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9-(Benzoyloximino)-xanthen | 18791-24-7

中文名称
——
中文别名
——
英文名称
9-(Benzoyloximino)-xanthen
英文别名
9H-Xanthen-9-one, O-benzoyloxime;(xanthen-9-ylideneamino) benzoate
9-(Benzoyloximino)-xanthen化学式
CAS
18791-24-7
化学式
C20H13NO3
mdl
——
分子量
315.328
InChiKey
MNBSGYYGPFEBNI-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):
    4.26
  • 重原子数:
    24.0
  • 可旋转键数:
    2.0
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    51.8
  • 氢给体数:
    0.0
  • 氢受体数:
    4.0

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:
    占吨酮盐酸羟胺 、 sodium hydride 作用下, 以 四氢呋喃乙醇 为溶剂, 生成 9-(Benzoyloximino)-xanthen
    参考文献:
    名称:
    Relationship Between Structure of Conjugated Oxime Esters and Their Ability to Cleave DNA
    摘要:
    The size and geometry of polycycles are critical to intercalation into DNA. This work involves the establishment of a new compound library that includes 35 O-benzoyl oxime esters with intercalators of five types. These conjugated compounds were synthesized by the condensation of substituted benzoyl chlorides (XC6H4COCl; X = H, Me, CN, F, and NO2) or naphthoyl chlorides with oximes of fluoren-9-one, 9,10-anthraquinone, xanthen-9-one, thioxanthen-9-one, and 9H-thioxanthen-9-one, 10,10-dioxide to give the corresponding esters in 80-99% yields. All of these compounds could cleave DNA when photolyzed by UV light. Of these conjugates, 9,10-anthraquinone-O-9-(4-fluorobenzoyl)oxime with a binding constant of 4.49 x 10(4) M-1 cleaved DNA most efficiently. Examination of the structure activity relationship supports a conclusion that two factors affect DNA-cleaving potency. These are (1) the planarity of the intercalating moiety, and (2) the size and substituents of the benzoyl ring. The DNA-cleaving ability followed the order 9,10-anthraquinone > fluoren-9-one >= xanthen-9-one similar to thioxanthen-9-one > 9H-thioxanthen-9-one 10,10-dioxide. The benzoyl-containing oxime ester conjugates were more active than the corresponding naphthoyl-containing conjugates. The potency that was associated with the different substituents on the benzoyl ring followed the order F > CN >= NO2 > Me similar to H.
    DOI:
    10.1021/bc400060h
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