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Assay Detail

CHEMBL803262

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

Binding
Inhibition of [3H]- 8-OH-DPAT binding to 5-HT1A-receptor from rat cerebral cortex membranes
15
Total Activities
15
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Organism Rattus norvegicus
Tissue Cerebral cortex
Subcellular Membrane
Confidence 9 — Direct single protein target
Curated By Expert

Target

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

Publication

C8-substituted derivatives of 2-(dipropylamino)tetralin: Palladium-catalyzed synthesis and interactions with 5-HT1A-receptors
Liu Y, Svensson BE, Yu H, Cortizo L, Ross SB, Lewander T, Hacksell U
Bioorg Med Chem Lett (1991) 1 : 257 -262
· DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
Ki 15 8.16 9.15

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL87195 1 9.15
CHEMBL90053 1 8.82
CHEMBL316050 1 8.77
CHEMBL87348 1 8.74
CHEMBL315684 1 8.55
CHEMBL89014 1 8.42
CHEMBL86648 1 8.37
CHEMBL87105 1 8.11
CHEMBL88994 1 8.02
CHEMBL88157 1 7.77
CHEMBL88997 1 7.62
CHEMBL316161 1 7.47
CHEMBL88504 1 7.25
CHEMBL88297 1 7.21
CHEMBL26922 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL87195 Ki = 0.7 nM 9.15
CHEMBL90053 Ki = 1.5 nM 8.82
CHEMBL316050 Ki = 1.7 nM 8.77
CHEMBL87348 Ki = 1.8 nM 8.74
CHEMBL315684 Ki = 2.8 nM 8.55
CHEMBL89014 Ki = 3.8 nM 8.42
CHEMBL86648 Ki = 4.3 nM 8.37
CHEMBL87105 Ki = 7.7 nM 8.11
CHEMBL88994 Ki = 9.5 nM 8.02
CHEMBL88157 Ki = 17.0 nM 7.77
CHEMBL88997 Ki = 24.0 nM 7.62
CHEMBL316161 Ki = 34.0 nM 7.47
CHEMBL88504 Ki = 56.0 nM 7.25
CHEMBL88297 Ki = 62.0 nM 7.21
CHEMBL26922 Ki > 300.0 nM -