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TargetNF-kappa-B inhibitor alpha
LigandBDBM50227494
Substrate/Competitorn/a
Meas. Tech.ChEMBL_465169 (CHEMBL946815)
EC50 17000±n/a nM
Citation Xie, YDeng, SThomas, CJLiu, YZhang, YQRinderspacher, AHuang, WGong, GWyler, MCayanis, EAulner, NTöbben, UChung, CPampou, SSouthall, NVidovic, DSchürer, SBranden, LDavis, REStaudt, LMInglese, JAustin, CPLandry, DWSmith, DHAuld, 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
More Info.:Get all data from this article,  Assay Method
 
NF-kappa-B inhibitor alpha
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
Blast this sequence in BindingDB or PDB
  Blast E-value cutoff:
BDBM50227494
n/a
NameBDBM50227494
Synonyms:CHEMBL257286 | N-(quinolin-8-yl)benzenesulfonamide | N-Quinolin-8-yl-benzenesulfonamide | cid_161167
TypeSmall organic molecule
Emp. Form.C15H12N2O2S
Mol. Mass.284.333
SMILESO=S(=O)(Nc1cccc2cccnc12)c1ccccc1
Structure
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