BDBM50317355 2-(3-stearoyl-1H-pyrazole-5-carboxamido)benzoic acid::CHEMBL1097720

SMILES CCCCCCCCCCCCCCCCCC(=O)c1cc([nH]n1)C(=O)Nc1ccccc1C(O)=O

InChI Key InChIKey=FIWRNZMEMMAYAC-UHFFFAOYSA-N

Data  5 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 5 hits for monomerid = 50317355   

TargetTyrosine-protein phosphatase non-receptor type 1(Human)
Chinese Academy of Sciences

Curated by ChEMBL
LigandPNGBDBM50317355(2-(3-stearoyl-1H-pyrazole-5-carboxamido)benzoic ac...)
Affinity DataIC50: 350nMAssay Description:Inhibition of PTP1BMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetM-phase inducer phosphatase 2(Human)
Chinese Academy of Sciences

Curated by ChEMBL
LigandPNGBDBM50317355(2-(3-stearoyl-1H-pyrazole-5-carboxamido)benzoic ac...)
Affinity DataIC50: 160nMAssay Description:Inhibition of CDC25BMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetTyrosine-protein phosphatase non-receptor type 2(Human)
Chinese Academy of Sciences

Curated by ChEMBL
LigandPNGBDBM50317355(2-(3-stearoyl-1H-pyrazole-5-carboxamido)benzoic ac...)
Affinity DataIC50: 1.30E+3nMAssay Description:Inhibition of TCPTPMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetTyrosine-protein phosphatase non-receptor type 6(Human)
Chinese Academy of Sciences

Curated by ChEMBL
LigandPNGBDBM50317355(2-(3-stearoyl-1H-pyrazole-5-carboxamido)benzoic ac...)
Affinity DataIC50: 1.06E+4nMAssay Description:Inhibition of SHP1More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetTyrosine-protein phosphatase non-receptor type 11(Human)
Chinese Academy of Sciences

Curated by ChEMBL
LigandPNGBDBM50317355(2-(3-stearoyl-1H-pyrazole-5-carboxamido)benzoic ac...)
Affinity DataIC50: 1.52E+4nMAssay Description:Inhibition of SHP2More data for this Ligand-Target Pair
In DepthDetails Article
PubMed