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Assay Detail

CHEMBL616573

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

Binding
Tested in vitro for binding affinity by measuring its ability to inhibit [3H]8-OH-DPAT binding at 5-hydroxytryptamine 1A receptor in rat cerebral cortex membranes.
38
Total Activities
38
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Tissue Cerebral cortex
Confidence 8 — Homologous single protein target
Curated By Expert

Target

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

Publication

Synthesis and structure-activity relationships of a new model of arylpiperazines. 2. Three-dimensional quantitative structure-activity relationships of hydantoin-phenylpiperazine derivatives with affinity for 5-HT1A and alpha 1 receptors. A comparison of CoMFA models.
López-Rodríguez ML, Rosado ML, Benhamú B, Morcillo MJ, Fernández E, Schaper KJ.
J Med Chem (1997) 40 : 1648 -1656
PubMed 9171874 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
Ki 38 6.86 8.62

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL46918 1 8.62
CHEMBL42706 1 8.42
CHEMBL43992 1 8.39
CHEMBL289873 1 8.36
CHEMBL42810 1 8.26
CHEMBL45253 1 8.24
CHEMBL42644 1 8.14
CHEMBL46881 1 8.06
CHEMBL417709 1 8.00
CHEMBL290039 1 7.95
CHEMBL290203 1 7.72
CHEMBL43332 1 7.61
CHEMBL296713 1 7.34
CHEMBL44786 1 7.27
CHEMBL416984 1 7.25
CHEMBL296413 1 7.24
CHEMBL42396 1 7.18
CHEMBL42404 1 7.11
CHEMBL46885 1 7.05
CHEMBL1202594 1 6.99
CHEMBL47200 1 6.91
CHEMBL46525 1 6.89
CHEMBL41978 1 6.81
CHEMBL46535 1 6.63
CHEMBL46802 1 6.38
CHEMBL45007 1 6.22
CHEMBL46677 1 5.93
CHEMBL291165 1 5.87
CHEMBL44876 1 5.59
CHEMBL296724 1 5.12

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL46918 Ki = 2.4 nM 8.62
CHEMBL42706 Ki = 3.8 nM 8.42
CHEMBL43992 Ki = 4.1 nM 8.39
CHEMBL289873 Ki = 4.4 nM 8.36
CHEMBL42810 Ki = 5.5 nM 8.26
CHEMBL45253 Ki = 5.7 nM 8.24
CHEMBL42644 Ki = 7.2 nM 8.14
CHEMBL46881 Ki = 8.8 nM 8.06
CHEMBL417709 Ki = 9.9 nM 8.00
CHEMBL290039 Ki = 11.3 nM 7.95
CHEMBL290203 Ki = 19.2 nM 7.72
CHEMBL43332 Ki = 24.8 nM 7.61
CHEMBL296713 Ki = 45.5 nM 7.34
CHEMBL44786 Ki = 53.6 nM 7.27
CHEMBL416984 Ki = 55.9 nM 7.25
CHEMBL296413 Ki = 57.9 nM 7.24
CHEMBL42396 Ki = 65.8 nM 7.18
CHEMBL42404 Ki = 78.5 nM 7.11
CHEMBL46885 Ki = 89.9 nM 7.05
CHEMBL1202594 Ki = 102.0 nM 6.99
CHEMBL47200 Ki = 123.0 nM 6.91
CHEMBL46525 Ki = 128.0 nM 6.89
CHEMBL41978 Ki = 154.0 nM 6.81
CHEMBL46535 Ki = 234.0 nM 6.63
CHEMBL46802 Ki = 418.0 nM 6.38
CHEMBL45007 Ki = 598.0 nM 6.22
CHEMBL46677 Ki = 1183.0 nM 5.93
CHEMBL291165 Ki = 1349.0 nM 5.87
CHEMBL44876 Ki = 2582.0 nM 5.59
CHEMBL296724 Ki = 7550.0 nM 5.12
CHEMBL289784 Ki = 19274.0 nM 4.71
CHEMBL432495 Ki = 23932.0 nM 4.62
CHEMBL47040 Ki = 23932.0 nM 4.62
CHEMBL298286 Ki = 30618.0 nM 4.51
CHEMBL42219 Ki = 93590.0 nM 4.03
CHEMBL46377 Ki = 168260.0 nM -
CHEMBL297882 Ki > 10000.0 nM -
CHEMBL46651 Ki = 501187.0 nM -