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8,2'-Cycloadenosin-3',3'-pyrophosphat | 55036-17-4

中文名称
——
中文别名
——
英文名称
8,2'-Cycloadenosin-3',3'-pyrophosphat
英文别名
diphosphoric acid 1,2-bis-((6aS)-4-amino-8t-hydroxymethyl-(6ar,9ac)-6a,7,8,9a-tetrahydro-furo[2',3':4,5]oxazolo[3,2-e]purin-7c-yl) ester;O3',O3'''-(1,2-dihydroxy-[1,2]diphosphoryl)-bis-(arabino-8,O2'-cyclo-adenosine)
8,2'-Cycloadenosin-3',3'-pyrophosphat化学式
CAS
55036-17-4
化学式
C20H22N10O13P2
mdl
——
分子量
672.401
InChiKey
IVRWBMITCVHBTQ-XSCBXMPGSA-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

反应信息

  • 作为产物:
    参考文献:
    名称:
    Polynucleotides. XXVI. Synthesis of an AUG analog, 8,2'-anhydro-8-oxy-9-.BETA.-D-arabinofuranosyladenine phosphoryl-(3'-5')-uridylyl-(3'-5')-guanosine.
    摘要:
    A triplet AUG analog containing 8, 2'-O-cycloadenosine in the first position was synthesized. Starting from 2'-O-(2, 4, 6-triisopropylbenzenesulfonyl)-8-bromoadenosine (I), 5'-monomethoxytrityl-8, 2'-O-cycloadenosine (IV) was synthesized via 8-oxy derivative (II) by the successive treatment with sodium acetate, monomethoxytrityl chloride and methanolic ammonia. Phosphorylation of compound IV with cyanoethyl phosphate and dicyclohexylcarbodiimide (DCC) at 18-20° for 5 days gave only 3'-cyanoethylphosphate (V) quantitatively. Treatment of V with methanolic ammonia gave 3'-phosphate (VI) in a relatively low yield with concomitant formation of 2', 3'-cyclic phosphate (VII). Compound VI was then condensed with 2'-O-benzoyluridylyl-(3'-5')-N2, 2', 3'-triisobutyrylguanosine (X) using DCC and after purification on a column of diethylaminoethyl (DEAE)-cellulose, 8, 2'-O-cycloadenylyl-(3'-5')-guanosine (XI) was obtained in a yield of 4.1%. Compound XI showed hypochromicity of 7.3% at 257 nm and circular dichroism (CD) spectra taken at 0° and 20° revealed that this trinucleotide exists in a rather freely rotatable, unstacked form both at these temperatures.
    DOI:
    10.1248/cpb.22.2578
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