Date published: 2026-2-22

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P2Y9 Activators

P2Y9 Activators comprise a group of compounds that modulate or enhance the activity of the P2Y9 receptor, a member of the purinergic receptor family primarily involved in various cellular communication and signaling processes. Adenosine Triphosphate (ATP) and Uridine Triphosphate (UTP), as endogenous agonists, play a crucial role in directly activating P2Y9. Their binding induces a conformational change in the receptor, facilitating the initiation of G-protein-mediated intracellular signaling cascades, thereby enhancing P2Y9's functional response in cellular signaling. Similarly, BzATP, a synthetic ATP analog, potentiates P2Y9 activation through enhanced signal transduction pathways, particularly in inflammatory signaling and nucleotide-mediated communication. MRS 2365, though primarily a P2Y1 agonist, can influence P2Y9 activity by enhancing receptor activation and subsequent calcium mobilization, implicating its role in calcium-dependent signaling pathways relevant to P2Y9. NF546 and NF157, interacting with P2Y11, indirectly influence P2Y9 activity; NF546 by enhancing P2Y9-mediated signaling through G-protein-coupled pathways and NF157 by shifting cellular signaling dynamics to potentially enhance P2Y9 pathways.

Further, the functional dynamics of P2Y9 are influenced by compounds that modulate other P2Y receptors, demonstrating the intricate interplay within the purinergic receptor family. Clopidogrel and Cangrelor, by inhibiting P2Y12 receptors, may indirectly upregulate P2Y9-mediated pathways, especially in platelet aggregation and vascular functions. Similarly, AR-C69931MX, as a potent P2Y12 antagonist, indirectly facilitates P2Y9 activity, particularly in platelet function and thrombosis. The presence of A2P5P, an ADP analog, and 2-MeSADP, a potent P2Y1 and P2Y12 agonist, in the signaling milieu could influence P2Y9 activity by altering receptor dynamics and favoring P2Y9-mediated signaling. Lastly, MRS2500, as a selective P2Y1 antagonist, subtly shifts purinergic signaling towards P2Y9, highlighting its potential role in enhancing P2Y9's function in platelets and vascular cells. Together, these activators, through their targeted effects on various P2Y receptors, underscore the complexity and significance of P2Y9 in purinergic signaling and its pivotal role in cellular communication mechanisms.

SEE ALSO...

Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

ATP

56-65-5sc-507511
5 g
$17.00
(0)

ATP acts as an endogenous agonist for P2Y receptors, including P2Y9. Binding to P2Y9, ATP facilitates receptor activation, initiating G-protein-mediated intracellular signaling cascades, which enhance P2Y9's functional response in cellular communication and signaling processes.

Uridine-5′-triphosphate, Trisodium Salt

19817-92-6sc-301964
sc-301964A
50 mg
1 g
$88.00
$120.00
2
(0)

UTP, a purine nucleotide like ATP, activates P2Y receptors such as P2Y9. This interaction induces receptor activation, leading to intracellular signaling pathways that elevate P2Y9's role in ion channel regulation and second messenger system activation.

Clopidogrel

113665-84-2sc-507403
1 g
$122.00
1
(0)

Clopidogrel, an antiplatelet compound, is metabolized to an active form that irreversibly inhibits P2Y12 receptors. This inhibition can indirectly enhance P2Y9 activity by reducing competitive binding or signaling through P2Y12, thereby potentially upregulating P2Y9-mediated pathways in platelet aggregation and vascular function.