Design, Synthesis and Evaluation of Riboflavin-Isoniazid Conjugate
Wavhale S R*, Shaikh A R
Department of Pharmaceutical Chemistry, MCE’s Allana College of Pharmacy, Pune, affiliated to Savitribai Phule Pune University, Pune-411001, India
Received: 30th Jun, 2025; Revised: 19th Aug, 2025; Accepted: 30th Aug, 2025; Available Online: 25th Sep, 2025
ABSTRACT
The infectious, contagious disease tuberculosis (TB), which is caused by the bacteria Mycobacterium tuberculosis (MT), frequently lasts the entirety of a person's life and results in the formation of tubercles in various parts of the body. This condition is exceedingly difficult to treat because of the complicated connections between different side effects and drug resistance. Along with AIDS and malaria, TB is a strain on healthcare systems in developing countries. Oxidoreductase enzyme was selected for molecular docking. The docking includes the comparison of docking results of Standard ligand that is 6TEV and molecular docking results of Riboflavin- Isoniazid Conjugate. The study used a linker (Riboflavin- Succinic Acid Linker) to create the molecule known as riboflavin-isoniazid conjugate. Melting point and TLC were used to verify the compound's purity. The final compound was confirmed using FTIR, NMR and HRMS study. Conjugate was tested for anti-tubercular activity using the Microplate Almar Blue Assay (MABA).
Keywords: Mycobacterium Tuberculosis, Molecular docking, Riboflavin-Isoniazid Conjugate, Anti-Tubercular activity.
How to cite this article: Wavhale S R, Shaikh A R. Design, Synthesis and Evaluation of Riboflavin-Isoniazid Conjugate. International Journal of Drug Delivery Technology. 2025;15(3):1304-09. doi: 10.25258/ijddt.15.3.51
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