5-(2-(4-chlorophenyl)hydrazono)pyrimidine-2,4,6(1H,3H,5H)-trione | 7293-30-3

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 二嗪类
• 英文名称: 5-(2-(4-chlorophenyl)hydrazono)pyrimidine-2,4,6(1H,3H,5H)-trione
• 英文别名: pyrimidinetetraone 5-[(4-chloro-phenyl)-hydrazone]；alloxan-5-(4-chloro-phenylhydrazone)；Alloxan-5-(4-chlor-phenylhydrazon)；5-(4-Chlor-phenylhydrazono)-barbitursaeure；5-(p-Chlorphenylhydrazono)-barbitursaeure；5-[(4-chlorophenyl)hydrazinylidene]-1,3-diazinane-2,4,6-trione
• CAS: 7293-30-3
• 化学式: C₁₀H₇ClN₄O₃
• mdl: MFCD00434898
• 分子量: 266.644
• InChiKey: KIJXOIQDPUUOBJ-UHFFFAOYSA-N

物化性质

• 密度：
  1.70±0.1 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  0.47
• 重原子数：
  18.0
• 可旋转键数：
  2.0
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.0
• 拓扑面积：
  99.66
• 氢给体数：
  3.0
• 氢受体数：
  5.0

反应信息

• 作为反应物：
  描述：

  5-(2-(4-chlorophenyl)hydrazono)pyrimidine-2,4,6(1H,3H,5H)-trione 、 乙二胺 以84%的产率得到
  参考文献：
  名称：

  DNA and BSA binding, anticancer and antimicrobial properties of Co(ii), Co(ii/iii), Cu(ii) and Ag(i) complexes of arylhydrazones of barbituric acid

  摘要：

  合成了新型苯肼酮衍生的巴比妥酸化合物，并制备了它们的水溶性AgI、CoII、CoII/III和CuII配合物。其中AgI化合物表现出显著的细胞毒性和抗菌活性。

  DOI：

  10.1039/c5ra20157h
• 作为产物：
  描述：

  巴比妥酸 、 4-氯-偶氮苯 生成 5-(2-(4-chlorophenyl)hydrazono)pyrimidine-2,4,6(1H,3H,5H)-trione
  参考文献：
  名称：

  KING; KING; SPENSLEY, Journal of the Chemical Society, 1947, vol. 25, p. 1247 - 1247

  摘要：

  DOI：

文献信息

• Preparation and hydrogen bonding studies of phenylhydrazone derivatives of alloxan: crystal and molecular structure of pyrimidine-2(1H),4(3H),5,6-tetraone 5-(2-nitrophenyl)hydrazone
  作者：Haydn G. Beaton、Gerald R. Willey、Michael G. B. Drew

  DOI：10.1039/p29870000469

  日期：——

  Eight phenylhydrazone derivatives of pyrimidine-2(1H),4(3H),5,6-tetraone, or 5-oxobarbituric acid (alloxan), are described. Spectroscopic pyrimidine (1H n.m.r., i.r.) data indicate the presence of extensive hydrogen bonding which, as shown by X-ray crystallographic data for the title hydrazone, includes both intra- and inter-molecular interactions. The title hydrazone, C10H7N5O5, is monoclinic, space

  描述了嘧啶-2（1 H），4（3 H），5,6-四酮或5-氧代巴比妥酸（四氧六环）的八种苯hydr衍生物。嘧啶光谱（1 H nmr，ir）数据表明存在广泛的氢键，如标题的X射线晶体学数据所示，该氢键包括分子内和分子间相互作用。标题C 10 H 7 N 5 O 5为单斜晶，空间群P 2 1 / a，a = 9.104（8），b = 17.975（13），c = 10.333（8）Å，β= 113.5（ 1）°，Z = 4.2145已在衍射仪上测量了独立反射，并通过直接方法确定了结构，并将其精炼为R 0.074。在不对称单元中有四个独立的氢键：两个分子内键将N（7）–H（7）连接到苯环的o -NO 2基团和巴比妥酸酯环的羰基上，两个分子间键连接通过对称中心将巴比妥酸酯环的NH位点连接至溶剂NN-二甲基甲酰胺氧原子和另一个巴比妥酸酯环的羰基氧原子。
• Synthesis, activity evaluation, and docking analysis of barbituric acid aryl hydrazone derivatives as RSK2 inhibitors
  作者：Mengzhu Xue、Minghao Xu、Weiqiang Lu、Jin Huang、Honglin Li、Yufang Xu、Xiaofeng Liu、Zhenjiang Zhao

  DOI：10.3109/14756366.2012.681651

  日期：2013.8.1

  The 90 kDa ribosomal S6 kinases (RSKs), especially RSK2, have attracted attention for the development of new anticancer agents. Through structural optimization of the hit compound 1 from our previous study, a series of barbituric acid aryl hydrazone analogues were designed and synthesized as potential RSK2 inhibitors. The most potent one, compound 9, showed a higher activity against RSK2 with an IC50 value of 1.95 mu M. To analyze and elucidate their structure-activity relationship, the homology model of RSK2 N-terminal kinase domain was built and molecular docking simulations were performed, which provide helpful clues to design new inhibitors with desired activities.
• KING; KING; SPENSLEY, Journal of the Chemical Society, 1947, vol. 25, p. 1247 - 1247
  作者：KING、KING、SPENSLEY

  DOI：——

  日期：——
• DNA and BSA binding, anticancer and antimicrobial properties of Co(<scp>ii</scp>), Co(<scp>ii</scp>/<scp>iii</scp>), Cu(<scp>ii</scp>) and Ag(<scp>i</scp>) complexes of arylhydrazones of barbituric acid
  作者：Jessica Palmucci、Kamran T. Mahmudov、M. Fátima C. Guedes da Silva、Fabio Marchetti、Claudio Pettinari、Dezemona Petrelli、Luca A. Vitali、Luana Quassinti、Massimo Bramucci、Giulio Lupidi、Armando J. L. Pombeiro

  DOI：10.1039/c5ra20157h

  日期：——

  Novel arylhydrazones of barbituric acid were synthesized and their water soluble Ag^I, Co^II, Co^II/III and Cu^II complexes obtained. The Ag^I compound shows remarkable cytotoxic and antibacterial activity.

  合成了新型苯肼酮衍生的巴比妥酸化合物，并制备了它们的水溶性AgI、CoII、CoII/III和CuII配合物。其中AgI化合物表现出显著的细胞毒性和抗菌活性。