diethyl 2-[(4-propoxyanilino)methylidene]propanedioate | 111185-76-3

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯酚醚
• 英文名称: diethyl 2-[(4-propoxyanilino)methylidene]propanedioate
• CAS: 111185-76-3
• 化学式: C₁₇H₂₃NO₅
• 分子量: 321.373
• InChiKey: IYVJLJHMGRVBDA-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.9
• 重原子数：
  23.0
• 可旋转键数：
  9.0
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.41
• 拓扑面积：
  73.86
• 氢给体数：
  1.0
• 氢受体数：
  6.0

反应信息

• 作为反应物：
  描述：

  diethyl 2-[(4-propoxyanilino)methylidene]propanedioate 在 sodium hydroxide 作用下， 以 various solvent(s) 为溶剂， 反应 2.0h， 生成 3-喹啉羧酸,1,4-二氢-4-羰基-6-丙氧基-
  参考文献：
  名称：

  Evaluation of 3-Carboxy-4(1H)-quinolones as Inhibitors of Human Protein Kinase CK2

  摘要：

  Due to the emerging role of protein kinase CK2 as a molecule that participates not only in the development of some cancers but also in viral infections and inflammatory failures, small organic inhibitors of CK2, besides application in scientific research, may have therapeutic significance. In this paper, we present a new class of CK2 inhibitorss3-carboxy-4(1H)-quinolones. This class of inhibitors has been selected via receptor-based virtual screening of the Otava compound library. It was revealed that the most active compounds, 5,6,8-trichloro-4-oxo-1,4-dihydroquinoline-3-carboxylic acid (7) (IC50 = 0.3 mu M) and 4-oxo-1,4-dihydrobenzo[h] quinoline-3-carboxylic acid (9) (IC50 = 1 AM), are ATP competitive (K-i values are 0.06 and 0.28 mu M, respectively). Evaluation of the inhibitors on seven protein kinases shows considerable selectivity toward CK2. According to theoretical calculations and experimental data, a structural model describing the key features of 3-carboxy-4(1H)-quinolones responsible for tight binding to CK2 active site has been developed.

  DOI：

  10.1021/jm050048t
• 作为产物：
  描述：

  diethyl 2-(((4-hydroxyphenyl)amino)methylene)malonate 、 溴丙烷 以82%的产率得到
  参考文献：
  名称：

  OZEKI KOHJI; ISHIZUKA YASUHIRO; SAWADA MASAHIRO; ICHIKAWA TERU; SATO MAKO+, J. PHARM. SOC. JAP., 107,(1987) N 2, 123-134

  摘要：

  DOI：