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新型铂配合物的结构-抗肿瘤活性关系

Structure-antitumour activity relationships for new platinum complexes.

作者信息

Craciunescu D G, Doadrio A, Furlani A, Scarcia V

出版信息

Chem Biol Interact. 1982 Nov;42(2):153-64. doi: 10.1016/0009-2797(82)90129-6.

Abstract

Fourteen platinum (Pt) coordination complexes with different ligands, which include both Pt(II) and Pt(IV) complexes, were prepared, characterized and tested for their in vitro cytotoxic effects on KB cells and for their antitumour activity against some tumour systems (L1210 and P388 leukaemia, ADJ/PC6A plasma cell tumour and Yoshida sarcoma). The majority of the ligands were derivatives of aniline or pyridine, but complexes with tranylcypromine, guanethidine and octodrine were also synthetized. Depending on cytotoxicity the Pt-compounds could be divided into 3 groups. The compounds with a high cytotoxicity (ED50 = 0.1-1 microgram/ml) were also active against L1210 and P-388 leukaemia; a correlation between cytotoxicity and antitumour activity was not always observed. In these complexes the oxidation state of the Pt appears to be critical for their activity.

摘要

制备了十四种具有不同配体的铂(Pt)配位络合物,其中包括Pt(II)和Pt(IV)络合物,对其进行了表征,并测试了它们对KB细胞的体外细胞毒性作用以及对某些肿瘤系统(L1210和P388白血病、ADJ/PC6A浆细胞瘤和吉田肉瘤)的抗肿瘤活性。大多数配体是苯胺或吡啶的衍生物,但也合成了与反苯环丙胺、胍乙啶和奥西君的络合物。根据细胞毒性,铂化合物可分为3组。具有高细胞毒性(ED50 = 0.1 - 1微克/毫升)的化合物对L1210和P - 388白血病也有活性;细胞毒性与抗肿瘤活性之间并不总是存在相关性。在这些络合物中,铂的氧化态似乎对其活性至关重要。

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