Triazolyl RuII, RhIII, OsII, and IrIII Complexes as Potential Anticancer Agents: Synthesis, Structure Elucidation, Cytotoxicity, and DNA Model Interaction Studies. Organometallics, 2019
收藏Figshare2020-05-05 更新2026-04-28 收录
下载链接:
https://figshare.com/articles/dataset/Triazolyl_RuII_RhIII_OsII_and_IrIII_Complexes_as_Potential_Anticancer_Agents_Synthesis_Structure_Elucidation_Cytotoxicity_and_DNA_Model_Interaction_Studies_Organometallics_2019/12040554
下载链接
链接失效反馈官方服务:
资源简介:
Novel conjugated ruthenium(II), rhodium-(III), and iridium(III) organometallic complexes of triazoles1 and 2 synthesized and evaluated for anticancer activityagainst cervical (HeLa), kidney (HEK293), nonsmall lungcancer (A549), and leukemia (MT4) cancer cell lines arereported herein. The complexes are κ2-N,C coordinated andhave the formula [ML(Ar)Cl] (where L is 1-benzyl-4-phenyl-1H-1,2,3-triazole for 1 and 1-benzyl-4-hydroxymethyl-1H-1,2,3-triazole for 2, Ar is p-cymene for RuII and OsII and Cp*for RhIII and IrIII, and M is metal). NMR studies, includingHMBC and NOESY, were employed to unambiguouslyelucidate their structures and provide their conformational information in solution. Single-crystal X-ray diffraction data havebeen used to establish the solid-state structures of selected complexes, which further confirm the structural elucidation by NMR.Dynamic NMR studies, such as differential transferred NOE, have been employed to distinguish between isomers 1a_I and1a_II of ruthenium(II) complexes of triazole 1. The rhodium(III) (1b) and iridium(III) (1c) complexes exhibited goodcytotoxic activities (CC50 = 4−6 μM) comparable to that of the drug auranofin against lung cancer A549 cell lines (CC50 = 4.69μM). While triazole 1 based ruthenium(II) (1a) and osmium(II) (1d) complexes displayed modest anticancer activities againstHeLa and HEK293 cell lines, the analogous rhodium(III) and iridium(III) complexes exhibited good potential (CC50 = 9−54μM versus auranofin (3−9 μM)) against these cancer cell lines. Insightful NMR studies on the interaction between the DNAmodel guanosine 5′-GMP and the complexes 1b,c reveal a possible mode of action of the aquated complexes involvingcarbenylation with DNA bases or purines through the triazolyl proton H-5. From the findings, these complexes could possiblyconfer their cytotoxic activities through intercalation with the DNA of pathological cells. Therefore, carbenylation of thetriazolylrhodium(III) and iridium(III) complexes by DNA guanosine 5′-GMP is proposed as a novel mode of DNAintercalation of these complexes in cancer cells.
创建时间:
2020-05-05



