(S)-6,7-bis(tert-butyldimethylsilyloxy)-1,2,3,4-tetrahydroisoquin-3-yl methanol | 1449406-03-4

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 四氢异喹啉
• 英文名称: (S)-6,7-bis(tert-butyldimethylsilyloxy)-1,2,3,4-tetrahydroisoquin-3-yl methanol
• 英文别名: [(3S)-6,7-bis[[tert-butyl(dimethyl)silyl]oxy]-1,2,3,4-tetrahydroisoquinolin-3-yl]methanol
• CAS: 1449406-03-4
• 化学式: C₂₂H₄₁NO₃Si₂
• 分子量: 423.743
• InChiKey: KEECNHKDKFHWDB-SFHVURJKSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  5.46
• 重原子数：
  28
• 可旋转键数：
  7
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.73
• 拓扑面积：
  50.7
• 氢给体数：
  2
• 氢受体数：
  4

反应信息

• 作为反应物：
  描述：

  [ruthenium(II)(η⁶-1-methyl-4-isopropyl-benzene)(chloride)(μ-chloride)]₂ 、 (S)-6,7-bis(tert-butyldimethylsilyloxy)-1,2,3,4-tetrahydroisoquin-3-yl methanol 在 三乙胺 作用下， 以 二氯甲烷 为溶剂， 反应 3.25h， 生成
  参考文献：
  名称：

  Anticancer activity of ruthenium(II) arene complexes bearing 1,2,3,4-tetrahydroisoquinoline amino alcohol ligands

  摘要：

  Ruthenium complexes offer potential reduced toxicity compared to current platinum anticancer drugs. 1,2,3,4-tetrahydrisoquinoline amino alcohol ligands were synthesised, characterised and coordinated to an organometallic Ru(II) centre. These complexes were evaluated for activity against the cancer cell lines MCF-7, A549 and MDA-MB-231 as well as for toxicity in the normal cell line MDBK. They were observed to be moderately active against only the MCF-7 cells with the best IC50 value of 34 mu M for the cis-diastereomeric complex C4. They also displayed excellent selectivity by being relatively inactive against the normal MDBK cell line with SI values ranging from 2.3 to 7.4. (C) 2013 Elsevier Masson SAS. All rights reserved.

  DOI：

  10.1016/j.ejmech.2013.05.048
• 作为产物：
  描述：

  左旋多巴 在 lithium aluminium tetrahydride 、 氯化亚砜 、 硫酸 、 N,N-二异丙基乙胺 作用下， 以 四氢呋喃 、 N,N-二甲基甲酰胺 为溶剂， 反应 9.58h， 生成 (S)-6,7-bis(tert-butyldimethylsilyloxy)-1,2,3,4-tetrahydroisoquin-3-yl methanol
  参考文献：
  名称：

  Anticancer activity of ruthenium(II) arene complexes bearing 1,2,3,4-tetrahydroisoquinoline amino alcohol ligands

  摘要：

  Ruthenium complexes offer potential reduced toxicity compared to current platinum anticancer drugs. 1,2,3,4-tetrahydrisoquinoline amino alcohol ligands were synthesised, characterised and coordinated to an organometallic Ru(II) centre. These complexes were evaluated for activity against the cancer cell lines MCF-7, A549 and MDA-MB-231 as well as for toxicity in the normal cell line MDBK. They were observed to be moderately active against only the MCF-7 cells with the best IC50 value of 34 mu M for the cis-diastereomeric complex C4. They also displayed excellent selectivity by being relatively inactive against the normal MDBK cell line with SI values ranging from 2.3 to 7.4. (C) 2013 Elsevier Masson SAS. All rights reserved.

  DOI：

  10.1016/j.ejmech.2013.05.048