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超氧离子和抗坏血酸盐与蒽环类抗生素相互作用的机制。

Mechanism of the interaction of superoxide ion and ascorbate with anthracycline antibiotics.

作者信息

Afanas'ev I B, Polozova N I, Kuprianova N S, Gunar V I

机构信息

All-Union Vitamin Research Institute, Moscow, USSR.

出版信息

Free Radic Res Commun. 1987;3(1-5):141-50. doi: 10.3109/10715768709069779.

Abstract

The interaction of superoxide ion and ascorbate anion with anthracycline antibiotics (adriamycin and aclacinimycin A) as well as with their Fe3+ complexes has been studied in aprotic and protic media. It was found that both superoxide and ascorbate reduce anthracyclines to deoxyaglycons via a one-electron transfer mechanism under all conditions studied. The reaction of ascorbate anion with adriamycin and aclacinomycin A in aqueous solution proceeded only in the presence of Fe3+ ions; it is supposed that an active catalytic species was Fe3+ adriamycin. It is also supposed that the reduction of anthracycline antibiotics by O2-. and ascorbate in cells may increase their anticancer effect.

摘要

在非质子和质子介质中,研究了超氧离子和抗坏血酸阴离子与蒽环类抗生素(阿霉素和阿克拉霉素A)及其Fe3+络合物的相互作用。发现在所有研究条件下,超氧离子和抗坏血酸均通过单电子转移机制将蒽环类抗生素还原为脱氧糖苷配基。抗坏血酸阴离子与阿霉素和阿克拉霉素A在水溶液中的反应仅在Fe3+离子存在下进行;据推测,活性催化物种是Fe3+阿霉素。还推测细胞中O2-和抗坏血酸对蒽环类抗生素的还原作用可能会增强它们的抗癌效果。

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