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(R)-(2,3,4,6-tetra-O-benzyl-α-D-mannopyranosyloxy)-2-methylpropionic acid N-hydroxysuccinimide ester | 1190373-33-1

中文名称
——
中文别名
——
英文名称
(R)-(2,3,4,6-tetra-O-benzyl-α-D-mannopyranosyloxy)-2-methylpropionic acid N-hydroxysuccinimide ester
英文别名
——
(R)-(2,3,4,6-tetra-O-benzyl-α-D-mannopyranosyloxy)-2-methylpropionic acid N-hydroxysuccinimide ester化学式
CAS
1190373-33-1
化学式
C42H45NO10
mdl
——
分子量
723.82
InChiKey
PTDIXRQIAQKROR-GLHVJAIESA-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):
    5.94
  • 重原子数:
    53.0
  • 可旋转键数:
    18.0
  • 环数:
    6.0
  • sp3杂化的碳原子比例:
    0.36
  • 拓扑面积:
    119.06
  • 氢给体数:
    0.0
  • 氢受体数:
    10.0

反应信息

  • 作为反应物:
    描述:
    (R)-(2,3,4,6-tetra-O-benzyl-α-D-mannopyranosyloxy)-2-methylpropionic acid N-hydroxysuccinimide ester 、 <2-acetamido-4-O-(2-acetamido-2-deoxy-β-D-glucopyranosyl)-2-deoxy-3-O-((D)-ethyl-1-carbonyl)-D-glucopyranose>-L-alanyl-D-isoglutaminyl-<(L)-meso-diaminopimeloyl-(D)-amide-(L)-D-alanyl-D-alanine> 在 三乙胺 作用下, 以 N,N-二甲基甲酰胺 为溶剂, 反应 49.0h, 生成 N-acetyl-β-D-glucosaminyl-(1->4)-N-acetylmuramyl-L-alanyl-D-iso-glutaminyl-{N(ε)-[(R)-3-(2,3,4,6-tetra-O-benzyl-α-D-mannopyranosyloxy)-2-methylpropanoyl]}-meso-2,6-diaminopimelyl-D-alanyl-D-alanine
    参考文献:
    名称:
    Novel mannosyl derivatives of peptidoglycan monomer: Synthesis and biological evaluation of immunomodulatory properties
    摘要:
    The aim of this work was to prepare mannosyl derivatives of peptidoglycan monomer (PGM, beta-D-GlcNAc( 1 -> 4)-D-MurNAc-L-Ala-D-isoGln-mesoDAP(epsilon NH(2))-D-Ala-D-Ala) in order to study the effects of mannosylation on adjuvant (immunostimulating) activity. Novel Man-OCH(2)CH(CH(3))CO-PGM isomers were substrates for N-acetylmuramyl-L-alanine amidase, like the parent PGM molecule. Adjuvant activity of Man-OCH(2)CH(CH(3)) CO-PGM was tested in the mouse model using ovalbumin as an antigen. (C) 2009 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmc.2009.06.016
  • 作为产物:
    描述:
    N-羟基丁二酰亚胺(R)-(2,3,4,6-tetra-O-benzyl-α-D-mannopyranosyloxy)-2-methylpropionic acid盐酸-N-乙基-Nˊ-(3-二甲氨基丙基)碳二亚胺 作用下, 以 二氯甲烷 为溶剂, 以172.6 mg的产率得到(R)-(2,3,4,6-tetra-O-benzyl-α-D-mannopyranosyloxy)-2-methylpropionic acid N-hydroxysuccinimide ester
    参考文献:
    名称:
    Novel mannosyl derivatives of peptidoglycan monomer: Synthesis and biological evaluation of immunomodulatory properties
    摘要:
    The aim of this work was to prepare mannosyl derivatives of peptidoglycan monomer (PGM, beta-D-GlcNAc( 1 -> 4)-D-MurNAc-L-Ala-D-isoGln-mesoDAP(epsilon NH(2))-D-Ala-D-Ala) in order to study the effects of mannosylation on adjuvant (immunostimulating) activity. Novel Man-OCH(2)CH(CH(3))CO-PGM isomers were substrates for N-acetylmuramyl-L-alanine amidase, like the parent PGM molecule. Adjuvant activity of Man-OCH(2)CH(CH(3)) CO-PGM was tested in the mouse model using ovalbumin as an antigen. (C) 2009 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmc.2009.06.016
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