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ethyl 3-{3-cyano-4-[((2R)-3-{[1,1-dimethyl-2-(2-naphthalenyl)-ethyl]amino}-2-hydroxypropyl)oxy]phenyl}propanoate hydrochloride | 1192845-62-7

中文名称
——
中文别名
——
英文名称
ethyl 3-{3-cyano-4-[((2R)-3-{[1,1-dimethyl-2-(2-naphthalenyl)-ethyl]amino}-2-hydroxypropyl)oxy]phenyl}propanoate hydrochloride
英文别名
Benzenepropanoic acid,3-cyano-4-[(2R)-3-[[1,1-dimethyl-2-(2-naphthalenyl)ethyl]amino]-2-hydroxypropoxy]-,ethyl ester,(Hydrochloride) (1:1);ethyl 3-[3-cyano-4-[(2R)-2-hydroxy-3-[(2-methyl-1-naphthalen-2-ylpropan-2-yl)amino]propoxy]phenyl]propanoate;hydrochloride
ethyl 3-{3-cyano-4-[((2R)-3-{[1,1-dimethyl-2-(2-naphthalenyl)-ethyl]amino}-2-hydroxypropyl)oxy]phenyl}propanoate hydrochloride化学式
CAS
1192845-62-7
化学式
C29H34N2O4*ClH
mdl
——
分子量
511.061
InChiKey
IFWPZKFWNGLFCD-UFTMZEDQSA-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):
    4.98
  • 重原子数:
    36
  • 可旋转键数:
    13
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.38
  • 拓扑面积:
    91.6
  • 氢给体数:
    3
  • 氢受体数:
    6

反应信息

  • 作为产物:
    参考文献:
    名称:
    Antagonists of the Calcium Receptor. 2. Amino Alcohol-Based Parathyroid Hormone Secretagogues
    摘要:
    When administered as a single agent to rats the previously reported calcium receptor antagonist 3 elicited a sustained elevation of plasma PTH resulting in no increase in overall bone mineral density. The lack of a bone building effect for analogue 3 was attributed to the large volume of distribution (V-dss(rat) = 11 L/kg) producing a protracted plasma PTH profile. Incorporation of a carboxylic acid functionality into the amino alcohol template led to the identification of 12 with a lower volume of distribution (V-dss(12) = 1.18 L/kg) and a shorter half-life. The zwitterionic nature of antagonist 12 necessitated the utility of an ester prodrug approach to increase overall permeability. Antagonist 12 elicited a rapid and transient increase in circulating levels of PTH following oral dosing of the ester prodrug 11 in the dog. The magnitude and duration of the increases in plasma levels of PTH would be expected to stimulate new bone formation.
    DOI:
    10.1021/jm900563e
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文献信息

  • Antagonists of the Calcium Receptor. 2. Amino Alcohol-Based Parathyroid Hormone Secretagogues
    作者:Robert W. Marquis、Amparo M. Lago、James F. Callahan、Attiq Rahman、Xiaoyang Dong、George B. Stroup、Sandra Hoffman、Maxine Gowen、Eric G. DelMar、Bradford C. Van Wagenen、Sarah Logan、Scott Shimizu、John Fox、Edward F. Nemeth、Theresa Roethke、Brian R. Smith、Keith W. Ward、Pradip Bhatnagar
    DOI:10.1021/jm900563e
    日期:2009.11.12
    When administered as a single agent to rats the previously reported calcium receptor antagonist 3 elicited a sustained elevation of plasma PTH resulting in no increase in overall bone mineral density. The lack of a bone building effect for analogue 3 was attributed to the large volume of distribution (V-dss(rat) = 11 L/kg) producing a protracted plasma PTH profile. Incorporation of a carboxylic acid functionality into the amino alcohol template led to the identification of 12 with a lower volume of distribution (V-dss(12) = 1.18 L/kg) and a shorter half-life. The zwitterionic nature of antagonist 12 necessitated the utility of an ester prodrug approach to increase overall permeability. Antagonist 12 elicited a rapid and transient increase in circulating levels of PTH following oral dosing of the ester prodrug 11 in the dog. The magnitude and duration of the increases in plasma levels of PTH would be expected to stimulate new bone formation.
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