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Assay Detail

CHEMBL807663

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

Binding
Inhibition of type-2 human steroid 5-alpha-reductase.
14
Total Activities
14
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

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

Target

3-oxo-5-alpha-steroid 4-dehydrogenase 2 (CHEMBL1856)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

A comparison of steroidal and non-steroidal inhibitors of human steroid 5-reductase: New tricyclic aryl acid inhibitors of the type-1 isozyme
Abell AD, Brandt M, Levy MA, Holt DA
Bioorg Med Chem Lett (1996) 6 : 481 -484
· DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
Ki 14 7.22 10.10

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL420020 1 10.10
CHEMBL138225 EPRISTERIDE 2.0 1 9.70
CHEMBL1627951 1 9.40
CHEMBL76192 1 9.05
CHEMBL143220 1 8.89
CHEMBL2298601 1 8.70
CHEMBL110001 1 7.52
CHEMBL25081 1 6.58
CHEMBL439804 1 5.80
CHEMBL356780 1 5.60
CHEMBL144346 1 5.00
CHEMBL341625 1 5.00
CHEMBL25578 1 5.00
CHEMBL97266 1 4.70

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL420020 Ki = 0.08 nM 10.10
CHEMBL138225 EPRISTERIDE Ki = 0.2 nM 9.70
CHEMBL1627951 Ki = 0.4 nM 9.40
CHEMBL76192 Ki = 0.89 nM 9.05
CHEMBL143220 Ki = 1.3 nM 8.89
CHEMBL2298601 Ki = 2.0 nM 8.70
CHEMBL110001 Ki = 30.0 nM 7.52
CHEMBL25081 Ki = 260.0 nM 6.58
CHEMBL439804 Ki = 1600.0 nM 5.80
CHEMBL356780 Ki = 2500.0 nM 5.60
CHEMBL144346 Ki = 10000.0 nM 5.00
CHEMBL341625 Ki = 10000.0 nM 5.00
CHEMBL25578 Ki = 10000.0 nM 5.00
CHEMBL97266 Ki = 20000.0 nM 4.70