摩熵化学
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

N1-methyl-2'-deoxy-3',5'-O-(1,1,3,3-tetraisopropyldisiloxane-1,3-diyl)-ψ-uridine | 80545-48-8

中文名称
——
中文别名
——
英文名称
N1-methyl-2'-deoxy-3',5'-O-(1,1,3,3-tetraisopropyldisiloxane-1,3-diyl)-ψ-uridine
英文别名
2'-deoxy-1-methyl-3',5'-O-(tetraisopropyldisiloxanyl)pseudouridine
N1-methyl-2'-deoxy-3',5'-O-(1,1,3,3-tetraisopropyldisiloxane-1,3-diyl)-ψ-uridine化学式
CAS
80545-48-8
化学式
C22H40N2O6Si2
mdl
——
分子量
484.74
InChiKey
AHKAGTKCMOYVNP-HSALFYBXSA-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

物化性质

  • 密度:
    1.11±0.1 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    3.86
  • 重原子数:
    32.0
  • 可旋转键数:
    5.0
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.82
  • 拓扑面积:
    91.78
  • 氢给体数:
    1.0
  • 氢受体数:
    7.0

反应信息

  • 作为反应物:
    描述:
    N1-methyl-2'-deoxy-3',5'-O-(1,1,3,3-tetraisopropyldisiloxane-1,3-diyl)-ψ-uridine四丁基氟化铵 作用下, 以 四氢呋喃 为溶剂, 以61%的产率得到5-(2-脱氧-BETA-D-赤式-呋喃戊糖基)-1-甲基-2,4(1H,3H)-嘧啶二酮
    参考文献:
    名称:
    Nucleosides. 121. Improved and general synthesis of 2'-deoxy-C-nucleosides. Synthesis of 5-(2-deoxy-.beta.-D-erythro-pentofuranosyl)uracil, -1-methyluracil, -1,3-dimethyluracil, and -isocytosine
    摘要:
    DOI:
    10.1021/jo00342a022
  • 作为产物:
    参考文献:
    名称:
    A Practical Synthesis ofN1-Methyl-2′-deoxy-ψ-uridine (ψ-Thymidine) and Its Incorporation into G-Rich Triple Helix Forming Oligonucleotides
    摘要:
    A convenient synthesis of N1-methyl-2'-deoxy-psi-uridine (psi-thymidine, psi T, 7a) has been accomplished in good yield. The structural conformation of 7a was derived by 2D NMR and 1D NOE experiments. The nucleoside 7a has been incorporated into G-rich tripler forming oligonucleotides (TFOs) by solid-support, phosphoramidite method. The tripler forming capabilities of the modified TFOs (S4, S5 and S6) containing psi T has been evaluated in antiparallel motif with a target duplex (duplex-31) 5'd(CTGAGACCGGGAAGGAGGAAGGGCCAGTGAC)3'-5d(GACTCTGGCCCTTCCTCCTTCCCGGTCACTG)3' (D1) at pH 7.6. The tripler formation of modified homopyrimidine-oligomers (S1, S2 and S3) has also been studied in parallel motif with a duplex-10 (A(10):T-10) at pH 7.0.
    DOI:
    10.1080/15257779508010690
点击查看最新优质反应信息