噻唑
化学
噻嗪
部分
组合化学
对接(动物)
三嗪
生物信息学
分子
立体化学
氯乙酰氯
氯化物
有机化学
生物化学
医学
护理部
基因
作者
Mohamed G. Badrey,Sobhi M. Gomha,Aboubakr H. Abdelmonsef,Ahmed A. M. El‐Reedy
标识
DOI:10.1080/10406638.2023.2173617
摘要
AbstractA number of new three-armed heterocycles as thiazoles and thiazines linked to triazine moiety was prepared starting from cyanuaric chloride and thiothemicarbazide which gave the target compound 1. The reaction of the tris-thiosemicarbazide with a variety of hydrazonoyl halides afforded thiazole derivatives. In addition, a thiazole derivative could be prepared from the reaction of the target compound 1 with DMAD. Moreover, thiazine derivatives were synthesized from compound 1 through its interaction with benzylidinemalonitrile. In this work, the molecular docking analysis of thirteen compounds against FTO (Fat mass and Obesity-Associated) protein is carried out to investigate the mode of their molecular interactions. Furthermore, in silico ADMET predictions for the new compounds were calculated with the objective to gain an insight into their pharmacokinetic, safety, and drug-likeness profile. The new compounds could be promising chemical scaffolds for the development of future anti-obesity drug candidates.Keywords: Triazinethiazoletriazolehydrazonoyl halidesthree-armedmolecular docking AcknowledgmentsThe authors are thankful to Cairo University for providing laboratory, chemicals, and supporting the research by facilitating the spectroscopic measurements.Disclosure statementNo potential conflict of interest was reported by the authors.
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