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- W4282024674 abstract "Cobalt complexes had exhibited the potential anti-diabetes abilities, but the mechanism is not so clear now. In this work, we synthesized and characterized a new cobalt(II) complex [Co(L)2Cl2]·1.5CH3OH·H2O (L=4-{[3-(pyridine-2-yl)-1H-pyrazol-1-yl]methyl}-benzoic acid). The crystal structure determination shows that the complex crystallizes in the triclinic system with P1¯ space group, where Co(II) center of the complex resides in a distorted octahedron with four N atoms from two pyridine-pyrazole ligands and two Cl− anions in a cis-configuration. The structure cohesion is ensured by intermolecular hydrogen bonds and intramolecular π···π stack interactions. Such a cobalt(II) complex shows moderate inhibition activity (IC50 = 35.6 µM) against T-cell protein tyrosine phosphatase (TCPTP), a potential target for therapy of diabetes. We speculate that the anti-diabetes ability of the cobalt complex may play its role by inhibiting the activity of TCPTP. Moreover, the MTT assays reveal that the complex exhibits relatively low cytotoxicity to cancer cell lines (MCF7, HepG2, and SW480) and the normal cell line (HL-7702)." @default.
- W4282024674 created "2022-06-13" @default.
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- W4282024674 date "2022-10-01" @default.
- W4282024674 modified "2023-10-14" @default.
- W4282024674 title "Crystal structure, TCPTP inhibition and cytotoxicity of the cobalt(II) complex with the 4‐{[3‐(pyridine‐2‐yl)‐1H‐pyrazol‐1‐yl]methyl}‐benzoic acid ligand" @default.
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- W4282024674 doi "https://doi.org/10.1016/j.molstruc.2022.133486" @default.
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