4.5 Article

Biosynthesized Selenium nanoparticles as a new catalyst in the synthesis of quinazoline derivatives in pentacyclic system with docking validation as (TRPV1) inhibitor

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JOURNAL OF ORGANOMETALLIC CHEMISTRY
卷 944, 期 -, 页码 -

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ELSEVIER SCIENCE SA
DOI: 10.1016/j.jorganchem.2021.121847

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Biosynthesis; Selenium; Quinazoline; Nanoparticles; Docking

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Selenium has been found to have many benefits for humans, animals, and chemical uses. Nano-Selenium was biosynthesized and characterized as a catalyst in the synthesis of N-bridged imidazo-quinazoline derivatives, showing highly efficient and facile properties. Molecular docking study was conducted to compare TRPV1 inhibitor activity with reference alkaloids ligands.
In recent years, a lot of benefits of Selenium have been discovered for humans, animals and chemical uses. Nano-Selenium was biosynthesized and characterized by using FTIR, UV/Vis., TEM/SAED, and mapping to ensure their crystallinity. The N-bridged imidazo-quinazoline derivatives were successfully synthesized in pentacyclic nonlinear ortho fused polynuclear by a one-pot reaction of aldehyde, beta-naphthol, and 2-aminobenzoimidazole in the presence of a catalytic amount of aqueous nano-Se as a highly efficient and facile catalyst at 70-80 degrees C. The molecular docking study as TRPV1 inhibitor compared with Rutaecarpine and Evodiamine as reference alkaloids ligands. (C) 2021 Elsevier B.V. All rights reserved.

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