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Assay Detail

CHEMBL642090

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

Binding
Binding affinity against native Alpha-1 adrenergic receptor from rat cerebral cortex using radioligand [3H]-prazosin binding assay
6
Total Activities
6
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

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

Target

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

Publication

Synthesis and biological profile of the enantiomers of [4-(4-amino-6,7-dimethoxyquinazolin-2-yl)-cis-octahydroquinoxalin- 1-yl]furan-2-ylmethanone (cyclazosin), a potent competitive alpha 1B- adrenoceptor antagonist.
Giardinà D, Crucianelli M, Romanelli R, Leonardi A, Poggesi E, Melchiorre C.
J Med Chem (1996) 39 : 4602 -4607
PubMed 8917649 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
Ki 6 8.43 9.25

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL97698 1 9.25
CHEMBL2 PRAZOSIN 4.0 1 9.13
CHEMBL423294 CYCLAZOSIN 1 9.10
CHEMBL342062 1 8.28
CHEMBL267930 SPIPERONE 2.0 1 8.16
CHEMBL140450 1 6.65

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL97698 Ki = 0.5623 nM 9.25
CHEMBL2 PRAZOSIN Ki = 0.7413 nM 9.13
CHEMBL423294 CYCLAZOSIN Ki = 0.7943 nM 9.10
CHEMBL342062 Ki = 5.248 nM 8.28
CHEMBL267930 SPIPERONE Ki = 6.918 nM 8.16
CHEMBL140450 Ki = 223.87 nM 6.65