Issue 45, 2025

Synthesis and cytotoxic activity of morpholino-s-triazine derivatives of POCOP-Ni(ii) pincers

Abstract

Six POCOP-Ni(II) complexes (2, 3a, 3b, 4, 5, and 6) bearing a morpholino-s-triazine moiety were synthesized and fully characterized. The structures of complexes 2 and 3a were determined by single-crystal X-ray diffraction, revealing a distorted square-planar geometry around the metal center. Based on these structures, a supramolecular analysis using Hirshfeld surfaces was also carried out, identifying intermolecular hydrogen bonding and π⋯π stacking interactions. The antiproliferative activity of all complexes was evaluated against six cancer cell lines and a non-cancerous cell line (COS7). Complexes 3a and 3b exhibited the highest antiproliferative activity mainly against leukemia (K562), with IC50 values of 0.55 ± 0.04 μM and 0.59 ± 0.04 μM, respectively. A study of the mechanism of action includes competitive displacement of ethidium bromide (EB) fluorescence within DNA, and molecular docking with DNA and PI3K.

Graphical abstract: Synthesis and cytotoxic activity of morpholino-s-triazine derivatives of POCOP-Ni(ii) pincers

Supplementary files

Article information

Article type
Paper
Submitted
05 Jun 2025
Accepted
14 Oct 2025
First published
14 Oct 2025
This article is Open Access
Creative Commons BY-NC license

Dalton Trans., 2025,54, 16836-16847

Synthesis and cytotoxic activity of morpholino-s-triazine derivatives of POCOP-Ni(II) pincers

J. S. Serrano-García, A. Amaya-Flórez, A. Arenaza-Corona, M. T. Ramírez-Apan, A. L. Orjuela, J. Alí-Torres, M. Flores-Alamo, S. Hernandez-Ortega, P. Cano-Sanchez and D. Morales-Morales, Dalton Trans., 2025, 54, 16836 DOI: 10.1039/D5DT01322D

This article is licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported Licence. You can use material from this article in other publications, without requesting further permission from the RSC, provided that the correct acknowledgement is given and it is not used for commercial purposes.

To request permission to reproduce material from this article in a commercial publication, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party commercial publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements