Sigma-Aldrich Nmda Antagonist Xi, N1-Dan

Assay

≥97% (HPLC)

Quality Level

100

Form

powder

Potency

0.31 μM IC₅₀

Manufacturer/Tradename

Calbiochem^®

Storage Condition

OK to freeze
protect from light

Color

yellow-white

Solubility

DMSO: 100 mg/mL

Storage Temp.

2-8°C

Smiles String

CN(C)C1=CC=CC2=C1C=CC=C2S(=O)(=O)NCCCNCCCCNCCCN

General Description

An N-sulfonyl-polyamine that acts as a potent and more specific antagonist of NMDA receptors expressed in Xenopus oocytes (IC₅₀= 310, 340 nM in NR1/NR2A and NR1/NR2B, respectively). The inhibition appears to be voltage-dependent and is non-competitive with respect to glutamate and glycine. Exhibits about 50-fold greater selectivity over NR1/NR2C and NR1/NR2D receptors (IC₅₀= 16 and 13 µM, respectively). Also shown to block c-AMP-dependent, calmodulin-activated phosphodiesterase (IC₅₀= 58 µM) and diminishes the induction of ornithine decarboxylase. At higher concentration (˜100 µM) it is shown to reduce spontaneous epileptiform activity in mouse cortical slices.

Biochem/Physiol Actions

Primary Target
NMDA

Packaging

Packaged under inert gas

Warning

Toxicity: Standard Handling (A)

Reconstitution

Following reconstitution, aliquot and freeze (-20°C). Stock solutions are stable for up to 3 months at -20°C.

Other Notes

Kirby, B.P., et Al. 2005,Eur. J. Pharmacol. 524,53.
Li, J., et Al. 2005,Brain Res. 1055,180.
Kirby, B. et Al. 2004,Brain Res. 1011,69.
Seiler, N., et Al. 1998,J. Biochem. Cell Biol. 30,393.

Chao, J., et Al. 1997,Mol. Pharm. 51,861.CALBIOCHEM is a registered trademark of Merck KGaA, Darmstadt, Germany