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二吡啶甲基胺磺酰胺衍生化铂配合物作为潜在抗癌剂的合成、表征及生物学评价

Synthesis, characterization and biological evaluation of dipicolylamine sulfonamide derivatized platinum complexes as potential anticancer agents.

作者信息

Thushara Nadini, Darshani Taniya, Samarakoon Sameera R, Perera Inoka C, Fronczek Frank R, Sameera W M C, Perera Theshini

机构信息

Department of Chemistry, University of Sri Jayewardenepura Sri Lanka

Institute of Biochemistry, Molecular Biology and Biotechnology, University of Colombo Sri Lanka.

出版信息

RSC Adv. 2021 May 14;11(29):17658-17668. doi: 10.1039/d1ra00842k. eCollection 2021 May 13.

Abstract

Three new Pt complexes, [PtCl(N(SO(2-nap))dpa)], [PtCl(N(SO(1-nap))dpa)] and [PtCl(N(SOpip)dpa)], containing a rare 8-membered ring were synthesized in good yield and high purity by utilizing the ligands N(SO(2-nap))dpa, N(SO(1-nap))dpa and N(SOpip)dpa, which contain a dipicolylamine moiety. Structural studies of all three complexes confirmed that the ligands are bound in a bidentate mode Pt-N bonds forming a rare 8-membered ring. The intense fluorescence displayed by the ligands is quenched upon coordination to Pt. According to time dependent density functional theory (TDDFT) calculations, the key excitations of N(SO(2-nap))dpa and [PtCl(N(SO(1-nap))dpa)] involve the 2-nap-ligand-centered π → π* excitations. While all six compounds have shown antiproliferative activity against human breast cancer cells (MCF-7), the N(SOpip)dpa and N(SO(2-nap))dpa ligands and [PtCl((NSOpip)dpa)] complex have shown significantly high cytotoxicity, directing them to be further investigated as potential anti-cancer drug leads.

摘要

利用含有二吡啶甲胺部分的配体N(SO(2 - nap))dpa、N(SO(1 - nap))dpa和N(SOpip)dpa,以良好的产率和高纯度合成了三种新的含有罕见八元环的铂配合物[PtCl(N(SO(2 - nap))dpa)]、[PtCl(N(SO(1 - nap))dpa)]和[PtCl(N(SOpip)dpa)]。对这三种配合物的结构研究证实,配体以双齿模式结合,Pt - N键形成一个罕见的八元环。配体显示的强烈荧光在与铂配位时被猝灭。根据含时密度泛函理论(TDDFT)计算,N(SO(2 - nap))dpa和[PtCl(N(SO(1 - nap))dpa)]的关键激发涉及2 - nap - 配体中心的π → π*激发。虽然所有六种化合物都对人乳腺癌细胞(MCF - 7)显示出抗增殖活性,但N(SOpip)dpa和N(SO(2 - nap))dpa配体以及[PtCl((NSOpip)dpa)]配合物显示出显著的高细胞毒性,这使得它们作为潜在的抗癌药物先导物有待进一步研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a9e9/9033217/f86646958fa1/d1ra00842k-s1.jpg

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