KR20140035383A - C형 간염 바이러스 억제제 - Google Patents
C형 간염 바이러스 억제제 Download PDFInfo
- Publication number
- KR20140035383A KR20140035383A KR1020137031994A KR20137031994A KR20140035383A KR 20140035383 A KR20140035383 A KR 20140035383A KR 1020137031994 A KR1020137031994 A KR 1020137031994A KR 20137031994 A KR20137031994 A KR 20137031994A KR 20140035383 A KR20140035383 A KR 20140035383A
- Authority
- KR
- South Korea
- Prior art keywords
- pyrrolo
- dioxo
- hexadecahydrocyclopropa
- dimethyl
- diazacyclopentadecin
- 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.)
- Abandoned
Links
- 0 CC(CCC=C)C[C@@](C)C1*CCC1 Chemical compound CC(CCC=C)C[C@@](C)C1*CCC1 0.000 description 9
- XHKVDLMHZLUDSK-UHFFFAOYSA-N COc(cc1)cc2c1c(Cl)cc(Cl)n2 Chemical compound COc(cc1)cc2c1c(Cl)cc(Cl)n2 XHKVDLMHZLUDSK-UHFFFAOYSA-N 0.000 description 2
- ZDQSQEFCHUWXQZ-UHFFFAOYSA-N CC(C)(C(F)(F)F)OC(N=C)O Chemical compound CC(C)(C(F)(F)F)OC(N=C)O ZDQSQEFCHUWXQZ-UHFFFAOYSA-N 0.000 description 1
- XTGDONQLSDEQGG-UHFFFAOYSA-N CC(C)(CC(F)(F)F)OC(Oc1ccccn1)=O Chemical compound CC(C)(CC(F)(F)F)OC(Oc1ccccn1)=O XTGDONQLSDEQGG-UHFFFAOYSA-N 0.000 description 1
- KNXKPRRNQTWULL-DHUWRJMKSA-N CC(C)N(C(c1ccccc11)=O)N=C1/[O]=C\C(C[C@H]1C(N[C@](C2)([C@@H]2/C=C\CC[C@@H](C)C[C@@H](C)[C@@H]2NC(OC(C)(C)C)=O)C(NS(C3CC3)(=O)=O)=O)=O)CN1C2=O Chemical compound CC(C)N(C(c1ccccc11)=O)N=C1/[O]=C\C(C[C@H]1C(N[C@](C2)([C@@H]2/C=C\CC[C@@H](C)C[C@@H](C)[C@@H]2NC(OC(C)(C)C)=O)C(NS(C3CC3)(=O)=O)=O)=O)CN1C2=O KNXKPRRNQTWULL-DHUWRJMKSA-N 0.000 description 1
- ZHGFWZQWIYANRM-ZPKFHAIKSA-N CC(C)Oc(cn1)c2c(Cl)cccc2c1O[C@H](C[C@H]1C(N[C@](C2)([C@@H]2/C=C\CC[C@@H](C)C[C@@H](C)[C@@H]2NC(OC(C)(C)C(F)(F)F)=O)C(NS(C3CC3)(=O)=O)=O)=O)CN1C2=O Chemical compound CC(C)Oc(cn1)c2c(Cl)cccc2c1O[C@H](C[C@H]1C(N[C@](C2)([C@@H]2/C=C\CC[C@@H](C)C[C@@H](C)[C@@H]2NC(OC(C)(C)C(F)(F)F)=O)C(NS(C3CC3)(=O)=O)=O)=O)CN1C2=O ZHGFWZQWIYANRM-ZPKFHAIKSA-N 0.000 description 1
- MCBUQXRNAMPSAU-UHFFFAOYSA-N CC1(CC1)S(NC=O)(=O)=O Chemical compound CC1(CC1)S(NC=O)(=O)=O MCBUQXRNAMPSAU-UHFFFAOYSA-N 0.000 description 1
- LZDDLHCQLFLHHV-AXVDGVBCSA-N CCC(C)(C)OC(N[C@@H]([C@H](C)C[C@H](C)CC/C=C\[C@H](C1)[C@]1(C(NS(C1(CF)CC1)(=O)=O)=O)NC([C@H](C1)N2C[C@@H]1Oc(nc1)c(cccc3)c3c1OC)=O)C2=O)=O Chemical compound CCC(C)(C)OC(N[C@@H]([C@H](C)C[C@H](C)CC/C=C\[C@H](C1)[C@]1(C(NS(C1(CF)CC1)(=O)=O)=O)NC([C@H](C1)N2C[C@@H]1Oc(nc1)c(cccc3)c3c1OC)=O)C2=O)=O LZDDLHCQLFLHHV-AXVDGVBCSA-N 0.000 description 1
- SDTPMYWNSRDUIX-HQKKBDCLSA-N CCCOc1nc(O[C@H](C[C@H]2C(N[C@](C3)([C@@H]3/C=C\CC[C@@H](C)C[C@@H](C)[C@@H]3NC(OC(C)(C)C(F)(F)F)=O)C(NS(C4CC4)(=O)=O)=O)=O)CN2C3=O)c(cccc2Cl)c2c1 Chemical compound CCCOc1nc(O[C@H](C[C@H]2C(N[C@](C3)([C@@H]3/C=C\CC[C@@H](C)C[C@@H](C)[C@@H]3NC(OC(C)(C)C(F)(F)F)=O)C(NS(C4CC4)(=O)=O)=O)=O)CN2C3=O)c(cccc2Cl)c2c1 SDTPMYWNSRDUIX-HQKKBDCLSA-N 0.000 description 1
- SDTPMYWNSRDUIX-GFLFNWCVSA-N CCCOc1nc(O[C@H](C[C@H]2C(N[C@](C3)([C@@H]3/C=C\CC[C@H](C)C[C@@H](C)[C@@H]3NC(OC(C)(C)C(F)(F)F)=O)C(NS(C4CC4)(=O)=O)=O)=O)CN2C3=O)c(cccc2Cl)c2c1 Chemical compound CCCOc1nc(O[C@H](C[C@H]2C(N[C@](C3)([C@@H]3/C=C\CC[C@H](C)C[C@@H](C)[C@@H]3NC(OC(C)(C)C(F)(F)F)=O)C(NS(C4CC4)(=O)=O)=O)=O)CN2C3=O)c(cccc2Cl)c2c1 SDTPMYWNSRDUIX-GFLFNWCVSA-N 0.000 description 1
- IRSJDVYTJUCXRV-UHFFFAOYSA-N CCOC(C(F)(F)Br)=O Chemical compound CCOC(C(F)(F)Br)=O IRSJDVYTJUCXRV-UHFFFAOYSA-N 0.000 description 1
- NDUSDWFZZYIZMS-JEKYGTNISA-N CCOc(cn1)c(cc(cc2)OC)c2c1O[C@H](C[C@H]1C(N[C@](C2)([C@@H]2/C=C\CC[C@H](C)C[C@@H](C)[C@@H]2NC(OC(C)(C)C(F)(F)F)=O)C(NS(C3(C)CC3)(=O)=O)=O)=O)CN1C2=O Chemical compound CCOc(cn1)c(cc(cc2)OC)c2c1O[C@H](C[C@H]1C(N[C@](C2)([C@@H]2/C=C\CC[C@H](C)C[C@@H](C)[C@@H]2NC(OC(C)(C)C(F)(F)F)=O)C(NS(C3(C)CC3)(=O)=O)=O)=O)CN1C2=O NDUSDWFZZYIZMS-JEKYGTNISA-N 0.000 description 1
- RJGHSWZLLLYXPG-QLYNWEGYSA-N CCOc(cn1)c(cccc2)c2c1O[C@H](C[C@H]1/C2=[O]\[C@@H](C[C@@H](C)[C@@H]3NC(Oc(ccc(F)c4)c4F)=O)CC/C=C\[C@H](C4)[C@]4(C(NS(C4(C)CC4)(=O)=O)=O)N2)CN1C3=O Chemical compound CCOc(cn1)c(cccc2)c2c1O[C@H](C[C@H]1/C2=[O]\[C@@H](C[C@@H](C)[C@@H]3NC(Oc(ccc(F)c4)c4F)=O)CC/C=C\[C@H](C4)[C@]4(C(NS(C4(C)CC4)(=O)=O)=O)N2)CN1C3=O RJGHSWZLLLYXPG-QLYNWEGYSA-N 0.000 description 1
- SGMUVALESKAJPB-LYKKTTPLSA-N CC[C@@H](CC(C)CCC=C)OS(c1ccc(C)cc1)(=O)=O Chemical compound CC[C@@H](CC(C)CCC=C)OS(c1ccc(C)cc1)(=O)=O SGMUVALESKAJPB-LYKKTTPLSA-N 0.000 description 1
- NVQHTNCEEMZHOS-UHFFFAOYSA-N CN(C(c1c2ccc(F)c1)F)C=C2OC1CC1 Chemical compound CN(C(c1c2ccc(F)c1)F)C=C2OC1CC1 NVQHTNCEEMZHOS-UHFFFAOYSA-N 0.000 description 1
- CDGRNRPARZOKOF-UHFFFAOYSA-N CN(C)c(c1cc(OC)ccc11)cnc1Cl Chemical compound CN(C)c(c1cc(OC)ccc11)cnc1Cl CDGRNRPARZOKOF-UHFFFAOYSA-N 0.000 description 1
- WYZYPWABLKFQRQ-UHFFFAOYSA-N CN(C)c(c1cc(OC)ccc11)cnc1O Chemical compound CN(C)c(c1cc(OC)ccc11)cnc1O WYZYPWABLKFQRQ-UHFFFAOYSA-N 0.000 description 1
- PIVZQDMZLIQYPD-UHFFFAOYSA-N COc(c(c1c2)ccc2F)cnc1Cl Chemical compound COc(c(c1c2)ccc2F)cnc1Cl PIVZQDMZLIQYPD-UHFFFAOYSA-N 0.000 description 1
- HEDFNPQWGLAXIU-FRNCZEFESA-N COc(c1c2cccc1)cnc2O[C@H](C1)CN[C@@H]1C(N[C@](C1)([C@@H]1C=C)C(NS(C1CC1)(=O)=O)=O)=O Chemical compound COc(c1c2cccc1)cnc2O[C@H](C1)CN[C@@H]1C(N[C@](C1)([C@@H]1C=C)C(NS(C1CC1)(=O)=O)=O)=O HEDFNPQWGLAXIU-FRNCZEFESA-N 0.000 description 1
- RUWKOLGTLOFEMK-UHFFFAOYSA-N COc(cc1)cc(N2)c1C(O)=CC2=O Chemical compound COc(cc1)cc(N2)c1C(O)=CC2=O RUWKOLGTLOFEMK-UHFFFAOYSA-N 0.000 description 1
- LRQYVYOFGDRVTH-UHFFFAOYSA-N COc(cc1)cc2c1c(Cl)cc(-[n]1nccc1)n2 Chemical compound COc(cc1)cc2c1c(Cl)cc(-[n]1nccc1)n2 LRQYVYOFGDRVTH-UHFFFAOYSA-N 0.000 description 1
- AGAHETWGCFCMDK-UHFFFAOYSA-N COc(cc1N)ccc1N Chemical compound COc(cc1N)ccc1N AGAHETWGCFCMDK-UHFFFAOYSA-N 0.000 description 1
- GVERQUMLAYWTMA-UHFFFAOYSA-N COc(cc1N2)ccc1N=CC2=O Chemical compound COc(cc1N2)ccc1N=CC2=O GVERQUMLAYWTMA-UHFFFAOYSA-N 0.000 description 1
- SYEUUDPGKMMKRU-UHFFFAOYSA-N COc(cc1N=C2)ccc1NC2=O Chemical compound COc(cc1N=C2)ccc1NC2=O SYEUUDPGKMMKRU-UHFFFAOYSA-N 0.000 description 1
- SXBLACDTTLNQHX-UHFFFAOYSA-N COc(ccc1c(nc2)O)cc1c2Br Chemical compound COc(ccc1c(nc2)O)cc1c2Br SXBLACDTTLNQHX-UHFFFAOYSA-N 0.000 description 1
- ZGADDIXVGQMXTP-UHFFFAOYSA-N COc(ccc1c(nc2)[O]=C)cc1c2OC=C Chemical compound COc(ccc1c(nc2)[O]=C)cc1c2OC=C ZGADDIXVGQMXTP-UHFFFAOYSA-N 0.000 description 1
- NCBZRJODKRCREW-UHFFFAOYSA-N COc1cc(N)ccc1 Chemical compound COc1cc(N)ccc1 NCBZRJODKRCREW-UHFFFAOYSA-N 0.000 description 1
- IQEWBMKALHPQID-UHFFFAOYSA-N COc1ccc2c(Cl)cc(N3CCCC3)nc2c1 Chemical compound COc1ccc2c(Cl)cc(N3CCCC3)nc2c1 IQEWBMKALHPQID-UHFFFAOYSA-N 0.000 description 1
- OEMPACGOUYYZCO-GFEOKLKBSA-N C[C@@H](CC/C=C\[C@H](C1)[C@]1(C(NS(C1(C)CC1)(=O)=O)=O)NC([C@H](C[C@H](C1)Oc2c(cccc3Cl)c3cc(OCC(F)F)n2)N1C1=O)=O)C[C@@H](C)[C@@H]1NC(OC(C)(C)C(F)(F)F)=O Chemical compound C[C@@H](CC/C=C\[C@H](C1)[C@]1(C(NS(C1(C)CC1)(=O)=O)=O)NC([C@H](C[C@H](C1)Oc2c(cccc3Cl)c3cc(OCC(F)F)n2)N1C1=O)=O)C[C@@H](C)[C@@H]1NC(OC(C)(C)C(F)(F)F)=O OEMPACGOUYYZCO-GFEOKLKBSA-N 0.000 description 1
- VOJQGXLLIAGPHW-MLQDOLLDSA-N C[C@@H](CC/C=C\[C@H](C1)[C@]1(C(NS(C1(CF)CC1)(=O)=O)=O)NC([C@H](C[C@H](C1)Oc2nc(OC)cc3c2ccc(OC)c3)N1C1=O)=O)C[C@@H](C)[C@@H]1NC(OC(C)(C)C(F)(F)F)=O Chemical compound C[C@@H](CC/C=C\[C@H](C1)[C@]1(C(NS(C1(CF)CC1)(=O)=O)=O)NC([C@H](C[C@H](C1)Oc2nc(OC)cc3c2ccc(OC)c3)N1C1=O)=O)C[C@@H](C)[C@@H]1NC(OC(C)(C)C(F)(F)F)=O VOJQGXLLIAGPHW-MLQDOLLDSA-N 0.000 description 1
- WDMOXEPEHPVMIB-PSZSXIAASA-N C[C@@H](CC/C=C\[C@H](C1)[C@]1(C(NS(C1CC1)(=O)=O)=O)NC([C@H](C[C@H](C1)Oc2c(ccc(OC)c3)c3ccn2)N1C1=O)=O)C[C@@H](C)[C@@H]1NC(OC(C)(C)C(F)(F)F)=O Chemical compound C[C@@H](CC/C=C\[C@H](C1)[C@]1(C(NS(C1CC1)(=O)=O)=O)NC([C@H](C[C@H](C1)Oc2c(ccc(OC)c3)c3ccn2)N1C1=O)=O)C[C@@H](C)[C@@H]1NC(OC(C)(C)C(F)(F)F)=O WDMOXEPEHPVMIB-PSZSXIAASA-N 0.000 description 1
- YKMAIDVFGIXTIO-LAGVYOHYSA-N C[C@@H](CCCC=C)[C@@H](C)C(C(O)=O)NC(OC(C)(C)C)=O Chemical compound C[C@@H](CCCC=C)[C@@H](C)C(C(O)=O)NC(OC(C)(C)C)=O YKMAIDVFGIXTIO-LAGVYOHYSA-N 0.000 description 1
- ZKNJNNKDTJMADK-JSHQXPJWSA-N C[C@H](CC/C=C\[C@H](C1)[C@]1(C(NS(C1(C)CC1)(=O)=O)=O)NC([C@H](C[C@H](C1)Oc(nc2)c(ccc(OC)c3)c3c2-c(cc2)cnc2OC)N1C1=O)=O)C[C@@H](C)[C@@H]1NC(OC(C)(C)C(F)(F)F)=O Chemical compound C[C@H](CC/C=C\[C@H](C1)[C@]1(C(NS(C1(C)CC1)(=O)=O)=O)NC([C@H](C[C@H](C1)Oc(nc2)c(ccc(OC)c3)c3c2-c(cc2)cnc2OC)N1C1=O)=O)C[C@@H](C)[C@@H]1NC(OC(C)(C)C(F)(F)F)=O ZKNJNNKDTJMADK-JSHQXPJWSA-N 0.000 description 1
- BSKLEWATXXVZLT-XXRAOSAGSA-N C[C@H](CC/C=C\[C@H](C1)[C@]1(C(NS(C1(C)CC1)(=O)=O)=O)NC([C@H](C[C@H](C1)Oc(nc2)c(ccc(OC)c3)c3c2OC)N1C1=O)=O)C[C@@H](C)[C@@H]1NC(OC(C)(C)C(F)(F)F)=O Chemical compound C[C@H](CC/C=C\[C@H](C1)[C@]1(C(NS(C1(C)CC1)(=O)=O)=O)NC([C@H](C[C@H](C1)Oc(nc2)c(ccc(OC)c3)c3c2OC)N1C1=O)=O)C[C@@H](C)[C@@H]1NC(OC(C)(C)C(F)(F)F)=O BSKLEWATXXVZLT-XXRAOSAGSA-N 0.000 description 1
- OEMPACGOUYYZCO-DHHITTSFSA-N C[C@H](CC/C=C\[C@H](C1)[C@]1(C(NS(C1(C)CC1)(=O)=O)=O)NC([C@H](C[C@H](C1)Oc2c(cccc3Cl)c3cc(OCC(F)F)n2)N1C1=O)=O)C[C@@H](C)[C@@H]1NC(OC(C)(C)C(F)(F)F)=O Chemical compound C[C@H](CC/C=C\[C@H](C1)[C@]1(C(NS(C1(C)CC1)(=O)=O)=O)NC([C@H](C[C@H](C1)Oc2c(cccc3Cl)c3cc(OCC(F)F)n2)N1C1=O)=O)C[C@@H](C)[C@@H]1NC(OC(C)(C)C(F)(F)F)=O OEMPACGOUYYZCO-DHHITTSFSA-N 0.000 description 1
- IREOCZPSBVGAFC-ITKUXEKXSA-N C[C@H](CC/C=C\[C@H](C1)[C@]1(C(NS(C1(CF)CC1)(=O)=O)=O)NC([C@H](C[C@H](C1)Oc2c(cc(c(OC)c3)F)c3ccn2)N1C1=O)=O)C[C@@H](C)[C@@H]1NC(OC(C)(C)C)=O Chemical compound C[C@H](CC/C=C\[C@H](C1)[C@]1(C(NS(C1(CF)CC1)(=O)=O)=O)NC([C@H](C[C@H](C1)Oc2c(cc(c(OC)c3)F)c3ccn2)N1C1=O)=O)C[C@@H](C)[C@@H]1NC(OC(C)(C)C)=O IREOCZPSBVGAFC-ITKUXEKXSA-N 0.000 description 1
- CBWYHVCPWLAFFL-SHYFOGMBSA-N C[C@H](CC/C=C\[C@H](C1)[C@]1(C(NS(C1(CF)CC1)(=O)=O)=O)NC([C@H](C[C@H](C1)Oc2c(ccc(OC)c3)c3cc(C(F)(F)F)n2)N1C1=O)=O)C[C@@H](C)[C@@H]1NC(OC(C)(C)C(C)(F)F)=O Chemical compound C[C@H](CC/C=C\[C@H](C1)[C@]1(C(NS(C1(CF)CC1)(=O)=O)=O)NC([C@H](C[C@H](C1)Oc2c(ccc(OC)c3)c3cc(C(F)(F)F)n2)N1C1=O)=O)C[C@@H](C)[C@@H]1NC(OC(C)(C)C(C)(F)F)=O CBWYHVCPWLAFFL-SHYFOGMBSA-N 0.000 description 1
- VOJQGXLLIAGPHW-NUTKTAOSSA-N C[C@H](CC/C=C\[C@H](C1)[C@]1(C(NS(C1(CF)CC1)(=O)=O)=O)NC([C@H](C[C@H](C1)Oc2c(ccc(OC)c3)c3cc(OC)n2)N1C1=O)=O)C[C@@H](C)[C@@H]1NC(OC(C)(C)C(F)(F)F)=O Chemical compound C[C@H](CC/C=C\[C@H](C1)[C@]1(C(NS(C1(CF)CC1)(=O)=O)=O)NC([C@H](C[C@H](C1)Oc2c(ccc(OC)c3)c3cc(OC)n2)N1C1=O)=O)C[C@@H](C)[C@@H]1NC(OC(C)(C)C(F)(F)F)=O VOJQGXLLIAGPHW-NUTKTAOSSA-N 0.000 description 1
- VRIDZGDXIMMGBK-UTWVIVDDSA-N C[C@H](CC/C=C\[C@H](C1)[C@]1(C(NS(C1(CF)CC1)(=O)=O)=O)NC([C@H](C[C@H](C1)Oc2nc(cc(cc3)OC)c3nc2)N1C1=O)=O)C[C@@H](C)[C@@H]1NC(OC(C)(C)C(F)(F)F)=O Chemical compound C[C@H](CC/C=C\[C@H](C1)[C@]1(C(NS(C1(CF)CC1)(=O)=O)=O)NC([C@H](C[C@H](C1)Oc2nc(cc(cc3)OC)c3nc2)N1C1=O)=O)C[C@@H](C)[C@@H]1NC(OC(C)(C)C(F)(F)F)=O VRIDZGDXIMMGBK-UTWVIVDDSA-N 0.000 description 1
- YYBSVXKCJKQRCT-LCEVOXARSA-N C[C@H](CC/C=C\[C@H](C1)[C@]1(C(NS(C1CC1)(=O)=O)=O)NC([C@H](C[C@H](C1)Oc(nc2)c(cc(c(OC)c3)F)c3c2OC)N1C1=O)=O)C[C@@H](C)[C@@H]1NC(OC(C)(C)C)=O Chemical compound C[C@H](CC/C=C\[C@H](C1)[C@]1(C(NS(C1CC1)(=O)=O)=O)NC([C@H](C[C@H](C1)Oc(nc2)c(cc(c(OC)c3)F)c3c2OC)N1C1=O)=O)C[C@@H](C)[C@@H]1NC(OC(C)(C)C)=O YYBSVXKCJKQRCT-LCEVOXARSA-N 0.000 description 1
- XWWVCPSZDZROEU-YJSFNWJYSA-N C[C@H](CC/C=C\[C@H](C1)[C@]1(C(NS(C1CC1)(=O)=O)=O)NC([C@H](C[C@H](C1)Oc(nc2)c(cccc3)c3c2OCCOC)N1C1=O)=O)C[C@@H](C)[C@@H]1NC(OC1CC(C2)[C@@H]2C1)=O Chemical compound C[C@H](CC/C=C\[C@H](C1)[C@]1(C(NS(C1CC1)(=O)=O)=O)NC([C@H](C[C@H](C1)Oc(nc2)c(cccc3)c3c2OCCOC)N1C1=O)=O)C[C@@H](C)[C@@H]1NC(OC1CC(C2)[C@@H]2C1)=O XWWVCPSZDZROEU-YJSFNWJYSA-N 0.000 description 1
- WDMOXEPEHPVMIB-HBJFQRDUSA-N C[C@H](CC/C=C\[C@H](C1)[C@]1(C(NS(C1CC1)(=O)=O)=O)NC([C@H](C[C@H](C1)Oc2c(ccc(OC)c3)c3ccn2)N1C1=O)=O)C[C@@H](C)[C@@H]1NC(OC(C)(C)C(F)(F)F)=O Chemical compound C[C@H](CC/C=C\[C@H](C1)[C@]1(C(NS(C1CC1)(=O)=O)=O)NC([C@H](C[C@H](C1)Oc2c(ccc(OC)c3)c3ccn2)N1C1=O)=O)C[C@@H](C)[C@@H]1NC(OC(C)(C)C(F)(F)F)=O WDMOXEPEHPVMIB-HBJFQRDUSA-N 0.000 description 1
- PUYOCGARVVBWFK-BEFMYCFFSA-N C[C@H](CC/C=C\[C@](C1)([C@]1(CNS(C1(C)CC1)(=O)=O)NC(C(C[C@H](C1)Oc2nc(cc(cc3)OC)c3nc2C)N1C1=O)=O)N=O)C[C@@H](C)[C@@H]1NC(OC(C)(C)C)=O Chemical compound C[C@H](CC/C=C\[C@](C1)([C@]1(CNS(C1(C)CC1)(=O)=O)NC(C(C[C@H](C1)Oc2nc(cc(cc3)OC)c3nc2C)N1C1=O)=O)N=O)C[C@@H](C)[C@@H]1NC(OC(C)(C)C)=O PUYOCGARVVBWFK-BEFMYCFFSA-N 0.000 description 1
- ZRQPDKAHJPCRRG-UHFFFAOYSA-N FC(Oc(cn1)c2c(Cl)cccc2c1Cl)F Chemical compound FC(Oc(cn1)c2c(Cl)cccc2c1Cl)F ZRQPDKAHJPCRRG-UHFFFAOYSA-N 0.000 description 1
- ODKYNOHKQZEDRZ-UHFFFAOYSA-N Fc(cc12)ccc1c(OC1CC1)cnc2Cl Chemical compound Fc(cc12)ccc1c(OC1CC1)cnc2Cl ODKYNOHKQZEDRZ-UHFFFAOYSA-N 0.000 description 1
- GVDOEFRAKCRLEL-UHFFFAOYSA-N O=C(OC1(COCCC1)C(F)(F)F)Oc1ncccc1 Chemical compound O=C(OC1(COCCC1)C(F)(F)F)Oc1ncccc1 GVDOEFRAKCRLEL-UHFFFAOYSA-N 0.000 description 1
- URUUZIAJVSGYRC-UHFFFAOYSA-N O=C1COCCC1 Chemical compound O=C1COCCC1 URUUZIAJVSGYRC-UHFFFAOYSA-N 0.000 description 1
- IRNDZVBNJTXDHF-UHFFFAOYSA-N O=S(CC(F)F)(OC(F)(F)F)=O Chemical compound O=S(CC(F)F)(OC(F)(F)F)=O IRNDZVBNJTXDHF-UHFFFAOYSA-N 0.000 description 1
- SOPGZIYGNDDLON-UHFFFAOYSA-N OC1(COCCC1)C(F)(F)F Chemical compound OC1(COCCC1)C(F)(F)F SOPGZIYGNDDLON-UHFFFAOYSA-N 0.000 description 1
- HISZXZFLXOUGGK-UHFFFAOYSA-N Oc(cn1)c2c(Cl)cccc2c1Cl Chemical compound Oc(cn1)c2c(Cl)cccc2c1Cl HISZXZFLXOUGGK-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K5/00—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
- C07K5/04—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing only normal peptide links
- C07K5/08—Tripeptides
- C07K5/0821—Tripeptides with the first amino acid being heterocyclic, e.g. His, Pro, Trp
- C07K5/0823—Tripeptides with the first amino acid being heterocyclic, e.g. His, Pro, Trp and Pro-amino acid; Derivatives thereof
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/13—Amines
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/47—Quinolines; Isoquinolines
- A61K31/4738—Quinolines; Isoquinolines ortho- or peri-condensed with heterocyclic ring systems
- A61K31/4745—Quinolines; Isoquinolines ortho- or peri-condensed with heterocyclic ring systems condensed with ring systems having nitrogen as a ring hetero atom, e.g. phenantrolines
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/70—Carbohydrates; Sugars; Derivatives thereof
- A61K31/7042—Compounds having saccharide radicals and heterocyclic rings
- A61K31/7052—Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides
- A61K31/7056—Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides containing five-membered rings with nitrogen as a ring hetero atom
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K38/00—Medicinal preparations containing peptides
- A61K38/04—Peptides having up to 20 amino acids in a fully defined sequence; Derivatives thereof
- A61K38/06—Tripeptides
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K38/00—Medicinal preparations containing peptides
- A61K38/16—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
- A61K38/17—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
- A61K38/19—Cytokines; Lymphokines; Interferons
- A61K38/20—Interleukins [IL]
- A61K38/2013—IL-2
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K38/00—Medicinal preparations containing peptides
- A61K38/16—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
- A61K38/17—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
- A61K38/19—Cytokines; Lymphokines; Interferons
- A61K38/20—Interleukins [IL]
- A61K38/204—IL-6
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K38/00—Medicinal preparations containing peptides
- A61K38/16—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
- A61K38/17—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
- A61K38/19—Cytokines; Lymphokines; Interferons
- A61K38/20—Interleukins [IL]
- A61K38/2053—IL-8
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K38/00—Medicinal preparations containing peptides
- A61K38/16—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
- A61K38/17—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
- A61K38/19—Cytokines; Lymphokines; Interferons
- A61K38/21—Interferons [IFN]
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K38/00—Medicinal preparations containing peptides
- A61K38/16—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
- A61K38/17—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
- A61K38/19—Cytokines; Lymphokines; Interferons
- A61K38/21—Interferons [IFN]
- A61K38/212—IFN-alpha
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K45/00—Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
- A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/12—Antivirals
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/12—Antivirals
- A61P31/14—Antivirals for RNA viruses
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/04—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K5/00—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
- C07K5/04—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing only normal peptide links
- C07K5/08—Tripeptides
- C07K5/0802—Tripeptides with the first amino acid being neutral
- C07K5/0804—Tripeptides with the first amino acid being neutral and aliphatic
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K5/00—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
- C07K5/04—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing only normal peptide links
- C07K5/08—Tripeptides
- C07K5/0827—Tripeptides containing heteroatoms different from O, S, or N
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K5/00—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
- C07K5/04—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing only normal peptide links
- C07K5/12—Cyclic peptides with only normal peptide bonds in the ring
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K38/00—Medicinal preparations containing peptides
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Chemical & Material Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Organic Chemistry (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- Epidemiology (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Gastroenterology & Hepatology (AREA)
- Immunology (AREA)
- Zoology (AREA)
- Molecular Biology (AREA)
- Biochemistry (AREA)
- Biophysics (AREA)
- Genetics & Genomics (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Virology (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Oncology (AREA)
- Communicable Diseases (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Peptides Or Proteins (AREA)
- Medicinal Preparation (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Medicines Containing Material From Animals Or Micro-Organisms (AREA)
- Plural Heterocyclic Compounds (AREA)
Applications Claiming Priority (7)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201161482658P | 2011-05-05 | 2011-05-05 | |
| US61/482,658 | 2011-05-05 | ||
| US201261611171P | 2012-03-15 | 2012-03-15 | |
| US61/611,171 | 2012-03-15 | ||
| US13/459,403 | 2012-04-30 | ||
| US13/459,403 US8957203B2 (en) | 2011-05-05 | 2012-04-30 | Hepatitis C virus inhibitors |
| PCT/US2012/035974 WO2012151195A1 (en) | 2011-05-05 | 2012-05-01 | Hepatitis c virus inhibitors |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| KR20140035383A true KR20140035383A (ko) | 2014-03-21 |
Family
ID=46172898
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| KR1020137031994A Abandoned KR20140035383A (ko) | 2011-05-05 | 2012-05-01 | C형 간염 바이러스 억제제 |
Country Status (31)
| Country | Link |
|---|---|
| US (2) | US8957203B2 (enExample) |
| EP (1) | EP2705049B1 (enExample) |
| JP (1) | JP6023178B2 (enExample) |
| KR (1) | KR20140035383A (enExample) |
| CN (1) | CN103797024B (enExample) |
| AR (1) | AR086290A1 (enExample) |
| AU (1) | AU2012250920B2 (enExample) |
| BR (1) | BR112013028487A2 (enExample) |
| CA (1) | CA2835105A1 (enExample) |
| CL (1) | CL2013003171A1 (enExample) |
| CO (1) | CO6821947A2 (enExample) |
| CY (1) | CY1118567T1 (enExample) |
| DK (1) | DK2705049T3 (enExample) |
| EA (1) | EA022624B1 (enExample) |
| ES (1) | ES2610967T3 (enExample) |
| HR (1) | HRP20161632T1 (enExample) |
| HU (1) | HUE033001T2 (enExample) |
| IL (1) | IL229270B (enExample) |
| LT (1) | LT2705049T (enExample) |
| MX (1) | MX2013012749A (enExample) |
| PE (1) | PE20141032A1 (enExample) |
| PH (1) | PH12013502190A1 (enExample) |
| PL (1) | PL2705049T3 (enExample) |
| PT (1) | PT2705049T (enExample) |
| RS (1) | RS55563B1 (enExample) |
| SG (1) | SG194749A1 (enExample) |
| SI (1) | SI2705049T1 (enExample) |
| SM (2) | SMT201700029T1 (enExample) |
| TW (1) | TWI542589B (enExample) |
| UY (1) | UY34057A (enExample) |
| WO (1) | WO2012151195A1 (enExample) |
Families Citing this family (18)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US8957203B2 (en) | 2011-05-05 | 2015-02-17 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
| US8691757B2 (en) | 2011-06-15 | 2014-04-08 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
| UA119315C2 (uk) | 2012-07-03 | 2019-06-10 | Гіліад Фармассет Елелсі | Інгібітори вірусу гепатиту с |
| CN104507912B (zh) | 2012-08-08 | 2016-09-28 | 默克专利股份公司 | (氮杂-)异喹啉酮衍生物 |
| JP6154474B2 (ja) * | 2012-10-19 | 2017-06-28 | ブリストル−マイヤーズ スクイブ カンパニーBristol−Myers Squibb Company | C型肝炎ウイルス阻害剤 |
| WO2014071007A1 (en) * | 2012-11-02 | 2014-05-08 | Bristol-Myers Squibb Company | Hepatitis c virus inhibitors |
| US9643999B2 (en) * | 2012-11-02 | 2017-05-09 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
| EP2914613B1 (en) | 2012-11-02 | 2017-11-22 | Bristol-Myers Squibb Company | Hepatitis c virus inhibitors |
| EP2914614B1 (en) * | 2012-11-05 | 2017-08-16 | Bristol-Myers Squibb Company | Hepatitis c virus inhibitors |
| EP2964664B1 (en) | 2013-03-07 | 2017-01-11 | Bristol-Myers Squibb Company | Hepatitis c virus inhibitors |
| JP6511432B2 (ja) | 2013-03-15 | 2019-05-15 | ギリアード サイエンシーズ, インコーポレイテッド | C型肝炎ウイルスの大環状二環式阻害剤 |
| CN108299425B (zh) * | 2015-03-24 | 2020-09-18 | 上海璎黎药业有限公司 | 稠环衍生物、其制备方法、中间体、药物组合物及应用 |
| US11072610B2 (en) | 2018-09-12 | 2021-07-27 | Novartis Ag | Antiviral pyridopyrazinedione compounds |
| CN113412249A (zh) | 2019-02-08 | 2021-09-17 | 大金工业株式会社 | 有机化合物的制造方法 |
| CN114667285B (zh) | 2019-09-26 | 2025-08-08 | 诺华股份有限公司 | 抗病毒吡唑并吡啶酮化合物 |
| US12083099B2 (en) | 2020-10-28 | 2024-09-10 | Accencio LLC | Methods of treating symptoms of coronavirus infection with viral protease inhibitors |
| EP4361142A4 (en) | 2021-06-25 | 2025-07-09 | Hangzhou Innogate Pharma Co Ltd | COMPOUND FOR USE AS A KIF18A INHIBITOR |
| US20240101531A1 (en) | 2022-06-08 | 2024-03-28 | Xenon Pharmaceuticals Inc. | Pyridinamine derivatives and their use as potassium channel modulators |
Family Cites Families (241)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0475255A3 (en) | 1990-09-12 | 1993-04-14 | F. Hoffmann-La Roche Ag | Process for the preparation of optically pure (s)-alpha-((tert-butylsulfonyl)methyl)hydro cinnamic acid |
| NZ335276A (en) | 1996-10-18 | 2000-09-29 | Vertex Pharma | Inhibitors of serine proteases, particularly hepatitis C virus (HCV) NS3 (Non Structural Protein 3) protease |
| PT1012180E (pt) | 1997-08-11 | 2005-04-29 | Boehringer Ingelheim Ca Ltd | Analogos de peptidos inibidores da hepatite c |
| IL134232A0 (en) | 1997-08-11 | 2001-04-30 | Boehringer Ingelheim Ca Ltd | Hepatitis c inhibitor peptides |
| US6323180B1 (en) | 1998-08-10 | 2001-11-27 | Boehringer Ingelheim (Canada) Ltd | Hepatitis C inhibitor tri-peptides |
| AR022061A1 (es) | 1998-08-10 | 2002-09-04 | Boehringer Ingelheim Ca Ltd | Peptidos inhibidores de la hepatitis c, una composicion farmaceutica que los contiene, el uso de los mismos para preparar una composicion farmaceutica, el uso de un producto intermedio para la preparacion de estos peptidos y un procedimiento para la preparacion de un peptido analogo de los mismos. |
| US6608027B1 (en) * | 1999-04-06 | 2003-08-19 | Boehringer Ingelheim (Canada) Ltd | Macrocyclic peptides active against the hepatitis C virus |
| UA74546C2 (en) * | 1999-04-06 | 2006-01-16 | Boehringer Ingelheim Ca Ltd | Macrocyclic peptides having activity relative to hepatitis c virus, a pharmaceutical composition and use of the pharmaceutical composition |
| US7244721B2 (en) | 2000-07-21 | 2007-07-17 | Schering Corporation | Peptides as NS3-serine protease inhibitors of hepatitis C virus |
| US7012066B2 (en) | 2000-07-21 | 2006-03-14 | Schering Corporation | Peptides as NS3-serine protease inhibitors of hepatitis C virus |
| MXPA03004299A (es) | 2000-11-20 | 2004-02-12 | Bristol Myers Squibb Co | Inhibidores de tripeptido de hepatitis c. |
| US6867185B2 (en) | 2001-12-20 | 2005-03-15 | Bristol-Myers Squibb Company | Inhibitors of hepatitis C virus |
| CA2369711A1 (en) | 2002-01-30 | 2003-07-30 | Boehringer Ingelheim (Canada) Ltd. | Macrocyclic peptides active against the hepatitis c virus |
| CA2370396A1 (en) | 2002-02-01 | 2003-08-01 | Boehringer Ingelheim (Canada) Ltd. | Hepatitis c inhibitor tri-peptides |
| CA2369970A1 (en) | 2002-02-01 | 2003-08-01 | Boehringer Ingelheim (Canada) Ltd. | Hepatitis c inhibitor tri-peptides |
| US6828301B2 (en) | 2002-02-07 | 2004-12-07 | Boehringer Ingelheim International Gmbh | Pharmaceutical compositions for hepatitis C viral protease inhibitors |
| PL215228B1 (pl) | 2002-05-20 | 2013-11-29 | Bristol Myers Squibb Co | Zwiazki tripeptydowe, ich zastosowanie i kompozycja farmaceutyczna je zawierajaca oraz jej zastosowanie |
| AU2003248535A1 (en) | 2002-05-20 | 2003-12-12 | Bristol-Myers Squibb Company | Heterocyclicsulfonamide hepatitis c virus inhibitors |
| ES2315568T3 (es) | 2002-05-20 | 2009-04-01 | Bristol-Myers Squibb Company | Inhibidores del virus de la hepatitis c basados en cicloalquilo p1' sustituido. |
| MY140680A (en) | 2002-05-20 | 2010-01-15 | Bristol Myers Squibb Co | Hepatitis c virus inhibitors |
| US20060199773A1 (en) | 2002-05-20 | 2006-09-07 | Sausker Justin B | Crystalline forms of (1R,2S)-N-[(1,1-dimethylethoxy)carbonyl]-3-methyl-L-valyl-(4R)-4-[(6-methoxy-1-isoquinolinyl)oxy]-L-prolyl-1-amino-N-(cyclopropylsulfonyl)-2-ethenyl-cyclopropanecarboxamide, monopotassium salt |
| US20040033959A1 (en) | 2002-07-19 | 2004-02-19 | Boehringer Ingelheim Pharmaceuticals, Inc. | Pharmaceutical compositions for hepatitis C viral protease inhibitors |
| US20050075279A1 (en) | 2002-10-25 | 2005-04-07 | Boehringer Ingelheim International Gmbh | Macrocyclic peptides active against the hepatitis C virus |
| US7601709B2 (en) | 2003-02-07 | 2009-10-13 | Enanta Pharmaceuticals, Inc. | Macrocyclic hepatitis C serine protease inhibitors |
| CN1771050A (zh) * | 2003-02-07 | 2006-05-10 | 益安药业 | 丙型肝炎丝氨酸蛋白酶的大环抑制剂 |
| JP4550824B2 (ja) | 2003-03-05 | 2010-09-22 | 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型肝炎抑制化合物 |
| DE602004029866D1 (de) | 2003-03-05 | 2010-12-16 | Boehringer Ingelheim Pharma | Peptidanaloga mit inhibitorischer wirkung auf hepatitis c |
| RS20050741A (sr) | 2003-04-02 | 2007-06-04 | Boehringer Ingelheim International Gmbh., | Farmaceutske kompozicije za inhibitore virusne proteaze hepatitisa c |
| ATE422895T1 (de) * | 2003-04-16 | 2009-03-15 | Bristol Myers Squibb Co | Makrocyclische isochinolinpeptidinhibitoren des hepatitis-c-virus |
| WO2004093798A2 (en) | 2003-04-18 | 2004-11-04 | Enanta Pharmaceuticals, Inc. | Quinoxalinyl macrocyclic hepatitis c serine protease inhibitors |
| CL2004001161A1 (es) | 2003-05-21 | 2005-04-08 | Boehringer Ingelheim Int | Compuestos describe compuestos derivados de quinolina; composicion farmaceutica; y su uso para tratar una enfermedad causada por el virus de la hepatitis c. |
| WO2004113365A2 (en) | 2003-06-05 | 2004-12-29 | Enanta Pharmaceuticals, Inc. | Hepatitis c serine protease tri-peptide inhibitors |
| US7125845B2 (en) | 2003-07-03 | 2006-10-24 | Enanta Pharmaceuticals, Inc. | Aza-peptide macrocyclic hepatitis C serine protease inhibitors |
| EP1673385B1 (en) | 2003-09-22 | 2011-03-02 | Boehringer Ingelheim International GmbH | Macrocyclic peptides active against the hepatitis c virus |
| NZ546663A (en) | 2003-10-10 | 2010-01-29 | Vertex Pharma | Inhibitors of serine proteases, particularly HCV NS3-NS4A protease |
| WO2005037214A2 (en) | 2003-10-14 | 2005-04-28 | Intermune, Inc. | Macrocyclic carboxylic acids and acylsulfonamides as inhibitors of hcv replication |
| US7132504B2 (en) | 2003-11-12 | 2006-11-07 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
| US7135462B2 (en) | 2003-11-20 | 2006-11-14 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
| MXPA06005683A (es) | 2003-11-20 | 2006-12-14 | Schering Corp | Inhibidores despeptidizados de la proteasa ns3 del virus de la hepatitis c. |
| US7309708B2 (en) | 2003-11-20 | 2007-12-18 | Birstol-Myers Squibb Company | Hepatitis C virus inhibitors |
| WO2005070955A1 (en) | 2004-01-21 | 2005-08-04 | Boehringer Ingelheim International Gmbh | Macrocyclic peptides active against the hepatitis c virus |
| ES2336009T3 (es) | 2004-01-30 | 2010-04-07 | Medivir Ab | Inhibidores de la ns-3 serina proteasa del vhc. |
| ES2338666T3 (es) | 2004-03-15 | 2010-05-11 | Boehringer Ingelheim International Gmbh | Procedimiento para la preparacion de dipeptidos macrociclicos adecuados para el tratamiento de infecciones viricas de la hepatitis c. |
| EP1749007A2 (en) | 2004-03-30 | 2007-02-07 | Intermune, Inc. | Macrocyclic compounds as inhibitors of viral replication |
| WO2006016930A2 (en) | 2004-05-14 | 2006-02-16 | Intermune, Inc. | Methods for treating hcv infection |
| EP1753775B1 (en) | 2004-05-25 | 2012-12-26 | Boehringer Ingelheim International GmbH | Process for preparing acyclic hcv protease inhibitors |
| JP4914348B2 (ja) | 2004-06-28 | 2012-04-11 | 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型肝炎インヒビターペプチド類似体 |
| KR20070034119A (ko) | 2004-07-16 | 2007-03-27 | 길리애드 사이언시즈, 인코포레이티드 | 항바이러스 화합물 |
| UY29016A1 (es) | 2004-07-20 | 2006-02-24 | Boehringer Ingelheim Int | Analogos de dipeptidos inhibidores de la hepatitis c |
| JP4914355B2 (ja) | 2004-07-20 | 2012-04-11 | 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型肝炎インヒビターペプチド類似体 |
| MX2007002371A (es) | 2004-08-27 | 2007-04-23 | Schering Corp | Compuestos de acilsulfonamida como inhibidores de la serina proteasa ns3 del virus de la hepatitis c. |
| US7375218B2 (en) | 2004-09-17 | 2008-05-20 | Boehringer Ingelheim International Gmbh | Process for preparing macrocyclic HCV protease inhibitors |
| WO2007001406A2 (en) | 2004-10-05 | 2007-01-04 | Chiron Corporation | Aryl-containing macrocyclic compounds |
| MX2007004783A (es) | 2004-10-21 | 2007-05-11 | Pfizer | Inhibidores de la proteasa del virus de la hepatitis c, y composiciones y tratamientos que los usan. |
| US7323447B2 (en) | 2005-02-08 | 2008-01-29 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
| CN103172697A (zh) | 2005-03-08 | 2013-06-26 | 贝林格尔.英格海姆国际有限公司 | 制备大环化合物的方法 |
| AU2006242475B2 (en) | 2005-05-02 | 2011-07-07 | Merck Sharp & Dohme Corp. | HCV NS3 protease inhibitors |
| US7592336B2 (en) | 2005-05-10 | 2009-09-22 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
| US20060276405A1 (en) | 2005-06-02 | 2006-12-07 | Schering Corporation | Methods for treating hepatitis C |
| WO2006130552A2 (en) | 2005-06-02 | 2006-12-07 | Schering Corporation | Methods of treating hepatitis c virus |
| US8119602B2 (en) | 2005-06-02 | 2012-02-21 | Schering Corporation | Administration of HCV protease inhibitors in combination with food to improve bioavailability |
| US20060281689A1 (en) | 2005-06-02 | 2006-12-14 | Schering Corporation | Method for modulating activity of HCV protease through use of a novel HCV protease inhibitor to reduce duration of treatment period |
| US20070004635A1 (en) | 2005-06-02 | 2007-01-04 | Schering Corporation | Method of treating interferon non-responders using HCV protease inhibitor |
| US20060276407A1 (en) | 2005-06-02 | 2006-12-07 | Schering Corporation | Methods of treating hepatitis C virus |
| JP2008545748A (ja) | 2005-06-02 | 2008-12-18 | シェーリング コーポレイション | C型肝炎ウイルスに関連する障害を処置するために有用な徐放処方物 |
| WO2006130666A2 (en) | 2005-06-02 | 2006-12-07 | Schering Corporation | Medicaments and methods combining a hcv protease inhibitor and an akr competitor |
| US20070021351A1 (en) | 2005-06-02 | 2007-01-25 | Schering Corporation | Liver/plasma concentration ratio for dosing hepatitis C virus protease inhibitor |
| US20060287248A1 (en) | 2005-06-02 | 2006-12-21 | Schering Corporation | Asymmetric dosing methods |
| US7772178B2 (en) | 2005-06-02 | 2010-08-10 | Schering Corporation | Pharmaceutical formulations and methods of treatment using the same |
| US7601686B2 (en) | 2005-07-11 | 2009-10-13 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
| TWI389908B (zh) | 2005-07-14 | 2013-03-21 | Gilead Sciences Inc | 抗病毒化合物類 |
| TW200738742A (en) | 2005-07-14 | 2007-10-16 | Gilead Sciences Inc | Antiviral compounds |
| US20080200497A1 (en) | 2005-07-20 | 2008-08-21 | Bailey Murray D | Hepatitis C Inhibitor Peptide Analogs |
| AR057456A1 (es) | 2005-07-20 | 2007-12-05 | Merck & Co Inc | Inhibidores de la proteasa ns3 del vhc |
| EP2305696A3 (en) | 2005-07-25 | 2011-10-12 | Intermune, Inc. | Macrocyclic inhibitors of Hepatitis C virus replication |
| PE20070343A1 (es) | 2005-07-29 | 2007-05-12 | Medivir Ab | Inhibidores macrociclicos del virus de la hepatitis c |
| AR055105A1 (es) | 2005-07-29 | 2007-08-08 | Tibotec Pharm Ltd | Inhibidores macrociclicos del virus de la hepatitis c |
| EP1919904B1 (en) | 2005-07-29 | 2014-01-08 | Janssen R&D Ireland | Macrocyclic inhibitors of hepatitis c virus |
| EP1910347A2 (en) | 2005-07-29 | 2008-04-16 | Medivir Ab | Macrocylic inhibitors of hepatitis c virus |
| PE20070210A1 (es) | 2005-07-29 | 2007-04-16 | Tibotec Pharm Ltd | Compuestos macrociclicos como inhibidores del virus de hepatitis c |
| BRPI0614637A2 (pt) | 2005-07-29 | 2011-04-12 | Tibotec Pharm Ltd | inibidores macrocìclicos do vìrus da hepatite c |
| PE20070211A1 (es) | 2005-07-29 | 2007-05-12 | Medivir Ab | Compuestos macrociclicos como inhibidores del virus de hepatitis c |
| JO2768B1 (en) | 2005-07-29 | 2014-03-15 | تيبوتيك فارماسيوتيكالز ليمتد | Large cyclic inhibitors of hepatitis C virus |
| WO2007014922A1 (en) | 2005-07-29 | 2007-02-08 | Tibotec Pharmaceuticals Ltd. | Macrocyclic inhibitors of hepatitis c virus |
| ATE496042T1 (de) | 2005-07-29 | 2011-02-15 | Tibotec Pharm Ltd | Makrocyclische inhibitoren des hepatitis-c-virus |
| RU2436787C2 (ru) | 2005-07-29 | 2011-12-20 | Тиботек Фармасьютикалз Лтд. | Макроциклические ингибиторы вируса гепатита с |
| US8278322B2 (en) | 2005-08-01 | 2012-10-02 | Merck Sharp & Dohme Corp. | HCV NS3 protease inhibitors |
| WO2007016476A2 (en) | 2005-08-01 | 2007-02-08 | Phenomix Corporation | Hepatitis c serine protease inhibitors and uses therefor |
| AR055395A1 (es) | 2005-08-26 | 2007-08-22 | Vertex Pharma | Compuestos inhibidores de la actividad de la serina proteasa ns3-ns4a del virus de la hepatitis c |
| EP1934243B1 (en) | 2005-09-09 | 2011-05-25 | Boehringer Ingelheim International GmbH | Ring-closing metathesis process for the preparation of macrocyclic peptides |
| EA200801050A1 (ru) | 2005-10-11 | 2008-12-30 | Интермьюн, Инк. | Соединения и способы ингибирования репликации вирусного гепатита с |
| US7772183B2 (en) | 2005-10-12 | 2010-08-10 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
| US7741281B2 (en) * | 2005-11-03 | 2010-06-22 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
| WO2007082131A1 (en) | 2006-01-09 | 2007-07-19 | Bristol-Myers Squibb Company | Process for the preparation of hydroxy substituted heterocycles |
| JP2009528353A (ja) | 2006-03-03 | 2009-08-06 | シェーリング コーポレイション | Hcvのプロテアーゼ阻害剤およびires阻害剤の医薬的組み合わせ |
| WO2007120595A2 (en) | 2006-04-11 | 2007-10-25 | Novartis Ag | Amines for the treatment of hcv |
| GB0609492D0 (en) | 2006-05-15 | 2006-06-21 | Angeletti P Ist Richerche Bio | Therapeutic agents |
| US8268776B2 (en) | 2006-06-06 | 2012-09-18 | Enanta Pharmaceuticals, Inc. | Macrocylic oximyl hepatitis C protease inhibitors |
| US20070281884A1 (en) | 2006-06-06 | 2007-12-06 | Ying Sun | Macrocyclic oximyl hepatitis C protease inhibitors |
| GB0612423D0 (en) | 2006-06-23 | 2006-08-02 | Angeletti P Ist Richerche Bio | Therapeutic agents |
| UY30437A1 (es) | 2006-06-26 | 2008-01-31 | Enanta Pharm Inc | Quinoxalinil macroceclicos inhibidores de serina proteasa del virus de la hepatitis c |
| RU2008152171A (ru) | 2006-07-05 | 2010-08-10 | Интермьюн, Инк. (Us) | Новые ингибиторы вирусной репликации гепатита с |
| US7893264B2 (en) | 2006-07-07 | 2011-02-22 | Gilead Sciences, Inc. | Antiviral phosphinate compounds |
| WO2008008776A2 (en) | 2006-07-11 | 2008-01-17 | Bristol-Myers Squibb Company | Hepatitis c virus inhibitors |
| ES2448494T3 (es) | 2006-07-13 | 2014-03-14 | Achillion Pharmaceuticals, Inc. | Péptidos de 4-amino-4-oxobutanoilo en calidad de inhibidores de la replicación viral |
| US20090035267A1 (en) | 2007-07-31 | 2009-02-05 | Moore Joel D | Acyclic, pyridazinone-derived hepatitis c serine protease inhibitors |
| CN101674844A (zh) | 2006-08-04 | 2010-03-17 | 英安塔制药有限公司 | 四唑基大环类c型肝炎丝氨酸蛋白酶抑制剂 |
| WO2008019303A2 (en) | 2006-08-04 | 2008-02-14 | Enanta Pharmaceuticals, Inc. | Pyridazinonyl macrocyclic hepatitis c serine protease inhibitors |
| US7635683B2 (en) | 2006-08-04 | 2009-12-22 | Enanta Pharmaceuticals, Inc. | Quinoxalinyl tripeptide hepatitis C virus inhibitors |
| WO2008021960A2 (en) | 2006-08-11 | 2008-02-21 | Enanta Pharmaceuticals, Inc. | Triazolyl macrocyclic hepatitis c serine protease inhibitors |
| US7582605B2 (en) | 2006-08-11 | 2009-09-01 | Enanta Pharmaceuticals, Inc. | Phosphorus-containing hepatitis C serine protease inhibitors |
| US7605126B2 (en) | 2006-08-11 | 2009-10-20 | Enanta Pharmaceuticals, Inc. | Acylaminoheteroaryl hepatitis C virus protease inhibitors |
| US20080038225A1 (en) | 2006-08-11 | 2008-02-14 | Ying Sun | Triazolyl acyclic hepatitis c serine protease inhibitors |
| US20090035268A1 (en) | 2007-08-01 | 2009-02-05 | Ying Sun | Tetrazolyl acyclic hepatitis c serine protease inhibitors |
| WO2008022006A2 (en) | 2006-08-11 | 2008-02-21 | Enanta Pharmaceuticals, Inc. | Arylalkoxyl hepatitis c virus protease inhibitors |
| CA2667165A1 (en) | 2006-10-24 | 2008-05-02 | Merck & Co., Inc. | Hcv ns3 protease inhibitors |
| US8138164B2 (en) | 2006-10-24 | 2012-03-20 | Merck Sharp & Dohme Corp. | HCV NS3 protease inhibitors |
| CN101583372A (zh) | 2006-10-24 | 2009-11-18 | 默克公司 | Hcv ns3蛋白酶抑制剂 |
| WO2008057208A2 (en) | 2006-10-27 | 2008-05-15 | Merck & Co., Inc. | Hcv ns3 protease inhibitors |
| JP5268927B2 (ja) | 2006-10-27 | 2013-08-21 | メルク・シャープ・アンド・ドーム・コーポレーション | Hcvns3プロテアーゼ阻害剤 |
| US8343477B2 (en) | 2006-11-01 | 2013-01-01 | Bristol-Myers Squibb Company | Inhibitors of hepatitis C virus |
| US20080107623A1 (en) | 2006-11-01 | 2008-05-08 | Bristol-Myers Squibb Company | Inhibitors of Hepatitis C Virus |
| US20080107625A1 (en) | 2006-11-01 | 2008-05-08 | Bristol-Myers Squibb Company | Inhibitors of Hepatitis C Virus |
| WO2008057995A2 (en) | 2006-11-02 | 2008-05-15 | Taigen Biotechnology Co., Ltd. | Hcv protease inhibitors |
| US7772180B2 (en) | 2006-11-09 | 2010-08-10 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
| US7763584B2 (en) | 2006-11-16 | 2010-07-27 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
| WO2008070358A2 (en) | 2006-11-16 | 2008-06-12 | Phenomix Corporation | N-cyclopropyl-hydroxyproline-based tripeptidic hepatitis c serine protease inhibitors containing an isoindole, pyrrolopyridine, pyrrolopyrimidine or pyrrolopyrazine heterocycle in the side chain |
| US8003604B2 (en) | 2006-11-16 | 2011-08-23 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
| US7888464B2 (en) | 2006-11-16 | 2011-02-15 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
| WO2008059046A1 (en) | 2006-11-17 | 2008-05-22 | Tibotec Pharmaceuticals Ltd. | Macrocyclic inhibitors of hepatitis c virus |
| US20100323953A1 (en) | 2007-01-08 | 2010-12-23 | Phenomix Corporation | Macrocyclic hepatitis c protease inhibitors |
| RU2483067C2 (ru) | 2007-02-01 | 2013-05-27 | Тиботек Фармасьютикалз Лтд. | Способы и промежуточные продукты для получения макроциклического ингибитора протеазы вируса гепатита с |
| SI2118098T1 (sl) | 2007-02-01 | 2015-01-30 | Janssen R&D Ireland | Polimorfne oblike makrocikličnega inhibitorja HCV |
| US20080207528A1 (en) | 2007-02-01 | 2008-08-28 | Syaulan Yang | Hcv protease inhibitors |
| WO2008096002A1 (en) | 2007-02-08 | 2008-08-14 | Tibotec Pharmaceuticals Ltd. | Hcv inhibiting macrocyclic phosphonates and amidophosphates |
| MX2009008541A (es) | 2007-02-08 | 2009-08-18 | Tibotec Pharm Ltd | Fenilcarbamatos macrociclicos que inhiben el virus de hepatitis c. |
| RU2481340C2 (ru) | 2007-02-08 | 2013-05-10 | Тиботек Фармасьютикалз Лтд. | Пиримидин-замещенные макроциклические ингибиторы hcv |
| JP2010518128A (ja) | 2007-02-16 | 2010-05-27 | 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ns3プロテアーゼのインヒビター |
| BRPI0807887A2 (pt) | 2007-02-20 | 2014-06-17 | Novartis Ag | Compostos macrocíclicos como inibidores de hcv ns3 protease. |
| EP2125113A2 (en) | 2007-02-26 | 2009-12-02 | Achillion Pharmaceuticals, Inc. | Tertiary amine substituted peptides useful as inhibitors of hcv replication |
| ES2355437T3 (es) | 2007-04-24 | 2011-03-25 | F. Hoffmann-La Roche Ag | Procedimiento para un intermediario de inhibidores de proteasa del vhc. |
| WO2008134395A1 (en) | 2007-04-26 | 2008-11-06 | Enanta Pharmaceuticals, Inc. | Aza-peptide macrocyclic hepatitis c serine protease inhibitors |
| WO2008134397A1 (en) | 2007-04-26 | 2008-11-06 | Enanta Pharmaceuticals, Inc. | Aza-tripeptide hepatitis c serine protease inhibitors |
| US20080292587A1 (en) | 2007-04-26 | 2008-11-27 | Ying Sun | Oximyl dipeptide hepatitis c protease inhibitors |
| US20080279821A1 (en) | 2007-04-26 | 2008-11-13 | Deqiang Niu | Arylpiperidinyl and arylpyrrolidinyl macrocyclic hepatitis c serine protease inhibitors |
| WO2008137779A2 (en) | 2007-05-03 | 2008-11-13 | Intermune, Inc. | Novel macrocyclic inhibitors of hepatitis c virus replication |
| CA2686546A1 (en) | 2007-05-10 | 2008-11-20 | Intermune, Inc. | Novel peptide inhibitors of hepatitis c virus replication |
| AR067180A1 (es) | 2007-06-29 | 2009-09-30 | Gilead Sciences Inc | Compuestos antivirales |
| NZ582096A (en) | 2007-06-29 | 2012-05-25 | Gilead Sciences Inc | Antiviral compounds that inhibit hepatitis c virus (hcv) |
| AR068794A1 (es) | 2007-06-29 | 2009-12-09 | Gilead Sciences Inc | Compuestos antivirales |
| CN101754974B (zh) | 2007-07-19 | 2016-02-03 | Msd意大利有限公司 | 作为抗病毒剂的大环化合物 |
| WO2009014730A1 (en) | 2007-07-26 | 2009-01-29 | Idenix Pharmaceuticals, Inc. | Macrocyclic serine protease inhibitors |
| KR101396696B1 (ko) | 2007-10-10 | 2014-05-16 | 노파르티스 아게 | 스피로피롤리딘, 및 hcv 및 hiv 감염에 대한 그의 용도 |
| WO2009053828A2 (en) | 2007-10-22 | 2009-04-30 | Enanta Pharmaceuticals, Inc. | P3 hydroxyamino macrocyclic hepatitis c serine protease inhibitors |
| US20090111757A1 (en) | 2007-10-25 | 2009-04-30 | Taigen Biotechnology Co., Ltd. | Hcv protease inhibitors |
| CL2008003384A1 (es) | 2007-11-14 | 2009-12-11 | Enanta Pharm Inc | Compuestos derivados de quinoxalina macrocíclica, inhibidores de serina proteasa; composicion farmaceutica que los comprende; y su uso en el tratamiento de la hepatitis c. |
| JP2011503201A (ja) | 2007-11-14 | 2011-01-27 | エナンタ ファーマシューティカルズ インコーポレイテッド | 大環状テトラゾリルc型肝炎セリンプロテアーゼ阻害剤 |
| US8263549B2 (en) | 2007-11-29 | 2012-09-11 | Enanta Pharmaceuticals, Inc. | C5-substituted, proline-derived, macrocyclic hepatitis C serine protease inhibitors |
| US8030307B2 (en) | 2007-11-29 | 2011-10-04 | Enanta Pharmaceuticals, Inc. | Bicyclic, C5-substituted proline derivatives as inhibitors of the hepatitis C virus NS3 protease |
| WO2009073713A1 (en) | 2007-12-05 | 2009-06-11 | Enanta Pharmaceuticals, Inc. | Oximyl macrocyclic derivatives |
| WO2009076166A2 (en) | 2007-12-05 | 2009-06-18 | Enanta Pharmaceuticals, Inc. | Oximyl hcv serine protease inhibitors |
| CA2708150A1 (en) | 2007-12-05 | 2009-06-18 | Enanta Pharmaceuticals, Inc. | Fluorinated tripeptide hcv serine protease inhibitors |
| MX2010006209A (es) | 2007-12-05 | 2010-08-10 | Enanta Pharm Inc | Derivados de quinoxalinilo. |
| CA2708047A1 (en) | 2007-12-06 | 2009-06-11 | Enanta Pharmaceuticals, Inc. | Process for making macrocyclic oximyl hepatitis c protease inhibitors |
| JP2011506472A (ja) | 2007-12-14 | 2011-03-03 | エナンタ ファーマシューティカルズ インコーポレイテッド | 大環状オキシミルc型肝炎セリンプロテアーゼ阻害剤 |
| WO2009079353A1 (en) | 2007-12-14 | 2009-06-25 | Enanta Pharmaceuticals, Inc. | Triazole-containing macrocyclic hcv serine protease inhibitors |
| US8293705B2 (en) | 2007-12-21 | 2012-10-23 | Avila Therapeutics, Inc. | HCV protease inhibitors and uses thereof |
| US8309685B2 (en) | 2007-12-21 | 2012-11-13 | Celgene Avilomics Research, Inc. | HCV protease inhibitors and uses thereof |
| CN104557880A (zh) | 2007-12-21 | 2015-04-29 | 阿维拉制药公司 | Hcv蛋白酶抑制剂和其用途 |
| AU2008340430B2 (en) | 2007-12-21 | 2013-01-24 | F. Hoffmann-La Roche Ag | Process for the preparation of a macrocycle |
| US8202996B2 (en) | 2007-12-21 | 2012-06-19 | Bristol-Myers Squibb Company | Crystalline forms of N-(tert-butoxycarbonyl)-3-methyl-L-valyl-(4R)-4-((7-chloro-4-methoxy-1-isoquinolinyl)oxy)-N- ((1R,2S)-1-((cyclopropylsulfonyl)carbamoyl)-2-vinylcyclopropyl)-L-prolinamide |
| WO2009082697A1 (en) | 2007-12-21 | 2009-07-02 | Avila Therapeutics, Inc. | Hcv protease inhibitors and uses thereof |
| CA2713005A1 (en) | 2008-01-24 | 2009-07-30 | Enanta Pharmaceuticals, Inc. | Difluorinated tripeptides as hcv serine protease inhibitors |
| JP2011510926A (ja) | 2008-01-24 | 2011-04-07 | エナンタ ファーマシューティカルズ インコーポレイテッド | ヘテロアリール含有トリペプチドhcvセリンプロテアーゼ阻害剤 |
| CA2714604A1 (en) | 2008-02-25 | 2009-09-03 | Merck Sharp & Dohme Corp. | Macrocyclic hcv ns3 protease inhibitors |
| CA2719008A1 (en) | 2008-03-20 | 2009-09-24 | Enanta Pharmaceuticals, Inc. | Fluorinated macrocyclic compounds as hepatitis c virus inhibitors |
| WO2009142842A2 (en) | 2008-04-15 | 2009-11-26 | Intermune, Inc. | Novel macrocyclic inhibitors of hepatitis c virus replication |
| US8163921B2 (en) | 2008-04-16 | 2012-04-24 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
| CN102014911A (zh) | 2008-04-28 | 2011-04-13 | 默沙东公司 | Hcv ns3蛋白酶抑制剂 |
| WO2009134987A1 (en) | 2008-04-30 | 2009-11-05 | Enanta Pharmaceuticals, Inc. | Difluoromethyl-containing macrocyclic compounds as hepatitis c virus inhibitors |
| US20090285773A1 (en) | 2008-05-15 | 2009-11-19 | Bristol-Myers Squibb Company | Hepatitis C Virus Inhibitors |
| US20090285774A1 (en) | 2008-05-15 | 2009-11-19 | Bristol-Myers Squibb Company | Hepatitis C Virus Inhibitors |
| CN101580535B (zh) | 2008-05-16 | 2012-10-03 | 太景生物科技股份有限公司 | 丙型肝炎病毒蛋白酶抑制剂 |
| US7964560B2 (en) | 2008-05-29 | 2011-06-21 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
| CN102046648A (zh) | 2008-05-29 | 2011-05-04 | 百时美施贵宝公司 | 丙型肝炎病毒抑制剂 |
| ES2392611T3 (es) | 2008-07-22 | 2012-12-12 | Merck Sharp & Dohme Corp. | Compuestos de quinoxalina macrocíclica como inhibidores de la proteasa NS3 del VHC |
| EP2323981B1 (en) | 2008-08-07 | 2014-03-12 | F. Hoffmann-La Roche AG | Process for the preparation of a macrocycle |
| UY32099A (es) | 2008-09-11 | 2010-04-30 | Enanta Pharm Inc | Inhibidores macrocíclicos de serina proteasas de hepatitis c |
| WO2010033466A1 (en) | 2008-09-16 | 2010-03-25 | Phenomix Corporation | Macrocyclic inhibitors of hepatitis c protease |
| TW201023858A (en) | 2008-09-18 | 2010-07-01 | Ortho Mcneil Janssen Pharm | Synergistic combinations of a macrocyclic inhibitor of HCV and a nucleoside |
| WO2010031832A2 (en) | 2008-09-18 | 2010-03-25 | Ortho-Mcneil-Janssen Pharmaceuticals, Inc | Synergistic combinations of a macrocyclic inhibitor of hcv and a thiophene-2-carboxylic acid derivative |
| EP2344487A4 (en) | 2008-09-23 | 2012-03-21 | Boehringer Ingelheim Int | HEPATITIS C INHIBITOR COMPOUNDS |
| US8563505B2 (en) | 2008-09-29 | 2013-10-22 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
| US8044087B2 (en) | 2008-09-29 | 2011-10-25 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
| US20100080770A1 (en) | 2008-09-29 | 2010-04-01 | Bristol-Myers Squibb Company | Hepatitis C Virus Inhibitors |
| JP5689810B2 (ja) | 2008-11-20 | 2015-03-25 | アキリオン ファーマシューティカルズ,インコーポレーテッド | C型肝炎ウイルス用の環状カルボキサミド化合物およびその類似体 |
| US20100272674A1 (en) | 2008-12-04 | 2010-10-28 | Bristol-Myers Squibb Company | Hepatitis C Virus Inhibitors |
| ES2527166T3 (es) | 2008-12-10 | 2015-01-21 | Achillion Pharmaceuticals, Inc. | Nuevos péptidos de 4-amino-4-oxobutanoílo como inhibidores de la replicación viral |
| US20100152103A1 (en) | 2008-12-10 | 2010-06-17 | Achillion Pharmaceuticals, Inc. | 4-amino-4-oxobutanoyl peptide cyclic analogues, inhibitors of viral replication |
| US8283310B2 (en) | 2008-12-15 | 2012-10-09 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
| MX2011006631A (es) | 2008-12-19 | 2011-09-06 | Gilead Sciences Inc | Inhibidores de proteasa ns3 del virus hcv. |
| AU2009330333A1 (en) | 2008-12-22 | 2011-07-07 | Gilead Sciences, Inc. | Antiviral compounds |
| JP2012516351A (ja) | 2009-01-30 | 2012-07-19 | アナコール ファーマシューティカルズ,インコーポレーテッド | 化合物 |
| US20110182850A1 (en) | 2009-04-10 | 2011-07-28 | Trixi Brandl | Organic compounds and their uses |
| US8512690B2 (en) | 2009-04-10 | 2013-08-20 | Novartis Ag | Derivatised proline containing peptide compounds as protease inhibitors |
| CA2761650C (en) | 2009-05-13 | 2015-05-26 | Enanta Pharmaceuticals, Inc. | Macrocyclic compounds as hepatitis c virus inhibitors |
| CN101921308A (zh) | 2009-06-16 | 2010-12-22 | 上海唐润医药科技有限公司 | 具有抗hcv活性的化合物及其用途 |
| US8232246B2 (en) | 2009-06-30 | 2012-07-31 | Abbott Laboratories | Anti-viral compounds |
| PE20120322A1 (es) | 2009-07-07 | 2012-04-14 | Boehringer Ingelheim Int | Composicion farmaceutica que comprende faldaprevir o una sal del mismo en un vehiculo auto-emulsionante |
| US8828930B2 (en) | 2009-07-30 | 2014-09-09 | Merck Sharp & Dohme Corp. | Hepatitis C virus NS3 protease inhibitors |
| EP2470189A4 (en) | 2009-08-27 | 2013-01-23 | Merck Sharp & Dohme | METHOD FOR PRODUCING PROTEASE INHIBITORS OF HEPATITIS C VIRUS |
| EP2477980B1 (en) | 2009-09-15 | 2016-06-08 | Taigen Biotechnology Co., Ltd. | Hcv protease inhibitors |
| MX2012003171A (es) | 2009-09-28 | 2012-04-11 | Hoffmann La Roche | Novedosos inhibidores macrociclicos de la replicacion del virus de hepatitis c. |
| CN105001302A (zh) | 2009-09-28 | 2015-10-28 | 英特穆恩公司 | C型肝炎病毒复制的环肽抑制剂 |
| TW201116540A (en) | 2009-10-01 | 2011-05-16 | Intermune Inc | Therapeutic antiviral peptides |
| US8415374B2 (en) | 2009-10-12 | 2013-04-09 | Bristol-Myers Squibb Company | Combinations of hepatitis C virus inhibitors |
| US9193740B2 (en) | 2009-10-19 | 2015-11-24 | Enanta Pharmaceuticals, Inc. | Bismacrocyclic compounds as hepatitis C virus inhibitors |
| JP2013511561A (ja) | 2009-11-24 | 2013-04-04 | 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 |
| WO2011063502A1 (en) | 2009-11-24 | 2011-06-03 | Boehringer Ingelheim International Gmbh | Hepatitis c inhibitor compounds |
| MX2012007076A (es) | 2009-12-18 | 2012-07-20 | Boehringer Ingelheim Int | Terapia combinada de hcv. |
| CA2788155C (en) | 2010-01-27 | 2018-04-24 | AB Pharma Ltd. | Polyheterocyclic compounds highly potent as hcv inhibitors |
| WO2011150190A2 (en) | 2010-05-26 | 2011-12-01 | Anacor Pharmaceuticals, Inc. | Hcv inhibitor compounds and methods of use thereof |
| EP2576564A4 (en) | 2010-06-07 | 2014-01-22 | Abbvie Inc | MACROCYCLIC HEPATITIS C SERIN PROTEASE INHIBITORS |
| US20120196794A1 (en) | 2010-08-06 | 2012-08-02 | Bristol-Myers Squibb Company | Combinations of Hepatitis C Virus Inhibitors |
| WO2012019299A1 (en) | 2010-08-11 | 2012-02-16 | Boehringer Ingelheim International Gmbh | Hepatitis c inhibitor compounds |
| WO2012037259A1 (en) | 2010-09-15 | 2012-03-22 | Intermune, Inc. | Novel inhibitors of hepatitis c virus replication |
| TWI523658B (zh) | 2010-09-21 | 2016-03-01 | 安塔製藥公司 | 巨環脯胺酸衍生之hcv絲胺酸蛋白酶抑制劑 |
| WO2012040040A1 (en) | 2010-09-21 | 2012-03-29 | Merck Sharp & Dohme Corp. | Hcv ns3 protease inhibitors |
| US20120095211A1 (en) | 2010-09-22 | 2012-04-19 | Intermune, Inc. | Substituted proline inhibitors of hepatitis c virus replication |
| WO2012047764A1 (en) | 2010-10-04 | 2012-04-12 | Intermune, Inc. | Therapeutic antiviral peptides |
| WO2012054874A1 (en) | 2010-10-22 | 2012-04-26 | Intermune, Inc. | Novel macrocyclic inhibitors of hepatitis c virus replication |
| CN103717067A (zh) | 2010-12-14 | 2014-04-09 | 默沙东公司 | 制备大环内酰胺的方法与中间体 |
| CN103534256B (zh) | 2010-12-30 | 2016-08-10 | 益安药业 | 大环丙型肝炎丝氨酸蛋白酶抑制剂 |
| KR20140003521A (ko) | 2010-12-30 | 2014-01-09 | 이난타 파마슈티칼스, 인코포레이티드 | 페난트리딘 매크로사이클릭 c형 간염 세린 프로테아제 억제제 |
| US8957203B2 (en) | 2011-05-05 | 2015-02-17 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
| WO2012166459A1 (en) | 2011-05-27 | 2012-12-06 | Bristol-Myers Squibb Company | Tripeptides incorporating deuterium as inhibitors of hepatitis c virus |
| US8691757B2 (en) | 2011-06-15 | 2014-04-08 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
| MX2014001945A (es) | 2011-08-19 | 2014-03-27 | Merck Sharp & Dohme | Procedimiento e intermedios para la preparacion de macrolactamas. |
| US9328138B2 (en) | 2011-11-15 | 2016-05-03 | Msd Italia S.R.L. | HCV NS3 protease inhibitors |
| US9040479B2 (en) | 2012-01-12 | 2015-05-26 | Cocrystal Pharma, Inc. | HCV NS3 protease inhibitors |
| CN102617705B (zh) | 2012-02-16 | 2014-12-31 | 上海纬诺医药科技有限公司 | 抑制丙肝病毒复制的大环类化合物 |
-
2012
- 2012-04-30 US US13/459,403 patent/US8957203B2/en active Active
- 2012-05-01 RS RS20170015A patent/RS55563B1/sr unknown
- 2012-05-01 EA EA201391637A patent/EA022624B1/ru not_active IP Right Cessation
- 2012-05-01 ES ES12723993T patent/ES2610967T3/es active Active
- 2012-05-01 CA CA2835105A patent/CA2835105A1/en not_active Abandoned
- 2012-05-01 SM SM20170029T patent/SMT201700029T1/it unknown
- 2012-05-01 DK DK12723993.7T patent/DK2705049T3/en active
- 2012-05-01 HR HRP20161632TT patent/HRP20161632T1/hr unknown
- 2012-05-01 KR KR1020137031994A patent/KR20140035383A/ko not_active Abandoned
- 2012-05-01 JP JP2014509359A patent/JP6023178B2/ja not_active Expired - Fee Related
- 2012-05-01 BR BR112013028487A patent/BR112013028487A2/pt not_active Application Discontinuation
- 2012-05-01 PE PE2013002447A patent/PE20141032A1/es not_active Application Discontinuation
- 2012-05-01 CN CN201280033363.4A patent/CN103797024B/zh not_active Expired - Fee Related
- 2012-05-01 PH PH1/2013/502190A patent/PH12013502190A1/en unknown
- 2012-05-01 MX MX2013012749A patent/MX2013012749A/es active IP Right Grant
- 2012-05-01 PT PT127239937T patent/PT2705049T/pt unknown
- 2012-05-01 SI SI201230766A patent/SI2705049T1/sl unknown
- 2012-05-01 SG SG2013081260A patent/SG194749A1/en unknown
- 2012-05-01 HU HUE12723993A patent/HUE033001T2/en unknown
- 2012-05-01 LT LTEP12723993.7T patent/LT2705049T/lt unknown
- 2012-05-01 EP EP12723993.7A patent/EP2705049B1/en active Active
- 2012-05-01 WO PCT/US2012/035974 patent/WO2012151195A1/en not_active Ceased
- 2012-05-01 AU AU2012250920A patent/AU2012250920B2/en not_active Ceased
- 2012-05-01 PL PL12723993T patent/PL2705049T3/pl unknown
- 2012-05-04 AR ARP120101594 patent/AR086290A1/es unknown
- 2012-05-04 UY UY0001034057A patent/UY34057A/es unknown
- 2012-05-04 TW TW101116051A patent/TWI542589B/zh not_active IP Right Cessation
-
2013
- 2013-11-05 CL CL2013003171A patent/CL2013003171A1/es unknown
- 2013-11-05 IL IL229270A patent/IL229270B/en active IP Right Grant
- 2013-12-02 CO CO13282452A patent/CO6821947A2/es not_active Application Discontinuation
-
2015
- 2015-01-08 US US14/592,313 patent/US9527885B2/en active Active
-
2017
- 2017-01-18 CY CY20171100073T patent/CY1118567T1/el unknown
- 2017-01-18 SM SM201700029T patent/SMT201700029B/it unknown
Also Published As
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| JP6023178B2 (ja) | C型肝炎ウイルス阻害剤 | |
| JP6154474B2 (ja) | C型肝炎ウイルス阻害剤 | |
| KR20100132078A (ko) | C형 간염 바이러스 억제제 | |
| WO2009140475A1 (en) | Hepatitis c virus inhibitors | |
| EP2283018A1 (en) | Hepatitis c virus inhibitors | |
| EP1863793A2 (en) | Hepatitis c virus inhibitors | |
| ES2650223T3 (es) | Tripéptidos que incorporan deuterio como inhibidores del virus de la hepatitis C | |
| JP2012511004A (ja) | C型肝炎ウイルス阻害剤 | |
| JP6342922B2 (ja) | C型肝炎ウイルス阻害剤 | |
| EP2914613A1 (en) | Hepatitis c virus inhibitors |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PA0105 | International application |
Patent event date: 20131202 Patent event code: PA01051R01D Comment text: International Patent Application |
|
| PG1501 | Laying open of application | ||
| A201 | Request for examination | ||
| PA0201 | Request for examination |
Patent event code: PA02012R01D Patent event date: 20170412 Comment text: Request for Examination of Application |
|
| E902 | Notification of reason for refusal | ||
| PE0902 | Notice of grounds for rejection |
Comment text: Notification of reason for refusal Patent event date: 20180516 Patent event code: PE09021S01D |
|
| E701 | Decision to grant or registration of patent right | ||
| PE0701 | Decision of registration |
Patent event code: PE07011S01D Comment text: Decision to Grant Registration Patent event date: 20181128 |
|
| NORF | Unpaid initial registration fee | ||
| PC1904 | Unpaid initial registration fee |