Cangrelor Tetrasodium

Catalog No.: A17919

P2Y12 receptors inhibitor

Cangrelor Tetrasodium

Cangrelor Tetrasodium Chemical Structure

CAS NO. 163706-36-3

Cangrelor Tetrasodium is a high-affinity, reversible inhibitor of P2Y12 receptors that causes almost complete inhibition of ADP-induced platelet aggregate. It is a modified ATP derivative stable to enzymatic degradation. Unlike clopidogrel (Plavix), which is a prodrug, cangrelor is an active drug not requiring metabolic conversion.

Availability: In stock

Package Price Qty
5 mg
$350.00
10 mg
$650.00
25 mg
$1,200.00
50 mg
$2,000.00
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Biological Activity

Cangrelor Tetrasodium is a high-affinity, reversible inhibitor of P2Y12 receptors that causes almost complete inhibition of ADP-induced platelet aggregate. It is a modified ATP derivative stable to enzymatic degradation. Unlike clopidogrel (Plavix), which is a prodrug, cangrelor is an active drug not requiring metabolic conversion.
Concentration / Solvent Volume / Mass 1 mg 5 mg 10 mg
0.1 mM 11.57 mL 57.85 mL 115.7 mL
0.5 mM 2.31 mL 11.57 mL 23.14 mL
1 mM 1.16 mL 5.79 mL 11.57 mL
5 mM 0.23 mL 1.16 mL 2.31 mL

*The above data is based on the productmolecular weight 864.27. Batch specific molecular weights may vary from batch to batch due to solvent of hydration, which will affect the solvent volumes required to prepare stock solutions.

Catalog Num A17919
Actions Inhibitor
M. Wt 864.27
Formula C17H21Cl2F3N5Na4O12P3S2
Solubility DMSO
Purity >98%
Storage at -20°C 3 years Powder
CAS No. 163706-36-3
Synonyms Cangrelor Tetrasodium; AR-C69931MX; AR C69931MX; ARC69931MX
SMILES CSCCNC1=NC(SCCC(F)(F)F)=NC2=C1N=CN2[[email protected]@H]3O[[email protected]](COP([O-])(OP([O-])(C(P([O-])([O-])=O)(Cl)Cl)=O)=O)[[email protected]@H](O)[[email protected]]3O.[Na+].[Na+].[Na+].[Na+]

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