The First Multimodal Anticancer Manganese(II) Complex of an Asymmetric Anthrahydrazone Triggers Apoptosis, Autophagy and Ferroptosis

A new nonsymmetric anthrahydrazone ligand (AAIH) was designed and synthesized, affording novel manganese(II) and cobalt(II) complexes, AAIH-Mn and AAIH-Co. Both complexes crystallized in the same centrosymmetric dinuclear coordination mode, however, AAIH-Mn exhibited much higher in vitro cytotoxicity (IC<sub>50</sub> = 1.64 μM against MGC-803 cells) than AAIH-Co (IC<sub>50</sub> = 10.05 μM) and AAIH (IC<sub>50</sub> = 18.82 μM), signifying the importance of the Mn(II) center. Furthermore, AAIH-Mn exerted anticancer activity via multiple pathways: S-phase cell cycle arrest, cell apoptosis, autophagy and notably, the emerging process of ferroptosis. AAIH-Mn also effectively inhibited 56% of tumor growth in vivo on MGC-803 xenografts at 16 mg/kg, without causing obvious toxicity. Low toxicity was further supported by zebrafish models, along with its anti-inflammatory activity and low cardiotoxicity. As the first Mn(II) complex inducing ferroptosis, AAIH-Mn provides a valuable example of a low-toxicity metal center to generate highly cytotoxic nonplatinum anticancer complex.

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Journal
Journal of Medicinal Chemistry
Published
2026-03-13
DOI
https://doi.org/10.1021/acs.jmedchem.5c03122
Primary Topic
Metal complexes synthesis and properties
Type
article
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article

The First Multimodal Anticancer Manganese(II) Complex of an Asymmetric Anthrahydrazone Triggers Apoptosis, Autophagy and Ferroptosis

Tongyan Ding, Tim Storr, Jiaxiu Xie, Changchun Wen et al.
Journal of Medicinal Chemistry
Metal complexes synthesis and properties
article

The First Multimodal Anticancer Manganese(II) Complex of an Asymmetric Anthrahydrazone Triggers Apoptosis, Autophagy and Ferroptosis

Tongyan Ding, Tim Storr, Jiaxiu Xie, Changchun Wen, Ying-Shu Wu, Yan‐Cheng Liu, Yue Huang, Xue-bin Bi, Sha-Sha Luo, Ru-yi Luo, Rui-Xue Liu, Dong-Mei Li, Hong Liang
article en

Abstract

A new nonsymmetric anthrahydrazone ligand (AAIH) was designed and synthesized, affording novel manganese(II) and cobalt(II) complexes, AAIH-Mn and AAIH-Co. Both complexes crystallized in the same centrosymmetric dinuclear coordination mode, however, AAIH-Mn exhibited much higher in vitro cytotoxicity (IC<sub>50</sub> = 1.64 μM against MGC-803 cells) than AAIH-Co (IC<sub>50</sub> = 10.05 μM) and AAIH (IC<sub>50</sub> = 18.82 μM), signifying the importance of the Mn(II) center. Furthermore, AAIH-Mn exerted anticancer activity via multiple pathways: S-phase cell cycle arrest, cell apoptosis, autophagy and notably, the emerging process of ferroptosis. AAIH-Mn also effectively inhibited 56% of tumor growth in vivo on MGC-803 xenografts at 16 mg/kg, without causing obvious toxicity. Low toxicity was further supported by zebrafish models, along with its anti-inflammatory activity and low cardiotoxicity. As the first Mn(II) complex inducing ferroptosis, AAIH-Mn provides a valuable example of a low-toxicity metal center to generate highly cytotoxic nonplatinum anticancer complex.

Journal of Medicinal ChemistryVol. 69(6)
Simon Fraser University (CA), Guangxi Normal University (CN), Guangxi University of Chinese Medicine (CN)
Openalex Percentile: Top 23%
Metal complexes synthesis and properties
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