GPR115 inhibitors are chemical compounds that target the GPR115 receptor, a member of the adhesion G protein-coupled receptor (GPCR) family. These receptors are characterized by their large extracellular domains, which are involved in cell adhesion and signaling. GPR115, also known as ADGRF4, is part of a subfamily of GPCRs that are often involved in diverse physiological processes, such as tissue development and immune responses. The inhibitors of GPR115 are typically small molecules or peptides that bind to the receptor, preventing its activation or interfering with its downstream signaling pathways. These compounds are designed to selectively modulate the activity of the receptor by interacting with its active sites, often resulting in changes in cellular responses.
Structurally, GPR115 inhibitors may exhibit a variety of chemical motifs depending on their mode of interaction with the receptor. They may target different parts of the receptor, such as the transmembrane regions or extracellular loops, depending on the mechanism by which they inhibit receptor function. Inhibitors of GPR115 are valuable tools for studying the receptor's role in cellular processes, allowing researchers to better understand the biochemical pathways in which GPR115 is involved. Additionally, these inhibitors are critical for dissecting the functional contributions of GPR115 to physiological systems, offering insights into its role in processes like cell adhesion, signaling cascades, and receptor-ligand interactions.
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Pertussis Toxin (islet-activating protein) | 70323-44-3 | sc-200837 | 50 µg | $451.00 | 3 | |
Inhibits Gi protein-coupled receptors, blocking downstream signaling. | ||||||
NF 023 | 104869-31-0 | sc-204124 sc-204124A | 10 mg 50 mg | $161.00 $629.00 | 1 | |
Inhibits G-protein α subunits, affecting multiple GPCRs. | ||||||
ML-7 hydrochloride | 110448-33-4 | sc-200557 sc-200557A | 10 mg 50 mg | $91.00 $267.00 | 13 | |
Inhibits myosin light chain kinase (MLCK), which can be activated by Gq signaling. | ||||||
Y-27632, free base | 146986-50-7 | sc-3536 sc-3536A | 5 mg 50 mg | $186.00 $707.00 | 88 | |
Inhibits ROCK, impacting cytoskeleton dynamics, related to G12/13 signaling. | ||||||
LY 294002 | 154447-36-6 | sc-201426 sc-201426A | 5 mg 25 mg | $123.00 $400.00 | 148 | |
Inhibitor of PI3K, affecting downstream Akt signaling of some GPCRs. | ||||||
Chelerythrine chloride | 3895-92-9 | sc-3547 sc-3547A | 5 mg 25 mg | $90.00 $317.00 | 17 | |
Broad-spectrum PKC inhibitor, affecting Gq-mediated activation. | ||||||
SQ 22536 | 17318-31-9 | sc-201572 sc-201572A | 5 mg 25 mg | $95.00 $363.00 | 13 | |
Adenylyl cyclase inhibitor, affecting Gs-mediated cAMP production. | ||||||
H-89 dihydrochloride | 130964-39-5 | sc-3537 sc-3537A | 1 mg 10 mg | $94.00 $186.00 | 71 | |
Protein kinase A (PKA) inhibitor, affecting Gs-mediated signaling. | ||||||
PD 116,948 | 102146-07-6 | sc-200115 sc-200115A | 25 mg 100 mg | $124.00 $228.00 | 6 | |
Adenosine A1 receptor antagonist, showing the approach of targeting specific GPCRs. | ||||||
Src kinase inhibitor I | 179248-59-0 | sc-204303 sc-204303A | 1 mg 10 mg | $53.00 $204.00 | 11 | |
Non-selective GPCR antagonist. | ||||||