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(+/-)-2-(cyclopropylmethyloxy)isodomesticine | 1340566-54-2

中文名称
——
中文别名
——
英文名称
(+/-)-2-(cyclopropylmethyloxy)isodomesticine
英文别名
Rac-2-(Cyclopropylmethyloxy)Isodomesticine;18-(cyclopropylmethoxy)-19-methoxy-13-methyl-5,7-dioxa-13-azapentacyclo[10.7.1.02,10.04,8.016,20]icosa-1(20),2,4(8),9,16,18-hexaene
(+/-)-2-(cyclopropylmethyloxy)isodomesticine化学式
CAS
1340566-54-2
化学式
C23H25NO4
mdl
——
分子量
379.456
InChiKey
YTUNBRIKVNISRV-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
  • 重原子数:
    28
  • 可旋转键数:
    4
  • 环数:
    6.0
  • sp3杂化的碳原子比例:
    0.48
  • 拓扑面积:
    40.2
  • 氢给体数:
    0
  • 氢受体数:
    5

反应信息

  • 作为产物:
    描述:
    三乙酰氧基硼氢化钠 、 zinc dibromide 作用下, 以 二氯甲烷 为溶剂, 生成 (+/-)-2-(cyclopropylmethyloxy)isodomesticine
    参考文献:
    名称:
    New aporphinoid 5-HT2A and α1A antagonists via structural manipulations of nantenine
    摘要:
    A series of Cl, C2, C3 and N6 analogs of nantenine (2) was synthesized and evaluated in 5-HT2A and alpha(1A) receptor functional assays. Alkyl substitution of the Cl and N6 methyl groups of nantenine provided selective 5-HT2A and alpha 1A antagonists, respectively. The C2 alkyloxy analogs studied were generally selective for alpha(1A) versus 5-HT2A. The C3 bromo analog 15 is one of the most potent aporphinoid 5-HT2A antagonists known presently. (C) 2011 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmc.2011.08.019
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文献信息

  • New aporphinoid 5-HT2A and α1A antagonists via structural manipulations of nantenine
    作者:Sandeep Chaudhary、Shashikanth Ponnala、Onica LeGendre、Junior A. Gonzales、Hernán A. Navarro、Wayne W. Harding
    DOI:10.1016/j.bmc.2011.08.019
    日期:2011.10
    A series of Cl, C2, C3 and N6 analogs of nantenine (2) was synthesized and evaluated in 5-HT2A and alpha(1A) receptor functional assays. Alkyl substitution of the Cl and N6 methyl groups of nantenine provided selective 5-HT2A and alpha 1A antagonists, respectively. The C2 alkyloxy analogs studied were generally selective for alpha(1A) versus 5-HT2A. The C3 bromo analog 15 is one of the most potent aporphinoid 5-HT2A antagonists known presently. (C) 2011 Elsevier Ltd. All rights reserved.
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