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Assay Detail

CHEMBL872066

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

Binding
Inhibition of recombinant rat adrenal 3-beta-hydroxy-delta-5-steroid dehydrogenase
4
Total Activities
4
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Confidence 0 — Uncurated / Unknown
Curated By Autocuration

Target

Unchecked (CHEMBL612545)
Type UNCHECKED

Publication

Structure-activity relationships for inhibition of type 1 and 2 human 5 alpha-reductase and human adrenal 3 beta-hydroxy-delta 5-steroid dehydrogenase/3-keto-delta 5-steroid isomerase by 6-azaandrost-4-en-3-ones: optimization of the C17 substituent.
Frye SV, Haffner CD, Maloney PR, Hiner RN, Dorsey GF, Noe RA, Unwalla RJ, Batchelor KW, Bramson HN, Stuart JD.
J Med Chem (1995) 38 : 2621 -2627
PubMed 7629802 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
Ki 4 7.00 7.30

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL327702 1 7.30
CHEMBL314953 1 7.01
CHEMBL277224 1 6.85
CHEMBL710 FINASTERIDE 4.0 1 6.82

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL327702 Ki = 50.0 nM 7.30
CHEMBL314953 Ki = 97.0 nM 7.01
CHEMBL277224 Ki = 140.0 nM 6.85
CHEMBL710 FINASTERIDE Ki = 150.0 nM 6.82