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(2-{6-[(4'-trifluoromethyl-biphenyl-2-carbonyl)-amino]-3,4-dihydro-1H-isoquinolin-2-yl}-ethyl)-carbamic acid methyl ester | 208590-81-2

中文名称
——
中文别名
——
英文名称
(2-{6-[(4'-trifluoromethyl-biphenyl-2-carbonyl)-amino]-3,4-dihydro-1H-isoquinolin-2-yl}-ethyl)-carbamic acid methyl ester
英文别名
CP-467688 free base;methyl N-[2-[6-[[2-[4-(trifluoromethyl)phenyl]benzoyl]amino]-3,4-dihydro-1H-isoquinolin-2-yl]ethyl]carbamate
(2-{6-[(4'-trifluoromethyl-biphenyl-2-carbonyl)-amino]-3,4-dihydro-1H-isoquinolin-2-yl}-ethyl)-carbamic acid methyl ester化学式
CAS
208590-81-2
化学式
C27H26F3N3O3
mdl
——
分子量
497.517
InChiKey
FJULIZHZIHXKSK-UHFFFAOYSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

计算性质

  • 辛醇/水分配系数(LogP):
    4.9
  • 重原子数:
    36
  • 可旋转键数:
    7
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.26
  • 拓扑面积:
    70.7
  • 氢给体数:
    2
  • 氢受体数:
    7

文献信息

  • Dibenzyl Amine Compounds and Derivatives
    申请人:Chang George
    公开号:US20070213371A1
    公开(公告)日:2007-09-13
    Dibenzyl amine compounds and derivatives, pharmaceutical compositions containing such compounds and the use of such compounds to elevate certain plasma lipid levels, including high density lipoprotein-cholesterol and to lower certain other plasma lipid levels, such as LDL-cholesterol and triglycerides and accordingly to treat diseases which are exacerbated by low levels of HDL cholesterol and/or high levels of LDL-cholesterol and triglycerides, such as atherosclerosis and cardiovascular diseases in some mammals, including humans.
    二苯基胺化合物及其衍生物,含有这种化合物的药物组合物以及使用这种化合物提高某些血浆脂质水平,包括高密度脂蛋白胆固醇,并降低其他一些血浆脂质水平,如低密度脂蛋白胆固醇和甘油三酯,并据此治疗由高密度脂蛋白胆固醇水平低和/或低密度脂蛋白胆固醇和甘油三酯水平高加重的疾病,如动脉粥样硬化和心血管疾病在某些哺乳动物,包括人类。
  • [EN] 1,2,4-SUBSTITUERTE 1,2,3,4-TETRAHYDRO-AND 1,2 DIHYDRO-QUINOLINE AND 1,2,3,4-TETRAHYDRO-QUINOXALINE DERIVATIVES AS CETP INHIBITORS FOR THE TREATMENT OF ATHEROSCLEROSIS AND OBESITY<br/>[FR] DERIVES DE 1,2,3,4-TETRAHYDRO- ET 1,2 DIHYDRO-QUINOLEINE ET 1,2,3,4-TETRAHYDRO-QUINOXALINE 1,2,4-SUBSTITUES, UTILES COMME INHIBITEURS DE CETP POUR LE TRAITEMENT DE L'ATHEROSCLEROSE ET DE L'OBESITE
    申请人:PFIZER PROD INC
    公开号:WO2004085401A1
    公开(公告)日:2004-10-07
    Quinoline and quinoxaline compounds of formula I and III wherein the subtituent are as defined in claims 1 and 15, pharmaceutical compositions containing such compounds and the use of such compounds to elevate certain plasma lipid levels, including high density lipoprotein-cholesterol and to lower certain other plasma lipid levels, such as LDL-cholesterol and triglycerides and accordingly to treat diseases which are exacerbated by low levels of HDL cholesterol and/or high levels of LDL-cholesterol and triglycerides, such as atherosclerosis and cardiovascular diseases in some mammals, including humans.
    喹啉和喹啉并喹啉化合物的公式I和III,其中取代基如权利要求1和15中所定义的,含有这种化合物的药物组合物以及使用这种化合物来提高某些血浆脂质水平,包括高密度脂蛋白胆固醇,并降低其他一些血浆脂质水平,如LDL胆固醇和甘油三酯,并因此治疗由HDL胆固醇水平低和/或LDL胆固醇和甘油三酯水平高加重的疾病,如动脉粥样硬化和心血管疾病在某些哺乳动物中,包括人类。
  • [EN] SUBSTITUTED HETEROARYL- AND PHENYLSULFAMOYL COMPOUNDS<br/>[FR] COMPOSES HETEROARYLE ET PHENYLSULFAMOYLE SUBSTITUES
    申请人:PFIZER PROD INC
    公开号:WO2005092845A1
    公开(公告)日:2005-10-06
    The present invention is directed at substituted heteroaryl- and phenylsulfamoyl compounds, pharmaceutical compositions containing such compounds and the use of such compounds as peroxisome proliferator activator receptor (PPAR) agonists. PPAR alpha activators, pharmaceutical compositions containing such compounds and the use of such compounds to elevate certain plasma lipid levels, including high density lipoprotein-cholesterol and to lower certain other plasma lipid levels, such as LDL-cholesterol and triglycerides and accordingly to treat diseases which are exacerbated by low levels of HDL cholesterol and/or high levels of LDL-cholesterol and triglycerides, such as atherosclerosis and cardiovascular diseases, in mammals, including humans. The compounds are also useful for the treatment of negative energy balance (NEB) and associated diseases in ruminants.
    本发明涉及取代杂环芳基和苯基磺酰胺化合物,含有这种化合物的药物组合物以及将这种化合物用作过氧化物酶增殖激活受体(PPAR)激动剂的用途。PPARα激活剂,含有这种化合物的药物组合物以及使用这种化合物提高特定血浆脂质水平,包括高密度脂蛋白胆固醇,并降低其他特定血浆脂质水平,如低密度脂蛋白胆固醇和甘油三酯,从而治疗由高密度脂蛋白胆固醇水平低和/或低密度脂蛋白胆固醇和甘油三酯水平高加重的疾病,如动脉粥样硬化和心血管疾病,在哺乳动物,包括人类中。这些化合物还可用于治疗反常能量平衡(NEB)和反常相关疾病的反刍动物。
  • Tetrahydroisoquinoline LXR modulators
    申请人:Yang Wu
    公开号:US20070093523A1
    公开(公告)日:2007-04-26
    A compound of formula I wherein X, R 1 , R 2a , R 3a , R 3b , R 4a , R 4b , R 4c and R 5 are defined herein.
    其中X,R1,R2a,R3a,R3b,R4a,R4b,R4c和R5在此处定义。
  • HETEROCYCLIC CETP INHIBITORS
    申请人:Salvati E. Mark
    公开号:US20070161685A1
    公开(公告)日:2007-07-12
    Compounds of formula Ia and Ib wherein A, B, C and R 1 are described herein.
    式Ia和Ib的化合物 其中A、B、C和R1 如本文所述。
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