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Target
Dual specificity protein phosphatase 3
Ligand
BDBM50096710
Substrate
n/a
Meas. Tech.
ChEBML_214527
IC50
22000±n/a nM
Citation
 Wipf, P; Aslan, DC; Southwick, EC; Lazo, JS Sulfonylated aminothiazoles as new small molecule inhibitors of protein phosphatases. Bioorg Med Chem Lett 11:313-7 (2001) [PubMed]  Article 
Target
Name:
Dual specificity protein phosphatase 3
Synonyms:
DUS3_HUMAN | DUSP3 | Dual specificity protein phosphatase (VHR) | Dual specificity protein phosphatase 3 | Dual specificity protein phosphatase VHR | Protein Tyrosine Phosphatase VHR | Tyrosine-protein phosphatase non-receptor type 1 | VHR
Type:
Hydrolase
Mol. Mass.:
20480.58
Organism:
Homo sapiens (Human)
Description:
n/a
Residue:
185
Sequence:
MSGSFELSVQDLNDLLSDGSGCYSLPSQPCNEVTPRIYVGNASVAQDIPKLQKLGITHVLNAAEGRSFMHVNTNANFYKDSGITYLGIKANDTQEFNLSAYFERAADFIDQALAQKNGRVLVHCREGYSRSPTLVIAYLMMRQKMDVKSALSIVRQNREIGPNDGFLAQLCQLNDRLAKEGKLKP
  
Inhibitor
Name:
BDBM50096710
Synonyms:
(E)-2-(3,4-Difluoro-phenyl)-ethenesulfonic acid (4-biphenyl-4-yl-5-propyl-thiazol-2-yl)-amide | CHEMBL324669
Type:
Small organic molecule
Emp. Form.:
C26H22F2N2O2S2
Mol. Mass.:
496.592
SMILES:
CCCc1sc(NS(=O)(=O)\C=C\c2ccc(F)c(F)c2)nc1-c1ccc(cc1)-c1ccccc1
Structure:
Search PDB for entries with ligand similarity: