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Bn(-2)[Bn(-3)]Fuc4Ac(a1-3)Ribf2S5S(b)-guanin-9-yl | 690623-84-8

中文名称
——
中文别名
——
英文名称
Bn(-2)[Bn(-3)]Fuc4Ac(a1-3)Ribf2S5S(b)-guanin-9-yl
英文别名
[(2S,3R,4R,5S,6S)-6-[(2R,3R,4R,5R)-5-(2-amino-6-oxo-1H-purin-9-yl)-4-sulfooxy-2-(sulfooxymethyl)oxolan-3-yl]oxy-2-methyl-4,5-bis(phenylmethoxy)oxan-3-yl] acetate
Bn(-2)[Bn(-3)]Fuc4Ac(a1-3)Ribf2S5S(b)-guanin-9-yl化学式
CAS
690623-84-8
化学式
C32H37N5O16S2
mdl
——
分子量
811.802
InChiKey
JTFYPFAVENLVNA-ZTQDMLQYSA-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):
    -0.5
  • 重原子数:
    55
  • 可旋转键数:
    16
  • 环数:
    6.0
  • sp3杂化的碳原子比例:
    0.44
  • 拓扑面积:
    302
  • 氢给体数:
    4
  • 氢受体数:
    18

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

  • 作为反应物:
    描述:
    Bn(-2)[Bn(-3)]Fuc4Ac(a1-3)Ribf2S5S(b)-guanin-9-ylpalladium dihydroxide 氢气溶剂黄146 作用下, 以 甲醇 为溶剂, 反应 15.0h, 以99%的产率得到3'-O-(4''-O-acetyl-α-L-fucopyranosyl)guanosine-2',5'-disulfate
    参考文献:
    名称:
    Structure and Total Synthesis of HF-7, a Neuroactive Glyconucleoside Disulfate from the Funnel-Web Spider Hololena curta
    摘要:
    Spider venom toxins have attracted considerable attention for their ability to block the action of excitatory amino acids such as glutamate and aspartate. A new neuroactive compound designated HF-7 was isolated in 1993 from the venom of a funnel-web spider, Hololena curta. HF-7 was shown to block kainate receptors and, albeit weakly, L-type calcium channels. Spectroscopic analysis established the structure of HF-7 as an unusual acetylated, disulfated fucopyranosyl guanosine, with the acetate ester attached at the 4-position of an alpha-linked fucose ring and two sulfates attached to the ribose ring. Because insufficient quantities of natural HF-7 were available for chemical degradation or X-ray diffraction analysis, total synthesis of three candidate structures was used to establish the identity of HF-7. Once HF-7 was fully characterized as 3'-O-(4 "-O-acetyl-alpha-L-fucopyranosyl)gnanosine-2',5-dusulfate, an improved, targeted synthesis of the natural product was developed.
    DOI:
    10.1021/ja990274q
  • 作为产物:
    参考文献:
    名称:
    Structure and Total Synthesis of HF-7, a Neuroactive Glyconucleoside Disulfate from the Funnel-Web Spider Hololena curta
    摘要:
    Spider venom toxins have attracted considerable attention for their ability to block the action of excitatory amino acids such as glutamate and aspartate. A new neuroactive compound designated HF-7 was isolated in 1993 from the venom of a funnel-web spider, Hololena curta. HF-7 was shown to block kainate receptors and, albeit weakly, L-type calcium channels. Spectroscopic analysis established the structure of HF-7 as an unusual acetylated, disulfated fucopyranosyl guanosine, with the acetate ester attached at the 4-position of an alpha-linked fucose ring and two sulfates attached to the ribose ring. Because insufficient quantities of natural HF-7 were available for chemical degradation or X-ray diffraction analysis, total synthesis of three candidate structures was used to establish the identity of HF-7. Once HF-7 was fully characterized as 3'-O-(4 "-O-acetyl-alpha-L-fucopyranosyl)gnanosine-2',5-dusulfate, an improved, targeted synthesis of the natural product was developed.
    DOI:
    10.1021/ja990274q
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