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| 1256921-78-4

中文名称
——
中文别名
——
英文名称
——
英文别名
——
化学式
CAS
1256921-78-4
化学式
C25H35NO4
mdl
——
分子量
413.557
InChiKey
QYAXMQORTCGCBF-VDKIKQQVSA-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):
    3.41
  • 重原子数:
    30.0
  • 可旋转键数:
    3.0
  • 环数:
    6.0
  • sp3杂化的碳原子比例:
    0.76
  • 拓扑面积:
    51.16
  • 氢给体数:
    1.0
  • 氢受体数:
    5.0

反应信息

  • 作为反应物:
    描述:
    盐酸 作用下, 以95%的产率得到(4bR,8aS,9R)-11-(cyclopentylmethyl)-8a-hydroxy-3-methoxy-8,8a,9,10-tetrahydro-5H-9,4b-(epiminoethano)phenanthren-6(7H)-one
    参考文献:
    名称:
    Design and synthesis of KNT-127, a δ-opioid receptor agonist effective by systemic administration
    摘要:
    We have reported previously the novel delta-opioid agonist, SN-28, which was more potent in in vitro assays than the prototype delta-agonists, TAN-67 and SNC-80. However, when administered by subcutaneous injection, this compound showed no analgesic effect at dosages greater than 30 mg/kg in the acetic acid writhing test. We speculated that SN-28 was not effective in the test because the presence of the charged ammonium groups prevented its penetration through the blood-brain barrier. On the basis of our proposal, we designed the novel delta-agonist, KNT-127, which was effective with systemic administration. (C) 2010 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2010.08.083
  • 作为产物:
    描述:
    在 lithium aluminium tetrahydride 作用下, 以 四氢呋喃 为溶剂, 生成
    参考文献:
    名称:
    Design and synthesis of KNT-127, a δ-opioid receptor agonist effective by systemic administration
    摘要:
    We have reported previously the novel delta-opioid agonist, SN-28, which was more potent in in vitro assays than the prototype delta-agonists, TAN-67 and SNC-80. However, when administered by subcutaneous injection, this compound showed no analgesic effect at dosages greater than 30 mg/kg in the acetic acid writhing test. We speculated that SN-28 was not effective in the test because the presence of the charged ammonium groups prevented its penetration through the blood-brain barrier. On the basis of our proposal, we designed the novel delta-agonist, KNT-127, which was effective with systemic administration. (C) 2010 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2010.08.083
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