JP2014505032A5 - - Google Patents

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Publication number
JP2014505032A5
JP2014505032A5 JP2013543340A JP2013543340A JP2014505032A5 JP 2014505032 A5 JP2014505032 A5 JP 2014505032A5 JP 2013543340 A JP2013543340 A JP 2013543340A JP 2013543340 A JP2013543340 A JP 2013543340A JP 2014505032 A5 JP2014505032 A5 JP 2014505032A5
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JP
Japan
Prior art keywords
alkyl
cycloalkyl
haloalkyl
juvenile
compound according
Prior art date
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Granted
Application number
JP2013543340A
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English (en)
Japanese (ja)
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JP2014505032A (ja
JP6050242B2 (ja
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Publication date
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Priority claimed from PCT/US2011/063945 external-priority patent/WO2012078869A1/en
Publication of JP2014505032A publication Critical patent/JP2014505032A/ja
Publication of JP2014505032A5 publication Critical patent/JP2014505032A5/ja
Application granted granted Critical
Publication of JP6050242B2 publication Critical patent/JP6050242B2/ja
Expired - Fee Related legal-status Critical Current
Anticipated expiration legal-status Critical

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JP2013543340A 2010-12-08 2011-12-08 ピリドニルグアニジンf1f0−atpアーゼ阻害剤およびその治療的使用 Expired - Fee Related JP6050242B2 (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US42093410P 2010-12-08 2010-12-08
US61/420,934 2010-12-08
PCT/US2011/063945 WO2012078869A1 (en) 2010-12-08 2011-12-08 Pyridonyl guanidine f1f0-atpase inhibitors and therapeutic uses thereof

Publications (3)

Publication Number Publication Date
JP2014505032A JP2014505032A (ja) 2014-02-27
JP2014505032A5 true JP2014505032A5 (enExample) 2015-01-29
JP6050242B2 JP6050242B2 (ja) 2016-12-21

Family

ID=46207514

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2013543340A Expired - Fee Related JP6050242B2 (ja) 2010-12-08 2011-12-08 ピリドニルグアニジンf1f0−atpアーゼ阻害剤およびその治療的使用

Country Status (10)

Country Link
US (2) US9000014B2 (enExample)
EP (1) EP2648710B1 (enExample)
JP (1) JP6050242B2 (enExample)
CN (1) CN103458886B (enExample)
AU (1) AU2011338304B2 (enExample)
CA (1) CA2820044A1 (enExample)
ES (1) ES2591156T3 (enExample)
IL (1) IL226790A (enExample)
MX (1) MX2013006398A (enExample)
WO (1) WO2012078869A1 (enExample)

Families Citing this family (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US9169199B2 (en) 2010-12-08 2015-10-27 Lycera Corporation Cycloalkyl guanidine F1F0-ATPase inhibitors and therapeutic uses thereof
HRP20171280T1 (hr) 2010-12-08 2018-01-12 Lycera Corporation Pirazolilgvanidinski inhibitori f1f0-atpaze i njihova upotreba u terapiji
WO2012078869A1 (en) 2010-12-08 2012-06-14 Lycera Corporation Pyridonyl guanidine f1f0-atpase inhibitors and therapeutic uses thereof
WO2013185046A1 (en) 2012-06-08 2013-12-12 Lycera Corporation Saturated acyl guanid1ne for inhibition of f1f0-atpase
US9221814B2 (en) 2012-06-08 2015-12-29 Lycera Corporation Heterocyclic guanidine F1F0-atpase inhibitors and therapeutic uses thereof
EP2866796A4 (en) 2012-06-08 2015-11-25 Lycera Corp PYRAZOLYL GUANIDINE F1FO ATPASE HEMMER AND THERAPEUTIC USES THEREOF
MX2016007445A (es) 2013-12-10 2016-09-09 Lycera Corp Inhibidores de f1f0-atpasa de trifluorometil pirazolil guanidina y usos terapeuticos de los mismos.
AU2014363958B2 (en) 2013-12-10 2018-11-08 Lycera Corporation Alkylpyrazolyl guanidine F1F0-ATPase inhibitors and therapeutic uses thereof
CA2931792A1 (en) 2013-12-10 2015-06-18 Lycera Corporation N-substituted pyrazolyl guanidine f1f0-atpase inhibitors and therapeutic uses thereof
US9553382B2 (en) * 2014-06-27 2017-01-24 Xiaomi Inc. Headphone socket assembly and electronic equipment including same

Family Cites Families (30)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4977189A (en) 1986-05-07 1990-12-11 American Cyanamid Company Substituted guanidinedicarbonyl derivatives
JPH07188197A (ja) 1993-11-17 1995-07-25 Fujisawa Pharmaceut Co Ltd オキサゾール誘導体
DE4344550A1 (de) 1993-12-24 1995-06-29 Hoechst Ag Substituierte 1-Oxo-1,2-dihydro-isochinolinoyl- und 1,1-Dioxo-2H-1,2-benzothiazinoylguanidine, Verfahrenzu ihrer Herstellung, ihre Verwendung als Medikamentt oder Diagnostikum sowie sie enthaltendes Medikamen
US7041702B1 (en) 1997-10-21 2006-05-09 Scion Pharmaceuticals, Inc. Pharmaceutically active compounds and methods of use
AU760174B2 (en) 1999-02-09 2003-05-08 Bristol-Myers Squibb Company Lactam inhibitors of FXa and method
US7276348B2 (en) 1999-04-30 2007-10-02 Regents Of The University Of Michigan Compositions and methods relating to F1F0-ATPase inhibitors and targets thereof
KR20020012310A (ko) 1999-07-15 2002-02-15 다께우찌 마사야쓰 복소 방향환 화합물
BR0111878A (pt) 2000-06-30 2005-05-24 Bristol Myers Squibb Co N-ureido-(heterociclo-alquil)-piperidinas como moduladores da atividade de receptores de quimiocinas
AU2002357137A1 (en) * 2001-12-10 2003-06-23 Bristol-Myers Squibb Company (1-phenyl-2-heteroaryl)ethyl-guanidine compounds as inhibitors of mitochondrial f1f0 atp hydrolase
GB0208224D0 (en) 2002-04-10 2002-05-22 Celltech R&D Ltd Chemical compounds
AU2003276648A1 (en) 2002-06-17 2003-12-31 Bristol-Myers Squibb Company Benzodiazepine inhibitors of mitochondial f¿1?f¿0? atp hydrolase and methods of inhibiting f¿1?f¿0? atp hydrolase
WO2004043362A2 (en) 2002-11-06 2004-05-27 Bristol-Myers Squibb Company Acyl guanidine compounds and use thereof
EP1590338B1 (en) 2002-12-04 2009-08-26 Ore Pharmaceuticals Inc. Modulators of melanocortin receptor
DE102004008141A1 (de) 2004-02-19 2005-09-01 Abbott Gmbh & Co. Kg Guanidinverbindungen und ihre Verwendung als Bindungspartner für 5-HT5-Rezeptoren
US20050272723A1 (en) 2004-04-27 2005-12-08 The Regents Of The University Of Michigan Methods and compositions for treating diseases and conditions associated with mitochondrial function
US20090275099A1 (en) 2004-04-27 2009-11-05 Regents Of The University Of Michigan Methods and compositions for treating diseases and conditions associated with mitochondrial function
TW200612948A (en) 2004-07-01 2006-05-01 Synta Pharmaceuticals Corp 2-substituted heteroaryl compounds
CA2659549C (en) 2006-06-09 2013-07-30 The Regents Of The University Of Michigan Compositions and methods relating to novel compounds and targets thereof
WO2009036175A2 (en) * 2007-09-14 2009-03-19 The Regents Of The University Of Michigan F1f0-atpase inhibitors and related methods
EP2219646A4 (en) 2007-12-21 2010-12-22 Univ Rochester PROCESS FOR EXTENDING THE LIFE OF EUKARYOTIC ORGANISMS
KR100982661B1 (ko) 2008-04-22 2010-09-17 전남대학교산학협력단 플라스멥신 ⅱ 활성을 저해하는 화합물을 유효성분으로함유하는 말라리아 예방 및 치료를 위한 약학 조성물 및이를 이용한 말라리아 치료방법
WO2010030891A2 (en) 2008-09-11 2010-03-18 The Regents Of The University Of Michigan Aryl guanidine f1f0-atpase inhibitors and related methods
HRP20171280T1 (hr) 2010-12-08 2018-01-12 Lycera Corporation Pirazolilgvanidinski inhibitori f1f0-atpaze i njihova upotreba u terapiji
US9169199B2 (en) 2010-12-08 2015-10-27 Lycera Corporation Cycloalkyl guanidine F1F0-ATPase inhibitors and therapeutic uses thereof
EP2648736A4 (en) 2010-12-08 2015-04-29 Lycera Corp CYCLOALKYL GUANIDINE F1F0 ATPASE INHIBITORS AND THERAPEUTIC USES THEREOF
WO2012078869A1 (en) 2010-12-08 2012-06-14 Lycera Corporation Pyridonyl guanidine f1f0-atpase inhibitors and therapeutic uses thereof
WO2013185046A1 (en) 2012-06-08 2013-12-12 Lycera Corporation Saturated acyl guanid1ne for inhibition of f1f0-atpase
EP2866796A4 (en) 2012-06-08 2015-11-25 Lycera Corp PYRAZOLYL GUANIDINE F1FO ATPASE HEMMER AND THERAPEUTIC USES THEREOF
US9221814B2 (en) 2012-06-08 2015-12-29 Lycera Corporation Heterocyclic guanidine F1F0-atpase inhibitors and therapeutic uses thereof
MX2016007445A (es) 2013-12-10 2016-09-09 Lycera Corp Inhibidores de f1f0-atpasa de trifluorometil pirazolil guanidina y usos terapeuticos de los mismos.

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