| 139656-21-6

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 吲哚及其衍生物
• CAS: 139656-21-6；139756-71-1
• 化学式: C₃₈H₄₀N₈O₁₆
• 分子量: 864.78
• InChiKey: HETFGKNKJBEKRA-LCBONGJFSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  -1.45
• 重原子数：
  62.0
• 可旋转键数：
  12.0
• 环数：
  7.0
• sp3杂化的碳原子比例：
  0.5
• 拓扑面积：
  310.96
• 氢给体数：
  3.0
• 氢受体数：
  19.0

反应信息

• 作为反应物：
  描述：

  在 Tetraacetyl-D-arabinoflavin 、 高氯酸 作用下， 以 乙腈 为溶剂， 生成 3-[3-(5-Methyl-2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl)-propyl]-2,6-dioxo-1,2,3,6-tetrahydro-pyrimidine-4-carboxylic acid 7-methyl-2,4-dioxo-10-((2S,3S,4R)-2,3,4,5-tetraacetoxy-pentyl)-2,3,4,10-tetrahydro-benzo[g]pteridin-8-ylmethyl ester
  参考文献：
  名称：

  A possible chain reaction in photosensitized splitting of pyrimidine dimers by a protonated, oxidized flavin

  摘要：

  Pyrimidine dimer cycloreversion was photosensitized by protonated 2',3',4',5'-tetraacetylriboflavin (ac4rfH+), whereas the protonated flavin radical (ac4rfH2.+) failed to sensitize detectable dimer splitting. In acetonitrile containing 0.075% perchloric acid, the ac4rf absorption bands at 375 nm and 445 nm are replaced by a new band at 390 nm due to ac4rfH+. Irradiation of ac4rfH+ in the presence of cis,syn- or trans,syn-1,3-dimethyluracil dimer resulted in efficient cycloreversion to 1,3-dimethyluracil, probably induced by electron abstraction from the dimer by ac4rfH+ to produce the dimer radical cation. The quantum yeilds of splitting were large (PHI(spl) = 0.35 and 1.5 for cis,syn and trans,syn isomers, respectively, at [dimer] = 1.2 mM). Splitting quantum yields increased with dimer concentration in a quadratic fashion. These results are consistent with the occurrence of a chain reaction propagated by monomer.+ + dimer --> monomer + dimer.+ in the case of the dimethyluracil dimers. The fluorescence of the protonated flavin (lambda(em) = 507 nm) was found to be quenched by the dimers. In the presence of small amounts of added water, however, both the fluorescence quenching and splitting were abolished. Two cis,syn dimers in which the N(1)- and N(1')-atoms were tethered via a trimethylene bridge exhibited quantum yields of approximately 0.02 at the above dimer concentration. A compound in which ac4rf is covalently bound to a pyrimidine dimer was also found to undergo splitting in acidified acetonitrile (PHI = 0.03). These values are more than 1 order of magnitude greater than those reported for unprotonated flavins.

  DOI：

  10.1021/jo00034a021
• 作为产物：
  描述：

  8α-Bromo-2',3',4',5'-tetraacetylriboflavin 、 N-benzyl-N,N-diethylethanaminium rac-(3a1R,6aR,6bS,6b1S)-6a-methyl-4,6,7,9-tetraoxodecahydro-1H-3a,5,8,9a-tetraazacyclohepta[def]biphenylene-6b1(3a1H)-carboxylate 以 乙腈 为溶剂， 反应 1.5h， 生成
  参考文献：
  名称：

  A possible chain reaction in photosensitized splitting of pyrimidine dimers by a protonated, oxidized flavin

  摘要：

  Pyrimidine dimer cycloreversion was photosensitized by protonated 2',3',4',5'-tetraacetylriboflavin (ac4rfH+), whereas the protonated flavin radical (ac4rfH2.+) failed to sensitize detectable dimer splitting. In acetonitrile containing 0.075% perchloric acid, the ac4rf absorption bands at 375 nm and 445 nm are replaced by a new band at 390 nm due to ac4rfH+. Irradiation of ac4rfH+ in the presence of cis,syn- or trans,syn-1,3-dimethyluracil dimer resulted in efficient cycloreversion to 1,3-dimethyluracil, probably induced by electron abstraction from the dimer by ac4rfH+ to produce the dimer radical cation. The quantum yeilds of splitting were large (PHI(spl) = 0.35 and 1.5 for cis,syn and trans,syn isomers, respectively, at [dimer] = 1.2 mM). Splitting quantum yields increased with dimer concentration in a quadratic fashion. These results are consistent with the occurrence of a chain reaction propagated by monomer.+ + dimer --> monomer + dimer.+ in the case of the dimethyluracil dimers. The fluorescence of the protonated flavin (lambda(em) = 507 nm) was found to be quenched by the dimers. In the presence of small amounts of added water, however, both the fluorescence quenching and splitting were abolished. Two cis,syn dimers in which the N(1)- and N(1')-atoms were tethered via a trimethylene bridge exhibited quantum yields of approximately 0.02 at the above dimer concentration. A compound in which ac4rf is covalently bound to a pyrimidine dimer was also found to undergo splitting in acidified acetonitrile (PHI = 0.03). These values are more than 1 order of magnitude greater than those reported for unprotonated flavins.

  DOI：

  10.1021/jo00034a021