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1,3,8,10,11-Pentahydroxy-6-methyl-naphthacene-5,12-dione

中文名称
——
中文别名
——
英文名称
1,3,8,10,11-Pentahydroxy-6-methyl-naphthacene-5,12-dione
英文别名
1,3,8,10,11-Pentahydroxy-6-methyltetracene-5,12-dione
1,3,8,10,11-Pentahydroxy-6-methyl-naphthacene-5,12-dione化学式
CAS
——
化学式
C19H12O7
mdl
——
分子量
352.3
InChiKey
QPTIGEXZMBTRSE-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):
    3.3
  • 重原子数:
    26
  • 可旋转键数:
    0
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.05
  • 拓扑面积:
    135
  • 氢给体数:
    5
  • 氢受体数:
    7

反应信息

  • 作为反应物:
    描述:
    乙酸酐1,3,8,10,11-Pentahydroxy-6-methyl-naphthacene-5,12-dione吡啶 作用下, 生成 Acetic acid 3,8,10-triacetoxy-12-hydroxy-5-methyl-6,11-dioxo-6,11-dihydro-naphthacen-1-yl ester
    参考文献:
    名称:
    Novel Selective Inhibitors for Human Topoisomerase I, BM2419-1 and -2 Derived from Saintopin.
    摘要:
    Compounds BM2419-1 and -2 were isolated from a culture broth of a fungus Paecilomyces sp. BM2419. It was shown that these novel compounds were artifacts derived from saintopin, a dual inhibitor of topoisomerase I and II by independent processes. In the human topoisomerase I inhibition assay using the recombinant Saccharomyces cerevisiae, BM2419-1 and -2 inhibited selectively the yeast growth dependent on human topoisomerase I induction with IC50 values of 0.3 ng/ml and 6.0 ng/ml, respectively.
    DOI:
    10.7164/antibiotics.51.1069
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文献信息

  • Novel Selective Inhibitors for Human Topoisomerase I, BM2419-1 and -2 Derived from Saintopin.
    作者:DAISUKE ISHIYAMA、KATUYUKI FUTAMATA、MATIKO FUTAMATA、OSAMU KASUYA、SHINYA KAMO、FUMIO YAMASHITA、SUSUMU KANAZAWA
    DOI:10.7164/antibiotics.51.1069
    日期:——
    Compounds BM2419-1 and -2 were isolated from a culture broth of a fungus Paecilomyces sp. BM2419. It was shown that these novel compounds were artifacts derived from saintopin, a dual inhibitor of topoisomerase I and II by independent processes. In the human topoisomerase I inhibition assay using the recombinant Saccharomyces cerevisiae, BM2419-1 and -2 inhibited selectively the yeast growth dependent on human topoisomerase I induction with IC50 values of 0.3 ng/ml and 6.0 ng/ml, respectively.
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