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| 1609449-86-6

中文名称
——
中文别名
——
英文名称
——
英文别名
——
化学式
CAS
1609449-86-6
化学式
C35H34O13
mdl
——
分子量
662.647
InChiKey
RYPPZLMPPOWUJA-HJIYDPOZSA-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

  • 沸点:
    782.7±60.0 °C(predicted)
  • 密度:
    1.37±0.1 g/cm3(Temp: 20 °C; Press: 760 Torr)(predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    4.94
  • 重原子数:
    48.0
  • 可旋转键数:
    8.0
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.34
  • 拓扑面积:
    163.1
  • 氢给体数:
    0.0
  • 氢受体数:
    13.0

反应信息

  • 作为反应物:
    描述:
    sodium cyanide 作用下, 以 甲醇 为溶剂, 反应 20.0h, 以77%的产率得到polycarcin V
    参考文献:
    名称:
    Total Synthesis of the Antitumor Natural Product Polycarcin V and Evaluation of Its DNA Binding Profile
    摘要:
    The convergent total synthesis of polycarcin V, a gilvocarcin-type natural product that shows significant cytotoxicity with selectivity for nonsmall-cell lung cancer, breast cancer, and melanoma cells, has been achieved in 13 steps from 7, 8, and 22; the sequence features a stereoselective alpha-C-glycosylation reaction for the union of protected carbohydrate 7' and naphthol 8. The association constant for the binding of polycarcin V to duplex DNA is similar to that previously reported for gilvocarcin V.
    DOI:
    10.1021/ol501095w
  • 作为产物:
    描述:
    2-硝基苯基丝氰酸酯三丁基膦双氧水 作用下, 以 四氢呋喃 为溶剂, 反应 0.67h, 以57%的产率得到
    参考文献:
    名称:
    Total Synthesis of the Antitumor Natural Product Polycarcin V and Evaluation of Its DNA Binding Profile
    摘要:
    The convergent total synthesis of polycarcin V, a gilvocarcin-type natural product that shows significant cytotoxicity with selectivity for nonsmall-cell lung cancer, breast cancer, and melanoma cells, has been achieved in 13 steps from 7, 8, and 22; the sequence features a stereoselective alpha-C-glycosylation reaction for the union of protected carbohydrate 7' and naphthol 8. The association constant for the binding of polycarcin V to duplex DNA is similar to that previously reported for gilvocarcin V.
    DOI:
    10.1021/ol501095w
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