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Assay Detail

CHEMBL645684

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

Binding
Percent inhibition against binding of [3H]prazosin to cloned mammalian Alpha-1 adrenergic receptor expressed in cultured cells or from rat whole brain at 1 uM
3
Total Activities
3
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Confidence 4 — Cell-line / Tissue
Curated By Autocuration

Target

Adrenergic receptor alpha-1 (CHEMBL1907610)
Type PROTEIN FAMILY
Organism Rattus norvegicus

Publication

(S)-(-)-4-[4-[2-(isochroman-1-yl)ethyl]-piperazin-1-yl] benzenesulfonamide, a selective dopamine D4 antagonist.
TenBrink RE, Bergh CL, Duncan JN, Harris DW, Huff RM, Lahti RA, Lawson CF, Lutzke BS, Martin IJ, Rees SA, Schlachter SK, Sih JC, Smith MW.
J Med Chem (1996) 39 : 2435 -2437
PubMed 8691438 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
Ki 3 6.66 7.42

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL81330 1 7.42
CHEMBL71724 1 5.89
CHEMBL69759 SONEPIPRAZOLE 2.0 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL81330 Ki = 38.0 nM 7.42
CHEMBL71724 Ki = 1280.0 nM 5.89
CHEMBL69759 SONEPIPRAZOLE Ki > 4900.0 nM -