KR20090082467A - C형 간염 바이러스 억제제 - Google Patents
C형 간염 바이러스 억제제 Download PDFInfo
- Publication number
- KR20090082467A KR20090082467A KR1020097011785A KR20097011785A KR20090082467A KR 20090082467 A KR20090082467 A KR 20090082467A KR 1020097011785 A KR1020097011785 A KR 1020097011785A KR 20097011785 A KR20097011785 A KR 20097011785A KR 20090082467 A KR20090082467 A KR 20090082467A
- Authority
- KR
- South Korea
- Prior art keywords
- methoxy
- carbamoyl
- oxy
- prolineamide
- isoquinolinyl
- 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.)
- Withdrawn
Links
- 0 CNC1(C*(*)C1)C(NS(*)(=O)=O)=O Chemical compound CNC1(C*(*)C1)C(NS(*)(=O)=O)=O 0.000 description 8
- WMSPXQIQBQAWLL-UHFFFAOYSA-N NS(C1CC1)(=O)=O Chemical compound NS(C1CC1)(=O)=O WMSPXQIQBQAWLL-UHFFFAOYSA-N 0.000 description 6
- RTKFCGMFEQPEMU-UHFFFAOYSA-N NS(C1(CC1)C1=CCCCC1)(=O)=O Chemical compound NS(C1(CC1)C1=CCCCC1)(=O)=O RTKFCGMFEQPEMU-UHFFFAOYSA-N 0.000 description 2
- JQLQQPTXRBSHPF-UHFFFAOYSA-N C=CCC1(CC1)S(N)(=O)=O Chemical compound C=CCC1(CC1)S(N)(=O)=O JQLQQPTXRBSHPF-UHFFFAOYSA-N 0.000 description 1
- KPGCMYRJDKUDCT-SVRRBLITSA-N C=C[C@H](C1)[C@H]1C(NS(C1CC1)(=O)=O)=O Chemical compound C=C[C@H](C1)[C@H]1C(NS(C1CC1)(=O)=O)=O KPGCMYRJDKUDCT-SVRRBLITSA-N 0.000 description 1
- VGHBWKACJXNKAF-HZGVNTEJSA-N C=C[C@H](C1)[C@]1(C(NS(C1CC1)(=O)=O)=O)N Chemical compound C=C[C@H](C1)[C@]1(C(NS(C1CC1)(=O)=O)=O)N VGHBWKACJXNKAF-HZGVNTEJSA-N 0.000 description 1
- SKKGMOAQEAQNGO-ZGBMLECWSA-N CC(C)(C)C(C(N(C[C@@H](C1)Oc(nc2)c(cc(cc3)Cl)c3c2OC)[C@@H]1C(N[C@](C1)([C@@H]1C=C)C(NS(C1CC1)(=O)=O)=O)=O)=O)Nc(cc1)cc(F)c1F Chemical compound CC(C)(C)C(C(N(C[C@@H](C1)Oc(nc2)c(cc(cc3)Cl)c3c2OC)[C@@H]1C(N[C@](C1)([C@@H]1C=C)C(NS(C1CC1)(=O)=O)=O)=O)=O)Nc(cc1)cc(F)c1F SKKGMOAQEAQNGO-ZGBMLECWSA-N 0.000 description 1
- KLOCPFINBSKKKA-MTYSSGSHSA-N CC(C)(C)C(C(N(C[C@@H](C1)Oc(nc2)c(cc(cc3)Cl)c3c2OC)[C@@H]1C(N[C@](C1)([C@@H]1C=C)C(NS(C1CC1)(=O)=O)=O)=O)=O)Nc(cn1)ccc1OC(F)F Chemical compound CC(C)(C)C(C(N(C[C@@H](C1)Oc(nc2)c(cc(cc3)Cl)c3c2OC)[C@@H]1C(N[C@](C1)([C@@H]1C=C)C(NS(C1CC1)(=O)=O)=O)=O)=O)Nc(cn1)ccc1OC(F)F KLOCPFINBSKKKA-MTYSSGSHSA-N 0.000 description 1
- LALJURJCIKBJGH-DQOAMNSGSA-N CC(C)(C)C(C(N(C[C@@H](C1)Oc(nc2)c(cc(cc3)Cl)c3c2OC)[C@@H]1C(N[C@](C1)([C@@H]1C=C)C(NS(C1CC1)(=O)=O)=O)=O)=O)Nc1cc(S(N(C)C)(=O)=O)ccc1 Chemical compound CC(C)(C)C(C(N(C[C@@H](C1)Oc(nc2)c(cc(cc3)Cl)c3c2OC)[C@@H]1C(N[C@](C1)([C@@H]1C=C)C(NS(C1CC1)(=O)=O)=O)=O)=O)Nc1cc(S(N(C)C)(=O)=O)ccc1 LALJURJCIKBJGH-DQOAMNSGSA-N 0.000 description 1
- XDPXYKMLGIKDGV-UHFFFAOYSA-N CC(C)(C)C(C(O)=O)Nc1ccccc1 Chemical compound CC(C)(C)C(C(O)=O)Nc1ccccc1 XDPXYKMLGIKDGV-UHFFFAOYSA-N 0.000 description 1
- KMYLDHSHCQGQHW-LDHQFIGFSA-N CC(C)(C)C[C@@H](C(N(C[C@@H](C1)Oc(c2c3ccc(Cl)c2)ncc3OC)[C@@H]1C(N[C@](C1)([C@@H]1C=C)C(NS(C1CC1)(=O)=O)=O)=O)=O)Nc1cc(C(N(C)C)=O)ccc1 Chemical compound CC(C)(C)C[C@@H](C(N(C[C@@H](C1)Oc(c2c3ccc(Cl)c2)ncc3OC)[C@@H]1C(N[C@](C1)([C@@H]1C=C)C(NS(C1CC1)(=O)=O)=O)=O)=O)Nc1cc(C(N(C)C)=O)ccc1 KMYLDHSHCQGQHW-LDHQFIGFSA-N 0.000 description 1
- SPGDRXRIVPMUCK-UHFFFAOYSA-N CC(C)(C)NS(CCCCl)(=O)=O Chemical compound CC(C)(C)NS(CCCCl)(=O)=O SPGDRXRIVPMUCK-UHFFFAOYSA-N 0.000 description 1
- QHHXJNLBANEKFF-UHFFFAOYSA-N CC(C)(C)OC(N(CC(C1)Oc2c(cc(cc3)Cl)c3ccn2)C1C(O)=O)=O Chemical compound CC(C)(C)OC(N(CC(C1)Oc2c(cc(cc3)Cl)c3ccn2)C1C(O)=O)=O QHHXJNLBANEKFF-UHFFFAOYSA-N 0.000 description 1
- PKFSEWUBSHYLOB-WUJWULDRSA-N CC(C)(C)OC(N(CC(C1)Oc2c(cc(cc3)F)c3ccn2)[C@@H]1C(O)=O)=O Chemical compound CC(C)(C)OC(N(CC(C1)Oc2c(cc(cc3)F)c3ccn2)[C@@H]1C(O)=O)=O PKFSEWUBSHYLOB-WUJWULDRSA-N 0.000 description 1
- ZQEBQGAAWMOMAI-ZETCQYMHSA-N CC(C)(C)OC(N(CCC1)[C@@H]1C(O)=O)=O Chemical compound CC(C)(C)OC(N(CCC1)[C@@H]1C(O)=O)=O ZQEBQGAAWMOMAI-ZETCQYMHSA-N 0.000 description 1
- BENKAPCDIOILGV-RQJHMYQMSA-N CC(C)(C)OC(N(C[C@@H](C1)O)[C@@H]1C(O)=O)=O Chemical compound CC(C)(C)OC(N(C[C@@H](C1)O)[C@@H]1C(O)=O)=O BENKAPCDIOILGV-RQJHMYQMSA-N 0.000 description 1
- YFRAGGNFPQCAPN-NPCAHTBFSA-N CC(C)(C)OC(N(C[C@@H](C1)Oc2c(C=CC(C3)OC)c3cc(OC)n2)C1C(O)=O)=O Chemical compound CC(C)(C)OC(N(C[C@@H](C1)Oc2c(C=CC(C3)OC)c3cc(OC)n2)C1C(O)=O)=O YFRAGGNFPQCAPN-NPCAHTBFSA-N 0.000 description 1
- RFDWVLAOYZWXGJ-QAPCUYQASA-N CC(C)(C)OC(N(C[C@@H](C1)Oc2c(ccc(OC)c3)c3c3OCCN(C)c3n2)[C@@H]1C([NH]=C)=O)=O Chemical compound CC(C)(C)OC(N(C[C@@H](C1)Oc2c(ccc(OC)c3)c3c3OCCN(C)c3n2)[C@@H]1C([NH]=C)=O)=O RFDWVLAOYZWXGJ-QAPCUYQASA-N 0.000 description 1
- DGMYUOIUPUZCDM-AEFFLSMTSA-N CC(C)(C)OC(N(C[C@@H](C1)Oc2c(ccc(OC)c3)c3cc(OC)n2)[C@@H]1C(C)=O)=O Chemical compound CC(C)(C)OC(N(C[C@@H](C1)Oc2c(ccc(OC)c3)c3cc(OC)n2)[C@@H]1C(C)=O)=O DGMYUOIUPUZCDM-AEFFLSMTSA-N 0.000 description 1
- NBXGDPBFRRQZEV-UHFFFAOYSA-N CC(C)(C)OC(NS(C1CC1)(=O)=O)=O Chemical compound CC(C)(C)OC(NS(C1CC1)(=O)=O)=O NBXGDPBFRRQZEV-UHFFFAOYSA-N 0.000 description 1
- CHQWLSPZWMQDMQ-SAUVGFCRSA-N CC(C)C(C(N(C[C@@H](C1)Oc2c(ccc(OC)c3)c3cc(OC)n2)[C@@H]1C(C)=O)=O)Nc1ccccc1 Chemical compound CC(C)C(C(N(C[C@@H](C1)Oc2c(ccc(OC)c3)c3cc(OC)n2)[C@@H]1C(C)=O)=O)Nc1ccccc1 CHQWLSPZWMQDMQ-SAUVGFCRSA-N 0.000 description 1
- JVLCLUQRUWCMGU-DBSPZYFTSA-N CC(C)C(C(N(C[C@@H](C1)Oc2c(ccc(OC)c3)c3ccn2)[C@@H]1C(N[C@](C1)([C@@H]1C=C)C(NS(C1CC1)(=O)=O)=O)=O)=O)Nc1nc(OC)cc(OC)n1 Chemical compound CC(C)C(C(N(C[C@@H](C1)Oc2c(ccc(OC)c3)c3ccn2)[C@@H]1C(N[C@](C1)([C@@H]1C=C)C(NS(C1CC1)(=O)=O)=O)=O)=O)Nc1nc(OC)cc(OC)n1 JVLCLUQRUWCMGU-DBSPZYFTSA-N 0.000 description 1
- DXQZISQNYYQIEU-BHKAWDCFSA-N CC(C)C(C(N(C[C@@H](C1)Oc2nccc3c2ccc(OC)c3)[C@@H]1C(N[C@](C1)([C@@H]1C=C)C(NS(C1CC1)(=O)=O)=O)=O)=O)Nc1ccc(C(F)(F)F)cn1 Chemical compound CC(C)C(C(N(C[C@@H](C1)Oc2nccc3c2ccc(OC)c3)[C@@H]1C(N[C@](C1)([C@@H]1C=C)C(NS(C1CC1)(=O)=O)=O)=O)=O)Nc1ccc(C(F)(F)F)cn1 DXQZISQNYYQIEU-BHKAWDCFSA-N 0.000 description 1
- YBOXXHKPMJKJLB-XYHZYDHVSA-N CC(C)[C@H](C(N(C[C@@H](C1)Oc2c(ccc(OC)c3)c3ccn2)[C@@H]1C(NC([C@@]1(C2)C=C)C12C(NS(C1CC1)(=O)=O)=O)=O)=O)Nc1nc(OC)nc(OC)n1 Chemical compound CC(C)[C@H](C(N(C[C@@H](C1)Oc2c(ccc(OC)c3)c3ccn2)[C@@H]1C(NC([C@@]1(C2)C=C)C12C(NS(C1CC1)(=O)=O)=O)=O)=O)Nc1nc(OC)nc(OC)n1 YBOXXHKPMJKJLB-XYHZYDHVSA-N 0.000 description 1
- CMQRMZLDLVWERJ-HIFRSBDPSA-N CC([C@H](C1)NC[C@@H]1Oc1c(ccc(OC)c2)c2cc(OC)n1)=O Chemical compound CC([C@H](C1)NC[C@@H]1Oc1c(ccc(OC)c2)c2cc(OC)n1)=O CMQRMZLDLVWERJ-HIFRSBDPSA-N 0.000 description 1
- KHEZKDIWDCVMTL-UHFFFAOYSA-N CCCNC(C1(CC1)S(N)(=O)=O)=O Chemical compound CCCNC(C1(CC1)S(N)(=O)=O)=O KHEZKDIWDCVMTL-UHFFFAOYSA-N 0.000 description 1
- PRBJPWWWRIEGTA-JFAAMYIWSA-N CCOc1n[s]nc1NC(C(C)(C)C)C(N(C[C@@H](C1)Oc(nc2)c(cc(cc3)Cl)c3c2OC)[C@@H]1C(N[C@](C1)([C@@H]1C=C)C(NS(C1CC1)(=O)=O)=O)=O)=O Chemical compound CCOc1n[s]nc1NC(C(C)(C)C)C(N(C[C@@H](C1)Oc(nc2)c(cc(cc3)Cl)c3c2OC)[C@@H]1C(N[C@](C1)([C@@H]1C=C)C(NS(C1CC1)(=O)=O)=O)=O)=O PRBJPWWWRIEGTA-JFAAMYIWSA-N 0.000 description 1
- VFYMVJNGXBABEF-UHFFFAOYSA-N COC(C(CC1)=C2C=C1N)=CCCC=C2[O]#C Chemical compound COC(C(CC1)=C2C=C1N)=CCCC=C2[O]#C VFYMVJNGXBABEF-UHFFFAOYSA-N 0.000 description 1
- PKGOAHVKZIEDOX-UHFFFAOYSA-N COc(cc(ccnc1Cl)c1c1)c1F Chemical compound COc(cc(ccnc1Cl)c1c1)c1F PKGOAHVKZIEDOX-UHFFFAOYSA-N 0.000 description 1
- SWPLDRGOIDIKQH-UHFFFAOYSA-N COc(cc1)cc2c1c(Cl)nc(-c1ncc[s]1)c2 Chemical compound COc(cc1)cc2c1c(Cl)nc(-c1ncc[s]1)c2 SWPLDRGOIDIKQH-UHFFFAOYSA-N 0.000 description 1
- WWJAKIIHTOQSBE-CGUBGCFPSA-N COc(cn1)c(ccc(Cl)c2)c2c1O[C@H](C[C@H]1C(N[C@](C2)([C@@H]2C=C)C(NS(C2CC2)(=O)=O)=O)=O)CN1C(C(CCCCCC=C)Nc(cn1)ccc1OC)=O Chemical compound COc(cn1)c(ccc(Cl)c2)c2c1O[C@H](C[C@H]1C(N[C@](C2)([C@@H]2C=C)C(NS(C2CC2)(=O)=O)=O)=O)CN1C(C(CCCCCC=C)Nc(cn1)ccc1OC)=O WWJAKIIHTOQSBE-CGUBGCFPSA-N 0.000 description 1
- DVHOIKSDQCZHOV-UHFFFAOYSA-N COc1c(ccnc2Cl)c2ccc1 Chemical compound COc1c(ccnc2Cl)c2ccc1 DVHOIKSDQCZHOV-UHFFFAOYSA-N 0.000 description 1
- DIAMRSWZRAZRSF-UHFFFAOYSA-N COc1ccc2c(Cl)nc(OC)cc2c1 Chemical compound COc1ccc2c(Cl)nc(OC)cc2c1 DIAMRSWZRAZRSF-UHFFFAOYSA-N 0.000 description 1
- AAYHAFZXFMIUSN-UHFFFAOYSA-N NS(C1CCCCC1)(=O)=O Chemical compound NS(C1CCCCC1)(=O)=O AAYHAFZXFMIUSN-UHFFFAOYSA-N 0.000 description 1
- YWUCOQGBXQHOJM-UHFFFAOYSA-N O=C(c1c2)NC=Cc1ccc2Cl Chemical compound O=C(c1c2)NC=Cc1ccc2Cl YWUCOQGBXQHOJM-UHFFFAOYSA-N 0.000 description 1
- WKCRTQPANFLWRL-UHFFFAOYSA-N O=C1NC=Cc2c(CCO3)c3ccc12 Chemical compound O=C1NC=Cc2c(CCO3)c3ccc12 WKCRTQPANFLWRL-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing three or more hetero rings
-
- 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
- A61K31/4709—Non-condensed quinolines and containing further heterocyclic rings
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing three or more hetero rings
-
- 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
- C07K5/0812—Tripeptides with the first amino acid being neutral and aromatic or cycloaliphatic
-
- 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
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Medicinal Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Molecular Biology (AREA)
- Biophysics (AREA)
- Biochemistry (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Genetics & Genomics (AREA)
- Pharmacology & Pharmacy (AREA)
- Virology (AREA)
- Animal Behavior & Ethology (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Communicable Diseases (AREA)
- Oncology (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Peptides Or Proteins (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Plural Heterocyclic Compounds (AREA)
Applications Claiming Priority (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US86503406P | 2006-11-09 | 2006-11-09 | |
| US60/865,034 | 2006-11-09 | ||
| US11/934,840 US7772180B2 (en) | 2006-11-09 | 2007-11-05 | Hepatitis C virus inhibitors |
| US11/934,840 | 2007-11-05 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| KR20090082467A true KR20090082467A (ko) | 2009-07-30 |
Family
ID=39304590
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| KR1020097011785A Withdrawn KR20090082467A (ko) | 2006-11-09 | 2007-11-08 | C형 간염 바이러스 억제제 |
Country Status (18)
| Country | Link |
|---|---|
| US (1) | US7772180B2 (enExample) |
| EP (1) | EP2086963B1 (enExample) |
| JP (1) | JP2010509359A (enExample) |
| KR (1) | KR20090082467A (enExample) |
| CN (1) | CN101541784B (enExample) |
| AR (1) | AR063653A1 (enExample) |
| AU (1) | AU2007319435A1 (enExample) |
| BR (1) | BRPI0718625A2 (enExample) |
| CA (1) | CA2669310A1 (enExample) |
| CL (1) | CL2007003250A1 (enExample) |
| EA (1) | EA200900676A1 (enExample) |
| IL (1) | IL198248A0 (enExample) |
| MX (1) | MX2009004888A (enExample) |
| NO (1) | NO20091591L (enExample) |
| NZ (1) | NZ576817A (enExample) |
| PE (1) | PE20081344A1 (enExample) |
| TW (1) | TW200826938A (enExample) |
| WO (1) | WO2008060927A2 (enExample) |
Families Citing this family (84)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| MY140680A (en) | 2002-05-20 | 2010-01-15 | Bristol Myers Squibb Co | Hepatitis c virus inhibitors |
| EP1831225A2 (en) | 2004-11-19 | 2007-09-12 | The Regents of the University of California | Anti-inflammatory pyrazolopyrimidines |
| JP2009532507A (ja) | 2006-04-04 | 2009-09-10 | ザ リージェンツ オブ ザ ユニバーシティ オブ カリフォルニア | Pi3キナーゼアンタゴニスト |
| AP2009005053A0 (en) * | 2007-05-03 | 2009-12-31 | Intermune Inc | Novel macrocyclic inhibitors of hepatitis c virus replication |
| MX2009012093A (es) * | 2007-05-10 | 2010-01-25 | Intermune Inc | Nuevos peptidos inhibidores de la replicacion del virus de la hepatitis c. |
| TW200918524A (en) * | 2007-06-29 | 2009-05-01 | Gilead Sciences Inc | Antiviral compounds |
| US20110160232A1 (en) | 2007-10-04 | 2011-06-30 | Pingda Ren | Certain chemical entities and therapeutic uses thereof |
| MX2010006738A (es) * | 2007-12-21 | 2010-10-15 | Avila Therapeutics Inc | Inhibidores de proteasa del virus de la hepatitis c (hcv) y usos de los mismos. |
| US8309685B2 (en) | 2007-12-21 | 2012-11-13 | Celgene Avilomics Research, Inc. | HCV protease inhibitors and uses thereof |
| US8293705B2 (en) | 2007-12-21 | 2012-10-23 | Avila Therapeutics, Inc. | HCV protease inhibitors and uses thereof |
| TW200932255A (en) | 2007-12-21 | 2009-08-01 | Avila Therapeutics Inc | HCV protease inhibitors and uses thereof |
| KR101660050B1 (ko) | 2008-01-04 | 2016-09-26 | 인텔리카인, 엘엘씨 | 특정 화학 물질, 조성물 및 방법 |
| US8193182B2 (en) | 2008-01-04 | 2012-06-05 | Intellikine, Inc. | Substituted isoquinolin-1(2H)-ones, and methods of use thereof |
| ES2437147T3 (es) * | 2008-02-04 | 2014-01-09 | Idenix Pharmaceuticals, Inc. | Inhibidores de serina proteasa macrocíclicos |
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| 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 |
| CA2644389A1 (en) | 2006-03-03 | 2007-09-20 | Schering Corporation | Pharmaceutical combinations of hcv-protease and -ires inhibitors |
| GB0609492D0 (en) | 2006-05-15 | 2006-06-21 | Angeletti P Ist Richerche Bio | Therapeutic agents |
| US7635683B2 (en) | 2006-08-04 | 2009-12-22 | Enanta Pharmaceuticals, Inc. | Quinoxalinyl tripeptide hepatitis C virus inhibitors |
| US7605126B2 (en) | 2006-08-11 | 2009-10-20 | Enanta Pharmaceuticals, Inc. | Acylaminoheteroaryl hepatitis C virus protease inhibitors |
| US7582605B2 (en) | 2006-08-11 | 2009-09-01 | Enanta Pharmaceuticals, Inc. | Phosphorus-containing hepatitis C serine protease inhibitors |
-
2007
- 2007-11-05 US US11/934,840 patent/US7772180B2/en active Active
- 2007-11-08 NZ NZ576817A patent/NZ576817A/en not_active IP Right Cessation
- 2007-11-08 EA EA200900676A patent/EA200900676A1/ru unknown
- 2007-11-08 BR BRPI0718625-8A patent/BRPI0718625A2/pt not_active IP Right Cessation
- 2007-11-08 EP EP07864081.0A patent/EP2086963B1/en active Active
- 2007-11-08 JP JP2009536467A patent/JP2010509359A/ja active Pending
- 2007-11-08 KR KR1020097011785A patent/KR20090082467A/ko not_active Withdrawn
- 2007-11-08 MX MX2009004888A patent/MX2009004888A/es active IP Right Grant
- 2007-11-08 CN CN2007800416231A patent/CN101541784B/zh not_active Expired - Fee Related
- 2007-11-08 CA CA002669310A patent/CA2669310A1/en not_active Abandoned
- 2007-11-08 AU AU2007319435A patent/AU2007319435A1/en not_active Abandoned
- 2007-11-08 WO PCT/US2007/084012 patent/WO2008060927A2/en not_active Ceased
- 2007-11-09 TW TW096142550A patent/TW200826938A/zh unknown
- 2007-11-09 CL CL200703250A patent/CL2007003250A1/es unknown
- 2007-11-09 PE PE2007001545A patent/PE20081344A1/es not_active Application Discontinuation
- 2007-11-09 AR ARP070105019A patent/AR063653A1/es not_active Application Discontinuation
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2009
- 2009-04-21 IL IL198248A patent/IL198248A0/en unknown
- 2009-04-22 NO NO20091591A patent/NO20091591L/no not_active Application Discontinuation
Also Published As
| Publication number | Publication date |
|---|---|
| JP2010509359A (ja) | 2010-03-25 |
| MX2009004888A (es) | 2009-05-19 |
| NZ576817A (en) | 2011-08-26 |
| TW200826938A (en) | 2008-07-01 |
| AU2007319435A1 (en) | 2008-05-22 |
| IL198248A0 (en) | 2009-12-24 |
| CN101541784B (zh) | 2013-04-24 |
| EP2086963B1 (en) | 2015-09-16 |
| US20080119461A1 (en) | 2008-05-22 |
| US7772180B2 (en) | 2010-08-10 |
| WO2008060927A2 (en) | 2008-05-22 |
| CA2669310A1 (en) | 2008-05-22 |
| EP2086963A2 (en) | 2009-08-12 |
| EA200900676A1 (ru) | 2010-02-26 |
| CL2007003250A1 (es) | 2008-05-23 |
| WO2008060927A3 (en) | 2008-07-03 |
| NO20091591L (no) | 2009-07-28 |
| CN101541784A (zh) | 2009-09-23 |
| PE20081344A1 (es) | 2008-09-18 |
| BRPI0718625A2 (pt) | 2014-04-01 |
| AR063653A1 (es) | 2009-02-04 |
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