Synthesis, spectroscopic characterization, DFT, molecular docking and in vitro antibacterial potential of novel quinoline derivatives

Bouzian Y., SERT Y., Khalid K., Van Meervelt L., Chkirate K., Mahi L., ...Daha Fazla

JOURNAL OF MOLECULAR STRUCTURE, cilt.1246, 2021 (SCI-Expanded) identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 1246
  • Basım Tarihi: 2021
  • Doi Numarası: 10.1016/j.molstruc.2021.131217
  • Dergi Adı: JOURNAL OF MOLECULAR STRUCTURE
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus, Academic Search Premier, Chemical Abstracts Core, INSPEC
  • Anahtar Kelimeler: Synthesis, Quinoline, Crystal structure, DFT, Antibacterial activity, Molecular docking, ANTIMICROBIAL ACTIVITY, CRYSTAL-STRUCTURE, INHIBITORS, COMPLEXES, CO(II)
  • Yozgat Bozok Üniversitesi Adresli: Evet

Özet

In this work, three new quinolone derivatives were prepared by alkylation of 2-oxo-1,2-dihydroquinoline-4-carboxylic acid with ethyl 2-bromoacetate. The synthesized compounds 2-4 were characterized by using FT-IR, H-1 NMR, C-13 NMR and mass spectrometry. Crystal structure of 4 was determined by single crystal X-ray diffraction. The optimized structures of 2-4 in gas phase, H-1 and C-13 NMR chemical shifts, molecular electrostatic potential (MEP), frontier orbitals and non-linear properties (NLO) have been investigated by using the B3LYP/6-311++G(d,p) method. All compounds were evaluated in vitro for their antibacterial activities against Pseudomonas aeruginosa ATCC 27853, Escherichia coli ATCC4157, Streptococcus faecalis ATCC 29212 and Staphylococcus aureus ATCC 25923 bacterial strains. The tested compounds exhibited a good to moderate antibacterial activity with MIC values between 6.25 and 50 mu g/mL, when compared to references Ampicillin and Chloramphenicol. Among the three compounds, compound 4 showed the most potent antibacterial activity against S. aureus with MIC value of 6.25 mu g/mL. In addition, molecular docking studies of compounds 2-4 were performed within the active site of PDB: 2ZCQ protein to analyze the binding interactions responsible for their activities. (C) 2021 Elsevier B.V. All rights reserved.