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Assay Detail

CHEMBL3058327

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

Binding
Displacement of [3H]-Ro 15-4513 from Homo sapiens (human) recombinant GABAA alpha6beta3gamma2 receptor expressed in Ltk- cells after 1 hr by liquid scintillation counting
18
Total Activities
18
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Organism Homo sapiens
Cell Type Ltk-
Confidence 7 — Homologous single protein target
Curated By Autocuration

Target

GABA-A receptor; alpha-6/beta-3/gamma-2 (CHEMBL2095190)
Type PROTEIN COMPLEX
Organism Homo sapiens

Publication

Development of Selective Ligands for Benzodiazepine Receptor Subtypes by Manipulating the Substituents at Positions 3- and 7- of Optically Active BzR Ligands
Li X, Yu J, Atack JR, Cook JM
Med Chem Res (2004) 13 : 259 -281
· DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
Ki 18 6.88 7.34

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL2261918 1 7.34
CHEMBL336377 1 7.34
CHEMBL2261919 1 7.24
CHEMBL2261922 1 7.14
CHEMBL52030 1 7.08
CHEMBL339163 1 6.90
CHEMBL2261631 1 6.60
CHEMBL2261633 1 6.54
CHEMBL2261920 1 6.51
CHEMBL2261634 1 6.50
CHEMBL129855 1 6.47
CHEMBL2261917 1 -
CHEMBL2261916 1 -
CHEMBL2261915 1 -
CHEMBL2261921 1 -
CHEMBL2261923 1 -
CHEMBL2261632 1 -
CHEMBL2261630 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL2261918 Ki = 46.0 nM 7.34
CHEMBL336377 Ki = 46.0 nM 7.34
CHEMBL2261919 Ki = 58.0 nM 7.24
CHEMBL2261922 Ki = 72.0 nM 7.14
CHEMBL52030 Ki = 83.0 nM 7.08
CHEMBL339163 Ki = 125.0 nM 6.90
CHEMBL2261631 Ki = 251.0 nM 6.60
CHEMBL2261633 Ki = 292.0 nM 6.54
CHEMBL2261920 Ki = 308.0 nM 6.51
CHEMBL2261634 Ki = 320.0 nM 6.50
CHEMBL129855 Ki = 340.0 nM 6.47
CHEMBL2261917 Ki > 333.0 nM -
CHEMBL2261916 Ki > 333.0 nM -
CHEMBL2261915 Ki > 333.0 nM -
CHEMBL2261921 Ki > 333.0 nM -
CHEMBL2261923 Ki > 333.0 nM -
CHEMBL2261632 Ki > 333.0 nM -
CHEMBL2261630 Ki > 333.0 nM -