BDBM50138040 (biphenyl-3-ylamino)methylenediphosphonic acid::BPH-218::CHEMBL55371::[(Biphenyl-3-ylamino)-phosphono-methyl]-phosphonic acid

SMILES OP(O)(=O)C(Nc1cccc(c1)-c1ccccc1)P(O)(O)=O

InChI Key InChIKey=IXFMBXNLOHKCPT-UHFFFAOYSA-N

Data  14 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 14 hits for monomerid = 50138040   

TargetDecaprenyl diphosphate synthase(Mycobacterium tuberculosis (strain CDC 1551 / Oshk...)
University of California San Diego

LigandPNGBDBM50138040([(Biphenyl-3-ylamino)-phosphono-methyl]-phosphonic...)
Affinity DataIC50: 6.30E+3nMpH: 7.5Assay Description:We screened an in-house library of 53 compounds using trans-FPP as substrate. Briefly, the condensation of IPP and GPP, FPP, or cis-FPP catalyzed by ...More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetCarbonic anhydrase 1(Human)
University of Bari Aldo Moro

Curated by ChEMBL
LigandPNGBDBM50138040([(Biphenyl-3-ylamino)-phosphono-methyl]-phosphonic...)
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
LigandPNGBDBM50138040([(Biphenyl-3-ylamino)-phosphono-methyl]-phosphonic...)
Affinity DataIC50: 9.37E+3nMAssay 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
LigandPNGBDBM50138040([(Biphenyl-3-ylamino)-phosphono-methyl]-phosphonic...)
Affinity DataIC50: 7.63E+3nMAssay 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
LigandPNGBDBM50138040([(Biphenyl-3-ylamino)-phosphono-methyl]-phosphonic...)
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
LigandPNGBDBM50138040([(Biphenyl-3-ylamino)-phosphono-methyl]-phosphonic...)
Affinity DataIC50: 309nMAssay 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
TargetPolyprenyl synthetase family protein(Leishmania donovani)
University of Illinois At Urbana-Champaign

Curated by ChEMBL
LigandPNGBDBM50138040([(Biphenyl-3-ylamino)-phosphono-methyl]-phosphonic...)
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibitory activity against Leishmania major Farnesyl diphosphate synthaseMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetPolyprenyl synthetase family protein(Leishmania donovani)
University of Illinois At Urbana-Champaign

Curated by ChEMBL
LigandPNGBDBM50138040([(Biphenyl-3-ylamino)-phosphono-methyl]-phosphonic...)
Affinity DataIC50: 1.15E+4nMAssay Description:Inhibitory activity against FPPS in Leishmania majorMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetPhosphotransferase(Trypanosoma cruzi)
University of Illinois At Urbana-Champaign

Curated by ChEMBL
LigandPNGBDBM50138040([(Biphenyl-3-ylamino)-phosphono-methyl]-phosphonic...)
Affinity DataIC50: 1.95E+3nMAssay Description:Inhibitory activity against Trypanosoma cruzi hexokinaseMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetFarnesyl pyrophosphate synthase(Human)
University of Illinois At Urbana-Champaign

Curated by ChEMBL
LigandPNGBDBM50138040([(Biphenyl-3-ylamino)-phosphono-methyl]-phosphonic...)
Affinity DataIC50: 8.50E+3nMAssay Description:Inhibition of human FPPSMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetH(+)-exporting diphosphatase(Trypanosoma brucei)
University of Illinois At Urbana-Champaign

Curated by ChEMBL
LigandPNGBDBM50138040([(Biphenyl-3-ylamino)-phosphono-methyl]-phosphonic...)
Affinity DataIC50: 4.30E+3nMAssay Description:Inhibition of recombinant Trypanosoma brucei soluble vacuolar pyrophosphatase expressed in Escherichia coliMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetMatrix metalloproteinase-14(Human)
University of Bari Aldo Moro

Curated by ChEMBL
LigandPNGBDBM50138040([(Biphenyl-3-ylamino)-phosphono-methyl]-phosphonic...)
Affinity DataIC50: 4.00E+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
TargetPhosphotransferase(Trypanosoma cruzi)
University of Illinois At Urbana-Champaign

Curated by ChEMBL
LigandPNGBDBM50138040([(Biphenyl-3-ylamino)-phosphono-methyl]-phosphonic...)
Affinity DataIC50: 810nMAssay Description:Inhibition of Trypanosoma cruzi hexokinaseMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetFarnesyl pyrophosphate synthase(Human)
University of Illinois At Urbana-Champaign

Curated by ChEMBL
LigandPNGBDBM50138040([(Biphenyl-3-ylamino)-phosphono-methyl]-phosphonic...)
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of human recombinant N-terminal-His6 tagged FPPS expressed in Escherichia coli BL21 using [14C]IPP and GPP as substrate incubated for 10 m...More data for this Ligand-Target Pair
In DepthDetails Article
PubMed