Name | NP10679 |
Description | NP10679 is an orally available, selective, brain-penetrating, potent, and pH-sensitive N-methyl-D-aspartate (NMDA) receptor inhibitor of the GluN2B subunit.NP10679 inhibits histamine H1, hERG channels, and CYP enzymes, and may be useful in the study of epilepsy and ischemic stroke. |
In vitro | NP10679 is an NMDA receptor inhibitor containing GluN2B that is more effective than physiological pH. It exhibits inhibitory effects on 5-HT2A, α1A adrenergic receptor, H1 histamine receptor, and hERG channels[2]. |
In vivo | In the Male C57BL/6 middle cerebral artery occlusion (MCAo) model of transient ischemia mice, NP10679 (2, 5, and 10 mg/kg; intraperitoneal injection; administered 15 minutes prior to transient ischemia) dose-dependently reduces infarct volumes, with an ED50 of 1 mg/kg[2]. |
Storage | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice. |
Solubility Information | DMSO : 80 mg/mL (177.99 mM), Sonication is recommended.
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Inhibitors Related | Tebuconazole | Meclizine dihydrochloride | Lidocaine | Apigenin | Famotidine | Fenofibrate | Naringin | Naringenin | Tauroursodeoxycholate | Alginic acid |
Related Compound Libraries | Bioactive Compound Library | Pain-Related Compound Library | Anti-Aging Compound Library | Bioactive Compounds Library Max | GPCR Compound Library |