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12-Cytisineacetic acid 2,6-dimethylanilide

中文名称
——
中文别名
——
英文名称
12-Cytisineacetic acid 2,6-dimethylanilide
英文别名
N-(2,6-dimethylphenyl)-2-[(1R,9S)-6-oxo-7,11-diazatricyclo[7.3.1.02,7]trideca-2,4-dien-11-yl]acetamide
12-Cytisineacetic acid 2,6-dimethylanilide化学式
CAS
——
化学式
C21H25N3O2
mdl
——
分子量
351.448
InChiKey
NDGMEEOCSKFWLJ-DLBZAZTESA-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):
    2.3
  • 重原子数:
    26
  • 可旋转键数:
    3
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.43
  • 拓扑面积:
    52.6
  • 氢给体数:
    1
  • 氢受体数:
    3

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为产物:
    描述:
    cytisine 、 alkaline earth salt of/the/ methylsulfuric acid 以 丙酮 为溶剂, 以26%的产率得到12-Cytisineacetic acid 2,6-dimethylanilide
    参考文献:
    名称:
    Synthesis and preliminary pharmacological evaluation of some cytisine derivatives
    摘要:
    Thirty-one N-derivatives of cytisine were prepared in order to modify its pharmacological profile and to obtain compounds of potential therapeutic interest either at a peripheral or central level, particularly as nicotinic ligands with improved ability to cross the blood-brain barrier. Actually, with the introduction of different kinds of substituent on the basic nitrogen of cytisine a variety of activities were observed, both in vivo (analgesic, dopamine antagonism, antihypertensive, inhibition of stress-induced ulcers, antiinflammatory, protection from PAF-induced mortality, hypoglycemic) and in vitro (positive cardio-inotropic, beta-adrenergic antagonism, alpha(1)- and alpha(2)-antagonism, inhibition of PAF-induced platelet aggregation). Six randomly selected compounds were tested for the ability to recognize a central nicotinic receptor and four of them exhibited K-i values; In the range 30-163 nM. (C) 1999 Elsevier Science S.A. All rights reserved.
    DOI:
    10.1016/s0014-827x(99)00049-x
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