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Assay Detail

CHEMBL749332

Review assay metadata, readout intent, target linkage, and publication context from the same page.

Binding
Compound was evaluated for the inhibition of [3H]-CGS-19,755 binding at N-methyl-D-aspartate glutamate receptor
5
Total Activities
5
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Confidence 4 — Cell-line / Tissue
Curated By Autocuration

Target

Glutamate NMDA receptor (CHEMBL1907608)
Type PROTEIN COMPLEX GROUP
Organism Rattus norvegicus

Publication

DL-tetrazol-5-ylglycine, a highly potent NMDA agonist: its synthesis and NMDA receptor efficacy.
Lunn WH, Schoepp DD, Calligaro DO, Vasileff RT, Heinz LJ, Salhoff CR, O'Malley PJ.
J Med Chem (1992) 35 : 4608 -4612
PubMed 1361579 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 5 6.35 7.01

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL140784 1 7.01
CHEMBL1437288 1 6.79
CHEMBL575060 GLUTAMIC ACID 3.0 1 6.76
CHEMBL274323 ASPARTIC ACID 3.0 1 5.79
CHEMBL291278 N-METHYL-D-ASPARTIC ACID (NMDA) 2.0 1 5.38

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL140784 IC50 = 98.0 nM 7.01
CHEMBL1437288 IC50 = 163.0 nM 6.79
CHEMBL575060 GLUTAMIC ACID IC50 = 172.0 nM 6.76
CHEMBL274323 ASPARTIC ACID IC50 = 1638.0 nM 5.79
CHEMBL291278 N-METHYL-D-ASPARTIC ACID (NMDA) IC50 = 4150.0 nM 5.38