assay
≥98% (HPLC)
Quality Level
form
solid
manufacturer/tradename
Calbiochem®
storage condition
OK to freeze, protect from light
color
white
solubility
1 M NaOH: 25 mM
storage temp.
2-8°C
InChI
1S/C7H8IN3O4/c8-3-1-11(2-4(9)6(13)14)7(15)10-5(3)12/h1,4H,2,9H2,(H,13,14)(H,10,12,15)/t4-/m0/s1
InChI key
AXXYLTBQIQBTES-BYPYZUCNSA-N
General description
A potent agonist highly selective for GluK1-containing subtype kainate receptors (EC50 = 0.06 and 0.21 µM for GluK1/K5 and GluK1, respectively) over GluK2-containing subtypes (EC50 = 0.47 and 30 µM for GluK1/K2 and GluK2/K5 respectively). Does not interact with GluK2, GluK6, and GluK7 receptors. Low affinity to AMPA receptors (EC50 = 1.5 and 33.6 µM for GluA2 and GluA1 respectively). Has been used in assessing the functional roles of GluK1-containing subtype kainate receptors in neuropathic pains, apoptosis, and necrosis.
Please note that the molecular weight for this compound is batch-specific due to variable water content.
Please note that the molecular weight for this compound is batch-specific due to variable water content.
Biochem/physiol Actions
Primary Target
GluK1
GluK1
Packaging
Packaged under inert gas
Preparation Note
Following reconstitution, aliquot and freeze (-20°C). Stock solutions are stable for up to 3 months at -20°C.
Other Notes
Bhangoo, K., et al. 2013. Mol. Pharmacol.83, 307.
Moldrich, X., et al. 2000. J. Neurosci. Res.59, 788.
Chittajallu, R., et al. 1999. Trends Pharmacol. Sci.20, 26.
Swanson, T., et al. 1998. Mol. Pharmacol.53, 942.
Moldrich, X., et al. 2000. J. Neurosci. Res.59, 788.
Chittajallu, R., et al. 1999. Trends Pharmacol. Sci.20, 26.
Swanson, T., et al. 1998. Mol. Pharmacol.53, 942.
Legal Information
CALBIOCHEM is a registered trademark of Merck KGaA, Darmstadt, Germany
Disclaimer
Toxicity: Standard Handling (A)
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_c
Not applicable
flash_point_f
Not applicable
法规信息
新产品
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全球贸易项目编号
| 货号 | GTIN |
|---|---|
| 5097070001 | 04055977241075 |