null

SMILES OC1=NC(=O)C(S1)=Cc1cc(Br)ccc1OCc1cc(cc(c1)C(F)(F)F)C(F)(F)F

InChI Key InChIKey=FZRDTEBLFOXQQJ-UHFFFAOYSA-N

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
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Similarity at least:  must be >=0.5
Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 8 hits for monomerid = 50299153   

TargetTyrosine-protein phosphatase non-receptor type 1(Homo sapiens (Human))
Inha University

Curated by ChEMBL
LigandPNGBDBM50299153((Z)-5-{2-[3,5-bis(trifluoromethyl)benzyloxy]-5-bro...)copy SMILEScopy InChI
Affinity DataKi:  2.10E+3nMAssay Description:Inhibition of PTP1BMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q20P102SPubMed
TargetTyrosine-protein phosphatase non-receptor type 6(Homo sapiens (Human))
Inha University

Curated by ChEMBL
LigandPNGBDBM50299153((Z)-5-{2-[3,5-bis(trifluoromethyl)benzyloxy]-5-bro...)copy SMILEScopy InChI
Affinity DataKi:  2.20E+3nMAssay Description:Inhibition of SHP1 catalytic domain expressed in Escherichia coliMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q20P102SPubMed
TargetTyrosine-protein phosphatase non-receptor type 2(Homo sapiens (Human))
Inha University

Curated by ChEMBL
LigandPNGBDBM50299153((Z)-5-{2-[3,5-bis(trifluoromethyl)benzyloxy]-5-bro...)copy SMILEScopy InChI
Affinity DataKi:  4.50E+3nMAssay Description:Inhibition of TC-PTPMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q20P102SPubMed
TargetPeroxisome proliferator-activated receptor gamma(Homo sapiens (Human))
Inha University

Curated by ChEMBL
LigandPNGBDBM50299153((Z)-5-{2-[3,5-bis(trifluoromethyl)benzyloxy]-5-bro...)copy SMILEScopy InChI
Affinity DataEC50:  870nMAssay Description:Agonist activity at PPARgamma expressed in HepG2 cells co-expressing PPRE assessed as transcriptional activation after 24 hrs by luciferase reporter ...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2FQ9X0GPubMed
TargetTyrosine-protein phosphatase non-receptor type 6(Homo sapiens (Human))
Inha University

Curated by ChEMBL
LigandPNGBDBM50299153((Z)-5-{2-[3,5-bis(trifluoromethyl)benzyloxy]-5-bro...)copy SMILEScopy InChI
Affinity DataIC50: 5.80E+3nMAssay Description:Inhibition of SHP1 catalytic domain expressed in Escherichia coliMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q20P102SPubMed
TargetTyrosine-protein phosphatase non-receptor type 2(Homo sapiens (Human))
Inha University

Curated by ChEMBL
LigandPNGBDBM50299153((Z)-5-{2-[3,5-bis(trifluoromethyl)benzyloxy]-5-bro...)copy SMILEScopy InChI
Affinity DataIC50: 1.60E+4nMAssay Description:Inhibition of TC-PTPMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q20P102SPubMed
TargetTyrosine-protein phosphatase non-receptor type 1(Homo sapiens (Human))
Inha University

Curated by ChEMBL
LigandPNGBDBM50299153((Z)-5-{2-[3,5-bis(trifluoromethyl)benzyloxy]-5-bro...)copy SMILEScopy InChI
Affinity DataIC50: 5.00E+3nMAssay Description:Inhibition of PTP1BMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q20P102SPubMed
TargetReceptor-type tyrosine-protein phosphatase F(Homo sapiens (Human))
Inha University

Curated by ChEMBL
LigandPNGBDBM50299153((Z)-5-{2-[3,5-bis(trifluoromethyl)benzyloxy]-5-bro...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibition of membrane proximal catalytic domain of LARMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q20P102SPubMed