Microwave-assisted synthesis of a zirconium-based MOF as an efficient catalyst for one-pot synthesis of xanthene derivatives: in silico study as a potential anti-HIV RNA

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Abstract

Firstly, construction and characterization of a novel Zr/VitB3 metal organic framework have been described. The physicochemical analysis and morphological properties of Zr-MOF has been accomplished by IR, SEM, EDX, TEM, and XRD. Cyclic diketones and various aromatic aldehydes were efficiently and ecologically benignly condensed in a single pot, yielding a range of tetrahydroxanthenediones in good to excellent yields. The utilization of a heterogeneous catalyst, solventless conditions, and a straightforward process that is atom-economical and yields low E-factor values are some of the benefits of this multicomponent reaction. The catalyst can be used up to three times and is completely recyclable. Advantages include a clean methodology, high yield, and straightforward catalyst preparation. Additionally, the study investigates the potential binding interactions of Zr-MOF with the HIV-RNA major groove, revealing its exceptional stability and strong binding affinity. The binding energy score of the Zr-MOF with HIV-RNA was found to be remarkably low at −12.32 kcal mol−1, indicating its potential to significantly outperform the reference molecule, nevirapine, which showed a higher E-score of −4.98 kcal mol−1. Xanthene derivatives were also evaluated for their binding affinity to the viral major groove, with energy scores ranging from −5.55 to −6.40 kcal mol−1, further indicating a promising potential for anti-HIV drug design. These findings underscore the potential of Zr-MOF and xanthene derivatives as potent candidates for HIV treatment, surpassing the reference molecule in terms of binding strength.

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Alsalhi, M. S., Tarek, M., Said, G. E., Almehizia, A. A., Naglah, A. M., & Khatab, T. K. (2025). Microwave-assisted synthesis of a zirconium-based MOF as an efficient catalyst for one-pot synthesis of xanthene derivatives: in silico study as a potential anti-HIV RNA. RSC Advances, 15(21), 16654–16666. https://doi.org/10.1039/d5ra02959g

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