2-methoxyamino-5-[1-quinolin-6-yl-meth-(Z)-ylidene]-thiazol-4-one

• 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-methoxyamino-5-[1-quinolin-6-yl-meth-(Z)-ylidene]-thiazol-4-one
• 英文别名: (2Z,5Z)-2-methoxyimino-5-(quinolin-6-ylmethylidene)-1,3-thiazolidin-4-one
• 化学式: C₁₄H₁₁N₃O₂S
• 分子量: 285.326
• InChiKey: HUBFHDCOBSCSRE-WQLSENKSSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3
• 重原子数：
  20
• 可旋转键数：
  2
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.07
• 拓扑面积：
  88.9
• 氢给体数：
  1
• 氢受体数：
  5

反应信息

• 作为产物：
  描述：

  喹啉-6-甲醛 在 sodium acetate 、 溶剂黄146 、 N,N-二异丙基乙胺 作用下， 以 乙醇 、 乙腈 为溶剂， 反应 36.33h， 生成 2-methoxyamino-5-[1-quinolin-6-yl-meth-(Z)-ylidene]-thiazol-4-one
  参考文献：
  名称：

  Synthesis and activity of quinolinyl-methylene-thiazolinones as potent and selective cyclin-dependent kinase 1 inhibitors

  摘要：

  A novel series of quinolinyl-methylene-thiazolinones has been identified as potent and selective cyclin-dependent kinase I (CDK1) inhibitors. Their synthesis and structure activity relationships (SAR) are described. Representative compounds from this class reversibly inhibit CDK1 activity in vitro, and block cell cycle progression in human tumor cell lines, suggesting a potential use as antitumor agents. (c) 2007 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2007.01.081

文献信息

• Thiazolinone unsubstituted quinolines
  申请人：Chen Li

  公开号：US20060004045A1

  公开（公告）日：2006-01-05

  Thiazolinone quinoline derivatives having no substitution on the quinoline ring active as CDK1 inhibitors which are useful as anti-proliferation agents such as for treating solid tumors.

  噻唑酮喹啉衍生物在喹啉环上没有取代基，作为CDK1抑制剂活性，可用作抗增殖剂，例如用于治疗实体肿瘤。
• THIAZOLINONE UNSUBSTITUTED QUINOLINES
  申请人：F.HOFFMANN-LA ROCHE AG

  公开号：EP1765817A1

  公开（公告）日：2007-03-28
• US7326786B2
  申请人：——

  公开号：US7326786B2

  公开（公告）日：2008-02-05
• [EN] THIAZOLINONE UNSUBSTITUTED QUINOLINES<br/>[FR] QUINOLINES INSUBSTITUEES THIAZOLINONE
  申请人：HOFFMANN LA ROCHE

  公开号：WO2006002829A1

  公开（公告）日：2006-01-12

  The present invention refers to thiazolinone quinoline derivatives of the formula (I) having no substitution on the quinoline ring, and being active as CDK1 inhibitors; to processes for the manufacture of said compounds as well as the use of said compounds for the production of medicaments.
• Synthesis and activity of quinolinyl-methylene-thiazolinones as potent and selective cyclin-dependent kinase 1 inhibitors
  作者：Shaoqing Chen、Li Chen、Nam T. Le、Chunlin Zhao、Achyutharao Sidduri、Jian Ping Lou、Christophe Michoud、Louis Portland、Nicole Jackson、Jin-Jun Liu、Fred Konzelmann、Feng Chi、Christian Tovar、Qing Xiang、Yingsi Chen、Yang Wen、Lyubomir T. Vassilev

  DOI：10.1016/j.bmcl.2007.01.081

  日期：2007.4

  A novel series of quinolinyl-methylene-thiazolinones has been identified as potent and selective cyclin-dependent kinase I (CDK1) inhibitors. Their synthesis and structure activity relationships (SAR) are described. Representative compounds from this class reversibly inhibit CDK1 activity in vitro, and block cell cycle progression in human tumor cell lines, suggesting a potential use as antitumor agents. (c) 2007 Elsevier Ltd. All rights reserved.