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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 IC(50) values ranging in between 0.8 ± 0.1–42.3 ± 0.8 μM when compared with the sta...
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| Udgivet i: | Molecules |
|---|---|
| Main Authors: | , , , , , , , , , , |
| Format: | Artigo |
| Sprog: | Inglês |
| Udgivet: |
MDPI
2019
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| Fag: | |
| Online adgang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6514607/ https://ncbi.nlm.nih.gov/pubmed/31003424 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/molecules24081528 |
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