Synthesis, Antibacterial Activity, and Cytotoxicity of Newly Synthesized N-Substituted 5,6-Dimethoxy-1H-indole Derivatives
- Authors: Raghavender M.1, Shankar B.1, Jalapathi P.1, Perugu S.2
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Affiliations:
- Department of Chemistry
- Department of Biotechnology
- Issue: Vol 89, No 7 (2019)
- Pages: 1496-1501
- Section: Article
- URL: https://journals.rcsi.science/1070-3632/article/view/223000
- DOI: https://doi.org/10.1134/S107036321907020X
- ID: 223000
Cite item
Abstract
A series of novel functionalized N-substituted 5, 6-dimethoxy-1H-indole derivatives is synthesized. All products are evaluated for antibacterial activity using rifampicin and ciprofloxacin as standard drugs and identified as the promising compounds for further studies. The products are screened for their anticancer activity against MCF7 cell line (breast cancer cell-line) using MTT assay. Two compounds display a significant activity against MCF7 cell line at a very low concentration. The structure-cytotoxicity relationship is supported by molecular docking studies of the active compounds against 3S7S receptor.
About the authors
M. Raghavender
Department of Chemistry
Email: pochampalli.ou.chemi@gmail.com
India, Hyderabad, Telagana, 500007
B. Shankar
Department of Chemistry
Email: pochampalli.ou.chemi@gmail.com
India, Hyderabad, Telagana, 500004
P. Jalapathi
Department of Chemistry
Author for correspondence.
Email: pochampalli.ou.chemi@gmail.com
India, Hyderabad, Telagana, 500007
S. Perugu
Department of Biotechnology
Email: pochampalli.ou.chemi@gmail.com
India, Warangal, Telagana, 506001