCCASQSFEME-UHFFFAOYSA-N 0.000 claims description 2
- 239000004474 valine Substances 0.000 claims description 2
- 239000000203 mixture Substances 0.000 claims 4
- 125000003588 lysine group Chemical group [H]N([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])(N([H])[H])C(*)=O 0.000 claims 3
- 150000001504 aryl thiols Chemical class 0.000 claims 2
- 150000001721 carbon Chemical group 0.000 claims 2
- 125000000586 2-(4-morpholinyl)ethoxy group Chemical group [H]C([H])(O*)C([H])([H])N1C([H])([H])C([H])([H])OC([H])([H])C1([H])[H] 0.000 claims 1
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 claims 1
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims 1
- 125000001028 difluoromethyl group Chemical group [H]C(F)(F)* 0.000 claims 1
- 229940042399 direct acting antivirals protease inhibitors Drugs 0.000 claims 1
- 229940047124 interferons Drugs 0.000 claims 1
- 0 *C(C1)C1(C(NS(O*)(=O)=O)=O)N(*)C(C(CC(*)C1)N1C(C(*)(*)N(*)*)=*)=* Chemical compound *C(C1)C1(C(NS(O*)(=O)=O)=O)N(*)C(C(CC(*)C1)N1C(C(*)(*)N(*)*)=*)=* 0.000 description 14
- NQRYJNQNLNOLGT-UHFFFAOYSA-N Piperidine Chemical group C1CCNCC1 NQRYJNQNLNOLGT-UHFFFAOYSA-N 0.000 description 8
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 description 4
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 description 3
- 125000002373 5 membered heterocyclic group Chemical group 0.000 description 3
- 125000004070 6 membered heterocyclic group Chemical group 0.000 description 3
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 description 2
- WMJPXKWIHDLOLK-UHFFFAOYSA-N CCc1nc(cccc2)c2nc1OC Chemical compound CCc1nc(cccc2)c2nc1OC WMJPXKWIHDLOLK-UHFFFAOYSA-N 0.000 description 2
- IVFRKPCKIWPVFX-UHFFFAOYSA-N COc1c(cccc2)c2c(N2CCCCC2)nn1 Chemical compound COc1c(cccc2)c2c(N2CCCCC2)nn1 IVFRKPCKIWPVFX-UHFFFAOYSA-N 0.000 description 2
- BAXABXIZQPAJEF-UHFFFAOYSA-N COc1nc(cccc2)c2nc1 Chemical compound COc1nc(cccc2)c2nc1 BAXABXIZQPAJEF-UHFFFAOYSA-N 0.000 description 2
- NXOFEFJRLUEJSH-UHFFFAOYSA-N COc1nc2ccccc2nc1NCc1ccccc1 Chemical compound COc1nc2ccccc2nc1NCc1ccccc1 NXOFEFJRLUEJSH-UHFFFAOYSA-N 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 125000006433 1-ethyl cyclopropyl group Chemical group [H]C([H])([H])C([H])([H])C1(*)C([H])([H])C1([H])[H] 0.000 description 1
- RPFPQLQEDIASGA-UHFFFAOYSA-N CC(C)N(Cc(cc(cc1)F)c1N1)C1=O Chemical compound CC(C)N(Cc(cc(cc1)F)c1N1)C1=O RPFPQLQEDIASGA-UHFFFAOYSA-N 0.000 description 1
- HCIFFIPSGMMRMU-UHFFFAOYSA-N CC(C)N(Cc1c(C2)c(OC)ccc1)C2=O Chemical compound CC(C)N(Cc1c(C2)c(OC)ccc1)C2=O HCIFFIPSGMMRMU-UHFFFAOYSA-N 0.000 description 1
- RZALQYQCABSXLA-UHFFFAOYSA-N CC(C)Nc1n[nH]cc1 Chemical compound CC(C)Nc1n[nH]cc1 RZALQYQCABSXLA-UHFFFAOYSA-N 0.000 description 1
- LQNPLTPLUNBILW-UHFFFAOYSA-N CCOc(cc1OC)nc2c1[s]cc2 Chemical compound CCOc(cc1OC)nc2c1[s]cc2 LQNPLTPLUNBILW-UHFFFAOYSA-N 0.000 description 1
- VBEUTEZVZKUGTD-UHFFFAOYSA-N CCOc(nc12)cc(OC)c1[s]cc2S=O Chemical compound CCOc(nc12)cc(OC)c1[s]cc2S=O VBEUTEZVZKUGTD-UHFFFAOYSA-N 0.000 description 1
- KOEZSCYKERBRCJ-UHFFFAOYSA-N CCOc1cc(OC)c2[s]c(C)c(C)c2n1 Chemical compound CCOc1cc(OC)c2[s]c(C)c(C)c2n1 KOEZSCYKERBRCJ-UHFFFAOYSA-N 0.000 description 1
- LFIUWMBUMYXYLM-UHFFFAOYSA-N CCOc1cc(OC)c2[s]c(C)cc2n1 Chemical compound CCOc1cc(OC)c2[s]c(C)cc2n1 LFIUWMBUMYXYLM-UHFFFAOYSA-N 0.000 description 1
- AZSAQDQHFDUEMX-UHFFFAOYSA-N Cc(c1nc(OCC=C)c2)c[s]c1c2OC Chemical compound Cc(c1nc(OCC=C)c2)c[s]c1c2OC AZSAQDQHFDUEMX-UHFFFAOYSA-N 0.000 description 1
- MTTGGOXMKRBJGP-UHFFFAOYSA-N FC(CC1(CC2)CCCC2NC1)(F)F Chemical compound FC(CC1(CC2)CCCC2NC1)(F)F MTTGGOXMKRBJGP-UHFFFAOYSA-N 0.000 description 1
- FWKQNCXZGNBPFD-UHFFFAOYSA-N Guaiazulene Chemical compound CC(C)C1=CC=C(C)C2=CC=C(C)C2=C1 FWKQNCXZGNBPFD-UHFFFAOYSA-N 0.000 description 1
- 102000006992 Interferon-alpha Human genes 0.000 description 1
- 108010047761 Interferon-alpha Proteins 0.000 description 1
- 206010034133 Pathogen resistance Diseases 0.000 description 1
- 229940123066 Polymerase inhibitor Drugs 0.000 description 1
- 229940124158 Protease/peptidase inhibitor Drugs 0.000 description 1
- 238000001727 in vivo Methods 0.000 description 1
- 230000002401 inhibitory effect Effects 0.000 description 1
Applications Claiming Priority (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US93775207P | 2007-06-29 | 2007-06-29 | |
| US60/937,752 | 2007-06-29 | ||
| US95969807P | 2007-07-16 | 2007-07-16 | |
| US60/959,698 | 2007-07-16 | ||
| PCT/US2008/007928 WO2009005677A2 (en) | 2007-06-29 | 2008-06-26 | Antiviral compounds |
Related Child Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2013124380A Division JP2013177452A (ja) | 2007-06-29 | 2013-06-13 | 抗ウイルス化合物 |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2010532352A JP2010532352A (ja) | 2010-10-07 |
| JP2010532352A5 true JP2010532352A5 (cg-RX-API-DMAC7.html) | 2011-10-27 |
| JP5465667B2 JP5465667B2 (ja) | 2014-04-09 |
Family
ID=40202103
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2010514802A Expired - Fee Related JP5465667B2 (ja) | 2007-06-29 | 2008-06-26 | 抗ウイルス化合物 |
| JP2013124380A Withdrawn JP2013177452A (ja) | 2007-06-29 | 2013-06-13 | 抗ウイルス化合物 |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2013124380A Withdrawn JP2013177452A (ja) | 2007-06-29 | 2013-06-13 | 抗ウイルス化合物 |
Country Status (19)
Families Citing this family (74)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| MY140680A (en) | 2002-05-20 | 2010-01-15 | Bristol Myers Squibb Co | Hepatitis c virus inhibitors |
| RU2008152171A (ru) | 2006-07-05 | 2010-08-10 | Интермьюн, Инк. (Us) | Новые ингибиторы вирусной репликации гепатита с |
| NZ587133A (en) * | 2008-02-04 | 2012-10-26 | Idenix Pharmaceuticals Inc | Macrocyclic serine protease inhibitor compounds for treating an HCV infection |
| US20090285773A1 (en) * | 2008-05-15 | 2009-11-19 | Bristol-Myers Squibb Company | Hepatitis C Virus Inhibitors |
| UY32099A (es) | 2008-09-11 | 2010-04-30 | Enanta Pharm Inc | Inhibidores macrocíclicos de serina proteasas de hepatitis c |
| AU2009293493B2 (en) | 2008-09-17 | 2014-09-18 | Boehringer Ingelheim International Gmbh | Combination of HCV NS3 protease inhibitor with interferon and ribavirin |
| JP2012502925A (ja) * | 2008-09-23 | 2012-02-02 | ベーリンガー インゲルハイム インターナショナル ゲゼルシャフト ミット ベシュレンクテル ハフツング | Ｃ型肝炎阻害化合物 |
| TW201034663A (en) * | 2008-12-19 | 2010-10-01 | Gilead Sciences Inc | HCV NS3 protease inhibitors |
| WO2010088394A1 (en) * | 2009-01-30 | 2010-08-05 | Glaxosmithkline Llc | Compounds |
| WO2010107965A1 (en) * | 2009-03-19 | 2010-09-23 | Boehringer Ingelheim International Gmbh | Process for preparing sulfonyl quinolines |
| CA2758072A1 (en) | 2009-04-08 | 2010-10-14 | Idenix Pharmaceuticals, Inc. | Macrocyclic serine protease inhibitors |
| KR20120026024A (ko) | 2009-04-24 | 2012-03-16 | 가부시키가이샤 가네카 | Ｎ-알콕시카르보닐-ｔｅｒｔ-류신의 제조법 |
| US8232246B2 (en) * | 2009-06-30 | 2012-07-31 | Abbott Laboratories | Anti-viral compounds |
| WO2011016576A1 (en) | 2009-08-04 | 2011-02-10 | Takeda Pharmaceutical Company Limited | Alanine derivatives as inhibitors of apoptosis proteins |
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- 2008-06-26 AU AU2008271117A patent/AU2008271117B2/en not_active Ceased
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- 2008-06-26 AR ARP080102758A patent/AR068794A1/es not_active Application Discontinuation
- 2008-06-26 TW TW097123925A patent/TW200914013A/zh unknown
- 2008-06-26 JP JP2010514802A patent/JP5465667B2/ja not_active Expired - Fee Related
- 2008-06-26 CA CA2692145A patent/CA2692145C/en not_active Expired - Fee Related
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2009
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2010
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- 2010-01-28 EC EC2010009906A patent/ECSP109906A/es unknown
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2013
- 2013-06-13 JP JP2013124380A patent/JP2013177452A/ja not_active Withdrawn
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