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o-aminobenzyl β-D-galactopyranoside | 1580000-43-6

中文名称
——
中文别名
——
英文名称
o-aminobenzyl β-D-galactopyranoside
英文别名
galacto-iteamine;(2R,3R,4S,5R,6R)-2-[(2-aminophenyl)methoxy]-6-(hydroxymethyl)oxane-3,4,5-triol
o-aminobenzyl β-D-galactopyranoside化学式
CAS
1580000-43-6
化学式
C13H19NO6
mdl
——
分子量
285.297
InChiKey
BQRRQISPSWTJIH-KSSYENDESA-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):
    -1.4
  • 重原子数:
    20
  • 可旋转键数:
    4
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.54
  • 拓扑面积:
    125
  • 氢给体数:
    5
  • 氢受体数:
    7

反应信息

  • 作为产物:
    描述:
    beta-D-半乳糖五乙酸酯 在 palladium 10% on activated carbon 、 氢溴酸氢气sodium methylate2,3-二氯-5,6-二氰基-1,4-苯醌 作用下, 以 甲醇乙醇二氯甲烷溶剂黄146乙腈 为溶剂, 反应 17.67h, 生成 o-aminobenzyl β-D-galactopyranoside
    参考文献:
    名称:
    Iteamine, the first alkaloid isolated from Itea virginica L. inflorescence
    摘要:
    Iteamine, o-aminobenzyl beta-D-glucopyranoside, is the first alkaloid to be isolated from Itea virginica. Itea is the sole plant source of D-psicose, a rare sugar likely to be a major dietary supplement. The structure of iteamine was established by NMR and confirmed by total synthesis. Iteamine and its galacto-analog (which was not found in Itea plants) showed no strong inhibition of any of the 15 glycosidases tested; unnatural galacto-iteamine was a weak inhibitor of chicken liver alpha-N-acetylgalactosaminidase. (C) 2014 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.phytochem.2014.01.012
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文献信息

  • Iteamine, the first alkaloid isolated from Itea virginica L. inflorescence
    作者:Benjamin J. Ayers、Jacqueline Hollinshead、Alexander W. Saville、Shinpei Nakagawa、Isao Adachi、Atsushi Kato、Ken Izumori、Barbara Bartholomew、George W.J. Fleet、Robert J. Nash
    DOI:10.1016/j.phytochem.2014.01.012
    日期:2014.4
    Iteamine, o-aminobenzyl beta-D-glucopyranoside, is the first alkaloid to be isolated from Itea virginica. Itea is the sole plant source of D-psicose, a rare sugar likely to be a major dietary supplement. The structure of iteamine was established by NMR and confirmed by total synthesis. Iteamine and its galacto-analog (which was not found in Itea plants) showed no strong inhibition of any of the 15 glycosidases tested; unnatural galacto-iteamine was a weak inhibitor of chicken liver alpha-N-acetylgalactosaminidase. (C) 2014 Elsevier Ltd. All rights reserved.
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