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

O6,5'-cyclo-5,6-dihydro-2',3'-O-isopropylideneuridine | 65820-77-1

中文名称
——
中文别名
——
英文名称
O6,5'-cyclo-5,6-dihydro-2',3'-O-isopropylideneuridine
英文别名
(6S)-O6,5'-cyclo-5,6-dihydro-2'3'-O-isopropylideneuridine;O6,5'-cyclo-5,6-dihydro-2',3'-O-isopropylideneuridine;Cyclouridine 5;(6Ξ)-O2',O3'-isopropylidene-5,6-dihydro-6,O5'-cyclo-uridine;(4R)-2,2-dimethyl-(3at,6aξ,12at)-4,5,6a,7,12,12a-hexahydro-3aH-4r,12c-epioxido-[1,3]dioxolo[4,5-e]pyrimido[6,1-b][1,3]oxazocine-8,10-dione
O6,5'-cyclo-5,6-dihydro-2',3'-O-isopropylideneuridine化学式
CAS
65820-77-1;118397-02-7
化学式
C12H16N2O6
mdl
——
分子量
284.269
InChiKey
LYMDREAKIVMIGF-XDSDWBQOSA-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):
    -0.47
  • 重原子数:
    20.0
  • 可旋转键数:
    0.0
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.83
  • 拓扑面积:
    86.33
  • 氢给体数:
    1.0
  • 氢受体数:
    6.0

反应信息

  • 作为产物:
    描述:
    5-formyl-2',3'-O-isopropylideneuridine 在 sodium cyanoborohydride 、 zinc(II) chloride 作用下, 25.0~200.0 ℃ 、666.61 Pa 条件下, 反应 36.83h, 生成 O6,5'-cyclo-5,6-dihydro-2',3'-O-isopropylideneuridine
    参考文献:
    名称:
    Insight into the Chemical Mechanism of Thymidylate Synthase-Catalyzed Reaction Through the Evaluation of Chemical Models: The Role of C6 Sulfhydryl Addition During the Reductive Elimination Step of the Reaction1
    摘要:
    Thymidylate synthase catalyzes the last step of the de novo synthesis of thymidine-5'-monophosphate (TMP), which has long been a target for the development of effective anticancer agents. Model compounds (15, 16, 17) were used to study the effect of C6 nucleophilic addition on the reductive elimination step of the TS-catalyzed reaction. Results suggest that C6 addition facilitates the reductive elimination of the H(2)folate moiety of the ternary intermediate (3). Therefore, the reaction pathway (pathway (b)) with the participation of C6 sulfhydryl addition during the reductive elimination process is the energetically favored process. Consequently, the elimination of the cysteine sulfhydryl group from the C6 position is the last step of the reaction before the dissociation of the products from the enzyme. (C) 1994 Academic Press, Inc.
    DOI:
    10.1006/bioo.1994.1034
点击查看最新优质反应信息

文献信息

  • Synthesis and chemistry of 5,6-dihydro-6-methoxyuridine derivatives. Access to O6,5′-cyclo-5,6-dihydrouridine
    作者:Jean-Louis Fourrey、Patrick Jouin
    DOI:10.1016/s0040-4039(01)83248-2
    日期:1977.1
查看更多