Table 1.
Direct NLRP3 inhibitors and their mechanisms.
Agent | Mechanism | Cell or animal model | Ref. |
---|---|---|---|
MNS | Inhibitory of NLRP3 ATPase activity | Bone-marrow derived macrophages | (94) |
CY-09 | Monocytes; mouse models of cryopyrin-associated autoinflammatory syndrome (CAPS) and type 2 diabetes | (93) | |
MCC950 | iPSC-Derived VCP Patient Myoblasts; VCPR155H/+ Mice;mouse model of Duchenne muscular dystrophy | (12, 86, 90, 91) | |
OLT1177 | LPS-stimulated human blood-derived macrophages; mouse model of LPS-induced systemic inflammation |
(71) | |
INF39 | Macrophages | (78) | |
Compound 6 | Dextran sulfate sodium (DSS)-induced colitis mouse model | (92) | |
BOT-4-one | Bone-marrow derived macrophages primed with LPS | (95) | |
Fluoxetine | Alu RNA-induced RPE degeneration in mice | (77) | |
β-OHB | Inhibitory of NLRP3 oligomerization | Human monocytes were stimulated with LPS; Mouses were primed with LPS | (72) |
RRx-001 | RRx-001 ameliorates inflammatory diseases by acting as a potent covalent NLRP3 inhibitor | (76) | |
Tranilast | BMDMs from C57BL/6 mice; mouse models of gouty arthritis, cryopyrin-associated autoinflammatory syndromes, and type 2 diabetes |
(96) | |
Oridonin | BMDMs treated with 50 ng/ml LPS | (79) |