A rhodanine derivative as a potential antibacterial and anticancer agent: Crystal structure, spectral characterization, DFT calculations, Hirshfeld surface analysis, in silico molecular docking and ADMET studies

被引:23
作者
Guerraoui, Amal [1 ]
Goudjil, Meriem [2 ,3 ]
Direm, Amani [4 ,5 ]
Guerraoui, Abdenour [4 ,5 ]
Sengun, Ilkin Yucel [6 ,7 ]
Parlak, Cemal [7 ,8 ]
Djedouani, Amel [9 ,10 ]
Chelazzi, Laura [11 ,12 ]
Monti, Filippo [13 ]
Lunedei, Eugenio [3 ]
Boumaza, Abdecharif [4 ,5 ]
机构
[1] Univ Batna 1, Fac Mat Sci, Lab Phys Radiat & Their Interact Matter, Batna 05000, Algeria
[2] Univ Florence, Dept Earth Sci, Via Giorgio La Pira 4, I-50121 Florence, FI, Italy
[3] CNR, ISMN, Via P Gobetti 101, Bologna, Italy
[4] Abbes Laghrour Univ, Fac Sci & Technol, Dept Matter Sci, Khenchela 40000, Algeria
[5] Abbes Laghrour Univ, Fac Sci & Technol, Lab Struct Properties & Interatom Interact LASPI2, Khenchela 40000, Algeria
[6] Ege Univ, Engn Fac, Food Engn Dept, TR-35040 Izmir, Turkiye
[7] Azerbaijan State Agr Univ, AZ-2000 Ganja, Azerbaijan
[8] Ege Univ, Fac Sci, Dept Phys, TR-35040 Izmir, Turkiye
[9] UFMC1, Lab Analyt Physicochem & Crystallochem Organometa, Constantine 25000, Algeria
[10] Univ Constantine 3, Higher Normal Sch Constantine, Constantine 25000, Algeria
[11] Univ Florence, Dept Chem U Schiff, Via Lastruccia 3-13, I-50019 Sesto Fiorentino, FI, Italy
[12] Univ Florence, Ctr Crystallog, Via Lastruccia 3, I-50019 Sesto Fiorentino, FI, Italy
[13] CNR, ISOF, Via P Gobetti 101, I-40129 Bologna, Italy
关键词
Rhodanine single crystal; Fluorescence microscopy; DFT; Hirshfeld surface analysis; In silico anticancer and antibacterial  inhibitory activity; ADMET properties; POLO-LIKE KINASES; DRUG DISCOVERY; THIAZOLIDINONE DERIVATIVES; PREDICTION; CLASSIFICATION; INHIBITORS; TOXICITY; SCAFFOLD; DESIGN; BINARY;
D O I
10.1016/j.molstruc.2023.135025
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
A novel rhodanine derivative, namely 5-(4-dimethylaminobenzylidene) rhodanine "C12H12N2OS2 ", was successfully crystallized from condensation route and characterized by NMR, FT-IR, UV-Vis spectral meth-ods as well as single-crystal X-ray diffraction. This rhodanine derivate crystallizes in the monoclinic P21/c space group, with the cell parameters: a = 3.93590(10), b = 11.2480(3), c = 26.6703(7) A and beta = 93.8530(10) degrees. The molecular structure displays intra-(C - S middotmiddotmiddotH) and intermolecular ( N - HmiddotmiddotmiddotO) hydrogen-bonding interactions. Micro-spectroscopy performed on single-crystals of the studied com-pound revealed the first absorption transition at 2.25 eV, and a well-structured luminescence peaked at 2.01 eV (0.15 eV broad). Density functional theory (DFT) calculations allowed the structure optimiza-tion, the electronic properties, the IR-vibrational modes and frequencies as well as the 1 H and 13 C NMR chemical shifts' calculation. Furthermore, time-dependent DFT (TD-DFT) calculations were performed for the vertical transition energies. Hirshfeld surface analysis (HSA) showed the presence of non-conventional C-H middotmiddotmiddotH-C, C-H middotmiddotmiddotn-and n-middotmiddotmiddotlp interactions and n--n-stacking. The anti-cancer and anti-bacterial activities of the studied compound towards the Polo-like kinase PLK1 and the Escherichia coli MurB enzymes were in silico evaluated by performing molecular docking simulations. The results suggest that the molecule can significantly inhibit the enzymes' active sites. Additionally, the physicochemical and pharmacokinetic characteristics of the molecule were evaluated through absorption, distribution, metabolism, excretion and toxicity (ADMET) analysis, and the results ensure its good drug-likeness properties.(c) 2023 Elsevier B.V. All rights reserved.
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页数:17
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