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新型抗叶酸剂N10-炔丙基-5,8-二去氮叶酸及其多聚谷氨酸对人二氢叶酸还原酶、人胸苷酸合成酶以及含有不同水平二氢叶酸还原酶的KB细胞的活性。

Activity of the new antifolate N10-propargyl-5,8-dideazafolate and its polyglutamates against human dihydrofolate reductase, human thymidylate synthetase, and KB cells containing different levels of dihydrofolate reductase.

作者信息

Cheng Y C, Dutschman G E, Starnes M C, Fisher M H, Nanavathi N T, Nair M G

出版信息

Cancer Res. 1985 Feb;45(2):598-600.

PMID:3917852
Abstract

The action of N10-propargyl-5,8-dideazafolate (PDDF) and its gamma-polyglutamyl analogues against human thymidylate synthetase and dihydrofolate reductase was examined. PDDF inhibited thymidylate synthetase in a noncompetitive fashion with respect to 5,10-methylenetetrahydrofolate and dihydrofolate reductase in a competitive fashion with respect to dihydrofolate. Ki values were estimated to be 20 and 250 nM, respectively. The addition of glutamyl moieties through gamma-linkage enhanced the inhibitory activity of PDDF against thymidylate synthetase without significant effect on dihydrofolate reductase. PDDF inhibited human KB cell growth, and its potency was found to be influenced less than that of methotrexate by the amount of cellular dihydrofolate reductase.

摘要

研究了N10-炔丙基-5,8-二氮杂叶酸(PDDF)及其γ-聚谷氨酰类似物对人胸苷酸合成酶和二氢叶酸还原酶的作用。PDDF对胸苷酸合成酶的抑制作用相对于5,10-亚甲基四氢叶酸呈非竞争性,对二氢叶酸还原酶的抑制作用相对于二氢叶酸呈竞争性。估计Ki值分别为20和250 nM。通过γ-连接添加谷氨酰部分增强了PDDF对胸苷酸合成酶的抑制活性,而对二氢叶酸还原酶没有显著影响。PDDF抑制人KB细胞生长,并且发现其效力受细胞二氢叶酸还原酶量的影响小于甲氨蝶呤。

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