Date published: 2026-5-19

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P2X Activators

Santa Cruz Biotechnology now offers a broad range of P2X Activators for use in various applications. P2X Activators target the P2X family of ligand-gated ion channels, which are activated by extracellular ATP. These receptors play a crucial role in mediating rapid ion fluxes across cell membranes, impacting numerous physiological processes such as neurotransmission, muscle contraction, and immune responses. By activating P2X receptors, researchers can delve into the intricate signaling pathways these channels govern and their broader effects on cellular function. P2X Activators are indispensable tools for studying the enhancement of synaptic transmission and the roles of P2X receptors in sensory perception, mechanotransduction, and inflammatory responses. They provide vital insights into the mechanisms of ATP-mediated signaling and its influence on cell communication and behavior. Utilizing P2X Activators allows scientists to explore the interactions between P2X receptors and other molecular pathways, explaining the comprehensive role of purinergic signaling in cellular physiology and adaptation to environmental changes. These activators are particularly valuable in understanding the regulation of ion homeostasis and the cellular responses to mechanical and osmotic stress. Moreover, P2X Activators facilitate detailed studies on receptor kinetics and the pharmacological properties of P2X channels, advancing our understanding of ion channel modulation and regulation. By leveraging P2X Activators, researchers can gain a deeper comprehension of the dynamic processes that drive cellular signaling and response mechanisms in various biological contexts. View detailed information on our available P2X Activators by clicking on the product name.

SEE ALSO...

Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

6-Benzylaminopurine

1214-39-7sc-202428
sc-202428A
1 g
5 g
$20.00
$52.00
(1)

6-Benzylaminopurine is a potent p2x modulator known for its unique ability to mimic adenine, engaging in specific interactions with purine receptors. This compound exhibits remarkable selectivity, influencing signal transduction pathways by stabilizing receptor conformations. Its kinetic profile reveals rapid binding and dissociation rates, facilitating dynamic cellular responses. Furthermore, its lipophilic nature enhances its affinity for lipid membranes, promoting effective cellular uptake and interaction with intracellular targets.

Adenosine 5′-Triphosphate, disodium salt

987-65-5sc-202040
sc-202040A
1 g
5 g
$39.00
$75.00
9
(1)

Adenosine 5'-Triphosphate, disodium salt, serves as a crucial energy currency in cellular processes, engaging in intricate interactions with various enzymes and proteins. Its triphosphate moiety enables high-energy bond cleavage, driving essential biochemical reactions. The compound exhibits unique conformational flexibility, allowing it to participate in diverse signaling pathways. Additionally, its solubility in aqueous environments enhances its bioavailability, facilitating rapid cellular energy transfer and metabolic regulation.

α,β-Methyleneadenosine 5′-triphosphate trisodium salt

7292-42-4sc-204428
1 mg
$471.00
(1)

α,β-Methyleneadenosine 5'-triphosphate trisodium salt acts as a potent P2X receptor agonist, influencing ion channel activity and cellular excitability. Its unique structure allows for specific binding interactions, promoting rapid conformational changes in receptor proteins. This compound exhibits distinct kinetic properties, facilitating swift signal transduction and modulation of intracellular calcium levels. Its high solubility enhances interaction with membrane proteins, amplifying its physiological effects.

P1,P5-Di(adenosine-5′-)pentaphosphate, Trilithium Salt

75522-97-3sc-204156
sc-204156A
sc-204156B
sc-204156C
25 mg
100 mg
250 mg
1 g
$264.00
$556.00
$917.00
$2295.00
1
(0)

P1,P5-Di(adenosine-5′-)pentaphosphate, Trilithium Salt serves as a selective modulator of P2X receptors, engaging in intricate molecular interactions that stabilize receptor conformations. Its unique pentaphosphate structure promotes enhanced binding affinity, leading to pronounced effects on ion permeability and cellular signaling pathways. The compound's rapid hydrolysis kinetics facilitate dynamic regulation of ATP-mediated responses, while its high ionic strength supports effective membrane interactions, influencing downstream signaling cascades.