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5-hydroxy-2-phenyl-7-(3-piperidin-1-yl-propoxy)-chromen-4-one

中文名称
——
中文别名
——
英文名称
5-hydroxy-2-phenyl-7-(3-piperidin-1-yl-propoxy)-chromen-4-one
英文别名
5-Hydroxy-2-phenyl-7-(3-piperidin-1-ylpropoxy)chromen-4-one
5-hydroxy-2-phenyl-7-(3-piperidin-1-yl-propoxy)-chromen-4-one化学式
CAS
——
化学式
C23H25NO4
mdl
——
分子量
379.456
InChiKey
AUNFBKIGPWRXQY-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:
    28
  • 可旋转键数:
    6
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.35
  • 拓扑面积:
    59
  • 氢给体数:
    1
  • 氢受体数:
    5

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

  • 作为产物:
    参考文献:
    名称:
    Synthesis and biological evaluation of novel C (7) modified chrysin analogues as antibacterial agents
    摘要:
    The natural product, chrysin (5,7-dihydroxy flavone), obtained from Oroxylum indicum, exhibits numerous biological activities including anticancer, anti-inflammatory, and antiallergic activities. Three series of chrysin analogues were prepared, in which chrysin and heterocyclic moieties are separated by 3-carbon, 4-carbon, and 6-carbon spacers. All the derivatives were screened for antibacterial activity against a panel of susceptible and resistant Gram-positive and Gram-negative organisms. It was observed that most of the derivatives displayed significant activity as compared to their parent compound (chrysin). (c) 2005 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2005.09.009
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文献信息

  • Natural agent for treatment of gastrointestinal toxicity, associated symptoms and ulcers
    申请人:Rao Madusudana Janaswamy
    公开号:US20070213281A1
    公开(公告)日:2007-09-13
    The present invention relates to identification of Oroxylum indicum , Indian medicinal plant as a rich source for flavanoid compounds. Mucoprotective and antigastric ulcer properties in the flavone class of compounds isolated therefrom have been identified along with a flavanoids mixture in substantial yields from hexane and acetone extracts. The hexane extract was fractionated, purified and the compounds identified as Oroxylin A, Chrysin and Baicalein. The acetone extract was purified and the compounds obtained identified as methoxy chrysin, Oroxyloside methyl ester and chrysin-7-O-methyl glycoside.
    本发明涉及将印度药用植物印度酸枝鉴定为一种丰富的类黄酮化合物来源。从中分离出的黄酮类化合物中已确定具有粘膜保护和抗胃溃疡特性,同时还从己烷和丙酮提取物中获得了大量的类黄酮混合物。己烷提取物经过分级、纯化,鉴定出的化合物为千里光素A、槲皮素和黄芩素。丙酮提取物经过纯化,获得的化合物被鉴定为甲氧基黄芩素、千里光苷甲酯和黄芩-7-O-甲基糖苷。
  • COMPOSITIONS AND METHODS FOR THE TREATMENT OF GASTROINTESTINAL INDICATIONS
    申请人:RAO Janaswamy Madusudana
    公开号:US20110059913A1
    公开(公告)日:2011-03-10
    The present invention relates to identification of Oroxylum indicum, Indian medicinal plant as a rich source for flavanoid compounds. Mucoprotective and antigastric ulcer properties in the flavone class of compounds isolated therefrom have been identified along with a flavanoids mixture in substantial yields from hexane and acetone extracts. The hexane extract was fractionated, purified and the compounds identified as Oroxylin A, Chrysin and Baicalein. The acetone extract was purified and the compounds obtained identified as methoxy chrysin, Oroxyloside methyl ester and chrysin-7-O-methyl glycoside.
  • Flavanoid Compounds and Process for Preparation Thereof
    申请人:Dab Pratap Kumar
    公开号:US20120022062A1
    公开(公告)日:2012-01-26
    The present invention relates to flavanoid compounds of general formula (X 1 ) wherein: R 1 is selected from a group consisting of morpholinyl, N-methyl piperizinyl, piperidinyl and N,N′-dimethylamino groups, and n ranges from 3 to 6, and process for preparation thereof. The present invention relates to the demonstration of anti Helicobacter pylori activity and gastric antisecretory activity of semisynthetically designed flavonoid compounds, to be used for the prevention and treatment of gastroduodenal disorders in general and peptic ulcer diseases in particular. The present invention also relates to a hetero-dimeric bi-functional molecule that can be used as monotherapy substituting/replacing/overcoming currently used triple/quadruple therapy, thereby implicating/anticipating/envisaging its commercial applicability.
  • FLAVANOID COMPOUNDS AND PROCESS FOR PREPARATION THEREOF
    申请人:Council of Scientific & Industrial Research
    公开号:US20150174135A1
    公开(公告)日:2015-06-25
    The present invention relates to flavanoid compounds of general formula (X 1 ) wherein: R 1 is selected from a group consisting of morpholinyl, N-methyl piperizinyl, piperidinyl and N,N′-dimethylamino groups, and n ranges from 3 to 6, and process for preparation thereof. The present invention relates to the demonstration of anti Helicobacter pylori activity and gastric antisecretory activity of semisynthetically designed flavonoid compounds, to be used for the prevention and treatment of gastroduodenal disorders in general and peptic ulcer diseases in particular. The present invention also relates to a hetero-dimeric bi-functional molecule that can be used as monotherapy substituting/replacing/overcoming currently used triple/quadruple therapy, thereby implicating/anticipating/envisaging its commercial applicability.
  • US7855200B2
    申请人:——
    公开号:US7855200B2
    公开(公告)日:2010-12-21
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