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首页> 外文期刊>Bioorganic and Medicinal Chemistry Letters >Synthesis, X-ray crystallographic analysis, and antitumor activity of 1-acyl-3,6-disubstituted phenyl-1,4-dihydro-1,2,4,5-tetrazines.
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Synthesis, X-ray crystallographic analysis, and antitumor activity of 1-acyl-3,6-disubstituted phenyl-1,4-dihydro-1,2,4,5-tetrazines.

机译:1-酰基-3,6-二取代的苯基-1,4-二氢-1,2,4,5-四嗪的合成,X射线晶体学分析和抗肿瘤活性。

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摘要

Eleven compounds of 1-acyl-3,6-disubstituted phenyl-1,4-dihydro-1,2,4,5-tetrazines were prepared from 3,6-disubstituted phenyl-1,2-dihydro-1,2,4,5-tetrazines and anhydrides or acyl chlorines, and their structures were confirmed by single-crystal X-ray diffraction and the semi-empirical calculation of PM3 method. This reaction yields the 1,4-dihydro derivatives rather than the 1,2-dihydro derivatives. The central six-membered ring of these compounds has an obvious boat conformation and therefore is not homoaromatic. Their antitumor activities were evaluated in vitro by the SRB method for A-549 cell and the MTT method for P-388 cells. The results show that there is one compound which is highly effective against A-549 cells and two compounds which are highly effective against P-388 cells. Thus, this compound possesses potential antitumor activities and is worth researching further.
机译:从3,6-二取代的苯基-1,2-二氢-1,2,4制备11种1-酰基-3,6-二取代的苯基-1,4-二氢-1,2,4,5-四嗪化合物通过单晶X射线衍射和PM3方法的半经验计算,确定了1,5-四嗪和酸酐或酰基氯的结构。该反应产生1,4-二氢衍生物而不是1,2-二氢衍生物。这些化合物的中央六元环具有明显的船形,因此不是纯芳香族的。通过SRB法对A-549细胞和MTT法对P-388细胞体外评价其抗肿瘤活性。结果表明,存在一种对A-549细胞高度有效的化合物和两种对P-388细胞高度有效的化合物。因此,该化合物具有潜在的抗肿瘤活性,值得进一步研究。

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