摩熵化学
数据开放平台 数据库官网
小程序
打开微信扫一扫
首页 分子通 化学资讯 化学百科 反应查询 关于我们
请输入关键词

(1R,2R,3R,4R,5S,6R)-2,3,4,5-tetrahydroxy-6-(D-mannopyranosyloxy)cyclohexyl phosphate

中文名称
——
中文别名
——
英文名称
(1R,2R,3R,4R,5S,6R)-2,3,4,5-tetrahydroxy-6-(D-mannopyranosyloxy)cyclohexyl phosphate
英文别名
[(1R,2R,3R,4R,5S,6R)-2,3,4,5-tetrahydroxy-6-[(3S,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxycyclohexyl] phosphate
(1R,2R,3R,4R,5S,6R)-2,3,4,5-tetrahydroxy-6-(D-mannopyranosyloxy)cyclohexyl phosphate化学式
CAS
——
化学式
C12H21O14P-2
mdl
——
分子量
420.26
InChiKey
UJXBXUSHOWRLIG-JDLYWALLSA-L
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):
    -6.6
  • 重原子数:
    27
  • 可旋转键数:
    4
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    253
  • 氢给体数:
    8
  • 氢受体数:
    14

反应信息

  • 作为产物:
    描述:
    a mannosylinositol-1-phospho-N-acyl-sphingoid base 、 生成 an N-acyl-sphingoid base 、 氢(+1)阳离子(1R,2R,3R,4R,5S,6R)-2,3,4,5-tetrahydroxy-6-(D-mannopyranosyloxy)cyclohexyl phosphate
    参考文献:
    名称:
    Identification of ISC1 (YER019w) as Inositol Phosphosphingolipid Phospholipase C inSaccharomyces cerevisiae
    摘要:
    Sphingolipids have emerged as novel bioactive mediators in eukaryotic cells including yeast. It has been proposed that sphingomyelin (SM) hydrolysis and the concomitant generation of ceramide are involved in various stress responses in mammalian cells, The yeast Saccharomyces cerevisiae has inositol phosphosphingolipids (IPS) instead of SM and glycolipids, and synthesis of IFS is indispensable to its growth. Although the genes responsible for the synthesis of IFS have been identified, the gene(s) for the degradation of IFS has not been reported, Here we show that ISC1 (YER019w), which has homology to bacterial neutral sphingomyelinase (SMase), encodes IFS phospholipase C (IPS-PLC). First, we observed that overexpression of ISC1 greatly increased neutral SMase activity, and this activity was dependent on the presence of phosphatidylserine. Cells deleted in ISC1 demonstrated negligible neutral SMase activity. Because yeast cells have IFS instead of SM, we investigated whether IFS are the physiologic substrates of this enzyme. Lysates of ISC1-overexpressing cells demonstrated very high PLC activities on IFS. Deletion of ISC1 eliminated endogenous IPS-PLC activities, Labeling yeast cells with [H-3]dihydrosphingosine showed that IFS were increased in the deletion mutant cells, This study identifies the first enzyme involved in catabolism of complex sphingolipids in S. cerevisiae.
    DOI:
    10.1074/jbc.m007721200
点击查看最新优质反应信息