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5β-pseudo-spirost-3β,15α,23α-triol 3-O-β-D-glucopyranosyl-(1→2)-β-D-galactopyranoside

中文名称
——
中文别名
——
英文名称
5β-pseudo-spirost-3β,15α,23α-triol 3-O-β-D-glucopyranosyl-(1→2)-β-D-galactopyranoside
英文别名
timosaponin Y
5β-pseudo-spirost-3β,15α,23α-triol 3-O-β-D-glucopyranosyl-(1→2)-β-D-galactopyranoside化学式
CAS
——
化学式
C39H64O15
mdl
——
分子量
772.928
InChiKey
PTLBKBIVYONQLJ-USSPPNTISA-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):
    -0.47
  • 重原子数:
    54.0
  • 可旋转键数:
    6.0
  • 环数:
    8.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    237.45
  • 氢给体数:
    9.0
  • 氢受体数:
    15.0

反应信息

  • 作为反应物:
    参考文献:
    名称:
    New steroidal glycosides from the rhizome of Anemarrhena asphodeloides
    摘要:
    Two new steroidal saponins, timosaponin X (1) and timosaponin Y (2), and one new pregnane glycoside, timopregnane B (3), were isolated from the rhizomes of Anemarrhena asphodeloides, as well as three known compounds 25S-timosaponin BII (4), protodesgalactotigonin (5), and timosaponin BII-a (6) isolated from this plant for the first time. By the detailed analysis of 1D, 2D NMR, MS spectra, and chemical evidences, the structures of new compounds were elucidated as 26-O-beta-D-glucopyranosyl-(25S)-5 beta-22-methoxy-furost-3 beta, 26-diol 3-O-beta-D-glucopyranosyl( 1 -> 2)-alpha-L-arabinopyranoside (1), 5 beta-pseudo-spirost-3 beta, 15 alpha, 23 alpha-triol 3-O-beta-D-glucopyranosyl-( 1 -> 2)-beta-D-galactopyranoside (2), (5 beta, 17 alpha)-Delta(16(17))-20-one-pregn-2 beta, 3 beta-diol 3-O-beta-D-glucopyranosyl-(1 -> 2)-beta-D-galactopyranoside (3).
    DOI:
    10.1080/10286020.2014.942658
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文献信息

  • New steroidal glycosides from the rhizome of <i>Anemarrhena asphodeloides</i>
    作者:Jian-Chao Yuan、Jie Zhang、Fang-Xu Wang、Xu Pang、Yang Zhao、Cheng-Qi Xiong、Bai-Ping Ma
    DOI:10.1080/10286020.2014.942658
    日期:2014.9.2
    Two new steroidal saponins, timosaponin X (1) and timosaponin Y (2), and one new pregnane glycoside, timopregnane B (3), were isolated from the rhizomes of Anemarrhena asphodeloides, as well as three known compounds 25S-timosaponin BII (4), protodesgalactotigonin (5), and timosaponin BII-a (6) isolated from this plant for the first time. By the detailed analysis of 1D, 2D NMR, MS spectra, and chemical evidences, the structures of new compounds were elucidated as 26-O-beta-D-glucopyranosyl-(25S)-5 beta-22-methoxy-furost-3 beta, 26-diol 3-O-beta-D-glucopyranosyl( 1 -> 2)-alpha-L-arabinopyranoside (1), 5 beta-pseudo-spirost-3 beta, 15 alpha, 23 alpha-triol 3-O-beta-D-glucopyranosyl-( 1 -> 2)-beta-D-galactopyranoside (2), (5 beta, 17 alpha)-Delta(16(17))-20-one-pregn-2 beta, 3 beta-diol 3-O-beta-D-glucopyranosyl-(1 -> 2)-beta-D-galactopyranoside (3).
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