Synthesis, Spectroscopic Characterization, DFT, Molecular Docking, Catechol Oxidase Activity, and Anti-SARS-CoV-2 of Acylhydrazone Derivatives

• Published in: POLYCYCLIC AROMATIC COMPOUNDS
• Main Authors: Anouar, El Hassane; Filali, Insaf; Shah, Syed Adnan Ali; Karrouchi, Khalid
• Format: Article; Early Access
• Language: English
• Published: TAYLOR & FRANCIS LTD 2024
• Subjects: Chemistry
• Online Access: https://www-webofscience-com.uitm.idm.oclc.org/wos/woscc/full-record/WOS:001296762900001

In the present work, five pyrazole-hydrazone biomolecule ligands (L1-L5) were synthesized by condensation between 1H-pyrazole-3-carbohydrazide (2) and aromatic benzaldehydes. Their corresponding structures were elucidated employing NMR and FT-IR spectra and ESI-MS data. Li-Cu(II) complexes (i = 1-5) were evaluated for catecholase activity in situ at standard conditions. The findings disclose that the catecholase oxidation rate varies with the substituted functional groups in ligand and the anion type in the copper (II) salt. Catecholase activity results showed that the L(i = 1-5)-Cu(II)SO4 complexes exhibited efficient catalytic activity, and a maximum activity of 105 +/- 42 mu M.min(-1) is obtained with L5-Cu(II)SO4. DFT and NBO calculations have been carried out to identify the global reactivity and the strength of interaction bonds between the donors and acceptors in L1-L5. The optimized structure of L1-L3 and L5 were found planar, while that of L4 is out of the molecular plan and forms a torsion angle of 18 degrees due to the presence of methoxy and hydroxyl group at meta and para. In L4, the 5-methyl-1H-pyrazole moiety. NBO findings show that the strongest interactions in L1-L5 are those involved in the electronic transition from pi-bonding -> pi*-antibonding and LP -> pi*- antibonding molecular orbitals. Further, the anti-SARS-CoV-2 of L1-L5 are investigated by estimating their binding affinities into its binding. The docking results reveal that L1-L5 may act as SARS-CoV-2 main protease inhibitors with estimated binding energies in the -6.00 to -8.0 kcal.mol(-1) range.