Date published: 2025-12-19

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OR4C12 Inhibitors

OR4C12 Inhibitors encompass a group of compounds that inhibit the functional activity of OR4C12 through various indirect mechanisms. These inhibitors do not target OR4C12 directly but affect the signaling pathways and cellular processes that are necessary for OR4C12 to function properly. For instance, LY294002 and U73122 target PI3K and PLC, respectively, which are enzymes that propagate signaling cascades initiated by GPCRs like OR4C12. The inhibition of these enzymes would prevent OR4C12 signaling. Other compounds, such as Brefeldin A and Monensin, interfere with cellular processes that are critical for GPCR function. Brefeldin A's disruption of protein transport could reduce the presence of OR4C12 on the cell surface, while Monensin's alteration of ion gradients could affect the receptor's conformation and signaling ability.Inhibitors that target specific signaling molecules downstream of GPCRs, such as Go 6983 and Chelerythrine Chloride (both targeting PKC), NF449 (targeting Gαs subunit), and Pertussis Toxin (targeting Gi/o proteins), could suppress OR4C12 signaling by preventing the receptor from triggering its associated G protein pathways.

Items 1 to 10 of 11 total

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Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

LY 294002

154447-36-6sc-201426
sc-201426A
5 mg
25 mg
$121.00
$392.00
148
(1)

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

20350-15-6sc-200861C
sc-200861
sc-200861A
sc-200861B
1 mg
5 mg
25 mg
100 mg
$30.00
$52.00
$122.00
$367.00
25
(3)

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

17090-79-8sc-362032
sc-362032A
5 mg
25 mg
$152.00
$515.00
(1)

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

133053-19-7sc-203432
sc-203432A
sc-203432B
1 mg
5 mg
10 mg
$103.00
$293.00
$465.00
15
(1)

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

627034-85-9sc-478179
sc-478179A
sc-478179B
10 mg
25 mg
100 mg
$199.00
$460.00
$1479.00
1
(0)

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)

70323-44-3sc-200837
50 µg
$442.00
3
(1)

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

3895-92-9sc-3547
sc-3547A
5 mg
25 mg
$88.00
$311.00
17
(1)

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

167869-21-8sc-3532
sc-3532A
1 mg
5 mg
$39.00
$90.00
212
(2)

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

152121-47-6sc-3533
sc-3533A
1 mg
5 mg
$88.00
$342.00
284
(5)

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

146986-50-7sc-3536
sc-3536A
5 mg
50 mg
$182.00
$693.00
88
(1)

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.