CN102414212A - 与环丙基稠合的吲哚并苯并氮杂*hcv ns5b抑制剂 - Google Patents
与环丙基稠合的吲哚并苯并氮杂*hcv ns5b抑制剂 Download PDFInfo
- Publication number
- CN102414212A CN102414212A CN2010800184448A CN201080018444A CN102414212A CN 102414212 A CN102414212 A CN 102414212A CN 2010800184448 A CN2010800184448 A CN 2010800184448A CN 201080018444 A CN201080018444 A CN 201080018444A CN 102414212 A CN102414212 A CN 102414212A
- Authority
- CN
- China
- Prior art keywords
- mmol
- cyclohexyl
- methoxy
- indolo
- carbonyl
- 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 10
- QWTZZAXPBKTYBQ-CABZTGNLSA-N COc(cc1)cc([C@H](C2)[C@]2(CO)C(O)=O)c1Br Chemical compound COc(cc1)cc([C@H](C2)[C@]2(CO)C(O)=O)c1Br QWTZZAXPBKTYBQ-CABZTGNLSA-N 0.000 description 2
- RRQITIHUHYCCJW-UHFFFAOYSA-N Bc(cc1)c(C=C)cc1OC Chemical compound Bc(cc1)c(C=C)cc1OC RRQITIHUHYCCJW-UHFFFAOYSA-N 0.000 description 1
- PJNPCKSPJXQBHH-UHFFFAOYSA-N CC(C)N(C)S(N)(=O)=O Chemical compound CC(C)N(C)S(N)(=O)=O PJNPCKSPJXQBHH-UHFFFAOYSA-N 0.000 description 1
- YWLMVVJLDHVRGZ-MIWMFXFDSA-N CC(C)S(NC(c1ccc(c(C2CCCCC2)c(-c(cc2)c([C@@H]3C4)cc2OC)[n]2C[C@]34C(N(C3)CC(C)(C4)C3(C)CN4C(OC)=O)=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(N(C3)CC(C)(C4)C3(C)CN4C(OC)=O)=O)c2c1)=O)(=O)=O YWLMVVJLDHVRGZ-MIWMFXFDSA-N 0.000 description 1
- KKWNNKQYKAGZDB-UHFFFAOYSA-N CCCC(CC)c1c(-c(cc2)c(CC(C3)C(N4CC(CN(C)C5)(CN(C)C6)C56C4)=O)cc2OC)[n]3c2cc(C(NS(N(C)C)(=O)=O)=O)ccc12 Chemical compound CCCC(CC)c1c(-c(cc2)c(CC(C3)C(N4CC(CN(C)C5)(CN(C)C6)C56C4)=O)cc2OC)[n]3c2cc(C(NS(N(C)C)(=O)=O)=O)ccc12 KKWNNKQYKAGZDB-UHFFFAOYSA-N 0.000 description 1
- UVKDKNDVWUAHIF-XKDCNZLGSA-N CCCC(CCC)c1c(-c(cc2)c(C(C3)C3(C3)C(N[C@@H]4C(CC5)C(C)(C)C5(C)C4)=O)cc2OC)[n]3c2cc(C(NS(N(C)C)(=O)=O)=O)ccc12 Chemical compound CCCC(CCC)c1c(-c(cc2)c(C(C3)C3(C3)C(N[C@@H]4C(CC5)C(C)(C)C5(C)C4)=O)cc2OC)[n]3c2cc(C(NS(N(C)C)(=O)=O)=O)ccc12 UVKDKNDVWUAHIF-XKDCNZLGSA-N 0.000 description 1
- NSVGSFIKEXKUAM-MIWMFXFDSA-N CN(C)C(N1CC(CC2)(CN(C3)C([C@@](C4)(C[n]5c6c7)[C@@H]4c(cc(cc4)OC)c4-c5c(C4CCCCC4)c6ccc7C(NS(N(C)C)(=O)=O)=O)=O)C23C1)=O Chemical compound CN(C)C(N1CC(CC2)(CN(C3)C([C@@](C4)(C[n]5c6c7)[C@@H]4c(cc(cc4)OC)c4-c5c(C4CCCCC4)c6ccc7C(NS(N(C)C)(=O)=O)=O)=O)C23C1)=O NSVGSFIKEXKUAM-MIWMFXFDSA-N 0.000 description 1
- IZPUCLUAOJYRDR-UHFFFAOYSA-N CN(C)S(NC(c1ccc(c(C2CCCCC2)c(-c(cc2)c(C3C4)cc2OC)[n]2CC34C(O)=O)c2c1)=O)(=O)=O Chemical compound CN(C)S(NC(c1ccc(c(C2CCCCC2)c(-c(cc2)c(C3C4)cc2OC)[n]2CC34C(O)=O)c2c1)=O)(=O)=O IZPUCLUAOJYRDR-UHFFFAOYSA-N 0.000 description 1
- XKEROFYDQBTACD-JJNMFGATSA-N CN(C)S(NC(c1ccc(c(C2CCCCC2)c(-c(cc2)c([C@@H]3C4)cc2OC)[n]2C[C@]34C(N(C3)CC4(CN(CC(F)(F)F)C5)C35COC4)=O)c2c1)=O)(=O)=O Chemical compound CN(C)S(NC(c1ccc(c(C2CCCCC2)c(-c(cc2)c([C@@H]3C4)cc2OC)[n]2C[C@]34C(N(C3)CC4(CN(CC(F)(F)F)C5)C35COC4)=O)c2c1)=O)(=O)=O XKEROFYDQBTACD-JJNMFGATSA-N 0.000 description 1
- VROIPRWOKWXWHZ-JJNMFGATSA-N CN(C)S(NC(c1ccc(c(C2CCCCC2)c(-c(cc2)c([C@@H]3C4)cc2OC)[n]2C[C@]34C(N3CC(CC4)(CN(CC(F)(F)F)C5)C45C3)=O)c2c1)=O)(=O)=O Chemical compound CN(C)S(NC(c1ccc(c(C2CCCCC2)c(-c(cc2)c([C@@H]3C4)cc2OC)[n]2C[C@]34C(N3CC(CC4)(CN(CC(F)(F)F)C5)C45C3)=O)c2c1)=O)(=O)=O VROIPRWOKWXWHZ-JJNMFGATSA-N 0.000 description 1
- OSUUUKNLAJLMSQ-KYRSZARQSA-N COC(C(/C=C/c1ccccc1)=N)=O Chemical compound COC(C(/C=C/c1ccccc1)=N)=O OSUUUKNLAJLMSQ-KYRSZARQSA-N 0.000 description 1
- JOSGHYFFIDRFIE-DWWIYJRSSA-N COC([C@](C1)([C@@H]1c1cc(OC)ccc1Br)/C=C/c1ccccc1)=O Chemical compound COC([C@](C1)([C@@H]1c1cc(OC)ccc1Br)/C=C/c1ccccc1)=O JOSGHYFFIDRFIE-DWWIYJRSSA-N 0.000 description 1
- ZHWKEWKOYIOCAE-UHFFFAOYSA-N COc(cc1)cc(C=C(C[n]2c3c4)C(N(C5)CC6(CNC7)C57COC6)=O)c1-c2c(C1CCCCC1)c3ccc4C(NS(C1CC1)(=O)=O)=O Chemical compound COc(cc1)cc(C=C(C[n]2c3c4)C(N(C5)CC6(CNC7)C57COC6)=O)c1-c2c(C1CCCCC1)c3ccc4C(NS(C1CC1)(=O)=O)=O ZHWKEWKOYIOCAE-UHFFFAOYSA-N 0.000 description 1
- VYUVVDXLSGKNSV-LUFONEFESA-N C[C@H](/C(/C=C)=C/C)N Chemical compound C[C@H](/C(/C=C)=C/C)N VYUVVDXLSGKNSV-LUFONEFESA-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 (1)
| Publication Number | Publication Date |
|---|---|
| CN102414212A true CN102414212A (zh) | 2012-04-11 |
Family
ID=42289577
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN2010800184448A Pending CN102414212A (zh) | 2009-02-26 | 2010-02-24 | 与环丙基稠合的吲哚并苯并氮杂*hcv ns5b抑制剂 |
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 (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN101103026A (zh) * | 2005-01-14 | 2008-01-09 | 健亚生物科技公司 | 用于治疗病毒感染的吲哚衍生物 |
| WO2008097796A1 (en) * | 2007-02-02 | 2008-08-14 | Bristol-Myers Squibb Company | Indolobenzazepine derivatives for the treatment of hepatitis c |
| 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 |
| US20090042860A1 (en) * | 2007-08-09 | 2009-02-12 | Bristol-Myers Squibb Company | Compounds for the Treatment of Hepatitis C |
Family Cites Families (54)
| 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 |
| 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 |
| 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 |
| 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 (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN101103026A (zh) * | 2005-01-14 | 2008-01-09 | 健亚生物科技公司 | 用于治疗病毒感染的吲哚衍生物 |
| WO2008097796A1 (en) * | 2007-02-02 | 2008-08-14 | Bristol-Myers Squibb Company | Indolobenzazepine derivatives for the treatment of hepatitis c |
| 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 |
| US20090042860A1 (en) * | 2007-08-09 | 2009-02-12 | Bristol-Myers Squibb Company | Compounds for the Treatment of Hepatitis C |
Non-Patent Citations (1)
| Title |
|---|
| VINCENZO SUMMA,等: "Discovery of a,γ-Diketo Acids as Potent Selective and Reversible Inhibitors of Hepatitis C Virus NS5b RNA-Dependent RNA Polymerase", 《JOURNAL OF MEDICINAL CHEMISTRY》 * |
Also Published As
| Publication number | Publication date |
|---|---|
| JP2012519173A (ja) | 2012-08-23 |
| EP2401280A1 (en) | 2012-01-04 |
| US8143244B2 (en) | 2012-03-27 |
| US20100216774A1 (en) | 2010-08-26 |
| EP2401280B1 (en) | 2013-05-01 |
| WO2010099159A1 (en) | 2010-09-02 |
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