Target3-phosphoshikimate 1-carboxyvinyltransferase(Escherichia coli (strain K12))
TBA
Curated by ChEMBL
TBA
Curated by ChEMBL
Affinity DataKi: 160nMAssay Description:Tested for the inhibition against Escherichia coli 5-enolpyruvyl-shikimate-3-phosphate synthase versus phosphoenolpyruvateMore data for this Ligand-Target Pair
Target3-phosphoshikimate 1-carboxyvinyltransferase(Escherichia coli (strain K12))
TBA
Curated by ChEMBL
TBA
Curated by ChEMBL
Affinity DataKi: 160nM Kd: 160nM Kon: 0.120M-1s-1 Koff: 7.80E+5s-1Assay Description:Tested for the dissociation constant against E. coli 5-enolpyruvyl-shikimate-3-phosphate synthaseMore data for this Ligand-Target Pair
Target3-phosphoshikimate 1-carboxyvinyltransferase(Escherichia coli (strain K12))
TBA
Curated by ChEMBL
TBA
Curated by ChEMBL
Affinity DataKi: 610nM Kd: 500nM Kon: 0.160M-1s-1 Koff: 3.20E+5s-1Assay Description:Tested for the dissociation constant against E. coli 5-enolpyruvyl-shikimate-3-phosphate synthaseMore data for this Ligand-Target Pair
Target3-phosphoshikimate 1-carboxyvinyltransferase(Escherichia coli (strain K12))
TBA
Curated by ChEMBL
TBA
Curated by ChEMBL
Affinity DataKi: 1.50E+3nMAssay Description:Dissociation constant of the compound was calculated for E. coli EPSP(5-enolpyruvyl-shikimate-3-phosphate) SynthaseMore data for this Ligand-Target Pair
Target3-phosphoshikimate 1-carboxyvinyltransferase(Escherichia coli (strain K12))
TBA
Curated by ChEMBL
TBA
Curated by ChEMBL
Affinity DataKi: 2.20E+3nMAssay Description:Tested for the dissociation constant against E. coli 5-enolpyruvyl-shikimate-3-phosphate synthaseMore data for this Ligand-Target Pair
Target3-phosphoshikimate 1-carboxyvinyltransferase(Escherichia coli (strain K12))
TBA
Curated by ChEMBL
TBA
Curated by ChEMBL
Affinity DataKi: 2.20E+3nMAssay Description:Tested for the dissociation constant against E. coli 5-enolpyruvyl-shikimate-3-phosphate synthaseMore data for this Ligand-Target Pair
Target3-phosphoshikimate 1-carboxyvinyltransferase(Escherichia coli (strain K12))
TBA
Curated by ChEMBL
TBA
Curated by ChEMBL
Affinity DataKi: 7.80E+4nMAssay Description:Tested for the dissociation constant against E. coli 5-enolpyruvyl-shikimate-3-phosphate synthaseMore data for this Ligand-Target Pair
Affinity DataIC50: 0.680nMAssay Description:Inhibition of recombinant HIV1 reverse transcriptase p66/p51 Y181C mutant expressed in Escherichia coli BL21 (DE3) pLysS cells preincubated followed ...More data for this Ligand-Target Pair
Affinity DataIC50: 1.10nMAssay Description:Inhibition of wild-type HIV-1 reverse transcriptase by fluorescence assayMore data for this Ligand-Target Pair
Affinity DataIC50: 2.70nMAssay Description:Inhibition of wild-type HIV-1 reverse transcriptase by fluorescence assayMore data for this Ligand-Target Pair
Affinity DataIC50: 3nMAssay Description:Inhibition of recombinant wild type HIV-1 reverse transcriptase using poly(rA)350/oligo(dT)16 as template/primer preincubated for 1 hr followed by su...More data for this Ligand-Target Pair
Affinity DataIC50: 3nMAssay Description:Competitive inhibition of C-Terminal histidine-tagged wild type heterodimeric HIV-1 reverse transcriptase p66/p51 assessed as inhibition of dTTP inco...More data for this Ligand-Target Pair
Affinity DataIC50: 3.30nMAssay Description:Inhibition of wild-type HIV-1 reverse transcriptase by fluorescence assayMore data for this Ligand-Target Pair
Affinity DataIC50: 3.80nMAssay Description:Inhibition of HIV1 3B reverse transcriptaseMore data for this Ligand-Target Pair
Affinity DataIC50: 4.30nMAssay Description:Inhibition of HIV-1 6His-tagged reverse transcriptase p66/p51-mediated TTP incorporation into D23/D36 primer/template preincubated for 15 mins follow...More data for this Ligand-Target Pair
Affinity DataIC50: 4.5nMAssay Description:Inhibition of recombinant HIV1 reverse transcriptase p66/p51 expressed in Escherichia coli BL21 (DE3) pLysS cells preincubated followed by primer/tem...More data for this Ligand-Target Pair
Affinity DataIC50: 5.5nMAssay Description:Inhibition of recombinant HIV1 reverse transcriptase p66/p51 Y181C mutant expressed in Escherichia coli BL21 (DE3) pLysS cells preincubated followed ...More data for this Ligand-Target Pair
Affinity DataIC50: 6nMAssay Description:Inhibition of HIV-1 6His-tagged reverse transcriptase p66/p51-mediated TTP incorporation into D23/D36 primer/template preincubated for 15 mins follow...More data for this Ligand-Target Pair
Affinity DataIC50: 9nMAssay Description:Competitive inhibition of C-Terminal histidine-tagged wild type heterodimeric HIV-1 reverse transcriptase p66/p51 assessed as inhibition of dGTP inco...More data for this Ligand-Target Pair
Affinity DataIC50: <10nMAssay Description:Inhibition of recombinant wildtype HIV-1 reverse transcriptase using r(A)350 as template and d(T)16 as primer preincubated with compound for 1 hrs fo...More data for this Ligand-Target Pair
Ligand Info
Affinity DataIC50: 11nMAssay Description:Inhibition of recombinant wildtype HIV-1 reverse transcriptase using r(A)350 as template and d(T)16 as primer preincubated with compound for 1 hrs fo...More data for this Ligand-Target Pair
Ligand Info
Affinity DataIC50: 13nMAssay Description:Competitive inhibition of C-Terminal histidine-tagged wild type heterodimeric HIV-1 reverse transcriptase p66/p51 assessed as inhibition of dTTP inco...More data for this Ligand-Target Pair
Affinity DataIC50: 15nMAssay Description:Inhibition of wild-type HIV-1 reverse transcriptase by fluorescence assayMore data for this Ligand-Target Pair
Affinity DataIC50: 15nMAssay Description:Covalent inhibition of recombinant wild type HIV-1 reverse transcriptase using poly(rA)350/oligo(dT)16 as template/primer preincubated followed by su...More data for this Ligand-Target Pair
Affinity DataIC50: 17nMAssay Description:Inhibition of recombinant wildtype HIV-1 reverse transcriptase using r(A)350 as template and d(T)16 as primer preincubated with compound for 1 hrs fo...More data for this Ligand-Target Pair
Ligand Info
Affinity DataIC50: 18nMAssay Description:Inhibition of proteolytic activity was tested using recombinant SARS-CoV-2Mpro, which was expressed and purified as previously described.8,12 For the...More data for this Ligand-Target Pair
Affinity DataIC50: 19nMAssay Description:Inhibition of HIV1 3B reverse transcriptaseMore data for this Ligand-Target Pair
Affinity DataIC50: 20nMAssay Description:Inhibition of proteolytic activity was tested using recombinant SARS-CoV-2Mpro, which was expressed and purified as previously described.8,12 For the...More data for this Ligand-Target Pair
Affinity DataIC50: 20nMAssay Description:Inhibition of recombinant wildtype HIV-1 reverse transcriptase using r(A)350 as template and d(T)16 as primer preincubated with compound for 1 hrs fo...More data for this Ligand-Target Pair
Ligand Info
TargetBifunctional dihydrofolate reductase-thymidylate synthase(Toxoplasma gondii)
Duquesne University
Curated by ChEMBL
Duquesne University
Curated by ChEMBL
Affinity DataIC50: 21nMAssay Description:Inhibition of wild type Toxoplasma gondii TS-DHFR expressed in Escherichia coli BL21 using dUMP and methylene-THF as substrate by kaleidagraph analys...More data for this Ligand-Target Pair
TargetBifunctional dihydrofolate reductase-thymidylate synthase(Toxoplasma gondii)
Duquesne University
Curated by ChEMBL
Duquesne University
Curated by ChEMBL
Affinity DataIC50: 23nMAssay Description:Inhibition of wild type Toxoplasma gondii TS-DHFR expressed in Escherichia coli BL21 using dUMP and methylene-THF as substrate by kaleidagraph analys...More data for this Ligand-Target Pair
Affinity DataIC50: 24nMAssay Description:Inhibition of HIV1 3B reverse transcriptaseMore data for this Ligand-Target Pair
Affinity DataIC50: 24nMAssay Description:Inhibition of proteolytic activity was tested using recombinant SARS-CoV-2Mpro, which was expressed and purified as previously described.8,12 For the...More data for this Ligand-Target Pair
Affinity DataIC50: 25nMAssay Description:Inhibition of proteolytic activity was tested using recombinant SARS-CoV-2Mpro, which was expressed and purified as previously described.8,12 For the...More data for this Ligand-Target Pair
Affinity DataIC50: 25nMAssay Description:Purified protein is diluted in reaction buffer to 100 nM in an opaque 96-well plate. The protein is incubated with or without compound in DMSO at dif...More data for this Ligand-Target Pair
Affinity DataIC50: 27nMAssay Description:Purified protein is diluted in reaction buffer to 100 nM in an opaque 96-well plate. The protein is incubated with or without compound in DMSO at dif...More data for this Ligand-Target Pair
Affinity DataIC50: 27nMAssay Description:Inhibition of HIV1 3B reverse transcriptaseMore data for this Ligand-Target Pair
Affinity DataIC50: 28nMAssay Description:Inhibition of HIV1 3B reverse transcriptaseMore data for this Ligand-Target Pair
Affinity DataIC50: 28nMAssay Description:Purified protein is diluted in reaction buffer to 100 nM in an opaque 96-well plate. The protein is incubated with or without compound in DMSO at dif...More data for this Ligand-Target Pair
Affinity DataIC50: 29nMAssay Description:Inhibition of human TS using dUMP and methylene-THF as substrate by kaleidagraph analysisMore data for this Ligand-Target Pair
Affinity DataIC50: 29nMAssay Description:Inhibition of human TS using dUMP and methylene-THF as substrate by kaleidagraph analysisMore data for this Ligand-Target Pair
Affinity DataIC50: 36nMAssay Description:Inhibition of proteolytic activity was tested using recombinant SARS-CoV-2Mpro, which was expressed and purified as previously described.8,12 For the...More data for this Ligand-Target Pair
Affinity DataIC50: 36nMAssay Description:Inhibition of proteolytic activity was tested using recombinant SARS-CoV-2Mpro, which was expressed and purified as previously described.8,12 For the...More data for this Ligand-Target Pair
TargetBifunctional dihydrofolate reductase-thymidylate synthase(Toxoplasma gondii)
Duquesne University
Curated by ChEMBL
Duquesne University
Curated by ChEMBL
Affinity DataIC50: 36nMAssay Description:Inhibition of wild type Toxoplasma gondii TS-DHFR expressed in Escherichia coli BL21 using dUMP and methylene-THF as substrate by kaleidagraph analys...More data for this Ligand-Target Pair
Affinity DataIC50: 37nMAssay Description:Inhibition of proteolytic activity was tested using recombinant SARS-CoV-2Mpro, which was expressed and purified as previously described.8,12 For the...More data for this Ligand-Target Pair
Affinity DataIC50: 37nMAssay Description:Inhibition of proteolytic activity was tested using recombinant SARS-CoV-2Mpro, which was expressed and purified as previously described.8,12 For the...More data for this Ligand-Target Pair
Affinity DataIC50: 37nMAssay Description:Purified protein is diluted in reaction buffer to 100 nM in an opaque 96-well plate. The protein is incubated with or without compound in DMSO at dif...More data for this Ligand-Target Pair
Affinity DataIC50: 38nMAssay Description:Purified protein is diluted in reaction buffer to 100 nM in an opaque 96-well plate. The protein is incubated with or without compound in DMSO at dif...More data for this Ligand-Target Pair
Affinity DataIC50: 38nMAssay Description:Inhibition of HIV1 reverse transcriptase-mediated thymidine incorporation into D23/D36 primer-template preincubated for 15 mins by polyacrylamide gel...More data for this Ligand-Target Pair
Affinity DataIC50: 38nMAssay Description:Covalent inhibition of recombinant wild type HIV-1 reverse transcriptase using poly(rA)350/oligo(dT)16 as template/primer preincubated followed by su...More data for this Ligand-Target Pair