ECSIT inhibitors belong to a specialized class of chemical compounds that are designed to interact with and modulate the activity of the EvC ciliary complex subunit 2 (ECSIT) protein. ECSIT holds a significant role in cellular processes, particularly in mitochondrial biology and innate immune signaling pathways. Within the mitochondria, ECSIT functions as an adaptor protein that facilitates the assembly and proper functioning of the respiratory chain complexes, notably by bridging the interaction between Complex I and Complex III. This interaction is crucial for efficient electron transport and ATP production through oxidative phosphorylation. In the context of innate immunity, ECSIT plays an instrumental role as a scaffold protein in the formation of the MAVS signalosome. This complex is pivotal for orchestrating antiviral immune responses by activating downstream signaling cascades, ultimately leading to the production of type I interferons and pro-inflammatory cytokines.
ECSIT's involvement in both mitochondrial function and antiviral immune responses.
ECSIT inhibitors are meticulously crafted molecules designed to bind to specific regions of the ECSIT protein, thereby modulating its activity and interactions with other molecules. By disrupting ECSIT-mediated interactions between respiratory chain complexes or interfering with its participation in innate immune signaling, these inhibitors have the potential to alter mitochondrial function and immune responses. The development and study of ECSIT inhibitors provide researchers with an invaluable toolkit to dissect the intricacies of ECSIT's contributions to cellular processes. Through these inhibitors, scientists can gain deeper insights into the mechanistic details of mitochondrial energy production, redox signaling, and immune responses.
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
GW4869 | 6823-69-4 | sc-218578 sc-218578A | 5 mg 25 mg | $203.00 $611.00 | 24 | |
Inhibits sphingomyelin synthase, disrupting ceramide-enriched membrane domains crucial for exosome biogenesis. | ||||||
Manumycin A | 52665-74-4 | sc-200857 sc-200857A | 1 mg 5 mg | $219.00 $634.00 | 5 | |
Blocks Ras farnesyltransferase, affecting exosome secretion due to its role in the endosomal sorting complex. | ||||||
Amiloride, 5-(N,N-Dimethyl)-, hydrochloride | 2235-97-4 | sc-202459 | 5 mg | $235.00 | 7 | |
Targets acid sphingomyelinase and neutral sphingomyelinase, impeding the formation of ceramide-rich exosomes. | ||||||
Spautin-1 | 1262888-28-7 | sc-507306 | 10 mg | $168.00 | ||
Inhibits autophagy by targeting BECN1 and VPS34, indirectly suppressing exosome release through disrupted pathways. | ||||||
GW 7647 | 265129-71-3 | sc-203068A sc-203068 sc-203068B sc-203068C | 1 mg 5 mg 10 mg 25 mg | $49.00 $170.00 $267.00 $661.00 | 6 | |
An agonist of PPARβ/δ, modulating cellular pathways that influence exosome release and cargo sorting. | ||||||
NSC 319726 | 71555-25-4 | sc-477736 | 10 mg | $159.00 | ||
Inhibits neutral sphingomyelinase, impacting ceramide generation and subsequently exosome biogenesis. | ||||||