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- W3028084557 abstract "Urease is a therapeutic target associated with several important diseases and health problems. Based on our previous work on the inhibition of glucosidase and other enzymes and exploiting the privileged structure assigned to the (thio)barbiturate (pyrimidine) scaffold, here we tested the capacity of two (thio)barbiturate-based compound collections to inhibit urease. Several compounds showed more activity than acetohydroxamic acid as a standard tested compound. In addition, by means of a conformational study and using the Density Functional Theory (DFT) method, we identified energetically low-lying conformers. Finally, we undertook a docking study to explore the binding mechanism of these new pyrimidine derivatives as urease inhibitors." @default.
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- W3028084557 date "2020-05-20" @default.
- W3028084557 modified "2023-09-27" @default.
- W3028084557 title "Enamine Barbiturates and Thiobarbiturates as a New Class of Bacterial Urease Inhibitors" @default.
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- W3028084557 doi "https://doi.org/10.3390/app10103523" @default.
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