肽
阳离子聚合
化学
齿合度
抗菌剂
组合化学
顺铂
铂金
癌细胞
配体(生物化学)
选择性
立体化学
生物化学
癌症
有机化学
受体
生物
金属
化疗
遗传学
催化作用
作者
James P. Parker,Marc Devocelle,Celine J. Marmion
标识
DOI:10.1002/zaac.201300109
摘要
Abstract This work focuses on the cationic antimicrobial peptide (CAP) DP18L with its known propensity to target and selectively kill cancer cells. DP18L was derivatised to dap‐DP18L where dap is 2,3‐diaminopropionic acid. Dap facilitated binding to Pt II via an ( N , N' ) bidentate ligand to afford the first reported Pt‐CAP complex, cis ‐[Pt(dap‐DP18L)Cl 2 )]. The syntheses of the peptides and the Pt‐peptide complex were carried out using solid phase chemistry. It was envisioned that the presence of the peptide in the complex would confer enhanced selectivity of the novel complex for neoplastic cells in addition to increasing the cellular uptake of the complex relative to cisplatin.
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