N-hexyl,N-methyl-3-(3',17'β-dihydroxy-1',3',5'(10')-estratrien-17'α-yl)-2-propynamide | 252955-46-7

• 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: N-hexyl,N-methyl-3-(3',17'β-dihydroxy-1',3',5'(10')-estratrien-17'α-yl)-2-propynamide
• 英文别名: 3-[(8R,9S,13S,14S,17S)-3,17-dihydroxy-13-methyl-7,8,9,11,12,14,15,16-octahydro-6H-cyclopenta[a]phenanthren-17-yl]-N-hexyl-N-methylprop-2-ynamide
• CAS: 252955-46-7
• 化学式: C₂₈H₃₉NO₃
• 分子量: 437.623
• InChiKey: HFSNRZOBVBIQSV-NHDOVPPCSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  5.8
• 重原子数：
  32
• 可旋转键数：
  6
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.68
• 拓扑面积：
  60.8
• 氢给体数：
  2
• 氢受体数：
  3

反应信息

• 作为反应物：
  描述：

  N-hexyl,N-methyl-3-(3',17'β-dihydroxy-1',3',5'(10')-estratrien-17'α-yl)-2-propynamide 在 palladium on activated charcoal 氢气 作用下， 以 乙酸乙酯 为溶剂， 以52%的产率得到N-hexyl,N-methyl-3-(3',17'β-dihydroxy-1',3',5'(10')-estratrien-17'α-yl)-propanamide
  参考文献：
  名称：

  17α-Alkan (or alkyn) amide derivatives of estradiol as inhibitors of steroid-sulfatase activity

  摘要：

  To develop inhibitors of steroid sulfatase without residual estrogenic activity, we have designed a series of estradiol (E-2) derivatives bearing an alkan (or alkyn) amide side chain at position 17 alpha. A hydrophobic alkyl group was selected from our previous study where 17 alpha-octyl-E-2 was found to inhibit strongly the steroid-sulfatase activity. Furthermore, it is known that an alkylamide side chain blocks the estrogen-receptor activation. Starting from ethynylestradiol, the chemical synthesis of target compounds was short and efficient with overall yields of 22-42% (3 or 4 steps). Among these compounds, N-octyl,N-methyl-3-(3',17' beta-dihydroxy-1',3',5'(10')-estratrien-17' alpha-yl)-propanamide (15) was the most potent inhibitor, with an IC50 value of 0.08 mu M for the transformation of estrone sulfate (E1S) to estrone (E-1) by homogenated JEG-3 cells. N-butyl, N-hexyl, and N,N-dioctyl propanamide derivatives of E-2 (IC50 values of 6.4, 2.8, and >20 mu M, respectively) were less potent inhibitors than N-octyl analog 15. Furthermore, the unsaturated propynamide analog of 15 gave lower inhibition (four times) than the saturated compound. Compound 15 is also about 100-fold more effective in interacting with the enzyme than substrate E1S itself. The ability of target compounds to bind the estrogen receptor, to stimulate the proliferation of estrogen-sensitive ZR-75-1 cells, or to inhibit the E-2-stimulation of ZR-75-1 cells was also evaluated. Although a mixed estrogenic/anti-estrogenic activity was obtained for tested compounds at 1 mu M, no estrogenic activity was observed at 0.03 mu M for 15. In conclusion, a promising inhibitor of steroid-sulfatase activity was obtained by introducing a hydrophobic octyl group in a 17 alpha-propanamide side chain of E-2, but further structure-activity relationships (SAR) studies are necessary to minimize the residual estrogenic activity. (C) 1999 Elsevier Science Inc. All rights reserved.

  DOI：

  10.1016/s0039-128x(99)00060-4
• 作为产物：
  描述：

  N-hexyl,N-methyl-3-[3'-(i-butyloxy-carbonyloxy)-17'β-hydroxy-1',3',5'(10')-estratrien-17'α-yl]-2-propynamide 在 水 、 potassium carbonate 作用下， 以 甲醇 为溶剂， 反应 3.0h， 以90%的产率得到N-hexyl,N-methyl-3-(3',17'β-dihydroxy-1',3',5'(10')-estratrien-17'α-yl)-2-propynamide
  参考文献：
  名称：

  17α-Alkan (or alkyn) amide derivatives of estradiol as inhibitors of steroid-sulfatase activity

  摘要：

  To develop inhibitors of steroid sulfatase without residual estrogenic activity, we have designed a series of estradiol (E-2) derivatives bearing an alkan (or alkyn) amide side chain at position 17 alpha. A hydrophobic alkyl group was selected from our previous study where 17 alpha-octyl-E-2 was found to inhibit strongly the steroid-sulfatase activity. Furthermore, it is known that an alkylamide side chain blocks the estrogen-receptor activation. Starting from ethynylestradiol, the chemical synthesis of target compounds was short and efficient with overall yields of 22-42% (3 or 4 steps). Among these compounds, N-octyl,N-methyl-3-(3',17' beta-dihydroxy-1',3',5'(10')-estratrien-17' alpha-yl)-propanamide (15) was the most potent inhibitor, with an IC50 value of 0.08 mu M for the transformation of estrone sulfate (E1S) to estrone (E-1) by homogenated JEG-3 cells. N-butyl, N-hexyl, and N,N-dioctyl propanamide derivatives of E-2 (IC50 values of 6.4, 2.8, and >20 mu M, respectively) were less potent inhibitors than N-octyl analog 15. Furthermore, the unsaturated propynamide analog of 15 gave lower inhibition (four times) than the saturated compound. Compound 15 is also about 100-fold more effective in interacting with the enzyme than substrate E1S itself. The ability of target compounds to bind the estrogen receptor, to stimulate the proliferation of estrogen-sensitive ZR-75-1 cells, or to inhibit the E-2-stimulation of ZR-75-1 cells was also evaluated. Although a mixed estrogenic/anti-estrogenic activity was obtained for tested compounds at 1 mu M, no estrogenic activity was observed at 0.03 mu M for 15. In conclusion, a promising inhibitor of steroid-sulfatase activity was obtained by introducing a hydrophobic octyl group in a 17 alpha-propanamide side chain of E-2, but further structure-activity relationships (SAR) studies are necessary to minimize the residual estrogenic activity. (C) 1999 Elsevier Science Inc. All rights reserved.

  DOI：

  10.1016/s0039-128x(99)00060-4