Synthesis of chromen-4-one-oxadiazole substituted analogs as potent β-glucuronidase inhibitors
Chromen-4-one substituted oxadiazole analogs 1–19 have been synthesized, characterized and evaluated for β-glucuronidase inhibition. All analogs exhibited a variable degree of β-glucuronidase inhibitory activity with IC50 values ranging in between 0.8 ± 0.1–42.3 ± 0.8 μM when compared with the stand...
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| Main Authors: | , , , , , , , , , , |
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| Formáid: | Article |
| Teanga: | English |
| Foilsithe: |
MDPI
2019
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| Rochtain Ar Líne: | http://psasir.upm.edu.my/id/eprint/38388/1/38388.pdf |
| Clibeanna: |
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