4-[5-Propan-2-yl-7-(2-propoxyquinolin-3-yl)quinolin-2-yl]morpholine | 1415663-69-2

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 喹啉及其衍生物
• 英文名称: 4-[5-Propan-2-yl-7-(2-propoxyquinolin-3-yl)quinolin-2-yl]morpholine
• 英文别名: 4-[5-propan-2-yl-7-(2-propoxyquinolin-3-yl)quinolin-2-yl]morpholine
• CAS: 1415663-69-2
• 化学式: C₂₈H₃₁N₃O₂
• 分子量: 441.573
• InChiKey: NNSULNYBTSFDTD-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  6.5
• 重原子数：
  33
• 可旋转键数：
  6
• 环数：
  5.0
• sp3杂化的碳原子比例：
  0.36
• 拓扑面积：
  47.5
• 氢给体数：
  0
• 氢受体数：
  5

反应信息

• 作为产物：
  描述：

  2-丙氧基喹啉 在 正丁基锂 、 [1,3-bis(2,6-diisopropylphenyl)imidazol-2-ylidene](3-chloropyridyl)palladium(ll) dichloride 、 potassium tert-butylate 、 水 、 氯化铵 、 二异丙胺 作用下， 以 四氢呋喃 、 正己烷 、 异丙醇 为溶剂， 反应 22.0h， 生成 4-[5-Propan-2-yl-7-(2-propoxyquinolin-3-yl)quinolin-2-yl]morpholine
  参考文献：
  名称：

  Synthesis and biological activities of polyquinoline derivatives: New Bcl-2 family protein modulators

  摘要：

  The synthesis of quinoline derivatives, designed to interact with BCl-x(L), and to inhibit its interaction with pro-apoptotic partners, is described and their biological effects investigated. We showed that 5 out of 28 synthetized compounds restored cell death of 3T3 cells overexpressing Bcl-x(L) following serum starvation. Active compounds were further characterized for their binding capacity to the anti-apoptotic member of the Bcl-2 family, Bcl-x(L) as well as Bcl-2, Bcl-x(L) and Mcl-1, and for their pro-apoptotic activities toward lymphoid tumor cells and peripheral blood mononuclear cells. Altogether our results indicate that dimeric, rather than trimeric quinoline derivatives, represent a new attractive class of BH3 mimetics for cancer therapy. (C) 2012 Elsevier Masson SAS. All rights reserved.

  DOI：

  10.1016/j.ejmech.2012.09.012