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Reaction Details
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TargetTumor necrosis factor
LigandBDBM50052601
Substrate/Competitorn/a
Meas. Tech.ChEMBL_212401 (CHEMBL815988)
IC50 120000±n/a nM
Citation Muller, GWCorral, LGShire, MGWang, HMoreira, AKaplan, GStirling, DI Structural modifications of thalidomide produce analogs with enhanced tumor necrosis factor inhibitory activity. J Med Chem39:3238-40 (1996) [PubMed]  Article
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:
BDBM50052601
n/a
NameBDBM50052601
Synonyms:3-(1,3-Dioxo-1,3-dihydro-isoindol-2-yl)-3-(3-methoxy-phenyl)-propionamide | CHEMBL111637
TypeSmall organic molecule
Emp. Form.C18H16N2O4
Mol. Mass.324.3306
SMILESCOc1cccc(c1)C(CC(N)=O)N1C(=O)c2ccccc2C1=O
Structure
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