KR101320907B1 - 바이러스 폴리머라제 억제제 - Google Patents
바이러스 폴리머라제 억제제 Download PDFInfo
- Publication number
- KR101320907B1 KR101320907B1 KR1020067019382A KR20067019382A KR101320907B1 KR 101320907 B1 KR101320907 B1 KR 101320907B1 KR 1020067019382 A KR1020067019382 A KR 1020067019382A KR 20067019382 A KR20067019382 A KR 20067019382A KR 101320907 B1 KR101320907 B1 KR 101320907B1
- Authority
- KR
- South Korea
- Prior art keywords
- mmol
- compound
- methyl
- formula
- alkyl
- 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
Links
- 0 C[n]1c(cc(cc2)C(NC(*)(*)c3nc(cc(*)c(*)c4)c4[n]3C)=O)c2c(*)c1* Chemical compound C[n]1c(cc(cc2)C(NC(*)(*)c3nc(cc(*)c(*)c4)c4[n]3C)=O)c2c(*)c1* 0.000 description 6
- NTLDVAXTMJJWKF-UHFFFAOYSA-N CC(C)(C)OC(NC1(CCC1)c([n](C)c1c2)nc1ccc2C(O1)=NNC1=O)=O Chemical compound CC(C)(C)OC(NC1(CCC1)c([n](C)c1c2)nc1ccc2C(O1)=NNC1=O)=O NTLDVAXTMJJWKF-UHFFFAOYSA-N 0.000 description 1
- IFHBYIUMLMXXND-SOFGYWHQSA-N CCOC(/C=C/c(cc1)cc2c1[n](C)c(C1(CCC1)N)n2)=O Chemical compound CCOC(/C=C/c(cc1)cc2c1[n](C)c(C1(CCC1)N)n2)=O IFHBYIUMLMXXND-SOFGYWHQSA-N 0.000 description 1
- ZNJUYUCIQPRDQL-GQCTYLIASA-N CNc(ccc(/C=C/C(OC)=O)c1)c1N Chemical compound CNc(ccc(/C=C/C(OC)=O)c1)c1N ZNJUYUCIQPRDQL-GQCTYLIASA-N 0.000 description 1
- WVOJTLCYJVZDQX-UHFFFAOYSA-N C[n](c1c2)c(-c3cnccn3)c(C3CCCC3)c1ccc2C(O)=O Chemical compound C[n](c1c2)c(-c3cnccn3)c(C3CCCC3)c1ccc2C(O)=O WVOJTLCYJVZDQX-UHFFFAOYSA-N 0.000 description 1
- MAINHSJYWMIERU-UHFFFAOYSA-N C[n]1c(Br)c(C2CCCC2)c(cc2)c1cc2C(OC)=O Chemical compound C[n]1c(Br)c(C2CCCC2)c(cc2)c1cc2C(OC)=O MAINHSJYWMIERU-UHFFFAOYSA-N 0.000 description 1
- NSIOTKYRKVHDJB-UHFFFAOYSA-N C[n]1c(cc(cc2)C(O3)=NN(C)C3=O)c2nc1C1(CCC1)N Chemical compound C[n]1c(cc(cc2)C(O3)=NN(C)C3=O)c2nc1C1(CCC1)N NSIOTKYRKVHDJB-UHFFFAOYSA-N 0.000 description 1
- BUIBQZJBSWDGMD-UKTHLTGXSA-N C[n]1c(ccc(/C=C/C(O)=O)c2)c2nc1C1(CCC1)NC(c(cc1)cc2c1c(C1CCCC1)c(-c1cnccn1)[n]2C)=O Chemical compound C[n]1c(ccc(/C=C/C(O)=O)c2)c2nc1C1(CCC1)NC(c(cc1)cc2c1c(C1CCCC1)c(-c1cnccn1)[n]2C)=O BUIBQZJBSWDGMD-UKTHLTGXSA-N 0.000 description 1
- GNSTYRWMMNGMGF-FNORWQNLSA-N C[n]1c(ccc(/C=C/C(OC)=O)c2)c2nc1C1(CCC1)N Chemical compound C[n]1c(ccc(/C=C/C(OC)=O)c2)c2nc1C1(CCC1)N GNSTYRWMMNGMGF-FNORWQNLSA-N 0.000 description 1
- DJMSQXVWGAJUPG-UKTHLTGXSA-N C[n]1c2ccc(/C=C/C(N)=O)cc2nc1C1(CCC1)NC(c1ccc(c(C2CCCC2)c(-c2cnccn2)[n]2C)c2c1)=O Chemical compound C[n]1c2ccc(/C=C/C(N)=O)cc2nc1C1(CCC1)NC(c1ccc(c(C2CCCC2)c(-c2cnccn2)[n]2C)c2c1)=O DJMSQXVWGAJUPG-UKTHLTGXSA-N 0.000 description 1
- XCQWRMHWLUCBTM-UHFFFAOYSA-N Cc(c(C(OC)=O)c1)cc(NC)c1N Chemical compound Cc(c(C(OC)=O)c1)cc(NC)c1N XCQWRMHWLUCBTM-UHFFFAOYSA-N 0.000 description 1
- XJHZLZSVKQRXQB-UHFFFAOYSA-N Cc(c(C(OC)=O)c1)cc(NC)c1[N+]([O-])=O Chemical compound Cc(c(C(OC)=O)c1)cc(NC)c1[N+]([O-])=O XJHZLZSVKQRXQB-UHFFFAOYSA-N 0.000 description 1
- WGBJWPWJLDXJLE-UHFFFAOYSA-N Cc(c(C(OC)=O)c1)cc([N+]([O-])=O)c1[N+]([O-])=O Chemical compound Cc(c(C(OC)=O)c1)cc([N+]([O-])=O)c1[N+]([O-])=O WGBJWPWJLDXJLE-UHFFFAOYSA-N 0.000 description 1
- RNTFKDBRMXYEPR-UHFFFAOYSA-N Cc(cc(cc1)[N+]([O-])=O)c1C#N Chemical compound Cc(cc(cc1)[N+]([O-])=O)c1C#N RNTFKDBRMXYEPR-UHFFFAOYSA-N 0.000 description 1
- JJHCLPDHYBSSHC-UHFFFAOYSA-N Cc(cc(cc1)[N+]([O-])=O)c1C(OC)=O Chemical compound Cc(cc(cc1)[N+]([O-])=O)c1C(OC)=O JJHCLPDHYBSSHC-UHFFFAOYSA-N 0.000 description 1
- VGPRNGGSKJHOFE-UHFFFAOYSA-N Cc(nc1)ncc1N Chemical compound Cc(nc1)ncc1N VGPRNGGSKJHOFE-UHFFFAOYSA-N 0.000 description 1
- VIWZMWZXCDYWRM-UHFFFAOYSA-N Cc1c(C2CCCC2)c(ccc(C(O)=O)c2)c2[n]1C Chemical compound Cc1c(C2CCCC2)c(ccc(C(O)=O)c2)c2[n]1C VIWZMWZXCDYWRM-UHFFFAOYSA-N 0.000 description 1
- DIBSZXYEIXRQAB-UHFFFAOYSA-N Cc1c(C2CCCC2)c(ccc(C(OC)=O)c2)c2[n]1C Chemical compound Cc1c(C2CCCC2)c(ccc(C(OC)=O)c2)c2[n]1C DIBSZXYEIXRQAB-UHFFFAOYSA-N 0.000 description 1
- XXXOBNJIIZQSPT-UHFFFAOYSA-N Cc1cc([N+]([O-])=O)ccc1C(O)=O Chemical compound Cc1cc([N+]([O-])=O)ccc1C(O)=O XXXOBNJIIZQSPT-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- 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
-
- 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
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/12—Antivirals
- A61P31/14—Antivirals for RNA viruses
- A61P31/18—Antivirals for RNA viruses for HIV
-
- 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
- A61P31/20—Antivirals for DNA 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
- 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
-
- 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
-
- 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
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—Ortho-condensed systems
Landscapes
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Virology (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Veterinary Medicine (AREA)
- Oncology (AREA)
- Communicable Diseases (AREA)
- Molecular Biology (AREA)
- Engineering & Computer Science (AREA)
- Biotechnology (AREA)
- AIDS & HIV (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Tropical Medicine & Parasitology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Plural Heterocyclic Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US54621304P | 2004-02-20 | 2004-02-20 | |
| US60/546,213 | 2004-02-20 | ||
| PCT/CA2005/000208 WO2005080388A1 (en) | 2004-02-20 | 2005-02-18 | Viral polymerase inhibitors |
Related Child Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| KR1020127014204A Division KR20120091276A (ko) | 2004-02-20 | 2005-02-18 | 바이러스 폴리머라제 억제제 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| KR20070005635A KR20070005635A (ko) | 2007-01-10 |
| KR101320907B1 true KR101320907B1 (ko) | 2013-10-22 |
Family
ID=34886250
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| KR1020127014204A Abandoned KR20120091276A (ko) | 2004-02-20 | 2005-02-18 | 바이러스 폴리머라제 억제제 |
| KR1020067019382A Expired - Fee Related KR101320907B1 (ko) | 2004-02-20 | 2005-02-18 | 바이러스 폴리머라제 억제제 |
Family Applications Before (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| KR1020127014204A Abandoned KR20120091276A (ko) | 2004-02-20 | 2005-02-18 | 바이러스 폴리머라제 억제제 |
Country Status (30)
| Country | Link |
|---|---|
| US (3) | US7582770B2 (enExample) |
| EP (2) | EP1718608B1 (enExample) |
| JP (4) | JP4648333B2 (enExample) |
| KR (2) | KR20120091276A (enExample) |
| CN (6) | CN101648944A (enExample) |
| AR (2) | AR047706A1 (enExample) |
| AU (1) | AU2005215829C1 (enExample) |
| BR (1) | BRPI0507861A (enExample) |
| CA (1) | CA2553879C (enExample) |
| DK (1) | DK1718608T3 (enExample) |
| EA (3) | EA013207B1 (enExample) |
| EC (1) | ECSP066780A (enExample) |
| ES (1) | ES2431314T3 (enExample) |
| HR (1) | HRP20130971T1 (enExample) |
| IL (2) | IL177537A (enExample) |
| IN (1) | IN2012DN04853A (enExample) |
| MY (1) | MY144718A (enExample) |
| NO (1) | NO20064004L (enExample) |
| NZ (1) | NZ549079A (enExample) |
| PE (1) | PE20051141A1 (enExample) |
| PL (1) | PL1718608T3 (enExample) |
| PT (1) | PT1718608E (enExample) |
| RS (1) | RS52931B (enExample) |
| SG (2) | SG184700A1 (enExample) |
| SI (1) | SI1718608T1 (enExample) |
| TW (2) | TWI368508B (enExample) |
| UA (2) | UA86962C2 (enExample) |
| UY (1) | UY28758A1 (enExample) |
| WO (1) | WO2005080388A1 (enExample) |
| ZA (1) | ZA200605151B (enExample) |
Families Citing this family (84)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN1133649C (zh) | 1996-10-18 | 2004-01-07 | 沃泰克斯药物股份有限公司 | 丝氨酸蛋白酶、特别是丙型肝炎病毒ns3蛋白酶的抑制剂 |
| SV2003000617A (es) | 2000-08-31 | 2003-01-13 | Lilly Co Eli | Inhibidores de la proteasa peptidomimetica ref. x-14912m |
| EP2335700A1 (en) | 2001-07-25 | 2011-06-22 | Boehringer Ingelheim (Canada) Ltd. | Hepatitis C virus polymerase inhibitors with a heterobicylic structure |
| US20050075279A1 (en) * | 2002-10-25 | 2005-04-07 | Boehringer Ingelheim International Gmbh | Macrocyclic peptides active against the hepatitis C virus |
| US7098231B2 (en) * | 2003-01-22 | 2006-08-29 | Boehringer Ingelheim International Gmbh | Viral polymerase inhibitors |
| US7223785B2 (en) * | 2003-01-22 | 2007-05-29 | Boehringer Ingelheim International Gmbh | Viral polymerase inhibitors |
| MY148123A (en) | 2003-09-05 | 2013-02-28 | Vertex Pharma | Inhibitors of serine proteases, particularly hcv ns3-ns4a protease |
| SG184700A1 (en) * | 2004-02-20 | 2012-10-30 | Boehringer Ingelheim Int | Viral polymerase inhibitors |
| US7772271B2 (en) | 2004-07-14 | 2010-08-10 | Ptc Therapeutics, Inc. | Methods for treating hepatitis C |
| US7781478B2 (en) | 2004-07-14 | 2010-08-24 | Ptc Therapeutics, Inc. | Methods for treating hepatitis C |
| JP2008506702A (ja) | 2004-07-14 | 2008-03-06 | ピーティーシー セラピューティクス,インコーポレーテッド | C型肝炎を治療するための方法 |
| US7868037B2 (en) | 2004-07-14 | 2011-01-11 | Ptc Therapeutics, Inc. | Methods for treating hepatitis C |
| NZ553329A (en) | 2004-07-22 | 2010-09-30 | Ptc Therapeutics Inc | Thienopyridines for treating hepatitis C |
| US7153848B2 (en) | 2004-08-09 | 2006-12-26 | Bristol-Myers Squibb Company | Inhibitors of HCV replication |
| MY141025A (en) | 2004-10-29 | 2010-02-25 | Vertex Pharma | Dose forms |
| CA2597680A1 (en) | 2005-02-11 | 2006-08-17 | Boehringer Ingelheim International Gmbh | Process for preparing 2,3-disubstituted indoles |
| CA2618682C (en) | 2005-08-12 | 2011-06-21 | Boehringer Ingelheim International Gmbh | Viral polymerase inhibitors |
| 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 |
| US7964624B1 (en) | 2005-08-26 | 2011-06-21 | Vertex Pharmaceuticals Incorporated | Inhibitors of serine proteases |
| US7816348B2 (en) | 2006-02-03 | 2010-10-19 | Boehringer Ingelheim International Gmbh | Viral polymerase inhibitors |
| US8039475B2 (en) | 2006-02-27 | 2011-10-18 | Vertex Pharmaceuticals Incorporated | Co-crystals and pharmaceutical compositions comprising the same |
| KR20080112303A (ko) | 2006-03-16 | 2008-12-24 | 버텍스 파마슈티칼스 인코포레이티드 | 중수소화 c형 간염 프로테아제 억제제 |
| GB0608928D0 (en) | 2006-05-08 | 2006-06-14 | Angeletti P Ist Richerche Bio | Therapeutic agents |
| CN101506167A (zh) | 2006-08-17 | 2009-08-12 | 贝林格尔.英格海姆国际有限公司 | 病毒聚合酶抑制剂 |
| US7999001B2 (en) * | 2007-01-15 | 2011-08-16 | The United States Of America As Represented By The Secretary Of The Army | Antiviral compounds and methods of using thereof |
| EP2134717A2 (en) | 2007-02-27 | 2009-12-23 | Vertex Pharmceuticals Incorporated | Inhibitors of serine proteases |
| PT2114924E (pt) | 2007-02-27 | 2012-04-03 | Vertex Pharma | Co-cristais e composições farmacêuticas que compreendem os mesmos |
| CN101815533A (zh) | 2007-05-04 | 2010-08-25 | 弗特克斯药品有限公司 | 用于治疗hcv感染的组合治疗 |
| AU2008277442A1 (en) | 2007-07-17 | 2009-01-22 | Istituto Di Ricerche Di Biologia Molecolare P. Angeletti Spa | Macrocyclic indole derivatives for the treatment of hepatitis C infections |
| US8242140B2 (en) | 2007-08-03 | 2012-08-14 | Boehringer Ingelheim International Gmbh | Viral polymerase inhibitors |
| JP5443360B2 (ja) | 2007-08-30 | 2014-03-19 | バーテックス ファーマシューティカルズ インコーポレイテッド | 共結晶体およびそれを含む医薬組成物 |
| CA2708150A1 (en) | 2007-12-05 | 2009-06-18 | Enanta Pharmaceuticals, Inc. | Fluorinated tripeptide hcv serine protease inhibitors |
| BRPI0821342A2 (pt) | 2007-12-19 | 2019-09-24 | Boehringer Ingelheim Int | inibidores da polimerase viral |
| AR072297A1 (es) | 2008-06-27 | 2010-08-18 | Novartis Ag | Derivados de indol-2-il-piridin-3-ilo, composicion farmaceutica que los comprende y su uso en medicamentos para el tratamiento de enfermedades mediadas por la sintasa aldosterona. |
| WO2010018131A1 (en) | 2008-08-11 | 2010-02-18 | Smithkline Beecham Corporation | Purine derivatives for use in the treatment of allergic, inflammatory and infectious diseases |
| UA103195C2 (uk) | 2008-08-11 | 2013-09-25 | Глаксосмитклайн Ллк | Похідні пурину для застосування у лікуванні алергій, запальних та інфекційних захворювань |
| CN102176911B (zh) | 2008-08-11 | 2014-12-10 | 葛兰素史密丝克莱恩有限责任公司 | 新的腺嘌呤衍生物 |
| CN102159245B (zh) * | 2008-09-17 | 2013-07-24 | 贝林格尔.英格海姆国际有限公司 | Hcv ns3蛋白酶抑制剂与干扰素和利巴韦林的组合 |
| JP2012051803A (ja) * | 2008-12-25 | 2012-03-15 | Kyorin Pharmaceutical Co Ltd | 環状アミノ安息香酸エステル誘導体の製造方法 |
| CN102271699A (zh) | 2009-01-07 | 2011-12-07 | 西尼克斯公司 | 用于治疗hcv和hiv感染的环孢菌素衍生物 |
| EP2396028A2 (en) | 2009-02-12 | 2011-12-21 | Vertex Pharmceuticals Incorporated | Hcv combination therapies comprising pegylated interferon, ribavirin and telaprevir |
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