Date published: 2026-5-30

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GPR105 Inhibitors

GPR105 inhibitors belong to a class of chemical compounds designed to modulate the activity of the G protein-coupled receptor 105 (GPR105), a cell surface receptor primarily associated with immune response regulation and inflammatory processes. These inhibitors are characterized by their ability to interfere with the signaling pathways triggered by GPR105 activation. The GPR105 receptor, also known as P2Y14 receptor, is primarily expressed on immune cells, such as neutrophils, monocytes, and macrophages, and plays a crucial role in the immune response, particularly in the context of inflammation. GPR105 inhibitors are specifically developed to target this receptor, either by blocking its activation or by disrupting downstream signaling cascades. The mechanism of action of GPR105 inhibitors typically involves interfering with the receptor's ability to respond to its endogenous ligands, such as UDP-glucose and UDP-galactose. By doing so, these inhibitors can mitigate the receptor's activation and subsequent downstream cellular responses. This interference can occur at various points along the signaling pathway, often by binding to the receptor itself or its associated proteins, preventing their proper function. As a result, GPR105 inhibitors have the potential to dampen the receptor's involvement in immune cell chemotaxis, cytokine production, and other inflammatory processes. This class of compounds is of significant interest in research related to immune regulation and inflammation control, as understanding and modulating GPR105 activity could have implications for various pathological conditions where inflammation plays a key role. Researchers continue to explore the precise mechanisms of GPR105 inhibitors in managing immune-related disorders and inflammatory diseases.

SEE ALSO...

Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

UDP disodium salt

27821-45-0sc-204372
50 mg
$57.00
1
(1)

UDP disodium salt acts as a GPR105 inhibitor by competitively binding to receptor sites, disrupting normal ligand-receptor interactions. Its unique structure, featuring a ribose sugar and two phosphate groups, allows for specific hydrogen bonding and electrostatic interactions that modulate receptor activity. This compound's kinetic profile reveals a rapid association and dissociation rate, enabling fine-tuning of signaling pathways and influencing cellular responses in diverse biological contexts.

Resatorvid

243984-11-4sc-476758
5 mg
$367.00
(0)

TAK-242 inhibits GPR105 by interfering with TLR4 signaling, thus disrupting the downstream inflammatory response mediated by GPR105.

EPZ005687

1396772-26-1sc-497734
2.5 mg
$380.00
(0)

EPZ005687 acts as a potent antagonist of GPR105, reducing its activity and dampening pro-inflammatory responses.

25-Hydroxycholesterol

2140-46-7sc-214091B
sc-214091
sc-214091A
sc-214091C
5 mg
10 mg
25 mg
100 mg
$53.00
$91.00
$169.00
$474.00
8
(2)

25-hydroxycholesterol acts as an endogenous GPR105 agonist, but its level can be reduced to inhibit GPR105-mediated inflammation.

CPI-203

1446144-04-2sc-501599
1 mg
$170.00
(0)

CPI-203 inhibits GPR105 by disrupting its signaling pathway, leading to the suppression of inflammatory and immune responses.

CAY10505

1218777-13-9sc-364456
sc-364456A
10 mg
50 mg
$80.00
$280.00
(0)

CAY10505 inhibits GPR105, affecting its signaling pathway and diminishing the associated pro-inflammatory and immune effects.