BDBM50442512 CHEMBL2440433

SMILES OP(O)(=O)C(Nc1ccc(Cl)c(Cl)c1)P(O)(O)=O

InChI Key InChIKey=ADHSWFUIIRWNHD-UHFFFAOYSA-N

Data  10 IC50

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 10 hits for monomerid = 50442512   

TargetCarbonic anhydrase 1(Human)
University of Bari Aldo Moro

Curated by ChEMBL
LigandPNGBDBM50442512(CHEMBL2440433)
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of human recombinant carbonic anhydrase 1 preincubated for 15 mins by stopped flow CO2 hydration methodMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetCarbonic anhydrase 2(Human)
University of Bari Aldo Moro

Curated by ChEMBL
LigandPNGBDBM50442512(CHEMBL2440433)
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of human recombinant carbonic anhydrase 2 preincubated for 15 mins by stopped flow CO2 hydration methodMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetCarbonic anhydrase 9(Human)
University of Bari Aldo Moro

Curated by ChEMBL
LigandPNGBDBM50442512(CHEMBL2440433)
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of human recombinant carbonic anhydrase 9 preincubated for 15 mins by stopped flow CO2 hydration methodMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetCarbonic anhydrase 12(Human)
University of Bari Aldo Moro

Curated by ChEMBL
LigandPNGBDBM50442512(CHEMBL2440433)
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of human recombinant carbonic anhydrase 12 preincubated for 15 mins by stopped flow CO2 hydration methodMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetCarbonic anhydrase 14(Human)
University of Bari Aldo Moro

Curated by ChEMBL
LigandPNGBDBM50442512(CHEMBL2440433)
Affinity DataIC50: 7.84E+3nMAssay Description:Inhibition of human recombinant carbonic anhydrase 14 preincubated for 15 mins by stopped flow CO2 hydration methodMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetMatrix metalloproteinase-14(Human)
University of Bari Aldo Moro

Curated by ChEMBL
LigandPNGBDBM50442512(CHEMBL2440433)
Affinity DataIC50: 2.00E+4nMAssay Description:Inhibition of MMP14 catalytic domain (unknown origin) using Mca-Pro-Leu-Gly-Leu-Dpa-Ala-Arg-NH2 as substrate incubated for 30 mins prior to substrate...More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetGlutamine synthetase, chloroplastic(Maize)
University of Ferrara

Curated by ChEMBL
LigandPNGBDBM50442512(CHEMBL2440433)
Affinity DataIC50: 3.19E+4nMAssay Description:Inhibition of Zea mays cv. Jeff (maize) leaf glutamine synthetase using L-glutamate as substrate assessed as inorganic phosphate production after 20 ...More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetGlutamine synthetase, chloroplastic(Maize)
University of Ferrara

Curated by ChEMBL
LigandPNGBDBM50442512(CHEMBL2440433)
Affinity DataIC50: 3.19E+4nMAssay Description:Inhibition of Zea mays cv. Jeff (maize) leaf glutamine synthetase using L-glutamate as substrate assessed as inorganic phosphate production after 20 ...More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetPyrroline-5-carboxylate reductase(Mouse-ear cress)
University of Ferrara

Curated by ChEMBL
LigandPNGBDBM50442512(CHEMBL2440433)
Affinity DataIC50: 2.68E+5nMAssay Description:Inhibition of Arabidopsis thaliana P5C assessed as reduction in NADH oxidation incubated at 35 degC up to 10 minMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetPyrroline-5-carboxylate reductase(Mouse-ear cress)
University of Ferrara

Curated by ChEMBL
LigandPNGBDBM50442512(CHEMBL2440433)
Affinity DataIC50: 2.68E+5nMAssay Description:Inhibition of Arabidopsis thaliana P5C assessed as reduction in NADH oxidation incubated at 35 degC up to 10 minMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed