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Assay Detail

CHEMBL3873357

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

Binding
Displacement of [3H]-flunitrazepam from rat brain GABA-A receptor benzodiazepine site after 20 mins by liquid scintillation counting
13
Total Activities
13
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Organism Rattus norvegicus
Confidence 0 — Uncurated / Unknown
Curated By Autocuration

Target

Unchecked (CHEMBL612545)
Type UNCHECKED

Publication

Design, synthesis, and biological evaluation of fluorinated imidazo[1,2-a]pyridine derivatives with potential antipsychotic activity.
Marcinkowska M, Kołaczkowski M, Kamiński K, Bucki A, Pawłowski M, Siwek A, Karcz T, Mordyl B, Starowicz G, Kubowicz P, Pękala E, Wesołowska A, Samochowiec J, Mierzejewski P, Bienkowski P.
Eur J Med Chem (2016) 124 : 456 -467
PubMed 27598234 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
Ki 13 6.86 7.60

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL3962969 1 7.60
CHEMBL911 ZOLPIDEM 4.0 1 7.36
CHEMBL3954951 1 7.25
CHEMBL3975584 1 7.24
CHEMBL3971200 1 7.22
CHEMBL3970126 1 7.17
CHEMBL3979360 1 6.89
CHEMBL3959035 1 6.85
CHEMBL3890007 1 6.75
CHEMBL3983568 1 6.31
CHEMBL3894769 1 6.29
CHEMBL3937382 1 6.14
CHEMBL3966116 1 6.08

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL3962969 Ki = 25.0 nM 7.60
CHEMBL911 ZOLPIDEM Ki = 44.0 nM 7.36
CHEMBL3954951 Ki = 55.6 nM 7.25
CHEMBL3975584 Ki = 57.5 nM 7.24
CHEMBL3971200 Ki = 59.6 nM 7.22
CHEMBL3970126 Ki = 68.0 nM 7.17
CHEMBL3979360 Ki = 130.0 nM 6.89
CHEMBL3959035 Ki = 140.0 nM 6.85
CHEMBL3890007 Ki = 180.0 nM 6.75
CHEMBL3983568 Ki = 487.0 nM 6.31
CHEMBL3894769 Ki = 510.0 nM 6.29
CHEMBL3937382 Ki = 730.0 nM 6.14
CHEMBL3966116 Ki = 830.0 nM 6.08