Date published: 2025-9-18

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P2X1 Inhibitors

P2X1 is a type of purinergic receptor, a class of ion channel receptors that are activated by ATP. It is predominantly expressed in smooth muscle cells, platelets, and certain types of neurons. Functionally, P2X1 is a ligand-gated ion channel that, upon binding ATP, opens to allow the flow of cations, particularly Ca and Na, into the cell. This influx of ions leads to various physiological responses, such as muscle contraction, platelet aggregation, and neurotransmission. In smooth muscle, P2X1 activation contributes to vasoconstriction, while in platelets, it plays a crucial role in thrombosis by mediating platelet activation. P2X1 is also involved in pain pathways and inflammatory responses, making it a potential target for intervention in conditions like hypertension, thrombosis, and pain management.Targeting P2X1 for disruption or inhibition using small molecules allows for detailed exploration of its role in various physiological and pathological processes. By selectively inhibiting P2X1, researchers can study its specific contributions to muscle contraction, particularly in vascular smooth muscle and the regulation of blood flow. In the context of platelet function, inhibiting P2X1 helps in understanding its role in thrombus formation and how its modulation could lead to novel antithrombotic therapies. The study of P2X1 inhibitors also aids in elucidating the receptor's involvement in pain and inflammatory signaling, potentially leading to new pain management strategies.

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