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2-O-(2-acetamido-2,6-dideoxy-β-D-glucopyranosyl)-3-O-carbamoyl-1-O-<<(R)-2-carboxy-2-(3,8,8,11,14,18-hexamethyl-nonadecyloxy)-ethoxy>-hydroxyphosphoryl>-α-D-galactopyranuronamide

中文名称
——
中文别名
——
英文名称
2-O-(2-acetamido-2,6-dideoxy-β-D-glucopyranosyl)-3-O-carbamoyl-1-O-<<(R)-2-carboxy-2-(3,8,8,11,14,18-hexamethyl-nonadecyloxy)-ethoxy>-hydroxyphosphoryl>-α-D-galactopyranuronamide
英文别名
2-O-(2-acetamido-2,6-dideoxy-β-D-glucopyranosyl)-3-O-carbamoyl-1-O-{[(R)-2-carboxy-2-(3,8,8,11,14,18-hexamethyl-nonadecyloxy)-ethoxy]-hydroxyphosphoryl}-α-D-galactopyranuronamide;(2R)-3-[[(2R,3R,4S,5R,6S)-3-[(2S,3R,4R,5S,6R)-3-acetamido-4,5-dihydroxy-6-methyloxan-2-yl]oxy-6-carbamoyl-4-carbamoyloxy-5-hydroxyoxan-2-yl]oxy-hydroxyphosphoryl]oxy-2-(3,8,8,11,14,18-hexamethylnonadecoxy)propanoic acid
2-O-(2-acetamido-2,6-dideoxy-β-D-glucopyranosyl)-3-O-carbamoyl-1-O-<<(R)-2-carboxy-2-(3,8,8,11,14,18-hexamethyl-nonadecyloxy)-ethoxy>-hydroxyphosphoryl>-α-D-galactopyranuronamide化学式
CAS
——
化学式
C43H80N3O17P
mdl
——
分子量
942.092
InChiKey
LUJAWAPOALAXQO-ROSGGTHOSA-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):
    6.1
  • 重原子数:
    64
  • 可旋转键数:
    31
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.91
  • 拓扑面积:
    315
  • 氢给体数:
    8
  • 氢受体数:
    17

反应信息

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文献信息

  • The first moenomycin antibiotic without the methyl-branched uronic acid constituent.- Unexpected structure activity relations
    作者:Martina Heßler-Klintz、Kurt Hobert、Armin Biallaß、Torsten Siegels、Monika Hiegemann、Armin Maulshagen、Dietrich Müller、Peter Welzel、Gerhard Huber、Dirk Böttger、Astrid Markus、Gerhard Seibert、Andreas Stärk、Hans-Wolfram Fehlhaber、Yveline van Heijenoort、Jean van Heijenoort
    DOI:10.1016/s0040-4020(01)87242-2
    日期:1993.8
    Isolation and structure elucidation of a new moenomycin antibiotic (C1, 1e) that lacks the branching methyl group in the 4-position of unit F are reported. The smallest antibiotically active degradation product of le is the trisaccharide derivative 3. This observation is in contrast to structure activity relations in the moenomycin A series where it was found that disaccharide 4a is fully active.
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