SG11201408739VA - Inhibitors of hepatitis c virus - Google Patents
Inhibitors of hepatitis c virusInfo
- Publication number
- SG11201408739VA SG11201408739VA SG11201408739VA SG11201408739VA SG11201408739VA SG 11201408739V A SG11201408739V A SG 11201408739VA SG 11201408739V A SG11201408739V A SG 11201408739VA SG 11201408739V A SG11201408739V A SG 11201408739VA SG 11201408739V A SG11201408739V A SG 11201408739VA
- Authority
- SG
- Singapore
- Prior art keywords
- foster city
- gilead sciences
- lakeside drive
- lakeside
- drive
- Prior art date
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- 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
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/498—Pyrazines or piperazines ortho- and peri-condensed with carbocyclic ring systems, e.g. quinoxaline, phenazine
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- 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
- A61K31/095—Sulfur, selenium, or tellurium compounds, e.g. thiols
- A61K31/10—Sulfides; Sulfoxides; Sulfones
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- 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
- A61K31/401—Proline; Derivatives thereof, e.g. captopril
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- 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
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- 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
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/4985—Pyrazines or piperazines ortho- or peri-condensed with heterocyclic ring systems
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- 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
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
- A61K31/506—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim not condensed and containing further heterocyclic rings
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- 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
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
- A61K31/519—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
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- 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
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- 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]
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- 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
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- 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
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- A—HUMAN NECESSITIES
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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- A61P31/10—Antimycotics
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- 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
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- 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
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- A—HUMAN NECESSITIES
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- 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
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D241/00—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings
- C07D241/36—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings condensed with carbocyclic rings or ring systems
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- 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
- C07D403/02—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 two hetero rings
- C07D403/12—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 two hetero rings linked by a chain containing hetero atoms as chain links
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- 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
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D498/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D498/12—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms in which the condensed system contains three hetero rings
- C07D498/16—Peri-condensed systems
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D498/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D498/22—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms in which the condensed system contains four or more hetero rings
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- 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
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- 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
- C07K5/0808—Tripeptides with the first amino acid being neutral and aliphatic the side chain containing 2 to 4 carbon atoms, e.g. Val, Ile, Leu
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- 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
- C07K5/081—Tripeptides with the first amino acid being neutral and aliphatic the side chain containing O or S as heteroatoms, e.g. Cys, Ser
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- 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
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- 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
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K2300/00—Mixtures or combinations of active ingredients, wherein at least one active ingredient is fully defined in groups A61K31/00 - A61K41/00
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K38/00—Medicinal preparations containing peptides
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- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- Epidemiology (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Molecular Biology (AREA)
- Biochemistry (AREA)
- Biophysics (AREA)
- Genetics & Genomics (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Gastroenterology & Hepatology (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Immunology (AREA)
- Oncology (AREA)
- Communicable Diseases (AREA)
- Zoology (AREA)
- Virology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Peptides Or Proteins (AREA)
- Micro-Organisms Or Cultivation Processes Thereof (AREA)
- Hydrogenated Pyridines (AREA)
- Plural Heterocyclic Compounds (AREA)
- Medicines Containing Material From Animals Or Micro-Organisms (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
- Enzymes And Modification Thereof (AREA)
Abstract
(12) INTERNATIONAL APPLICATION PUBLISHED UNDER THE PATENT COOPERATION TREATY (PCT) (19) World Intellectual Property Organization International Bureau (43) International Publication Date 9 January 2014 (09.01.2014) WIPOIPCT (10) International Publication Number WO 2014/008285 A1 (51) International Patent Classification: C07D 491/18 (2006.01) A61K31/4995 (2006.01) A61P 31/14 ( 2006.01) (21) International Application Number: (22) International Filing Date: (25) Filing Language: (26) Publication Language: PCT/US2013/049119 2 July 2013 (02.07.2013) English English (30) Priority Data: 61/667,806 61/798,524 3 July 2012 (03.07.2012) 15 March 2013 (15.03.2013) (71) Applicant: GILEAD SCIENCES, INC. [US/US]; Lakeside Drive, Foster City, CA 94404 (US). US US 333 (72) Inventors: BJORNSON, Kyla; c/o Gilead Sciences, Inc., 333 Lakeside Drive, Foster City, CA 94404 (US). CANALES, Eda; c/o Gilead Sciences, Inc., 333 Lakeside Drive, Foster City, CA 94404 (US). COTTELL, Jeromy, J.; c/o Gilead Sciences, Inc., 333 Lakeside Drive, Foster City, CA 94404 (US). KARKI, Kapil, Kumar; c/o Gilead Sciences, Inc., 333 Lakeside Drive, Foster City, CA 94404 (US). KATANA, Ashley, Anne; c/o Gilead Sciences, Inc., 333 Lakeside Drive, Foster City, CA 94404 (US). KATO, Darryl; c/o Gilead Sciences, Inc., 333 Lakeside Drive, Foster City, CA 94404 (US). KOBAYASHI, Tetsuya; c/o Gilead Sciences, Inc., 333 Lakeside Drive, Foster City, CA 94404 (US). LINK, John, O.; c/o Gilead Sciences, Inc., 333 Lakeside Drive, Foster City, CA 94404 (US). MAR TINEZ, Ruben; c/o Gilead Sciences, Inc., 333 Lakeside Drive, Foster City, CA 94404 (US). PHILLIPS, Barton, W.; c/o Gilead Sciences, Inc., 333 Lakeside Drive, Foster City, CA 94404 (US). PYUN, Hyung-jung; c/o Gilead Sciences, Inc., 333 Lakeside Drive, Foster City, CA 94404 (US). SANGI, Michael; c/o Gilead Sciences, Inc., 333 Lakeside Drive, Foster City, CA 94404 (US). SCHRIER, Adam, James; c/o Gilead Sciences, Inc., 333 Lakeside Drive, Foster City, CA 94404 (US). SIEGEL, Dustin; c/o Gilead Sciences, Inc., 333 Lakeside Drive, Foster City, CA 94404 (US). TAYLOR, James, G.; c/o Gilead Sciences, Inc., 333 Lakeside Drive, Foster City, CA 94404 (US). TRAN, Chinh, Viet; c/o Gilead Sciences, Inc., 333 Lakeside Drive, Foster City, CA 94404 (US). TREJO MARTIN, Teresa, Alejandra; c/o Gilead Sciences, Inc., 333 Lakeside Drive, Foster City, CA 94404 (US). VIVI AN, Randall, W.; c/o Gilead Sciences, Inc., 333 Lakeside Drive, Foster City, CA 94404 (US). YANG, Zheng-Yu; c/o Gilead Sciences, Inc., 333 Lakeside Drive, Foster City, CA 94404 (US). ZABLOCKI, Jeff; c/o Gilead Sciences, Inc., 333 Lakeside Drive, Foster City, CA 94404 (US). ZIPFEL, Sheila; c/o Gilead Sciences, Inc., 333 Lakeside Drive, Foster City, CA 94404 (US). (74) Agent: TANNER, Lorna L.; Sheppard Mullin Richter & Hampton LLP, 379 Lytton Avenue, Palo Alto, CA 94301- 1479 (US). (81) Designated States (unless otherwise indicated, for every kind of national protection available)'. AE, AG, AL, AM, AO, AT, AU, AZ, BA, BB, BG, BH, BN, BR, BW, BY, BZ, CA, CH, CL, CN, CO, CR, CU, CZ, DE, DK, DM, DO, DZ, EC, EE, EG, ES, FI, GB, GD, GE, GH, GM, GT, HN, HR, HU, ID, IL, IN, IS, JP, KE, KG, KN, KP, KR, KZ, LA, LC, LK, LR, LS, LT, LU, LY, MA, MD, ME, [Continued on next page] (54) Title: INHIBITORS OF HEPATITIS C VIRUS N^G oo CJ 00 o o o CJ (57) Abstract: Compounds of Formula I are disclosed, As well as pharmaceutically acceptable salts thereof. Methods of using said compounds and pharmaceutical compositions containing said compounds are also disclosed. WO 2014/008285 A11II llll IIII III III Hill III III III Hill Hill lllll lllll llll 111 mill llll 111 llll MG, MK, MN, MW, MX, MY, MZ, NA, NG, NI, NO, NZ, OM, PA, PE, PG, PH, PL, PT, QA, RO, RS, RU, RW, SC, SD, SE, SG, SK, SL, SM, ST, SV, SY, TH, TJ, TM, TN, TR, TT, TZ, UA, UG, US, UZ, VC, VN, ZA, ZM, ZW. (84) Designated States (unless otherwise indicated, for every kind of regional protection available): ARIPO (BW, GH, GM, KE, LR, LS, MW, MZ, NA, RW, SD, SL, SZ, TZ, UG, ZM, ZW), Eurasian (AM, AZ, BY, KG, KZ, RU, TJ, TM), European (AL, AT, BE, BG, CH, CY, CZ, DE, DK, EE, ES, FI, FR, GB, GR, HR, HU, IE, IS, IT, LT, LU, LV, MC, MK, MT, NL, NO, PL, PT, RO, RS, SE, SI, SK, SM, TR), OAPI (BF, BJ, CF, CG, CI, CM, GA, GN, GQ, GW, KM, ML, MR, NE, SN, TD, TG). Declarations under Rule 4.17: — as to applicant's entitlement to apply for and be granted a patent (Rule 4.17(H)) — as to the applicant's entitlement to claim the priority of the earlier application (Rule 4.17(iii)) Published: — with international search report (Art. 21(3)) — before the expiration of the time limit for amending the claims and to be republished in the event of receipt of amendments (Rule 48.2(h))
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US201261667806P | 2012-07-03 | 2012-07-03 | |
US201361798524P | 2013-03-15 | 2013-03-15 | |
PCT/US2013/049119 WO2014008285A1 (en) | 2012-07-03 | 2013-07-02 | Inhibitors of hepatitis c virus |
Publications (1)
Publication Number | Publication Date |
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SG11201408739VA true SG11201408739VA (en) | 2015-01-29 |
Family
ID=48803614
Family Applications (3)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
SG10201702950TA SG10201702950TA (en) | 2012-07-03 | 2013-07-02 | Inhibitors of hepatitis c virus |
SG10201912269YA SG10201912269YA (en) | 2012-07-03 | 2013-07-02 | Inhibitors of hepatitis c virus |
SG11201408739VA SG11201408739VA (en) | 2012-07-03 | 2013-07-02 | Inhibitors of hepatitis c virus |
Family Applications Before (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
SG10201702950TA SG10201702950TA (en) | 2012-07-03 | 2013-07-02 | Inhibitors of hepatitis c virus |
SG10201912269YA SG10201912269YA (en) | 2012-07-03 | 2013-07-02 | Inhibitors of hepatitis c virus |
Country Status (41)
Families Citing this family (29)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
TWI568722B (en) | 2012-06-15 | 2017-02-01 | 葛蘭馬克製藥公司 | Triazolone compounds as mpges-1 inhibitors |
UA119315C2 (en) | 2012-07-03 | 2019-06-10 | Гіліад Фармассет Елелсі | Inhibitors of hepatitis c virus |
KR20150074051A (en) | 2012-10-19 | 2015-07-01 | 브리스톨-마이어스 스큅 컴퍼니 | Hepatitis c virus inhibitors |
US9334279B2 (en) | 2012-11-02 | 2016-05-10 | 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 |
US9409943B2 (en) | 2012-11-05 | 2016-08-09 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
HUE047777T2 (en) | 2013-01-31 | 2020-05-28 | Gilead Pharmasset Llc | Combination formulation of two antiviral compounds |
JP6342922B2 (en) | 2013-03-07 | 2018-06-13 | ブリストル−マイヤーズ スクイブ カンパニーBristol−Myers Squibb Company | Hepatitis C virus inhibitor |
CN105073758B (en) * | 2013-03-15 | 2017-08-11 | 吉利德科学公司 | Hepatitis c virus inhibitors |
JP2016529293A (en) | 2013-08-27 | 2016-09-23 | ギリアド ファーマセット エルエルシー | Combination preparation of two antiviral compounds |
WO2015100144A1 (en) | 2013-12-23 | 2015-07-02 | Gilead Sciences, Inc. | Crystalline forms of a macrocyclic hcv ns3 inhibiting tripeptide |
WO2015100145A1 (en) | 2013-12-23 | 2015-07-02 | Gilead Sciences, Inc. | Synthesis of a macrocyclic hcv ns3 inhibiting tripeptide |
US10059969B1 (en) | 2014-10-03 | 2018-08-28 | Abbvie Inc. | Process for the preparation of (S)-2-amino-non-8-enoic acid |
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WO2016132805A1 (en) * | 2015-02-16 | 2016-08-25 | セントラル硝子株式会社 | PRACTICAL PROCESSES FOR PRODUCING FLUORINATED α-KETOCARBOXYLIC ESTERS AND ANALOGUES THEREOF |
WO2017184670A2 (en) | 2016-04-22 | 2017-10-26 | Gilead Sciences, Inc. | Methods for treating zika virus infections |
CN109562107A (en) | 2016-05-10 | 2019-04-02 | C4医药公司 | Heterocycle degron body for target protein degradation |
EP3454862B1 (en) | 2016-05-10 | 2024-09-11 | C4 Therapeutics, Inc. | Spirocyclic degronimers for target protein degradation |
CN109641874A (en) | 2016-05-10 | 2019-04-16 | C4医药公司 | C for target protein degradation3The glutarimide degron body of carbon connection |
WO2017205078A1 (en) | 2016-05-27 | 2017-11-30 | Gilead Sciences, Inc. | Methods for treating hepatitis b virus infections using ns5a, ns5b or ns3 inhibitors |
BR102017011025A2 (en) | 2016-06-02 | 2017-12-19 | Gilead Pharmasset Llc | FORMULATION OF COMBINATION OF THREE ANTIVIRAL COMPOUNDS |
JOP20190052A1 (en) | 2016-09-22 | 2019-03-21 | Astrazeneca Ab | 5-[2-(pyridin-2-ylamino)-1,3-thiazol-5-yl]-2,3-dihydro-1 h-isoindol-1 -one derivatives and their use as dual inhibitors of phosphatidylinositol 3-kinase delta & gamma |
CN110461812A (en) * | 2017-02-01 | 2019-11-15 | 艾伯维公司 | It is used to prepare the enzymatic method of (±) -2- (difluoromethyl) -1- (alkoxy carbonyl)-cyclopropane-carboxylic acid He (±) -2- (vinyl) -1- (alkoxy carbonyl)-cyclopropane-carboxylic acid |
CA3082191C (en) | 2017-12-07 | 2021-09-21 | Emory University | N4-hydroxycytidine and derivatives and anti-viral uses related thereto |
CN111018795B (en) * | 2019-12-25 | 2023-03-28 | 上海彩迩文生化科技有限公司 | Method for synthesizing quinoxaline-3-ketone under alkaline condition |
US20230218644A1 (en) | 2020-04-16 | 2023-07-13 | Som Innovation Biotech, S.A. | Compounds for use in the treatment of viral infections by respiratory syndrome-related coronavirus |
US12083099B2 (en) | 2020-10-28 | 2024-09-10 | Accencio LLC | Methods of treating symptoms of coronavirus infection with viral protease inhibitors |
EP4382529A1 (en) | 2022-12-07 | 2024-06-12 | Bayer Consumer Care AG | A process for preparing pure (3s)-pyrrolidin-3-ol and pure (3s)-pyrrolidin-3-ol hydrochloride |
Family Cites Families (111)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP4368581B2 (en) | 2000-12-12 | 2009-11-18 | シェーリング コーポレイション | Diaryl peptides as NS3-serine protease inhibitors of hepatitis C virus |
BR0213562A (en) | 2001-10-26 | 2004-08-31 | Aventis Pharma Inc | Benzimidazoles and analogs and their use as protein kinase inhibitors |
US6867185B2 (en) | 2001-12-20 | 2005-03-15 | Bristol-Myers Squibb Company | Inhibitors of hepatitis C virus |
EP1506000B9 (en) | 2002-05-20 | 2011-08-31 | Bristol-Myers Squibb Company | Heterocyclicsulfonamide hepatitis c virus inhibitors |
ATE413411T1 (en) | 2002-05-20 | 2008-11-15 | Bristol Myers Squibb Co | SUBSTITUTED CYCLOALKYL P1' HEPATITIS C VIRUS INHIBITORS |
MY140680A (en) | 2002-05-20 | 2010-01-15 | Bristol Myers Squibb Co | Hepatitis c virus inhibitors |
AU2003299519A1 (en) | 2002-05-20 | 2004-05-04 | Bristol-Myers Squibb Company | Hepatitis c virus inhibitors |
EP1629000B1 (en) | 2003-04-16 | 2009-02-18 | Bristol-Myers Squibb Company | Macrocyclic isoquinoline peptide inhibitors of hepatitis c virus |
ES2335887T3 (en) | 2003-04-18 | 2010-04-06 | Enanta Pharmaceuticals, Inc. | MACROCYCLIC QUINOXALINYL COMPOUNDS THAT INHIBIT THE SERINE PROTEASES OF HEPATITIS C. |
US7176208B2 (en) | 2003-04-18 | 2007-02-13 | Enanta Pharmaceuticals, Inc. | Quinoxalinyl macrocyclic hepatitis C serine protease inhibitors |
MY143076A (en) | 2003-05-21 | 2011-02-28 | Boehringer Ingelheim Int | Hepatitis c inhibitors compounds |
US7135462B2 (en) | 2003-11-20 | 2006-11-14 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
WO2006020276A2 (en) | 2004-07-16 | 2006-02-23 | Gilead Sciences, Inc. | Antiviral compounds |
WO2007001406A2 (en) | 2004-10-05 | 2007-01-04 | Chiron Corporation | Aryl-containing macrocyclic compounds |
WO2006119061A2 (en) | 2005-05-02 | 2006-11-09 | Merck & Co., Inc. | Hcv ns3 protease inhibitors |
AR057456A1 (en) | 2005-07-20 | 2007-12-05 | Merck & Co Inc | HCV PROTEASA NS3 INHIBITORS |
JP5249028B2 (en) | 2005-07-25 | 2013-07-31 | インターミューン・インコーポレーテッド | Novel macrocyclic inhibitor of hepatitis C virus replication |
PE20070211A1 (en) | 2005-07-29 | 2007-05-12 | Medivir Ab | MACROCYCLIC COMPOUNDS AS INHIBITORS OF HEPATITIS C VIRUS |
CA2615896C (en) * | 2005-08-01 | 2012-11-13 | Merck & Co., Inc. | Macrocyclic peptides as hcv ns3 protease inhibitors |
CN101233148A (en) * | 2005-08-01 | 2008-07-30 | 默克公司 | Macrocyclic peptides as HCV NS3 protease inhibitors |
MX2008004754A (en) | 2005-10-11 | 2009-03-02 | Intermune Inc | Compounds and methods for inhibiting hepatitis c viral replication. |
US7772183B2 (en) | 2005-10-12 | 2010-08-10 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
GB0609492D0 (en) | 2006-05-15 | 2006-06-21 | Angeletti P Ist Richerche Bio | Therapeutic agents |
GB0612423D0 (en) | 2006-06-23 | 2006-08-02 | Angeletti P Ist Richerche Bio | Therapeutic agents |
RU2008152171A (en) | 2006-07-05 | 2010-08-10 | Интермьюн, Инк. (Us) | NEW HEPATITIS C VIRAL REPLICATION INHIBITORS |
EP2079479B1 (en) | 2006-10-24 | 2014-11-26 | Merck Sharp & Dohme Corp. | Hcv ns3 protease inhibitors |
US8309540B2 (en) | 2006-10-24 | 2012-11-13 | Merck Sharp & Dohme Corp. | HCV NS3 protease inhibitors |
AU2007309546A1 (en) | 2006-10-24 | 2008-05-02 | Istituto Di Ricerche Di Biologia Molecolare P. Angeletti S.P.A. | HCV NS3 protease inhibitors |
MX2009004556A (en) | 2006-10-27 | 2009-07-10 | Merck & Co Inc | Hcv ns3 protease inhibitors. |
CA2667032A1 (en) | 2006-10-27 | 2008-05-15 | Merck & Co., Inc. | Hcv ns3 protease inhibitors |
US7888464B2 (en) | 2006-11-16 | 2011-02-15 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
US20080287449A1 (en) | 2007-04-26 | 2008-11-20 | Deqiang Niu | Aza-tripeptide hepatitis c serine protease inhibitors |
KR20100024920A (en) | 2007-05-03 | 2010-03-08 | 인터뮨, 인크. | Novel macrocyclic inhibitors of hepatitis c virus replication |
CL2008001381A1 (en) | 2007-05-10 | 2008-11-03 | Intermune Inc Y Array Biopharma Inc | Compounds derived from tripeptides containing nitrogen heterocycles; pharmaceutical composition comprising said compounds; and use to treat a hepatitis c or hiv infection. |
US20090005387A1 (en) | 2007-06-26 | 2009-01-01 | Deqiang Niu | Quinoxalinyl macrocyclic hepatitis c virus serine protease inhibitors |
EP2162432A2 (en) | 2007-06-29 | 2010-03-17 | Gilead Sciences, Inc. | Antiviral compounds |
AU2008271116B2 (en) | 2007-06-29 | 2012-09-20 | Gilead Sciences, Inc. | Antiviral compounds |
US8927569B2 (en) | 2007-07-19 | 2015-01-06 | Merck Sharp & Dohme Corp. | Macrocyclic compounds as antiviral agents |
WO2009014730A1 (en) | 2007-07-26 | 2009-01-29 | Idenix Pharmaceuticals, Inc. | Macrocyclic serine protease inhibitors |
US8163693B2 (en) | 2007-09-24 | 2012-04-24 | Achillion Pharmaceuticals, Inc. | Urea-containing peptides as inhibitors of viral replication |
US8106059B2 (en) | 2007-10-24 | 2012-01-31 | Virobay, Inc. | Substituted pyrazines that inhibit protease cathepsin S and HCV replication |
US20090111757A1 (en) | 2007-10-25 | 2009-04-30 | Taigen Biotechnology Co., Ltd. | Hcv protease inhibitors |
CL2008003384A1 (en) | 2007-11-14 | 2009-12-11 | Enanta Pharm Inc | Macrocyclic quinoxaline derived compounds, serine protease inhibitors; pharmaceutical composition comprising them; and its use in the treatment of hepatitis c. |
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 |
WO2009070692A1 (en) | 2007-11-29 | 2009-06-04 | Enanta Pharmaceuticals, Inc. | C5-substituted, proline-derived, macrocyclic hepatitis c serine protease inhibitors |
WO2009073719A1 (en) | 2007-12-05 | 2009-06-11 | Enanta Pharmaceuticals, Inc. | Quinoxalinyl derivatives |
US8273709B2 (en) | 2007-12-14 | 2012-09-25 | Enanta Pharmaceuticals, Inc. | Triazole-containing macrocyclic HCV serine protease inhibitors |
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 |
MX2010006736A (en) | 2007-12-21 | 2010-10-15 | 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 |
US8293705B2 (en) | 2007-12-21 | 2012-10-23 | 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 |
RU2490272C2 (en) | 2008-02-04 | 2013-08-20 | Айденикс Фармасьютикалз, Инк. | Macrocyclic serine protease inhibitors |
US8591878B2 (en) | 2008-02-25 | 2013-11-26 | Merck Sharp & Dohme Corp. | Therapeutic compounds |
US8431733B2 (en) | 2008-03-12 | 2013-04-30 | Virobay, Inc. | Process for the preparation of (3S)-3-amino-N-cyclopropyl-2-hydroxyalkanamide derivatives |
EP2268619A4 (en) | 2008-03-20 | 2012-04-04 | Enanta Pharm Inc | Fluorinated macrocyclic compounds as hepatitis c virus inhibitors |
JP2011519364A (en) | 2008-04-15 | 2011-07-07 | インターミューン・インコーポレーテッド | Novel macrocyclic inhibitor of hepatitis C virus replication |
US8163921B2 (en) | 2008-04-16 | 2012-04-24 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
JP2011518882A (en) | 2008-04-28 | 2011-06-30 | メルク・シャープ・エンド・ドーム・コーポレイション | HCV NS3 protease inhibitor |
WO2009134987A1 (en) | 2008-04-30 | 2009-11-05 | Enanta Pharmaceuticals, Inc. | Difluoromethyl-containing macrocyclic compounds as hepatitis c virus inhibitors |
PL2310095T3 (en) * | 2008-07-22 | 2013-03-29 | Msd Italia Srl | Macrocyclic quinoxaline compounds as hcv ns3 protease inhibitors |
CA2732091A1 (en) | 2008-08-07 | 2010-02-11 | F. Hoffmann-La Roche Ag | Process for the preparation of a macrocycle |
US8765667B2 (en) | 2008-08-20 | 2014-07-01 | Michael Eissenstat | HCV protease inhibitors |
UY32099A (en) | 2008-09-11 | 2010-04-30 | Enanta Pharm Inc | HEPATITIS C SERINA PROTEASAS MACROCYCLIC INHIBITORS |
WO2010033466A1 (en) | 2008-09-16 | 2010-03-25 | Phenomix Corporation | Macrocyclic inhibitors of hepatitis c protease |
SI2331538T1 (en) | 2008-09-16 | 2014-06-30 | Boehringer Ingelheim International Gmbh | Crystalline forms of a 2-thiazolyl- 4-quinolinyl-oxy derivative, a potent hcv inhibitor |
US8044087B2 (en) | 2008-09-29 | 2011-10-25 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
US8563505B2 (en) | 2008-09-29 | 2013-10-22 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
US20100080770A1 (en) | 2008-09-29 | 2010-04-01 | Bristol-Myers Squibb Company | Hepatitis C Virus Inhibitors |
KR20110075019A (en) | 2008-10-15 | 2011-07-05 | 인터뮨, 인크. | Therapeutic antiviral peptides |
WO2010048468A1 (en) | 2008-10-23 | 2010-04-29 | Concert Pharmaceuticals, Inc. | Deuterated macrocyclic inhibitors of viral ns3 protease |
CA2743912A1 (en) | 2008-11-20 | 2010-05-27 | Achillion Pharmaceuticals, Inc. | Cyclic carboxamide compounds and analogues thereof as of hepatitis c virus |
BRPI0921070A2 (en) | 2008-11-21 | 2019-09-24 | Boehringer Ingelheim Int | liquid pharmaceutical composition of a potent hcv inhibitor for oral administration |
US20100272674A1 (en) | 2008-12-04 | 2010-10-28 | Bristol-Myers Squibb Company | Hepatitis C Virus Inhibitors |
CN102245598B (en) | 2008-12-10 | 2014-01-29 | 艾其林医药公司 | 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 |
CN102300871A (en) | 2008-12-19 | 2011-12-28 | 吉里德科学公司 | Hcv ns3 protease inhibitors |
US8927722B2 (en) | 2008-12-23 | 2015-01-06 | Janssen Pharmaceutica N.V. | Processes and intermediates for preparing a macrocyclic protease inhibitor of HCV |
MX2011012155A (en) | 2009-05-13 | 2012-02-28 | Enanta Pharm Inc | Macrocyclic compounds as hepatitis c virus inhibitors. |
CA2763122A1 (en) | 2009-05-22 | 2010-11-25 | Sequoia Pharmaceuticals Inc. | Bimacrocyclic hcv ns3 protease inhibitors |
WO2011014487A1 (en) | 2009-07-30 | 2011-02-03 | Merck Sharp & Dohme Corp. | Hepatitis c virus ns3 protease inhibitors |
CA2768232A1 (en) | 2009-07-31 | 2011-02-03 | Cadila Healthcare Limited | Substituted benzamide derivatives as glucokinase (gk) activators |
AU2010286681A1 (en) | 2009-08-27 | 2012-02-09 | Merck Sharp & Dohme Corp. | Processes for preparing protease inhibitors of hepatitis C virus |
AU2010298028A1 (en) | 2009-09-28 | 2012-04-19 | Intermune, Inc. | Cyclic peptide inhibitors of hepatitis C virus replication |
WO2011041551A1 (en) | 2009-10-01 | 2011-04-07 | Intermune, Inc. | Therapeutic antiviral peptides |
WO2011049908A2 (en) | 2009-10-19 | 2011-04-28 | Enanta Pharmaceuticals, Inc. | Bismacrokyclic compounds as hepatitis c virus inhibitors |
WO2011112558A2 (en) | 2010-03-10 | 2011-09-15 | Abbott Laboratories | Solid compositions |
US8530497B2 (en) | 2010-03-11 | 2013-09-10 | Boehringer Ingelheim International Gmbh | Crystalline salts of a potent HCV inhibitor |
WO2011156337A2 (en) | 2010-06-07 | 2011-12-15 | Abbott Laboratories | Macrocyclic hepatitis c serine protease 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 |
HUE028384T2 (en) * | 2010-09-21 | 2016-12-28 | Enanta Pharm Inc | Macrocyclic proline derived hcv serine protease inhibitors |
US20130178413A1 (en) | 2010-09-21 | 2013-07-11 | John A. McCauley | 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 |
US20120101032A1 (en) | 2010-10-22 | 2012-04-26 | Intermune, Inc. | Novel macrocyclic inhibitors of hepatitis c virus replication |
BR112013010836A2 (en) | 2010-11-01 | 2019-09-24 | Genoscience Pharma | hcv ns3 protease specific inhibitors |
AU2011344075A1 (en) | 2010-12-14 | 2013-05-09 | Merck Sharp & Dohme Corp. | Process and intermediates for preparing macrolactams |
CN103534256B (en) | 2010-12-30 | 2016-08-10 | 益安药业 | Macrocyclic hepatitis c serine protease inhibitors |
EP2658858A4 (en) | 2010-12-30 | 2014-06-25 | Enanta Pharm Inc | Phenanthridine macrocyclic hepatitis c serine protease inhibitors |
US8957203B2 (en) | 2011-05-05 | 2015-02-17 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
ES2650223T3 (en) | 2011-05-27 | 2018-01-17 | Bristol-Myers Squibb Company | Tripeptides incorporating deuterium as hepatitis C virus inhibitors |
US8691757B2 (en) | 2011-06-15 | 2014-04-08 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
WO2012171332A1 (en) | 2011-06-16 | 2012-12-20 | 爱博新药研发(上海)有限公司 | Macrocyclic heterocyclic compound for inhibiting hepatitis c virus and preparation and use thereof |
US8912141B2 (en) | 2011-06-23 | 2014-12-16 | Panmed Ltd. | Treatment of hepatitis C virus |
RU2014110400A (en) | 2011-08-19 | 2015-09-27 | Мерк Шарп И Доум Корп. | METHOD AND INTERMEDIATE COMPOUNDS FOR MAKING MACROLACTS |
AU2012332832A1 (en) | 2011-10-31 | 2014-04-17 | Msd Italia S.R.L. | Compositions useful for the treatment of viral diseases |
EP2780026B1 (en) | 2011-11-15 | 2019-10-23 | Merck Sharp & Dohme Corp. | Hcv ns3 protease inhibitors |
SG11201404042VA (en) | 2012-01-12 | 2014-08-28 | Boehringer Ingelheim Int | Stabilized pharmaceutical formulations of a potent hcv inhibitor |
UA119315C2 (en) | 2012-07-03 | 2019-06-10 | Гіліад Фармассет Елелсі | Inhibitors of hepatitis c virus |
CN105073758B (en) | 2013-03-15 | 2017-08-11 | 吉利德科学公司 | Hepatitis c virus inhibitors |
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2021
- 2021-06-23 AU AU2021204238A patent/AU2021204238A1/en not_active Abandoned
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