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FC726 | 198343-05-4

中文名称
——
中文别名
——
英文名称
FC726
英文别名
Paradisin A;4-[(E,6R)-6-hydroxy-7-[(E,3R)-2-hydroxy-2,6-dimethyl-8-(7-oxofuro[3,2-g]chromen-4-yl)oxyoct-6-en-3-yl]oxy-3,7-dimethyloct-2-enoxy]furo[3,2-g]chromen-7-one
FC726化学式
CAS
198343-05-4
化学式
C42H46O11
mdl
——
分子量
726.821
InChiKey
AGWWNHLHAZTYCS-OBKSYJDZSA-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):
    7.7
  • 重原子数:
    53
  • 可旋转键数:
    16
  • 环数:
    6.0
  • sp3杂化的碳原子比例:
    0.38
  • 拓扑面积:
    147
  • 氢给体数:
    2
  • 氢受体数:
    11

反应信息

  • 作为反应物:
    描述:
    乙酸酐FC726吡啶 作用下, 反应 12.0h, 生成 Acetic acid (E)-(R)-1-{1-[(E)-(R)-1-(1-hydroxy-1-methyl-ethyl)-4-methyl-6-(7-oxo-7H-furo[3,2-g]chromen-4-yloxy)-hex-4-enyloxy]-1-methyl-ethyl}-4-methyl-6-(7-oxo-7H-furo[3,2-g]chromen-4-yloxy)-hex-4-enyl ester
    参考文献:
    名称:
    Dihydroxybergamottin Caproate as a Potent and Stable CYP3A4 Inhibitor
    摘要:
    We investigated the inhibitory activity of the furanocoumarin derivatives from grapefruit juice to the drug metabolizing enzyme, cytochrome P450 (CYP) 3A4. Although two known furanocoumarin dimers GF-I-1 (1) and GF-I-4 (2) showed potent CYP3A4 inhibition with IC50 value of 0.07 muM. a semi-synthetic dihydroxybergamottin caproate (11), which was more stable and more simple than the dimers. exhibited comparable activity against CYP3A4. (C) 2002 Elsevier Science Ltd. All rights reserved.
    DOI:
    10.1016/s0968-0896(01)00362-5
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文献信息

  • Dihydroxybergamottin Caproate as a Potent and Stable CYP3A4 Inhibitor
    作者:Tomihisa Ohta、Minoru Nagahashi、Shinzo Hosoi、Sachiko Tsukamoto
    DOI:10.1016/s0968-0896(01)00362-5
    日期:2002.4
    We investigated the inhibitory activity of the furanocoumarin derivatives from grapefruit juice to the drug metabolizing enzyme, cytochrome P450 (CYP) 3A4. Although two known furanocoumarin dimers GF-I-1 (1) and GF-I-4 (2) showed potent CYP3A4 inhibition with IC50 value of 0.07 muM. a semi-synthetic dihydroxybergamottin caproate (11), which was more stable and more simple than the dimers. exhibited comparable activity against CYP3A4. (C) 2002 Elsevier Science Ltd. All rights reserved.
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