(1R,9R,10R)-17-(cyclobutylmethyl)-4-(3-{[(1R,9R,10R)-17-(cyclobutylmethyl)-17-azatetracyclo[7.5.3.0^{1,10}.0^{2,7}]heptadeca-2,4,6-trien-4-yl]oxy}propoxy)-17-azatetracyclo[7.5.3.0^{1,10}.0^{2,7}]heptadeca-2,4,6-triene | 1221440-81-8

• 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: (1R,9R,10R)-17-(cyclobutylmethyl)-4-(3-{[(1R,9R,10R)-17-(cyclobutylmethyl)-17-azatetracyclo[7.5.3.0^{1,10}.0^{2,7}]heptadeca-2,4,6-trien-4-yl]oxy}propoxy)-17-azatetracyclo[7.5.3.0^{1,10}.0^{2,7}]heptadeca-2,4,6-triene
• 英文别名: (1R,9R,10R)-17-(cyclobutylmethyl)-4-[3-[[(1R,9R,10R)-17-(cyclobutylmethyl)-17-azatetracyclo[7.5.3.01,10.02,7]heptadeca-2(7),3,5-trien-4-yl]oxy]propoxy]-17-azatetracyclo[7.5.3.01,10.02,7]heptadeca-2(7),3,5-triene
• CAS: 1221440-81-8
• 化学式: C₄₅H₆₂N₂O₂
• 分子量: 662.999
• InChiKey: ITYQNXWROCRMOE-GZALVWPRSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  11.2
• 重原子数：
  49
• 可旋转键数：
  10
• 环数：
  10.0
• sp3杂化的碳原子比例：
  0.73
• 拓扑面积：
  24.9
• 氢给体数：
  0
• 氢受体数：
  4

反应信息

• 作为产物：
  描述：

  1,3-丙二醇-二-间-甲苯磺酸盐 、 butorphan 在 sodium hydride 作用下， 以 N,N-二甲基甲酰胺 为溶剂， 以66%的产率得到(1R,9R,10R)-17-(cyclobutylmethyl)-4-(3-{[(1R,9R,10R)-17-(cyclobutylmethyl)-17-azatetracyclo[7.5.3.0^{1,10}.0^{2,7}]heptadeca-2,4,6-trien-4-yl]oxy}propoxy)-17-azatetracyclo[7.5.3.0^{1,10}.0^{2,7}]heptadeca-2,4,6-triene
  参考文献：
  名称：

  Effect of linker substitution on the binding of butorphan univalent and bivalent ligands to opioid receptors

  摘要：

  A series of bivalent hydroxy ether butorphan ligands were prepared and their binding affinities at the opioid receptors determined. Addition of a hydroxy group to a hydrocarbon chain can potentiate binding affinity up to 27- and 86-fold at the mu and kappa opioid receptors, respectively. Two bivalent ligands with sub-nanomolar binding affinity at the mu and kappa opioid receptors were discovered. (C) 2010 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2010.01.101

文献信息

• Effect of linker substitution on the binding of butorphan univalent and bivalent ligands to opioid receptors
  作者：Brian S. Fulton、Brian L. Knapp、Jean M. Bidlack、John L. Neumeyer

  DOI：10.1016/j.bmcl.2010.01.101

  日期：2010.3

  A series of bivalent hydroxy ether butorphan ligands were prepared and their binding affinities at the opioid receptors determined. Addition of a hydroxy group to a hydrocarbon chain can potentiate binding affinity up to 27- and 86-fold at the mu and kappa opioid receptors, respectively. Two bivalent ligands with sub-nanomolar binding affinity at the mu and kappa opioid receptors were discovered. (C) 2010 Elsevier Ltd. All rights reserved.