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(Z)-N-(4-morpholinophenyl)-2-(2-oxoindolin-3-ylidene)hydrazine-1-carbothioamide | 100891-82-5

中文名称
——
中文别名
——
英文名称
(Z)-N-(4-morpholinophenyl)-2-(2-oxoindolin-3-ylidene)hydrazine-1-carbothioamide
英文别名
——
(Z)-N-(4-morpholinophenyl)-2-(2-oxoindolin-3-ylidene)hydrazine-1-carbothioamide化学式
CAS
100891-82-5
化学式
C19H19N5O2S
mdl
——
分子量
381.458
InChiKey
NLXRHVISMAEFPA-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):
    2.17
  • 重原子数:
    27.0
  • 可旋转键数:
    3.0
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.21
  • 拓扑面积:
    77.99
  • 氢给体数:
    3.0
  • 氢受体数:
    5.0

文献信息

  • Isatin-β-thiosemicarbazones as potent herpes simplex virus inhibitors
    作者:Iou-Jiun Kang、Li-Wen Wang、Tsu-An Hsu、Andrew Yueh、Chung-Chi Lee、Yen-Chun Lee、Ching-Yin Lee、Yu-Sheng Chao、Shin-Ru Shih、Jyh-Haur Chern
    DOI:10.1016/j.bmcl.2011.02.037
    日期:2011.4
    A series of isatin-beta-thiosemicarbazones have been designed and evaluated for antiviral activity against herpes simplex virus type 1 (HSV-1) and type 2 (HSV-2) in a plaque reduction assay. Their cytotoxicity was examined using human rhabdomyosarcoma cells (RD cells). Several derivatives of isatin-beta-thiosemicarbazone exhibited significant and selective antiviral activity with low cytotoxicity. It was found that the thiourea group at thiosemicarbazone and the NH functionality at isatin were essential for their anti-herpetic activity. The synthesis and structure-activity relationship studies are presented. (C) 2011 Elsevier Ltd. All rights reserved.
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