Home Categories
S8915814

opticalpurityopticalpurity:≥95%(HPLC,Marfey′sreagent) , 23052-81-5

Synonym(s):
L-AP-4;Cartilage-Derived Morphogenetic Protein-1;CDMP-1;LAP4;L-AP4

CAS NO.:23052-81-5

Empirical Formula: C4H10NO5P

Molecular Weight: 183.1

MDL number: MFCD00083244

EINECS: 200-258-5

Pack Size Price Stock Quantity
0.5MG RMB932.93 In Stock
1mg RMB1528.34 In Stock
others     Enquire
Update time: 2022-07-08

PRODUCT Properties

Melting point: 207-215 °C
Boiling point: 491.7±55.0 °C(Predicted)
Density  1.628±0.06 g/cm3(Predicted)
storage temp.  0-6°C
solubility  H2O : 50 mg/mL (273.07 mM; Need ultrasonic)
pka 2.19±0.10(Predicted)
form  solid
color  White
Water Solubility  Soluble to 5 mM in water and to 100 mM in 1eq. NaOH
Sensitive  Light Sensitive
CAS DataBase Reference 23052-81-5(CAS DataBase Reference)

Description and Uses

Metabotropic glutamate receptors (mGluR) function to modulate excitatory synaptic transmission in the brain. Eight subtypes (1-8) and multiple splice variants of the mGluR have been identified and grouped based on their pharmacological properties. Group I mGluRs (subtypes 1 and 5) activate the phosphatidyl inositol pathway, while Group II (2 and 3) and Group III (4, 6, 7, and 8) inhibit adenylyl cyclase. L-AP4, an analog of L-glutamic acid, is a selective Group III mGluR agonist that functions presynaptically to suppress glutamate release (IC50 = 2.5 μM). L-AP4 has been shown to depress synaptic transmission in glutamatergic pathways in the hippocampus, olfactory bulb, and retina as well as act as an agonist at the quisqualate-sensitized AP6 site in hippocampus.

Metabotropic glutamate receptors (mGluR) function to modulate excitatory synaptic transmission in the brain. Eight subtypes (1-8) and multiple splice variants of the mGluR have been identified and grouped based on their pharmacological properties. Group I mGluRs (subtypes 1 and 5) activate the phosphatidyl inositol pathway, while Group II (2 and 3) and Group III (4, 6, 7, and 8) inhibit adenylyl cyclase. L-AP4, an analog of L-glutamic acid, is a selective Group III mGluR agonist that functions presynaptically to suppress glutamate release (IC50 = 2.5 μM). L-AP4 has been shown to depress synaptic transmission in glutamatergic pathways in the hippocampus, olfactory bulb, and retina as well as act as an agonist at the quisqualate-sensitized AP6 site in hippocampus.

Safety

Symbol(GHS) 
GHS07
Signal word  Warning
Hazard statements  H315-H319-H335
Precautionary statements  P261-P280a-P304+P340-P305+P351+P338-P405-P501a
Hazard Codes  Xi
Risk Statements  36/37/38
Safety Statements  26-36
WGK Germany  3
RTECS  ES7191700

RELATED PRODUCTS