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Assay Detail

CHEMBL749324

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

Binding
Competitive inhibition (at 100 uM) of NMDA receptor site was assessed by its ability to displace [3H]CPP from its binding site in rat synaptic membranes
1
Total Activities
1
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

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

Target

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

Publication

Design, synthesis, SAR, and biological evaluation of highly potent benzimidazole-spaced phosphono-alpha-amino acid competitive NMDA antagonists of the AP-6 type.
Baudy RB, Fletcher H, Yardley JP, Zaleska MM, Bramlett DR, Tasse RP, Kowal DM, Katz AH, Moyer JA, Abou-Gharbia M.
J Med Chem (2001) 44 : 1516 -1529
PubMed 11334562 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 1 6.41 6.41

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL274440 AP-7 1 6.41

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL274440 AP-7 IC50 = 388.0 nM 6.41