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Assay Detail

CHEMBL5376053

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

Binding
Inhibition of human recombinant aromatase in JEG-3 cells using [1beta-3H]androstenedione as substarte incubated for 3 hr by scintillation counting analysis
4
Total Activities
4
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Organism Homo sapiens
Cell Type JEG-3
Confidence 9 — Direct single protein target
Curated By Autocuration

Target

Aromatase (CHEMBL1978)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

Combating breast cancer with non-steroidal aromatase inhibitors (NSAIs): Understanding the chemico-biological interactions through comparative SAR/QSAR study.
Adhikari N, Amin SA, Saha A, Jha T.
Eur J Med Chem (2017) 137 : 365 -438
PubMed 28622580 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 4 4.20 4.20

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL3622062 1 4.20
CHEMBL3622063 1 -
CHEMBL5397563 1 -
CHEMBL5398997 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL3622062 IC50 = 62517.27 nM 4.20
CHEMBL3622063 IC50 = 99083194.49 nM -
CHEMBL5397563 IC50 = 156675107.01 nM -
CHEMBL5398997 IC50 = 749894209.33 nM -