Flavonol is a cholinesterase (ChE) inhibitor, demonstrating an IC50 of 120 μM and a Ki value of 74 μM. This compound exhibits notable antioxidant, free radical-scavenging, and antibacterial activities, while also modulating immune responses. Flavonol effectively inhibits the PriA helicase in Staphylococcus aureus and reduces nitric oxide (NO) production in LPS-activated RAW 264.7 cells by downregulating iNOS expression. Its protective and analgesic effects in murine models suggest potential applications in research focused on tumors and atherosclerosis.
Flavonol is a cholinesterase (ChE) inhibitor, demonstrating an IC50 of 120 μM and a Ki value of 74 μM. This compound exhibits notable antioxidant, free radical-scavenging, and antibacterial activities, while also modulating immune responses. Flavonol effectively inhibits the PriA helicase in Staphylococcus aureus and reduces nitric oxide (NO) production in LPS-activated RAW 264.7 cells by downregulating iNOS expression. Its protective and analgesic effects in murine models suggest potential applications in research focused on tumors and atherosclerosis.
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