glyceryl 1,2,3-tris<3-(3-amino-2,4,6-triiodophenyl)propionate> | 103959-75-7

• 分子结构分类: 有机化合物 - 脂质和类脂质分子 - 甘油脂
• 英文名称: glyceryl 1,2,3-tris<3-(3-amino-2,4,6-triiodophenyl)propionate>
• 英文别名: 2,3-Bis[3-(3-amino-2,4,6-triiodophenyl)propanoyloxy]propyl 3-(3-amino-2,4,6-triiodophenyl)propanoate
• CAS: 103959-75-7
• 化学式: C₃₀H₂₆I₉N₃O₆
• 分子量: 1666.69
• InChiKey: SEOOQMZJKWGIBW-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  9.4
• 重原子数：
  48
• 可旋转键数：
  17
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.3
• 拓扑面积：
  157
• 氢给体数：
  3
• 氢受体数：
  9

反应信息

• 作为产物：
  描述：

  3-(3-氨基-2,4,6-三碘-苯基)丙酸 、 甘油 在 4-二甲氨基吡啶 、 N,N'-二环己基碳二亚胺 作用下， 以 二氯甲烷 为溶剂， 反应 96.0h， 以38%的产率得到glyceryl 1,2,3-tris<3-(3-amino-2,4,6-triiodophenyl)propionate>
  参考文献：
  名称：

  Potential tumor- or organ-imaging agents. 27. Polyiodinated 1,3-disubstituted and 1,2,3-trisubstituted triacylglycerols

  摘要：

  A series of glyceryl 1,3-bis- and 1,2,3-tris[omega-(3-amino-2,4,6-triiodophenyl)alkanoates] were synthesized, radioiodinated with iodine-125, and evaluated for their ability to selectively localize in the liver for potential use as hepatographic imaging agents. Of the nine target compounds synthesized and evaluated in rats, glyceryl 1,2,3-tris[3-(3-amino-2,4,6-triiodophenyl)propionate] (5b) displayed rapid and sustained liver specificity. This agent was found to accumulate in the liver in concentrations of 60, 75, and 86% of the administered dose at 5 min, 30 min, and 24 h, respectively. Moreover, the 24-h liver-to-blood ratio of 235 justifies further studies in higher animal species.

  DOI：

  10.1021/jm00162a007

文献信息

• Potential tumor- or organ-imaging agents. 27. Polyiodinated 1,3-disubstituted and 1,2,3-trisubstituted triacylglycerols
  作者：Jamey P. Weichert、Michael P. Groziak、Marc A. Longino、Susan W. Schwendner、Raymond E. Counsell

  DOI：10.1021/jm00162a007

  日期：1986.12

  A series of glyceryl 1,3-bis- and 1,2,3-tris[omega-(3-amino-2,4,6-triiodophenyl)alkanoates] were synthesized, radioiodinated with iodine-125, and evaluated for their ability to selectively localize in the liver for potential use as hepatographic imaging agents. Of the nine target compounds synthesized and evaluated in rats, glyceryl 1,2,3-tris[3-(3-amino-2,4,6-triiodophenyl)propionate] (5b) displayed rapid and sustained liver specificity. This agent was found to accumulate in the liver in concentrations of 60, 75, and 86% of the administered dose at 5 min, 30 min, and 24 h, respectively. Moreover, the 24-h liver-to-blood ratio of 235 justifies further studies in higher animal species.