| 93135-46-7

• 分子结构分类: 有机化合物 - 有机氧化合物
• CAS: 93135-46-7
• 化学式: C₁₈H₂₄N₄O₁₅P₂S₂
• 分子量: 662.486
• InChiKey: NOAYHWMAMDQZNB-JOSLGPENSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  -1.93
• 重原子数：
  41.0
• 可旋转键数：
  12.0
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.56
• 拓扑面积：
  313.63
• 氢给体数：
  8.0
• 氢受体数：
  17.0

反应信息

• 作为产物：
  描述：

  tiazofurin 5'-monophosphate 在 三正丁胺 作用下， 以 N,N-二甲基甲酰胺 为溶剂， 反应 51.0h， 生成
  参考文献：
  名称：

  Ribavirin, tiazofurin, and selenazofurin: mononucleotides and nicotinamide adenine dinucleotide analogs. Synthesis, structure, and interactions with IMP dehydrogenase

  摘要：

  A series of dinucleotides, analogous to nicotinamide adenine dinucleotide but containing the five-membered base nucleosides tiazofurin (1a), selenazofurin (1b), ribavirin (2), and AICAR (3) in place of nicotinamide ribonucleoside, were prepared in greater than 50% yield by reacting the corresponding nucleotide imidazolidates (6a-d) with adenosine 5'-monophosphate (AMP). The symmetric dinucleotides of tiazofurin (TTD, 8e) and selenazofurin (SSD, 8f) were also prepared by a similar methodology. These dinucleotides were characterized by 1H NMR and fast atom bombardment MS and were evaluated for their inhibitory potency against a partially purified preparation of tumoral inosine monophosphate dehydrogenase (IMPD) from P388 cells. The order of potency found was SAD (8b) greater than TAD (8a) much greater than SSD (8f) congruent to TTD (8e) congruent to RAD (8c) much much greater than ZAD (8d). On kinetic analysis none of the dinucleotides produced competitive inhibition of IMPD with NAD as a variable substrate. In addition to their superior IMPD inhibitory activity, SAD and TAD appear to be the only dinucleotides, besides NAD, that are formed naturally by the NAD pyrophosphorylase from P388 lymphoblasts.

  DOI：

  10.1021/jm00379a018

文献信息

• Potent Inhibitors of Human Inosine Monophosphate Dehydrogenase Type II. Fluorine-Substituted Analogs of Thiazole-4-carboxamide Adenine Dinucleotide
  作者：Andrzej Zatorski、Barry M. Goldstein、Thomas D. Colby、Jeffery P. Jones、Krzysztof W. Pankiewicz

  DOI：10.1021/jm00007a007

  日期：1995.3

  best cofactor-type inhibitor, beta-CH2-TAD (Ki = 0.11 microM). Interestingly, the level of inhibition of horse liver alcohol dehydrogenase by these compounds was found to be much lower (0.1 mM for 1 and 2 and no inhibition up to 10 mM for 3). These findings show that inhibition of tumor-induced inosine monophosphate dehydrogenase type II is selective and may be of therapeutic interest.

  噻唑-4-羧酰胺腺嘌呤二核苷酸（TAD）（1-3）的三个类似物分别在腺嘌呤核苷的C2'（核糖和阿拉伯糖构型）和C3'（核糖构型）中含有氟原子。由2'-脱氧-2'-氟腺苷（9），9-（2-脱氧-2-氟-β-D-阿拉伯呋喃糖基）-腺嘌呤（17）和3的相应5'-单磷酸盐高收率合成'-deoxy-3'-氟腺苷（14）。通过将被保护的噻唑呋喃磷酸化，然后用羰基二咪唑处理并进行HPLC纯化，获得纯的2'，3'-O-异亚丙基-噻唑呋喃5'-磷酸咪唑啉（8）。8在DMF-d7中（由1H和31P NMR监测）中的9与9的反应得到所需的二核苷酸12，在脱异丙基化之后，其收率为82％，为1。在主要产品12的HPLC纯化过程中，还分离出少量对称的二核苷酸AppA（10，7.2％）和TRppTR（11，8.0％）。以类似的方式，通过将8与14和C偶联，得到化合物2和3。分别以80％和76％的收率排名第17位。我们早