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N-{[6-(dansylamino)hexyl]aminohexyl}-3,4-O-isopropylidene-1,5-dideoxy-1,5-imino-D-galactitol | 1320341-40-9

中文名称
——
中文别名
——
英文名称
N-{[6-(dansylamino)hexyl]aminohexyl}-3,4-O-isopropylidene-1,5-dideoxy-1,5-imino-D-galactitol
英文别名
——
N-{[6-(dansylamino)hexyl]aminohexyl}-3,4-O-isopropylidene-1,5-dideoxy-1,5-imino-D-galactitol化学式
CAS
1320341-40-9
化学式
C33H54N4O6S
mdl
——
分子量
634.881
InChiKey
KPSRQLJXSYNCOL-FZSDTKOLSA-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):
    3.45
  • 重原子数:
    44.0
  • 可旋转键数:
    18.0
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.7
  • 拓扑面积:
    123.6
  • 氢给体数:
    4.0
  • 氢受体数:
    9.0

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
  • 下游产品
    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:
    N-{[6-(dansylamino)hexyl]aminohexyl}-3,4-O-isopropylidene-1,5-dideoxy-1,5-imino-D-galactitol吡啶盐酸 作用下, 以 二氯甲烷 为溶剂, 反应 2.5h, 生成 1-{6-[N-[6-(dansylamino)hexyl]-N-(octanoyl)amino]hexyl}-1,5-dideoxy-1,5-imino-D-galactitol dihydrochloride
    参考文献:
    名称:
    1-Deoxy-d-galactonojirimycins with dansyl capped N-substituents as β-galactosidase inhibitors and potential probes for GM1 gangliosidosis affected cell lines
    摘要:
    Two simple and reliably accessible intermediates, N-carboxypentyl- and N-aminohexyl-1-deoxy-D-galactonojirimycin were employed for the synthesis of a set of terminally N-dansyl substituted derivatives. Reaction of the terminal carboxylic acid of N-carboxypentyl-1-deoxy-D-galactonojirimycin with N-dansyl-1,6-diaminohexane provided the chain-extended fluorescent derivative. Employing bis(6-dansylaminohexyl)amine, the corresponding branched di-N-dansyl compound was obtained. Partially protected N-aminohexyl-1-deoxy-D-galactonojirimycin served as intermediate for two additional chain-extended fluorescent 1-deoxy-D-galactonojirimycin (1-DGJ) derivatives featuring terminal dansyl groups in the N-alkyl substituent. These new compounds are strong inhibitors of D-galactosidases and may serve as leads en route to pharmacological chaperones for GM1-gangliosidosis. (C) 2011 Published by Elsevier Ltd.
    DOI:
    10.1016/j.carres.2011.05.010
  • 作为产物:
    描述:
    N-dansyl-O-mesyl-6-aminohexanolN-(6-amimohexyl)-3,4-O-isopropylidene-1-deoxy-D-galactonojirimycinsodium carbonate 作用下, 以 N,N-二甲基甲酰胺 为溶剂, 反应 44.0h, 以47%的产率得到N-{[6-(dansylamino)hexyl]aminohexyl}-3,4-O-isopropylidene-1,5-dideoxy-1,5-imino-D-galactitol
    参考文献:
    名称:
    1-Deoxy-d-galactonojirimycins with dansyl capped N-substituents as β-galactosidase inhibitors and potential probes for GM1 gangliosidosis affected cell lines
    摘要:
    Two simple and reliably accessible intermediates, N-carboxypentyl- and N-aminohexyl-1-deoxy-D-galactonojirimycin were employed for the synthesis of a set of terminally N-dansyl substituted derivatives. Reaction of the terminal carboxylic acid of N-carboxypentyl-1-deoxy-D-galactonojirimycin with N-dansyl-1,6-diaminohexane provided the chain-extended fluorescent derivative. Employing bis(6-dansylaminohexyl)amine, the corresponding branched di-N-dansyl compound was obtained. Partially protected N-aminohexyl-1-deoxy-D-galactonojirimycin served as intermediate for two additional chain-extended fluorescent 1-deoxy-D-galactonojirimycin (1-DGJ) derivatives featuring terminal dansyl groups in the N-alkyl substituent. These new compounds are strong inhibitors of D-galactosidases and may serve as leads en route to pharmacological chaperones for GM1-gangliosidosis. (C) 2011 Published by Elsevier Ltd.
    DOI:
    10.1016/j.carres.2011.05.010
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