通过母体化合物4-氨基吡啶(4-AP)与N-二异丙基磷酰化氨基酸(DiPP-AA)在Ph3P 和C2Cl6体系下的缩合反应, 将具有生物活性的氨基吡啶环引入到磷酸化氨基酸结构中, 设计、合成了5 个N-二异丙基磷酰化氨基酸-N-4-氨基吡啶衍生物A1～A5. 所有目标化合物均经IR, 1H NMR, 13C NMR, 31P NMR, MS 的表征. 初步生物活性测试结果表明: 目标化合物对河豚毒素(TTX)中毒的小鼠均有一定的解毒作用, 并不同程度地延长了生存时间, 而且毒性比母体化合物降低了.
方华
,
陈伟珠
,
洪碧红
,
张怡评
,
易瑞灶
. N-二异丙基磷酰化氨基酸-N-4-氨基吡啶衍生物的合成及对河豚毒素(TTX)解毒生物活性的研究[J]. 有机化学, 2012
, 32(01)
: 178
-182
.
DOI: 10.6023/cjoc1105102
Some novel 4-aminopyridine derivatives of the title compounds containing the unit of N-diisopropyloxyphosphoryl amino acids were synthesized. Their structures were confirmed by IR, 1H NMR, 13C NMR, and mass spectra. In the present work, a group of 4-aminopyridine derivatives were synthesized in order to find novel structure with higher antagonize effects and lower toxity. On the other hand, their fragmentation behaviors were investigated by positive ion electrospray ionization mass spectrometry in conjunction with tandem mass spectrometry. The preliminary bioassay results showed that chemical modification of 4-aminopyridine possessed stronger bioactivity of antidote tetrodotoxin intoxication.
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