JP5731004B2 - C型肝炎ウイルスの阻害剤 - Google Patents

C型肝炎ウイルスの阻害剤 Download PDF

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JP5731004B2
JP5731004B2 JP2013536688A JP2013536688A JP5731004B2 JP 5731004 B2 JP5731004 B2 JP 5731004B2 JP 2013536688 A JP2013536688 A JP 2013536688A JP 2013536688 A JP2013536688 A JP 2013536688A JP 5731004 B2 JP5731004 B2 JP 5731004B2
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JP2014500861A (ja
JP2014500861A5 (enExample
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ゾン,ミン
リ,レピング
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プレシディオ ファーマシューティカルズ インコーポレイテッド
プレシディオ ファーマシューティカルズ インコーポレイテッド
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    • C07ORGANIC CHEMISTRY
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    • C07D491/00Heterocyclic 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
    • C07D491/02Heterocyclic 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 two hetero rings
    • C07D491/04Ortho-condensed systems
    • C07D491/044Ortho-condensed systems with only one oxygen atom as ring hetero atom in the oxygen-containing ring
    • C07D491/048Ortho-condensed systems with only one oxygen atom as ring hetero atom in the oxygen-containing ring the oxygen-containing ring being five-membered
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    • C07D491/02Heterocyclic 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 two hetero rings
    • C07D491/04Ortho-condensed systems
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    • A61K31/33Heterocyclic compounds
    • A61K31/335Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin
    • A61K31/34Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having five-membered rings with one oxygen as the only ring hetero atom, e.g. isosorbide
    • A61K31/343Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having five-membered rings with one oxygen as the only ring hetero atom, e.g. isosorbide condensed with a carbocyclic ring, e.g. coumaran, bufuralol, befunolol, clobenfurol, amiodarone
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    • A61K31/407Heterocyclic 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 condensed with other heterocyclic ring systems, e.g. ketorolac, physostigmine
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    • A61K31/4353Heterocyclic 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 ortho- or peri-condensed with heterocyclic ring systems
    • A61K31/4355Heterocyclic 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 ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system containing a five-membered ring having oxygen as a ring hetero atom
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    • A61K31/4353Heterocyclic 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 ortho- or peri-condensed with heterocyclic ring systems
    • A61K31/437Heterocyclic 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 ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system containing a five-membered ring having nitrogen as a ring hetero atom, e.g. indolizine, beta-carboline
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    • A61K31/47Quinolines; Isoquinolines
    • A61K31/4738Quinolines; Isoquinolines ortho- or peri-condensed with heterocyclic ring systems
    • A61K31/4741Quinolines; Isoquinolines ortho- or peri-condensed with heterocyclic ring systems condensed with ring systems having oxygen as a ring hetero atom, e.g. tubocuraran derivatives, noscapine, bicuculline
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    • A61K31/55Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole
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    • A61K31/55Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole
    • A61K31/551Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole having two nitrogen atoms, e.g. dilazep
    • A61K31/55131,4-Benzodiazepines, e.g. diazepam or clozapine
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    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/55Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole
    • A61K31/553Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole having at least one nitrogen and one oxygen as ring hetero atoms, e.g. loxapine, staurosporine
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    • A61K31/7052Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides
    • A61K31/7056Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides containing five-membered rings with nitrogen as a ring hetero atom
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    • C07D307/78Benzo [b] furans; Hydrogenated benzo [b] furans
    • C07D307/82Benzo [b] furans; Hydrogenated benzo [b] furans with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to carbon atoms of the hetero ring
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    • C07D471/02Heterocyclic 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
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    • C07D471/12Heterocyclic 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 three hetero rings
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  • Communicable Diseases (AREA)
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  • Immunology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Micro-Organisms Or Cultivation Processes Thereof (AREA)
  • Measuring Or Testing Involving Enzymes Or Micro-Organisms (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
JP2013536688A 2010-10-26 2011-10-21 C型肝炎ウイルスの阻害剤 Expired - Fee Related JP5731004B2 (ja)

Applications Claiming Priority (7)

Application Number Priority Date Filing Date Title
US40697210P 2010-10-26 2010-10-26
US61/406,972 2010-10-26
US201161438429P 2011-02-01 2011-02-01
US61/438,429 2011-02-01
US201161524220P 2011-08-16 2011-08-16
US61/524,220 2011-08-16
PCT/US2011/057398 WO2012058125A1 (en) 2010-10-26 2011-10-21 Inhibitors of hepatitis c virus

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JP2014500861A JP2014500861A (ja) 2014-01-16
JP2014500861A5 JP2014500861A5 (enExample) 2014-12-11
JP5731004B2 true JP5731004B2 (ja) 2015-06-10

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JP2013536688A Expired - Fee Related JP5731004B2 (ja) 2010-10-26 2011-10-21 C型肝炎ウイルスの阻害剤

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US (4) US20130302282A1 (enExample)
EP (1) EP2632261B1 (enExample)
JP (1) JP5731004B2 (enExample)
KR (1) KR101594166B1 (enExample)
CN (1) CN103269586B (enExample)
AR (1) AR083565A1 (enExample)
AU (1) AU2011320696B2 (enExample)
BR (1) BR112013009789A2 (enExample)
CA (1) CA2815537A1 (enExample)
CL (1) CL2013001141A1 (enExample)
CO (1) CO6700883A2 (enExample)
EA (1) EA025151B1 (enExample)
IL (1) IL225853A0 (enExample)
MX (1) MX2013004655A (enExample)
NZ (1) NZ609564A (enExample)
PE (1) PE20140109A1 (enExample)
PH (1) PH12013500770A1 (enExample)
SG (1) SG189985A1 (enExample)
TW (1) TWI486348B (enExample)
WO (1) WO2012058125A1 (enExample)
ZA (1) ZA201303752B (enExample)

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JP2012533569A (ja) 2009-07-16 2012-12-27 ヴァーテックス ファーマシューティカルズ、 インコーポレイテッド フラビウイルス感染症を治療又は予防するためのベンゾイミダゾール類似体
MX344373B (es) * 2010-01-27 2016-12-13 Ab Pharma Ltd * Compuestos policiclicos heterociclicos se puede utilizar como inhibidores eficaces para virus de la hepatitis c.
JP2013522375A (ja) 2010-03-24 2013-06-13 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 フラビウイルス感染を処置または予防するためのアナログ
JP5731004B2 (ja) 2010-10-26 2015-06-10 プレシディオ ファーマシューティカルズ インコーポレイテッド C型肝炎ウイルスの阻害剤
SG2014011670A (en) * 2011-10-21 2014-10-30 Abbvie Inc Combination treatment (eg. with abt-072 or abt -333) of daas for use in treating hcv
WO2013163466A1 (en) * 2012-04-25 2013-10-31 Presidio Pharmaceuticals, Inc. Inhibitors of hepatitis c virus
JP2016505011A (ja) 2013-01-10 2016-02-18 ブリストル−マイヤーズ スクイブ カンパニーBristol−Myers Squibb Company C型肝炎の治療用の大環状ベンゾフランおよびアザベンゾフラン化合物
US9914739B2 (en) 2014-03-21 2018-03-13 Bristol-Myers Squibb Company 6H-furo[2,3-E]indole compounds for the treatment of hepatitis C
US9920036B2 (en) * 2014-03-21 2018-03-20 Bristol-Myers Squibb Company Cyanoamino (aza)benzofuran compounds for the treatment of hepatitis C
PE20161224A1 (es) 2014-03-21 2016-11-12 Bristol Myers Squibb Co Compuestos de azabenzofurano que contienen ciano para el tratamiento de la hepatitis c
EP3145932B1 (en) 2014-05-21 2018-08-15 Bristol-Myers Squibb Company 2-(aryl- or heteroaryl-)phenyl (aza)benzofuran compounds for the treatment of hepatitis c
WO2015191653A1 (en) 2014-06-11 2015-12-17 Bristol-Myers Squibb Company Substituted 2-phenyl (aza)benzofuran compounds for the treatment of hepatitis c
US9957278B2 (en) 2014-08-05 2018-05-01 Bristol-Myers Squibb Company Furopyridine compounds for the treatment of hepatitis C
WO2016054299A1 (en) 2014-10-02 2016-04-07 Bristol-Myers Squibb Company Macrocyclic benzofuran compounds for the treatment of hepatitis c
US10570108B2 (en) 2015-02-19 2020-02-25 Bristol-Myers Squibb Company Substituted benzofuran compounds for the treatment of hepatitis C
WO2016133948A1 (en) 2015-02-19 2016-08-25 Bristol-Myers Squibb Company Benzofuran compounds for the treatment of hepatitis c
WO2016133970A1 (en) 2015-02-19 2016-08-25 Bristol-Myers Squibb Company Benzofurans substituted with primary benzamide as hcv inhibitors
US10125137B2 (en) 2015-02-19 2018-11-13 Bristol-Myers Squibb Company Benzofurans substituted with bicyclic secondary benzamide as HCV inhibitors
WO2016133963A1 (en) 2015-02-19 2016-08-25 Bristol-Myers Squibb Company Benzofurans substituted with secondary benzamide as hcv inhibitors
US11831699B2 (en) * 2016-09-08 2023-11-28 Harmonic, Inc. Using web-based protocols to assist graphic presentations when providing digital video
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US9085587B2 (en) 2015-07-21
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