KR101475189B1 - C형 간염 바이러스 억제제 - Google Patents
C형 간염 바이러스 억제제 Download PDFInfo
- Publication number
- KR101475189B1 KR101475189B1 KR1020147010437A KR20147010437A KR101475189B1 KR 101475189 B1 KR101475189 B1 KR 101475189B1 KR 1020147010437 A KR1020147010437 A KR 1020147010437A KR 20147010437 A KR20147010437 A KR 20147010437A KR 101475189 B1 KR101475189 B1 KR 101475189B1
- Authority
- KR
- South Korea
- Prior art keywords
- mmol
- tfa
- methanol
- water
- vacuo
- 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.)
- Expired - Fee Related
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- 0 C*(C)C1*C(C)N(*)C1 Chemical compound C*(C)C1*C(C)N(*)C1 0.000 description 11
- VVUABVJPAULPES-INIZCTEOSA-N CC(C)(C)OC(N(CCC1)[C@@H]1c1ncc(-c(cc2)cc(C)c2Br)[nH]1)=O Chemical compound CC(C)(C)OC(N(CCC1)[C@@H]1c1ncc(-c(cc2)cc(C)c2Br)[nH]1)=O VVUABVJPAULPES-INIZCTEOSA-N 0.000 description 1
- BPTITUGGDAOTMW-BCRBLDSWSA-N CC(C)(C)OC(N(CCC1)[C@@H]1c1ncc(-c(cc2)ccc2-c(ccc(-c2cnc([C@H](CCC3)N3C(OC(C)(C)C)=O)[nH]2)c2)c2C(OCc2ccccc2)=O)[nH]1)=O Chemical compound CC(C)(C)OC(N(CCC1)[C@@H]1c1ncc(-c(cc2)ccc2-c(ccc(-c2cnc([C@H](CCC3)N3C(OC(C)(C)C)=O)[nH]2)c2)c2C(OCc2ccccc2)=O)[nH]1)=O BPTITUGGDAOTMW-BCRBLDSWSA-N 0.000 description 1
- YDAFLAFNFGJYJQ-KYJUHHDHSA-N CC(C)(C)OC(N(CCC1)[C@@H]1c1ncc(-c(cc2)ccc2-c2cc(-c3cnc([C@H](CCC4)N4C(OC(C)(C)C)=O)[nH]3)ccc2)[nH]1)=O Chemical compound CC(C)(C)OC(N(CCC1)[C@@H]1c1ncc(-c(cc2)ccc2-c2cc(-c3cnc([C@H](CCC4)N4C(OC(C)(C)C)=O)[nH]3)ccc2)[nH]1)=O YDAFLAFNFGJYJQ-KYJUHHDHSA-N 0.000 description 1
- HJLYKRGXTOVWFL-SNVBAGLBSA-N CC(C)(C)OC([C@@H](c1ccccc1)N)=O Chemical compound CC(C)(C)OC([C@@H](c1ccccc1)N)=O HJLYKRGXTOVWFL-SNVBAGLBSA-N 0.000 description 1
- HQDWPVYKOJWACL-OAHLLOKOSA-N CC(C)(C)OC([C@@H](c1ccccc1)NC(NC1CCCC1)=O)=O Chemical compound CC(C)(C)OC([C@@H](c1ccccc1)NC(NC1CCCC1)=O)=O HQDWPVYKOJWACL-OAHLLOKOSA-N 0.000 description 1
- CVIZSYUSRYEOHC-YDPTYEFTSA-N CC(C)[C@@H](C(N(CC(C1)(F)F)[C@@H]1c1ncc(-c(cc2)ccc2-c(cc2)ccc2-c2cnc([C@H](CC(C3)(F)F)N3C([C@H](C(C)C)NC(OC)=O)=O)[nH]2)[nH]1)=O)NC(OC)=O Chemical compound CC(C)[C@@H](C(N(CC(C1)(F)F)[C@@H]1c1ncc(-c(cc2)ccc2-c(cc2)ccc2-c2cnc([C@H](CC(C3)(F)F)N3C([C@H](C(C)C)NC(OC)=O)=O)[nH]2)[nH]1)=O)NC(OC)=O CVIZSYUSRYEOHC-YDPTYEFTSA-N 0.000 description 1
- GRBFQDZJQZRPQD-CHQNGUEUSA-N CC(C)[C@@H](C(N(CCC1)[C@@H]1c1ncc(-c(cc2)ccc2-c(cc2)ccc2-c2cnc([C@H](CCC3)N3C(OC(C)(C)C)=O)[nH]2)[nH]1)=O)N Chemical compound CC(C)[C@@H](C(N(CCC1)[C@@H]1c1ncc(-c(cc2)ccc2-c(cc2)ccc2-c2cnc([C@H](CCC3)N3C(OC(C)(C)C)=O)[nH]2)[nH]1)=O)N GRBFQDZJQZRPQD-CHQNGUEUSA-N 0.000 description 1
- BZMZTFGKATWNGH-DNPKDEDDSA-N CC(C)[C@@H](C(N(CCC1)[C@@H]1c1ncc(-c(cc2)ccc2-c(cc2)ccc2-c2cnc([C@H](CCC3)N3C([C@H](CC(N3CCN(C)CC3)=O)NC(OC)=O)=O)[nH]2)[nH]1)=O)NC(OC)=O Chemical compound CC(C)[C@@H](C(N(CCC1)[C@@H]1c1ncc(-c(cc2)ccc2-c(cc2)ccc2-c2cnc([C@H](CCC3)N3C([C@H](CC(N3CCN(C)CC3)=O)NC(OC)=O)=O)[nH]2)[nH]1)=O)NC(OC)=O BZMZTFGKATWNGH-DNPKDEDDSA-N 0.000 description 1
- BHLPGQSNBFUPQA-FMYROPPKSA-N CC(C)[C@@H](C(N(CCC1)[C@@H]1c1ncc(-c(cc2)ccc2-c(cc2)ccc2-c2cnc([C@H]3NCCC3)[nH]2)[nH]1)=O)NC(OC)=O Chemical compound CC(C)[C@@H](C(N(CCC1)[C@@H]1c1ncc(-c(cc2)ccc2-c(cc2)ccc2-c2cnc([C@H]3NCCC3)[nH]2)[nH]1)=O)NC(OC)=O BHLPGQSNBFUPQA-FMYROPPKSA-N 0.000 description 1
- BITWNWQEFDHWMO-LETRWZBTSA-N CN(C)[C@@H](C(N(CCC1)[C@@H]1c1ncc(-c(cc2)ccc2-c(nc2)ccc2-c2cnc([C@H](CCC3)N3C([C@@H](c3ccccc3)N(C)C)=O)[nH]2)[nH]1)=O)c1ccccc1 Chemical compound CN(C)[C@@H](C(N(CCC1)[C@@H]1c1ncc(-c(cc2)ccc2-c(nc2)ccc2-c2cnc([C@H](CCC3)N3C([C@@H](c3ccccc3)N(C)C)=O)[nH]2)[nH]1)=O)c1ccccc1 BITWNWQEFDHWMO-LETRWZBTSA-N 0.000 description 1
- NWQCAAUPWUXELC-JJZFGKISSA-N CN(C)[C@@H](C(N(CSC1)[C@@H]1c1ncc(-c(cc2)ccc2-c(cc2)ccc2-c2cnc([C@H](CSC3)N3C(C(c3ccccc3)N(C)C)=O)[nH]2)[nH]1)=O)c1ccccc1 Chemical compound CN(C)[C@@H](C(N(CSC1)[C@@H]1c1ncc(-c(cc2)ccc2-c(cc2)ccc2-c2cnc([C@H](CSC3)N3C(C(c3ccccc3)N(C)C)=O)[nH]2)[nH]1)=O)c1ccccc1 NWQCAAUPWUXELC-JJZFGKISSA-N 0.000 description 1
- JCWUTEGWHABTTF-VIFPVBQESA-N CN(C)[C@H](C(O)=O)c1ccccc1F Chemical compound CN(C)[C@H](C(O)=O)c1ccccc1F JCWUTEGWHABTTF-VIFPVBQESA-N 0.000 description 1
- WQASUPQWFDYCLJ-LBPRGKRZSA-N CN(CC(C1)(F)F)[C@@H]1c1ncc(-c(cc2)ccc2Br)[nH]1 Chemical compound CN(CC(C1)(F)F)[C@@H]1c1ncc(-c(cc2)ccc2Br)[nH]1 WQASUPQWFDYCLJ-LBPRGKRZSA-N 0.000 description 1
- GOJLQSAREKTKPT-MRVPVSSYSA-N COC(N[C@@H](C(O)=O)c1ccccc1)=O Chemical compound COC(N[C@@H](C(O)=O)c1ccccc1)=O GOJLQSAREKTKPT-MRVPVSSYSA-N 0.000 description 1
- MFXTWNXRAFHHRD-DEOSSOPVSA-N COC(N[C@@H](Cc1ccc(CNC(OCC2c3ccccc3-c3c2cccc3)=O)cc1)C(O)=O)=O Chemical compound COC(N[C@@H](Cc1ccc(CNC(OCC2c3ccccc3-c3c2cccc3)=O)cc1)C(O)=O)=O MFXTWNXRAFHHRD-DEOSSOPVSA-N 0.000 description 1
- JAFZODJINWJNPZ-VKHMYHEASA-N C[C@@H](C(O)=O)NC(OC)=O Chemical compound C[C@@H](C(O)=O)NC(OC)=O JAFZODJINWJNPZ-VKHMYHEASA-N 0.000 description 1
- GFRABURJAGGVIU-GUYCJALGSA-N C[C@@H](c1ccccc1)OC([C@H](c(cccc1)c1F)N(C)C)=O Chemical compound C[C@@H](c1ccccc1)OC([C@H](c(cccc1)c1F)N(C)C)=O GFRABURJAGGVIU-GUYCJALGSA-N 0.000 description 1
- ISWCOMWHZGPUFB-OXPNQDLOSA-N O=C([C@@H](c1ccccc1)NC([C@@H]1OCCC1)=O)N(CCC1)[C@@H]1c1ncc(-c(cc2)ccc2-c(cc2)ccc2-c2cnc([C@H](CCC3)N3C([C@H]3OCCC3)=O)[nH]2)[nH]1 Chemical compound O=C([C@@H](c1ccccc1)NC([C@@H]1OCCC1)=O)N(CCC1)[C@@H]1c1ncc(-c(cc2)ccc2-c(cc2)ccc2-c2cnc([C@H](CCC3)N3C([C@H]3OCCC3)=O)[nH]2)[nH]1 ISWCOMWHZGPUFB-OXPNQDLOSA-N 0.000 description 1
- RPTRFSADOICSSK-UHFFFAOYSA-N OC(Cc1ccccc1F)=O Chemical compound OC(Cc1ccccc1F)=O RPTRFSADOICSSK-UHFFFAOYSA-N 0.000 description 1
- OWJLCJLXRSNPJK-GFCCVEGCSA-N OC([C@@H](c1ccccc1)NC(NC1CCCC1)=O)=O Chemical compound OC([C@@H](c1ccccc1)NC(NC1CCCC1)=O)=O OWJLCJLXRSNPJK-GFCCVEGCSA-N 0.000 description 1
- LVEOHQUIVQGCIM-VXKWHMMOSA-N OC(c(cc(cc1)-c2cnc([C@H]3NCCC3)[nH]2)c1-c(cc1)ccc1-c1cnc([C@H]2NCCC2)[nH]1)=O Chemical compound OC(c(cc(cc1)-c2cnc([C@H]3NCCC3)[nH]2)c1-c(cc1)ccc1-c1cnc([C@H]2NCCC2)[nH]1)=O LVEOHQUIVQGCIM-VXKWHMMOSA-N 0.000 description 1
- JDRNPWZKSMNMEB-GOTSBHOMSA-N OCc(cc(cc1)-c2cnc([C@H]3NCCC3)[nH]2)c1-c(cc1)ccc1-c1cnc([C@H]2NCCC2)[nH]1 Chemical compound OCc(cc(cc1)-c2cnc([C@H]3NCCC3)[nH]2)c1-c(cc1)ccc1-c1cnc([C@H]2NCCC2)[nH]1 JDRNPWZKSMNMEB-GOTSBHOMSA-N 0.000 description 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
- C07D233/54—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
- C07D233/64—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with substituted hydrocarbon radicals attached to ring carbon atoms, e.g. histidine
-
- 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
- A61K31/40—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
- A61K31/4025—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil not condensed and containing further heterocyclic rings, e.g. cromakalim
-
- 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
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/4164—1,3-Diazoles
-
- 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
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/4164—1,3-Diazoles
- A61K31/4178—1,3-Diazoles not condensed 1,3-diazoles and containing further heterocyclic rings, e.g. pilocarpine, nitrofurantoin
-
- 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
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/16—Drugs for disorders of the alimentary tract or the digestive system for liver or gallbladder disorders, e.g. hepatoprotective agents, cholagogues, litholytics
-
- 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
-
- 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
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/14—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
- C07D409/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero rings
-
- 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
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F5/00—Compounds containing elements of Groups 3 or 13 of the Periodic Table
- C07F5/02—Boron compounds
- C07F5/025—Boronic and borinic acid compounds
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F7/00—Compounds containing elements of Groups 4 or 14 of the Periodic Table
- C07F7/02—Silicon compounds
- C07F7/08—Compounds having one or more C—Si linkages
- C07F7/0803—Compounds with Si-C or Si-Si linkages
- C07F7/081—Compounds with Si-C or Si-Si linkages comprising at least one atom selected from the elements N, O, halogen, S, Se or Te
- C07F7/0812—Compounds with Si-C or Si-Si linkages comprising at least one atom selected from the elements N, O, halogen, S, Se or Te comprising a heterocyclic ring
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D207/00—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D207/02—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D207/04—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
- C07D207/10—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D207/16—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Epidemiology (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Virology (AREA)
- Oncology (AREA)
- Communicable Diseases (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Molecular Biology (AREA)
- Gastroenterology & Hepatology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Peptides Or Proteins (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Medicines Containing Material From Animals Or Micro-Organisms (AREA)
- Medicinal Preparation (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Applications Claiming Priority (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US83699606P | 2006-08-11 | 2006-08-11 | |
| US60/836,996 | 2006-08-11 | ||
| US11/835,462 | 2007-08-08 | ||
| US11/835,462 US8329159B2 (en) | 2006-08-11 | 2007-08-08 | Hepatitis C virus inhibitors |
| PCT/US2007/075544 WO2008021927A2 (en) | 2006-08-11 | 2007-08-09 | Hepatitis c virus inhibitors |
Related Parent Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| KR1020097004970A Division KR101450352B1 (ko) | 2006-08-11 | 2007-08-09 | C형 간염 바이러스 억제제 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| KR20140066768A KR20140066768A (ko) | 2014-06-02 |
| KR101475189B1 true KR101475189B1 (ko) | 2014-12-22 |
Family
ID=38812845
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| KR1020097004970A Expired - Fee Related KR101450352B1 (ko) | 2006-08-11 | 2007-08-09 | C형 간염 바이러스 억제제 |
| KR1020147010437A Expired - Fee Related KR101475189B1 (ko) | 2006-08-11 | 2007-08-09 | C형 간염 바이러스 억제제 |
Family Applications Before (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| KR1020097004970A Expired - Fee Related KR101450352B1 (ko) | 2006-08-11 | 2007-08-09 | C형 간염 바이러스 억제제 |
Country Status (31)
| Country | Link |
|---|---|
| US (7) | US8329159B2 (OSRAM) |
| EP (5) | EP2049522B1 (OSRAM) |
| JP (3) | JP5235882B2 (OSRAM) |
| KR (2) | KR101450352B1 (OSRAM) |
| CN (1) | CN104447707B (OSRAM) |
| AR (1) | AR063684A1 (OSRAM) |
| AU (1) | AU2007286222B2 (OSRAM) |
| BR (1) | BRPI0716483B8 (OSRAM) |
| CA (1) | CA2660520C (OSRAM) |
| CL (1) | CL2007002327A1 (OSRAM) |
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| WO (1) | WO2008021927A2 (OSRAM) |
| ZA (1) | ZA200900962B (OSRAM) |
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Patent Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2006133326A1 (en) | 2005-06-06 | 2006-12-14 | Bristol-Myers Squibb Company | Inhibitors of hcv replication |
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