摩熵化学
数据库官网
小程序
打开微信扫一扫
首页 分子通 化学资讯 化学百科 反应查询 关于我们
请输入关键词

4-aminophenyl S-β-D-glucopyranosyl-(1->4)-S-4-thio-β-D-glucopyranosyl-(1->4)-1,4-dithio-β-D-glucopyranoside | 116307-19-8

中文名称
——
中文别名
——
英文名称
4-aminophenyl S-β-D-glucopyranosyl-(1->4)-S-4-thio-β-D-glucopyranosyl-(1->4)-1,4-dithio-β-D-glucopyranoside
英文别名
——
4-aminophenyl S-β-D-glucopyranosyl-(1->4)-S-4-thio-β-D-glucopyranosyl-(1->4)-1,4-dithio-β-D-glucopyranoside化学式
CAS
116307-19-8
化学式
C24H37NO13S3
mdl
——
分子量
643.755
InChiKey
LYEWPYLHDSWMQM-FVLBVTBHSA-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):
    -3.76
  • 重原子数:
    41.0
  • 可旋转键数:
    9.0
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.75
  • 拓扑面积:
    256.01
  • 氢给体数:
    11.0
  • 氢受体数:
    17.0

反应信息

  • 作为反应物:
    描述:
    乙酸酐4-aminophenyl S-β-D-glucopyranosyl-(1->4)-S-4-thio-β-D-glucopyranosyl-(1->4)-1,4-dithio-β-D-glucopyranoside吡啶 作用下, 以87%的产率得到4-acetamidophenyl S-(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl)-(1->4)-S-(2,3,6-tri-O-acetyl-4-thio-β-D-glucopyranosyl)-(1->4)-2,3,6-tri-O-acetyl-1,4-dithio-β-D-glucopyranoside
    参考文献:
    名称:
    4-Thiocellooligosaccharides. Their synthesis and use as ligands for the separation of cellobiohydrolases of Trichoderma reesei by affinity chromatography
    摘要:
    4-Aminophenyl 1,4-dithio-beta-cellobioside (6) was obtained by treatment of methyl 2,3,6-tri-O-benzoyl-4-O-triflyl-alpha-D-galactopyranoside with the sodium salt of 1-thio-beta-D-glucopyranose, followed by acetolysis and glycosylation of the corresponding bromide with 4-aminobenzenethiol and subsequent deacylation. A similar synthesis starting with the 1-thiolate of 1,4-dithio-beta-cellobiose led to the trisaccharide 4-aminophenyl 1,4,4'-trithiocellotrioside (16). The 4-acetamidophenyl di- and tri-thiocellooligosaccharides were found to be excellent competitive inhibitors of the hydrolysis of 4-methylumbelliferyl beta-lactoside with respective K(i) values of 25 and 6.5mM. The two 4-aminophenyl oligosaccharides 6 and 16 were coupled to CH-Sepharose 4B, and the affinity gels were used for the purification of cellobiohydrolases from a crude commercial cellulolytic extract of T. reesei. Cellobiohydrolases I or II were selectively desorbed from gels bearing ligands 6 and 16.
    DOI:
    10.1016/0008-6215(92)84090-f
  • 作为产物:
    参考文献:
    名称:
    4-Thiocellooligosaccharides. Their synthesis and use as ligands for the separation of cellobiohydrolases of Trichoderma reesei by affinity chromatography
    摘要:
    4-Aminophenyl 1,4-dithio-beta-cellobioside (6) was obtained by treatment of methyl 2,3,6-tri-O-benzoyl-4-O-triflyl-alpha-D-galactopyranoside with the sodium salt of 1-thio-beta-D-glucopyranose, followed by acetolysis and glycosylation of the corresponding bromide with 4-aminobenzenethiol and subsequent deacylation. A similar synthesis starting with the 1-thiolate of 1,4-dithio-beta-cellobiose led to the trisaccharide 4-aminophenyl 1,4,4'-trithiocellotrioside (16). The 4-acetamidophenyl di- and tri-thiocellooligosaccharides were found to be excellent competitive inhibitors of the hydrolysis of 4-methylumbelliferyl beta-lactoside with respective K(i) values of 25 and 6.5mM. The two 4-aminophenyl oligosaccharides 6 and 16 were coupled to CH-Sepharose 4B, and the affinity gels were used for the purification of cellobiohydrolases from a crude commercial cellulolytic extract of T. reesei. Cellobiohydrolases I or II were selectively desorbed from gels bearing ligands 6 and 16.
    DOI:
    10.1016/0008-6215(92)84090-f
点击查看最新优质反应信息