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2-acetamido-4-O-(2-acetamido-2-deoxy-β-D-glucopyranosyl)-1,6-anhydro-2-deoxy-3-O-[(1R)-1-(amido)ethyl]-β-D-glucopyranose | 1449311-45-8

中文名称
——
中文别名
——
英文名称
2-acetamido-4-O-(2-acetamido-2-deoxy-β-D-glucopyranosyl)-1,6-anhydro-2-deoxy-3-O-[(1R)-1-(amido)ethyl]-β-D-glucopyranose
英文别名
——
2-acetamido-4-O-(2-acetamido-2-deoxy-β-D-glucopyranosyl)-1,6-anhydro-2-deoxy-3-O-[(1R)-1-(amido)ethyl]-β-D-glucopyranose化学式
CAS
1449311-45-8
化学式
C19H31N3O11
mdl
——
分子量
477.469
InChiKey
GGABGZHHRMDPCK-STFZFCBQSA-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

反应信息

  • 作为产物:
    描述:
    2-acetamido-4-O-(2-acetamido-2-deoxy-β-D-glucopyranosyl)-1,6-anhydro-2-deoxy-3-O-[(1R)-1-(methoxycarbonyl)ethyl]-β-D-glucopyranose 在 作用下, 以 甲醇 为溶剂, 反应 8.0h, 以96%的产率得到2-acetamido-4-O-(2-acetamido-2-deoxy-β-D-glucopyranosyl)-1,6-anhydro-2-deoxy-3-O-[(1R)-1-(amido)ethyl]-β-D-glucopyranose
    参考文献:
    名称:
    Active Site Plasticity within the Glycoside Hydrolase NagZ Underlies a Dynamic Mechanism of Substrate Distortion
    摘要:
    NagZ is a glycoside hydrolase that participates in peptidoglycan (PG) recycling by removing beta-N-acetylglucosamine from PG fragments that are excised from the bacterial cell wall during growth. Notably, the products formed by NagZ, 1,6-anhydroMurNAc-peptides, activate beta-lactam resistance in many Gram-negative bacteria, making this enzyme of interest as a potential therapeutic target. Crystal structure determinations of NagZ from Salmonella typhimurium and Bacillus subtilis in complex with natural substrate, trapped as a glycosyl-enzyme intermediate, and bound to product, define the reaction coordinate of the NagZ family of enzymes. The structures, combined with kinetic studies, reveal an uncommon degree of structural plasticity within the active site of a glycoside hydrolase, and unveil how NagZ drives substrate distortion using a highly mobile loop that contains a conserved histidine that has been proposed as the general acid/base.
    DOI:
    10.1016/j.chembiol.2012.09.016
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