Ki Summary BindingDB logo
myBDB logout
Reaction Details
Report a problem with these data
TargetDual specificity protein phosphatase 22
LigandBDBM50205436
Substrate/Competitorn/a
Meas. Tech.ChEMBL_438363 (CHEMBL887465)
IC50>40000±n/a nM
Citation Zhang, LQiu, BXiong, BLi, XLi, JWang, XLi, JShen, J Quinoxalinylurea derivatives as a novel class of JSP-1 inhibitors. Bioorg Med Chem Lett17:2118-22 (2007) [PubMed]  Article
More Info.:Get all data from this article,  Assay Method
 
Dual specificity protein phosphatase 22
Name:Dual specificity protein phosphatase 22
Synonyms:DUS22_HUMAN | DUSP22 | Dual specificity phosphatase 22 | Dual specificity protein phosphatase (MKPX) | Dual specificity protein phosphatase 22 | Dual specificity protein phosphatase 22 (VHX) | Dual specificity protein phosphatase VHX (VHX) | JSP1 | LMWDSP2 | MKPX | Mitogen-activated protein kinase phosphatase x | VHX
Type:Protein
Mol. Mass.:20915.83
Organism:Homo sapiens (Human)
Description:Q9NRW4
Residue:184
Sequence:
MGNGMNKILPGLYIGNFKDARDAEQLSKNKVTHILSVHDSARPMLEGVKYLCIPAADSPS
QNLTRHFKESIKFIHECRLRGESCLVHCLAGVSRSVTLVIAYIMTVTDFGWEDALHTVRA
GRSCANPNVGFQRQLQEFEKHEVHQYRQWLKEEYGESPLQDAEEAKNILAAPGILKFWAF
LRRL
Blast this sequence in BindingDB or PDB
  Blast E-value cutoff:
BDBM50205436
n/a
NameBDBM50205436
Synonyms:CHEMBL230362 | N-(2,3-bis(4-bromophenyl)quinoxalin-6-yl)-3-(pyrrolidine-1-carbonyl)piperidine-1-carboxamide
TypeSmall organic molecule
Emp. Form.C31H29Br2N5O2
Mol. Mass.663.402
SMILESBrc1ccc(cc1)-c1nc2ccc(NC(=O)N3CCCC(C3)C(=O)N3CCCC3)cc2nc1-c1ccc(Br)cc1 |w:20.23|
Structure
Search PDB for entries with ligand similarity:Similarity to this molecule at least: