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Assay Detail

CHEMBL4672389

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

Binding
Inhibition of N-His6-tagged human AspH (315-755) expressed in Escherichia coli BL21 (DE3) using 1 uM hFX-CP as substrate mixture with high 200 uM 2OG, 100 uM L-ascorbic acid and 2 uM FAS incubated for 35 mins by MS analysis
12
Total Activities
12
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

Aspartyl/asparaginyl beta-hydroxylase (CHEMBL4680030)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

Small-molecule active pharmaceutical ingredients of approved cancer therapeutics inhibit human aspartate/asparagine-β-hydroxylase.
Brewitz L,Tumber A,Zhang X,Schofield CJ
Bioorg Med Chem (2020) 28 : 115675 -115675
PubMed 33069066 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 12 5.48 7.00

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL316034 1 7.00
CHEMBL51483 GOSSYPOL 3.0 1 6.60
CHEMBL443684 NAVITOCLAX 3.0 1 5.88
CHEMBL3137309 VENETOCLAX 4.0 1 5.82
CHEMBL6067492 BLEOMYCIN 4.0 1 5.42
CHEMBL376408 ABT 737 1.0 1 5.35
CHEMBL356769 TUBACIN 1 5.25
CHEMBL408513 BELINOSTAT 4.0 1 4.95
CHEMBL608533 MIDOSTAURIN 4.0 1 4.91
CHEMBL257619 1 4.91
CHEMBL1229517 VEMURAFENIB 4.0 1 4.82
CHEMBL4777255 1 4.79

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL316034 IC50 = 100.0 nM 7.00
CHEMBL51483 GOSSYPOL IC50 = 250.0 nM 6.60
CHEMBL443684 NAVITOCLAX IC50 = 1330.0 nM 5.88
CHEMBL3137309 VENETOCLAX IC50 = 1520.0 nM 5.82
CHEMBL6067492 BLEOMYCIN IC50 = 3810.0 nM 5.42
CHEMBL376408 ABT 737 IC50 = 4470.0 nM 5.35
CHEMBL356769 TUBACIN IC50 = 5690.0 nM 5.25
CHEMBL408513 BELINOSTAT IC50 = 11200.0 nM 4.95
CHEMBL608533 MIDOSTAURIN IC50 = 12400.0 nM 4.91
CHEMBL257619 IC50 = 12200.0 nM 4.91
CHEMBL1229517 VEMURAFENIB IC50 = 15100.0 nM 4.82
CHEMBL4777255 IC50 = 16400.0 nM 4.79