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2,5-anhydro-1-deoxy-1-(uracil-1'-yl)-6-(5''-(4'''-aminomethyl-1H,1''',2''',3'''-triazol-1'''-yl)-1'',5''-dideoxy-2'',3''-O-isopentylidene-β-D-ribos-1''-yl)-D-glucitol | 1237748-15-0

中文名称
——
中文别名
——
英文名称
2,5-anhydro-1-deoxy-1-(uracil-1'-yl)-6-(5''-(4'''-aminomethyl-1H,1''',2''',3'''-triazol-1'''-yl)-1'',5''-dideoxy-2'',3''-O-isopentylidene-β-D-ribos-1''-yl)-D-glucitol
英文别名
1-[[(2S,3S,4S,5R)-5-[[(2R,3R,4S,5R)-5-[[4-(aminomethyl)triazol-1-yl]methyl]-3,4-dihydroxyoxolan-2-yl]oxymethyl]-3,4-dihydroxyoxolan-2-yl]methyl]pyrimidine-2,4-dione
2,5-anhydro-1-deoxy-1-(uracil-1'-yl)-6-(5''-(4'''-aminomethyl-1H,1''',2''',3'''-triazol-1'''-yl)-1'',5''-dideoxy-2'',3''-O-isopentylidene-β-D-ribos-1''-yl)-D-glucitol化学式
CAS
1237748-15-0
化学式
C18H26N6O9
mdl
——
分子量
470.439
InChiKey
QFWBLYWHEMVKLJ-CFGOVTMJSA-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):
    -5.5
  • 重原子数:
    33
  • 可旋转键数:
    8
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.67
  • 拓扑面积:
    215
  • 氢给体数:
    6
  • 氢受体数:
    12

反应信息

  • 作为产物:
    描述:
    2,5-anhydro-1-deoxy-1-(uracil-1'-yl)-6-(5''-(4'''-(N,N-di-tertbutyloxyaminomethyl)-1H,1''',2''',3'''-triazol-1'''-yl)-1'',5''-dideoxy-2'',3''-O-isopentylidene-β-D-ribos-1''-yl)-D-glucitol三氟乙酸 作用下, 以47%的产率得到2,5-anhydro-1-deoxy-1-(uracil-1'-yl)-6-(5''-(4'''-aminomethyl-1H,1''',2''',3'''-triazol-1'''-yl)-1'',5''-dideoxy-2'',3''-O-isopentylidene-β-D-ribos-1''-yl)-D-glucitol
    参考文献:
    名称:
    Bacterial transferase MraY inhibitors: Synthesis and biological evaluation
    摘要:
    New inhibitors of the bacterial transferase MraY are described. Their structure is based on an aminoribosyl-O-uridine like scaffold, readily obtained in two key steps. The amino group can be coupled with proline or guanylated. Alternatively, these amino, prolinyl or guanidinyl groups can be introduced through a triazole linker. Biological evaluation of these compounds on MraY from Bacillus subtilis revealed interesting inhibitory activity for both amino compounds. (C) 2010 Published by Elsevier Ltd.
    DOI:
    10.1016/j.bmc.2010.04.023
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