JP2010521483A - シクロプロピル縮合インドロベンゾアゼピンhcvインヒビター - Google Patents
シクロプロピル縮合インドロベンゾアゼピンhcvインヒビター Download PDFInfo
- Publication number
- JP2010521483A JP2010521483A JP2009553765A JP2009553765A JP2010521483A JP 2010521483 A JP2010521483 A JP 2010521483A JP 2009553765 A JP2009553765 A JP 2009553765A JP 2009553765 A JP2009553765 A JP 2009553765A JP 2010521483 A JP2010521483 A JP 2010521483A
- Authority
- JP
- Japan
- Prior art keywords
- alkyl
- hcv
- inhibitor
- piperazinyl
- cycloalkyl
- 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.)
- Pending
Links
- 0 CN(C)S(=O)#*C(c1ccc(c(C2CCCCC2)c(-c2c(C3C4)cc(*)cc2)[n]2CC34C(O)=O)c2c1)=O Chemical compound CN(C)S(=O)#*C(c1ccc(c(C2CCCCC2)c(-c2c(C3C4)cc(*)cc2)[n]2CC34C(O)=O)c2c1)=O 0.000 description 3
- IWYAULVVEFYJRL-UHFFFAOYSA-N CCC(C)S(NC(c1ccc(c(C2CCCCC2)c(-c(cc2)c(C3C4)cc2OC)[n]2CC34C(OC)=O)c2c1)=O)(=O)=O Chemical compound CCC(C)S(NC(c1ccc(c(C2CCCCC2)c(-c(cc2)c(C3C4)cc2OC)[n]2CC34C(OC)=O)c2c1)=O)(=O)=O IWYAULVVEFYJRL-UHFFFAOYSA-N 0.000 description 1
- DRMSAMZUMYPHHW-UHFFFAOYSA-N CN(C)CC(c1ccccc1)N(C)C(C1(C[n](c2c3)c(-c(cc4)c5cc4OC)c(C4CCCCC4)c2ccc3C(NS(N(C)C)(=O)=O)=O)C5=C1)=O Chemical compound CN(C)CC(c1ccccc1)N(C)C(C1(C[n](c2c3)c(-c(cc4)c5cc4OC)c(C4CCCCC4)c2ccc3C(NS(N(C)C)(=O)=O)=O)C5=C1)=O DRMSAMZUMYPHHW-UHFFFAOYSA-N 0.000 description 1
- BZKAQFPZOAMTNR-UHFFFAOYSA-N CN(C)S(NC(c(cc1)cc2c1c(C1CCCCC1)c(-c(c(C1C3)c4)ccc4OC)[n]2CC13C(N(CC1)CCC1c1cccc(Cl)c1)=O)=O)(=O)=O Chemical compound CN(C)S(NC(c(cc1)cc2c1c(C1CCCCC1)c(-c(c(C1C3)c4)ccc4OC)[n]2CC13C(N(CC1)CCC1c1cccc(Cl)c1)=O)=O)(=O)=O BZKAQFPZOAMTNR-UHFFFAOYSA-N 0.000 description 1
- LEBGTJIHOCUXDT-UHFFFAOYSA-N CN(C)S(NC(c1ccc(C(C(c(c(C2C3)c4)ccc4OC)N4CC23C(N(CC2)CCC2c2cccc(O)c2)=O)C2CCCCC2)c4c1)=O)(=O)=O Chemical compound CN(C)S(NC(c1ccc(C(C(c(c(C2C3)c4)ccc4OC)N4CC23C(N(CC2)CCC2c2cccc(O)c2)=O)C2CCCCC2)c4c1)=O)(=O)=O LEBGTJIHOCUXDT-UHFFFAOYSA-N 0.000 description 1
- LSAWFTOYTMSDCO-UHFFFAOYSA-N CN(C)S(NC(c1ccc(c(C2CCCCC2)c(-c(c(C2C3)c4)ccc4OC)[n]4CC23C(N(CC2)CCC2c(cc2)ccc2Cl)=O)c4c1)=O)(=O)=O Chemical compound CN(C)S(NC(c1ccc(c(C2CCCCC2)c(-c(c(C2C3)c4)ccc4OC)[n]4CC23C(N(CC2)CCC2c(cc2)ccc2Cl)=O)c4c1)=O)(=O)=O LSAWFTOYTMSDCO-UHFFFAOYSA-N 0.000 description 1
- ZGUNCAYHERGYMM-UHFFFAOYSA-N CN(C)S(NC(c1ccc(c(C2CCCCC2)c(-c(cc2)c(C3C4)cc2OC)[n]2CC34C(N(C)CC3(CCCCC3)N3CCCCC3)=O)c2c1)=O)(=O)=O Chemical compound CN(C)S(NC(c1ccc(c(C2CCCCC2)c(-c(cc2)c(C3C4)cc2OC)[n]2CC34C(N(C)CC3(CCCCC3)N3CCCCC3)=O)c2c1)=O)(=O)=O ZGUNCAYHERGYMM-UHFFFAOYSA-N 0.000 description 1
- OCWGEDJBLXZWCX-UHFFFAOYSA-N CN(C)S(NC(c1ccc(c(C2CCCCC2)c(-c(cc2)c(C3C4)cc2OC)[n]2CC34C(N(CC3)CCC3c(cc3)ccc3C#N)=O)c2c1)=O)(=O)=O Chemical compound CN(C)S(NC(c1ccc(c(C2CCCCC2)c(-c(cc2)c(C3C4)cc2OC)[n]2CC34C(N(CC3)CCC3c(cc3)ccc3C#N)=O)c2c1)=O)(=O)=O OCWGEDJBLXZWCX-UHFFFAOYSA-N 0.000 description 1
- YTBSILWTGITJJS-UHFFFAOYSA-N CN(C)S(NC(c1ccc(c(C2CCCCC2)c(-c(cc2)c(C3C4)cc2OC)[n]2CC34C(N(CC3)CCC3c3cccc(F)c3)=O)c2c1)=O)(=O)=O Chemical compound CN(C)S(NC(c1ccc(c(C2CCCCC2)c(-c(cc2)c(C3C4)cc2OC)[n]2CC34C(N(CC3)CCC3c3cccc(F)c3)=O)c2c1)=O)(=O)=O YTBSILWTGITJJS-UHFFFAOYSA-N 0.000 description 1
- XKVIPZGECAXKKM-UHFFFAOYSA-N CN(C)S(NC(c1ccc(c(C2CCCCC2)c(-c(cc2)c(C3C4)cc2OC)[n]2CC34C(N(CC3)CCC3c3ccccc3)=O)c2c1)=O)(=O)=O Chemical compound CN(C)S(NC(c1ccc(c(C2CCCCC2)c(-c(cc2)c(C3C4)cc2OC)[n]2CC34C(N(CC3)CCC3c3ccccc3)=O)c2c1)=O)(=O)=O XKVIPZGECAXKKM-UHFFFAOYSA-N 0.000 description 1
- ZBCLSGVDIXMBIQ-UHFFFAOYSA-N CN(C)S(NC(c1ccc(c(C2CCCCC2)c(-c(cc2)c(C3C4)cc2OC)[n]2CC34C(NCC3NCCC3)=O)c2c1)=O)(=O)=O Chemical compound CN(C)S(NC(c1ccc(c(C2CCCCC2)c(-c(cc2)c(C3C4)cc2OC)[n]2CC34C(NCC3NCCC3)=O)c2c1)=O)(=O)=O ZBCLSGVDIXMBIQ-UHFFFAOYSA-N 0.000 description 1
- HAHULJMPMRAZNA-UHFFFAOYSA-N CN(C)S(NC(c1ccc(c(C2CCCCC2)c-2[n]3CC(C(OC)=O)=Cc4c-2ccc(OC)c4)c3c1)=O)(=O)=O Chemical compound CN(C)S(NC(c1ccc(c(C2CCCCC2)c-2[n]3CC(C(OC)=O)=Cc4c-2ccc(OC)c4)c3c1)=O)(=O)=O HAHULJMPMRAZNA-UHFFFAOYSA-N 0.000 description 1
- REJZTBBROOPALB-UHFFFAOYSA-N COC(C(C1)(C[n]2c3c4)C1c(cc(cc1)OC)c1-c2c(C1CCCCC1)c3ccc4C(NS(C1CCCC1)(=O)=O)=O)=O Chemical compound COC(C(C1)(C[n]2c3c4)C1c(cc(cc1)OC)c1-c2c(C1CCCCC1)c3ccc4C(NS(C1CCCC1)(=O)=O)=O)=O REJZTBBROOPALB-UHFFFAOYSA-N 0.000 description 1
- OEKRRSJKHMJSOT-UHFFFAOYSA-N COC(C(C[n]1c2c3)=Cc(cc(cc4)OC)c4-c1c(C1CCCCC1)c2ccc3C(O)=O)=O Chemical compound COC(C(C[n]1c2c3)=Cc(cc(cc4)OC)c4-c1c(C1CCCCC1)c2ccc3C(O)=O)=O OEKRRSJKHMJSOT-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
-
- 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
- C07D519/00—Heterocyclic compounds containing more than one system of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring system not provided for in groups C07D453/00 or C07D455/00
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Public Health (AREA)
- Animal Behavior & Ethology (AREA)
- Veterinary Medicine (AREA)
- General Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Pharmacology & Pharmacy (AREA)
- Virology (AREA)
- Oncology (AREA)
- Communicable Diseases (AREA)
- Molecular Biology (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US89488907P | 2007-03-14 | 2007-03-14 | |
| US98952207P | 2007-11-21 | 2007-11-21 | |
| PCT/US2008/056789 WO2008112851A1 (en) | 2007-03-14 | 2008-03-13 | Cyclopropyl fused indolobenzazepine hcv inhibitors |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2010521483A true JP2010521483A (ja) | 2010-06-24 |
| JP2010521483A5 JP2010521483A5 (enExample) | 2011-04-14 |
Family
ID=39541177
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2009553765A Pending JP2010521483A (ja) | 2007-03-14 | 2008-03-13 | シクロプロピル縮合インドロベンゾアゼピンhcvインヒビター |
Country Status (6)
| Country | Link |
|---|---|
| US (1) | US7538102B2 (enExample) |
| EP (1) | EP2118110B1 (enExample) |
| JP (1) | JP2010521483A (enExample) |
| CN (1) | CN101790533B (enExample) |
| ES (1) | ES2390191T3 (enExample) |
| WO (1) | WO2008112851A1 (enExample) |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2011503229A (ja) * | 2007-11-20 | 2011-01-27 | ブリストル−マイヤーズ スクイブ カンパニー | シクロプロピル縮合インドロベンズアゼピンhcvns5b阻害剤 |
| JP2011504179A (ja) * | 2007-11-21 | 2011-02-03 | ブリストル−マイヤーズ スクイブ カンパニー | C型肝炎治療のための化合物 |
| JP2015528008A (ja) * | 2012-07-18 | 2015-09-24 | ブリストル−マイヤーズ・スクイブ・ホールディングス・アイルランドBristol−Myers Squibb Holdings Ireland | (4bS,5aR)−12−シクロヘキシル−N−(N,N−ジメチルスルファモイル)−3−メトキシ−5a−((1R,5S)−3−メチル−3,8−ジアザビシクロ[3.2.1]オクタン−8−カルボニル)−4b,5,5a,6−テトラヒドロベンゾ[3,4]シクロプロパ[5,6]アゼピノ[1,2−A]インドール−9−カルボキサミドを製造するための新規な方法および中間体 |
Families Citing this family (17)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPWO2005049622A1 (ja) * | 2003-11-19 | 2007-06-07 | 日本たばこ産業株式会社 | 5−5員縮合複素環化合物及びそのhcvポリメラーゼ阻害剤としての用途 |
| US20070049593A1 (en) * | 2004-02-24 | 2007-03-01 | Japan Tobacco Inc. | Tetracyclic fused heterocyclic compound and use thereof as HCV polymerase inhibitor |
| US7659263B2 (en) | 2004-11-12 | 2010-02-09 | Japan Tobacco Inc. | Thienopyrrole compound and use thereof as HCV polymerase inhibitor |
| US7521443B2 (en) * | 2006-05-17 | 2009-04-21 | Bristol-Myers Squibb Company | Cyclopropyl fused indolobenzazepine HCV NS5B inhibitors |
| US7642251B2 (en) * | 2007-08-09 | 2010-01-05 | Bristol-Myers Squibb Company | Compounds for the treatment of hepatitis C |
| US8143243B2 (en) * | 2007-08-09 | 2012-03-27 | Bristol-Myers Squibb Company | Compounds for the treatment of hepatitis C |
| US7652004B2 (en) * | 2007-08-09 | 2010-01-26 | Bristol-Myers Squibb Company | Compounds for the treatment of hepatitis C |
| US8124601B2 (en) * | 2007-11-21 | 2012-02-28 | Bristol-Myers Squibb Company | Compounds for the treatment of Hepatitis C |
| EP2280978B1 (en) * | 2008-03-27 | 2013-04-24 | Bristol-Myers Squibb Company | Pyrrolidine fused indolobenzadiazepine hcv ns5b inhibitors |
| WO2009120745A1 (en) * | 2008-03-27 | 2009-10-01 | Bristol-Myers Squibb Company | Compounds for the treatment of hepatitis c |
| EP2268643B1 (en) | 2008-03-27 | 2014-08-06 | Bristol-Myers Squibb Company | Dioxolane and dioxolanone fused indolobenzadiazepine hcv ns5b inhibitors |
| US8133884B2 (en) * | 2008-05-06 | 2012-03-13 | Bristol-Myers Squibb Company | Compounds for the treatment of hepatitis C |
| US8143244B2 (en) * | 2009-02-26 | 2012-03-27 | Bristol-Myers Squibb Company | Cyclopropyl fused indolobenzazepine HCV NS5B inhibitors |
| EP2655362A1 (en) | 2010-12-22 | 2013-10-30 | Abbvie Inc. | Hepatitis c inhibitors and uses thereof |
| CN102659668B (zh) * | 2012-05-03 | 2014-04-09 | 苏州汉德创宏生化科技有限公司 | 1-烷基-哌啶-4-磺酰苄胺的合成方法 |
| EP2968280A4 (en) | 2013-03-14 | 2016-08-10 | Genentech Inc | SUBSTITUTED TRIAZOLOPYRIDINES AND METHOD OF USE THEREOF |
| US12274700B1 (en) | 2020-10-30 | 2025-04-15 | Accencio LLC | Methods of treating symptoms of coronavirus infection with RNA polymerase inhibitors |
Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP5211078B2 (ja) * | 2007-03-13 | 2013-06-12 | ブリストル−マイヤーズ スクイブ カンパニー | シクロプロピル縮合インドロベンズアゼピンhcvns5b阻害剤 |
Family Cites Families (14)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| PT1719773E (pt) | 2004-02-24 | 2009-06-03 | Japan Tobacco Inc | Compostos heterotetracíclicos fundidos e a sua utilização como inibidores da polimerase do hcv |
| US7153848B2 (en) * | 2004-08-09 | 2006-12-26 | Bristol-Myers Squibb Company | Inhibitors of HCV replication |
| US7348425B2 (en) | 2004-08-09 | 2008-03-25 | Bristol-Myers Squibb Company | Inhibitors of HCV replication |
| JP2008517986A (ja) | 2004-10-26 | 2008-05-29 | イステイチユート・デイ・リチエルケ・デイ・ビオロジア・モレコラーレ・ピ・アンジエレツテイ・エツセ・ピー・アー | 抗ウイルス薬としての四環式インドール誘導体 |
| GB0518390D0 (en) | 2005-09-09 | 2005-10-19 | Angeletti P Ist Richerche Bio | Therapeutic compounds |
| US7399758B2 (en) * | 2005-09-12 | 2008-07-15 | Meanwell Nicholas A | Cyclopropyl fused indolobenzazepine HCV NS5B inhibitors |
| US7473688B2 (en) * | 2005-09-13 | 2009-01-06 | Bristol-Myers Squibb Company | Indolobenzazepine HCV NS5B inhibitors |
| US7456165B2 (en) * | 2006-02-08 | 2008-11-25 | Bristol-Myers Squibb Company | HCV NS5B inhibitors |
| GB0608928D0 (en) | 2006-05-08 | 2006-06-14 | Angeletti P Ist Richerche Bio | Therapeutic agents |
| US7456166B2 (en) * | 2006-05-17 | 2008-11-25 | Bristol-Myers Squibb Company | Cyclopropyl fused indolobenzazepine HCV NS5B inhibitors |
| US7521441B2 (en) * | 2006-05-22 | 2009-04-21 | Bristol-Myers Squibb Company | Cyclopropyl fused indolobenzazepine HCV NS5B inhibitors |
| ATE469155T1 (de) * | 2006-05-25 | 2010-06-15 | Bristol Myers Squibb Co | Cyclopropyl-fusionierte indolbenzazepin-hcv-ns5b- hemmer |
| US7521442B2 (en) * | 2006-05-25 | 2009-04-21 | Bristol-Myers Squibb Company | Cyclopropyl fused indolobenzazepine HCV NS5B inhibitors |
| US7452876B2 (en) * | 2006-06-08 | 2008-11-18 | Bristol-Myers Squibb Company | Cyclopropyl fused indolobenzazepine HCV NS5B inhibitors |
-
2008
- 2008-03-11 US US12/046,030 patent/US7538102B2/en active Active
- 2008-03-13 ES ES08743824T patent/ES2390191T3/es active Active
- 2008-03-13 EP EP08743824A patent/EP2118110B1/en not_active Not-in-force
- 2008-03-13 WO PCT/US2008/056789 patent/WO2008112851A1/en not_active Ceased
- 2008-03-13 JP JP2009553765A patent/JP2010521483A/ja active Pending
- 2008-03-13 CN CN2008800159152A patent/CN101790533B/zh not_active Expired - Fee Related
Patent Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP5211078B2 (ja) * | 2007-03-13 | 2013-06-12 | ブリストル−マイヤーズ スクイブ カンパニー | シクロプロピル縮合インドロベンズアゼピンhcvns5b阻害剤 |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2011503229A (ja) * | 2007-11-20 | 2011-01-27 | ブリストル−マイヤーズ スクイブ カンパニー | シクロプロピル縮合インドロベンズアゼピンhcvns5b阻害剤 |
| JP2011504179A (ja) * | 2007-11-21 | 2011-02-03 | ブリストル−マイヤーズ スクイブ カンパニー | C型肝炎治療のための化合物 |
| JP2015528008A (ja) * | 2012-07-18 | 2015-09-24 | ブリストル−マイヤーズ・スクイブ・ホールディングス・アイルランドBristol−Myers Squibb Holdings Ireland | (4bS,5aR)−12−シクロヘキシル−N−(N,N−ジメチルスルファモイル)−3−メトキシ−5a−((1R,5S)−3−メチル−3,8−ジアザビシクロ[3.2.1]オクタン−8−カルボニル)−4b,5,5a,6−テトラヒドロベンゾ[3,4]シクロプロパ[5,6]アゼピノ[1,2−A]インドール−9−カルボキサミドを製造するための新規な方法および中間体 |
Also Published As
| Publication number | Publication date |
|---|---|
| CN101790533B (zh) | 2013-02-27 |
| EP2118110A1 (en) | 2009-11-18 |
| US20080226592A1 (en) | 2008-09-18 |
| EP2118110B1 (en) | 2012-07-25 |
| CN101790533A (zh) | 2010-07-28 |
| US7538102B2 (en) | 2009-05-26 |
| WO2008112851A1 (en) | 2008-09-18 |
| ES2390191T3 (es) | 2012-11-07 |
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