NLR

NLR

The host's innate immune system and immune homeostasis depend heavily on the cytoplasmic pattern-recognition receptors (PRRs) known as nucleotide oligomerization domain (NOD)-like receptors (NLRs). Humans have 23 members of the NLR family, while mice have at least 34 NLR genes. Although many cell types, including immune and epithelial cells, express NLRs, some NLR family members, such as macrophages and neutrophils, express them primarily in phagocytes. The NLR family is most frequently divided into one of four subfamilies based on their N-terminal domains: NLRA, NLRB, NLRC, and NLRP.

The NLRs are capable of recognizing a wide range of ligands, including those produced by microbial pathogens (peptidoglycan, flagellin, viral RNA, fungal hyphae, etc.), host cells (ATPs, cholesterol crystals, uric acid, etc.), and environmental sources (alum, asbestos, silica, alloy particles, UV radiation, skin irritants, etc.). Most NLRs function as PRRs, identifying the aforementioned ligands and inciting inflammatory reactions. Some NLRs, however, might not function as PRRs and instead react to cytokines like interferons. Four broad categories of functions performed by the activated NLRs include inflammasome formation, signal transduction, transcription activation, and autophagy.

NLR related products

Structure Cat No. Product Name CAS No. Product Description
V75164 (±)11(12)-EET (11,12-EET) 123931-40-8 (±)11(12)-EET is an inhibitor (blocker/antagonist) of the NLRP3 inflammasome.
V75174 (±)11(12)-EET-d11 ((±)11,12-EET-d11) 2699607-19-5 (±)11(12)-EET-d11 is the deuterated form of (±)11(12)-EET.
V75186 ADS032 2757333-37-0 ADS032 is a dual (bifunctional) inhibitor of NLRP1 and NLRP3 that can rapidly, reversibly and stably inhibit inflammasome formation.
V74293 D359-0396 1031977-31-7 D359-0396 is an orally bioactive NLRP3 inflammasome inhibitor.
V75166 Emlenoflast (MCC7840) 1995067-59-8 Emlenoflast (MCC7840), a sulfonylurea, is a potent and specific inhibitor of the NLRP3 inflammasome with IC50 of less than 100 nM.
V75161 GSK717 1595278-21-9 GSK717 is a potent and specific NOD2 (nucleotide-binding oligomerization domain 2) inhibitor.
V80371 INF200 INF200 (compound 5) is a sulfonylurea-based inhibitor that can suppress NLRP3 and NLRP3-mediated pyroptosis.
V2031 INF39 866028-26-4 INF39 (INF-39; INF 39), an acrylate derivative, is a potent, irreversible andnontoxic inhibitor of NLRP3 with potential anti-inflammatory activity.
V51067 JC2-11 937820-89-8 inhibitor of inflammatory corpuscles
V79924 JT001 sodium (NLRP3-IN-19 sodium) JT001 (NLRP3-IN-19) sodium is a potent, specific and orally bioactive NLRP3 inhibitor.
V75180 JT002 2238820-43-2 JT002 is an orally bioactive NLRP3 inflammasome inhibitor.
V75181 M-TriDAP (N-Acetylmuramyl-L-Ala-γ-D-Glu-meso-diaminopimelic acid) 60230-21-9 M-TriDAP (N-Acetylmuramyl-L-Ala-γ-D-Glu-meso-diaminopimelic acid) is a biologically active peptide.
V3786 MCC950 210826-40-7 MCC950 (also known asMCC-950, CP-456773or CRID3) isa potent, selective, small-molecule inhibitor of NLRP3 that has the potential for the treatment of inflammatory diseases and diabetic encephalopathy (DEP).
V3026 MCC950 sodium 256373-96-3 MCC950 sodium, the sodium salt of MCC950 (also known asMCC-950, CP-456773or CRID3), isa potent, selective, small-molecule inhibitor of NLRP3 that has the potential for the treatment of inflammatory diseases and diabetic encephalopathy (DEP).
V76767 Mifamurtide TFA (Mifamurtide TFA salt; MTP-PE TFA; L-MTP-PE TFA; CGP 19835 TFA) Mifamurtide TFA (MTP-PE TFA) is an analog of mularchi dipeptide (MDP), a non-specific immunomodulator that works by stimulating immune responses by activating macrophages and monocytes.
V75172 NLRP3 agonist 1 2454019-69-1 NLRP3 agonist 1 (compound 23) is a potent and orally bioactive NLRP3 agonist.
V80206 NLRP3 agonist 2 NLRP3 agonist 2 (compound 22) is an orally bioactive NLRP3 agonist.
V75189 NLRP3 modulators 1 2143015-87-4 NLRP3 modulators 1 is a potent modulator of NLRP3.
V75163 NLRP3-IN-11 2769040-91-5 NLRP3-IN-11 is an NLRP3 protein inhibitor.
V80953 NLRP3-IN-12 NLRP3-IN-12 is a specific NLRP3 inflammasome inhibitor.
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