Potent, selective and competitive NMDA receptor antagonist which reversibly binds to the glutamate binding site. Crosses the blood brain barrier and is active in vivo. Shows various effects (e.g. supresses seizure activity, interferes with addiction paradigms, blocks LTP and LTD and impairs learning and memory). (R)-CPP also available.
Solubility & Handling
Solubility overview
Soluble in water (100mM)
Storage instructions
Room temperature (desiccate)
Storage of solutions
Prepare and use solutions on the same day if possible. Store solutions at -20°C for up to one month if storage is required. Equilibrate to RT and ensure the solution is precipitate free before use.
Shipping Conditions
Stable for ambient temperature shipping. Follow storage instructions on receipt.
Important
This product is for RESEARCH USE ONLY and is not intended for therapeutic or diagnostic use. Not for human or veterinary use.
Action of 3-((+/-)-2-carboxypiperazin-4-yl)-propyl-1-phosphonic acid (CPP): a new and highly potent antagonist of N-methyl-D-aspartate receptors in the hippocampus.
CPP, a new potent and selective NMDA antagonist. Depression of central neuron responses, affinity for [3H]D-AP5 binding sites on brain membranes and anticonvulsant activity.
FMRP regulates experience-dependent maturation of callosal synaptic connections and bilateral cortical synchrony
Huber et al (2021) bioRxiv https://doi.org/10.1101/2021.06.25.449490 : doi
Dysregulated clock gene expression and abnormal diurnal regulation of hippocampal inhibitory transmission and spatial memory in amyloid precursor protein transgenic mice
Fusilier AR et al (2021) Neurobiol Dis 158 : 105454
Different glutamate sources and endogenous co-agonists activate extrasynaptic NMDA receptors on amacrine cells of the rod pathway microcircuitBeltran-Matas et al
Beltran-Matas et al (2021) Eur J Neurosci. : 54(2)