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人嘌呤核苷磷酸化酶抑制剂。2,5 - 二氨基噻唑并[5,4 - d]嘧啶 - 7(6H) - 酮和2,5 - 二氨基噻唑并[4,5 - d]嘧啶 - 7(6H) - 酮的合成、嘌呤核苷磷酸化酶抑制作用及T细胞细胞毒性。8 - 氨基鸟嘌呤的两种硫代类似物。

Inhibitors of human purine nucleoside phosphorylase. Synthesis, purine nucleoside phosphorylase inhibition, and T-cell cytotoxicity of 2,5-diaminothiazolo[5,4-d]pyrimidin-7(6H)-one and 2,5-diaminothiazolo[4,5-d]pyrimidin-7(6H)-one. Two thio isosteres of 8-aminoguanine.

作者信息

Sircar J C, Suto M J, Scott M E, Dong M K, Gilbertsen R B

出版信息

J Med Chem. 1986 Sep;29(9):1804-6. doi: 10.1021/jm00159a045.

Abstract

8-Aminoguanine is a potent inhibitor of purine nucleoside phosphorylase (PNP) and also a substrate of PNP. Two thio isosteres of 8-aminoguanine, 2,5-diaminothiazolo[5,4-d]pyrimidin-7(6H)-one (2) and 2,4-diaminothiazolo[4,5-d]pyrimidin-7(6H)-one (3), which cannot be substrates of PNP, were synthesized and evaluated for their inhibitory activity against PNP. They were found to be weak inhibitors of PNP and to be noncytotoxic for MOLT-4 T-cells in culture.

摘要

8-氨基鸟嘌呤是嘌呤核苷磷酸化酶(PNP)的强效抑制剂,也是PNP的底物。合成了8-氨基鸟嘌呤的两种硫代类似物,2,5-二氨基噻唑并[5,4-d]嘧啶-7(6H)-酮(2)和2,4-二氨基噻唑并[4,5-d]嘧啶-7(6H)-酮(3),它们不能作为PNP的底物,并对其对PNP的抑制活性进行了评估。发现它们是PNP的弱抑制剂,并且对培养中的MOLT-4 T细胞无细胞毒性。

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