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2-trans-pentenyl diphosphate | 929531-71-5

中文名称
——
中文别名
——
英文名称
2-trans-pentenyl diphosphate
英文别名
[(E)-pent-2-enyl] phosphono hydrogen phosphate
2-trans-pentenyl diphosphate化学式
CAS
929531-71-5
化学式
C5H12O7P2
mdl
——
分子量
246.094
InChiKey
WZDSLOCYZQFUGM-ONEGZZNKSA-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):
    -1.3
  • 重原子数:
    14
  • 可旋转键数:
    6
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.6
  • 拓扑面积:
    113
  • 氢给体数:
    3
  • 氢受体数:
    7

反应信息

  • 作为反应物:
    描述:
    (R)-benzodiazepinedione2-trans-pentenyl diphosphate 在 recombinant AnaPT 、 三羟甲基氨基甲烷盐酸盐二甲基亚砜甘油 、 calcium chloride 作用下, 反应 16.0h, 以26.8%的产率得到
    参考文献:
    名称:
    Breaking Cyclic Dipeptide Prenyltransferase Regioselectivity by Unnatural Alkyl Donors
    摘要:
    The behavior of five cyclic dipeptide prenyltransferases, responsible for C2-regular, C2-reverse, or C3-reverse prenylation, was investigated In the presence of the unnatural alkyl donors monomethylallyl and 2-pentenyl diphosphate. Both substrates were well accepted by the tested enzymes. Interestingly, C2-reverse and C3-reverse monoalkylated derivatives were identified as enzyme products In all of the enzyme assays. These findings indicate their similar reaction characteristics in the presence of unnatural alkyl donors.
    DOI:
    10.1021/ol401247s
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文献信息

  • Breaking Cyclic Dipeptide Prenyltransferase Regioselectivity by Unnatural Alkyl Donors
    作者:Mike Liebhold、Xiulan Xie、Shu-Ming Li
    DOI:10.1021/ol401247s
    日期:2013.6.21
    The behavior of five cyclic dipeptide prenyltransferases, responsible for C2-regular, C2-reverse, or C3-reverse prenylation, was investigated In the presence of the unnatural alkyl donors monomethylallyl and 2-pentenyl diphosphate. Both substrates were well accepted by the tested enzymes. Interestingly, C2-reverse and C3-reverse monoalkylated derivatives were identified as enzyme products In all of the enzyme assays. These findings indicate their similar reaction characteristics in the presence of unnatural alkyl donors.
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