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2-(4-hydroxy-3-methoxyphenyl)-3,7-dimethoxy-4H-chromen-4-one | 93876-57-4

中文名称
——
中文别名
——
英文名称
2-(4-hydroxy-3-methoxyphenyl)-3,7-dimethoxy-4H-chromen-4-one
英文别名
2-(4-hydroxy-3-methoxy-phenyl)-3,7-dimethoxy-chromen-4-one;2-(4-Hydroxy-3-methoxy-phenyl)-3,7-dimethoxy-chromen-4-on;4'-Hydroxy-3,3',7-trimethoxy-flavon;2-(4-hydroxy-3-methoxyphenyl)-3,7-dimethoxychromen-4-one
2-(4-hydroxy-3-methoxyphenyl)-3,7-dimethoxy-4H-chromen-4-one化学式
CAS
93876-57-4
化学式
C18H16O6
mdl
——
分子量
328.321
InChiKey
IWTORDMFPIOXBT-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

物化性质

  • 熔点:
    173-174 °C
  • 沸点:
    537.4±50.0 °C(Predicted)
  • 密度:
    1.36±0.1 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    2.9
  • 重原子数:
    24
  • 可旋转键数:
    4
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.17
  • 拓扑面积:
    74.2
  • 氢给体数:
    1
  • 氢受体数:
    6

反应信息

  • 作为反应物:
    描述:
    乌洛托品2-(4-hydroxy-3-methoxyphenyl)-3,7-dimethoxy-4H-chromen-4-one溶剂黄146 作用下, 生成 5-(3,7-dimethoxy-4-oxo-4H-chromen-2-yl)-2-hydroxy-3-methoxy-benzaldehyde
    参考文献:
    名称:
    Nuclear oxidation in flavones and related compounds
    摘要:
    DOI:
    10.1007/bf03171364
  • 作为产物:
    描述:
    丹皮酚 在 palladium 10% on activated carbon 、 氢气双氧水potassium carbonate 、 potassium hydroxide 、 sodium hydroxide 作用下, 以 四氢呋喃甲醇乙醇丙酮 为溶剂, 反应 1.0h, 生成 2-(4-hydroxy-3-methoxyphenyl)-3,7-dimethoxy-4H-chromen-4-one
    参考文献:
    名称:
    3′-Hydroxy-3,4′-dimethoxyflavone blocks tubulin polymerization and is a potent apoptotic inducer in human SK-MEL-1 melanoma cells
    摘要:
    Flavonoids are naturally occurring polyphenolic compounds and are among the most promising anticancer agents. A series of flavonols and their 3-methyl ether derivatives were synthesized and assessed for cytotoxicity. It was found that 3'-hydroxy-3,4'-dimethoxyflavone (flavonoid 7a) displayed strong cytotoxicity against human SK-MEL-1 melanoma cells and blocked tubulin polymerization, but had no significant cytotoxic effects against quiescent or proliferating human peripheral blood mononuclear cells. Our analyses showed that flavonoid 7a induces G2-M cell cycle arrest and apoptosis in melanoma cells which is associated with cytochrome c release and activation of both extrinsic and intrinsic apoptotic pathways of cell death. (C) 2017 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmc.2017.09.043
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文献信息

  • Exploration of Pharmacophore in Chrysosplenol C as Activator in Ventricular Myocyte Contraction
    作者:Eeda Venkateswararao、Min-Jeong Son、Niti Sharma、Manoj Manickam、PullaReddy Boggu、Young Ho Kim、Sun-Hee Woo、Sang-Hun Jung
    DOI:10.1021/acsmedchemlett.5b00043
    日期:2015.7.9
    Chrysosplenol C (4',5,6-trihydroxy-3,3',7-tri-methoxyflavone) isolated from Miliusa balansae has unique structural features as a reversible inotropic agent independent of beta-adrenergic signaling and with selective activation of cardiac myosin ATPase. Hence, a series of chrysosplenol analogues were synthesized and explored for identification of pharmacophore that is essential for the increasing contractility in rat ventricular myocytes. Analogue 7-chloro-2-(3-hydroxypheny1)-3-methoxy-4H-chromen-4-one showed highly potent contractility (54.8% at 10 mu M) through activating cardiac myosin ATPase (38.7% at 10 mu M). Our systematic structure activity relationship study revealed that flavonoid nucleus of chrososplenol C appears to be an essential basic skeleton and hydrophobic substituent at position 7 of chromenone such as methoxy or chloro enhances the activity. Additionally, our ATPase study suggested that these chrysosplenol analogues have selectivity toward cardiac myosin activation. Thus, the novel flavonone with 3-/7-hydrophobic substituent and 3'-hydrogen bonding donor function is a novel scaffold for discovery of a new positive inotropic agent.
  • Nuclear oxidation in flavones and related compounds
    作者:L. Ramachandra Row、T. R. Seshadri、T. R. Thiruvengadam
    DOI:10.1007/bf03171364
    日期:1949.3
  • 3′-Hydroxy-3,4′-dimethoxyflavone blocks tubulin polymerization and is a potent apoptotic inducer in human SK-MEL-1 melanoma cells
    作者:Francisco Estévez-Sarmiento、Mercedes Said、Ignacio Brouard、Francisco León、Celina García、José Quintana、Francisco Estévez
    DOI:10.1016/j.bmc.2017.09.043
    日期:2017.11
    Flavonoids are naturally occurring polyphenolic compounds and are among the most promising anticancer agents. A series of flavonols and their 3-methyl ether derivatives were synthesized and assessed for cytotoxicity. It was found that 3'-hydroxy-3,4'-dimethoxyflavone (flavonoid 7a) displayed strong cytotoxicity against human SK-MEL-1 melanoma cells and blocked tubulin polymerization, but had no significant cytotoxic effects against quiescent or proliferating human peripheral blood mononuclear cells. Our analyses showed that flavonoid 7a induces G2-M cell cycle arrest and apoptosis in melanoma cells which is associated with cytochrome c release and activation of both extrinsic and intrinsic apoptotic pathways of cell death. (C) 2017 Elsevier Ltd. All rights reserved.
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表征谱图

  • 氢谱
    1HNMR
  • 质谱
    MS
  • 碳谱
    13CNMR
  • 红外
    IR
  • 拉曼
    Raman
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mass
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ir
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  • 峰位数据
  • 峰位匹配
  • 表征信息
Shift(ppm)
Intensity
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Assign
Shift(ppm)
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测试频率
样品用量
溶剂
溶剂用量
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