Discodermolide-7-acetate

• 分子结构分类: 有机化合物 - 脂质和类脂质分子 - 异戊烯醇脂质
• 英文名称: Discodermolide-7-acetate
• 英文别名: [(2S,3Z,5S,6S,7S,8Z,11S,12R,13S,14S,15S,16Z)-14-carbamoyloxy-6,12-dihydroxy-1-[(2S,3R,4S,5R)-4-hydroxy-3,5-dimethyl-6-oxooxan-2-yl]-5,7,9,11,13,15-hexamethylnonadeca-3,8,16,18-tetraen-2-yl] acetate
• 化学式: C₃₅H₅₇NO₉
• 分子量: 635.839
• InChiKey: XDSYTCKUOLOFAP-WSJTUFDFSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  6
• 重原子数：
  45
• 可旋转键数：
  19
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.69
• 拓扑面积：
  166
• 氢给体数：
  4
• 氢受体数：
  9

反应信息

• 作为产物：
  描述：

  乙酸酐 、 盘皮海绵内酯 在 吡啶 作用下， 以1.0 mg的产率得到Discodermolide-3,11-diacetate
  参考文献：
  名称：

  Acetylated Analogues of the Microtubule-Stabilizing Agent Discodermolide:  Preparation and Biological Activity

  摘要：

  A series of eight discodermolide acetates have been prepared using natural (+)-discodermolide and evaluated for in vitro cytotoxicity against the cultured murine P-388 leukemia cells. The acetylated analogues showed a significant variation of cytotoxicity and suggested the importance of C-11 and C-17 hydroxyl groups for potency. The preparation and structure elucidation of the new analogues are described.

  DOI：

  10.1021/np000423e

文献信息

• Acetylated Analogues of the Microtubule-Stabilizing Agent Discodermolide:  Preparation and Biological Activity
  作者：Sarath P. Gunasekera、Ross E. Longley、Richard A. Isbrucker

  DOI：10.1021/np000423e

  日期：2001.2.1

  A series of eight discodermolide acetates have been prepared using natural (+)-discodermolide and evaluated for in vitro cytotoxicity against the cultured murine P-388 leukemia cells. The acetylated analogues showed a significant variation of cytotoxicity and suggested the importance of C-11 and C-17 hydroxyl groups for potency. The preparation and structure elucidation of the new analogues are described.