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Assay Detail

CHEMBL983954

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

Binding
Inhibition of human recombinant IKK2
20
Total Activities
20
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

Publication

4-Phenyl-7-azaindoles as potent and selective IKK2 inhibitors.
Liddle J, Bamborough P, Barker MD, Campos S, Cousins RP, Cutler GJ, Hobbs H, Holmes DS, Ioannou C, Mellor GW, Morse MA, Payne JJ, Pritchard JM, Smith KJ, Tape DT, Whitworth C, Williamson RA.
Bioorg Med Chem Lett (2009) 19 : 2504 -2508
PubMed 19349179 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 20 7.01 7.80

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL520473 1 7.80
CHEMBL483165 1 7.70
CHEMBL519965 1 7.70
CHEMBL482747 1 7.70
CHEMBL483557 1 7.70
CHEMBL482539 1 7.50
CHEMBL473080 1 7.40
CHEMBL483166 1 7.40
CHEMBL482540 1 7.40
CHEMBL520308 1 7.40
CHEMBL485145 1 7.20
CHEMBL482746 1 7.10
CHEMBL453707 1 6.80
CHEMBL520954 1 6.70
CHEMBL520655 1 6.60
CHEMBL484966 1 6.50
CHEMBL519028 1 6.50
CHEMBL504261 1 6.20
CHEMBL482538 1 5.50
CHEMBL482553 1 5.30

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL520473 IC50 = 15.85 nM 7.80
CHEMBL483165 IC50 = 19.95 nM 7.70
CHEMBL519965 IC50 = 19.95 nM 7.70
CHEMBL482747 IC50 = 19.95 nM 7.70
CHEMBL483557 IC50 = 19.95 nM 7.70
CHEMBL482539 IC50 = 31.62 nM 7.50
CHEMBL473080 IC50 = 39.81 nM 7.40
CHEMBL483166 IC50 = 39.81 nM 7.40
CHEMBL482540 IC50 = 39.81 nM 7.40
CHEMBL520308 IC50 = 39.81 nM 7.40
CHEMBL485145 IC50 = 63.1 nM 7.20
CHEMBL482746 IC50 = 79.43 nM 7.10
CHEMBL453707 IC50 = 158.49 nM 6.80
CHEMBL520954 IC50 = 199.53 nM 6.70
CHEMBL520655 IC50 = 251.19 nM 6.60
CHEMBL484966 IC50 = 316.23 nM 6.50
CHEMBL519028 IC50 = 316.23 nM 6.50
CHEMBL504261 IC50 = 630.96 nM 6.20
CHEMBL482538 IC50 = 3162.28 nM 5.50
CHEMBL482553 IC50 = 5011.87 nM 5.30