Reaction Details | |||
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Target | Inhibitor of nuclear factor kappa-B kinase subunit beta | ||
Ligand | BDBM50357884 | ||
Substrate/Competitor | n/a | ||
Meas. Tech. | ChEMBL_786761 (CHEMBL1919602) | ||
IC50 | >10000±n/a nM | ||
Citation | Lumeras, W; Vidal, L; Vidal, B; Balagué, C; Orellana, A; Maldonado, M; Domínguez, M; Segarra, V; Caturla, F 1,7-Naphthyridine 1-oxides as novel potent and selective inhibitors of p38 mitogen activated protein kinase. J Med Chem54:7899-910 (2011) [PubMed] Article | ||
More Info.: | Get all data from this article, Assay Method | ||
Inhibitor of nuclear factor kappa-B kinase subunit beta | |||
Name: | Inhibitor of nuclear factor kappa-B kinase subunit beta | ||
Synonyms: | I-kappa-B Kinase 2 (IKK-beta) | I-kappa-B kinase 2 | I-kappa-B-kinase beta | I-kappa-B-kinase beta (IKKB) | IKBKB | IKK-B | IKK-beta | IKK2 | IKK2/IKK1 | IKKB | IKKB_HUMAN | Inhibitor of NF-kappa-B kinase alpha/beta | Inhibitor of nuclear factor kappa B kinase beta subunit | NFKBIKB | Nuclear factor NF-kappa-B inhibitor kinase beta | ||
Type: | Serine/threonine-protein kinase | ||
Mol. Mass.: | 86554.39 | ||
Organism: | Homo sapiens (Human) | ||
Description: | GST-tagged IKK-2 was expressed in High Five cells and purified. | ||
Residue: | 756 | ||
Sequence: |
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BDBM50357884 | |||
n/a | |||
Name | BDBM50357884 | ||
Synonyms: | CHEMBL1916359 | ||
Type | Small organic molecule | ||
Emp. Form. | C20H10Cl3FN2O | ||
Mol. Mass. | 419.664 | ||
SMILES | [O-][n+]1ccc2c(ccnc2c1-c1c(Cl)cccc1Cl)-c1ccc(F)cc1Cl |(12.75,-22.82,;14.08,-22.05,;14.08,-20.51,;15.41,-19.74,;16.75,-20.5,;18.08,-19.73,;19.42,-20.51,;19.42,-22.05,;18.08,-22.82,;16.74,-22.05,;15.42,-22.83,;15.42,-24.36,;14.08,-25.13,;12.75,-24.36,;14.09,-26.67,;15.42,-27.44,;16.76,-26.66,;16.75,-25.12,;18.08,-24.34,;18.08,-18.2,;19.42,-17.43,;19.42,-15.89,;18.08,-15.12,;18.08,-13.58,;16.75,-15.89,;16.75,-17.43,;15.42,-18.2,)| | ||
Structure |