IndraLab
Statements
Flufenamic acid inhibits NLRP3. 9 / 9
|
9
reach
"Different NLRP3 inflammasome inhibitors, including sulforaphane, β-hydroxybutyrate, glyburide, flufenamic acid, mefenamic acid, parthenolide, BAY 11-7082, INF39, and MCC950 have been developed, but there is no evidence demonstrating that these compounds directly and specifically target NLRP3 itself (212)."
reach
"Various Cl - channel inhibitors, including 4,4 '-diisothiocyano-2,2 ' stilbene-disulfonic acid (DIDS), 5-nitro-(3-phenylpropylamino) benzoic acid (NPPB), flufenamic acid, mefenamic acid, and indanyloxyacetic acid 94 (IAA94), block the NLRP3 inflammasome but can not block the NLRC4 or AIM2 inflammasomes."
reach
"A few NLRP3 inflammasome inhibitors, including sulforaphane, isoliquiritigenin, beta-hydroxybutyrate (BHB), flufenamic acid, mefenamic acid, 3,4-methylenedioxy-beta-nitrostyrene (MNS), parthenolide, BAY 11-7082, INF39, and MCC950, have been developed, but there is no evidence showing that these compounds can specifically and directly inhibit NLRP3 itself."
reach
"Daniels et al. demonstrated that the nonsteroidal anti-inflammatory drugs flufenamic acid, meclofenamic acid and mefenamic acid inhibited the NLRP3 inflammasome by inhibiting volume-regulated anion channels in macrophages, and mefenamic acid ameliorated Alzheimer’s disease in a mouse model (39)."
reach
"This signaling induces mitochondrial fragmentation and generation of ROS, thereby activating the NLRP3 inflammasome.In addition, this signaling pathway is inhibited in microglia by flufenamic acid (FA), a type of non‐steroidal anti‐inflammatory drugs (NSAIDs), thereby regulating the Aβ‐induced activation of microglial inflammasome."