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Assay Detail

CHEMBL644947

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

Binding
The concentration required to inhibit 3[H]prazosin binding to Alpha-1 adrenergic receptor in rat brain membranes was measured (in vitro)
1
Total Activities
1
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

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

Target

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

Publication

Naphthosultam derivatives: a new class of potent and selective 5-HT2 antagonists.
Malleron JL, Comte MT, Gueremy C, Peyronel JF, Truchon A, Blanchard JC, Doble A, Piot O, Zundel JL, Huon C.
J Med Chem (1991) 34 : 2477 -2483
PubMed 1908521 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 1 7.96 7.96

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL82826 1 7.96

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL82826 IC50 = 11.0 nM 7.96