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Merck
CN

C1835

(S)-(+)-4-Carboxyphenylglycine

别名:

(S)-α-Amino-4-carboxyphenylacetic acid, L-α-(4-Carboxyphenyl)glycine, S-4CPG

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关于此项目

经验公式(希尔记法):
C9H9NO4
化学文摘社编号:
分子量:
195.17
UNSPSC Code:
12352103
MDL number:
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solubility

0.1 M NaOH: 15 mg/mL

Biochem/physiol Actions

Competitive mGluR1 metabotropic glutamate receptor antagonist; mGluR2 metabotropic glutamate receptor agonist.


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S A Eaton et al.
European journal of pharmacology, 244(2), 195-197 (1993-01-15)
Two phenylglycine derivates, (S)-4-carboxyphenylglycine and (RS)-alpha-methyl-4-carboxyphenylglycine, competitively antagonised (1S,3R)-1-aminocyclopentane-1,3-dicarboxylate (ACPD)-stimulated phosphoinositide hydrolysis in rat cerebral cortical slices. The same phenylglycine derivatives selectively antagonized ACPD-induced depolarization in neonatal rat spinal motoneurones and rate thalamic neurones relative to depolarization or excitation induced
Pharmacological analysis of carboxyphenyl-glycines at metabotropic glutamate receptors.
Cavanni, et al.
Eur. J. Pharmacol., Molec. Pharmacol. Sec., 269, 9-9 (1994)
E F Birse et al.
Neuroscience, 52(3), 481-488 (1993-02-01)
The possible roles of G-protein coupled metabotropic glutamate receptors in central nervous function are currently the focus of intensive investigation. The complexity of effects produced by agonists at these receptors probably reflects the activity of a range of sub-types. The