1-[(4-nitrophenyl)methylideneamino]-3-[(2-oxoindol-3-yl)amino]thiourea | 1452579-94-0

• 分子结构分类: 有机化合物 - 有机酸及其衍生物 - 羧酸及其衍生物
• 英文名称: 1-[(4-nitrophenyl)methylideneamino]-3-[(2-oxoindol-3-yl)amino]thiourea
• CAS: 1452579-94-0；508226-58-2
• 化学式: C₁₆H₁₂N₆O₃S
• 分子量: 368.376
• InChiKey: YOUBSUUCIAEJDT-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  1.75
• 重原子数：
  26.0
• 可旋转键数：
  4.0
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.0
• 拓扑面积：
  121.02
• 氢给体数：
  3.0
• 氢受体数：
  6.0

反应信息

• 作为产物：
  描述：

  靛红 、 1-Amino-3-[(4-nitrophenyl)methylideneamino]thiourea 在 溶剂黄146 作用下， 以 乙醇 为溶剂， 反应 0.03h， 以75%的产率得到1-[(4-nitrophenyl)methylideneamino]-3-[(2-oxoindol-3-yl)amino]thiourea
  参考文献：
  名称：

  Microwave Assisted Synthesis, Characterization of Some New Isatin and Thiophene Derivatives as Cytotoxic and Chemopreventive Agents

  摘要：

  In obtaining some new cytotoxic and chemopreventive agents with potent antiproliferative activity against cancer cells, a series of new beta-isatin aldehyde-N,N'-thiocarbohydrazone, bis-beta-isatin thiocarbohydrazones, bis-beta-isatin carbohydrazones, N,2-bis(thiophen-2-ylmethylidene) thiocarbohydrazone and N,2-bis(thiophen-2-ylmethylidene) carbohydrazone derivatives was synthesized by microwave oriented reaction and evaluated for their in vitro cytotoxic activity. The newly synthesized compounds were characterized based on spectral (FT-IR, NMR, MS) analyses. The inhibitory effects of synthesized compounds on the proliferation of murine leukemia cells (L1210), human T-lymphocyte cells (CEM) and human cervix carcinoma cells (HeLa) were assayed by using MTT assay. The compounds were also tested for their inhibitory effects on Epstein-Barr virus early antigen (EBV-EA) activation induced by 12-O-tetradecanoylphorbol-13-acetate (TPA). In vitro evaluation of these schiff bases revealed mild to moderate cytotoxic activity in a dose dependent manner. The results of the in vitro inhibitory activities of synthetic compounds against EBV-EA activation with IC50 ranges from 485-535 (mol ratio/32pmol/TPA). Chlorine group containing derivatives did not show increased inhibitory activity against tumor promoter TPA induction. Sulphur containing derivatives also did not show a high inhibitory potency in this system.

  DOI：

  10.2174/157018012804586950

文献信息

• Synthesis of thiocarbohydrazide and carbohydrazide derivatives as possible biologically active agents
  作者：Kiran Gangarapu、Sarangapani Manda、Anvesh Jallapally、Sreekanth Thota、Subhas S. Karki、Jan Balzarini、Erik De Clercq、Harukuni Tokuda

  DOI：10.1007/s00044-013-0684-3

  日期：2014.2

  AbstractA series of new β-isatin aldehyde-N,N′-thiocarbohydrazone, bis-β-isatin thiocarbohydrazones, bis-β-isatin carbohydrazones was synthesized by condensation of 5-substituted isatin with thiocarbohydrazide or carbohydrazide. The chemical structures of the newly synthesized compounds were confirmed by FT-IR, 1H NMR, and mass spectral analysis. The synthesized compounds were evaluated for in vitro antiviral

  摘要5-取代靛红与硫代卡巴肼或碳酰肼缩合合成了一系列新的β-靛红醛-N、N′-硫代羰腙、双-β-靛红硫代羰腙、双-β-靛红羰腙。新合成化合物的化学结构经FT-IR、1 H NMR和质谱分析证实。评估了合成的化合物对各种 DNA 和 RNA 病毒株的体外抗病毒活性，但与参考化合物相比显示出中等的抗病毒活性。在所有化合物中，6c在两阶段小鼠皮肤致癌试验中表现出最高的化学预防活性。 图形概要