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Assay Detail

CHEMBL2340951

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

Binding
Inhibition of human CYP17 expressed in Escherichia coli co-expressing rat NADPH-P450-reductase using progesterone as substrate
17
Total Activities
17
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

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

Target

Steroid 17-alpha-hydroxylase/17,20 lyase (CHEMBL3522)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

Modulation of cytochromes P450 with xanthone-based molecules: from aromatase to aldosterone synthase and steroid 11β-hydroxylase inhibition.
Gobbi S, Hu Q, Negri M, Zimmer C, Belluti F, Rampa A, Hartmann RW, Bisi A.
J Med Chem (2013) 56 : 1723 -1729
PubMed 23363058 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 17 6.40 7.38

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL78322 1 7.38
CHEMBL254328 ABIRATERONE 3.0 1 7.14
CHEMBL307160 1 6.89
CHEMBL442373 1 6.66
CHEMBL2333326 1 6.58
CHEMBL2333336 1 6.31
CHEMBL2333329 1 6.21
CHEMBL2333331 1 5.90
CHEMBL2333327 1 5.87
CHEMBL2333337 1 5.76
CHEMBL2333328 1 5.72
CHEMBL2333332 1 -
CHEMBL2333330 1 -
CHEMBL2333333 1 -
CHEMBL2333334 1 -
CHEMBL2333335 1 -
CHEMBL9298 FADROZOLE 2.0 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL78322 IC50 = 42.0 nM 7.38
CHEMBL254328 ABIRATERONE IC50 = 72.0 nM 7.14
CHEMBL307160 IC50 = 130.0 nM 6.89
CHEMBL442373 IC50 = 220.0 nM 6.66
CHEMBL2333326 IC50 = 260.0 nM 6.58
CHEMBL2333336 IC50 = 493.0 nM 6.31
CHEMBL2333329 IC50 = 610.0 nM 6.21
CHEMBL2333331 IC50 = 1250.0 nM 5.90
CHEMBL2333327 IC50 = 1346.0 nM 5.87
CHEMBL2333337 IC50 = 1737.0 nM 5.76
CHEMBL2333328 IC50 = 1886.0 nM 5.72
CHEMBL2333332 IC50 > 5000.0 nM -
CHEMBL2333330 IC50 > 5000.0 nM -
CHEMBL2333333 IC50 > 5000.0 nM -
CHEMBL2333334 IC50 > 5000.0 nM -
CHEMBL2333335 IC50 > 5000.0 nM -
CHEMBL9298 FADROZOLE IC50 > 5000.0 nM -