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[1,3]Thiazolo[3,2-a]pyrimidin-4-ium

中文名称
——
中文别名
——
英文名称
[1,3]Thiazolo[3,2-a]pyrimidin-4-ium
英文别名
——
[1,3]Thiazolo[3,2-a]pyrimidin-4-ium化学式
CAS
——
化学式
C6H5N2S+
mdl
——
分子量
137.18
InChiKey
ZOYQGPGGBMOMMD-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):
    2.2
  • 重原子数:
    9
  • 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:
    45.2
  • 氢给体数:
    0
  • 氢受体数:
    2

文献信息

  • NOVEL HETEROCYCLIC SYSTEMS AND PHARMACEUTICAL COMPOSITIONS THEREOF
    申请人:University of Sharjah
    公开号:EP3774819A2
    公开(公告)日:2021-02-17
  • [EN] NOVEL HETEROCYCLIC SYSTEMS AND PHARMACEUTICAL COMPOSITIONS THEREOF<br/>[FR] NOUVEAUX SYSTÈMES HÉTÉROCYCLIQUES ET COMPOSITIONS PHARMACEUTIQUES ASSOCIÉES
    申请人:UNIV OF SHARJAH
    公开号:WO2019186384A2
    公开(公告)日:2019-10-03
    Novel heterocyclic systems are herein disclosed, which possess many biological activities, including but not limited to anticancer activity. The disclosed compounds are useful in the treatment of many disease states related to cell proliferation. In particular, new pyran derivatives are provided along with processes for their preparations and methods for their pharmaceutical applications, for example, as anticancer agents. These compounds were found to have antiproliferative effects against multiple cancer cell lines and showed low toxicity to normal fibroblasts. The disclosed compounds also exhibited anticancer properties by inducing caspase-mediated cell death mechanisms and arresting cancer cell progression. Further, these novel compounds were able to target multiple key proteins/enzymes, including thioredoxin reductase, glutathione reductase, transferrin receptors, inisitol-3-phosphate synthase, cystolic aminopeptidase, and transketolase, which are over-expressed in tumor cells.
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