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Assay Detail

CHEMBL615971

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

Binding
In vitro binding affinity against 5-hydroxytryptamine 1A receptor using [3H]8-OH-DPAT
11
Total Activities
11
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Organism Rattus norvegicus
Confidence 9 — Direct single protein target
Curated By Expert

Target

5-hydroxytryptamine receptor 1A (CHEMBL273)
Type SINGLE PROTEIN
Organism Rattus norvegicus

Publication

(S)- and (R)-8-(di-n-propylamino)-6,7,8,9-tetrahydro-3H-benz[e]indole-1- carbaldehyde: a new class of orally active 5-HT1A-receptor agonists.
Stjernlöf P, Gullme M, Elebring T, Andersson B, Wikström H, Lagerquist S, Svensson K, Ekman A, Carlsson A, Sundell S.
J Med Chem (1993) 36 : 2059 -2065
PubMed 8340910 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
Ki 11 7.83 8.89

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL304426 1 8.89
CHEMBL65274 1 8.85
CHEMBL63449 1 8.70
CHEMBL302172 1 8.15
CHEMBL41436 1 8.08
CHEMBL65196 1 7.92
CHEMBL302171 1 7.85
CHEMBL303339 1 7.60
CHEMBL413105 1 7.18
CHEMBL292274 1 6.72
CHEMBL305341 1 6.24

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL304426 Ki = 1.3 nM 8.89
CHEMBL65274 Ki = 1.4 nM 8.85
CHEMBL63449 Ki = 2.0 nM 8.70
CHEMBL302172 Ki = 7.0 nM 8.15
CHEMBL41436 Ki = 8.4 nM 8.08
CHEMBL65196 Ki = 12.0 nM 7.92
CHEMBL302171 Ki = 14.0 nM 7.85
CHEMBL303339 Ki = 25.0 nM 7.60
CHEMBL413105 Ki = 66.0 nM 7.18
CHEMBL292274 Ki = 190.0 nM 6.72
CHEMBL305341 Ki = 570.0 nM 6.24