1-(4-methoxyphenyl)pyrimidine-2,4,6(1H,3H,5H)-trione | 69457-35-8

• 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: 1-(4-methoxyphenyl)pyrimidine-2,4,6(1H,3H,5H)-trione
• 英文别名: 1-(4-methoxyphenyl)pyrimidin-2,4,6(1H,3H,5H)-trione；1-(4-Methoxyphenyl)-1,3-diazinane-2,4,6-trione
• CAS: 69457-35-8
• 化学式: C₁₁H₁₀N₂O₄
• mdl: MFCD00552564
• 分子量: 234.211
• InChiKey: QQZJAOVFTGBDSP-UHFFFAOYSA-N

物化性质

• 熔点：
  190 °C
• 密度：
  1.367±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  0.5
• 重原子数：
  17
• 可旋转键数：
  2
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.181
• 拓扑面积：
  75.7
• 氢给体数：
  1
• 氢受体数：
  4

反应信息

• 作为反应物：
  描述：

  1-(4-methoxyphenyl)pyrimidine-2,4,6(1H,3H,5H)-trione 在 溴 作用下， 生成 5,5-dibromo-1-(4-methoxyphenyl)-1,3-diazinane-2,4,6-trione
  参考文献：
  名称：

  Synthesis of Novel Galactopyranosyl‐Derived Spiro Barbiturates

  摘要：

  Malonic acid undergoes condensation readily with ureas to yield barbituric acids 2, which on bromination give 5,5-dibromobarbituric acids 3. Reaction of alpha-D-galactose with these 5,5-dibromo barbituric acids afforded 2,3-alpha-D-galactopyrano-1,4-dioxo-7,9-diaza-spiro[4,5]deca-6,8,10-triones 4. The structures of the products have been assigned on the basis of H-1 NMR, C-13 NMR, FAB-MS, optical activity, and elemental analysis. The title compounds are found to have antibacterial and antifungal activities.

  DOI：

  10.1080/07328300601039328
• 作为产物：
  描述：

  甲氧苯胺 在 sodium 、 溶剂黄146 、 尿素 作用下， 以 乙醇 、 水 为溶剂， 反应 5.0h， 生成 1-(4-methoxyphenyl)pyrimidine-2,4,6(1H,3H,5H)-trione
  参考文献：
  名称：

  优化用于治疗急性早幼粒细胞白血病的有效的，选择性的，可逆的LSD1抑制剂5-亚芳基巴比妥酸盐

  摘要：

  组蛋白赖氨酸特异性脱甲基酶1（LSD1）在各种血液系统疾病中过表达，被公认为是血液药物的有希望的靶标。在这项研究中，结合生物评估的基于分子对接的虚拟筛选被用来鉴定5-芳基巴比妥酸酯的新骨架作为LSD1的小分子抑制剂。在合成的衍生物中，12a 对MAO-A和MAO-B表现出可逆和有效的抑制作用（IC 50 = 0.41μM）和高选择性。值得注意的是，12a强烈诱导了对急性早幼粒细胞白血病NB4细胞系的分化作用，并明显提高了组蛋白3赖氨酸4（H3K4）的甲基化水平。我们的研究结果表明5-芳基巴比妥酸酯可能代表了LSD1抑制剂的新骨架和12a应该作为进一步研究的有希望的媒介。

  DOI：

  10.1016/j.bmc.2018.08.026

文献信息

• 발모촉진용 조성물
  申请人：Pusan National University Industry-University Cooperation Foundation 부산대학교 산학협력단(220040044843) BRN ▼621-82-06530

  公开号：KR101732929B1

  公开（公告）日：2017-05-11

  본 발명은 신규한 바비투르산(Barbiturate) 및 싸이오바비투르산(thiobarbiturate) 유도체 및 이를 이용한 발모촉진용 조성물에 관한 것으로, 상기 바비투르산(Barbiturate) 및 싸이오바비투르산(thiobarbiturate) 유도체들은 동물모델에서 모발성장을 촉진할 뿐 아니라, Wnt/β-카테닌과 모발성장인자의 신호전달 조절을 촉진시키고 세포 사멸기전을 억제함으로써 모발의 생장을 촉진하여 우수한 발모 효과를 나타냄에 따라, 본 발명의 바비투르산(Barbiturate) 및 싸이오바비투르산(thiobarbiturate) 유도체는 발모촉진용 조성물로 사용될 수 있다.

  本发明涉及一种新的巴比妥酸（Barbiturate）和硫代巴比妥酸（thiobarbiturate）衍生物以及它们用于促进头发生长的组合物，所述的巴比妥酸（Barbiturate）和硫代巴比妥酸（thiobarbiturate）衍生物不仅可以促进动物模型中的毛发生长，还可以通过促进Wnt/β-连环蛋白和毛发生长因子的信号传导调节，抑制细胞凋亡机制，从而促进头发生长，显示出优异的促发效果，因此，本发明的巴比妥酸（Barbiturate）和硫代巴比妥酸（thiobarbiturate）衍生物可用作促进头发生长的组合物。
• A new method for the synthesis of 5-amidinobarbiturates
  作者：I. V. Paramonov、N. A. Belyaev、V. A. Bakulev

  DOI：10.1007/s11172-007-0253-3

  日期：2007.8

  The reactions of 5-[arylamino(methylthio)methylene]pyrimidine-2,4,6(1H,3H,5H)-triones with different aliphatic and aromatic amines were studied. A series of 5-amidinobarbiturates was synthesized. A new and preparatively convenient method for their synthesis appropriate for the use in the combinatorial chemistry was developed.

  研究了5-[芳基氨基(甲硫基)亚甲基]嘧啶-2,4,6(1H,3H,5H)-triones与不同脂肪族和芳香族胺的反应。合成了一系列 5-脒基巴比妥酸盐。开发了一种新的、制备方便的合成方法，适用于组合化学。
• Aggregated dyes for radiation-sensitive elements
  申请人：EASTMAN KODAK COMPANY

  公开号：EP0778493A1

  公开（公告）日：1997-06-11

  A dispersion comprising an aqueous medium having dispersed therein an aggregated dye of the Formula (I): wherein X is oxygen or sulfur; R1-R4 each independently represent an unsubstituted or substituted alkyl group, an unsubstituted or substituted aryl group or an unsubstituted or substituted heteroaryl group; L1, L2 and L3 each independently represent substituted or unsubstituted methine groups; M+ represents a proton or an inorganic or organic cation; and n is 0, 1, 2 or 3 and wherein the aggregated dye in the dispersion has an absorption halfbandwidth of less than 55 nm.

  一种分散体，包括一种水介质，其中分散有式(I)的聚集染料： 其中 X 是氧或硫；R1-R4 各自独立地代表未取代或取代的烷基、未取代或取代的芳基或未取代或取代的杂芳基；L1、L2 和 L3 各自独立地代表取代或未取代的甲基；M+ 代表质子或无机或有机阳离子；n 是 0、1、2 或 3，其中分散液中的聚集染料的吸收半带宽小于 55 nm。
• ——
  作者：K. A. Krasnov、V. G. Kartsev、E. E. Santarovich

  DOI：10.1023/a:1019973404301

  日期：——
• Synthesis and antitumor evaluation of novel cyclic arylsulfonylureas: ADME-T and pharmacophore prediction
  作者：Ibrahim M. El-Deeb、Said M. Bayoumi、Magda A. El-Sherbeny、Alaa A.-M. Abdel-Aziz

  DOI：10.1016/j.ejmech.2010.02.038

  日期：2010.6

  Novel derivatives of 5-(substituted)benzylidene-3-(4-substituted)phenylsulfonylimidazolidine-2,4-diones (3a-r), 1-(4-substituted)phenylsulfonyl-3-(4-substituted)phenylpyrimidine-2,4,6-(1H,3H,5H)-triones (6a-l), and 3-(4-substituted)phenyl-1-(4-substituted)phenylsulfonylquinazoline-2,4(1H,3H)-diones (8a-l) have been synthesized and tested for their antitumor activity against 60 tumor cell lines taken from 9 different organs. The tested compounds have showed good inhibitory effect at the ovarian cancer (IGROV1) cell line. A significant inhibition for (RXF393) renal cancer cells was observed with series 3 compounds, while in the other two series 6 and 8, there was a significant inhibition of ovarian cancer cells (OVCAR-8) and melanoma cells (SK-MEL-2). Interestingly, beside the strong inhibition of compound 3q to IGROV1 and RXF393 cells, a great inhibition (199 62%) for (M14) Melanoma cells was observed at the tested concentration (10 mu M) ADME-T and pharmacophore prediction methodology were used to study the antitumor activity of the most active compounds and to identify the structural features required for antitumor activity.