摩熵化学
数据库官网
小程序
打开微信扫一扫
首页 分子通 化学资讯 化学百科 反应查询 关于我们
请输入关键词

3-benzyloxy-2-(4-benzyloxy-3,5-dimethoxy-phenyl)-7-decyl-chromen-4-one | 649551-79-1

中文名称
——
中文别名
——
英文名称
3-benzyloxy-2-(4-benzyloxy-3,5-dimethoxy-phenyl)-7-decyl-chromen-4-one
英文别名
7-decyl-2-(3,5-dimethoxy-4-phenylmethoxyphenyl)-3-phenylmethoxychromen-4-one
3-benzyloxy-2-(4-benzyloxy-3,5-dimethoxy-phenyl)-7-decyl-chromen-4-one化学式
CAS
649551-79-1
化学式
C41H46O6
mdl
——
分子量
634.813
InChiKey
XOEFSBHRLSYVFW-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

  • 沸点:
    756.4±60.0 °C(Predicted)
  • 密度:
    1.17±0.1 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    11.4
  • 重原子数:
    47
  • 可旋转键数:
    18
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.34
  • 拓扑面积:
    63.2
  • 氢给体数:
    0
  • 氢受体数:
    6

SDS

SDS:e9fb6cd9c231a37f6f729e4cd83c9a14
查看

上下游信息

  • 下游产品
    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:
    3-benzyloxy-2-(4-benzyloxy-3,5-dimethoxy-phenyl)-7-decyl-chromen-4-one三溴化硼 作用下, 以 甲醇二氯甲烷 为溶剂, 反应 20.0h, 以95%的产率得到7-decyl-3-hydroxy-2-(3,4,5-trihydroxy-phenyl)-chromen-4-one
    参考文献:
    名称:
    [EN] FLAVONOID COMPOUNDS AS THERAPEUTIC ANTIOXIDANTS
    [FR] COMPOSES FLAVONOIDES EN TANT QU'ANTIOXYDANTS THERAPEUTIQUES
    摘要:
    描述了具有抗氧化活性的新型黄酮类化合物。公式(1)。已经证明这些化合物在生物系统中展现出抗氧化特性,其在防晒霜或护肤品中的用途,或用于治疗涉及氧化损伤的情况,特别是治疗或预防治疗阿尔茨海默病或缺血再灌注和损伤的情况。
    公开号:
    WO2004007475A1
  • 作为产物:
    描述:
    1-(2-羟基-4-碘苯基)乙酮氢氧化钾sodium hydroxide 、 9-borabicyclo[3.3.1]nonane dimer 、 双氧水potassium carbonate 、 potassium iodide 作用下, 以 四氢呋喃甲醇乙醇丙酮 为溶剂, 反应 110.0h, 生成 3-benzyloxy-2-(4-benzyloxy-3,5-dimethoxy-phenyl)-7-decyl-chromen-4-one
    参考文献:
    名称:
    Potential therapeutic antioxidants that combine the radical scavenging ability of myricetin and the lipophilic chain of vitamin E to effectively inhibit microsomal lipid peroxidation
    摘要:
    The flavonol myricetin, reacts with oxygen-centred galvinoxyl radicals 28 times faster than d-alpha-tocopherol (vitamin E), the main lipid-soluble antioxidant in biological membranes. Moreover, each myricetin molecule reduces twice as many such radicals as vitamin E. However, myricetin fails to protect vitamin E-deficient microsomes from lipid peroxidation as assessed by the formation of thiobarbituric acid reactive substances (TBARS). Novel and potentially therapeutic antioxidants have been prepared that combine the radical-scavenging ability of a myricetin-like head group with a lipophilic chain similar to that of vitamin E. C-6-C-12 alkyl chains are attached to the A-ring of either a 3,3',4',5'-tetrahydroxyflavone or a 3,2',4',5'-tetrahydroxyflavone head group to give lipophilic flavonoids (Clog P = 4 to 10) that markedly inhibit iron-ADP catalysed oxidation of microsomal preparations. Orientation of the head group as well as total lipophilicity are important determinants of antioxidant efficacy. MM2 models indicate that our best straight chain 7-alkylflavonoids embed to the same depth in the membrane as vitamin E. The flavonoid head groups are prepared by aldol condensation followed by Algar-Flynn-Oyamada (AFO) oxidation or by Baker-Venkataraman re-arrangement. The alkyl tails are introduced by Suzuki or Negishi palladium-catalysed cross-coupling or by cross-metathesis catalysed by first generation Grubbs catalyst, which tolerate phenolic hydroxyl and ketone groups. (C) 2004 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmc.2004.02.031
点击查看最新优质反应信息

文献信息

  • [EN] FLAVONOID COMPOUNDS AS THERAPEUTIC ANTIOXIDANTS<br/>[FR] COMPOSES FLAVONOIDES EN TANT QU'ANTIOXYDANTS THERAPEUTIQUES
    申请人:ROWETT RES INST
    公开号:WO2004007475A1
    公开(公告)日:2004-01-22
    Novel flavonoid compounds having anti-oxidant activity are described. Formula (1). The compounds have been shown to exhibit anti-oxidative properties in biological systems and their utility in a sunscreen or skincare composition or to treat conditions involving oxidative damage, especially curative or prophylactic treatment of Alzheimer's disease or ischaemia-reperfusion and injury, is described.
    描述了具有抗氧化活性的新型黄酮类化合物。公式(1)。已经证明这些化合物在生物系统中展现出抗氧化特性,其在防晒霜或护肤品中的用途,或用于治疗涉及氧化损伤的情况,特别是治疗或预防治疗阿尔茨海默病或缺血再灌注和损伤的情况。
  • Flavonoid compounds as therapeutic antioxidants
    申请人:Caldwell Thomas Stuart
    公开号:US20060137207A1
    公开(公告)日:2006-06-29
    Novel flavonoid compounds having anti-oxidant activity are described. Formula 1. The compounds have been shown to exhibit anti-oxidative properties in biological systems and their utility in a sunscreen or skincare composition or to treat conditions involving oxidative damage, especially curative or prophylactic treatment of Alzheimer's disease or ischaemia-reperfusion injury, is described.
    描述了具有抗氧化活性的新型黄酮类化合物。公式1。已经证明这些化合物在生物系统中表现出抗氧化性质,并描述了它们在防晒霜或护肤组合物中的实用性,或用于治疗涉及氧化损伤的疾病,特别是治疗阿尔茨海默病或缺血再灌注损伤的治疗或预防。
  • COMPOUNDS
    申请人:Kong Thoo Lin Paul
    公开号:US20100151508A1
    公开(公告)日:2010-06-17
    Flavonoid-type compounds of the Formula (II); in which R 1 is alkyl C 2 to C 20 , R 2 , R 3 , R 4 and R 5 are any one or more of hydrogen, alkyl, alkenyl, alkynyl, phenyl or benzyl, especially 7-decyl-3-hydroxy-2-(3,4,5-trihydroxyphenyl)-4H-1-benzopy-ran-4-one or 7-ethyl-3-hydroxy-2-(3,4,5-trihydroxyphenyl)-4H-1-benzopyran-4-one provide fluorescent probes and antioxidants, and are useful in discriminating healthy and stressed cells.
    公式(II)中的黄酮类化合物;其中R1是烷基C2到C20,R2,R3,R4和R5是氢,烷基,烯基,炔基,苯基或苄基中的任何一个或多个,特别是7-癸基-3-羟基-2-(3,4,5-三羟基苯基)-4H-1-苯并吡喃-4-酮或7-乙基-3-羟基-2-(3,4,5-三羟基苯基)-4H-1-苯并吡喃-4-酮提供荧光探针和抗氧化剂,并且对于区分健康和受压力细胞非常有用。
  • FLAVONOID COMPOUNDS AS THERAPEUTIC ANTIOXIDANTS
    申请人:The Rowett Research Institute
    公开号:EP1534698B1
    公开(公告)日:2007-09-19
  • US7601754B2
    申请人:——
    公开号:US7601754B2
    公开(公告)日:2009-10-13
查看更多