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RM-6424 | 206536-36-9

中文名称
——
中文别名
——
英文名称
RM-6424
英文别名
Rm6424;3-(3-Bromophenyl)-5,7-dihydroxy-chromen-4-one;3-(3-bromophenyl)-5,7-dihydroxychromen-4-one
RM-6424化学式
CAS
206536-36-9
化学式
C15H9BrO4
mdl
——
分子量
333.138
InChiKey
OEQTWUDMGAVSPZ-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):
    3.7
  • 重原子数:
    20
  • 可旋转键数:
    1
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    66.8
  • 氢给体数:
    2
  • 氢受体数:
    4

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:
    描述:
    RM-6424sodium hydroxidepotassium carbonate 作用下, 以 丙酮 为溶剂, 反应 19.0h, 生成 RM-6450
    参考文献:
    名称:
    Identification of Isoflavone Derivatives as Effective Anticryptosporidial Agents in Vitro and in Vivo
    摘要:
    We report the preparation and antiparasitic activity in vitro and in vivo of a series of isoflavone derivatives related to genistein. These analogues retain the 5,7-dihydroxyisoflavone core of genistein: direct genistein analogues (2-H isoflavones), 2-carboethoxy isoflavones, and the precursor deoxybenzoins were all evaluated. Excellent in vitro activity against Cryptosporidium parvum was observed for both classes of isoflavones in cell cultures, and the lead compound 19, RM6427, shows high in vivo efficacy against an experimental infection.
    DOI:
    10.1021/jm050973f
  • 作为产物:
    描述:
    间苯三酚盐酸三氟化硼乙醚甲基磺酰氯 、 zinc(II) chloride 作用下, 以 乙醚 为溶剂, 生成 RM-6424
    参考文献:
    名称:
    Identification of Isoflavone Derivatives as Effective Anticryptosporidial Agents in Vitro and in Vivo
    摘要:
    We report the preparation and antiparasitic activity in vitro and in vivo of a series of isoflavone derivatives related to genistein. These analogues retain the 5,7-dihydroxyisoflavone core of genistein: direct genistein analogues (2-H isoflavones), 2-carboethoxy isoflavones, and the precursor deoxybenzoins were all evaluated. Excellent in vitro activity against Cryptosporidium parvum was observed for both classes of isoflavones in cell cultures, and the lead compound 19, RM6427, shows high in vivo efficacy against an experimental infection.
    DOI:
    10.1021/jm050973f
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文献信息

  • Identification of Isoflavone Derivatives as Effective Anticryptosporidial Agents in Vitro and in Vivo
    作者:Andrew V. Stachulski、Neil G. Berry、A. C. Lilian Low、Shelley L. Moores、Eleanor Row、David C. Warhurst、Ipemida S. Adagu、Jean-François Rossignol
    DOI:10.1021/jm050973f
    日期:2006.2.1
    We report the preparation and antiparasitic activity in vitro and in vivo of a series of isoflavone derivatives related to genistein. These analogues retain the 5,7-dihydroxyisoflavone core of genistein: direct genistein analogues (2-H isoflavones), 2-carboethoxy isoflavones, and the precursor deoxybenzoins were all evaluated. Excellent in vitro activity against Cryptosporidium parvum was observed for both classes of isoflavones in cell cultures, and the lead compound 19, RM6427, shows high in vivo efficacy against an experimental infection.
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