蛋白质数据库
化学
三唑
自动停靠
对接(动物)
点击化学
糖基
组合化学
催化作用
立体化学
有机化学
生物化学
医学
基因
护理部
生物信息学
作者
Anjaneyulu Bendi,G. B. Dharma Rao
出处
期刊:Letters in Organic Chemistry
[Bentham Science]
日期:2023-01-12
卷期号:20 (6): 568-578
被引量:7
标识
DOI:10.2174/1570178620666230111103902
摘要
Abstract: In the present study, we have introduced an efficient solvent-free protocol for the synthesis of glycosyl annulated phosphorylated/thiophosphorylated 1,2,3-triazole derivatives using reusable CuFe2O4 magnetic nanoparticles as a heterogeneous catalyst with the protocols of popular click chemistry approach. Quantum chemical calculations of all the reactants and products have been calculated using density functional theory with Spartan-18 software. In addition, the molecular docking studies of all the glycosyl annulated phosphorylated/thiophosphorylated 1,2,3- triazole derivatives have been studied as effective fungicides against CaCYP51 (PDB ID 5EQB), protein of P. infestans effector target site (PDB ID: 2NAR), and SsCYP51(PDB code: 6CR2) using Autodock Vina and Discovery Studio software. Among the three different proteins, the binding energies of the compounds (5a-d) with CaCYP51 (PDB ID 5EQB) have shown better results in the range of 7.0 to 7.4 kcal/mol. Hence, these compounds may be used as strong fungicides for the inhibition of CaCYP51 (PDB ID 5EQB). In conclusion, the synthesized compounds may be better useful in agrochemical applications as vital fungicides.
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