TargetHistone-lysine N-methyltransferase PRDM9(Homo sapiens)
Daiichi Sankyo Co., Ltd
Curated by ChEMBL
Daiichi Sankyo Co., Ltd
Curated by ChEMBL
Affinity DataIC50: 1nMAssay Description:Inhibition of human PRDM9 using Histone H3 and [3H]SAM as substrate incubated for 30 mins to 1 hr by HotSpot kinase assayMore data for this Ligand-Target Pair
TargetHistone-lysine N-methyltransferase PRDM9(Homo sapiens)
Daiichi Sankyo Co., Ltd
Curated by ChEMBL
Daiichi Sankyo Co., Ltd
Curated by ChEMBL
Affinity DataIC50: 1nMAssay Description:Inhibition of human PRDM9 using Histone H3 and [3H]SAM as substrate incubated for 30 mins to 1 hr by HotSpot kinase assayMore data for this Ligand-Target Pair
TargetHistone-lysine N-methyltransferase PRDM9(Homo sapiens)
Daiichi Sankyo Co., Ltd
Curated by ChEMBL
Daiichi Sankyo Co., Ltd
Curated by ChEMBL
Affinity DataKi: 65nMAssay Description:Competitive inhibition of PRDM9 (unknown origin) assessed as inhibition constant in presence of varying concentration of SAM and peptide substrateMore data for this Ligand-Target Pair
TargetHistone-lysine N-methyltransferase PRDM9(Homo sapiens)
Daiichi Sankyo Co., Ltd
Curated by ChEMBL
Daiichi Sankyo Co., Ltd
Curated by ChEMBL
Affinity DataIC50: 80nMAssay Description:Inhibition of PRDM9 (unknown origin) (195 to 415 residues) using biotin-tagged Histone H3 (1 to 25) and 3H-SAM as substrate incubated for 30 mins by ...More data for this Ligand-Target Pair
TargetHistone-lysine N-methyltransferase PRDM9(Homo sapiens)
Daiichi Sankyo Co., Ltd
Curated by ChEMBL
Daiichi Sankyo Co., Ltd
Curated by ChEMBL
Affinity DataKd: 87nMAssay Description:Binding affinity to PRDM9 (unknown origin) (195 to 415 residues) assessed as dissociation constant measured at 60 to 120 secs in presence of SAM by b...More data for this Ligand-Target Pair
TargetHistone-lysine N-methyltransferase PRDM9(Homo sapiens)
Daiichi Sankyo Co., Ltd
Curated by ChEMBL
Daiichi Sankyo Co., Ltd
Curated by ChEMBL
Affinity DataIC50: 800nMAssay Description:Inhibition of FLAG tagged PRDM9 transfected in HEK293T cells assessed as reduction in trimethylation of ectopic H3K4 measured after 20 hrs by Western...More data for this Ligand-Target Pair
Affinity DataKd: 3.60E+3nMpH: 8.5 T: 2°CAssay Description:In this assay [3H]AdoMet (PerkinElmer Life Sciences; catalog number NET155V250UC)was used as a methyl donor to methylate biotinylated histone peptide...More data for this Ligand-Target Pair
Affinity DataKd: 4.10E+3nMpH: 8.5 T: 2°CAssay Description:In this assay [3H]AdoMet (PerkinElmer Life Sciences; catalog number NET155V250UC)was used as a methyl donor to methylate biotinylated histone peptide...More data for this Ligand-Target Pair
Affinity DataKd: 4.20E+3nMpH: 8.5 T: 2°CAssay Description:In this assay [3H]AdoMet (PerkinElmer Life Sciences; catalog number NET155V250UC)was used as a methyl donor to methylate biotinylated histone peptide...More data for this Ligand-Target Pair
Affinity DataKd: 4.60E+3nMpH: 8.5 T: 2°CAssay Description:In this assay [3H]AdoMet (PerkinElmer Life Sciences; catalog number NET155V250UC)was used as a methyl donor to methylate biotinylated histone peptide...More data for this Ligand-Target Pair
Affinity DataKd: 4.70E+3nMpH: 8.5 T: 2°CAssay Description:In this assay [3H]AdoMet (PerkinElmer Life Sciences; catalog number NET155V250UC)was used as a methyl donor to methylate biotinylated histone peptide...More data for this Ligand-Target Pair
TargetHistone-lysine N-methyltransferase PRDM9(Homo sapiens)
Daiichi Sankyo Co., Ltd
Curated by ChEMBL
Daiichi Sankyo Co., Ltd
Curated by ChEMBL
Affinity DataIC50: 5.00E+3nMAssay Description:Inhibition of Saccharomyces cerevisiae GST-tagged Fab1 incubated for 15 mins in presence of ATPMore data for this Ligand-Target Pair
Affinity DataKd: 5.80E+3nMpH: 8.5 T: 2°CAssay Description:In this assay [3H]AdoMet (PerkinElmer Life Sciences; catalog number NET155V250UC)was used as a methyl donor to methylate biotinylated histone peptide...More data for this Ligand-Target Pair
Affinity DataKd: 9.60E+3nMpH: 8.5 T: 2°CAssay Description:In this assay [3H]AdoMet (PerkinElmer Life Sciences; catalog number NET155V250UC)was used as a methyl donor to methylate biotinylated histone peptide...More data for this Ligand-Target Pair
TargetHistone-lysine N-methyltransferase PRDM9(Homo sapiens)
Daiichi Sankyo Co., Ltd
Curated by ChEMBL
Daiichi Sankyo Co., Ltd
Curated by ChEMBL
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of PRDM9 (unknown origin) methyltransferase activity measuredMore data for this Ligand-Target Pair
TargetHistone-lysine N-methyltransferase PRDM9(Homo sapiens)
Daiichi Sankyo Co., Ltd
Curated by ChEMBL
Daiichi Sankyo Co., Ltd
Curated by ChEMBL
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of PRDM9 (unknown origin) methyltransferase activity measuredMore data for this Ligand-Target Pair
TargetHistone-lysine N-methyltransferase PRDM9(Homo sapiens)
Daiichi Sankyo Co., Ltd
Curated by ChEMBL
Daiichi Sankyo Co., Ltd
Curated by ChEMBL
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of PRDM9 (unknown origin) methyltransferase activity measuredMore data for this Ligand-Target Pair
TargetHistone-lysine N-methyltransferase PRDM9(Homo sapiens)
Daiichi Sankyo Co., Ltd
Curated by ChEMBL
Daiichi Sankyo Co., Ltd
Curated by ChEMBL
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of Saccharomyces cerevisiae GST-tagged Fab1 incubated for 15 mins in presence of ATPMore data for this Ligand-Target Pair
Affinity DataKd: 1.20E+4nMpH: 8.5 T: 2°CAssay Description:In this assay [3H]AdoMet (PerkinElmer Life Sciences; catalog number NET155V250UC)was used as a methyl donor to methylate biotinylated histone peptide...More data for this Ligand-Target Pair















