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9-(3-O-(tert-butyldimethylsilyl)-2,5-dideoxy-2-methylene-β-D-glycero-pent-4-enofuranosyl)adenine | 137058-87-8

中文名称
——
中文别名
——
英文名称
9-(3-O-(tert-butyldimethylsilyl)-2,5-dideoxy-2-methylene-β-D-glycero-pent-4-enofuranosyl)adenine
英文别名
9-[3-O-(tert-butyldimethylsilyl)-2,5-dideoxy-2-methylene-β-D-glycero-pent-4-enofuranosyl]adenine;9-[(2R,4S)-4-[tert-butyl(dimethyl)silyl]oxy-3,5-dimethylideneoxolan-2-yl]purin-6-amine
9-(3-O-(tert-butyldimethylsilyl)-2,5-dideoxy-2-methylene-β-D-glycero-pent-4-enofuranosyl)adenine化学式
CAS
137058-87-8
化学式
C17H25N5O2Si
mdl
——
分子量
359.503
InChiKey
ZIHRWYCWWQHANC-XJKSGUPXSA-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):
    3.4
  • 重原子数:
    25.0
  • 可旋转键数:
    3.0
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.47
  • 拓扑面积:
    88.08
  • 氢给体数:
    1.0
  • 氢受体数:
    7.0

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为产物:
    参考文献:
    名称:
    Nucleic acid related compounds. 70. Synthesis of 2'(and 3')-deoxy-2'(and 3')-methyleneadenosines and bis(methylene)furan 4',5'-didehydro-5'-deoxy-2'(and 3')-methyleneadenosines. Inhibitors of S-adenosyl-L-homocysteine hydrolase and ribonucleotide reductase
    摘要:
    Wittig treatment of 3',5'(or 2',5')-bis-O-silyl-2'(or 3')-ketoadenosine derivatives with methylenetriphenylphosphorane and deprotection gave the 2'(or 3')-deoxy-2'(or 3')-methyleneadenosines, respectively. Enzymatic deamination afforded the 2'(or 3')-deoxy-2'(or 3')-methyleneinosines. Treatment of 2'-O-(tert-butyldimethylsilyl)-3'-deoxy-3'-methylene-5'-O-tosyladenosine (14) with sodium 2-methyl-2-butoxide and deprotection gave 9-(3,5-dideoxy-3-methylene-beta-D-glycero-pent-4-enofuranosyl)adenine (20). Analogous treatment of a protected 2',5'-dideoxy-5'-iodo-2'-methyleneadenosine derivative gave 9-(2,5-dideoxy-2-methylene-beta-D-glycero-pent-4-enofuranosyl)adenine (22). Biochemical aspects of the putative mechanism-based inhibition of S-adenosyl-L-homocysteine hydrolase and ribonucleotide reductase by these compounds are discussed.
    DOI:
    10.1021/jo00025a029
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