A square planar cobalt(II)-thiosemicarbazone complex. Synthesis, characterization, antiviral and anti-inflammatory potential

被引:1
|
作者
Atasever-Arslan, Belkis [1 ]
Kaya, Busra [2 ]
Sahin, Onur [3 ]
Ulkuseven, Bahri [2 ]
机构
[1] Uskudar Univ, Fac Engn & Nat Sci, Dept Mol Biol & Genet, Istanbul, Turkiye
[2] Istanbul Univ Cerrahpasa, Dept Chem, Engn Fac, TR-34320 Avcilar, Istanbul, Turkiye
[3] Sinop Univ, Fac Hlth Sci, Dept Occupat Hlth & Safety, TR-57000 Sinop, Turkiye
关键词
SARS-CoV-2; Inflammation; IL8; Thiosemicarbazone; Cobalt; COVID19; BRONCHIAL EPITHELIAL-CELLS; PALLADIUM(II) COMPLEXES; DERIVATIVES; THIOSEMICARBAZONE; VIRUS; EXPRESSION; IRON;
D O I
10.1016/j.molstruc.2024.140109
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Considering the possible antiviral effect of cobalt compounds and known pharmacological potential of thiosemicarbazones, a new combination containing cobalt(II) ions and tetradentate thiosemicarbazone was synthesized and structurally analyzed. In the complex structure (Co1), the cobalt ion is in 2+ + oxidation state and is coordinated with ONNO donor set on the thiosemicarbazone backbone. The complex molecule crystallizes in the space group P21/m and the environment of the cobalt center tends to square planar geometry. The inhibitory performance of SARS-CoV-2 and the anti-inflammatory impact of the complex molecule were investigated. It was found that Co1 has high inhibitory effects on the SARS-CoV-2 virus's 3CL main protease enzyme, ACE2:SARSCoV2 Spike RBD interaction, and IL8. Also, it showed significant anti-inflammatory effects on the release of IL6, IL8, IL10, and TGF beta 1 beta 1 cytokines and wound healing during in vitro TNF-alpha-induced inflammation. Experimental evidence demonstrates that Co1 diminishes both IL8 gene expression and protein levels. According to in silico and experimental results, it has a drug potential. Assessing the in vivo impacts of Co1 might contribute to understanding its potential as an antiviral and anti-inflammatory agent.
引用
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页数:13
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