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bis(4,5,6,7-tetrahydrobenzo[d]thiazol-2-yl)disulfide | 23888-56-4

中文名称
——
中文别名
——
英文名称
bis(4,5,6,7-tetrahydrobenzo[d]thiazol-2-yl)disulfide
英文别名
2-(4,5,6,7-Tetrahydro-1,3-benzothiazol-2-yldisulfanyl)-4,5,6,7-tetrahydro-1,3-benzothiazole;2-(4,5,6,7-tetrahydro-1,3-benzothiazol-2-yldisulfanyl)-4,5,6,7-tetrahydro-1,3-benzothiazole
bis(4,5,6,7-tetrahydrobenzo[d]thiazol-2-yl)disulfide化学式
CAS
23888-56-4
化学式
C14H16N2S4
mdl
——
分子量
340.558
InChiKey
ILEZYMARHZUBGD-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

  • 熔点:
    102-105 °C
  • 沸点:
    553.2±60.0 °C(predicted)
  • 密度:
    1.44±0.1 g/cm3(Temp: 20 °C; Press: 760 Torr)(predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    4.9
  • 重原子数:
    20
  • 可旋转键数:
    3
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.57
  • 拓扑面积:
    133
  • 氢给体数:
    0
  • 氢受体数:
    6

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为产物:
    描述:
    2-溴环己酮 在 ammonium persulfate 作用下, 以 四氢呋喃乙醇 为溶剂, 反应 1.5h, 生成 bis(4,5,6,7-tetrahydrobenzo[d]thiazol-2-yl)disulfide
    参考文献:
    名称:
    Development of the First Generation of Disulfide-Based Subtype-Selective and Potent Covalent Pyruvate Dehydrogenase Kinase 1 (PDK1) Inhibitors
    摘要:
    Pyruvate dehydrogenase kinases (PDKs) are overexpressed in most cancer cells and are responsible for aberrant glucose metabolism. We previously described bis(4-morpholinyl thiocarbonyl)-disulfide (JX06, 16) as the first covalent inhibitor of PDK1. Here, on the basis of the scaffold of 16, we identify two novel types of disulfide-based PDK1 inhibitors. The most potent analogue, 3a, effectively inhibits PDK1 both at the molecular (k(mact)/K-i = 4.17 x 10(3) M-1 s(-1)) and the cellular level (down to 0.1 mu M). In contrast to 16, 3a is a potent and subtype-selective inhibitor of PDK1 with >40-fold selectivity for PDK2-4. 3a also significantly alters glucose metabolic pathways in A549 cells by decreasing ECAR and increasing ROS. Moreover, in the xenograft models, 3a shows significant antitumor activity with no negative effect to the mice weight. Collectively, these data demonstrate that 3a may be an excellent lead compound for the treatment of cancer as a first-generation subtype-selective and covalent PDK1 inhibitor.
    DOI:
    10.1021/acs.jmedchem.6b01245
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文献信息

  • Vulcanization accelerator
    申请人:FIRESTONE TIRE & RUBBER CO
    公开号:US02445724A1
    公开(公告)日:1948-07-20
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