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2,2-dioxo-1H-thieno[3,2-c][1,2,6]thiadiazin-4-one | 250281-23-3

中文名称
——
中文别名
——
英文名称
2,2-dioxo-1H-thieno[3,2-c][1,2,6]thiadiazin-4-one
英文别名
——
2,2-dioxo-1H-thieno[3,2-c][1,2,6]thiadiazin-4-one化学式
CAS
250281-23-3
化学式
C5H4N2O3S2
mdl
——
分子量
204.23
InChiKey
UNAOACRYFCFFIQ-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

物化性质

  • 密度:
    1.689±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    0.1
  • 重原子数:
    12
  • 可旋转键数:
    0
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    112
  • 氢给体数:
    2
  • 氢受体数:
    5

反应信息

  • 作为反应物:
    描述:
    2,2-dioxo-1H-thieno[3,2-c][1,2,6]thiadiazin-4-one(氯甲基)萘碳酸氢钠 作用下, 以 为溶剂, 反应 24.0h, 生成 1-(Naphthalen-1-ylmethyl)-2,2-dioxothieno[3,2-c][1,2,6]thiadiazin-4-one
    参考文献:
    名称:
    CODES, a novel procedure for ligand-based virtual screening: PDE7 inhibitors as an application example
    摘要:
    Phosphodiesterase (PDE) 7 is a high affinity cAMP-specific PDE whose functional role in T-cells has been the subject of some controversy. Recent findings on tissue distribution, however, support the hypothesis that PDE7 could be a good target for the treatment of airway diseases, T-cell related diseases or central nervous system (CNS) disorders. Therefore, the identification of selective inhibitors targeted against PDE7 enzyme has become an attractive area of research. We report here the first use of the descriptors generated by the CODES program for ligand-based virtual screening. This program codifies molecules from a topological point of view and the generated descriptors are related to the chemical nature of the atoms, the atomic bonds and the connectivity with the rest of the molecule. They are also able to distinguish among stereoisomers. By using this approach, 173 compounds were codified, and their similarity with the reference compound was analysed. Based on the analysis, new potential PDE7 inhibitors have been identified, synthesized and biologically evaluated confirming that CODES descriptors are valid for ligand-based virtual screening and provided new lead compounds for further optimization as potent and selective PDE7 inhibitors. (c) 2007 Elsevier Masson SAS. All rights reserved.
    DOI:
    10.1016/j.ejmech.2007.10.027
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