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(4R,4aS)-4,8-Dihydroxy-6-methyl-9-oxo-1,4,9,9a-tetrahydro-xanthene-4a-carboxylic acid methyl ester | 200409-34-3

中文名称
——
中文别名
——
英文名称
(4R,4aS)-4,8-Dihydroxy-6-methyl-9-oxo-1,4,9,9a-tetrahydro-xanthene-4a-carboxylic acid methyl ester
英文别名
——
(4R,4aS)-4,8-Dihydroxy-6-methyl-9-oxo-1,4,9,9a-tetrahydro-xanthene-4a-carboxylic acid methyl ester化学式
CAS
200409-34-3
化学式
C16H16O6
mdl
——
分子量
304.299
InChiKey
SQQVLPAZXRNECF-MGHJCYNESA-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):
    1.12
  • 重原子数:
    22.0
  • 可旋转键数:
    1.0
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.38
  • 拓扑面积:
    93.06
  • 氢给体数:
    2.0
  • 氢受体数:
    6.0

上下游信息

  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    参考文献:
    名称:
    Syntheses of novel antitumor dihydroxanthone derivatives with inhibitory activity against DNA topoisomerase II
    摘要:
    A series of methoxycarbonyl group modified nidulalin A analogs were synthesized to improve stability against esterases. The amide derivatives showed cytotoxic activity along with inhibitory activity against DNA topoisomerase II. Among the analogs, amide 9a exhibited antitumor activity in Colon 26 murine tumor model. (C) 1999 Elsevier Science Ltd. All rights reserved.
    DOI:
    10.1016/s0960-894x(99)00440-0
  • 作为产物:
    描述:
    nidulalin A 在 sodium tetrahydroborate 作用下, 以 甲醇 为溶剂, 以87%的产率得到(4R,4aS)-4,8-Dihydroxy-6-methyl-9-oxo-1,4,9,9a-tetrahydro-xanthene-4a-carboxylic acid methyl ester
    参考文献:
    名称:
    Syntheses of novel antitumor dihydroxanthone derivatives with inhibitory activity against DNA topoisomerase II
    摘要:
    A series of methoxycarbonyl group modified nidulalin A analogs were synthesized to improve stability against esterases. The amide derivatives showed cytotoxic activity along with inhibitory activity against DNA topoisomerase II. Among the analogs, amide 9a exhibited antitumor activity in Colon 26 murine tumor model. (C) 1999 Elsevier Science Ltd. All rights reserved.
    DOI:
    10.1016/s0960-894x(99)00440-0
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