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Assay Detail

CHEMBL650290

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

Binding
In vitro inhibition of 3[H]Diazepam binding to Benzodiazepine receptor from rat cerebral cortical membranes; value ranges from 4-12 nM
1
Total Activities
1
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Organism Rattus norvegicus
Subcellular Membrane
Confidence 5 — Multiple protein complex / RNA
Curated By Autocuration

Target

GABA-A receptor; anion channel (CHEMBL1907607)
Type PROTEIN COMPLEX GROUP
Organism Rattus norvegicus

Publication

Synthetic and computer-assisted analyses of the pharmacophore for the benzodiazepine receptor inverse agonist site.
Allen MS, Tan YC, Trudell ML, Narayanan K, Schindler LR, Martin MJ, Schultz C, Hagen TJ, Koehler KF, Codding PW.
J Med Chem (1990) 33 : 2343 -2357
PubMed 2167977 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 1 8.40 8.40

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL53651 1 8.40

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL53651 IC50 = 4.0 nM 8.40