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Assay Detail

CHEMBL838856

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

Binding
In vitro ability to displace the radioligand [3H]-OH-DPAT from binding to rat 5-hydroxytryptamine 1A receptor
10
Total Activities
10
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

The impact of spacer structure on 5-HT7 and 5-HT1A receptor affinity in the group of long-chain arylpiperazine ligands.
Bojarski AJ, Duszyńska B, Kołaczkowski M, Kowalski P, Kowalska T.
Bioorg Med Chem Lett (2004) 14 : 5863 -5866
PubMed 15501057 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
Ki 10 7.59 9.22

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL8618 NAN-190 1 9.22
CHEMBL186334 1 8.30
CHEMBL279841 1 8.19
CHEMBL441313 1 8.10
CHEMBL187270 1 7.82
CHEMBL365412 1 7.54
CHEMBL365201 1 7.11
CHEMBL186734 1 6.80
CHEMBL185988 1 6.39
CHEMBL185936 1 6.38

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL8618 NAN-190 Ki = 0.6 nM 9.22
CHEMBL186334 Ki = 5.0 nM 8.30
CHEMBL279841 Ki = 6.4 nM 8.19
CHEMBL441313 Ki = 8.0 nM 8.10
CHEMBL187270 Ki = 15.2 nM 7.82
CHEMBL365412 Ki = 29.0 nM 7.54
CHEMBL365201 Ki = 77.0 nM 7.11
CHEMBL186734 Ki = 157.0 nM 6.80
CHEMBL185988 Ki = 405.0 nM 6.39
CHEMBL185936 Ki = 415.0 nM 6.38