P2 Receptor Modulators

Cat.No.	Product Name	Information	Product Use Citations
S1415	Clopidogrel (SR-25990C) Bisulfate	Clopidogrel (SR-25990C) Bisulfate is an oral, thienopyridine class antiplatelet agent.	Nat Commun, 2025, 16(1):7974 J Immunother Cancer, 2024, 12(11)e009805 Cell Mol Life Sci, 2024, 81(1):116
S3368	Uridine-5'-diphosphate disodium salt	Uridine-5'-diphosphate (UDP) disodium salt is a potent, selective and natural agonist of P2Y₆ receptor with EC50 = 300 nM and pEC50 of 6.52, respectively. Uridine-5'-diphosphate (UDP) disodium salt is also an antagonist of P2Y₁₄ receptor with pEC50 of 7.28.
S1351	Ivermectin	Ivermectin is a glutamate-gated chloride channel (GluCls) activator, used as a broad-spectrum antiparasitic drug. This compound is a specific positive allosteric effector of P2X4 and α7 nicotinic acetylcholine receptors (nAChRs). It is a specific inhibitor of Impα/β1-mediated nuclear import and has potent antiviral activity towards both HIV-1 and dengue virus. This chemical induces autophagy through the AKT/mTOR signaling pathway and mitophagy.	Nat Commun, 2025, 16(1):7156 J Adv Res, 2025, S2090-1232(25)00874-4 Biomed Pharmacother, 2025, 189:118248

Cat.No.

Product Name

Information

Product Use Citations

Product Validations

S1415

Clopidogrel (SR-25990C) Bisulfate

Clopidogrel (SR-25990C) Bisulfate is an oral, thienopyridine class antiplatelet agent.

Nat Commun, 2025, 16(1):7974

J Immunother Cancer, 2024, 12(11)e009805

Cell Mol Life Sci, 2024, 81(1):116

Verified customer review of Clopidogrel (SR-25990C) Bisulfate

S3368

Uridine-5'-diphosphate disodium salt

Uridine-5'-diphosphate (UDP) disodium salt is a potent, selective and natural agonist of P2Y₆ receptor with EC50 = 300 nM and pEC50 of 6.52, respectively. Uridine-5'-diphosphate (UDP) disodium salt is also an antagonist of P2Y₁₄ receptor with pEC50 of 7.28.

S1351

Ivermectin

Ivermectin is a glutamate-gated chloride channel (GluCls) activator, used as a broad-spectrum antiparasitic drug. This compound is a specific positive allosteric effector of P2X4 and α7 nicotinic acetylcholine receptors (nAChRs). It is a specific inhibitor of Impα/β1-mediated nuclear import and has potent antiviral activity towards both HIV-1 and dengue virus. This chemical induces autophagy through the AKT/mTOR signaling pathway and mitophagy.

Nat Commun, 2025, 16(1):7156

J Adv Res, 2025, S2090-1232(25)00874-4

Biomed Pharmacother, 2025, 189:118248