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rac-dihydrokadsurenone | 104832-96-4

中文名称
——
中文别名
——
英文名称
rac-dihydrokadsurenone
英文别名
9,10-Dihydrokadsurenone;(2S,3R,3aS)-2-(3,4-dimethoxyphenyl)-3a-methoxy-3-methyl-5-propyl-2,3-dihydro-1-benzofuran-6-one
rac-dihydrokadsurenone化学式
CAS
104832-96-4
化学式
C21H26O5
mdl
——
分子量
358.434
InChiKey
SLMFJWTXIZCNBN-UBWHGVKJSA-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):
    3.4
  • 重原子数:
    26
  • 可旋转键数:
    6
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.48
  • 拓扑面积:
    54
  • 氢给体数:
    0
  • 氢受体数:
    5

反应信息

  • 作为产物:
    描述:
    (E)-3-(3,4-二甲氧基苯基)烯丙醇 在 palladium on activated charcoal lead(IV) acetate氢气三苯基膦N,N-二乙基苯胺偶氮二甲酸二乙酯 作用下, 以 四氢呋喃乙酸乙酯 为溶剂, 25.0~225.0 ℃ 、137.9 kPa 条件下, 反应 16.5h, 生成 rac-dihydrokadsurenone
    参考文献:
    名称:
    Structure-activity relationships of kadsurenone analogues
    摘要:
    Kadsurenone, a specific receptor antagonist of platelet-activating factor (PAF), and its analogues were prepared from derivatives of cinnamyl alcohol and (allyloxy)phenol. Racemic kadsurenone, resolvable by a Chiralpak column at low temperatures, has an IC50 value of 2 X 10(-7) M, which is about 50% of the activity of the natural product (IC50 = 1 X 10(-7) M). The structural specificity of kadsurenone was further demonstrated by the low PAF-receptor-blocking activities of denudatin B, mirandin A, desallylkadsurenone, and the 2-epimer of kadsurenone.
    DOI:
    10.1021/jm00384a023
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文献信息

  • Structure-activity relationships of kadsurenone analogues
    作者:Mitree M. Ponpipom、Robert L. Bugianesi、David R. Brooker、Bao-zhen Yue、San-bao Hwang、Tsung-ying Shen
    DOI:10.1021/jm00384a023
    日期:1987.1
    Kadsurenone, a specific receptor antagonist of platelet-activating factor (PAF), and its analogues were prepared from derivatives of cinnamyl alcohol and (allyloxy)phenol. Racemic kadsurenone, resolvable by a Chiralpak column at low temperatures, has an IC50 value of 2 X 10(-7) M, which is about 50% of the activity of the natural product (IC50 = 1 X 10(-7) M). The structural specificity of kadsurenone was further demonstrated by the low PAF-receptor-blocking activities of denudatin B, mirandin A, desallylkadsurenone, and the 2-epimer of kadsurenone.
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