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5-((2R,3R,4S,5R,6R)-3,4,5-Trihydroxy-6-hydroxymethyl-tetrahydro-pyran-2-ylcarbamoyl)-pentanoic acid | 198149-55-2

中文名称
——
中文别名
——
英文名称
5-((2R,3R,4S,5R,6R)-3,4,5-Trihydroxy-6-hydroxymethyl-tetrahydro-pyran-2-ylcarbamoyl)-pentanoic acid
英文别名
6-oxo-6-[[(2R,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]amino]hexanoic acid
5-((2R,3R,4S,5R,6R)-3,4,5-Trihydroxy-6-hydroxymethyl-tetrahydro-pyran-2-ylcarbamoyl)-pentanoic acid化学式
CAS
198149-55-2
化学式
C12H21NO8
mdl
——
分子量
307.301
InChiKey
FHPNSCMOLLOIBS-LTVFLDSHSA-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):
    -2.4
  • 重原子数:
    21
  • 可旋转键数:
    7
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.83
  • 拓扑面积:
    157
  • 氢给体数:
    6
  • 氢受体数:
    8

反应信息

  • 作为反应物:
    描述:
    单-6-O-氨基-Β-环糊精5-((2R,3R,4S,5R,6R)-3,4,5-Trihydroxy-6-hydroxymethyl-tetrahydro-pyran-2-ylcarbamoyl)-pentanoic acid1-羟基苯并三唑一水物N,N'-二环己基碳二亚胺 作用下, 以 N,N-二甲基甲酰胺 为溶剂, 以52%的产率得到mono-6-[6-(β-D-galactopyranosylamino)-1,6-dioxohexyl]amino-6-deoxy-β-cyclodextrin
    参考文献:
    名称:
    Synthesis of Cyclodextrin Derivatives Carrying Bio-Recognisable Saccharide Antennae
    摘要:
    The use of coupling saccharide antenna onto cyclodextrins allows mobility for the biologically active galactose head group, and allows the recognition process by the lectin (KbCWL). This paper reports a chemical synthesis of beta-CD derivatives using spacer arms 3, 4, 5, 6 and 9 carbon atoms. Preliminary results suggested that recognition is strongly dependent on the length of the spacer chain between the cyclodextrin and the sugar head group. (C) 1997 Elsevier Science Ltd.
    DOI:
    10.1016/s0040-4039(97)10033-8
  • 作为产物:
    描述:
    5-((2R,3R,4S,5R,6R)-3,4,5-Trihydroxy-6-hydroxymethyl-tetrahydro-pyran-2-ylcarbamoyl)-pentanoic acid methyl ester 在 sodium hydroxide 作用下, 以 甲醇 为溶剂, 以54%的产率得到5-((2R,3R,4S,5R,6R)-3,4,5-Trihydroxy-6-hydroxymethyl-tetrahydro-pyran-2-ylcarbamoyl)-pentanoic acid
    参考文献:
    名称:
    Synthesis of Cyclodextrin Derivatives Carrying Bio-Recognisable Saccharide Antennae
    摘要:
    The use of coupling saccharide antenna onto cyclodextrins allows mobility for the biologically active galactose head group, and allows the recognition process by the lectin (KbCWL). This paper reports a chemical synthesis of beta-CD derivatives using spacer arms 3, 4, 5, 6 and 9 carbon atoms. Preliminary results suggested that recognition is strongly dependent on the length of the spacer chain between the cyclodextrin and the sugar head group. (C) 1997 Elsevier Science Ltd.
    DOI:
    10.1016/s0040-4039(97)10033-8
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