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Reaction Details
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TargetTumor necrosis factor
LigandBDBM50081332
Substrate/Competitorn/a
Meas. Tech.ChEMBL_212403 (CHEMBL816155)
IC50>25000±n/a nM
Citation Chao, QDeng, LShih, HLeoni, LMGenini, DCarson, DACottam, HB Substituted isoquinolines and quinazolines as potential antiinflammatory agents. Synthesis and biological evaluation of inhibitors of tumor necrosis factor alpha. J Med Chem42:3860-73 (1999) [PubMed]
More Info.:Get all data from this article,  Assay Method
 
Tumor necrosis factor
Name:Tumor necrosis factor
Synonyms:Cachectin | TNF | TNF-a | TNF-alpha | TNFA | TNFA_HUMAN | TNFSF2 | Tumor necrosis factor (TNF-alpha) | Tumor necrosis factor (TNFa) | Tumor necrosis factor alpha (TNFα) | Tumor necrosis factor ligand superfamily member 2 | Tumor necrosis factor, membrane form | Tumor necrosis factor, soluble form | tumor necrosis factor alpha
Type:Enzyme
Mol. Mass.:25645.11
Organism:Homo sapiens (Human)
Description:P01375
Residue:233
Sequence:
MSTESMIRDVELAEEALPKKTGGPQGSRRCLFLSLFSFLIVAGATTLFCLLHFGVIGPQR
EEFPRDLSLISPLAQAVRSSSRTPSDKPVAHVVANPQAEGQLQWLNRRANALLANGVELR
DNQLVVPSEGLYLIYSQVLFKGQGCPSTHVLLTHTISRIAVSYQTKVNLLSAIKSPCQRE
TPEGAEAKPWYEPIYLGGVFQLEKGDRLSAEINRPDYLDFAESGQVYFGIIAL
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  Blast E-value cutoff:
BDBM50081332
n/a
NameBDBM50081332
Synonyms:4-(5-Azido-6,7-dimethoxy-4-oxo-4H-quinazolin-3-yl)-butyric acid ethyl ester | CHEMBL338340
TypeSmall organic molecule
Emp. Form.C16H19N5O5
Mol. Mass.361.3526
SMILESCCOC(=O)CCCn1cnc2cc(OC)c(OC)c(N=[N+]=[N-])c2c1=O
Structure
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