| Cat.No. | Name | Information |
|---|---|---|
| M5986 | Suramin sodium salt | Suramin Sodium Salt (Suramin hexasodium salt) is a reversible inhibitor of competitive protein tyrosine phosphatases (PTPases). |
| M10064 | Uridine 5'-diphosphoglucose disodium salt | Uridine 5'-diphosphoglucose disodium salt is an agonist of the P2Y14 receptor, with EC50 of 0.35 μM. Uridine 5′-diphosphoglucose disodium salt (UDP-Glucose sodium salt) can also bind to and activate GPR17, inducing oligodendrocyte differentiation at a maximal concentration of 100 μM. |
| M3069 | Ticagrelor | Ticagrelor is the first reversibly binding oral P2Y12 receptor antagonist with Ki of 2 nM respectively. |
| M2234 | Prasugrel | Prasugrel is a platelet inhibitor irreversibly binding to P2Y12 receptors. |
| M3280 | Clopidogrel | Clopidogrel is an oral, thienopyridine class antiplatelet agent used to inhibit blood clots in coronary artery disease, peripheral vascular disease, and cerebrovascular disease. |
| M1909 | GW 791343 dihydrochloride | GW 791343 dihydrochloride is a non-competitive inhibitor of human P2X(7) receptor. |
| M1895 | Prasugrel hydrochloride | Prasugrel hydrochloride is a novel inhibitor of platelet activation and aggregation. |
| M59078 | 2-Methylthio-AMP | 2-Methylthio-AMP (2-MeSAMP) is a selective and direct P2Y12 antagonist. 2-Methylthio-AMP is an inhibitor of ADP-dependent platelet aggregation. |
| M56550 | NF449 | NF449 is a highly potent P2X1 receptor antagonist, with IC50s of 0.28, 0.69, and 120 nM for rP2X1, rP2X1+5, P2X2+3, respectively. |
| M56549 | NF279 | NF279 is a potent selective and reversible P2X1 receptor antagonist, with an IC50 of 19 nM. |
| M56548 | NF110 | NF110 is a P2X3 receptor antagonist (Ki = 36 nM) and inactive toward P2Y receptors stably expressed (IC50s > 10 M). |
| M56547 | PSB-12062 | PSB-12062 is a potent and selective P2X4 antagonist with an IC50 of 1.38 μM for human P2X4. |
| M56545 | α,β-Methylene-ATP | α,β-Methylene ATP, a phosphonic analog of ATP, is a P2X3 and P2X7 receptor ligand. |
| M56544 | Iso-PPADS tetrasodium | Iso-PPADS tetrasodium is a P2X-purinoceptor antagonist. |
| M56543 | α,β-Methylene-ATP dilithium | α,β-Methylene ATP dilithium, a phosphonic analog of ATP, is a P2X3 and P2X7 receptor ligand. |
| M56542 | α,β-Methylene-ATP trisodium | α,β-Methylene-ATP trisodium, a phosphonic analog of ATP, is a P2X3 and P2X7 receptor ligand. |
| M56306 | PIT | PIT (2,2'-Pyridylisatogen tosylate) is a selective and non-competitive antagonist of P2Y1 receptor with an IC50 value of 0.14 μM for human P2Y1 receptor. |
| M56305 | 2-Thio-UTP | 2-Thio-UTP is a selective P2Y2 inhibitor with an EC50 value of 50 nM. |
| M56304 | MRS2693 ammonium | MRS2693 ammonium is the ammonium dalt form of MRS2693. |
| M56303 | PSB-1114 tetrasodium | PSB-1114 tetrasodium is a potent, enzymatically stable, and subtype-selective P2Y2 receptor agonist with an EC50 of 134 nM. |
| M56301 | Adenosine 2',5'-diphosphate sodium | Adenosine 2',5'-diphosphate sodium is a competitive P2Y1 antagonist. |
| M52754 | Purotoxin 1 | Purotoxin 1 is a P2X3 receptor inhibitor. |
| M42223 | P2X2/3 modulator-1 | P2X2/3 modulator-1 is a P2X2/3 modulator. |
| M42222 | P2X7-IN-2 TFA | P2X7-IN-2 TFA is a P2X7 receptor inhibitor. |
| M42221 | NP-1815-PX | NP-1815-PX is a potent and selective P2X4R antagonist. |
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