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glucosyl-γ-CD | 104723-63-9

中文名称
——
中文别名
——
英文名称
glucosyl-γ-CD
英文别名
(1S,3R,5R,6S,8R,10R,11S,13R,15R,16S,18R,20R,21S,23R,25R,26S,28R,30R,31S,33R,35R,36S,38R,40R,41R,42R,43R,44R,45R,46R,47R,48R,49R,50R,51R,52R,53R,54R,55R,56R)-5,10,15,20,30,35,40-heptakis(hydroxymethyl)-25-[[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]-2,4,7,9,12,14,17,19,22,24,27,29,32,34,37,39-hexadecaoxanonacyclo[36.2.2.23,6.28,11.213,16.218,21.223,26.228,31.233,36]hexapentacontane-41,42,43,44,45,46,47,48,49,50,51,52,53,54,55,56-hexadecol
glucosyl-γ-CD化学式
CAS
104723-63-9
化学式
C54H90O45
mdl
——
分子量
1459.28
InChiKey
SPSGWVFQAVINCT-FXWIDUTLSA-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):
    -18.8
  • 重原子数:
    99
  • 可旋转键数:
    11
  • 环数:
    31.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    712
  • 氢给体数:
    27
  • 氢受体数:
    45

反应信息

  • 作为反应物:
    描述:
    glucosyl-γ-CD 反应 1.0h, 以9.5%的产率得到
    参考文献:
    名称:
    Preparation, isolation, and characterization of novel heterogeneous branched cyclomalto-oligosaccharides having β-d-galactosyl residue(s) on the side chain
    摘要:
    Transgalactosylated products of branched cyclodextrins (glucosyl-alphaCD, -betaCD, -gammaCD, and maltosyl-alphaCD, -betaCD, -gammaCD)were synthesized by beta-D-galactosidases from Bacillus circulans and Penicillium multicolor using lactose as a donor substrate and branched CDs as acceptors. Eighteen beta-D-galactosylated branched CDs were isolated and purified by HPLC. Their structures were elucidated by FABMS and C-13 NMR spectroscopies, and methylation analysis. The chromatographic behavior of these novel heterogeneous branched CDs on three HPLC columns of different separation modes was compared.
    DOI:
    10.1016/0008-6215(93)87006-e
  • 作为产物:
    描述:
    (1S,3R,5R,6S,8R,10R,11S,13R,15R,16S,18R,20R,21S,23R,25R,26S,28R,30R,31S,33R,35R,36S,38R,40R,41R,42R,43R,44R,45R,46R,47R,48R,49R,50R,51R,52R,53R,54R,55R,56R)-20-[[(2S,3R,4R,5S,6R)-5-[(2R,3R,4R,5S,6R)-3,4-dihydroxy-6-(hydroxymethyl)-5-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-3,4-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]-5,10,15,25,30,35,40-heptakis(hydroxymethyl)-2,4,7,9,12,14,17,19,22,24,27,29,32,34,37,39-hexadecaoxanonacyclo[36.2.2.23,6.28,11.213,16.218,21.223,26.228,31.233,36]hexapentacontane-41,42,43,44,45,46,47,48,49,50,51,52,53,54,55,56-hexadecol 生成 glucosyl-γ-CD
    参考文献:
    名称:
    OKADA, YASUYO;KUBOTA, YOKO;KOIZUMI, KYOKO;HIZUKURI, SUSUMU;OHFUJI, TAKEHI+, CHEM. AND PHARM. BULL., 36,(1988) N 6, C. 2176-2185
    摘要:
    DOI:
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