Date published: 2025-10-15

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P2Y Inhibitors

Santa Cruz Biotechnology now offers a broad range of P2Y Inhibitors for use in various applications. P2Y Inhibitors target the P2Y family of G-protein-coupled receptors, which are activated by extracellular nucleotides such as ATP, ADP, UTP, and UDP. These receptors play critical roles in various cellular processes, including signal transduction, cell communication, and the regulation of immune responses. By inhibiting P2Y receptors, researchers can explore the complex signaling pathways mediated by these receptors and their impact on cellular functions. P2Y Inhibitors are essential tools for studying the modulation of platelet aggregation, inflammation, and vascular tone, offering insights into the biochemical mechanisms underlying these processes. They are particularly valuable in investigating the roles of P2Y receptors in purinergic signaling, a system crucial for maintaining cellular homeostasis and responding to physiological stress. Utilizing P2Y Inhibitors allows scientists to dissect the interactions between P2Y receptors and other signaling molecules, revealing how these receptors influence intracellular pathways and cellular outcomes. These inhibitors are also instrumental in understanding the regulation of neurotransmission and synaptic plasticity, as P2Y receptors are involved in modulating neurotransmitter release and neuronal communication. By leveraging P2Y Inhibitors, researchers can gain a deeper understanding of the dynamic processes that govern cellular signaling and function in various biological contexts. View detailed information on our available P2Y Inhibitors by clicking on the product name.

SEE ALSO...

Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

2-Methylthioadenosine 5′-monophosphate triethylammonium salt

22140-20-1 (non-salt)sc-213854
5 mg
$1200.00
(0)

2-Methylthioadenosine 5'-monophosphate triethylammonium salt acts as a potent modulator of P2Y receptors, characterized by its unique methylthio group that influences receptor affinity and selectivity. This compound engages in specific molecular interactions that can alter downstream signaling pathways, particularly those related to cellular energy metabolism. Its triethylammonium salt form enhances solubility, promoting effective cellular penetration and facilitating rapid kinetic responses in signaling networks.