ArtNr |
HY-112461A-10mg |
Hersteller |
MedChem Express
|
CAS-Nr. |
627034-85-9 |
Menge |
10 mg |
Quantity options |
100 mg
10 mg
1 mg
25 mg
50 mg
5 mg
|
Kategorie |
|
Typ |
Inhibitors |
Specific against |
other |
Purity |
99.0 |
Formula |
C41H24N6Na8O29S8 |
Citations |
[1]Rettinger J, et al. Profiling at recombinant homomeric and heteromeric rat P2X receptors identifies the suramin analogue NF449 as a highly potent P2X1 receptor antagonist. Neuropharmacology. 2005;48(3):461-468. [2]Hechler B, et al. Inhibition of platelet functions and thrombosis through selective or nonselective inhibition of the platelet P2 receptors with increasing doses of NF449 [4,4',4'',4'''-(carbonylbis(imino-5,1,3-benzenetriylbis-(carbonylimino)))tetrakis-benzene-1,3-disulfonic acid octasodium salt]. J Pharmacol Exp Ther. 2005;314(1):232-243. [3]Hohenegger M, et al. Gsalpha-selective G protein antagonists. Proc Natl Acad Sci U S A. 1998;95(1):346-351. |
Smiles |
O=C(NC1=CC(C(NC2=CC=C(S(=O)(O[Na])=O)C=C2S(=O)(O[Na])=O)=O)=CC(C(NC3=CC=C(S(=O)(O[Na])=O)C=C3S(=O)(O[Na])=O)=O)=C1)NC4=CC(C(NC5=CC=C(S(=O)(O[Na])=O)C=C5S(=O)(O[Na])=O)=O)=CC(C(NC6=CC=C(S(=O)(O[Na])=O)C=C6S(=O)(O[Na])=O)=O)=C4 |
ECLASS 10.1 |
32160490 |
ECLASS 11.0 |
32160490 |
UNSPSC |
12000000 |
Versandbedingung |
Gekühlt |
Lieferbar |
|
Manufacturer - Type |
Reference compound |
Manufacturer - Applications |
Neuroscience-Neuromodulation |
Manufacturer - Targets |
P2X Receptor |
Shipping Temperature |
Blue Ice |
Storage Conditions |
-20°C (Powder, stored under nitrogen) |
Molecular Weight |
1505.09 |
Product Description |
NF449 octasodium is a highly potent P2X1 receptor antagonist, with IC50s of 0.28, 0.69, and 120 nM for rP2X1, rP2X1+5, P2X2+3, respectively. NF449 octasodium is a Gsα-selective G Protein antagonist. NF449 octasodium suppresses the rate of GTP[γS] binding to Gsα-s, inhibits the stimulation of adenylyl cyclase activity, and blocks the coupling of β-adrenergic receptors to Gs[1][2]. |
Manufacturer - Research Area |
Cardiovascular Disease |
Solubility |
H2O : 10 mg/mL (ultrasonic; warming)|DMSO : 10 mg/mL (ultrasonic; warming; heat to 60°C) |
Manufacturer - Pathway |
Membrane Transporter/Ion Channel |
Isoform |
P2X1 Receptor |
Clinical information |
No Development Reported |
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