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2'-Hydroxy-3,4'-dibenzyloxy-4,5'-dimethoxychalkone | 82298-12-2

中文名称
——
中文别名
——
英文名称
2'-Hydroxy-3,4'-dibenzyloxy-4,5'-dimethoxychalkone
英文别名
(E)-1-(2-hydroxy-5-methoxy-4-phenylmethoxyphenyl)-3-(4-methoxy-3-phenylmethoxyphenyl)prop-2-en-1-one
2'-Hydroxy-3,4'-dibenzyloxy-4,5'-dimethoxychalkone化学式
CAS
82298-12-2
化学式
C31H28O6
mdl
——
分子量
496.56
InChiKey
LDSGCWAWQUFLGM-FYWRMAATSA-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):
    6.8
  • 重原子数:
    37
  • 可旋转键数:
    11
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.13
  • 拓扑面积:
    74.2
  • 氢给体数:
    1
  • 氢受体数:
    6

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

  • 作为反应物:
    描述:
    2'-Hydroxy-3,4'-dibenzyloxy-4,5'-dimethoxychalkone 在 palladium on activated charcoal selenium(IV) oxide 、 氢气 作用下, 以 异戊醇 为溶剂, 生成 abrectorin
    参考文献:
    名称:
    Bhardwaj, D. K.; Gupta, A. K.; Sharma, A. K., Indian Journal of Chemistry - Section B Organic and Medicinal Chemistry, 1982, vol. 21, # 2, p. 98 - 100
    摘要:
    DOI:
  • 作为产物:
    描述:
    2,4-二羟基苯乙酮sodium hydroxide 、 dipotassium peroxodisulfate 、 potassium carbonate 作用下, 以 吡啶乙醇丙酮 为溶剂, 反应 18.0h, 生成 2'-Hydroxy-3,4'-dibenzyloxy-4,5'-dimethoxychalkone
    参考文献:
    名称:
    Structure−Activity Requirements for Flavone Cytotoxicity and Binding to Tubulin
    摘要:
    A series of 79 flavones related to centaureidin (3,6,4'-trimethoxy-5,7,3'-trihydroxyflavone 1) was screened for cytotoxicity in the NCI in vitro 60-cell line human tumor screen. The resulting cytotoxicity profiles of these flavones were compared for degree of similarity to the profile of 1. Selected compounds were further evaluated with in vitro assays of tubulin polymerization and [H-3]colchicine binding to tubulin. Maximum potencies for tubulin interaction and production of differential cytotoxicity profiles characteristic of 1 were observed only with compounds containing hydroxyl substituents at C-3' and C-5 and methoxyl groups at C-3 and C-4'.
    DOI:
    10.1021/jm970842h
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文献信息

  • Structure−Activity Requirements for Flavone Cytotoxicity and Binding to Tubulin
    作者:John A. Beutler、Ernest Hamel、Arnold J. Vlietinck、Achiel Haemers、Padinchare Rajan、James N. Roitman、John H. Cardellina、Michael R. Boyd
    DOI:10.1021/jm970842h
    日期:1998.6.1
    A series of 79 flavones related to centaureidin (3,6,4'-trimethoxy-5,7,3'-trihydroxyflavone 1) was screened for cytotoxicity in the NCI in vitro 60-cell line human tumor screen. The resulting cytotoxicity profiles of these flavones were compared for degree of similarity to the profile of 1. Selected compounds were further evaluated with in vitro assays of tubulin polymerization and [H-3]colchicine binding to tubulin. Maximum potencies for tubulin interaction and production of differential cytotoxicity profiles characteristic of 1 were observed only with compounds containing hydroxyl substituents at C-3' and C-5 and methoxyl groups at C-3 and C-4'.
  • Bhardwaj, D. K.; Gupta, A. K.; Sharma, A. K., Indian Journal of Chemistry - Section B Organic and Medicinal Chemistry, 1982, vol. 21, # 2, p. 98 - 100
    作者:Bhardwaj, D. K.、Gupta, A. K.、Sharma, A. K.
    DOI:——
    日期:——
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