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2'-hydroxy-3,4-dimethoxy-4',6'-di[(2-methoxyethoxy)methoxy]chalcone | 1456788-17-2

中文名称
——
中文别名
——
英文名称
2'-hydroxy-3,4-dimethoxy-4',6'-di[(2-methoxyethoxy)methoxy]chalcone
英文别名
——
2'-hydroxy-3,4-dimethoxy-4',6'-di[(2-methoxyethoxy)methoxy]chalcone化学式
CAS
1456788-17-2
化学式
C25H32O10
mdl
——
分子量
492.523
InChiKey
JYKMAUIZRVSWPE-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):
    3.3
  • 重原子数:
    35.0
  • 可旋转键数:
    17.0
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.4
  • 拓扑面积:
    111.14
  • 氢给体数:
    1.0
  • 氢受体数:
    10.0

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-dimethoxy-4',6'-di[(2-methoxyethoxy)methoxy]chalconesodium periodate 作用下, 以 二甲基亚砜 为溶剂, 反应 72.0h, 以44%的产率得到3',4'-dimethoxy-5,7-di[(2-methoxyethoxy)methoxy]flavone
    参考文献:
    名称:
    Modulation of human neutrophils' oxidative burst by flavonoids
    摘要:
    Inflammation is a normal response towards tissue injury, but may become deleterious to the organism if uncontrolled. The overproduction of reactive species during the inflammatory process may cause or magnify the damage at inflammatory sites. Flavonoids have been suggested as therapeutic agents to avoid such damage, as these compounds exhibit anti-inflammatory activity, through the modulation of oxidative stress and signalling pathways. Both effects may attenuate neutrophils' activities at inflammatory sites. In this study, we investigated the structure/activity relationship of a series of flavonoids on the oxidative burst of human neutrophils in vitro, as a measure of its anti-inflammatory potential. Neutrophils were stimulated with phorbol-12-myristate-13-acetate, and fluorescence and chemiluminescence techniques were used to evaluate the generation of reactive oxygen species. All the tested flavonoids revealed the ability to modulate the neutrophil's oxidative burst. From the obtained results, the pivotal role of the catechol group in the B-ring was evidenced as well as the minor importance of the hydroxylations in the A-ring, which did not appear to be determinant for the activity, although clearly influencing the lipophilicity of the tested flavonoids. It is also clarified the importance of the methylation in the OH group at the B-ring catechol moiety. In conclusion, the obtained results uncover new possible strategies for the resolution of inflammatory processes, using flavonoids to modulate neutrophil's oxidative burst. (C) 2013 Elsevier Masson SAS. All rights reserved.
    DOI:
    10.1016/j.ejmech.2013.06.019
  • 作为产物:
    描述:
    3,4-二甲氧基苯甲醛2'-hydroxy-4',6'-bis[(2-methoxyethoxy)methoxy]acetophenone 在 sodium hydroxide 作用下, 以 甲醇 为溶剂, 反应 4.0h, 以86%的产率得到2'-hydroxy-3,4-dimethoxy-4',6'-di[(2-methoxyethoxy)methoxy]chalcone
    参考文献:
    名称:
    Modulation of human neutrophils' oxidative burst by flavonoids
    摘要:
    Inflammation is a normal response towards tissue injury, but may become deleterious to the organism if uncontrolled. The overproduction of reactive species during the inflammatory process may cause or magnify the damage at inflammatory sites. Flavonoids have been suggested as therapeutic agents to avoid such damage, as these compounds exhibit anti-inflammatory activity, through the modulation of oxidative stress and signalling pathways. Both effects may attenuate neutrophils' activities at inflammatory sites. In this study, we investigated the structure/activity relationship of a series of flavonoids on the oxidative burst of human neutrophils in vitro, as a measure of its anti-inflammatory potential. Neutrophils were stimulated with phorbol-12-myristate-13-acetate, and fluorescence and chemiluminescence techniques were used to evaluate the generation of reactive oxygen species. All the tested flavonoids revealed the ability to modulate the neutrophil's oxidative burst. From the obtained results, the pivotal role of the catechol group in the B-ring was evidenced as well as the minor importance of the hydroxylations in the A-ring, which did not appear to be determinant for the activity, although clearly influencing the lipophilicity of the tested flavonoids. It is also clarified the importance of the methylation in the OH group at the B-ring catechol moiety. In conclusion, the obtained results uncover new possible strategies for the resolution of inflammatory processes, using flavonoids to modulate neutrophil's oxidative burst. (C) 2013 Elsevier Masson SAS. All rights reserved.
    DOI:
    10.1016/j.ejmech.2013.06.019
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同类化合物

(2Z)-1,3-二苯基-2-丙烯-1-酮,2-丙烯-1-酮,1,3-二苯基-,(2Z)- 龙血素D 龙血素A 龙血素 B 黄色当归醇F 黄色当归醇B 黄腐醇; 黄腐酚 黄腐醇 D; 黄腐酚 D 黄腐酚B 黄腐酚 黄腐酚 黄卡瓦胡椒素 C 高紫柳查尔酮 阿普非农 阿司巴汀 阿伏苯宗 金鸡菊查耳酮 邻肉桂酰苯甲酸 达泊西汀杂质25 豆蔻明 补骨脂色烯查耳酮 补骨脂查耳酮 补骨脂呋喃查耳酮 补骨脂乙素 蜡菊亭; 4,2',4'-三羟基-6'-甲氧基查耳酮 苯酚,4-[3-(2-羟基苯基)-1-苯基丙基]-2-(3-苯基丙基)- 苯磺酰胺,N-[4-[3-(3-羟基苯基)-1-羰基-2-丙烯基]苯基]- 苯磺酰胺,N-[3-[3-(4-羟基-3-甲氧苯基)-1-羰基-2-丙烯基]苯基]- 苯磺酰胺,4-甲氧基-N,N-二甲基-2-(3-羰基-3-苯基-1-丙烯基)-,(E)- 苯磺酰氯化,4,5-二甲氧基-2-(3-羰基-3-苯基-1-丙烯基)-,(E)- 苯磺酰氯,4-甲氧基-3-(3-羰基-3-苯基-1-丙烯基)-,(E)- 苯甲醇,4-甲氧基-a-[2-(4-甲氧苯基)乙烯基]- 苯甲酸-[4-(3-氧代-3-苯基-丙烯基)-苯胺] 苯甲酸,3-[3-(4-溴苯基)-1-羰基-2-丙烯基]-4-羟基- 苯甲酰(2-羟基苯酰)甲烷 苯甲腈,4-(1-羟基-3-羰基-3-苯基丙基)- 苯基[2-(1-萘基)乙烯基]甲酮 苯基-(三苯基-丙-2-炔基)-醚 苯基-(2-苯基-2,3-二氢-苯并噻唑-2-基)-甲酮 苯亚甲基苯乙酮 苯乙酰腈,a-(1-氨基-2-苯基亚乙基)- 苯丙酸,a-苯甲酰-b-羰基-,苯基(苯基亚甲基)酰肼 苯,1-(2,2-二甲基-3-苯基丙基)-2-甲基- 苏木查耳酮 苄桂哌酯 苄基(4-氯-2-(3-氧代-1,3-二苯基丙基)苯基)氨基甲酸酯 芦荟提取物 腈苯唑 胀果甘草宁C 聚磷酸根皮酚