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N-(2-nitrophenyl)-N'-(N-phenylpiperazin-4-yl)urea | 1394922-00-9

中文名称
——
中文别名
——
英文名称
N-(2-nitrophenyl)-N'-(N-phenylpiperazin-4-yl)urea
英文别名
N-(2-nitrophenyl)-4-phenylpiperazine-1-carboxamide
N-(2-nitrophenyl)-N'-(N-phenylpiperazin-4-yl)urea化学式
CAS
1394922-00-9
化学式
C17H18N4O3
mdl
——
分子量
326.355
InChiKey
BEOVSJAAHWICRV-UHFFFAOYSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

计算性质

  • 辛醇/水分配系数(LogP):
    2.95
  • 重原子数:
    24.0
  • 可旋转键数:
    3.0
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.24
  • 拓扑面积:
    78.72
  • 氢给体数:
    1.0
  • 氢受体数:
    4.0

反应信息

  • 作为产物:
    描述:
    N-苯基哌嗪异腈酸2-硝基苯1,4-二氧六环 为溶剂, 以71%的产率得到N-(2-nitrophenyl)-N'-(N-phenylpiperazin-4-yl)urea
    参考文献:
    名称:
    取代的尿素衍生物:一类有效的抗抑郁药
    摘要:
    合成了一系列十四(14)种N-硝基苯基-N'-(烷基/芳基)脲和对称的1,3-二取代的脲衍生物,并评估了它们在小鼠中的抗抑郁活性。其中,N-(4-硝基苯基)-N'-(1'-苯乙基)脲(1)具有很强的抗抑郁作用,其固定时间显着减少(89.83%),而化合物2-6具有活性值在36%至59%之间,也比标准苯乙嗪大。化合物7-9在将小鼠的不动周期减少26.20至31.01%方面不太有效。抗抑郁活性的这种变化幅度似乎与硝基相对于母体分子1、2和8的位置有关。硝基处在对位的化合物1被证明是最有效的抗抑郁剂。但是,活动减少了
    DOI:
    10.2174/157340612800786615
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文献信息

  • Antiproliferative effects of novel urea derivatives against human prostate and lung cancer cells; and their inhibition of β-glucuronidase activity
    作者:Shahnaz Perveen、Sana Mustafa、Kehkashan Qamar、Ahsana Dar、Khalid M. Khan、Muhammad Iqbal Choudhary、Ajmal Khan、Wolfgang Voelter
    DOI:10.1007/s00044-013-0702-5
    日期:2014.3
    Twenty-one novel urea derivatives were synthesized and their structures characterized by mass, NMR, IR, and UV spectroscopy. These compounds were evaluated for their antiproliferative profile against human PC-3 (prostate) and NCI-H460 (lung) cancer cell lines. Among them, compound 21 N-(3-nitrophenyl)-N'-(1-phenylethyl)urea was found to be active against both PC-3 (IC50 +/- A SEM: 20.13 +/- A 0.91 mu M) and NCI-H460 (GI(50): 22 +/- A 2.6 mu M) cell lines; hence has the potential to be further studied as anticancer agent. These compounds were also investigated for their ability to inhibit urease, beta-glucuronidase, and phosphodiesterase enzymes. N-(2,6-Dimethylphenyl)-N'-(4'-nitrophenyl)urea (1) demonstrated 90 % inhibition of beta-glucuronidase enzyme (IC50 +/- A SEM: 3.38 +/- A 0.043 mu M).
  • Perveen, Shahnaz; Mustafa, Sana; Khan, Khalid Mohammed, Journal of the Chemical Society of Pakistan, 2013, vol. 35, # 6, p. 1603 - 1611
    作者:Perveen, Shahnaz、Mustafa, Sana、Khan, Khalid Mohammed、Choudhary, Muhammad Iqbal
    DOI:——
    日期:——
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