Synthesis, DFT calculations, biological investigation, molecular docking studies of beta-lactam derivatives

Mermer A., Bayrak H., Alyar S., Alagumuthu M.

JOURNAL OF MOLECULAR STRUCTURE, cilt.1208, 2020 (SCI-Expanded) identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 1208
  • Basım Tarihi: 2020
  • Doi Numarası: 10.1016/j.molstruc.2020.127891
  • Dergi Adı: JOURNAL OF MOLECULAR STRUCTURE
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus, Academic Search Premier, Chimica, Compendex, INSPEC
  • Anahtar Kelimeler: DFT calculation, beta-lactam, Molecular docking, Urease inhibition, MICROWAVE IRRADIATED SYNTHESIS, UREASE, ANTIBACTERIAL, ANTIFUNGAL, COMPLEXES
  • Karadeniz Teknik Üniversitesi Adresli: Evet

Özet

In this study beta-lactam derivatives which include 1,3,4-thiadiazole and 1,3,4-oxadiazole structure (8a,b) have been achieved by cyclocondensation reaction. The synthesized compounds were investigated for antioxidant capacity and in vitro antiurease activity. The obtained compounds displayed good-moderate urease inhibiton results in comparison with thiourea, standard drug. Also, frontier molecular orbital analysis, reactivity descriptors (such as ionization energy (I), electron affinity(A), electro negativity(chi), chemical hardnesses (eta) and chemical softness (S), chemical potential (mu) and global electrophilicity index (omega)), nonlinear optical properties (NLO) and molecular electrostatic potential (MEP) studied with DFT approach and B3LYP/6-311++G (d,p) level of theory. Nonlinear optical calculations presented that 7b and 8b have very large nonlinear optical activity. In addition, molecular docking studies were performed. (C) 2020 Elsevier B.V. All rights reserved.