Date published: 2026-4-1

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GPR87 Activators

GPR87 activators refer to a class of chemical compounds that specifically enhance the functional activity of the G protein-coupled receptor 87 (GPR87) through various biochemical mechanisms. GPR87 is a cell surface receptor implicated in numerous intracellular signaling cascades that regulate diverse cellular functions. Activators of GPR87 typically exert their effects by binding to the receptor, leading to a conformational change that triggers the association of G proteins with the intracellular domain of GPR87. This association subsequently activates the G proteins, which then go on to modulate downstream effectors and second messenger systems such as cyclic adenosine monophosphate (cAMP), inositol trisphosphate (IP3), and diacylglycerol (DAG). The result of this activation is an enhancement of the receptor's signaling capabilities, which can influence various physiological processes that GPR87 is known to be involved in, such as cell growth, survival, and metabolism.

The activators of GPR87 are diverse in structure and origin, yet they share the common feature of specificity in enhancing receptor activity without directly affecting gene expression or protein translation. By binding to the extracellular domain of GPR87, these activators can induce a favorable environment for the receptor's active conformation, ensuring efficient signal transduction. Additionally, some activators may influence the lipid microenvironment of the receptor, facilitating optimal receptor conformation and function. The specificity of these activators is crucial, as it allows for the discrete regulation of GPR87's signaling pathways without cross-activating other G protein-coupled receptors or cellular pathways. Through these finely tuned mechanisms, GPR87 activators are capable of selectively amplifying the receptor's natural signaling processes, which play a vital role in maintaining cellular homeostasis and responding to various extracellular signals.

SEE ALSO...

Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

Lysophosphatidic Acid

325465-93-8sc-201053
sc-201053A
5 mg
25 mg
$98.00
$341.00
50
(3)

Lysophosphatidic acid (LPA) binds to GPR87 and activates it, triggering downstream G-protein coupled signaling events which can lead to cell proliferation and survival.

Oleylethanolamide

111-58-0sc-201400
sc-201400A
10 mg
50 mg
$90.00
$194.00
1
(1)

Oleoylethanolamide, a fatty acid ethanolamide, has affinity for GPR87 and can enhance its signaling, influencing cellular processes related to energy homeostasis.

D-erythro-Sphingosine-1-phosphate

26993-30-6sc-201383
sc-201383D
sc-201383A
sc-201383B
sc-201383C
1 mg
2 mg
5 mg
10 mg
25 mg
$165.00
$322.00
$570.00
$907.00
$1727.00
7
(1)

Sphingosine 1-phosphate is an endogenous ligand for GPR87, enhancing its activity and thereby affecting cellular processes such as migration and angiogenesis.

FTY720

162359-56-0sc-202161
sc-202161A
sc-202161B
1 mg
5 mg
25 mg
$33.00
$77.00
$120.00
14
(1)

FTY720 is phosphorylated in vivo to form a compound that acts on GPR87, potentially enhancing cell survival and proliferation pathways that GPR87 is implicated in.

Ursolic Acid

77-52-1sc-200383
sc-200383A
50 mg
250 mg
$56.00
$180.00
8
(1)

Ursolic acid has been shown to bind to and activate GPR87, potentially influencing anti-inflammatory and anticarcinogenic processes.

Resolvin D1

872993-05-0sc-204877
sc-204877A
10 µg
25 µg
$262.00
$614.00
1
(1)

Resolvin D1 is involved in resolving inflammation and may activate GPR87 to promote anti-inflammatory signaling pathways.

Rosiglitazone

122320-73-4sc-202795
sc-202795A
sc-202795C
sc-202795D
sc-202795B
25 mg
100 mg
500 mg
1 g
5 g
$120.00
$326.00
$634.00
$947.00
$1259.00
38
(1)

As a PPARγ agonist, rosiglitazone may indirectly enhance GPR87 activity, implicating it in the modulation of glucose metabolism.

D,L-Sulforaphane

4478-93-7sc-207495A
sc-207495B
sc-207495C
sc-207495
sc-207495E
sc-207495D
5 mg
10 mg
25 mg
1 g
10 g
250 mg
$153.00
$292.00
$489.00
$1325.00
$8465.00
$933.00
22
(1)

Sulforaphane may enhance GPR87 activation, contributing to its role in cytoprotective responses to oxidative stress.