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Cangrelor tetrasodium salt

Cat. No. M8762
Cangrelor tetrasodium salt Structure
Size Price Availability Quantity
1mg USD 50  USD50 In stock
5mg USD 115  USD115 In stock
10mg USD 175  USD175 In stock
50mg USD 540  USD540 In stock
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Quality Control & Documentation
Biological Activity

Canrelor is an adenosine triphosphate analog as well as a potent and selective platelet P2Y12 antagonist and a non-specific GPR17 antagonist.

Chemical Information
Molecular Weight 864.29
Formula C17H21Cl2F3N5O12P3S2·Na4
CAS Number 163706-36-3
Form Solid
Solubility (25°C) Water: 2 mg/mL
Storage Powder          -20°C   3 years ;  4°C   2 years
In solvent       -80°C   6 months ;  -20°C   1 month
Conversion of different model animals based on BSA (PMID: 27057123)
Species Mouse Rat Rabbit Guinea pig Hamster Dog
Weight (kg) 0.02 0.15 1.8 0.4 0.08 10
Body Surface Area (m2) 0.007 0.025 0.15 0.05 0.02 0.5
Km factor 3 6 12 8 5 20
Animal A (mg/kg) = Animal B (mg/kg) multiplied by  Animal B Km
Animal A Km

For example, to modify the dose of Compound A used for a mouse (20 mg/kg) to a dose based on the BSA for a rat, multiply 20 mg/kg by the Km factor for a mouse and then divide by the Km factor for a rat. This calculation results in a rat equivalent dose for Compound A of 10 mg/kg.

References

[1] Kurt Huber, et al. Antiplatelet and anticoagulation agents in acute coronary syndromes: what is the current status and what does the future hold?

[2] Binggang Xiang, et al. The P2Y(12) antagonists, 2MeSAMP and cangrelor, inhibit platelet activation through P2Y(12)/G(i)-dependent mechanism

[3] Chiara Tamburrelli, et al. Epoprostenol inhibits human platelet-leukocyte mixed conjugate and platelet microparticle formation in whole blood

[4] Subhashini Srinivasan, et al. The P2Y12 antagonists, 2-methylthioadenosine 5'-monophosphate triethylammonium salt and cangrelor (ARC69931MX), can inhibit human platelet aggregation through a Gi-independent increase in cAMP levels

[5] M Bayes, et al. Gateways to clinical trials

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