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methyl 6-(5-chloro-3-oxoisothiazol-2(3H)-yl)hexanoate | 1134642-86-6

中文名称
——
中文别名
——
英文名称
methyl 6-(5-chloro-3-oxoisothiazol-2(3H)-yl)hexanoate
英文别名
methyl 6-(5-chloro-3-oxo-1,2-thiazol-2-yl)hexanoate
methyl 6-(5-chloro-3-oxoisothiazol-2(3H)-yl)hexanoate化学式
CAS
1134642-86-6
化学式
C10H14ClNO3S
mdl
——
分子量
263.745
InChiKey
INYRXSOKQIQGSK-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):
    1.8
  • 重原子数:
    16
  • 可旋转键数:
    7
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.6
  • 拓扑面积:
    71.9
  • 氢给体数:
    0
  • 氢受体数:
    4

反应信息

  • 作为产物:
    描述:
    3,3'-dithiobis[N-(methyl 2-aminohexanoate)propanamide] 在 磺酰氯 作用下, 以 二氯甲烷 为溶剂, 反应 2.0h, 以61%的产率得到methyl 6-(5-chloro-3-oxoisothiazol-2(3H)-yl)hexanoate
    参考文献:
    名称:
    Inhibition of the PCAF histone acetyl transferase and cell proliferation by isothiazolones
    摘要:
    Small molecule HAT inhibitors are useful tools to unravel the role of histone acetyl transferases (HATs) in the cell and have relevance for oncology. We present a systematic investigation of the inhibition of the HAT p300/CBP Associated Factor (PCAF) by isothiazolones with different substitutions. 5-chloroisothiazolones proved to be the most potent inhibitors of PCAF. The growth inhibition of 4 different cell lines was studied and the growth of two cell lines (A2780 and HEK 293) was inhibited at micromolar concentrations by 5-chloroisothiazolones. Furthermore, the 5-chloroisothiazolone preservative Kathon (TM) CG that is used in cosmetics inhibited PCAF and the growth of cell lines A2780 and HEK 293, which indicates that this preservative should be applied with care. (C) 2008 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmc.2008.12.008
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文献信息

  • Inhibition of the PCAF histone acetyl transferase and cell proliferation by isothiazolones
    作者:Frank J. Dekker、Massimo Ghizzoni、Nanette van der Meer、Rosalina Wisastra、Hidde J. Haisma
    DOI:10.1016/j.bmc.2008.12.008
    日期:2009.1
    Small molecule HAT inhibitors are useful tools to unravel the role of histone acetyl transferases (HATs) in the cell and have relevance for oncology. We present a systematic investigation of the inhibition of the HAT p300/CBP Associated Factor (PCAF) by isothiazolones with different substitutions. 5-chloroisothiazolones proved to be the most potent inhibitors of PCAF. The growth inhibition of 4 different cell lines was studied and the growth of two cell lines (A2780 and HEK 293) was inhibited at micromolar concentrations by 5-chloroisothiazolones. Furthermore, the 5-chloroisothiazolone preservative Kathon (TM) CG that is used in cosmetics inhibited PCAF and the growth of cell lines A2780 and HEK 293, which indicates that this preservative should be applied with care. (C) 2008 Elsevier Ltd. All rights reserved.
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