Chalcones bearing nitrogen-containing heterocyclics as multi-targeted inhibitors: Design, synthesis, biological evaluation and molecular docking studies.
Yusuf SicakHüseyin KekeçmuhammedAyşegül Karaküçük IyidoğanTugba Taskin TokEmine Elçin Oruç EmreMehmet ÖztürkPublished in: Journal of molecular recognition : JMR (2023)
In this work, a series of chalcones (1a-d, 2a-d, 3a-d, 4a-d, and 5a-d) were designed and synthesized by Claisen-Schmidt condensation. Also, their chemical structures were elucidated using UV-Vis, FT IR, 1 H NMR, 13 C NMR, MS spectral data, and elemental analyses. Subsequently, the anticholinesterase, tyrosinase, urease inhibitory activities and antioxidant activities of all chalcones were evaluated. The inhibitory potential of all chalcones in terms of IC 50 value was observed to range from 7.18 ± 0.43 to 29.62 ± 0.30 μM against BChE by comparing with Galantamine (IC 50 46.06 ± 0.10 μM) as a reference drug. Also, compounds 2c, 3c, 4c, 4b, and 4d exhibited high anticholinesterase activity against both AChE and BChE enzymes. The tyrosinase inhibitory activity results revealed that three compounds (IC 50 1.75 ± 0.83 μM for 2b, IC 50 2.24 ± 0.11 μM for 3b, and IC 50 1.90 ± 0.64 μM for 4b) displayed good inhibitory activity against tyrosinase compared with kojic acid (IC 50 0.64 ± 0.12 μM). In addition, other different three chalcones (IC 50 22.34 ± 0.25 μM for 2c, IC 50 20.98 ± 0.08 μM for 3c, and IC 50 18.26 ± 0.13 μM for 4c) showed excellent inhibitory activity against the urease by comparing with thiourea (IC 50 23.08 ± 0.19 μM). Compounds 3c and 4c showed the best potency in all antioxidant activity tests. In light of these findings, the structure-activity relationship for compounds was also described. Furthermore, molecular modeling studies, including molecular docking, absorption, distribution, metabolism, excretion, and toxicity (ADMET), and pharmacophore analyses of compounds, gave important information about the interactions and drug-likeness properties. As a result, all chalcones exhibited suitable ADMET findings, predicting good oral bioavailability.
Keyphrases
- molecular docking
- molecular dynamics simulations
- magnetic resonance
- oxidative stress
- high resolution
- emergency department
- mass spectrometry
- healthcare
- drug delivery
- ms ms
- multiple sclerosis
- computed tomography
- risk assessment
- magnetic resonance imaging
- anti inflammatory
- machine learning
- molecular dynamics
- electronic health record
- human health
- single cell