[(3R,5R,8R,9S,10S,12S,13S,14S,17R)-12-acetyloxy-17-[(2S)-1-(benzylamino)propan-2-yl]-10,13-dimethyl-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-yl] acetate | 1059124-55-8

• 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: [(3R,5R,8R,9S,10S,12S,13S,14S,17R)-12-acetyloxy-17-[(2S)-1-(benzylamino)propan-2-yl]-10,13-dimethyl-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-yl] acetate
• CAS: 1059124-55-8
• 化学式: C₃₃H₄₉NO₄
• 分子量: 523.756
• InChiKey: ALXOQCMPDLIDDN-BPRGTMDCSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  7.3
• 重原子数：
  38
• 可旋转键数：
  9
• 环数：
  5.0
• sp3杂化的碳原子比例：
  0.76
• 拓扑面积：
  64.6
• 氢给体数：
  1
• 氢受体数：
  5

反应信息

• 作为产物：
  描述：

  苄胺 、 acetic acid (3R,5R,8R,9S,10S,12S,13S,14S,17R)-3-acetoxy-10,13-dimethyl-17-((S)-1-methyl-2-oxoethyl)-hexadecahydrocyclopenta[a]phenanthren-12-yl ester 在 三乙酰氧基硼氢化钠 、 溶剂黄146 作用下， 以 二氯甲烷 为溶剂， 反应 9.5h， 以50%的产率得到[(3R,5R,8R,9S,10S,12S,13S,14S,17R)-12-acetyloxy-17-[(2S)-1-(benzylamino)propan-2-yl]-10,13-dimethyl-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-yl] acetate
  参考文献：
  名称：

  Amino steroids as antimalarial agents

  摘要：

  Using easily accessible deoxycholic acid as the starting material, amino compounds 8a-e and 9a-c were prepared and screened against P. falciparum in vitro. Amino steroid 8d was the most active of the series with a minimum inhibiting concentration (MIC) of 0.5 mu g/mL.

  DOI：

  10.1007/s00044-007-9068-x

文献信息

• Amino steroids as antimalarial agents
  作者：Upasana Sharma、Kumkum Srivastava、Sunil K. Puri、Chandan Singh

  DOI：10.1007/s00044-007-9068-x

  日期：2008.6

  Using easily accessible deoxycholic acid as the starting material, amino compounds 8a-e and 9a-c were prepared and screened against P. falciparum in vitro. Amino steroid 8d was the most active of the series with a minimum inhibiting concentration (MIC) of 0.5 mu g/mL.