Items 1 to 10 of 11 total
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
LY 294002 | 154447-36-6 | sc-201426 sc-201426A | 5 mg 25 mg | $121.00 $392.00 | 148 | |
LY294002 is a potent inhibitor of the phosphoinositide 3-kinases (PI3Ks). OR4C12 is a G protein-coupled receptor (GPCR) that, upon activation, can initiate PI3K signaling. By inhibiting PI3K, LY294002 prevents the downstream signaling required for OR4C12 to exert its cellular effects. | ||||||
Brefeldin A | 20350-15-6 | sc-200861C sc-200861 sc-200861A sc-200861B | 1 mg 5 mg 25 mg 100 mg | $30.00 $52.00 $122.00 $367.00 | 25 | |
Brefeldin A disrupts protein transportation by blocking the transition from the endoplasmic reticulum to the Golgi apparatus, thus potentially reducing the cell surface expression of GPCRs like OR4C12, lowering its functional activity. | ||||||
Monensin A | 17090-79-8 | sc-362032 sc-362032A | 5 mg 25 mg | $152.00 $515.00 | ||
Monensin is an ionophore that disrupts proton and sodium ion gradients across cellular membranes. This disruption can affect GPCR function including OR4C12, as ion gradients are essential for maintaining the receptor's conformation and activity. | ||||||
Gö 6983 | 133053-19-7 | sc-203432 sc-203432A sc-203432B | 1 mg 5 mg 10 mg | $103.00 $293.00 $465.00 | 15 | |
Go 6983 is a protein kinase C (PKC) inhibitor. PKC is often involved in the phosphorylation and regulation of GPCRs. By inhibiting PKC, Go 6983 can prevent OR4C12 from undergoing the phosphorylation required for normal receptor internalization and desensitization. | ||||||
NF449 | 627034-85-9 | sc-478179 sc-478179A sc-478179B | 10 mg 25 mg 100 mg | $199.00 $460.00 $1479.00 | 1 | |
NF449 is a selective Gαs subunit inhibitor. If OR4C12 is coupled to Gαs, inhibition of this subunit by NF449 would result in decreased signaling of the receptor. | ||||||
Pertussis Toxin (islet-activating protein) | 70323-44-3 | sc-200837 | 50 µg | $442.00 | 3 | |
Pertussis Toxin inhibits Gi/o type G proteins. If OR4C12 associates with Gi/o proteins, this toxin would prevent the receptor from inhibiting adenylyl cyclase, thereby reducing OR4C12-mediated signaling. | ||||||
Chelerythrine chloride | 3895-92-9 | sc-3547 sc-3547A | 5 mg 25 mg | $88.00 $311.00 | 17 | |
Chelerythrine Chloride is a selective inhibitor of PKC. Similar to Go 6983, it would inhibit the phosphorylation events required for proper OR4C12 receptor regulation, affecting its signaling efficacy. | ||||||
PD 98059 | 167869-21-8 | sc-3532 sc-3532A | 1 mg 5 mg | $39.00 $90.00 | 212 | |
PD 98059 selectively inhibits MEK, which is involved in the MAPK/ERK pathway. While not directly linked to OR4C12, inhibition of this pathway could influence cellular responses to OR4C12 activation by altering the cellular context in which OR4C12 operates. | ||||||
SB 203580 | 152121-47-6 | sc-3533 sc-3533A | 1 mg 5 mg | $88.00 $342.00 | 284 | |
SB 203580 is a selective inhibitor of p38 MAPK. Inhibition of p38 MAPK can modulate the cellular response to stress and inflammation, which could indirectly affect the signaling and regulation of receptors such as OR4C12. | ||||||
Y-27632, free base | 146986-50-7 | sc-3536 sc-3536A | 5 mg 50 mg | $182.00 $693.00 | 88 | |
Y27632 is a Rho-associated protein kinase (ROCK) inhibitor. By inhibiting ROCK, Y27632 can alter actin cytoskeleton dynamics, which may influence GPCR function including OR4C12 by affecting receptor trafficking and cell surface expression. | ||||||