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Assay Detail

CHEMBL859877

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Binding
Inhibitory activity against IKK1
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 Expert

Publication

Design and preparation of 2-benzamido-pyrimidines as inhibitors of IKK.
Waelchli R, Bollbuck B, Bruns C, Buhl T, Eder J, Feifel R, Hersperger R, Janser P, Revesz L, Zerwes HG, Schlapbach A.
Bioorg Med Chem Lett (2006) 16 : 108 -112
PubMed 16236504 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 20 6.20 7.52

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL199837 1 7.52
CHEMBL382945 1 7.52
CHEMBL372736 1 7.00
CHEMBL200229 1 6.82
CHEMBL200027 1 6.70
CHEMBL199980 1 6.40
CHEMBL381041 1 6.30
CHEMBL200106 1 6.30
CHEMBL371543 1 6.16
CHEMBL200462 1 6.00
CHEMBL371967 1 5.92
CHEMBL200832 1 5.92
CHEMBL370166 1 5.43
CHEMBL382752 1 5.42
CHEMBL200946 1 5.30
CHEMBL372160 1 4.52
CHEMBL372345 1 -
CHEMBL200892 1 -
CHEMBL200860 1 -
CHEMBL200191 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL199837 IC50 = 30.0 nM 7.52
CHEMBL382945 IC50 = 30.0 nM 7.52
CHEMBL372736 IC50 = 100.0 nM 7.00
CHEMBL200229 IC50 = 150.0 nM 6.82
CHEMBL200027 IC50 = 200.0 nM 6.70
CHEMBL199980 IC50 = 400.0 nM 6.40
CHEMBL381041 IC50 = 500.0 nM 6.30
CHEMBL200106 IC50 = 500.0 nM 6.30
CHEMBL371543 IC50 = 700.0 nM 6.16
CHEMBL200462 IC50 = 1000.0 nM 6.00
CHEMBL371967 IC50 = 1200.0 nM 5.92
CHEMBL200832 IC50 = 1200.0 nM 5.92
CHEMBL370166 IC50 = 3700.0 nM 5.43
CHEMBL382752 IC50 = 3800.0 nM 5.42
CHEMBL200946 IC50 = 5000.0 nM 5.30
CHEMBL372160 IC50 = 30000.0 nM 4.52
CHEMBL372345 IC50 > 100000.0 nM -
CHEMBL200892 IC50 - -
CHEMBL200860 IC50 - -
CHEMBL200191 IC50 - -