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(1S,2S,4S)-2-(2-{[3-(4,7-dimethoxy-1H-benzoimidazol-2-yl)-propyl]-methyl-amino}-ethyl)-5-phenyl-bicyclo[2.2.2]oct-5-en-2-ol | 1075744-60-3

中文名称
——
中文别名
——
英文名称
(1S,2S,4S)-2-(2-{[3-(4,7-dimethoxy-1H-benzoimidazol-2-yl)-propyl]-methyl-amino}-ethyl)-5-phenyl-bicyclo[2.2.2]oct-5-en-2-ol
英文别名
(1S,2S,4S)-2-[2-[3-(4,7-dimethoxy-1H-benzimidazol-2-yl)propyl-methylamino]ethyl]-5-phenylbicyclo[2.2.2]oct-5-en-2-ol
(1S,2S,4S)-2-(2-{[3-(4,7-dimethoxy-1H-benzoimidazol-2-yl)-propyl]-methyl-amino}-ethyl)-5-phenyl-bicyclo[2.2.2]oct-5-en-2-ol化学式
CAS
1075744-60-3
化学式
C29H37N3O3
mdl
——
分子量
475.631
InChiKey
QLZMGKRVULIOSP-IHMCZWCLSA-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):
    4.6
  • 重原子数:
    35
  • 可旋转键数:
    10
  • 环数:
    6.0
  • sp3杂化的碳原子比例:
    0.48
  • 拓扑面积:
    70.6
  • 氢给体数:
    2
  • 氢受体数:
    5

文献信息

  • BENZIMIDAZOLE DERIVATIVES AS CALCIUM CHANNEL BLOCKERS
    申请人:Hubler Francis
    公开号:US20110039905A1
    公开(公告)日:2011-02-17
    The invention relates to compounds of formula (I) wherein R 1 represents aryl, which is unsubstituted, or mono-, di-, or tri-substituted wherein the substituents are independently selected from the group consisting of (C 1-4 )alkyl, (C 1-4 )alkoxy, halogen, and trifluoromethyl; R 2 represents hydrogen, or —CO—R 21 ; R 21 represents (C 1-5 )alkyl, (C 1-3 )fluoroalkyl, or (C 3-6 )cycloalkyl; m represents the integer 2, or 3; p represents the integer 2 or 3; and R 3 represents hydrogen, or (C 1-5 )alkyl; and pharmaceutically acceptable salts of such compounds. These compounds are useful as calcium channel blockers.
    该发明涉及以下式(I)的化合物,其中R1代表芳基,未取代,或者单取代、双取代或三取代,其中取代基独立地选自(C1-4)烷基,(C1-4)氧烷基,卤素和三甲基组成的组;R2代表氢,或者—CO—R21;R21代表(C1-5)烷基,(C1-3)氟烷基或(C3-6)环烷基;m表示整数2或3;p表示整数2或3;和R3代表氢,或者(C1-5)烷基;以及这些化合物的药用盐。这些化合物可用作钙通道阻滞剂
  • [EN] BENZIMIDAZOLE DERIVATIVES AS CALCIUM CHANNEL BLOCKERS<br/>[FR] DÉRIVÉS DE BENZIMIDAZOLE EN TANT QUE BLOQUEURS DES CANAUX CALCIQUES
    申请人:ACTELION PHARMACEUTICALS LTD
    公开号:WO2009130679A1
    公开(公告)日:2009-10-29
    The invention relates to compounds of formula (I) wherein R1 represents aryl, which is unsubstituted, or mono-, di-, or tri-substituted wherein the substituents are independently selected from the group consisting of (C1-4alkyl, (C1-4)alkoxy, halogen, and trifluoromethyl; R2 represents hydrogen, or -CO-R21; R21 represents (C1-5)alkyl, (C1-3)fluoroalkyl, or (C3-6)cycloalkyl; m represents the integer 2, or 3; p represents the integer 2 or 3; and R3 represents hydrogen, or (C1-5)alkyl; and pharmaceutically acceptable salts of such compounds. These compounds are useful as calcium channel blockers.
    该发明涉及具有以下结构的化合物(I),其中R1代表芳基,该芳基未经取代,或者经过单取代、双取代或三取代,其中取代基可独立地选择自(C1-4烷基)、(C1-4)烷氧基、卤素和三甲基的组成部分;R2代表氢,或-CO-R21;R21代表(C1-5)烷基、(C1-3)氟烷基或(C3-6)环烷基;m代表整数2或3;p代表整数2或3;R3代表氢,或(C1-5)烷基;以及这些化合物的药用盐。这些化合物可用作钙通道阻滞剂
  • BRIDGED SIX-MEMBERED RING COMPOUNDS
    申请人:Hilpert Kurt
    公开号:US20100130545A1
    公开(公告)日:2010-05-27
    The invention relates to compounds of formula (I), wherein R 1 , R 2 , R 1a , R 2a , R 3 , R 4 , A, B, X, W and n are as defined in the description, and pharmaceutically acceptable salts of such compounds. These compounds are useful as calcium channel blockers.
    本发明涉及式(I)的化合物,其中R1、R2、R1a、R2a、R3、R4、A、B、X、W和n如描述中所定义,并且这些化合物的药学上可接受的盐。这些化合物可用作钙通道阻滞剂
  • SALTS OF ISOBUTYRIC ACID (1R*,2R*,4R*)-2-(2-{[3-(4,7-DIMETHOXY-1 H-BENZOIMIDAZOL-2-YL)-PROPYL]-METHYL-AMINO}-ETHYL)-5-PHENYL-BICYCLO[2.2.2]OCT-5-EN-2-YL ESTER
    申请人:Actelion Pharmaceuticals Ltd.
    公开号:EP2344461B1
    公开(公告)日:2016-12-14
  • JP2011518821A
    申请人:——
    公开号:JP2011518821A
    公开(公告)日:2011-06-30
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