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Design, Synthesis, Molecular Docking and Antimicrobial Activity of Novel Thiazolo[5,4-c]Pyridine Glycoside and Thiazolo[4,5-d]Pyrimidin Glycoside
被引:2
|作者:
Ghoneim, Amira Atef
[1
,2
]
Zafar, Rehman
[3
]
El-Farargy, Ahmed F.
[2
]
机构:
[1] Jouf Univ, Coll Sci, Chem Dept, Sakaka, Saudi Arabia
[2] Zagazig Univ, Fac Sci, Chem Dept, Zagazig, Egypt
[3] Riphah Int Univ, Riphah Inst Pharmaceut Sci, Dept Chem, Islamabad, Pakistan
关键词:
Synthesis;
analysis;
thiazolo[45-d]pyrimidine;
thioglycoside;
N-glycoside and thiazolo[45-b]pyridine;
DERIVATIVES;
D O I:
10.1080/10406638.2021.1903953
中图分类号:
O62 [有机化学];
学科分类号:
070303 ;
081704 ;
摘要:
In this research, we study here, the synthesis of 5-arylidenethiazolidin-4-one derivatives 5 which was used as a base for the synthesis of new thiazolo[4,5-d]thiopyrimidine derivatives and thiazolo[4,5-b] pyridine derivatives. New of their thioglycoside and N-glycoside derivatives were also studies. All the newly synthesized compounds exhibited high antimicrobial activity toward certain some microorganisms (bacteria and fungi). Some of these newly synthesized compounds were docked within the protein surface of 5AF1. The reports of this docking study revealed that the new compounds exhibit good antimicrobial activity. The structure of the newly synthesized compounds was characterized by spectral analysis such as IR spectrum, H-1 NMR spectrum, and C-13 HNMR spectrum.
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页码:4599 / 4620
页数:22
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