Chakraborty B K, Biswas N, Choudhury K, Neogy R K, Das Sarma B
Chemotherapy. 1985;31(1):55-9. doi: 10.1159/000238314.
A group of cis-ethylenediammine platinum (II) complexes were synthesized and their activity against Sarcoma-180 ascites tumour cells in mouse was tested. One of the compounds, Pt(HOCH2CH2NHCH2CH2NH2)Cl2, showed significant antitumour activity having little toxicity to the host. Like the parent compound, cis-DDP, it binds to DNA, but transcription is not the primary process inhibited by these compounds. The drug-DNA complex, though less toxic, was not more effective than the free drug.
合成了一组顺式乙二胺铂(II)配合物,并测试了它们对小鼠肉瘤-180腹水肿瘤细胞的活性。其中一种化合物,Pt(HOCH2CH2NHCH2CH2NH2)Cl2,显示出显著的抗肿瘤活性,对宿主毒性很小。与母体化合物顺铂一样,它与DNA结合,但转录不是这些化合物抑制的主要过程。药物-DNA复合物虽然毒性较小,但并不比游离药物更有效。