JP2011511089A5 - - Google Patents

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Publication number
JP2011511089A5
JP2011511089A5 JP2010545997A JP2010545997A JP2011511089A5 JP 2011511089 A5 JP2011511089 A5 JP 2011511089A5 JP 2010545997 A JP2010545997 A JP 2010545997A JP 2010545997 A JP2010545997 A JP 2010545997A JP 2011511089 A5 JP2011511089 A5 JP 2011511089A5
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JP
Japan
Prior art keywords
alkyl
amino
optionally substituted
halo
heteroaryl
Prior art date
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Application number
JP2010545997A
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English (en)
Japanese (ja)
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JP2011511089A (ja
JP5718647B2 (ja
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Publication date
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Priority claimed from PCT/US2009/033229 external-priority patent/WO2009100225A1/en
Publication of JP2011511089A publication Critical patent/JP2011511089A/ja
Publication of JP2011511089A5 publication Critical patent/JP2011511089A5/ja
Application granted granted Critical
Publication of JP5718647B2 publication Critical patent/JP5718647B2/ja
Active legal-status Critical Current
Anticipated expiration legal-status Critical

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JP2010545997A 2008-02-07 2009-02-05 カテプシンbの阻害剤 Active JP5718647B2 (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US2700708P 2008-02-07 2008-02-07
US61/027,007 2008-02-07
PCT/US2009/033229 WO2009100225A1 (en) 2008-02-07 2009-02-05 Inhibitors of cathepsin b

Related Child Applications (1)

Application Number Title Priority Date Filing Date
JP2014209108A Division JP2015051985A (ja) 2008-02-07 2014-10-10 カテプシンbの阻害剤

Publications (3)

Publication Number Publication Date
JP2011511089A JP2011511089A (ja) 2011-04-07
JP2011511089A5 true JP2011511089A5 (cg-RX-API-DMAC7.html) 2012-03-29
JP5718647B2 JP5718647B2 (ja) 2015-05-13

Family

ID=40939419

Family Applications (2)

Application Number Title Priority Date Filing Date
JP2010545997A Active JP5718647B2 (ja) 2008-02-07 2009-02-05 カテプシンbの阻害剤
JP2014209108A Withdrawn JP2015051985A (ja) 2008-02-07 2014-10-10 カテプシンbの阻害剤

Family Applications After (1)

Application Number Title Priority Date Filing Date
JP2014209108A Withdrawn JP2015051985A (ja) 2008-02-07 2014-10-10 カテプシンbの阻害剤

Country Status (9)

Country Link
US (1) US8211897B2 (cg-RX-API-DMAC7.html)
EP (1) EP2237793A4 (cg-RX-API-DMAC7.html)
JP (2) JP5718647B2 (cg-RX-API-DMAC7.html)
CN (1) CN101969973B (cg-RX-API-DMAC7.html)
BR (1) BRPI0907729A2 (cg-RX-API-DMAC7.html)
CA (1) CA2713108A1 (cg-RX-API-DMAC7.html)
EA (1) EA201001262A1 (cg-RX-API-DMAC7.html)
MX (1) MX2010008371A (cg-RX-API-DMAC7.html)
WO (1) WO2009100225A1 (cg-RX-API-DMAC7.html)

Families Citing this family (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7932277B2 (en) 2007-05-10 2011-04-26 Intermune, Inc. Peptide inhibitors of hepatitis C virus replication
EA201071034A1 (ru) 2008-04-15 2011-06-30 Интермьюн, Инк. Новые макроциклические ингибиторы репликаций вируса гепатита с
AR075584A1 (es) 2009-02-27 2011-04-20 Intermune Inc COMPOSICIONES TERAPEUTICAS QUE COMPRENDEN beta-D-2'-DESOXI-2'-FLUORO-2'-C-METILCITIDINA Y UN DERIVADO DE ACIDO ISOINDOL CARBOXILICO Y SUS USOS. COMPUESTO.
CN103946213A (zh) * 2011-11-25 2014-07-23 霍夫曼-拉罗奇有限公司 作为组织蛋白酶抑制剂的新吡咯烷衍生物
WO2014164844A1 (en) * 2013-03-11 2014-10-09 Virobay, Inc. Cathepsin inhibitors
BR112018012914B1 (pt) 2015-12-22 2023-04-18 SHY Therapeutics LLC Composto, uso de um composto e composição farmacêutica
KR102595723B1 (ko) 2016-06-21 2023-10-27 오리온 옵탈몰로지 엘엘씨 헤테로시클릭 프롤린아미드 유도체
WO2017222914A1 (en) 2016-06-21 2017-12-28 Inception 4, Inc. Carbocyclic prolinamide derivatives
JP2019526563A (ja) * 2016-08-23 2019-09-19 エフ.ホフマン−ラ ロシュ アーゲーF. Hoffmann−La Roche Aktiengesellschaft Htra1阻害剤としての新規ジフルオロケタミド誘導体
US10834908B2 (en) * 2017-04-26 2020-11-17 InfiCure Bio AB Model animal for fibrosis
AU2018288841B2 (en) 2017-06-21 2022-09-29 SHY Therapeutics LLC Compounds that interact with the Ras superfamily for the treatment of cancers, inflammatory diseases, Rasopathies, and fibrotic disease
CN111447940A (zh) * 2017-07-17 2020-07-24 科罗拉多大学评议会 预防或治疗由辐射或放射疗法引起的辐射诱发的旁观者效应的组合物和方法
WO2020132071A1 (en) 2018-12-19 2020-06-25 Shy Therapeutics. Llc Compounds that interact with the ras superfamily for the treatment of cancers, inflammatory diseases, rasopathies, and f1brotic disease

Family Cites Families (14)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
HRP20000286A2 (en) 1997-11-11 2000-12-31 Pfizer Prod Inc Thienopyrimidine and thienopyridine derivatives useful as anticancer agents
US6404397B1 (en) 1998-08-10 2002-06-11 Raytheon Company Compact all-weather electromagnetic imaging system
US6323180B1 (en) * 1998-08-10 2001-11-27 Boehringer Ingelheim (Canada) Ltd Hepatitis C inhibitor tri-peptides
US6608027B1 (en) 1999-04-06 2003-08-19 Boehringer Ingelheim (Canada) Ltd Macrocyclic peptides active against the hepatitis C virus
EP1254901A4 (en) * 2000-01-26 2003-03-05 Ono Pharmaceutical Co 5-CHAIN CYCLIC COMPOUNDS, CONTAINING NITROGEN, AND MEDICINAL PRODUCTS CONTAINING THE SAME AS ACTIVE INGREDIENTS
CA2369970A1 (en) 2002-02-01 2003-08-01 Boehringer Ingelheim (Canada) Ltd. Hepatitis c inhibitor tri-peptides
ATE500264T1 (de) 2003-09-22 2011-03-15 Boehringer Ingelheim Int Makrozyklische peptide mit wirkung gegen das hepatitis-c-virus
WO2006113942A2 (en) 2005-04-20 2006-10-26 Schering Corporation Method of inhibiting cathepsin activity
WO2006130552A2 (en) 2005-06-02 2006-12-07 Schering Corporation Methods of treating hepatitis c virus
US20060287248A1 (en) 2005-06-02 2006-12-21 Schering Corporation Asymmetric dosing methods
WO2006130554A2 (en) 2005-06-02 2006-12-07 Schering Corporation Methods of treating hepatitis c virus
US7608592B2 (en) * 2005-06-30 2009-10-27 Virobay, Inc. HCV inhibitors
RU2008152171A (ru) * 2006-07-05 2010-08-10 Интермьюн, Инк. (Us) Новые ингибиторы вирусной репликации гепатита с
US20080161254A1 (en) 2007-01-03 2008-07-03 Virobay, Inc. Hcv inhibitors

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