SDZ 220-581
Tocris Bioscience, part of Bio-Techne | Catalog # 1250
Competitive NMDA antagonist
Discontinued Product
1250 has been discontinued.
View all NMDA Receptor Antagonists products.
Product Description
SDZ 220-581 is a competitive NMDA receptor antagonist (pKi = 7.7). Centrally active following oral administration (ED50 < 3.2 mg/kg for protection against MES-induced seizures).Licensing Information
Sold with the permission of Novartis Pharma AGProduct Specifications
Molecular Weight
369.74
Formula
C16H17ClNO5P
Storage
Store at RT
Purity
≥98% (HPLC)
Chemical Name
(S)-α-Amino-2'-chloro-5-(phosphonomethyl)[1,1'-biphenyl]-3-propanoic acid
CAS Number
174575-17-8
PubChem ID
128019
InChI Key
VBRJFXSFCYEZMQ-HNNXBMFYSA-N
SMILES
OC([C@@H](N)CC1=CC(C2=CC=CC=C2Cl)=CC(CP(O)(O)=O)=C1)=O
The technical data provided above is for guidance only. For batch specific data refer to the Certificate of Analysis.
Solubility
| Solvent | Max Conc. mg/mL | Max Conc. mM | |
|---|---|---|---|
| Solubility | |||
| 1.1eq. NaOH | 36.97 | 100 | |
| DMSO | 9.24 | 25 with gentle warming |
Preparing Stock Solutions
for SDZ 220-581
The following data is based on the product molecular weight 369.74
Batch specific molecular weights may vary from batch to batch due to the degree of hydration, which all affect the solvent volumes required to prepare stock solutions.
| Concentration / Solvent Volume / Mass | 1 mg | 5 mg | 10 mg |
|---|---|---|---|
| 1 mM | 2.70 mL | 13.52 mL | 27.05 mL |
| 5 mM | 0.54 mL | 2.70 mL | 5.41 mL |
| 10 mM | 0.27 mL | 1.35 mL | 2.70 mL |
| 50 mM | 0.05 mL | 0.27 mL | 0.54 mL |
Calculators
Molarity Calculator
Dilution Calculator
Reconstitution Calculator
Background References
References are publications that support the biological activity of the product.
- Urwyler Biphenyl-derivatives of 2-amino-7-phosphono-heptanoic acid, a novel class of potent competitive N-MthD.-aspartate receptor antagonists - I. Pharmacological characterization in vitro. Neuropharmacology 1996 PMID: 8887974
- Urwyler Biphenyl-derivatives of 2-amino-7-phosphono-heptanoic acid, a novel class of potent competitive N-MthD.-aspartate receptor antagonists - II. Pharmacological characterization in vivo. Neuropharmacology 1996 PMID: 8887975
- Bakshi Disruption of prepulse inhibition and increases in locomotor activity by competitive N-MthD.-aspartate receptor antagonists in rats. J.Pharmacol.Exp.Ther. 1999 PMID: 9918570
Product Specific Notices for SDZ 220-581
For research use only
Loading...
Loading...