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pipertramine

中文名称
——
中文别名
——
英文名称
pipertramine
英文别名
1-[(2-methoxyphenyl)methyl]-4-[1-[8-[4-[1-[(2-methoxyphenyl)methyl]piperidin-4-yl]piperidin-1-yl]octyl]piperidin-4-yl]piperidine
pipertramine化学式
CAS
——
化学式
C44H70N4O2
mdl
——
分子量
687.065
InChiKey
HECAWZFPXYNICY-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):
    8.8
  • 重原子数:
    50
  • 可旋转键数:
    17
  • 环数:
    6.0
  • sp3杂化的碳原子比例:
    0.73
  • 拓扑面积:
    31.4
  • 氢给体数:
    0
  • 氢受体数:
    6

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:
    N-boc-4,4-联哌啶盐酸potassium carbonate 、 potassium iodide 作用下, 以 甲醇 为溶剂, 反应 30.0h, 生成 pipertramine
    参考文献:
    名称:
    Design, Synthesis, and Biological Activity of Methoctramine-Related Polyamines as Putative Gi Protein Activators
    摘要:
    The universal template approach provided a prospect of modifying methoctramine (2) structure. Thus, polyamines 3-7 were designed in which the flexibility of the diamino-hexane spacer of 2 was replaced by a bipiperidinyl moiety. In electrically stimulated guinea pig left atria, these novel polyamines, unlike prototype 2, displayed a potent intrinsic activity, which was in contrast with the muscarinic antagonism shown in binding studies by some of them (3 and 4) and was inhibited by benzalkonium chloride, an inhibitor of G(i) proteins.
    DOI:
    10.1021/jm0155594
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文献信息

  • Design, Synthesis, and Biological Activity of Methoctramine-Related Polyamines as Putative G<sub>i</sub> Protein Activators
    作者:Carlo Melchiorre、Maria L. Bolognesi、Roberta Budriesi、Carla Ghelardini、Alberto Chiarini、Anna Minarini、Michela Rosini、Vincenzo Tumiatti、Erik J. Wade
    DOI:10.1021/jm0155594
    日期:2001.11.1
    The universal template approach provided a prospect of modifying methoctramine (2) structure. Thus, polyamines 3-7 were designed in which the flexibility of the diamino-hexane spacer of 2 was replaced by a bipiperidinyl moiety. In electrically stimulated guinea pig left atria, these novel polyamines, unlike prototype 2, displayed a potent intrinsic activity, which was in contrast with the muscarinic antagonism shown in binding studies by some of them (3 and 4) and was inhibited by benzalkonium chloride, an inhibitor of G(i) proteins.
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