8'-amino-6,7-didehydro-3-methoxy-17-methylquinolino[2',3':6,7]morphinan-14β-ol | 1403215-55-3

• 分子结构分类: 有机化合物 - 生物碱及其衍生物 - 吗啡烷
• 英文名称: 8'-amino-6,7-didehydro-3-methoxy-17-methylquinolino[2',3':6,7]morphinan-14β-ol
• CAS: 1403215-55-3
• 化学式: C₂₅H₂₇N₃O₂
• 分子量: 401.508
• InChiKey: BVOBRRDEMIRXBY-QLBJFCOMSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.85
• 重原子数：
  30.0
• 可旋转键数：
  1.0
• 环数：
  6.0
• sp3杂化的碳原子比例：
  0.4
• 拓扑面积：
  71.61
• 氢给体数：
  2.0
• 氢受体数：
  5.0

反应信息

• 作为产物：
  描述：

  6,6-ethylenedioxy-3-methoxy-17-(2,2,2-trichloroethoxycarbonyl)morphinan-14β-yl acetate 在 盐酸 、 lithium aluminium tetrahydride 、 甲烷磺酸 、 氢气 作用下， 以 四氢呋喃 、 乙醇 为溶剂， 反应 30.0h， 生成 8'-amino-6,7-didehydro-3-methoxy-17-methylquinolino[2',3':6,7]morphinan-14β-ol
  参考文献：
  名称：

  Synthesis of quinolinomorphinan derivatives as highly selective δ opioid receptor ligands

  摘要：

  We have reported previously the novel delta opioid agonist KNT-127 which showed high affinity and selectivity for the delta receptor. Moreover, the analgesic effect of subcutaneously administered KNT-127 was more potent than that of a prototypical delta agonist (-)-TAN-67 in the acetic acid writhing test. This study of the structure-activity relationship of KNT-127 derivatives focused on the introduction of substituents onto the 5'-, 6'-, 7'- or 8'-position of the quinoline ring and revealed that many derivatives with 5'- or 8'-substituents showed high affinities and selectivities for the delta receptor. Especially, SYK-153 with an 8'-OH group showed the highest affinity and the most balanced and highest selectivity for the delta receptor among the synthesized compounds. (C) 2012 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmc.2012.08.004