Synthesis, Characterization, and Biological Evaluation of Benzimidazole Derivatives as Potential Anxiolytics
Nannapaneni DT1★, Gupta Atyam VSSS2, Reddy MI1, Sarva Raidu Ch2★ Corresponding author
- 1Department of Pharmaceutical Chemistry, Mallareddy College of Pharmacy, Dhullapally Village, Hyderabad, INDIA.
- 2Department of Pharmacology, Joginpally B.R Pharmacy College, Yenkapally (P.O), Moinabad (Mandal), Ranga Reddy (Dist), Andhra Pradesh, INDIA.
CORRESPONDENCE
Nannapaneni DT
Department of Pharmaceutical Chemistry, Mallareddy College of Pharmacy, Dhullapally Village, Hyderabad , INDIA.
Volume 2, Issue 3 · pp. 273–279 · PUBLISHED · DOI: 10.4103/0975-1483.66809
ABSTRACT
The synthesized benzimidazoles compounds were prepared from the condensation reaction between o-Phenylenediamine and various carbonyl compounds, in the presence of ammonium chloride as a catalyst. Ammonium chloride is a commercial and environmentally benign catalyst. The yield of all benzimidazole derivatives was found to be in the range of 75 – 94%. The purity of the compounds was ascertained by melting point and TLC. The synthesized compounds were characterized by using IR, 1H NMR, and MASS spectral data together with elemental analysis. The synthesized benzimidazole compounds were screened for acute and chronic anti-anxiety activity in Wistar rats by using an elevated plus maze model with standard Diazepam. The synthesized compounds ZB, ZE, ZF, ZG, and ZH showed potent anti-anxiety activity when compared to the standard Diazepam. The compound ZH exhibited a higher anti-anxiety activity when compared to other prepared benzimidazoles. The results were subjected to statistical analysis by using one-way ANOVA followed by the Tukey-Kramer test, to calculate the significance.
KEYWORDS
REFERENCES
As publishedShowing references and in-text citations exactly as published.
Cite this article
SELECT FORMAT
DT, N., VSSS, G. A., MI, R., & Ch, S. R. (). Synthesis, Characterization, and Biological Evaluation of Benzimidazole Derivatives as Potential Anxiolytics. Journal of Young Pharmacists, 2(3), 273–279. https://doi.org/10.4103/0975-1483.66809