Design, synthesis of 1,2,4-triazine derivatives as antidepressant and antioxidant agents: In vitro, in vivo and in silico studies.
Bioorg Chem
; 131: 106284, 2023 02.
Article
en En
| MEDLINE
| ID: mdl-36444791
ABSTRACT
The novel series of substituted-N-(5,6-diphenyl-1,2,4-triazin-3-yl) benzamides (R 1-12) were designed, synthesized and evaluated for in-vitro and in-vivo antidepressant-like activity. In MAO-A inhibition assay, compound R 5 and R 9 displayed most potent activity with IC50 = 0.12 and 0.30 µM. R 5 and R 9 were also evaluated for in-vivo antidepressant using FST and TST. In both models, the test samples R 5 and R 9 showed noteworthy antidepressant effect. R 5 showed 46.48 % and 45.96 % reduction in immobility in FST and TST respectively at dosage of 30 mg/kg (p.o). Whereas compound R 9 reduced the immobility time by 52.76 % and 47.14 % as compared to control in FST and TST, respectively at same dosage. Both the compounds were also tested for behavioural study using actophotometer and grip tests. None of compounds exhibited decrease in locomotor activity. Further, these compounds were subjected to in silico studies to determine their ADME properties along with binding energies and binding orientions. In ADME studies none of the compounds violated the Lipinski rule and all other parameters were also within the acceptable ranges. In docking study R 5 (-10.7) and R 9 (-10.4) were also displayed highest docking score. These encouraging results present the pharmacophoric features of substituted-N-(5,6-diphenyl-1,2,4-triazin-3-yl) benzamides as interesting lead for further development of new antidepressant drug molecules.
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Banco de datos:
MEDLINE
Asunto principal:
Natación
/
Antioxidantes
Tipo de estudio:
Prognostic_studies
Idioma:
En
Año:
2023
Tipo del documento:
Article