[17(20)E]-N-[(3β-hydroxy)-21-oxopregna-5,17(20)-dien-21-yl]glycine dimethyl amide | 1428124-54-2

• 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: [17(20)E]-N-[(3β-hydroxy)-21-oxopregna-5,17(20)-dien-21-yl]glycine dimethyl amide
• 英文别名: 2-[[(2E)-2-[(3S,8R,9S,10R,13S,14S)-3-hydroxy-10,13-dimethyl-1,2,3,4,7,8,9,11,12,14,15,16-dodecahydrocyclopenta[a]phenanthren-17-ylidene]acetyl]amino]-N,N-dimethylacetamide
• CAS: 1428124-54-2
• 化学式: C₂₅H₃₈N₂O₃
• 分子量: 414.588
• InChiKey: FQIXGPSOAGOLOU-LQKWLNOTSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.1
• 重原子数：
  30
• 可旋转键数：
  3
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.76
• 拓扑面积：
  69.6
• 氢给体数：
  2
• 氢受体数：
  3

反应信息

• 作为产物：
  描述：

  2-[[(2E)-2-[(3S,8R,9S,10R,13S,14S)-3-hydroxy-10,13-dimethyl-1,2,3,4,7,8,9,11,12,14,15,16-dodecahydrocyclopenta[a]phenanthren-17-ylidene]acetyl]amino]acetic acid 在 三乙胺 作用下， 以 乙醇 、 二氯甲烷 为溶剂， 反应 4.17h， 生成 [17(20)E]-N-[(3β-hydroxy)-21-oxopregna-5,17(20)-dien-21-yl]glycine dimethyl amide
  参考文献：
  名称：

  Pregna-5,17(20)-dien-21-oyl amides affecting sterol and triglyceride biosynthesis in Hep G2 cells

  摘要：

  Synthesis of series [17(20)Z]- and [17(20)E]-pregna-5,17(20)-dien-21-oyl amides, containing polar substituents in amide moiety, based on rearrangement of 17 alpha-bromo-21-iodo-3 beta-acetoxypregn-5-en-20-one caused by amines, is presented. The titled compounds were evaluated for their potency to regulate sterol and triglyceride biosynthesis in human hepatoma Hep G2 cells in comparison with 25-hydroxycholesterol. Three [17(20)E]-pregna-5,17(20)-dien-21-oyl amides at a concentrations of 5 mu M inhibited sterol biosynthesis and stimulated triglyceride biosynthesis; their regulatory potency was dependent on the structure of amide moiety; the isomeric [17(20)Z]-pregna-5,17(20)-dien-21-oyl amides were inactive. (C) 2013 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2013.02.026

文献信息

• Pregna-5,17(20)-dien-21-oyl amides affecting sterol and triglyceride biosynthesis in Hep G2 cells
  作者：Sergey V. Stulov、Olga V. Mankevich、Nikita O. Dugin、Roman A. Novikov、Vladimir P. Timofeev、Alexander Yu. Misharin

  DOI：10.1016/j.bmcl.2013.02.026

  日期：2013.4

  Synthesis of series [17(20)Z]- and [17(20)E]-pregna-5,17(20)-dien-21-oyl amides, containing polar substituents in amide moiety, based on rearrangement of 17 alpha-bromo-21-iodo-3 beta-acetoxypregn-5-en-20-one caused by amines, is presented. The titled compounds were evaluated for their potency to regulate sterol and triglyceride biosynthesis in human hepatoma Hep G2 cells in comparison with 25-hydroxycholesterol. Three [17(20)E]-pregna-5,17(20)-dien-21-oyl amides at a concentrations of 5 mu M inhibited sterol biosynthesis and stimulated triglyceride biosynthesis; their regulatory potency was dependent on the structure of amide moiety; the isomeric [17(20)Z]-pregna-5,17(20)-dien-21-oyl amides were inactive. (C) 2013 Elsevier Ltd. All rights reserved.