2-Ethoxy-5-propan-2-yl-7-(2-pyrrolidin-1-ylquinolin-3-yl)quinoline | 1415663-47-6

• 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: 2-Ethoxy-5-propan-2-yl-7-(2-pyrrolidin-1-ylquinolin-3-yl)quinoline
• 英文别名: 2-ethoxy-5-propan-2-yl-7-(2-pyrrolidin-1-ylquinolin-3-yl)quinoline
• CAS: 1415663-47-6
• 化学式: C₂₇H₂₉N₃O
• 分子量: 411.547
• InChiKey: SWGZWBMKPMUYCA-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  6.8
• 重原子数：
  31
• 可旋转键数：
  5
• 环数：
  5.0
• sp3杂化的碳原子比例：
  0.33
• 拓扑面积：
  38.2
• 氢给体数：
  0
• 氢受体数：
  4

反应信息

• 作为反应物：
  描述：

  2-Ethoxy-5-propan-2-yl-7-(2-pyrrolidin-1-ylquinolin-3-yl)quinoline 在 bis-triphenylphosphine-palladium(II) chloride 、 正丁基锂 、 水 、 sodium carbonate 、 氯化铵 、 二异丙胺 作用下， 以 四氢呋喃 、 正己烷 、 水 为溶剂， 反应 19.33h， 生成 4-[7-[2-Ethoxy-5-propan-2-yl-7-(2-pyrrolidin-1-ylquinolin-3-yl)quinolin-3-yl]-5-propan-2-ylquinolin-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
• 作为产物：
  描述：

  7-bromo-2-ethoxy-5-isopropylquinoline 在 三叔丁基膦 、 palladium diacetate 、 sodium carbonate 作用下， 以 1,4-二氧六环 、 水 为溶剂， 反应 2.0h， 生成 2-Ethoxy-5-propan-2-yl-7-(2-pyrrolidin-1-ylquinolin-3-yl)quinoline
  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

文献信息

• Chemical entities that kill senescent cells for use in treating age-related disease
  申请人：Unity Biotechnology, Inc.

  公开号：US10195213B2

  公开（公告）日：2019-02-05

  Disclosed herein are compounds that are effective for treatment of various disease states associated with senescence. The disclosed compounds can be used to eliminate senescent cells for disease treatment. The dosing of the compounds includes both single administration and regimens of cycling dosages.

  本文公开的化合物可有效治疗与衰老有关的各种疾病状态。所公开的化合物可用于消除衰老细胞以治疗疾病。化合物的给药方式包括单次给药和循环给药。
• COMPOUNDS AND THERAPEUTIC USES
  申请人：Unity Biotechnology, Inc.

  公开号：US20170281649A1

  公开（公告）日：2017-10-05

  Disclosed herein are compounds that are effective for treatment of various disease states associated with senescence. The disclosed compounds can be used to eliminate senescent cells for disease treatment. The dosing of the compounds includes both single administration and regimens of cycling dosages.
• Synthesis and biological activities of polyquinoline derivatives: New Bcl-2 family protein modulators
  作者：Emmanuelle Saugues、Anne-Laure Debaud、Fabrice Anizon、Nathalie Bonnefoy、Pascale Moreau

  DOI：10.1016/j.ejmech.2012.09.012

  日期：2012.11

  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.