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4-(2,3-Dichloro-phenyl)-2-[2-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-ethoxymethyl]-6-methyl-1,4-dihydro-pyridine-3,5-dicarboxylic acid 3-ethyl ester 5-isopropyl ester | 103198-43-2

中文名称
——
中文别名
——
英文名称
4-(2,3-Dichloro-phenyl)-2-[2-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-ethoxymethyl]-6-methyl-1,4-dihydro-pyridine-3,5-dicarboxylic acid 3-ethyl ester 5-isopropyl ester
英文别名
——
4-(2,3-Dichloro-phenyl)-2-[2-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-ethoxymethyl]-6-methyl-1,4-dihydro-pyridine-3,5-dicarboxylic acid 3-ethyl ester 5-isopropyl ester化学式
CAS
103198-43-2
化学式
C30H30Cl2N2O7
mdl
——
分子量
601.483
InChiKey
NVDAUSRYZFHOMQ-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

物化性质

  • 沸点:
    684.3±55.0 °C(Predicted)
  • 密度:
    1.326±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    5.04
  • 重原子数:
    41.0
  • 可旋转键数:
    10.0
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.33
  • 拓扑面积:
    111.24
  • 氢给体数:
    1.0
  • 氢受体数:
    8.0

SDS

SDS:b7352cef42a32aaa856eb3048051cd13
查看

反应信息

  • 作为反应物:
    参考文献:
    名称:
    Long-acting dihydropyridine calcium antagonists. 9. Structure activity relationships around amlodipine
    摘要:
    The preparation of a range of 1,4-dihydropyridine analogues of amlodipine has been undertaken and their calcium antagonist activities on rat aorta have been evaluated. Increasing the size of the C5 ester group dramatically reduces calcium antagonist activity, a trend which would be compatible with the carbonyl group of that ester binding to the DHP receptor. Amlodipine analogues with extended C3 ester substituents also have lower potency than amlodipine, possibly because of disruption of a favourable interaction between the protonated amino group on the 2-substituent and the DHP receptor. Replacement of the 6-methyl substituent in amlodipine by alkoxyalkyl groups or electron-withdrawing groups is also detrimental to calcium antagonist activity.
    DOI:
    10.1016/0223-5234(91)90132-7
  • 作为产物:
    参考文献:
    名称:
    Long-acting dihydropyridine calcium antagonists. 9. Structure activity relationships around amlodipine
    摘要:
    The preparation of a range of 1,4-dihydropyridine analogues of amlodipine has been undertaken and their calcium antagonist activities on rat aorta have been evaluated. Increasing the size of the C5 ester group dramatically reduces calcium antagonist activity, a trend which would be compatible with the carbonyl group of that ester binding to the DHP receptor. Amlodipine analogues with extended C3 ester substituents also have lower potency than amlodipine, possibly because of disruption of a favourable interaction between the protonated amino group on the 2-substituent and the DHP receptor. Replacement of the 6-methyl substituent in amlodipine by alkoxyalkyl groups or electron-withdrawing groups is also detrimental to calcium antagonist activity.
    DOI:
    10.1016/0223-5234(91)90132-7
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同类化合物

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