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1-[2'-hydroxy-4'-(2''',3''',4''',6'''-tetra-O-acetyl-β-D-glucopyranosyloxy)phenyl]-3-phenyl-propane-1,3-dione | 121965-40-0

中文名称
——
中文别名
——
英文名称
1-[2'-hydroxy-4'-(2''',3''',4''',6'''-tetra-O-acetyl-β-D-glucopyranosyloxy)phenyl]-3-phenyl-propane-1,3-dione
英文别名
1-[2-hydroxy-4-(tetra-O-acetyl-β-D-glucopyranosyloxy)-phenyl]-3-phenyl-propane-1,3-dione;1-[2-Hydroxy-4-(tetra-O-acetyl-β-D-glucopyranosyloxy)-phenyl]-3-phenyl-propan-1,3-dion;[(2R,3R,4S,5R,6S)-3,4,5-triacetyloxy-6-[3-hydroxy-4-(3-oxo-3-phenylpropanoyl)phenoxy]oxan-2-yl]methyl acetate
1-[2'-hydroxy-4'-(2''',3''',4''',6'''-tetra-O-acetyl-β-D-glucopyranosyloxy)phenyl]-3-phenyl-propane-1,3-dione化学式
CAS
121965-40-0
化学式
C29H30O13
mdl
——
分子量
586.549
InChiKey
HYOFZBXRVTWEOW-XYPQWYOHSA-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):
    2.9
  • 重原子数:
    42
  • 可旋转键数:
    15
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.38
  • 拓扑面积:
    178
  • 氢给体数:
    1
  • 氢受体数:
    13

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:
    1-[2'-hydroxy-4'-(2''',3''',4''',6'''-tetra-O-acetyl-β-D-glucopyranosyloxy)phenyl]-3-phenyl-propane-1,3-dione甲醇sodium methylate 作用下, 以 甲醇 为溶剂, 反应 10.0h, 以69%的产率得到1-(4'-β-D-glucopyranosyloxy-2'-hydroxyphenyl)-3-phenylpropane-1,3-dione
    参考文献:
    名称:
    Synthesis, biopharmaceutical characterization, antimicrobial and antioxidant activities of 1-(4′-O-β-d-glucopyranosyloxy-2′-hydroxyphenyl)-3-aryl-propane-1,3-diones
    摘要:
    This research communication is toward the investigation of the antibacterial, antifungal and antioxidant activities of the synthesized compounds 1-(4'-O-beta-D-glucopyranosyloxy-2'-hydroxyphenyl)-3-aryl-propane-1,3-diones (5a)-(5h). These compounds have been obtained by the interaction of alpha-acetobromoglucose with 1-(2',4'-dihydroxyphenyl)-3-aryl-propane-1,3-diones (3a)-(3h) under anhydrous condition and at lower temperature. The structures of these newly synthesized O-beta-D-glucopyranosides were established on the basis of chemical, elemental, and spectral analyses. Further, the compounds (5b), (5c), (5d) and (5g) showed potent antibacterial and antifungal activity. A good correlation was obtained between the theoretical predictions of bioavailability using Lipinski's rule-of-five and experimental verification. (c) 2011 Elsevier Masson SAS. All rights reserved.
    DOI:
    10.1016/j.ejmech.2011.01.068
  • 作为产物:
    描述:
    参考文献:
    名称:
    Reichel; Henning, Justus Liebigs Annalen der Chemie, 1959, vol. 621, p. 72,77
    摘要:
    DOI:
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文献信息

  • Baker et al., Journal of the Chemical Society, 1952, p. 1505
    作者:Baker et al.
    DOI:——
    日期:——
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