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Assay Detail

CHEMBL860939

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Binding
Inhibition of human CYP11B1 expressed in V79 11B1 cells
18
Total Activities
18
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Organism Homo sapiens
Cell Type V79
Confidence 9 — Direct single protein target
Curated By Expert

Target

Cytochrome P450 11B1, mitochondrial (CHEMBL1908)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

Synthesis and evaluation of heteroaryl-substituted dihydronaphthalenes and indenes: potent and selective inhibitors of aldosterone synthase (CYP11B2) for the treatment of congestive heart failure and myocardial fibrosis.
Voets M, Antes I, Scherer C, Müller-Vieira U, Biemel K, Marchais-Oberwinkler S, Hartmann RW.
J Med Chem (2006) 49 : 2222 -2231
PubMed 16570918 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 18 6.10 8.00

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL9298 FADROZOLE 2.0 1 8.00
CHEMBL157101 KETOCONAZOLE 4.0 1 6.65
CHEMBL206125 1 6.54
CHEMBL206550 1 6.30
CHEMBL206351 1 6.24
CHEMBL208471 1 6.19
CHEMBL207751 1 6.12
CHEMBL206283 1 5.90
CHEMBL206070 1 5.89
CHEMBL205250 1 5.79
CHEMBL205881 1 5.76
CHEMBL205503 1 5.67
CHEMBL205782 1 5.62
CHEMBL425054 1 5.60
CHEMBL206300 1 5.25
CHEMBL377576 1 -
CHEMBL206273 1 -
CHEMBL207829 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL9298 FADROZOLE IC50 = 10.0 nM 8.00
CHEMBL157101 KETOCONAZOLE IC50 = 224.0 nM 6.65
CHEMBL206125 IC50 = 288.0 nM 6.54
CHEMBL206550 IC50 = 503.0 nM 6.30
CHEMBL206351 IC50 = 578.0 nM 6.24
CHEMBL208471 IC50 = 639.0 nM 6.19
CHEMBL207751 IC50 = 763.0 nM 6.12
CHEMBL206283 IC50 = 1268.0 nM 5.90
CHEMBL206070 IC50 = 1291.0 nM 5.89
CHEMBL205250 IC50 = 1615.0 nM 5.79
CHEMBL205881 IC50 = 1729.0 nM 5.76
CHEMBL205503 IC50 = 2117.0 nM 5.67
CHEMBL205782 IC50 = 2391.0 nM 5.62
CHEMBL425054 IC50 = 2529.0 nM 5.60
CHEMBL206300 IC50 = 5684.0 nM 5.25
CHEMBL377576 IC50 - -
CHEMBL206273 IC50 - -
CHEMBL207829 IC50 - -