Novel aldehyde and thiosemicarbazone derivatives: Synthesis, spectroscopic characterization, structural studies and molecular docking studies

KARAKURT T., Tahtaci H., SUBAŞI CANBAZ N. T., Er M., Ağar E.

JOURNAL OF MOLECULAR STRUCTURE, cilt.1125, ss.470-480, 2016 (SCI-Expanded) identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 1125
  • Basım Tarihi: 2016
  • Doi Numarası: 10.1016/j.molstruc.2016.07.013
  • Dergi Adı: JOURNAL OF MOLECULAR STRUCTURE
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Sayfa Sayıları: ss.470-480
  • Anahtar Kelimeler: Aldehyde, Thiosemicarbazone, NMR, B3LYP, Beta-lactam, EFFECTIVE CORE POTENTIALS, BIOLOGICAL-ACTIVITY, IN-VITRO, CYCLIZATION REACTIONS, BETA-LACTAMASES, COMPLEXES, ANTICONVULSANT, SEMICARBAZONE, INHIBITORS, OPTIMIZATION
  • Ondokuz Mayıs Üniversitesi Adresli: Evet

Özet

In this study our purpose is that, synthesis and characterization of compounds containing the aldehyde and thiosemicarbazone groups and comparison of the theoretical results with the experimental results. The structures of all synthesized compounds were elucidated by IR, H-1 NMR, C-13 NMR, elemental analyses techniques. The structure of compound (4) (C9H8N4O2S) was also elucidated by X-ray diffraction analysis. In addition, the theoretical IR spectrum, H-1 NMR and C-13 NMR chemical shift values, frontier molecular orbital values (FMO) of these molecules were analyzed by using Becke-3- Lee-Yang-Parr (B3LYP) method with LanL2DZ basis set. Finally, molecular docking studies were performed on synthesized compounds using the 4DKI beta-lactam protein structure to determine the potential binding mode of inhibitors. (C) 2016 Elsevier B.V. All rights reserved.