TargetL-lactate dehydrogenase B chain(Homo sapiens (Human))
University Of New Mexico School Of Medicine
Curated by ChEMBL
University Of New Mexico School Of Medicine
Curated by ChEMBL
Affinity DataKi: 50nMAssay Description:inhibitory activity against Human Lactate Dehydrogenase (LDH-M)More data for this Ligand-Target Pair
TargetL-lactate dehydrogenase B chain(Homo sapiens (Human))
University Of New Mexico School Of Medicine
Curated by ChEMBL
University Of New Mexico School Of Medicine
Curated by ChEMBL
Affinity DataKi: 100nMAssay Description:inhibitory activity against Human Lactate Dehydrogenase (LDH-M)More data for this Ligand-Target Pair
TargetL-lactate dehydrogenase A chain(Homo sapiens (Human))
University Of New Mexico School Of Medicine
Curated by ChEMBL
University Of New Mexico School Of Medicine
Curated by ChEMBL
Affinity DataKi: 100nMAssay Description:inhibitory activity against P. falciparum lactate dehydrogenase (pLDH)More data for this Ligand-Target Pair
TargetL-lactate dehydrogenase A chain(Homo sapiens (Human))
University Of New Mexico School Of Medicine
Curated by ChEMBL
University Of New Mexico School Of Medicine
Curated by ChEMBL
Affinity DataKi: 200nMAssay Description:inhibitory activity against P. falciparum lactate dehydrogenase (pLDH)More data for this Ligand-Target Pair
TargetL-lactate dehydrogenase B chain(Homo sapiens (Human))
University Of New Mexico School Of Medicine
Curated by ChEMBL
University Of New Mexico School Of Medicine
Curated by ChEMBL
Affinity DataKi: 200nMAssay Description:inhibitory activity against Human Lactate Dehydrogenase (LDH-M)More data for this Ligand-Target Pair
TargetL-lactate dehydrogenase A chain(Homo sapiens (Human))
University Of New Mexico School Of Medicine
Curated by ChEMBL
University Of New Mexico School Of Medicine
Curated by ChEMBL
Affinity DataKi: 300nMAssay Description:inhibitory activity against P. falciparum lactate dehydrogenase (pLDH)More data for this Ligand-Target Pair
TargetL-lactate dehydrogenase B chain(Homo sapiens (Human))
University Of New Mexico School Of Medicine
Curated by ChEMBL
University Of New Mexico School Of Medicine
Curated by ChEMBL
Affinity DataKi: 500nMAssay Description:inhibitory activity against Human Lactate Dehydrogenase (LDH-M)More data for this Ligand-Target Pair
TargetL-lactate dehydrogenase A chain(Homo sapiens (Human))
University Of New Mexico School Of Medicine
Curated by ChEMBL
University Of New Mexico School Of Medicine
Curated by ChEMBL
Affinity DataKi: 700nMAssay Description:inhibitory activity against P. falciparum lactate dehydrogenase (pLDH)More data for this Ligand-Target Pair
TargetL-lactate dehydrogenase B chain(Homo sapiens (Human))
University Of New Mexico School Of Medicine
Curated by ChEMBL
University Of New Mexico School Of Medicine
Curated by ChEMBL
Affinity DataKi: 1.00E+3nMAssay Description:inhibitory activity against Human Lactate Dehydrogenase (LDH-M)More data for this Ligand-Target Pair
TargetL-lactate dehydrogenase B chain(Homo sapiens (Human))
University Of New Mexico School Of Medicine
Curated by ChEMBL
University Of New Mexico School Of Medicine
Curated by ChEMBL
Affinity DataKi: 1.00E+3nMAssay Description:inhibitory activity against Human Lactate Dehydrogenase (LDH-H)More data for this Ligand-Target Pair
TargetL-lactate dehydrogenase A chain(Homo sapiens (Human))
University Of New Mexico School Of Medicine
Curated by ChEMBL
University Of New Mexico School Of Medicine
Curated by ChEMBL
Affinity DataKi: 1.00E+3nMAssay Description:inhibitory activity against P. falciparum lactate dehydrogenase (pLDH)More data for this Ligand-Target Pair
TargetL-lactate dehydrogenase B chain(Homo sapiens (Human))
University Of New Mexico School Of Medicine
Curated by ChEMBL
University Of New Mexico School Of Medicine
Curated by ChEMBL
Affinity DataKi: 2.00E+3nMAssay Description:inhibitory activity against Human Lactate Dehydrogenase (LDH-M)More data for this Ligand-Target Pair
TargetL-lactate dehydrogenase A chain(Homo sapiens (Human))
University Of New Mexico School Of Medicine
Curated by ChEMBL
University Of New Mexico School Of Medicine
Curated by ChEMBL
Affinity DataKi: 2.00E+3nMAssay Description:inhibitory activity against P. falciparum lactate dehydrogenase (pLDH)More data for this Ligand-Target Pair
TargetL-lactate dehydrogenase B chain(Homo sapiens (Human))
University Of New Mexico School Of Medicine
Curated by ChEMBL
University Of New Mexico School Of Medicine
Curated by ChEMBL
Affinity DataKi: 3.00E+3nMAssay Description:inhibitory activity against Human Lactate Dehydrogenase (LDH-M)More data for this Ligand-Target Pair
TargetL-lactate dehydrogenase B chain(Homo sapiens (Human))
University Of New Mexico School Of Medicine
Curated by ChEMBL
University Of New Mexico School Of Medicine
Curated by ChEMBL
Affinity DataKi: 4.00E+3nMAssay Description:inhibitory activity against Human Lactate Dehydrogenase (LDH-M)More data for this Ligand-Target Pair
TargetL-lactate dehydrogenase A chain(Homo sapiens (Human))
University Of New Mexico School Of Medicine
Curated by ChEMBL
University Of New Mexico School Of Medicine
Curated by ChEMBL
Affinity DataKi: 6.00E+3nMAssay Description:inhibitory activity against P. falciparum lactate dehydrogenase (pLDH)More data for this Ligand-Target Pair
TargetL-lactate dehydrogenase B chain(Homo sapiens (Human))
University Of New Mexico School Of Medicine
Curated by ChEMBL
University Of New Mexico School Of Medicine
Curated by ChEMBL
Affinity DataKi: 7.00E+3nMAssay Description:inhibitory activity against Human Lactate Dehydrogenase (LDH-H)More data for this Ligand-Target Pair
TargetL-lactate dehydrogenase A chain(Homo sapiens (Human))
University Of New Mexico School Of Medicine
Curated by ChEMBL
University Of New Mexico School Of Medicine
Curated by ChEMBL
Affinity DataKi: 8.00E+3nMAssay Description:inhibitory activity against P. falciparum lactate dehydrogenase (pLDH)More data for this Ligand-Target Pair
TargetL-lactate dehydrogenase A chain(Homo sapiens (Human))
University Of New Mexico School Of Medicine
Curated by ChEMBL
University Of New Mexico School Of Medicine
Curated by ChEMBL
Affinity DataKi: 1.30E+4nMAssay Description:inhibitory activity against P. falciparum lactate dehydrogenase (pLDH)More data for this Ligand-Target Pair
TargetL-lactate dehydrogenase B chain(Homo sapiens (Human))
University Of New Mexico School Of Medicine
Curated by ChEMBL
University Of New Mexico School Of Medicine
Curated by ChEMBL
Affinity DataKi: 1.30E+4nMAssay Description:inhibitory activity against Human Lactate Dehydrogenase (LDH-M)More data for this Ligand-Target Pair
TargetL-lactate dehydrogenase B chain(Homo sapiens (Human))
University Of New Mexico School Of Medicine
Curated by ChEMBL
University Of New Mexico School Of Medicine
Curated by ChEMBL
Affinity DataKi: 1.90E+4nMAssay Description:inhibitory activity against Human Lactate Dehydrogenase (LDH-H)More data for this Ligand-Target Pair
TargetL-lactate dehydrogenase A chain(Homo sapiens (Human))
University Of New Mexico School Of Medicine
Curated by ChEMBL
University Of New Mexico School Of Medicine
Curated by ChEMBL
Affinity DataKi: 2.20E+4nMAssay Description:inhibitory activity against P. falciparum lactate dehydrogenase (pLDH)More data for this Ligand-Target Pair
TargetL-lactate dehydrogenase B chain(Homo sapiens (Human))
University Of New Mexico School Of Medicine
Curated by ChEMBL
University Of New Mexico School Of Medicine
Curated by ChEMBL
Affinity DataKi: 3.40E+4nMAssay Description:inhibitory activity against Human Lactate Dehydrogenase (LDH-M)More data for this Ligand-Target Pair
TargetL-lactate dehydrogenase B chain(Homo sapiens (Human))
University Of New Mexico School Of Medicine
Curated by ChEMBL
University Of New Mexico School Of Medicine
Curated by ChEMBL
Affinity DataKi: 3.90E+4nMAssay Description:inhibitory activity against Human Lactate Dehydrogenase (LDH-H)More data for this Ligand-Target Pair
TargetL-lactate dehydrogenase B chain(Homo sapiens (Human))
University Of New Mexico School Of Medicine
Curated by ChEMBL
University Of New Mexico School Of Medicine
Curated by ChEMBL
Affinity DataKi: 4.90E+4nMAssay Description:inhibitory activity against Human Lactate Dehydrogenase (LDH-H)More data for this Ligand-Target Pair
TargetL-lactate dehydrogenase B chain(Homo sapiens (Human))
University Of New Mexico School Of Medicine
Curated by ChEMBL
University Of New Mexico School Of Medicine
Curated by ChEMBL
Affinity DataKi: 7.80E+4nMAssay Description:inhibitory activity against Human Lactate Dehydrogenase (LDH-H)More data for this Ligand-Target Pair
TargetL-lactate dehydrogenase B chain(Homo sapiens (Human))
University Of New Mexico School Of Medicine
Curated by ChEMBL
University Of New Mexico School Of Medicine
Curated by ChEMBL
Affinity DataKi: 8.10E+4nMAssay Description:inhibitory activity against Human Lactate Dehydrogenase (LDH-H)More data for this Ligand-Target Pair
TargetL-lactate dehydrogenase B chain(Homo sapiens (Human))
University Of New Mexico School Of Medicine
Curated by ChEMBL
University Of New Mexico School Of Medicine
Curated by ChEMBL
Affinity DataKi: 9.10E+4nMAssay Description:inhibitory activity against Human Lactate Dehydrogenase (LDH-H)More data for this Ligand-Target Pair
TargetL-lactate dehydrogenase B chain(Homo sapiens (Human))
University Of New Mexico School Of Medicine
Curated by ChEMBL
University Of New Mexico School Of Medicine
Curated by ChEMBL
Affinity DataKi: 1.90E+5nMAssay Description:inhibitory activity against Human Lactate Dehydrogenase (LDH-H)More data for this Ligand-Target Pair
TargetL-lactate dehydrogenase B chain(Homo sapiens (Human))
University Of New Mexico School Of Medicine
Curated by ChEMBL
University Of New Mexico School Of Medicine
Curated by ChEMBL
Affinity DataKi: >2.50E+5nMAssay Description:inhibitory activity against Human Lactate Dehydrogenase (LDH-H)More data for this Ligand-Target Pair
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit gamma isoform(Homo sapiens (Human))
The Institute Of Cancer Research
Curated by ChEMBL
The Institute Of Cancer Research
Curated by ChEMBL
Affinity DataIC50: 44nMAssay Description:Inhibition of human recombinant PI3K p110gamma after 1 hr by radiometric scintillation proximity assayMore data for this Ligand-Target Pair
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform(Homo sapiens (Human))
The Institute Of Cancer Research
Curated by ChEMBL
The Institute Of Cancer Research
Curated by ChEMBL
Affinity DataIC50: 62nMAssay Description:Inhibition of human recombinant PI3K p110alpha after 1 hr by radiometric scintillation proximity assayMore data for this Ligand-Target Pair
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit beta isoform(Homo sapiens (Human))
The Institute Of Cancer Research
Curated by ChEMBL
The Institute Of Cancer Research
Curated by ChEMBL
Affinity DataIC50: 100nMAssay Description:Inhibition of human recombinant PI3K p110beta after 1 hr by radiometric scintillation proximity assayMore data for this Ligand-Target Pair
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform(Homo sapiens (Human))
The Institute Of Cancer Research
Curated by ChEMBL
The Institute Of Cancer Research
Curated by ChEMBL
Affinity DataIC50: 110nMAssay Description:Inhibition of human recombinant PI3K p110alpha after 1 hr by radiometric scintillation proximity assayMore data for this Ligand-Target Pair
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform(Homo sapiens (Human))
The Institute Of Cancer Research
Curated by ChEMBL
The Institute Of Cancer Research
Curated by ChEMBL
Affinity DataIC50: 140nMAssay Description:Inhibition of human recombinant PI3K p110alpha after 1 hr by radiometric scintillation proximity assayMore data for this Ligand-Target Pair
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform(Homo sapiens (Human))
The Institute Of Cancer Research
Curated by ChEMBL
The Institute Of Cancer Research
Curated by ChEMBL
Affinity DataIC50: 140nMAssay Description:Inhibition of human recombinant PI3K p110alpha after 1 hr by radiometric scintillation proximity assayMore data for this Ligand-Target Pair
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit gamma isoform(Homo sapiens (Human))
The Institute Of Cancer Research
Curated by ChEMBL
The Institute Of Cancer Research
Curated by ChEMBL
Affinity DataIC50: 150nMAssay Description:Inhibition of human recombinant PI3K p110gamma after 1 hr by radiometric scintillation proximity assayMore data for this Ligand-Target Pair
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform(Homo sapiens (Human))
The Institute Of Cancer Research
Curated by ChEMBL
The Institute Of Cancer Research
Curated by ChEMBL
Affinity DataIC50: 180nMAssay Description:Inhibition of human recombinant PI3K p110alpha after 1 hr by radiometric scintillation proximity assayMore data for this Ligand-Target Pair
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit beta isoform(Homo sapiens (Human))
The Institute Of Cancer Research
Curated by ChEMBL
The Institute Of Cancer Research
Curated by ChEMBL
Affinity DataIC50: 200nMAssay Description:Inhibition of human recombinant PI3K p110beta after 1 hr by radiometric scintillation proximity assayMore data for this Ligand-Target Pair
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform(Homo sapiens (Human))
The Institute Of Cancer Research
Curated by ChEMBL
The Institute Of Cancer Research
Curated by ChEMBL
Affinity DataIC50: 200nMAssay Description:Inhibition of human recombinant PI3K p110alpha after 1 hr by radiometric scintillation proximity assayMore data for this Ligand-Target Pair
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform(Homo sapiens (Human))
The Institute Of Cancer Research
Curated by ChEMBL
The Institute Of Cancer Research
Curated by ChEMBL
Affinity DataIC50: 230nMAssay Description:Inhibition of human recombinant PI3K p110alpha after 1 hr by radiometric scintillation proximity assayMore data for this Ligand-Target Pair
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform(Homo sapiens (Human))
The Institute Of Cancer Research
Curated by ChEMBL
The Institute Of Cancer Research
Curated by ChEMBL
Affinity DataIC50: 250nMAssay Description:Inhibition of human recombinant PI3K p110alpha after 1 hr by radiometric scintillation proximity assayMore data for this Ligand-Target Pair
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform(Homo sapiens (Human))
The Institute Of Cancer Research
Curated by ChEMBL
The Institute Of Cancer Research
Curated by ChEMBL
Affinity DataIC50: 250nMAssay Description:Inhibition of human recombinant PI3K p110alpha after 1 hr by radiometric scintillation proximity assayMore data for this Ligand-Target Pair
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform(Homo sapiens (Human))
The Institute Of Cancer Research
Curated by ChEMBL
The Institute Of Cancer Research
Curated by ChEMBL
Affinity DataIC50: 260nMAssay Description:Inhibition of human recombinant PI3K p110alpha after 1 hr by radiometric scintillation proximity assayMore data for this Ligand-Target Pair
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform(Homo sapiens (Human))
The Institute Of Cancer Research
Curated by ChEMBL
The Institute Of Cancer Research
Curated by ChEMBL
Affinity DataIC50: 260nMAssay Description:Inhibition of human recombinant PI3K p110alpha after 1 hr by radiometric scintillation proximity assayMore data for this Ligand-Target Pair
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit gamma isoform(Homo sapiens (Human))
The Institute Of Cancer Research
Curated by ChEMBL
The Institute Of Cancer Research
Curated by ChEMBL
Affinity DataIC50: 340nMAssay Description:Inhibition of human recombinant PI3K p110gamma after 1 hr by radiometric scintillation proximity assayMore data for this Ligand-Target Pair
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit beta isoform(Homo sapiens (Human))
The Institute Of Cancer Research
Curated by ChEMBL
The Institute Of Cancer Research
Curated by ChEMBL
Affinity DataIC50: 370nMAssay Description:Inhibition of human recombinant PI3K p110beta after 1 hr by radiometric scintillation proximity assayMore data for this Ligand-Target Pair
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit gamma isoform(Homo sapiens (Human))
The Institute Of Cancer Research
Curated by ChEMBL
The Institute Of Cancer Research
Curated by ChEMBL
Affinity DataIC50: 380nMAssay Description:Inhibition of human recombinant PI3K p110gamma after 1 hr by radiometric scintillation proximity assayMore data for this Ligand-Target Pair
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform(Homo sapiens (Human))
The Institute Of Cancer Research
Curated by ChEMBL
The Institute Of Cancer Research
Curated by ChEMBL
Affinity DataIC50: 440nMAssay Description:Inhibition of human recombinant PI3K p110alpha after 1 hr by radiometric scintillation proximity assayMore data for this Ligand-Target Pair
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit beta isoform(Homo sapiens (Human))
The Institute Of Cancer Research
Curated by ChEMBL
The Institute Of Cancer Research
Curated by ChEMBL
Affinity DataIC50: 440nMAssay Description:Inhibition of human recombinant PI3K p110beta after 1 hr by radiometric scintillation proximity assayMore data for this Ligand-Target Pair