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(2R,3R,4R,5S,6R)-5-[(2S,3R,4S,5S,6R)-6-[(2-chloro-4-nitrophenoxy)methyl]-3,4,5-trihydroxyoxan-2-yl]oxy-6-(hydroxymethyl)oxane-2,3,4-triol

中文名称
——
中文别名
——
英文名称
(2R,3R,4R,5S,6R)-5-[(2S,3R,4S,5S,6R)-6-[(2-chloro-4-nitrophenoxy)methyl]-3,4,5-trihydroxyoxan-2-yl]oxy-6-(hydroxymethyl)oxane-2,3,4-triol
英文别名
——
(2R,3R,4R,5S,6R)-5-[(2S,3R,4S,5S,6R)-6-[(2-chloro-4-nitrophenoxy)methyl]-3,4,5-trihydroxyoxan-2-yl]oxy-6-(hydroxymethyl)oxane-2,3,4-triol化学式
CAS
——
化学式
C18H24ClNO13
mdl
——
分子量
497.8
InChiKey
WKUMKRUDPNZIEN-KFRZSCGFSA-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):
    -2.5
  • 重原子数:
    33
  • 可旋转键数:
    6
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.67
  • 拓扑面积:
    224
  • 氢给体数:
    7
  • 氢受体数:
    13

文献信息

  • Cellulase assay
    申请人:Megazyme IP Limited
    公开号:EP2719758A1
    公开(公告)日:2014-04-16
    The invention involves the development of a substrate and assay procedure for the scientific measurement of cellulase in admixture with other enzymes active on cellulose or 1,4-β-D-gluco-oligosaccharides, or in various levels of purity of the cellulase. This substrate being characterised by the fact that it contains at least 2 glucose units linked β-1,4-, with the reducing end glucose unit linked β- or α- to a compound which exhibits an optically measurable change on cleavage of the bond between it and the adjacent D-glucosyl residue and the non-reducing terminal D-glucosyl unit is covalently linked to a blocking substituent which inhibits cleavage by exo-acting enzymes of the bond between the terminal and non-reducing end, penultimate D-glucose unit.
    本发明涉及开发一种底物和测定程序,用于科学测定纤维素酶与其他对纤维素或 1,4-β-D-葡聚寡糖有活性的酶混合的情况,或不同纯度的纤维素酶。这种底物的特点是,它至少含有 2 个连接在 β-1,4-上的葡萄糖单元,其中还原端的葡萄糖单元与一种化合物连接在 β- 或 α-上,这种化合物在裂解它与相邻 D-葡萄糖残基之间的键时显示出可测量的光学变化,而非还原端的 D-葡萄糖单元与一种阻断取代基共价连接,这种取代基抑制外作用酶裂解末端和非还原端、倒数第二个 D-葡萄糖单元之间的键。
  • Cellulase Assay
    申请人:Megazyme IP Limited
    公开号:US20140154721A1
    公开(公告)日:2014-06-05
    The invention involves the development of a substrate and assay procedure for the scientific measurement of cellulase in admixture with other enzymes active on cellulose or 1,4-β-D-cello-oligosaccharides, or in various levels of purity of the cellulase. This substrate being characterised by the fact that it contains at least 2 glucose units linked β-1,4-, with the reducing end glucose unit linked β- or α- to a compound which exhibits an optically measurable change on cleavage of the bond between it and the adjacent D-glucosyl residue and the non-reducing terminal D-glucosyl unit is covalently linked to a blocking substituent which inhibits cleavage by exo-acting enzymes of the bond between the terminal and non-reducing end, penultimate D-glucose unit.
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