Reaction Details |
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Target | NF-kappa-B inhibitor alpha |
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Ligand | BDBM50227494 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_465171 (CHEMBL945841) |
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EC50 | 20000±n/a nM |
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Citation | Xie, Y; Deng, S; Thomas, CJ; Liu, Y; Zhang, YQ; Rinderspacher, A; Huang, W; Gong, G; Wyler, M; Cayanis, E; Aulner, N; Többen, U; Chung, C; Pampou, S; Southall, N; Vidovic, D; Schürer, S; Branden, L; Davis, RE; Staudt, LM; Inglese, J; Austin, CP; Landry, DW; Smith, DH; Auld, DS Identification of N-(quinolin-8-yl)benzenesulfonamides as agents capable of down-regulating NFkappaB activity within two separate high-throughput screens of NFkappaB activation. Bioorg Med Chem Lett18:329-35 (2008) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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NF-kappa-B inhibitor alpha |
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Name: | NF-kappa-B inhibitor alpha |
Synonyms: | I-kappa-B-alpha | IKBA | IKBA_HUMAN | MAD3 | NF-kappa-B inhibitor alpha | NFKBI | NFKBIA |
Type: | GST fusion protein |
Mol. Mass.: | 35584.84 |
Organism: | Homo sapiens (Human) |
Description: | It was produced in E. coli as GST-tagged fusion protein (Santa Cruz Biotechnology). |
Residue: | 317 |
Sequence: | MFQAAERPQEWAMEGPRDGLKKERLLDDRHDSGLDSMKDEEYEQMVKELQEIRLEPQEVP
RGSEPWKQQLTEDGDSFLHLAIIHEEKALTMEVIRQVKGDLAFLNFQNNLQQTPLHLAVI
TNQPEIAEALLGAGCDPELRDFRGNTPLHLACEQGCLASVGVLTQSCTTPHLHSILKATN
YNGHTCLHLASIHGYLGIVELLVSLGADVNAQEPCNGRTALHLAVDLQNPDLVSLLLKCG
ADVNRVTYQGYSPYQLTWGRPSTRIQQQLGQLTLENLQMLPESEDEESYDTESEFTEFTE
DELPYDDCVFGGQRLTL
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BDBM50227494 |
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n/a |
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Name | BDBM50227494 |
Synonyms: | CHEMBL257286 | N-(quinolin-8-yl)benzenesulfonamide | N-Quinolin-8-yl-benzenesulfonamide | cid_161167 |
Type | Small organic molecule |
Emp. Form. | C15H12N2O2S |
Mol. Mass. | 284.333 |
SMILES | O=S(=O)(Nc1cccc2cccnc12)c1ccccc1 |
Structure |
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