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PPADS Tetrasodium Salt

Cat. No. M2954
PPADS Tetrasodium Salt Structure
Size Price Availability
5mg USD 320  USD320 4-7 Days
10mg USD 600  USD600 4-7 Days
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Quality Control & Documentation
Biological Activity

PPADS tetrasodium salt is a non-selective P2 purinergic antagonist blocking recombinant P2X1, P2X2, P2X3, P2X5 with IC50 of 1-2.6 μM, native P2Y2-like with IC50 of ~ 0.9 mM, and recombinant P2Y4 receptors with IC50 of ~ 15 mM.

Chemical Information
Molecular Weight 599.3
Formula C14H10N3Na4O12PS2
CAS Number 149017-66-3
Solubility (25°C) Water 6 mg/mL
Storage -20°C, dry, sealed
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] Hong Huo, et al. J Biol Chem. Mapping the binding site of the P2X receptor antagonist PPADS reveals the importance of orthosteric site charge and the cysteine-rich head region

[2] Edgar Flores-Soto, et al. Eur J Pharmacol. PPADS, a P2X receptor antagonist, as a novel inhibitor of the reverse mode of the Na⁺/Ca²⁺ exchanger in guinea pig airway smooth muscle

[3] Sylvia Rost, et al. Kidney Int. P2 receptor antagonist PPADS inhibits mesangial cell proliferation in experimental mesangial proliferative glomerulonephritis

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Keywords: PPADS Tetrasodium Salt supplier, P2 Receptor, inhibitors, activators


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