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嘌呤无环核苷酸类似物的遗传毒性。

Genotoxicity of purine acyclic nucleotide analogs.

作者信息

Otová B, Holý A, Votruba I, Sladká M, Bílá V, Mejsnarová B, Lesková V

机构信息

Department of Biology, 1st Faculty of Medicine, Charles University, Prague, Czech Republic.

出版信息

Folia Biol (Praha). 1997;43(6):225-9.

PMID:9595265
Abstract

The genotoxic and embryotoxic effects of phosphonomethoxyalkylpurines, a new group of antiviral agents, decrease in the following order: PMEG > PMEthioG > PMEDAP > PMEA > (R)-PMPDAP = (R)-PMPA. Results of the present study are fully consistent with the previously found efficacy of their diphosphates to inhibit the replicative DNA polymerases. The marked genotoxicity of PMEG and PMEthioG is comparable to that of mitomycin C, whereas the moderate genotoxicity of PMEA is comparable to that of AZT. (R)-PMPDAP and (R)-PMPA did not induce any structural aberrations of chromosomes under the experimental conditions.

摘要

新型抗病毒药物膦酰甲氧基烷基嘌呤的遗传毒性和胚胎毒性作用按以下顺序降低

PMEG>PMEthioG>PMEDAP>PMEA>(R)-PMPDAP = (R)-PMPA。本研究结果与先前发现的其二磷酸盐抑制复制性DNA聚合酶的效力完全一致。PMEG和PMEthioG的显著遗传毒性与丝裂霉素C相当,而PMEA的中度遗传毒性与齐多夫定相当。在实验条件下,(R)-PMPDAP和(R)-PMPA未诱导任何染色体结构畸变。

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