Reaction Details | |||
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Target | Transcription factor Jun | ||
Ligand | BDBM50279698 | ||
Substrate/Competitor | n/a | ||
Meas. Tech. | ChEMBL_545230 (CHEMBL1019824) | ||
IC50 | 5500±n/a nM | ||
Citation | Giri, RS; Thaker, HM; Giordano, T; Williams, J; Rogers, D; Sudersanam, V; Vasu, KK Design, synthesis and characterization of novel 2-(2,4-disubstituted-thiazole-5-yl)-3-aryl-3H-quinazoline-4-one derivatives as inhibitors of NF-kappaB and AP-1 mediated transcription activation and as potential anti-inflammatory agents. Eur J Med Chem44:2184-9 (2009) [PubMed] Article | ||
More Info.: | Get all data from this article, Assay Method | ||
Transcription factor Jun | |||
Name: | Transcription factor Jun | ||
Synonyms: | AP1 | Activator protein 1 | JUN | JUN_HUMAN | Proto-oncogene c-JUN | Transcription factor AP-1 | Transcription factor AP1 | V-jun avian sarcoma virus 17 oncogene homolog | p39 | ||
Type: | n/a | ||
Mol. Mass.: | 35683.24 | ||
Organism: | Homo sapiens (Human) | ||
Description: | P05412 | ||
Residue: | 331 | ||
Sequence: |
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BDBM50279698 | |||
n/a | |||
Name | BDBM50279698 | ||
Synonyms: | 2-(4-Methyl-2-methylamino-thiazol-5-yl)-3-o-tolyl-3H-quinazolin-4-one | CHEMBL515276 | ||
Type | Small organic molecule | ||
Emp. Form. | C20H18N4OS | ||
Mol. Mass. | 362.448 | ||
SMILES | CNc1nc(C)c(s1)-c1nc2ccccc2c(=O)n1-c1ccccc1C |(32.14,-.5,;31.37,.83,;29.84,.83,;29.07,-.51,;27.56,-.19,;26.42,-1.22,;27.4,1.34,;28.8,1.97,;26.07,2.11,;24.72,1.33,;23.38,2.1,;22.04,1.33,;20.71,2.1,;20.71,3.65,;22.04,4.42,;23.38,3.65,;24.71,4.44,;24.7,5.98,;26.06,3.66,;27.39,4.44,;28.73,3.67,;30.06,4.44,;30.05,5.98,;28.71,6.75,;27.38,5.97,;26.05,6.73,)| | ||
Structure |