7α-N-(3,20-dioxopregn-4-en-7-carbonyloxy)-N'-[6-(6-amino-9H-purin-9-yl)hexyl]succinamide | 1408059-09-5

• 分子结构分类: 有机化合物 - 脂质和类脂质分子 - 类固醇和类固醇衍生物
• 英文名称: 7α-N-(3,20-dioxopregn-4-en-7-carbonyloxy)-N'-[6-(6-amino-9H-purin-9-yl)hexyl]succinamide
• 英文别名: [[4-[6-(6-aminopurin-9-yl)hexylamino]-4-oxobutanoyl]amino] (7R,8S,9S,10R,13S,14S,17S)-17-acetyl-10,13-dimethyl-3-oxo-1,2,6,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthrene-7-carboxylate
• CAS: 1408059-09-5
• 化学式: C₃₇H₅₁N₇O₆
• 分子量: 689.855
• InChiKey: SHRHLFDDEDTKDC-MEQRUPAYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.9
• 重原子数：
  50
• 可旋转键数：
  14
• 环数：
  6.0
• sp3杂化的碳原子比例：
  0.68
• 拓扑面积：
  188
• 氢给体数：
  3
• 氢受体数：
  10

反应信息

• 作为产物：
  描述：

  N-羟基丁二酰亚胺 、 progesterone-7α-carboxylic acid 、 9-(6-aminohexyl)adenine 在 N,N'-二环己基碳二亚胺 、 N,N-二异丙基乙胺 作用下， 以 N,N-二甲基甲酰胺 为溶剂， 反应 19.0h， 以37%的产率得到7α-[6-(6-amino-9H-purin-9-yl)hexylcarbamoyl]pregn-4-en-3,20-dione
  参考文献：
  名称：

  Progesterone–adenine hybrids as bivalent inhibitors of P-glycoprotein-mediated multidrug efflux: Design, synthesis, characterization and biological evaluation

  摘要：

  Bivalent ligands were designed on the basis of the described close proximity of the ATP-site and the putative steroid-binding site of P-glycoprotein (ABCB1). The syntheses of 19 progesterone-adenine hybrids are described. Their abilities to inhibit P-glycoprotein-mediated daunorubicin efflux in K562/R7 human leukemic cells overexpressing P-glycoprotein were evaluated versus progesterone. The hybrid with a hexamethylene linker chain showed the best inhibitory potency. The efficiency of these progesterone-adenine hybrids depends on two main factors: (i) the nature of the linker and (ii) its attachment point on the steroid skeleton. (C) 2012 Elsevier Inc. All rights reserved.

  DOI：

  10.1016/j.steroids.2012.07.010

文献信息

• Progesterone–adenine hybrids as bivalent inhibitors of P-glycoprotein-mediated multidrug efflux: Design, synthesis, characterization and biological evaluation
  作者：Waël Zeinyeh、Zahia Mahiout、Sylvie Radix、Thierry Lomberget、Axel Dumoulin、Roland Barret、Catherine Grenot、Luc Rocheblave、Eva-Laure Matera、Charles Dumontet、Nadia Walchshofer

  DOI：10.1016/j.steroids.2012.07.010

  日期：2012.10

  Bivalent ligands were designed on the basis of the described close proximity of the ATP-site and the putative steroid-binding site of P-glycoprotein (ABCB1). The syntheses of 19 progesterone-adenine hybrids are described. Their abilities to inhibit P-glycoprotein-mediated daunorubicin efflux in K562/R7 human leukemic cells overexpressing P-glycoprotein were evaluated versus progesterone. The hybrid with a hexamethylene linker chain showed the best inhibitory potency. The efficiency of these progesterone-adenine hybrids depends on two main factors: (i) the nature of the linker and (ii) its attachment point on the steroid skeleton. (C) 2012 Elsevier Inc. All rights reserved.