BDBM50184993 CHEMBL3824236

SMILES COC(=O)CN(c1ccc(CN(c2ccc(OCc3ccccc3)c(c2)C(=O)OC)S(=O)(=O)Cc2ccccc2)cc1)S(C)(=O)=O

InChI Key InChIKey=DZTSPUIXGGCGGS-UHFFFAOYSA-N

Data  3 IC50

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
Find this compound or compounds like it in BindingDB:
   Substructure
Similarity at least:  must be >=0.5
Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 3 hits for monomerid = 50184993   

TargetTyrosine-protein phosphatase non-receptor type 1(Human)
Qilu University of Technology

Curated by ChEMBL
LigandPNGBDBM50184993(CHEMBL3824236)
Affinity DataIC50: 355nMAssay Description:Inhibition of recombinant PTP1B (unknown origin) using pNPP as substrate incubated for 30 minsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
10/2/2017
Entry Details Article
PubMed
TargetTyrosine-protein phosphatase non-receptor type 2(Human)
Qilu University of Technology

Curated by ChEMBL
LigandPNGBDBM50184993(CHEMBL3824236)
Affinity DataIC50: 427nMAssay Description:Inhibition of human TCPTP using pNPP as substrate incubated for 30 minsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
10/2/2017
Entry Details Article
PubMed
TargetTyrosine-protein phosphatase non-receptor type 6(Human)
Qilu University of Technology

Curated by ChEMBL
LigandPNGBDBM50184993(CHEMBL3824236)
Affinity DataIC50: 6.46E+3nMAssay Description:Inhibition of human SHP1 using pNPP as substrate incubated for 30 minsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
10/2/2017
Entry Details Article
PubMed