Protein Kinase Inhibitory Potential and Anti-Fungal Activities of Metal Complexes of Anti-Viral Drug Ribavirin
Background: Ribavirin, a known antiviral drug, potentially recognised for a number of pathological conditions like hepatitis C, Lassa fever and Hanta virus infection. It predominantly works by inhibiting viral RNA synthesis that in turn stop viral multiplication. The best prosperous derivative of this drug is Taribavirin (3-carboxamidine derivative).
Objective: In this research, we aim to synthesize the metal complexes of already marketed drug ribavirin, because the complexation of such approved marketed drug will save time and currency that may spend in relation to clinical development of new drug molecule.
Method: Eleven derivatives (S-01-S-11) of ribavirin were synthesized in combination with di/tri organotin, Zn, Cu and Fe. Characterization was done through IR and H1 NMR spectrophotometer and these compounds were analysed for in vitro biological activities including anti-microbial, anti-fungal and protein kinase inhibition assay.
Results: Research revealed that addition of trace metals to approved marketed drug have enhanced the biological properties of unbound drug.
Conclusion: Outcomes of this research clearly indicates the enhancement of biological activities of free drug through immersion of metals which could be further analysed for toxicity studies.
Copyright (c) 2019 RADS Journal of Pharmacy and Pharmaceutical Sciences
This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License.
Submitting a manuscript to a journal implies that the work has not previously been published in any other journal, printed or online (save as an abstract or an academic thesis), and that it is not currently being considered for publication elsewhere.