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A-317491

Cat. No. M11206
A-317491  Structure
Size Price Availability Quantity
10mg USD 175  USD175 In stock
50mg USD 580  USD580 In stock
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Quality Control & Documentation
Biological Activity

A-317491 is a potent, selective and non-nucleotide antagonist of P2X3 and P2X2/3 receptors, with Kis of 22, 22, 9, and 92 nM for hP2X3, rP2X3, hP2X2/3, and rP2X2/3, respectively. A-317491 is highly selective for other P2 receptors and neurotransmitter receptors, ion channels, and enzymes (IC50>10 μM). A-317491 blocks P2X by3 AND P2X2/3 receptor-mediated calcium fluxes reduce inflammatory and neuropathic pain.

Chemical Information
Molecular Weight 565.57
Formula C33H27NO8
CAS Number 475205-49-3
Form Solid
Solubility (25°C) DMSO ≥ 60 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] Ming Yuan, et al. Int J Nanomedicine. Effect of A-317491 delivered by glycolipid-like polymer micelles on endometriosis pain

[2] Gang Wu, et al. Eur J Pharmacol. A-317491, a selective P2X3/P2X2/3 receptor antagonist, reverses inflammatory mechanical hyperalgesia through action at peripheral receptors in rats

[3] Michael F Jarvis, et al. J Pharmacol Exp Ther. [3H]A-317491, a novel high-affinity non-nucleotide antagonist that specifically labels human P2X2/3 and P2X3 receptors

[4] Steve McGaraughty, et al. Br J Pharmacol. Effects of A-317491, a novel and selective P2X3/P2X2/3 receptor antagonist, on neuropathic, inflammatory and chemogenic nociception following intrathecal and intraplantar administration

[5] Michael F Jarvis, et al. Proc Natl Acad Sci U S A. A-317491, a novel potent and selective non-nucleotide antagonist of P2X3 and P2X2/3 receptors, reduces chronic inflammatory and neuropathic pain in the rat

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  Catalog
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Keywords: A-317491 supplier, P2 Receptor, inhibitors, activators


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