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Assay Detail

CHEMBL796735

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

Functional
Inhibition of [3H]spiroperidol binding to rat striatal membrane using 0.5 nM ligand.
4
Total Activities
4
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Functional
Organism Rattus norvegicus
Tissue Striatum
Subcellular Membrane
Confidence 1 — Organism
Curated By Intermediate

Target

Rattus norvegicus (CHEMBL376)
Type ORGANISM
Organism Rattus norvegicus

Publication

4a,9b-trans-8-Fluoro-5-(4-fluorophenyl)-2-[4-(4-fluorophenyl)-4-hydroxybutyl]-2,3,4,4a,5,9b-hexahydro-1H-pyrido[4,3-b]indole hydrochloride, a new potent neuroleptic.
Welch WM, Ewing FE, Harbert CA, Weissman A, Koe BK.
J Med Chem (1980) 23 : 949 -952
PubMed 6105220 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 4 7.61 7.85

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL57241 FLUTROLINE 2.0 1 7.85
CHEMBL175301 1 7.66
CHEMBL174762 1 7.64
CHEMBL71 CHLORPROMAZINE 4.0 1 7.29

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL57241 FLUTROLINE IC50 = 14.0 nM 7.85
CHEMBL175301 IC50 = 22.0 nM 7.66
CHEMBL174762 IC50 = 23.0 nM 7.64
CHEMBL71 CHLORPROMAZINE IC50 = 51.0 nM 7.29