D-AP5.Na

SKU:BHB11900199
Suppliers
StressMarq Biosciences Inc.
StressMarq Biosciences Inc.
Details Products
Overview
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D-AP5.Na (D-amino-5-phosphonopentaoic acid sodium salt) is a research-grade small-molecule antagonist of NMDA receptor supporting Neuroscience and Ion Channels research. Supplied as a white solid with >99.5 purity (CAS 14375-45-2, MW 219.11) soluble in 1 M NH4OH; store at -20°C. For research use only.
Cas No. 14375-45-2
Molecular Formula C5H12NO5P.Na
Purity >99.5
Application Notes NMDA receptor antagonist
Options selector
Catalog no. Size
SIH-412-5MG 5 mg
SIH-412-25MG 25 mg
Available Options

Select the variant that best fits your experiment. Availability and lead time may vary by option.

  • Options: Size (2) — 25 mg, 5 mg.
  • Lead time: options listed as “in stock at manufacturer” typically ship in 2-3 business days; other statuses may take longer.
  • Storage: -20ºC
  • Shipping: ships at ambient temperature.
  • Upon receipt: store at the recommended temperature as soon as possible.
  • Sales terms and conditions: Please review prior to ordering.
Field Specification
Mfr No SIH-412
Activity
  • Antagonist
Alternative Names D-amino-5-phosphonopentaoic acid sodium salt
Cas No. 14375-45-2
Form White solid
Molecular Weight 219.11
Product Type
  • Biochemicals
  • Small Molecules
Purity >99.5
Shipping Shipped Ambient
SMILES [C@@H]([NH3+])(CCC[P]([O-])([O-])=O)C([O-])=O
Solubility Soluble in 1 M NH4OH (50 mg/ml); water (9 mg/ml).
Source Synthetic
Storage -20ºC

D-AP5.Na (D-(-)-2-Amino-5-phosphonopentanoic acid sodium salt) is a selective NMDA receptor antagonist that inhibits glutamate binding at the receptor site. NMDA receptors are critical for synaptic plasticity, learning, and memory, but their overactivation leads to excitotoxicity—a major contributor to neuronal death in neurodegenerative diseases such as Alzheimer’s, Huntington’s, and ALS. D-AP5.Na is widely used in neuroscience to study NMDA receptor-mediated signaling and to explore neuroprotective strategies by blocking calcium influx and excitotoxic damage. Its sodium salt form enhances solubility and stability for in vitro and in vivo applications.

Classification: Not WHMIS controlled.

Safety Phrases:

  • S22 - Do not breathe dust.
  • S24/25 - Avoid contact with skin and eyes.
  • S36/37/39 - Wear suitable protective clothing, gloves and eye/face protection.

D-AP5.Na (StressMarq Biosciences Inc., Victoria BC CANADA, Catalog # SIH-412)

Need this compound in a format that drops straight into your assay? We can tailor formulation, chemistry, and documentation so your results stay consistent across runs and re-orders.

  • Format options: solid or pre-dissolved solution (choose solvent), target concentration, aliquots, light/moisture-protected packaging
  • Chemistry options: free base/acid vs salt forms, hydrate/solvate preference, stereoisomer control (single enantiomer or racemate), close analogs
  • Add-on labels & handles: D/¹³C/¹⁵N isotopes (LC-MS/internal standards), azide/alkyne or other functional handles for conjugation
  • QC & documentation: standard COA or enhanced analytical pack (HPLC/LC-MS/NMR), chiral purity, residual solvents, water content (KF), method-specific specs
  • Scale & continuity: mg to gram scale, bulk pricing, lot reservation, repeat-order continuity

To quote quickly, tell us: compound name + CAS/structure (SMILES or mol file), intended assay context, solvent preference, salt/stereochemistry requirements, purity/QC level, and the amount (mg–g).

Can’t find the compound you’re looking for?
Send the CAS or structure and your specs. We can help source it, suggest close equivalents, or discuss custom synthesis with the right QC documentation (RUO).

1. Davies J., & Watkins J. (1982) Brain Res. 378-86.
2. Schulte M., Roon R., Chalmers D., Sunter D., & Koerner J. (1994) Brain Res. 203-7.

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