JP2012519173A - シクロプロピル縮合インドロベンズアゼピンhcvns5b阻害剤 - Google Patents
シクロプロピル縮合インドロベンズアゼピンhcvns5b阻害剤 Download PDFInfo
- Publication number
- JP2012519173A JP2012519173A JP2011552097A JP2011552097A JP2012519173A JP 2012519173 A JP2012519173 A JP 2012519173A JP 2011552097 A JP2011552097 A JP 2011552097A JP 2011552097 A JP2011552097 A JP 2011552097A JP 2012519173 A JP2012519173 A JP 2012519173A
- Authority
- JP
- Japan
- Prior art keywords
- mmol
- cyclohexyl
- methoxy
- indolo
- benzazepine
- 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)CC1(CC2)*2C*C1 Chemical compound CN(C)CC1(CC2)*2C*C1 0.000 description 11
- ZUTVCRWKOXXRIS-UHFFFAOYSA-N CC(C)C[S+2]([NH2+]C(c1ccc(c(C2CCCCC2)c(-c(cc2)c(C3C4)cc2OC)[n]2CC34C(OC)=O)c2c1)=O)=O Chemical compound CC(C)C[S+2]([NH2+]C(c1ccc(c(C2CCCCC2)c(-c(cc2)c(C3C4)cc2OC)[n]2CC34C(OC)=O)c2c1)=O)=O ZUTVCRWKOXXRIS-UHFFFAOYSA-N 0.000 description 1
- RDNPHYZQNKJQLV-JJNMFGATSA-N CC(C)S(NC(c1ccc(c(C2CCCCC2)c(-c(cc2)c([C@@H]3C4)cc2OC)[n]2C[C@]34C(N3CC(CC4)(CNC5)C45C3)=O)c2c1)=O)(=O)=O Chemical compound CC(C)S(NC(c1ccc(c(C2CCCCC2)c(-c(cc2)c([C@@H]3C4)cc2OC)[n]2C[C@]34C(N3CC(CC4)(CNC5)C45C3)=O)c2c1)=O)(=O)=O RDNPHYZQNKJQLV-JJNMFGATSA-N 0.000 description 1
- QVCFGUZJHCUXKH-HWILGKNMSA-N CC(S(NC(c1ccc(c(C2CCCCC2)c(-c(cc2)c([C@@H]3C4)cc2OC)[n]2C[C@]34C(N3CC(COC)(CN(C)C4)[C@]4(COC)C3)=O)c2c1)=O)(=O)=O)=C Chemical compound CC(S(NC(c1ccc(c(C2CCCCC2)c(-c(cc2)c([C@@H]3C4)cc2OC)[n]2C[C@]34C(N3CC(COC)(CN(C)C4)[C@]4(COC)C3)=O)c2c1)=O)(=O)=O)=C QVCFGUZJHCUXKH-HWILGKNMSA-N 0.000 description 1
- XKYAOFAJGZWBMX-UHFFFAOYSA-N CN(C1)CC2(CN(C3)C(C(Cc4c-5ccc(OC)c4)C[n](c4c6)c-5c(C5CCCCC5)c4ccc6C(NS(C4CC4)(=O)=O)=O)=O)C13COC2 Chemical compound CN(C1)CC2(CN(C3)C(C(Cc4c-5ccc(OC)c4)C[n](c4c6)c-5c(C5CCCCC5)c4ccc6C(NS(C4CC4)(=O)=O)=O)=O)C13COC2 XKYAOFAJGZWBMX-UHFFFAOYSA-N 0.000 description 1
- FOFBNFHKSZROTE-UHFFFAOYSA-N CN(C1CC1)S(NC(c1ccc(c(C2CCCCC2)c(-c(cc2)c(C3C4)cc2OC)[n]2CC34C(OC)=O)c2c1)=O)(=O)=O Chemical compound CN(C1CC1)S(NC(c1ccc(c(C2CCCCC2)c(-c(cc2)c(C3C4)cc2OC)[n]2CC34C(OC)=O)c2c1)=O)(=O)=O FOFBNFHKSZROTE-UHFFFAOYSA-N 0.000 description 1
- UJKGRUFGEKWYGH-UHFFFAOYSA-N CNCC1(C2)C2(CNC)CN(C)C1 Chemical compound CNCC1(C2)C2(CNC)CN(C)C1 UJKGRUFGEKWYGH-UHFFFAOYSA-N 0.000 description 1
- HPSGILHSWFUPSL-AOOOYVTPSA-N COC[C@]1(CNC2)[C@]2(COC)CNC1 Chemical compound COC[C@]1(CNC2)[C@]2(COC)CNC1 HPSGILHSWFUPSL-AOOOYVTPSA-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
- 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
- A61P31/14—Antivirals for RNA viruses
-
- 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
- C07D487/12—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 three hetero rings
- C07D487/18—Bridged systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D491/00—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
- C07D491/12—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains three hetero rings
- C07D491/18—Bridged systems
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)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Health & Medical Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Oncology (AREA)
- Virology (AREA)
- Communicable Diseases (AREA)
- Molecular Biology (AREA)
- Gastroenterology & Hepatology (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US15563409P | 2009-02-26 | 2009-02-26 | |
| US61/155,634 | 2009-02-26 | ||
| PCT/US2010/025169 WO2010099159A1 (en) | 2009-02-26 | 2010-02-24 | Cyclopropyl fused indolobenzazepine hcv ns5b inhibitors |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2012519173A true JP2012519173A (ja) | 2012-08-23 |
| JP2012519173A5 JP2012519173A5 (https=) | 2013-03-21 |
Family
ID=42289577
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2011552097A Pending JP2012519173A (ja) | 2009-02-26 | 2010-02-24 | シクロプロピル縮合インドロベンズアゼピンhcvns5b阻害剤 |
Country Status (5)
| Country | Link |
|---|---|
| US (1) | US8143244B2 (https=) |
| EP (1) | EP2401280B1 (https=) |
| JP (1) | JP2012519173A (https=) |
| CN (1) | CN102414212A (https=) |
| WO (1) | WO2010099159A1 (https=) |
Families Citing this family (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20070049593A1 (en) | 2004-02-24 | 2007-03-01 | Japan Tobacco Inc. | Tetracyclic fused heterocyclic compound and use thereof as HCV polymerase inhibitor |
| WO2009120733A1 (en) * | 2008-03-27 | 2009-10-01 | Bristol-Myers Squibb Company | Pyrrolidine fused indolobenzadiazepine hcv ns5b inhibitors |
| JP2011515486A (ja) * | 2008-03-27 | 2011-05-19 | ブリストル−マイヤーズ スクイブ カンパニー | C型肝炎の治療用化合物 |
| US8138171B2 (en) * | 2008-03-27 | 2012-03-20 | Bristol-Myers Squibb Company | Dioxolane and dioxolanone fused indolobenzadiazepine HCV NS5B inhibitors |
| ES2747768T3 (es) | 2017-03-20 | 2020-03-11 | Forma Therapeutics Inc | Composiciones de pirrolopirrol como activadores de quinasa de piruvato (PKR) |
| ES2989438T3 (es) | 2018-09-19 | 2024-11-26 | Novo Nordisk Healthcare Ag | Activación de la piruvato cinasa R |
| US12053458B2 (en) | 2018-09-19 | 2024-08-06 | Novo Nordisk Health Care Ag | Treating sickle cell disease with a pyruvate kinase R activating compound |
| US20220378756A1 (en) | 2019-09-19 | 2022-12-01 | Forma Therapeutics, Inc. | Activating pyruvate kinase r |
| US12128035B2 (en) | 2021-03-19 | 2024-10-29 | Novo Nordisk Health Care Ag | Activating pyruvate kinase R |
| EP4269332A1 (de) | 2022-04-26 | 2023-11-01 | GasConTec GmbH | Verfahren und anlage zur herstellung von ammoniak |
Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2008112841A1 (en) * | 2007-03-14 | 2008-09-18 | Bristol-Myers Squibb Company | Compounds for the treatment of hepatitis c |
| WO2008112848A1 (en) * | 2007-03-14 | 2008-09-18 | Bristol-Myers Squibb Company | Compounds for the treatment of hepatitis c |
Family Cites Families (57)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| NZ533057A (en) * | 2001-10-26 | 2005-11-25 | Angeletti P Ist Richerche Bio | N-substituted hydroxypyrimidinone carboxamide inhibitors of HIV integrase |
| EP1441734B1 (en) * | 2001-10-26 | 2007-02-28 | Istituto di Richerche di Biologia Molecolare P. Angeletti S.p.A. | Dihydroxypyrimidine carboxamide inhibitors of hiv integrase |
| GB0201179D0 (en) | 2002-01-18 | 2002-03-06 | Angeletti P Ist Richerche Bio | Therapeutic agents |
| CN1731993A (zh) | 2002-11-01 | 2006-02-08 | 维洛药品公司 | 苯并呋喃化合物、组合物以及治疗和预防丙型肝炎病毒感染及相关疾病的方法 |
| US6745521B1 (en) * | 2002-12-13 | 2004-06-08 | Klemming Ulf Jp | Gazebo |
| EP1578748B1 (en) * | 2002-12-27 | 2010-09-15 | Istituto Di Ricerche Di Biologia Molecolare P. Angeletti S.P.A. | Tetrahydro-4h-pyrido[1,2-a]pyrimidines and related compounds useful as hiv integrase inhibitors |
| WO2004062613A2 (en) * | 2003-01-13 | 2004-07-29 | Bristol-Myers Squibb Company | Hiv integrase inhibitors |
| US7223785B2 (en) | 2003-01-22 | 2007-05-29 | Boehringer Ingelheim International Gmbh | Viral polymerase inhibitors |
| JP2004244320A (ja) | 2003-02-10 | 2004-09-02 | Shionogi & Co Ltd | 含窒素複素環抗ウイルス剤 |
| US7037908B2 (en) * | 2003-04-24 | 2006-05-02 | Bristol-Myers Squibb Company | HIV integrase inhibitors |
| AR046938A1 (es) | 2003-12-12 | 2006-01-04 | Merck & Co Inc | Procedimiento para preparar hexahidropirimido[1,2-a]azepin-2-carboxilatos y compuetos similares |
| TW200526635A (en) | 2003-12-22 | 2005-08-16 | Shionogi & Co | Hydroxypyrimidinone derivative having HIV integrase inhibitory activity |
| MXPA06007906A (es) | 2004-01-12 | 2007-02-14 | Gilead Sciences Inc | Compuestos antivirales de fosfonato de pirimidilo y metodos de uso. |
| HRP20090250T1 (hr) | 2004-02-24 | 2009-06-30 | Japan Tobacco | Kondenzirani heterociklički spojevi i njihova upotreba kao inhibitora hcv polimeraze |
| US7273859B2 (en) * | 2004-05-12 | 2007-09-25 | Bristol-Myers Squibb Company | HIV integrase inhibitors: cyclic pyrimidinone compounds |
| US7115601B2 (en) * | 2004-05-18 | 2006-10-03 | Bristol-Myers Squibb Company | HIV integrase inhibitors |
| US7192948B2 (en) * | 2004-05-28 | 2007-03-20 | Bristol-Myers Squibb Company | Bicyclic heterocycles as HIV integrase inhibitors |
| US7173022B2 (en) * | 2004-05-28 | 2007-02-06 | Bristol-Myers Squibb Company | Bicyclic heterocycles as HIV integrase inhibitors |
| US7176196B2 (en) * | 2004-05-28 | 2007-02-13 | Bristol-Myers Squibb Company | Bicyclic heterocycles as HIV integrase inhibitors |
| 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 |
| EP1807403A2 (en) | 2004-10-26 | 2007-07-18 | Istituto di Richerche di Biologia Molecolare P. Angeletti S.p.A. | Tetracyclic indole derivatives as antiviral agents |
| ZA200705872B (en) * | 2005-01-14 | 2008-09-25 | Genelabs Tecnologies Inc | Indole derivatives for treating viral infections |
| CN101146811B (zh) | 2005-03-31 | 2012-01-11 | P.安杰莱蒂分子生物学研究所 | Hiv整合酶抑制剂 |
| CA2607151C (en) | 2005-05-10 | 2012-06-19 | Merck & Co., Inc. | Hiv integrase inhibitors |
| CA2616314A1 (en) | 2005-07-27 | 2007-02-01 | Gilead Sciences, Inc. | Antiviral phosphonate conjugates for inhibition of hiv |
| US7494984B2 (en) * | 2005-08-31 | 2009-02-24 | Bristol-Myers Squibb Company | Substituted imidazo[1,2-a]pyrimidines as HIV viral DNA integrase inhibitors |
| 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 |
| US7897592B2 (en) * | 2005-11-15 | 2011-03-01 | Bristol-Myers Squibb Company | HIV integrase inhibitors |
| US7902182B2 (en) * | 2005-11-16 | 2011-03-08 | Bristol-Myers Squibb Company | HIV integrase inhibitors |
| US8039458B2 (en) | 2005-11-17 | 2011-10-18 | Bristol-Myers Squibb Company | HIV integrase inhibitors |
| US20070129379A1 (en) * | 2005-12-01 | 2007-06-07 | Bristol-Myers Squibb Company | Hiv integrase 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 |
| US7521443B2 (en) * | 2006-05-17 | 2009-04-21 | Bristol-Myers Squibb Company | Cyclopropyl fused indolobenzazepine HCV NS5B inhibitors |
| 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 |
| WO2007140200A2 (en) * | 2006-05-25 | 2007-12-06 | Bristol-Myers Squibb Company | Cyclopropyl fused indolobenzazepine hcv ns5b inhibitors |
| JP5205370B2 (ja) * | 2006-05-25 | 2013-06-05 | 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ゾアゼピンhcvns5b阻害剤 |
| US7897593B2 (en) * | 2006-05-30 | 2011-03-01 | Bristol-Myers Squibb Company | HIV integrase inhibitors |
| US7452876B2 (en) | 2006-06-08 | 2008-11-18 | Bristol-Myers Squibb Company | Cyclopropyl fused indolobenzazepine HCV NS5B inhibitors |
| US7893055B2 (en) * | 2006-06-28 | 2011-02-22 | Bristol-Myers Squibb Company | HIV integrase inhibitors |
| US7541351B2 (en) * | 2007-01-11 | 2009-06-02 | Bristol-Myers Squibb Company | Compounds for the treatment of hepatitis C |
| US7541352B2 (en) | 2007-02-02 | 2009-06-02 | Bristol-Myers Squibb Company | Compounds for the treatment of hepatitis C |
| US7517872B2 (en) * | 2007-02-22 | 2009-04-14 | Bristol-Myers Squibb Company | Compounds for the treatment of hepatitis C |
| US7998951B2 (en) * | 2007-03-05 | 2011-08-16 | Bristol-Myers Squibb Company | HCV NS5B inhibitors |
| US7547690B2 (en) * | 2007-03-14 | 2009-06-16 | Bristol-Myers Squibb Company | Compounds for the treatment of Hepatitis C |
| US7538102B2 (en) * | 2007-03-14 | 2009-05-26 | Bristol-Myers Squibb Company | Compounds for the treatment of Hepatitis C |
| US7538103B2 (en) * | 2007-03-15 | 2009-05-26 | Bristol-Myers Squibb Company | Compounds for the treatment of hepatitis C |
| US20090018163A1 (en) * | 2007-07-11 | 2009-01-15 | Bristol-Myers Squibb Company | Substituted Heterocyclic Ethers and Their Use in CNS Disorders |
| US7642251B2 (en) * | 2007-08-09 | 2010-01-05 | 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 |
| US8129367B2 (en) * | 2007-11-21 | 2012-03-06 | Bristol-Myers Squibb Company | Compounds for the treatment of Hepatitis C |
| US8129398B2 (en) * | 2008-03-19 | 2012-03-06 | Bristol-Myers Squibb Company | HIV integrase inhibitors |
| JP2011515486A (ja) | 2008-03-27 | 2011-05-19 | ブリストル−マイヤーズ スクイブ カンパニー | C型肝炎の治療用化合物 |
-
2010
- 2010-02-23 US US12/710,527 patent/US8143244B2/en active Active
- 2010-02-24 CN CN2010800184448A patent/CN102414212A/zh active Pending
- 2010-02-24 WO PCT/US2010/025169 patent/WO2010099159A1/en not_active Ceased
- 2010-02-24 EP EP10722809.0A patent/EP2401280B1/en not_active Not-in-force
- 2010-02-24 JP JP2011552097A patent/JP2012519173A/ja active Pending
Patent Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2008112841A1 (en) * | 2007-03-14 | 2008-09-18 | Bristol-Myers Squibb Company | Compounds for the treatment of hepatitis c |
| WO2008112848A1 (en) * | 2007-03-14 | 2008-09-18 | Bristol-Myers Squibb Company | Compounds for the treatment of hepatitis c |
Also Published As
| Publication number | Publication date |
|---|---|
| EP2401280A1 (en) | 2012-01-04 |
| US8143244B2 (en) | 2012-03-27 |
| CN102414212A (zh) | 2012-04-11 |
| US20100216774A1 (en) | 2010-08-26 |
| EP2401280B1 (en) | 2013-05-01 |
| WO2010099159A1 (en) | 2010-09-02 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| CN101490054B (zh) | 环丙基稠合的吲哚并苯并氮杂*hcv ns5b抑制剂 | |
| JP5343011B2 (ja) | C型肝炎の治療のための化合物 | |
| KR101417145B1 (ko) | 시클로프로필 융합된 인돌로벤즈아제핀 hcv ns5b 억제제 | |
| US7521441B2 (en) | Cyclopropyl fused indolobenzazepine HCV NS5B inhibitors | |
| JP5306230B2 (ja) | C型肝炎の治療用化合物 | |
| JP5301473B2 (ja) | C型肝炎の治療のための化合物 | |
| JP5232178B2 (ja) | C型肝炎の治療のための化合物 | |
| JP5209647B2 (ja) | C型肝炎の治療のための化合物 | |
| JP5416710B2 (ja) | シクロプロピル縮合インドロベンズアゼピンhcvns5b阻害剤 | |
| JP2012519173A (ja) | シクロプロピル縮合インドロベンズアゼピンhcvns5b阻害剤 | |
| JP5306366B2 (ja) | C型肝炎治療のための化合物 | |
| WO2007140200A2 (en) | Cyclopropyl fused indolobenzazepine hcv ns5b inhibitors | |
| JP2010521483A (ja) | 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 | |
| JP2011504178A (ja) | C型肝炎治療のための化合物 | |
| CN101646674B (zh) | 用于治疗丙型肝炎的吲哚并苯并氮杂*衍生物 | |
| CN101981038B (zh) | 二氧戊环和二氧戊环酮稠合的吲哚并苯并二氮杂*hcv ns5b抑制剂 |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20130125 |
|
| A621 | Written request for application examination |
Free format text: JAPANESE INTERMEDIATE CODE: A621 Effective date: 20130125 |
|
| A131 | Notification of reasons for refusal |
Free format text: JAPANESE INTERMEDIATE CODE: A131 Effective date: 20140408 |
|
| A02 | Decision of refusal |
Free format text: JAPANESE INTERMEDIATE CODE: A02 Effective date: 20140909 |