A New Approach For The Synthesis Of Bis(Indolyl) Derivatives And The Evaluation Of Antioxidant And Antiulcer Activity

  • Unique Paper ID: 165106
  • Volume: 11
  • Issue: 1
  • PageNo: 1458-1473
  • Abstract:
  • This study introduces an efficient synthesis method for bis(indolyl) derivatives, highlighting their potential as anti-ulcer and antioxidant agents. The novel approach involves reacting indoles with aldehydes/ ketones in the presence of TBAHS as a catalyst and Ethyl Acetate as a solvent at 95°C for 60-90 minutes. This method offers advantages such as cost efficiency, minimal reagent consumption, one-pot synthesis, and high yield. The synthesized derivatives were characterized using IR to confirm their structures and purity. Subsequent in silico and in vitro experiments assessed their biological activities. The antioxidant activity, evaluated via phosphomolybdate assay, revealed that compounds 1, 2, and 5 exhibit strong antioxidant properties, which may contribute to their anti-ulcer effects by mitigating oxidative stress. The anti-ulcer activity was assessed using an acid neutralizing capacity assay, where compounds 1 and 2 at 50 mg, 1, 2, 3, and 5 at 100 mg, and 2 and 4 at 150 mg demonstrated the highest ANC. These findings suggest that several synthesized compounds could reduce ulcer formation and promote healing, indicating their potential as therapeutic agents.

Copyright & License

Copyright © 2025 Authors retain the copyright of this article. This article is an open access article distributed under the Creative Commons Attribution License which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

BibTeX

@article{165106,
        author = {Dr Kesari Lakshmi Manasa and Arjun Acharya and Andabatla Usha and G. Bhumika and Dr G Tulja Rani},
        title = {A New Approach For The Synthesis Of Bis(Indolyl) Derivatives And The Evaluation Of Antioxidant And Antiulcer Activity },
        journal = {International Journal of Innovative Research in Technology},
        year = {},
        volume = {11},
        number = {1},
        pages = {1458-1473},
        issn = {2349-6002},
        url = {https://ijirt.org/article?manuscript=165106},
        abstract = {This study introduces an efficient synthesis method for bis(indolyl) derivatives, highlighting their potential as anti-ulcer and antioxidant agents. The novel approach involves reacting indoles with aldehydes/ ketones in the presence of TBAHS as a catalyst and Ethyl Acetate as a solvent at 95°C for 60-90 minutes. This method offers advantages such as cost efficiency, minimal reagent consumption, one-pot synthesis, and high yield. The synthesized derivatives were characterized using IR to confirm their structures and purity. Subsequent in silico and in vitro experiments assessed their biological activities. The antioxidant activity, evaluated via phosphomolybdate assay, revealed that compounds 1, 2, and 5 exhibit strong antioxidant properties, which may contribute to their anti-ulcer effects by mitigating oxidative stress. The anti-ulcer activity was assessed using an acid neutralizing capacity assay, where compounds 1 and 2 at 50 mg, 1, 2, 3, and 5 at 100 mg, and 2 and 4 at 150 mg demonstrated the highest ANC. These findings suggest that several synthesized compounds could reduce ulcer formation and promote healing, indicating their potential as therapeutic agents.},
        keywords = {BisIndole, One pot, Anti-ulcer activity, Anti-oxidant activity},
        month = {},
        }

Related Articles