MX2011000276A - Derivados de indol macrociclicos utiles como inhibidores del virus de la hepatitis c. - Google Patents

Derivados de indol macrociclicos utiles como inhibidores del virus de la hepatitis c.

Info

Publication number
MX2011000276A
MX2011000276A MX2011000276A MX2011000276A MX2011000276A MX 2011000276 A MX2011000276 A MX 2011000276A MX 2011000276 A MX2011000276 A MX 2011000276A MX 2011000276 A MX2011000276 A MX 2011000276A MX 2011000276 A MX2011000276 A MX 2011000276A
Authority
MX
Mexico
Prior art keywords
compound
compounds
formula
hcv
methyl
Prior art date
Application number
MX2011000276A
Other languages
English (en)
Spanish (es)
Inventor
Abdellah Tahri
Pierre Jean-Marie Bernard Raboisson
Katie Ingrid Eduard Amssoms
Sandrine Marie Helene Vendeville
Tse-I Lin
Original Assignee
Tibotec Pharm Ltd
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Tibotec Pharm Ltd filed Critical Tibotec Pharm Ltd
Publication of MX2011000276A publication Critical patent/MX2011000276A/es

Links

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • 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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D513/00Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00
    • C07D513/12Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00 in which the condensed system contains three hetero rings
    • C07D513/14Ortho-condensed systems
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K45/00Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
    • A61K45/06Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/12Antivirals
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/12Antivirals
    • A61P31/14Antivirals for RNA viruses
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/12Antivirals
    • A61P31/14Antivirals for RNA viruses
    • A61P31/18Antivirals for RNA viruses for HIV
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/12Antivirals
    • A61P31/20Antivirals for DNA viruses
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D513/00Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00
    • C07D513/12Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00 in which the condensed system contains three hetero rings
    • C07D513/18Bridged systems
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D513/00Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00
    • C07D513/22Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00 in which the condensed system contains four or more hetero rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D515/00Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen, oxygen, and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00
    • C07D515/12Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen, oxygen, and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00 in which the condensed system contains three hetero rings
    • C07D515/18Bridged systems

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • General Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Animal Behavior & Ethology (AREA)
  • Virology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Oncology (AREA)
  • Communicable Diseases (AREA)
  • Molecular Biology (AREA)
  • Epidemiology (AREA)
  • Engineering & Computer Science (AREA)
  • Tropical Medicine & Parasitology (AREA)
  • AIDS & HIV (AREA)
  • Biotechnology (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
  • Micro-Organisms Or Cultivation Processes Thereof (AREA)
MX2011000276A 2008-07-08 2009-07-08 Derivados de indol macrociclicos utiles como inhibidores del virus de la hepatitis c. MX2011000276A (es)

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
EP08159965 2008-07-08
EP08160254 2008-07-11
EP08161743 2008-08-04
PCT/EP2009/004942 WO2010003658A1 (en) 2008-07-08 2009-07-08 Macrocyclic indole derivatives useful as hepatitis c virus inhibitors

Publications (1)

Publication Number Publication Date
MX2011000276A true MX2011000276A (es) 2011-03-02

Family

ID=40972916

Family Applications (1)

Application Number Title Priority Date Filing Date
MX2011000276A MX2011000276A (es) 2008-07-08 2009-07-08 Derivados de indol macrociclicos utiles como inhibidores del virus de la hepatitis c.

Country Status (32)

Country Link
US (2) US8921355B2 (US20070167479A1-20070719-C00034.png)
EP (1) EP2310396B1 (US20070167479A1-20070719-C00034.png)
JP (2) JP5426671B2 (US20070167479A1-20070719-C00034.png)
KR (1) KR101640374B1 (US20070167479A1-20070719-C00034.png)
CN (1) CN102089314B (US20070167479A1-20070719-C00034.png)
AP (1) AP2743A (US20070167479A1-20070719-C00034.png)
AR (1) AR072726A1 (US20070167479A1-20070719-C00034.png)
AU (1) AU2009267389B8 (US20070167479A1-20070719-C00034.png)
BR (1) BRPI0915887B8 (US20070167479A1-20070719-C00034.png)
CA (1) CA2729307C (US20070167479A1-20070719-C00034.png)
CL (1) CL2011000032A1 (US20070167479A1-20070719-C00034.png)
CO (1) CO6351793A2 (US20070167479A1-20070719-C00034.png)
CR (1) CR20110076A (US20070167479A1-20070719-C00034.png)
DK (1) DK2310396T3 (US20070167479A1-20070719-C00034.png)
EA (1) EA019008B1 (US20070167479A1-20070719-C00034.png)
EC (1) ECSP11010750A (US20070167479A1-20070719-C00034.png)
ES (1) ES2651038T3 (US20070167479A1-20070719-C00034.png)
HK (1) HK1155734A1 (US20070167479A1-20070719-C00034.png)
HN (1) HN2011000072A (US20070167479A1-20070719-C00034.png)
HR (1) HRP20171892T1 (US20070167479A1-20070719-C00034.png)
HU (1) HUE035244T2 (US20070167479A1-20070719-C00034.png)
IL (1) IL210086A (US20070167479A1-20070719-C00034.png)
LT (1) LT2310396T (US20070167479A1-20070719-C00034.png)
MX (1) MX2011000276A (US20070167479A1-20070719-C00034.png)
NI (1) NI201100010A (US20070167479A1-20070719-C00034.png)
NO (1) NO2310396T3 (US20070167479A1-20070719-C00034.png)
NZ (2) NZ603343A (US20070167479A1-20070719-C00034.png)
SI (1) SI2310396T1 (US20070167479A1-20070719-C00034.png)
SV (1) SV2011003796A (US20070167479A1-20070719-C00034.png)
TW (1) TWI454476B (US20070167479A1-20070719-C00034.png)
UY (1) UY31973A (US20070167479A1-20070719-C00034.png)
WO (1) WO2010003658A1 (US20070167479A1-20070719-C00034.png)

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BRPI0821836A2 (pt) 2007-12-24 2015-06-16 Tibotec Pharm Ltd Indóis macrocíclicos como inibidores do vírus da hepatite c
TWI454476B (zh) * 2008-07-08 2014-10-01 Tibotec Pharm Ltd 用作c型肝炎病毒抑制劑之巨環吲哚衍生物
UA108211C2 (uk) * 2009-11-04 2015-04-10 Янссен Рід Айрленд Бензімідазолімідазольні похідні
CN102844028B (zh) * 2010-04-13 2016-04-06 杨森制药公司 Hcv大环抑制剂、非核苷和核苷的组合
EP2585438B1 (en) * 2010-06-24 2014-08-20 Janssen R&D Ireland PREPARATION OF 13-CYCLOHEXYL-3-METHOXY-6-[METHYL-(2-{2-[METHYL-(SULPHAMOYL)-AMINO]-ETHOXY}-ETHYL)-CARBAMOYL]-7H-INDOLO-[2,1-a]-[2]-BENZAZEPINE-10-CARBOXYLIC ACID
EP2760821B1 (en) 2011-09-02 2017-10-11 Novartis AG Choline salt of an anti-inflammatory substituted cyclobutenedione compound
US8716275B2 (en) * 2011-10-20 2014-05-06 Bristol-Myers Squibb Company Compound for the treatment of hepatitis C
RU2015111491A (ru) 2012-08-31 2016-10-20 Янссен Фармасьютикалз, Инк. Комбинация макроциклического ингибитора протеазы hcv, ненуклеозидного ингибитора hcv и ритонавира
WO2014152275A1 (en) * 2013-03-14 2014-09-25 Concert Pharmaceuticals, Inc. Deuterium modified derivatives of the ns5b polymerase inhibitor tmc647055
US10450263B2 (en) 2017-02-10 2019-10-22 Southern Research Institute Benzo annulenes as antiviral agents
KR101974388B1 (ko) 2017-06-23 2019-05-02 (주)에니켐텍 알킬 디에틸렌 트리아민 유도체 및 이의 제조방법
US11066357B2 (en) 2017-12-26 2021-07-20 Southern Research Institute Benzoannulene derivatives as antiviral agents
US12060148B2 (en) 2022-08-16 2024-08-13 Honeywell International Inc. Ground resonance detection and warning system and method

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US20050267836A1 (en) * 1996-03-25 2005-12-01 Cfph, Llc Method and system for transacting with a trading application
NZ332405A (en) 1996-04-23 2000-06-23 Vertex Pharma oxazolyl, thiazolyl or phenyl urea derivatives as inhibitors of inosine monophosphate dehydrogenase enzyme
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PE20070211A1 (es) 2005-07-29 2007-05-12 Medivir Ab Compuestos macrociclicos como inhibidores del virus de hepatitis c
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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
TWI454476B (zh) * 2008-07-08 2014-10-01 Tibotec Pharm Ltd 用作c型肝炎病毒抑制劑之巨環吲哚衍生物
TW201023858A (en) 2008-09-18 2010-07-01 Ortho Mcneil Janssen Pharm Synergistic combinations of a macrocyclic inhibitor of HCV and a nucleoside
HUE031738T2 (en) 2009-02-27 2017-07-28 Janssen Pharmaceuticals Inc Amorphous salts of the HCV macrocyclic inhibitor
CN102844028B (zh) 2010-04-13 2016-04-06 杨森制药公司 Hcv大环抑制剂、非核苷和核苷的组合
EP2585438B1 (en) 2010-06-24 2014-08-20 Janssen R&D Ireland PREPARATION OF 13-CYCLOHEXYL-3-METHOXY-6-[METHYL-(2-{2-[METHYL-(SULPHAMOYL)-AMINO]-ETHOXY}-ETHYL)-CARBAMOYL]-7H-INDOLO-[2,1-a]-[2]-BENZAZEPINE-10-CARBOXYLIC ACID
RU2015111491A (ru) 2012-08-31 2016-10-20 Янссен Фармасьютикалз, Инк. Комбинация макроциклического ингибитора протеазы hcv, ненуклеозидного ингибитора hcv и ритонавира

Also Published As

Publication number Publication date
HN2011000072A (es) 2013-09-01
TWI454476B (zh) 2014-10-01
CN102089314B (zh) 2014-07-23
US8921355B2 (en) 2014-12-30
HRP20171892T1 (hr) 2018-01-12
ECSP11010750A (es) 2011-08-31
IL210086A0 (en) 2011-02-28
EP2310396B1 (en) 2017-09-06
US9427440B2 (en) 2016-08-30
UY31973A (es) 2010-01-29
EP2310396A1 (en) 2011-04-20
CA2729307A1 (en) 2010-01-14
TW201014865A (en) 2010-04-16
US20110105473A1 (en) 2011-05-05
NZ590073A (en) 2012-11-30
DK2310396T3 (en) 2017-12-11
NO2310396T3 (US20070167479A1-20070719-C00034.png) 2018-02-03
JP5426671B2 (ja) 2014-02-26
SI2310396T1 (en) 2018-01-31
AP2743A (en) 2013-09-30
BRPI0915887A2 (pt) 2015-11-03
CL2011000032A1 (es) 2011-07-15
LT2310396T (lt) 2017-12-27
JP2014028818A (ja) 2014-02-13
BRPI0915887B8 (pt) 2021-05-25
NZ603343A (en) 2013-08-30
KR101640374B1 (ko) 2016-07-18
EA201170153A1 (ru) 2011-08-30
EA019008B1 (ru) 2013-12-30
NI201100010A (es) 2011-09-07
AP2010005521A0 (en) 2010-12-31
SV2011003796A (es) 2011-04-08
ES2651038T3 (es) 2018-01-23
AR072726A1 (es) 2010-09-15
AU2009267389B2 (en) 2013-05-30
CO6351793A2 (es) 2011-12-20
IL210086A (en) 2014-05-28
US20140107101A1 (en) 2014-04-17
KR20110040889A (ko) 2011-04-20
AU2009267389B8 (en) 2013-07-04
BRPI0915887B1 (pt) 2020-02-18
WO2010003658A1 (en) 2010-01-14
CA2729307C (en) 2017-08-29
HK1155734A1 (en) 2012-05-25
CR20110076A (es) 2011-11-10
HUE035244T2 (hu) 2018-05-02
JP5808370B2 (ja) 2015-11-10
JP2011527299A (ja) 2011-10-27
AU2009267389A8 (en) 2013-07-04
AU2009267389A1 (en) 2010-01-14
CN102089314A (zh) 2011-06-08

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