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Assay Detail

CHEMBL880029

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

Binding
Inhibition of solubilized, purified rat liver HMG-CoA reductase.
20
Total Activities
20
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Confidence 8 — Homologous single protein target
Curated By Expert

Target

3-hydroxy-3-methylglutaryl-coenzyme A reductase (CHEMBL3247)
Type SINGLE PROTEIN
Organism Rattus norvegicus

Publication

3-Hydroxy-3-methylglutaryl-coenzyme A reductase inhibitors. 4. Side chain ester derivatives of mevinolin.
Hoffman WF, Alberts AW, Anderson PS, Chen JS, Smith RL, Willard AK.
J Med Chem (1986) 29 : 849 -852
PubMed 3634830 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 20 8.08 9.05

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL3349544 1 9.05
CHEMBL3349956 1 8.85
CHEMBL3349944 1 8.85
CHEMBL3349955 1 8.72
CHEMBL333443 1 8.66
CHEMBL3349951 1 8.66
CHEMBL3349950 1 8.57
CHEMBL3349954 1 8.54
CHEMBL3349952 1 8.46
CHEMBL3349946 1 8.42
CHEMBL3349949 1 8.27
CHEMBL3349960 1 8.11
CHEMBL3349958 1 8.06
CHEMBL3085466 1 7.72
CHEMBL3349945 1 7.56
CHEMBL3349948 1 7.43
CHEMBL3349953 1 7.41
CHEMBL3349947 1 7.08
CHEMBL3349957 1 6.57
CHEMBL3349959 1 6.53

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL3349544 IC50 = 0.9 nM 9.05
CHEMBL3349956 IC50 = 1.4 nM 8.85
CHEMBL3349944 IC50 = 1.4 nM 8.85
CHEMBL3349955 IC50 = 1.9 nM 8.72
CHEMBL333443 IC50 = 2.2 nM 8.66
CHEMBL3349951 IC50 = 2.2 nM 8.66
CHEMBL3349950 IC50 = 2.7 nM 8.57
CHEMBL3349954 IC50 = 2.9 nM 8.54
CHEMBL3349952 IC50 = 3.5 nM 8.46
CHEMBL3349946 IC50 = 3.8 nM 8.42
CHEMBL3349949 IC50 = 5.4 nM 8.27
CHEMBL3349960 IC50 = 7.7 nM 8.11
CHEMBL3349958 IC50 = 8.7 nM 8.06
CHEMBL3085466 IC50 = 19.0 nM 7.72
CHEMBL3349945 IC50 = 27.3 nM 7.56
CHEMBL3349948 IC50 = 37.0 nM 7.43
CHEMBL3349953 IC50 = 38.6 nM 7.41
CHEMBL3349947 IC50 = 83.0 nM 7.08
CHEMBL3349957 IC50 = 269.0 nM 6.57
CHEMBL3349959 IC50 = 295.0 nM 6.53