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| 1223461-45-7

中文名称
——
中文别名
——
英文名称
——
英文别名
——
化学式
CAS
1223461-45-7
化学式
C31H28Cl3F2NO4
mdl
——
分子量
622.923
InChiKey
NKMYVOKQDPXKIT-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):
    8.07
  • 重原子数:
    41.0
  • 可旋转键数:
    12.0
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.29
  • 拓扑面积:
    55.84
  • 氢给体数:
    0.0
  • 氢受体数:
    4.0

反应信息

  • 作为反应物:
    描述:
    乙腈正丁基锂copper(l) iodide 作用下, 反应 3.25h, 以66%的产率得到
    参考文献:
    名称:
    Design and optimization of a substituted amino propanamide series of renin inhibitors for the treatment of hypertension
    摘要:
    The discovery and SAR of a new series of substituted amino propanamide renin inhibitors are herein described. This work has led to the preparation of compounds with in vitro and in vivo profiles suitable for further development. Specifically, challenges pertaining to oral bioavailability, covalent binding and time-dependent CYP 3A4 inhibition were overcome thereby culminating in the identification of compound 50 as an optimized renin inhibitor with good efficacy in the hypertensive double-transgenic rat model. (C) 2010 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2010.02.036
  • 作为产物:
    描述:
    参考文献:
    名称:
    Design and optimization of a substituted amino propanamide series of renin inhibitors for the treatment of hypertension
    摘要:
    The discovery and SAR of a new series of substituted amino propanamide renin inhibitors are herein described. This work has led to the preparation of compounds with in vitro and in vivo profiles suitable for further development. Specifically, challenges pertaining to oral bioavailability, covalent binding and time-dependent CYP 3A4 inhibition were overcome thereby culminating in the identification of compound 50 as an optimized renin inhibitor with good efficacy in the hypertensive double-transgenic rat model. (C) 2010 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2010.02.036
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