CGP 37849

CAT: 0804-HY-107702-01Size: 1 mgDry Ice: NoHazardous: No
CAT#:0804-HY-107702-01Size:1 mg
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Description
CGP 37849 is a potent, competitive and orally active N-methyl-D-aspartate (NMDA) receptor antagonist. CGP 37849 is an anticonvulsant in rodents and has antidepressant and anxiolytic-like effects[1].
CAS Number
[127910-31-0]
UNSPSC
12352211
Hazard Statement
H302, H315, H319, H335
Target
IGluR
Type
Reference compound
Related Pathways
Membrane Transporter/Ion Channel; Neuronal Signaling
Applications
Neuroscience-Neurodegeneration
Field of Research
Neurological Disease
Assay Protocol
https://www.medchemexpress.com/cgp-37849.html
Purity
99.0
Solubility
H2O : 20.91 mg/mL (ultrasonic)
Smiles
O=P(O)(O)C/C(C)=C/C(N)C(O)=O
Molecular Formula
C6H12NO5P
Molecular Weight
209.14
Precautions
H302, H315, H319, H335
References & Citations
[1]Fagg GE, et al. CGP 37849 and CGP 39551: novel and potent competitive N-methyl-D-aspartate receptor antagonists with oral activity. Br J Pharmacol. 1990 Apr;99 (4) :791-7.|[2]Schmutz M, et al. The competitive NMDA receptor antagonists CGP 37849 and CGP 39551 are potent, orally-active anticonvulsants in rodents. Naunyn Schmiedebergs Arch Pharmacol. 1990 Jul;342 (1) :61-6.|[3]Papp M, et al. Antidepressant activity of non-competitive and competitive NMDA receptor antagonists in a chronic mild stress model of depression. Eur J Pharmacol. 1994 Sep 22;263 (1-2) :1-7.|[4]Przegaliński E, et al. The influence of the benzodiazepine receptor antagonist flumazenil on the anxiolytic-like effects of CGP 37849 and ACPC in rats. Neuropharmacology. 2000 Jul 24;39 (10) :1858-64.
Shipping Conditions
Room Temperature
Storage Conditions
4°C (Powder, sealed storage, away from moisture)
Scientific Category
Reference compound1
Clinical Information
Phase 1
Isoform
NMDA Receptor

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