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2,4-二氨基-6-(取代苄基)-5-甲基吡啶[2,3-d]并嘧啶衍生物的合成及抗癌活性的研究

SYNTHESIS AND STUDIES ON THE ANTITUMOR BIOLOGICAL ACTIVITIES OF 2,4-DIAMINO-6-SUBSTITUTED BENZYL-5-METHYL PYRIDO[2,3-d]PYRIMIDINE DERIVATIVES

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【摘要】 二氨基吡啶并嘧啶类化合物具有很强的抑制二氢叶酸还原酶的作用。这类化合物中BW301u已进行临床试验以治疗癌症。本文报道了17个2,4-二氨基-6-取代苄基-5-甲基-吡啶[2,3-d]并嘧啶类化合物的合成及对L1210细胞的抑制作用。合成化合物的结构经由MS-EI,1H-NMR及元素分析确证。以MTT法测定了它们对L1210细胞的抑制作用。

【Abstract】 Diamino pyridopyrimidines possess potent inhibitory activity against dihydrofolate reductase. One of this kind of compounds BW301U is now used in the clinical trail of cancer diseases. In this paper, 17 target compounds of 2, 4-diamino-6-substituted benzyl-5-methyl pyrido[2,3-d]pyrimidines were synthesized and the structures of these compounds were determined by means of MS-EI,H-NMR,Elemental Analysis. The MTT method was applied to the tests of biological activities of these compounds in the inhibitation to L1210 cell.

【基金】 国家自然科学基金
  • 【文献出处】 中国药物化学杂志 ,Chinese Journal of Medicinal Chemistry , 编辑部邮箱 ,1993年02期
  • 【下载频次】99
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