NLRP3
NLRP3 inflammasome activation inhibitor
Product Specifications
Background
NLRP3 (MCC950) was originally found to act as a cytokine release inhibitory drug (CRID), arresting activated monocytes and preventing activation of caspase-1(1). Discovered to be a novel inhibitor of the NLRP3 and AIM2 inflammasomes(2). Blocks canonical and noncanonical NLRP3 activation at nanomolar concentrations3. Inhibits interleukin 1β (IL-1β) secretion in vivo and attenuates the severity of experimental autoimmune encephalomyelitis (an MS disease model)(3). Disrupts the interaction between AIM2 and ASC in a reconstituted cell-free inflammasome(4). A valuable new tool for exploring the pathophysiology of NLRP3. It may contribute to additional alpha synuclein aggregation and cell loss in PD (5).
Product Name Alternative
N-[[(1,2,3,5,6,7-Hexahydro-s-indacen-4-yl)amino]carbonyl]-4-(1-hydroxy-1-methylethyl)-2-furansulfonamide sodium salt; CRID3; CP-456773 sodium salt
UNSPSC
41116105
Source
Synthetic
Purity
>98% (HPLC); NMR (Conforms)
Weight
0.005
Format
White powder
Solubility
May be dissolved in water (30 mg/ml): or DMSO (40 mg/ml)
Molecular Formula
C20H23N2O5S ∙ Na
Molecular Weight
426.5
Precautions
Not for use in humans. Not for use in diagnostics or therapeutics. For in vitro research use only.
References & Citations
1. Laliberte R.E. et al. (2003) J. Biol. Chem. 278(19):16567-78.
2. Coll R.C., et al. (2011) PLoS One. 6(12):e29539.
3. Coll R.C., et al. (2015) Nat. Med. 21(3):248-255.
4. Kaneko N., et al. (2015) J. Immunol. Methods. 426:76-81. 5. Nguyen L., et al. (2022) J Parkinsons Dis. 12(7): 2117-2133.
CAS Number
256373-96-3
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