摩熵化学
数据库官网
小程序
打开微信扫一扫
首页 分子通 化学资讯 化学百科 反应查询 关于我们
请输入关键词

6-Methyl-2-oxo-4-thiophen-2-yl-8-[1-thiophen-2-yl-meth-(E)-ylidene]-1,2,5,6,7,8-hexahydro-[1,6]naphthyridine-3-carbonitrile

中文名称
——
中文别名
——
英文名称
6-Methyl-2-oxo-4-thiophen-2-yl-8-[1-thiophen-2-yl-meth-(E)-ylidene]-1,2,5,6,7,8-hexahydro-[1,6]naphthyridine-3-carbonitrile
英文别名
(8E)-6-methyl-2-oxo-4-thiophen-2-yl-8-(thiophen-2-ylmethylidene)-5,7-dihydro-1H-1,6-naphthyridine-3-carbonitrile
6-Methyl-2-oxo-4-thiophen-2-yl-8-[1-thiophen-2-yl-meth-(E)-ylidene]-1,2,5,6,7,8-hexahydro-[1,6]naphthyridine-3-carbonitrile化学式
CAS
——
化学式
C19H15N3OS2
mdl
——
分子量
365.48
InChiKey
UVZQXAKBCIKLBZ-XYOKQWHBSA-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):
    1.6
  • 重原子数:
    25
  • 可旋转键数:
    2
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.16
  • 拓扑面积:
    113
  • 氢给体数:
    1
  • 氢受体数:
    5

反应信息

  • 作为产物:
    参考文献:
    名称:
    Synthesis and Biological Evaluation of Certain α,β-Unsaturated Ketones and Their Corresponding Fused Pyridines as Antiviral and Cytotoxic Agents
    摘要:
    A new series of 3,5-bis(arylidene)-4-piperidones, as chalcone analogues carrying variety of aryl and heteroaryl groups, pyrazolo[4,3-c]pyridines, pyrido[4,3-d]pyrimidines, and pyrido[3,2-c]-pyridines, carrying an arylidene moiety, and a series of pyrano[3,2-c]pyridines, as flavone and coumarin isosteres, were synthesized and screened for their in vitro antiviral and antitumor activities at the National Cancer Institute (NCI). Compounds 9 and 18 proved to be active against herpes simplex virus-1 (HSV-1), while compound 13 showed moderate activity against human immunodeficiency virus-1 (HIV-1). Compounds 14, 26, 28, 33, and 35 exhibited a broad spectrum antitumor activity. In addition, compounds 26, 33, and 35 proved to be of moderate selectivity toward leukemia cell lines. The pyrano[3,2-c]pyridines heterocyclic system proved to be the most active antitumors among the investigated heterocycles.
    DOI:
    10.1021/jm000038m
点击查看最新优质反应信息