3-oxa-7-thiaPGE1 methyl ester 11,15-bis(tert-butyldimethylsilyl ether) | 433213-13-9

• 分子结构分类: 有机化合物 - 有机金属化合物 - 有机类金属化合物
• 英文名称: 3-oxa-7-thiaPGE1 methyl ester 11,15-bis(tert-butyldimethylsilyl ether)
• 英文别名: 3-oxa-7-thiaPGE₁ methyl ester 11,15-bis(tert-butyldimethylsilyl ether)
• CAS: 433213-13-9
• 化学式: C₃₁H₆₀O₆SSi₂
• 分子量: 617.051
• InChiKey: WGSPMJXDLCUSOT-VXOUFEQFSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  8.17
• 重原子数：
  40.0
• 可旋转键数：
  17.0
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.87
• 拓扑面积：
  71.06
• 氢给体数：
  0.0
• 氢受体数：
  7.0

反应信息

• 作为反应物：
  描述：

  3-oxa-7-thiaPGE1 methyl ester 11,15-bis(tert-butyldimethylsilyl ether) 在 porcine liver esterase 、 (HF)n*Py 作用下， 以 phosphate buffer 、 乙醇 、 乙腈 为溶剂， 反应 4.5h， 生成 {3-[(1R,2S,3R)-3-Hydroxy-2-((E)-(S)-3-hydroxy-oct-1-enyl)-5-oxo-cyclopentylsulfanyl]-propoxy}-acetic acid
  参考文献：
  名称：

  Design and synthesis of a selective EP4-Receptor agonist. Part 1: discovery of 3,7-DithiaPGE1 derivatives and identification of Their ω chains

  摘要：

  Improvement of EP4-receptor selectivity and the agonist activity by introduction of heteroatoms into the a chain of PGE(1) was investigated. Among the compounds tested, 3,7-dithiaPGE(1) 4a exhibited good EP4-receptor selectivity and agonist activity. Further modification of the omega chain of 3,7-dithiaPGE(1) was performed to improve EP4-receptor selectivity and agonist activity. Of the compounds produced, 16-phenyl-omega-tetranor-3.7-dithiaPGE(1) 4p possessing moderate EP4-receptor selectivity and agonist activity. was identified as a new chemical lead for further optimization by modification of the aromatic moiety. (C) 2002 Elsevier Science Ltd. All rights reserved.

  DOI：

  10.1016/s0968-0896(01)00351-0
• 作为产物：
  描述：

  methyl 6-mercapto-3-oxahexanoate 在 aluminum oxide 、 叔丁基锂 作用下， 以 乙醚 、 正己烷 、 正戊烷 为溶剂， 反应 2.0h， 生成 3-oxa-7-thiaPGE1 methyl ester 11,15-bis(tert-butyldimethylsilyl ether)
  参考文献：
  名称：

  Design and synthesis of a selective EP4-Receptor agonist. Part 1: discovery of 3,7-DithiaPGE1 derivatives and identification of Their ω chains

  摘要：

  Improvement of EP4-receptor selectivity and the agonist activity by introduction of heteroatoms into the a chain of PGE(1) was investigated. Among the compounds tested, 3,7-dithiaPGE(1) 4a exhibited good EP4-receptor selectivity and agonist activity. Further modification of the omega chain of 3,7-dithiaPGE(1) was performed to improve EP4-receptor selectivity and agonist activity. Of the compounds produced, 16-phenyl-omega-tetranor-3.7-dithiaPGE(1) 4p possessing moderate EP4-receptor selectivity and agonist activity. was identified as a new chemical lead for further optimization by modification of the aromatic moiety. (C) 2002 Elsevier Science Ltd. All rights reserved.

  DOI：

  10.1016/s0968-0896(01)00351-0