KR100827470B1 - 히스타민 h3 길항제로서 유용한(1-4-피페리디닐)벤즈이미다졸 유도체 - Google Patents

히스타민 h3 길항제로서 유용한(1-4-피페리디닐)벤즈이미다졸 유도체 Download PDF

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KR100827470B1
KR100827470B1 KR1020047016508A KR20047016508A KR100827470B1 KR 100827470 B1 KR100827470 B1 KR 100827470B1 KR 1020047016508 A KR1020047016508 A KR 1020047016508A KR 20047016508 A KR20047016508 A KR 20047016508A KR 100827470 B1 KR100827470 B1 KR 100827470B1
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KR20040099445A (ko
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젱큉베이
아슬라니안로버트쥐.
벌린마이클와이.
보이스크리스토퍼더블류.
카오지안후아
코즐로브스키조셉에이.
맨지아라시나피트로
맥코믹케빈디.
무타히망지더블류.
로젠블룸스튜어트비.
쉬이넹-양
솔로몬다니엘엠.
톰윙씨.
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쉐링 코포레이션
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    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/06Antimigraine agents
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    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/18Antipsychotics, i.e. neuroleptics; Drugs for mania or schizophrenia
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    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
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    • C07DHETEROCYCLIC COMPOUNDS
    • C07D405/00Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
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    • C07D409/00Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
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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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  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
KR1020047016508A 2002-04-18 2003-04-16 히스타민 h3 길항제로서 유용한(1-4-피페리디닐)벤즈이미다졸 유도체 Expired - Fee Related KR100827470B1 (ko)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US37373102P 2002-04-18 2002-04-18
US60/373,731 2002-04-18
PCT/US2003/011672 WO2003088967A1 (en) 2002-04-18 2003-04-16 (1-4-piperidinyl) benzimidazole derivatives useful as histamine h3 antagonists

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KR20040099445A KR20040099445A (ko) 2004-11-26
KR100827470B1 true KR100827470B1 (ko) 2008-05-06

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EP (1) EP1499316B1 (https=)
JP (1) JP4384918B2 (https=)
KR (1) KR100827470B1 (https=)
CN (1) CN100522166C (https=)
AR (1) AR040405A1 (https=)
AT (1) ATE389406T1 (https=)
AU (1) AU2003223627B2 (https=)
BR (1) BR0309348A (https=)
CA (1) CA2481940A1 (https=)
CY (1) CY1110363T1 (https=)
DE (1) DE60319813T2 (https=)
DK (1) DK1499316T3 (https=)
EC (1) ECSP045367A (https=)
ES (1) ES2301791T3 (https=)
IL (1) IL164584A (https=)
MX (1) MXPA04010173A (https=)
NO (1) NO20045002L (https=)
NZ (1) NZ535763A (https=)
PE (1) PE20040684A1 (https=)
PL (1) PL373889A1 (https=)
PT (1) PT1499316E (https=)
RU (1) RU2323935C2 (https=)
SI (1) SI1499316T1 (https=)
TW (1) TW200306183A (https=)
WO (1) WO2003088967A1 (https=)
ZA (1) ZA200407984B (https=)

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JP5080970B2 (ja) 2004-06-17 2012-11-21 サイトキネティクス・インコーポレーテッド 心疾患を治療するための置換尿素誘導体
US7176222B2 (en) 2004-07-27 2007-02-13 Cytokinetics, Inc. Syntheses of ureas
WO2006038738A1 (ja) * 2004-10-08 2006-04-13 Takeda Pharmaceutical Company Limited 受容体機能調節剤
CN101107231A (zh) 2005-01-21 2008-01-16 先灵公司 用作组胺h3拮抗剂的咪唑和苯并咪唑衍生物
EP1896453B1 (en) * 2005-06-20 2009-12-02 Schering Corporation Carbon-linked substituted piperidines and derivatives thereof useful as histamine h3 antagonists
DE602006010870D1 (de) 2005-06-20 2010-01-14 Schering Corp Als antagonisten von histamin h3 geeignete piperidinderivate
US7538223B2 (en) 2005-08-04 2009-05-26 Cytokinetics, Inc. Compounds, compositions and methods
JP4860700B2 (ja) * 2005-09-20 2012-01-25 シェーリング コーポレイション ヒスタミンH3アンタゴニストとして有用な、1−[[1−[(2−アミノ−6−メチル−4−ピリジニル)メチル]−4−フルオロ−4−ピペリジニル]カルボニル]−4−[2−(2−ピリジニル)−3H−イミダゾ[4,5−b]ピリジン−3−イル]ピペリジン
CN101273026A (zh) 2005-09-30 2008-09-24 霍夫曼-拉罗奇有限公司 作为mch受体拮抗剂的茚满衍生物
US7825120B2 (en) 2005-12-15 2010-11-02 Cytokinetics, Inc. Certain substituted ((piperazin-1-ylmethyl)benzyl)ureas
TW200808321A (en) 2005-12-15 2008-02-16 Cytokinetics Inc Certain chemical entities, compositions and methods
EP1959962A2 (en) 2005-12-16 2008-08-27 Cytokinetics, Inc. Certain chemical entities, compositions, and methods
EP1962852B1 (en) 2005-12-19 2017-01-25 Cytokinetics, Inc. Compounds, compositions and methods
US20070142369A1 (en) * 2005-12-21 2007-06-21 Margaret Van Heek Combination of an H3 antagonist/inverse agonist and an appetite suppressant
JP2009521448A (ja) 2005-12-21 2009-06-04 シェーリング コーポレイション ヒスタミンh3アンタゴニストとして有用なフェノキシピペリジンおよびそのアナログ
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DK2519522T3 (en) 2009-12-30 2014-12-08 Arqule Inc SUBSTITUTED IDAZOPYRIDINYL AMINOPYRIDINE COMPOUNDS
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US8552253B2 (en) 2011-09-02 2013-10-08 Korea Advanced Institute Of Science And Technology Screening of drug for attention deficit hyperactive disorder by using GIT1 knock-out mice as a novel ADHD mouse model

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PL373889A1 (en) 2005-09-19
PE20040684A1 (es) 2004-10-05
AU2003223627C1 (en) 2003-11-03
EP1499316B1 (en) 2008-03-19
JP4384918B2 (ja) 2009-12-16
MXPA04010173A (es) 2005-02-03
CY1110363T1 (el) 2012-05-23
ECSP045367A (es) 2004-11-26
AU2003223627A1 (en) 2003-11-03
ATE389406T1 (de) 2008-04-15
NO20045002L (no) 2005-01-18
DE60319813T2 (de) 2009-04-23
NZ535763A (en) 2007-06-29
PT1499316E (pt) 2008-06-30
RU2004133764A (ru) 2005-07-20
SI1499316T1 (sl) 2008-08-31
IL164584A (en) 2010-12-30
JP2005529116A (ja) 2005-09-29
ZA200407984B (en) 2005-10-18
BR0309348A (pt) 2005-03-01
CN100522166C (zh) 2009-08-05
KR20040099445A (ko) 2004-11-26
AR040405A1 (es) 2005-04-06
DK1499316T3 (da) 2008-07-21
WO2003088967A1 (en) 2003-10-30
CA2481940A1 (en) 2003-10-30
RU2323935C2 (ru) 2008-05-10
IL164584A0 (en) 2005-12-18
HK1067981A1 (en) 2005-04-22
EP1499316A1 (en) 2005-01-26
TW200306183A (en) 2003-11-16
DE60319813D1 (de) 2008-04-30
AU2003223627B2 (en) 2006-10-12
CN1658874A (zh) 2005-08-24

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