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2-(3,4-二羟基苯基)-3-(alpha-D-吡喃半乳糖基氧基)-5,7-二羟基-4H-1-苯并吡喃-4-酮 | 65549-68-0

中文名称
2-(3,4-二羟基苯基)-3-(alpha-D-吡喃半乳糖基氧基)-5,7-二羟基-4H-1-苯并吡喃-4-酮
中文别名
——
英文名称
quercetin-3-O-galactoside
英文别名
3-quercetin-galactoside;hyperoside;hyperin;4H-1-Benzopyran-4-one, 2-(3,4-dihydroxyphenyl)-3-(alpha-D-galactopyranosyloxy)-5,7-dihydroxy-;2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2R,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one
2-(3,4-二羟基苯基)-3-(alpha-D-吡喃半乳糖基氧基)-5,7-二羟基-4H-1-苯并吡喃-4-酮化学式
CAS
65549-68-0
化学式
C21H20O12
mdl
——
分子量
464.383
InChiKey
OVSQVDMCBVZWGM-PRPRGGMHSA-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):
    0.4
  • 重原子数:
    33
  • 可旋转键数:
    4
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.29
  • 拓扑面积:
    207
  • 氢给体数:
    8
  • 氢受体数:
    12

SDS

SDS:53be90d2ee7b7776e906e6f3aa4a00a9
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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:
    描述:
    尿苷 5’-二二氧磷基半乳糖二钠盐槲皮素 在 recombinant poplar flavonoid galactosyltransferase PtUGT78L1 作用下, 以 aq. buffer 为溶剂, 反应 0.5h, 生成 2-(3,4-二羟基苯基)-3-(alpha-D-吡喃半乳糖基氧基)-5,7-二羟基-4H-1-苯并吡喃-4-酮
    参考文献:
    名称:
    Molecular cloning and biochemical characterization of two UDP-glycosyltransferases from poplar
    摘要:
    Two pathogen-induced uridine diphosphate glycosyltransferases (UGTs) identified previously via co-expression with induced proanthocyanidin (PA) synthesis in poplar were cloned and characterized. Phylogenetic analysis grouped both genes with other known flavonoid UGTs that act on flavonols and anthocyanins. Recombinant enzymes were produced in order to test if they could glycoslate flavonoids. PtUGT78L1 accepted the flavonols quercetin and kaempferol as well as cyanidin, and used UDP-galactose as a sugar donor. PtUGT78M1 did not accept any of the flavonoids tested as a substrate, but did transfer glucose from UDP-glucose to the universal substrate 2,4,6-trichlorophenol. However, neither enzyme acted on the flavan-3-ols catechin or epicatechin, intermediates in the PA biosynthetic pathway. (C) 2013 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.phytochem.2012.12.012
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文献信息

  • Molecular cloning and biochemical characterization of two UDP-glycosyltransferases from poplar
    作者:Vasko Veljanovski、C. Peter Constabel
    DOI:10.1016/j.phytochem.2012.12.012
    日期:2013.7
    Two pathogen-induced uridine diphosphate glycosyltransferases (UGTs) identified previously via co-expression with induced proanthocyanidin (PA) synthesis in poplar were cloned and characterized. Phylogenetic analysis grouped both genes with other known flavonoid UGTs that act on flavonols and anthocyanins. Recombinant enzymes were produced in order to test if they could glycoslate flavonoids. PtUGT78L1 accepted the flavonols quercetin and kaempferol as well as cyanidin, and used UDP-galactose as a sugar donor. PtUGT78M1 did not accept any of the flavonoids tested as a substrate, but did transfer glucose from UDP-glucose to the universal substrate 2,4,6-trichlorophenol. However, neither enzyme acted on the flavan-3-ols catechin or epicatechin, intermediates in the PA biosynthetic pathway. (C) 2013 Elsevier Ltd. All rights reserved.
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