Corrigendum to ‘Mitochondria localizing high-spin iron complexes of curcumin for photo-induced drug release’ [Inorg. Chim. Acta 483 (2018) 571–578]

Jana, Avishek; Verma, Brijesh Kumar; Garai, Aditya; Kondaiah, Paturu; Chakravarty, Akhil R.

doi:10.1016/j.ica.2019.04.052

Cited by 2 publications

(1 citation statement)

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“…However, compared with Cu-P1, a new band has arisen in the spectra of CuP-2 (or CuP-3) at 1556 cm −1 (or 1595 cm −1 ); it is mainly because of complex's carbonyl oxygen coordinate with metal ion. [42,43]…”

Section: Synthesis Of Porphyrin Cu-p1mentioning

confidence: 99%

DNA interactive and selective anticancer activity studies of copper(II) complexes decorated water‐soluble porphyrin

Zhang

Hou

et al. 2020

Applied Organom Chemis

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Cancer is one of the diseases that seriously threaten the health of peoples. As a representative of metal drugs, cisplatin has considerable promise for the treatment of cancer. However, side effects are one of major problems for cisplatin due to their poor selectivity for cancer cells. We report here, for the first time, the syntheses of three new water‐soluble porphyrin‐modified copper(II) complexes Cu‐P1, Cu‐P2, and Cu‐P3. Results from calf thymus DNA (ct‐DNA)‐binding efficiency tests show that three copper(II) complexes could obviously interact with ct‐DNA and Cu‐P1 characterized the strongest bound performance. Besides, their function on anticancer against A549, H1975, HepG2, and T47D cells were analyzed, they show the best anticancer activity against lung cancer cells H1975, Cu‐P1 exhibited the greatest cytotoxic effect among the series, and the ligand L was less active against cancer cells. Furthermore, the cytotoxicities of ligand L, complexes Cu‐P1, Cu‐P2, Cu‐P3, and cisplatin were further evaluated against the breast cells Hs 578Bst and complexes more negligible cytotoxicity than ligand L and cisplatin. The anticancer mechanism is discussed by flow cytometer. Then, density functional theory (DFT) calculations analysis further proved the biological activities of the target compounds. Therefore, preliminary research suggests that these copper(II) complexes can inhibit human malignancy cells.

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Section: Synthesis Of Porphyrin Cu-p1mentioning

confidence: 99%

DNA interactive and selective anticancer activity studies of copper(II) complexes decorated water‐soluble porphyrin

Zhang

Hou

et al. 2020

Applied Organom Chemis

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Coordination compounds of biogenic metals as cytotoxic agents in cancer therapy

Guk¹,

Krasnovskaya²,

Белоглазкина³

2021

Russ. Chem. Rev.

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The review summarizes the data on the structures and methods for the synthesis of compounds with anticancer activity based on biogenic metals, which can replace platinum drugs prevailing in cytotoxic therapy. The main focus is given to the comparison of the mechanisms of the cytotoxic action of these complexes, their efficacy and prospects of their use in clinical practice. This is the first systematic review of cytotoxic zinc, iron, cobalt and copper compounds. The structure–activity relationships and the mechanisms of antitumour action are formulated for each type of metal complexes. The bibliography includes 181 references.

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Corrigendum to ‘Mitochondria localizing high-spin iron complexes of curcumin for photo-induced drug release’ [Inorg. Chim. Acta 483 (2018) 571–578]

Cited by 2 publications

References 0 publications

DNA interactive and selective anticancer activity studies of copper(II) complexes decorated water‐soluble porphyrin

DNA interactive and selective anticancer activity studies of copper(II) complexes decorated water‐soluble porphyrin

Coordination compounds of biogenic metals as cytotoxic agents in cancer therapy

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