KR101328306B1 - 염증 치료를 위한 lta4h의 바이아릴 치환된헤테로사이클 억제제 - Google Patents

염증 치료를 위한 lta4h의 바이아릴 치환된헤테로사이클 억제제 Download PDF

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KR101328306B1
KR101328306B1 KR1020087009260A KR20087009260A KR101328306B1 KR 101328306 B1 KR101328306 B1 KR 101328306B1 KR 1020087009260 A KR1020087009260 A KR 1020087009260A KR 20087009260 A KR20087009260 A KR 20087009260A KR 101328306 B1 KR101328306 B1 KR 101328306B1
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mmol
pyrrolidine
phenoxymethyl
substituted
mixture
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KR20080050500A (ko
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자스비 씽
빈센트 산다나야카
마크 거니
펭 유
루이스 베델
비욘 마마트
레이 즈하오
라마 케이. 미슈라
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디코드 제네틱스 이에이치에프
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    • A61K31/40Heterocyclic 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
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    • C07D207/22Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having one double bond between ring members or between a ring member and a non-ring member 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 ring carbon atoms
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KR1020087009260A 2005-09-21 2006-06-23 염증 치료를 위한 lta4h의 바이아릴 치환된헤테로사이클 억제제 Expired - Fee Related KR101328306B1 (ko)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US71901605P 2005-09-21 2005-09-21
US60/719,016 2005-09-21
PCT/US2006/024393 WO2007040682A1 (en) 2005-09-21 2006-06-23 Biaryl substituted heterocycle inhibitors of lta4h for treating inflammation

Publications (2)

Publication Number Publication Date
KR20080050500A KR20080050500A (ko) 2008-06-05
KR101328306B1 true KR101328306B1 (ko) 2013-11-11

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US (3) US20070078263A1 (enExample)
EP (1) EP1926708B1 (enExample)
JP (1) JP5133889B2 (enExample)
KR (1) KR101328306B1 (enExample)
CN (1) CN101312948B (enExample)
AU (1) AU2006297798B2 (enExample)
BR (1) BRPI0616187A2 (enExample)
CA (1) CA2623348A1 (enExample)
EA (1) EA017618B1 (enExample)
IL (1) IL190372A0 (enExample)
NO (1) NO20081829L (enExample)
NZ (1) NZ566788A (enExample)
SG (1) SG166769A1 (enExample)
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HUE031972T2 (en) * 2005-12-29 2017-08-28 Celtaxsys Inc Diamine derivatives as inhibitors of leukotriene a4 hydrolase
US8653115B2 (en) * 2006-06-13 2014-02-18 Shanghai Institute Of Materia Medica, Chinese Academy Of Sciences Heterocyclic non-nucleoside compounds, their preparation, pharmaceutical composition and their use as antiviral agents
WO2008019302A1 (en) * 2006-08-04 2008-02-14 Decode Genetics Ehf Pyrazolylphenyl and pyrrolylphenyl inhibitors of lta4h for treating inflammation
BRPI0813837A2 (pt) * 2007-07-27 2015-01-06 Hoffmann La Roche 2-azetidinametanoaminas e 2-pirrolidinametanoaminas como ligantes de taar
UY31443A1 (es) * 2007-10-31 2009-04-30 Diaminas en puente o fusionadas sustituidas con arilo como moduladores de leucotrieno a4 hidrolasa
US20090312558A1 (en) * 2008-06-13 2009-12-17 Reliance Life Sciences Pvt. Ltd. Process for the preparation of arylcyclopropoane carboxylic carbonitriles, and compounds derived therefrom
WO2010045633A2 (en) * 2008-10-17 2010-04-22 National Jewish Health Measurement and analysis of leukotrienes
AU2010249041B2 (en) * 2009-05-14 2014-11-13 Janssen Pharmaceutica Nv Compounds with two fused bicyclic heteroaryl moieties as modulators of leukotriene A4 hydrolase
WO2011011598A1 (en) 2009-07-24 2011-01-27 Decode Genetics Ehf Process for preparing 4- { (s) -2- (4-(4-chlorophenoxy) phenoxymethyl) pyrrolidin-1-yl) } butyric acid and salts thereof
CN102666490A (zh) 2009-12-25 2012-09-12 宇部兴产株式会社 氨基吡啶化合物
CN103338767B (zh) 2010-08-04 2018-06-22 弗吉尼亚大学专利基金会 治疗炎症性疾病的组合物和方法
CN103415513B (zh) 2011-03-14 2016-01-20 勃林格殷格翰国际有限公司 白三烯产物的苯并二氧杂环己烷抑制剂
EP2734516B1 (en) 2011-07-19 2015-06-17 Boehringer Ingelheim International GmbH Arylpyrazole ethers as inhibitors of leukotriene a4 hydrolase
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