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PPADS

Cat. No. M14247

All AbMole products are for research use only, cannot be used for human consumption.

PPADS Structure

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Quality Control & Documentation
Biological Activity

PPADS is a non-selective P2X receptor antagonist. PPADS blocks recombinant P2X1, -2, -3, -5 with IC50s ranging from 1 to 2.6 μM. PPADS blocks native P2Y2-like (IC50~0.9 mM) and recombinant P2Y4 (IC50~15 mM) receptors. PPADS is an inhibitor of the reverse mode of the Na/Ca2+ exchanger in guinea pig airway smooth muscle.

Chemical Information
Molecular Weight 511.38
Formula C14H14N3O12PS2
CAS Number 149017-66-3
Storage Powder          -20°C   3 years ;  4°C   2 years
In solvent       -80°C   6 months ;  -20°C   1 month
References

[1] H C Ferreira-Neto, et al. Purinergic P2 and glutamate NMDA receptor coupling contributes to osmotically driven excitability in hypothalamic magnocellular neurosecretory neurons

[2] Hildebrando Candido Ferreira-Neto, et al. ATP stimulates rat hypothalamic sympathetic neurons by enhancing AMPA receptor-mediated currents

[3] Marie E Gibbs, et al. ATP derived from astrocytes modulates memory in the chick

[4] Brian D Gulbransen, et al. Purinergic neuron-to-glia signaling in the enteric nervous system

[5] Yanpeng Lin, et al. P2 receptor antagonist PPADS confers neuroprotection against glutamate/NMDA toxicity

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PPADS Tetrasodium

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

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Keywords: PPADS supplier, P2 Receptor, inhibitors, activators

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