ChemicalBook--->CAS DataBase List--->170846-89-6

170846-89-6

170846-89-6 Structure

170846-89-6 Structure
IdentificationBack Directory
[Name]

E4CPG
[CAS]

170846-89-6
[Synonyms]

E4CPG
(RS)-α-Ethyl-4-carboxyphenylglycine
4-(1-amino-1-carboxypropyl)benzoic acid
(RS)-ALPHA-ETHYL-4-CARBOXYPHENYLGLYCINE
Benzeneacetic acid, α-amino-4-carboxy-α-ethyl-
[Molecular Formula]

C11H13NO4
[MDL Number]

MFCD01074798
[MOL File]

170846-89-6.mol
[Molecular Weight]

223.23
Chemical PropertiesBack Directory
[Boiling point ]

431.3±40.0 °C(Predicted)
[density ]

1.337±0.06 g/cm3(Predicted)
[storage temp. ]

Store at RT
[solubility ]

H2O : < 0.1 mg/mL (insoluble)DMSO : < 1 mg/mL (insoluble or slightly soluble)
[form ]

Powder
[pka]

1.76±0.10(Predicted)
[color ]

White to off-white
Hazard InformationBack Directory
[Uses]

E4CPG is a group I/group II metabotropic glutamate receptor antagonist.
[in vivo]

E4CPG (3-30 nmol/site (i.t.), 1-10 μmol/paw (i.pl.), and 1-10 nmol/site (i.c.v.)) significantly inhibits the nociception induced by the Glutamate-injection (i.pl.; 30 μmol/paw), and the maximal inhibition values for the antinociceptive action of E4CPG in Glutamate-induced nociception are 48% (i.pl.), 49% (i.t.) and 40% (i.c.v.) [4].
E4CPG (35 nM/3.5 μL, i.c.v.) completely blocks long-term depression (LTD) induced by the group I mGluR agonist Dihydroxyphenylglycine (DHPG, 100 nM/5 μL, i.c.v.) in male Sprague-Dawley rats[5].

Animal Model:Male Swiss mice (25-35 g)[4]
Dosage:3-30 nmol/site (i.t.), 1-10 μmol/paw (i.pl.) and 1-10 nmol/ site (i.c.v.)
Administration:Single injection
Result:The maximal inhibition values for the antinociceptive action of E4CPG in glutamate-induced nociception were 48% (i.pl.), 49% (i.t.) and 40% (i.c.v.).
Animal Model:Male Sprague-Dawley rats[5]
Dosage:35 nM/3.5 μL
Administration:Single injection, i.c.v.
Result:Completely blocked LTD induced by the group I mGluR agonist dihydroxyphenylglycine (DHPG).
[IC 50]

mGluR
[storage]

Room temperature
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