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NF 279

Names

[ CAS No. ]:
202983-32-2

[ Name ]:
NF 279

[Synonym ]:
cc-368
1,3,5-Naphthalenetrisulfonic acid, 8,8'-[carbonylbis(imino-4,1-phenylenecarbonylimino-4,1-phenylenecarbonylimino)]bis-, sodium salt (1:6)
Hexasodium 8-[(4-{[4-({[4-({4-[(4,6,8-trisulfonato-1-naphthyl)carbamoyl]phenyl}carbamoyl)phenyl]carbamoyl}amino)benzoyl]amino}benzoyl)amino]naphthalene-1,3,5-trisulfonate
Hexasodium 8,8'-[carbonylbis(imino-4,1-phenylenecarbonylimino-4,1-phenylenecarbonylimino)]di(1,3,5-naphthalenetrisulfonate)
NF 279

Biological Activity

[Description]:

NF279 is a potent selective and reversible P2X1 receptor antagonist, with an IC50 of 19 nM. NF279 displays good selectivity over P2X2, P2X3 (IC50=1.62 μM), P2X4 (IC50>300 μM). NF279 is a dual HIV-1 coreceptor inhibitor that interferes with the functional engagement of CCR5 and CXCR4 by Env[1][2].

[Related Catalog]:

Signaling Pathways >> Anti-infection >> HIV
Research Areas >> Infection
Signaling Pathways >> Membrane Transporter/Ion Channel >> P2X Receptor

[Target]

HIV


[References]

[1]. Rettinger J, Schmalzing G, Damer S, Müller G, Nickel P, Lambrecht G. The suramin analogue NF279 is a novel and potent antagonist selective for the P2X(1) receptor. Neuropharmacology. 2000;39(11):2044-2053.

[2]. Giroud C, et al. P2X1 Receptor Antagonists Inhibit HIV-1 Fusion by Blocking Virus-Coreceptor Interactions. J Virol. 2015;89(18):9368-9382.

Chemical & Physical Properties

[ Molecular Formula ]:
C49H30N6Na6O23S6

[ Molecular Weight ]:
1401.118

[ Exact Mass ]:
1399.907227

[ PSA ]:
551.01000

[ LogP ]:
10.99360

[ Storage condition ]:
-20°C

Related Compounds