NF 279

Catalog # Availability Size / Price Qty
1199/10
1199/50
NF 279 | CAS No. 202983-32-2 | P2X Receptor Antagonists
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Description: Potent and selective P2X1 antagonist

Chemical Name: 8,8'-[Carbonylbis(imino-4,1-phenylenecarbonylimino-4,1-phenylenecarbonylimino)]bis-1,3,5-naphthalenetrisulfonic acid hexasodium salt

Purity: ≥95%

Product Details
Citations (9)
Supplemental Products
Reviews

Biological Activity

NF 279 is a a potent and selective P2X1 antagonist (IC50 = 19 nM). Displays good selectivity over P2X2,(IC50 = 0.76 μM), P2X3 (IC50 = 1.62μM), P2X4 (IC50 > 300 μM), P2Y receptors and ecto-nucleotidases.

This product is supplied with a high degree of hydration and some residual NaCl, the amount of which are batch dependent. Please refer to the Certificate of Analysis to obtain the batch specific Net Product Content.

Technical Data

M.Wt:
1401.1
Formula:
C49H30N6Na6O23S6
Solubility:
Soluble to 25 mg/ml in water
Purity:
≥95%
Storage:
Store at -20°C
CAS No:
202983-32-2

The technical data provided above is for guidance only. For batch specific data refer to the Certificate of Analysis.
Tocris products are intended for laboratory research use only, unless stated otherwise.

Background References

  1. Purinergic receptors are required for HIV-1 infection of primary human macrophages.
    Hazleton JE, Berman JW, Eugenin EA
    J. Immunol., 2012;188(9):4488-95.
  2. NF279: a novel potent and selective antagonist of P2X receptor-mediated responses.
    Damer et al.
    Eur.J.Pharmacol., 1998;350:R5
  3. Antagonism by the suramin analogue NF 279 on human P2X1 and P2X7 receptors.
    Klapperstuck et al.
    Eur.J.Pharmacol., 2000;387:245
  4. The suramin analogue NF279 is a novel and potent antagonist selective for the P2X1 receptor.
    Rettinger et al.
    Neuropharmacology, 2000;39:2044

Product Datasheets

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Citations for NF 279

The citations listed below are publications that use Tocris products. Selected citations for NF 279 include:

9 Citations: Showing 1 - 9

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