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(2S,5S,6S)-2-((R)-1-(((2R,3R,4S,5R)-5-(aminomethyl)-3,4-dihydroxytetrahydrofuran-2-yl)oxy)ethyl)-1,4-dimethyl-3-oxo-6-(palmitoyloxy)-1,4-diazepane-5-carboxylic acid compound with 2,2,2-trifluoroacetic acid (1:1) | 1037307-56-4

中文名称
——
中文别名
——
英文名称
(2S,5S,6S)-2-((R)-1-(((2R,3R,4S,5R)-5-(aminomethyl)-3,4-dihydroxytetrahydrofuran-2-yl)oxy)ethyl)-1,4-dimethyl-3-oxo-6-(palmitoyloxy)-1,4-diazepane-5-carboxylic acid compound with 2,2,2-trifluoroacetic acid (1:1)
英文别名
——
(2S,5S,6S)-2-((R)-1-(((2R,3R,4S,5R)-5-(aminomethyl)-3,4-dihydroxytetrahydrofuran-2-yl)oxy)ethyl)-1,4-dimethyl-3-oxo-6-(palmitoyloxy)-1,4-diazepane-5-carboxylic acid compound with 2,2,2-trifluoroacetic acid (1:1)化学式
CAS
1037307-56-4
化学式
C2HF3O2*C31H57N3O9
mdl
——
分子量
729.832
InChiKey
KTFAYSUWFBVKMW-GDNNDYQPSA-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):
    3.05
  • 重原子数:
    50.0
  • 可旋转键数:
    20.0
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.88
  • 拓扑面积:
    209.39
  • 氢给体数:
    5.0
  • 氢受体数:
    11.0

反应信息

  • 作为产物:
    描述:
    tert-butyl (2S,5S,6S)-2-((R)-1-(((3aR,4R,6R,6aR)-6-(((tert-butoxycarbonyl)amino)methyl)-2,2-diethyltetrahydrofuro[3,4-d][1,3]dioxol-4-yl)oxy)ethyl)-1,4-dimethyl-3-oxo-6-(palmitoyloxy)-1,4-diazepane-5-carboxylate 三氟乙酸 为溶剂, 反应 24.0h, 以100%的产率得到(2S,5S,6S)-2-((R)-1-(((2R,3R,4S,5R)-5-(aminomethyl)-3,4-dihydroxytetrahydrofuran-2-yl)oxy)ethyl)-1,4-dimethyl-3-oxo-6-(palmitoyloxy)-1,4-diazepane-5-carboxylic acid compound with 2,2,2-trifluoroacetic acid (1:1)
    参考文献:
    名称:
    Structure–activity relationship of truncated analogs of caprazamycins as potential anti-tuberculosis agents
    摘要:
    Systematic structure-activity relationship studies of caprazamycin (CPZ) analogs, including the aminoribose-truncated 5 and the uridine-truncated 6, have been carried out. Both 5 and 6 were synthesized efficiently via diazepanone ring construction by intramolecular reductive alkylation of aminoaldehyde derivatives. The antibacterial activity of a range of analogs, including 5 and 6, against Mycobacteriumosis was evaluated, and it was found that the uridine, the aminoribose, and the fatty acyl side chains are crucial for antibacterial activity. This study would be a guide for designing novel anti-tuberculosis agents based on the 6'-N-alkyl-5'-beta-O-aminoribosyl-glycyluridine class of antibiotics including the CPZs. (C) 2008 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmc.2008.03.020
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