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SMILES: FC(F)(F)c1ccccc1S(=O)(=O)Nc1ccc(cc1)-c1nc2ccccc2o1

InChI Key: InChIKey=JESCTCQPDHESJC-UHFFFAOYSA-N

Find this compound or compounds like it in BindingDB or PDB:
   Substructure
Similarity at least:  must be >=0.5
Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 8 hits for monomerid = 50522524   
Target/Host
(Institution)
LigandTarget/Host
Links
Ligand
Links
Trg + Lig
Links
Ki
nM
ΔG°
kcal/mole
IC50
nM
Kd
nM
EC50/IC50
nM
koff
s-1
kon
M-1s-1
pHTemp
°C
Malate dehydrogenase, mitochondrial


(Sus scrofa (pig))
BDBM50522524
PNG
(CHEMBL4462640)
Show SMILES FC(F)(F)c1ccccc1S(=O)(=O)Nc1ccc(cc1)-c1nc2ccccc2o1
Show InChI InChI=1S/C20H13F3N2O3S/c21-20(22,23)15-5-1-4-8-18(15)29(26,27)25-14-11-9-13(10-12-14)19-24-16-6-2-3-7-17(16)28-19/h1-12,25H
PDB
MMDB

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n/an/a>6.30E+4n/an/an/an/an/an/a



Indiana University School of Medicine

Curated by ChEMBL


Assay Description
Inhibition of refolded pig heart mitochondrial MDH preincubated with Escherichia coli GroEL/GroES for 45 mins using sodium mesoxalate as substrate fo...


Bioorg Med Chem Lett 29: 1665-1672 (2019)


Article DOI: 10.1016/j.bmcl.2019.04.034
More data for this
Ligand-Target Pair
Tyrosine-protein phosphatase non-receptor type 5


(Homo sapiens (Human))
BDBM50522524
PNG
(CHEMBL4462640)
Show SMILES FC(F)(F)c1ccccc1S(=O)(=O)Nc1ccc(cc1)-c1nc2ccccc2o1
Show InChI InChI=1S/C20H13F3N2O3S/c21-20(22,23)15-5-1-4-8-18(15)29(26,27)25-14-11-9-13(10-12-14)19-24-16-6-2-3-7-17(16)28-19/h1-12,25H
PDB
MMDB

KEGG

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UniChem
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PubMed
n/an/a 5.30E+4n/an/an/an/an/an/a



Indiana University School of Medicine

Curated by ChEMBL


Assay Description
Inhibition of human PTPN5 expressed in Escherichia coli Rosetta 2 (DE3) using pNPP as substrate after 45 mins by spectrophotometric method


Bioorg Med Chem Lett 29: 1665-1672 (2019)


Article DOI: 10.1016/j.bmcl.2019.04.034
More data for this
Ligand-Target Pair
Co-chaperonin GroES


(Escherichia coli)
BDBM50522524
PNG
(CHEMBL4462640)
Show SMILES FC(F)(F)c1ccccc1S(=O)(=O)Nc1ccc(cc1)-c1nc2ccccc2o1
Show InChI InChI=1S/C20H13F3N2O3S/c21-20(22,23)15-5-1-4-8-18(15)29(26,27)25-14-11-9-13(10-12-14)19-24-16-6-2-3-7-17(16)28-19/h1-12,25H
PDB

UniProtKB/TrEMBL

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UniChem
Article
PubMed
n/an/a 7.50E+4n/an/an/an/an/an/a



Indiana University School of Medicine

Curated by ChEMBL


Assay Description
Inhibition of Escherichia coli GroEL expressed in Escherichia coliDH5alpha/Escherichia coli GroES expressed in Escherichia coli BL21 (DE3) assessed a...


Bioorg Med Chem Lett 29: 1665-1672 (2019)


Article DOI: 10.1016/j.bmcl.2019.04.034
More data for this
Ligand-Target Pair
60 kDa heat shock protein, mitochondrial


(Homo sapiens)
BDBM50522524
PNG
(CHEMBL4462640)
Show SMILES FC(F)(F)c1ccccc1S(=O)(=O)Nc1ccc(cc1)-c1nc2ccccc2o1
Show InChI InChI=1S/C20H13F3N2O3S/c21-20(22,23)15-5-1-4-8-18(15)29(26,27)25-14-11-9-13(10-12-14)19-24-16-6-2-3-7-17(16)28-19/h1-12,25H
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UniProtKB/SwissProt

antibodypedia
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UniChem
Article
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n/an/a 7.40E+4n/an/an/an/an/an/a



Indiana University School of Medicine

Curated by ChEMBL


Assay Description
Inhibition of human HSP60 expressed in Escherichia coli Rosetta 2(DE3)/human HSP10 expressed in Escherichia coli Rosetta 2(DE3) pLysS cells assessed ...


Bioorg Med Chem Lett 29: 1665-1672 (2019)


Article DOI: 10.1016/j.bmcl.2019.04.034
More data for this
Ligand-Target Pair
Tyrosine-protein phosphatase non-receptor type 2


(Homo sapiens (Human))
BDBM50522524
PNG
(CHEMBL4462640)
Show SMILES FC(F)(F)c1ccccc1S(=O)(=O)Nc1ccc(cc1)-c1nc2ccccc2o1
Show InChI InChI=1S/C20H13F3N2O3S/c21-20(22,23)15-5-1-4-8-18(15)29(26,27)25-14-11-9-13(10-12-14)19-24-16-6-2-3-7-17(16)28-19/h1-12,25H
PDB
MMDB

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UniProtKB/SwissProt

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antibodypedia
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PC cid
PC sid
UniChem
Article
PubMed
n/an/a 6.10E+4n/an/an/an/an/an/a



Indiana University School of Medicine

Curated by ChEMBL


Assay Description
Inhibition of human PTPN2 expressed in Escherichia coli Rosetta 2 (DE3) using pNPP as substrate after 45 mins by spectrophotometric method


Bioorg Med Chem Lett 29: 1665-1672 (2019)


Article DOI: 10.1016/j.bmcl.2019.04.034
More data for this
Ligand-Target Pair
TYR_PHOSPHATASE_2 domain-containing protein


(Mycobacterium tuberculosis)
BDBM50522524
PNG
(CHEMBL4462640)
Show SMILES FC(F)(F)c1ccccc1S(=O)(=O)Nc1ccc(cc1)-c1nc2ccccc2o1
Show InChI InChI=1S/C20H13F3N2O3S/c21-20(22,23)15-5-1-4-8-18(15)29(26,27)25-14-11-9-13(10-12-14)19-24-16-6-2-3-7-17(16)28-19/h1-12,25H
PDB
MMDB

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UniProtKB/TrEMBL

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UniChem
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n/an/a 5.80E+4n/an/an/an/an/an/a



Indiana University School of Medicine

Curated by ChEMBL


Assay Description
Inhibition of Mycobacterium tuberculosis His-tagged PtpB expressed in Escherichia coli Rosetta 2 (DE3) using pNPP as substrate after 30 mins by spect...


Bioorg Med Chem Lett 29: 1665-1672 (2019)


Article DOI: 10.1016/j.bmcl.2019.04.034
More data for this
Ligand-Target Pair
Co-chaperonin GroES


(Escherichia coli)
BDBM50522524
PNG
(CHEMBL4462640)
Show SMILES FC(F)(F)c1ccccc1S(=O)(=O)Nc1ccc(cc1)-c1nc2ccccc2o1
Show InChI InChI=1S/C20H13F3N2O3S/c21-20(22,23)15-5-1-4-8-18(15)29(26,27)25-14-11-9-13(10-12-14)19-24-16-6-2-3-7-17(16)28-19/h1-12,25H
PDB

UniProtKB/TrEMBL

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PC cid
PC sid
UniChem
Article
PubMed
n/an/a 1.66E+5n/an/an/an/an/an/a



Indiana University School of Medicine

Curated by ChEMBL


Assay Description
Inhibition of Escherichia coli GroEL expressed in Escherichia coli DH5alpha/Escherichia coli GroES expressed in Escherichia coli BL21 (DE3) assessed ...


Bioorg Med Chem Lett 29: 1665-1672 (2019)


Article DOI: 10.1016/j.bmcl.2019.04.034
More data for this
Ligand-Target Pair
Tyrosine-protein phosphatase non-receptor type 1


(Homo sapiens (Human))
BDBM50522524
PNG
(CHEMBL4462640)
Show SMILES FC(F)(F)c1ccccc1S(=O)(=O)Nc1ccc(cc1)-c1nc2ccccc2o1
Show InChI InChI=1S/C20H13F3N2O3S/c21-20(22,23)15-5-1-4-8-18(15)29(26,27)25-14-11-9-13(10-12-14)19-24-16-6-2-3-7-17(16)28-19/h1-12,25H
PDB
MMDB

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PC cid
PC sid
UniChem
Article
PubMed
n/an/a 4.40E+4n/an/an/an/an/an/a



Indiana University School of Medicine

Curated by ChEMBL


Assay Description
Inhibition of human PTPN1 expressed in Escherichia coli Rosetta 2 (DE3) using pNPP as substrate after 45 mins by spectrophotometric method


Bioorg Med Chem Lett 29: 1665-1672 (2019)


Article DOI: 10.1016/j.bmcl.2019.04.034
More data for this
Ligand-Target Pair