BDBM50075071 CHEMBL3414619
SMILES CCCc1cc(C)[nH]c(=O)c1CNC(=O)c1cc(cc2n(ncc12)C(C)C)-c1ccc(nc1)N1CCN(CC1)C(C)C
InChI Key InChIKey=DPJNKUOXBZSZAI-UHFFFAOYSA-N
Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB
Found 39 hits for monomerid = 50075071
Affinity DataIC50: 2nMAssay Description:Inhibition of EZH2 in PRC2 complex (unknown origin) using biotinylated peptide as substrate in presence of S-adenosylmethionineMore data for this Ligand-Target Pair
Affinity DataKi: 4.60nMAssay Description:Competitive inhibition of EZH2 (unknown origin) using biotinylated-histone H3 (1 to 24) as substrate by Lineweaver-Burk plot analysis in presence of ...More data for this Ligand-Target Pair
Affinity DataKi: 4.60nMAssay Description:Competitive inhibition of EZH2 methyltransferase activity (unknown origin) in PRC2 complex assessed as inhibition constant in presence of cofactor SA...More data for this Ligand-Target Pair
Affinity DataIC50: 10nMAssay Description:Inhibition of human EZH2 in human MCF-10A cells assessed as reduction in H3K27me3 levels incubated for 72 hrs by Western blot analysisMore data for this Ligand-Target Pair
Affinity DataIC50: 10nMAssay Description:Inhibition of EZH2 methyltransferase activity (unknown origin) in PRC2 complex using 3H-SAM as substrate by Scintillation proximity assayMore data for this Ligand-Target Pair
Affinity DataIC50: 10nMAssay Description:Inhibition of EZH2 (unknown origin)More data for this Ligand-Target Pair
Affinity DataIC50: 10nMAssay Description:Inhibition of EZH2 histone methyltransferase activity of EZH2/EED/SUZ12 protein complex (unknown origin) using histone H3 peptide as substrate (21 to...More data for this Ligand-Target Pair
Affinity DataIC50: 10nMAssay Description:Inhibition of EZH2 (unknown origin)More data for this Ligand-Target Pair
Affinity DataIC50: 10nMAssay Description:Inhibition of EZH2 (unknown origin) in PRC2 complex using H3 (1 to 24 residues) and 3H-SAM as substrate incubated for 1 hrs by Scintillation proximit...More data for this Ligand-Target Pair
Affinity DataIC50: 10nMAssay Description:Inhibition of EZH2 (unknown origin) using biotinylated-histone H3 (1 to 24) as substrate after 1 hr by scintillation proximity assay in presence of [...More data for this Ligand-Target Pair
Affinity DataIC50: 10nMAssay Description:Inhibition of human EZH2 using core histone as substrate incubated for 1 hr by fluorescence based assayMore data for this Ligand-Target Pair
Affinity DataIC50: 15nMAssay Description:Inhibition of EZH2 Y641F mutant (unknown origin) using HMT as substrate incubated for 60 mins by luminescence based analysisMore data for this Ligand-Target Pair
TargetHistone-lysine N-methyltransferase EZH1(Human)
Case Western Reserve University
Curated by ChEMBL
Case Western Reserve University
Curated by ChEMBL
Affinity DataIC50: 45nMAssay Description:Inhibition of EZH1 (unknown origin)More data for this Ligand-Target Pair
TargetHistone-lysine N-methyltransferase EZH1(Human)
Case Western Reserve University
Curated by ChEMBL
Case Western Reserve University
Curated by ChEMBL
Affinity DataIC50: 45nMAssay Description:Inhibition of wildtype EZH1 expressed in human MCF-10A cells assessed as reduction in H3K27me3 level incubated for 1 hr by Western blot analysisMore data for this Ligand-Target Pair
TargetHistone-lysine N-methyltransferase EZH1(Human)
Case Western Reserve University
Curated by ChEMBL
Case Western Reserve University
Curated by ChEMBL
Affinity DataIC50: 45nMAssay Description:Inhibition of EZH1 methyltransferase activity (unknown origin) in PRC2 complex using 3H-SAM as substrate by Scintillation proximity assayMore data for this Ligand-Target Pair
TargetHistone-lysine N-methyltransferase EZH1(Human)
Case Western Reserve University
Curated by ChEMBL
Case Western Reserve University
Curated by ChEMBL
Affinity DataIC50: 45nMAssay Description:Inhibition of human recombinant full length EZH1 measured after 30 mins by scintillation proximity assayMore data for this Ligand-Target Pair
Affinity DataKi: 65nMAssay Description:Binding affinity to sigma 2 receptor (unknown origin) assessed as inhibition constantMore data for this Ligand-Target Pair
TargetHistone-lysine N-methyltransferase EZH1(Human)
Case Western Reserve University
Curated by ChEMBL
Case Western Reserve University
Curated by ChEMBL
Affinity DataIC50: 69nMAssay Description:Inhibition of EZH1 histone methyltransferase activity of EZH1/EED/SUZ12/RBBP4/AEBP2 protein complex (unknown origin) using histone H3 peptide as subs...More data for this Ligand-Target Pair
Affinity DataIC50: 124nMAssay Description:Inhibition of human EZH2 in human MCF-10A cells assessed as reduction in H3K27me3 levels incubated for 72 hrs by In-cell western assayMore data for this Ligand-Target Pair
Affinity DataIC50: 124nMAssay Description:Inhibition of human EZH2 in human MCF-10A cells assessed as reduction in H3K27me3 levels incubated for 72 hrs by In-cell western assayMore data for this Ligand-Target Pair
Affinity DataIC50: 124nMAssay Description:Inhibition of EZH2 in human MCF10A cells assessed as reduction of H3K27me3 level after 72 hrs by Western blot analysisMore data for this Ligand-Target Pair
Affinity DataKi: 300nMAssay Description:Binding affinity to H3 receptor (unknown origin) assessed as inhibition constantMore data for this Ligand-Target Pair
TargetSodium-dependent noradrenaline transporter(Human)
UNC Eshelman School of Pharmacy
Curated by ChEMBL
UNC Eshelman School of Pharmacy
Curated by ChEMBL
Affinity DataKi: 1.50E+3nMAssay Description:Binding affinity to NET (unknown origin) assessed as inhibition constantMore data for this Ligand-Target Pair
TargetSigma non-opioid intracellular receptor 1(Human)
UNC Eshelman School of Pharmacy
Curated by ChEMBL
UNC Eshelman School of Pharmacy
Curated by ChEMBL
Affinity DataKi: 4.70E+3nMAssay Description:Binding affinity to sigma 1 receptor (unknown origin) assessed as inhibition constantMore data for this Ligand-Target Pair
TargetHistone-lysine N-methyltransferase EHMT2(Human)
UNC Eshelman School of Pharmacy
Curated by ChEMBL
UNC Eshelman School of Pharmacy
Curated by ChEMBL
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibition of G9a (unknown origin) using [3H-SAM] as substrate incubated for 1 hr by scintillation proximity assayMore data for this Ligand-Target Pair
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibition of SMYD2 (unknown origin) using [3H-SAM] as substrate incubated for 1 hr by scintillation proximity assayMore data for this Ligand-Target Pair
TargetHistone-lysine N-methyltransferase SETD7(Human)
UNC Eshelman School of Pharmacy
Curated by ChEMBL
UNC Eshelman School of Pharmacy
Curated by ChEMBL
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibition of SETD7 (unknown origin) using [3H-SAM] as substrate incubated for 1 hr by scintillation proximity assayMore data for this Ligand-Target Pair
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibition of SETD8 (unknown origin) using [3H-SAM] as substrate incubated for 1 hr by scintillation proximity assayMore data for this Ligand-Target Pair
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibition of PRMT5 (unknown origin) using [3H-SAM] as substrate incubated for 1 hr by scintillation proximity assayMore data for this Ligand-Target Pair
TargetHistone-lysine N-methyltransferase SUV39H2(Human)
UNC Eshelman School of Pharmacy
Curated by ChEMBL
UNC Eshelman School of Pharmacy
Curated by ChEMBL
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibition of SUV39H2 (unknown origin) using [3H-SAM] as substrate incubated for 1 hr by scintillation proximity assayMore data for this Ligand-Target Pair
TargetHistone-lysine N-methyltransferase KMT5B(Human)
UNC Eshelman School of Pharmacy
Curated by ChEMBL
UNC Eshelman School of Pharmacy
Curated by ChEMBL
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibition of SUV420H1 (unknown origin) using [3H-SAM] as substrate incubated for 1 hr by scintillation proximity assayMore data for this Ligand-Target Pair
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibition of PRMT1 (unknown origin) using [3H-SAM] as substrate incubated for 1 hr by scintillation proximity assayMore data for this Ligand-Target Pair
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibition of MLL1 (unknown origin) using [3H-SAM] as substrate incubated for 1 hr by scintillation proximity assayMore data for this Ligand-Target Pair
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibition of PRMT3 (unknown origin) using [3H-SAM] as substrate incubated for 1 hr by scintillation proximity assayMore data for this Ligand-Target Pair
TargetHistone-lysine N-methyltransferase, H3 lysine-79 specific(Human)
UNC Eshelman School of Pharmacy
Curated by ChEMBL
UNC Eshelman School of Pharmacy
Curated by ChEMBL
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibition of DOT1L (unknown origin) using [3H-SAM] as substrate incubated for 1 hr by scintillation proximity assayMore data for this Ligand-Target Pair
TargetHistone-lysine N-methyltransferase EHMT1(Human)
UNC Eshelman School of Pharmacy
Curated by ChEMBL
UNC Eshelman School of Pharmacy
Curated by ChEMBL
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibition of EHMT1 (unknown origin) using [3H-SAM] as substrate incubated for 1 hr by scintillation proximity assayMore data for this Ligand-Target Pair
TargetHistone-lysine N-methyltransferase KMT5C(Human)
UNC Eshelman School of Pharmacy
Curated by ChEMBL
UNC Eshelman School of Pharmacy
Curated by ChEMBL
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibition of SUV420H2 (unknown origin) using [3H-SAM] as substrate incubated for 1 hr by scintillation proximity assayMore data for this Ligand-Target Pair
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibition of DNMT1 (unknown origin) using hemimethylated dsDNA as substrate incubated for 1 hr by scintillation proximity assayMore data for this Ligand-Target Pair
TargetHistone-lysine N-methyltransferase SETDB1(Human)
UNC Eshelman School of Pharmacy
Curated by ChEMBL
UNC Eshelman School of Pharmacy
Curated by ChEMBL
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibition of SETDB1 (unknown origin) using [3H-SAM] as substrate incubated for 1 hr by scintillation proximity assayMore data for this Ligand-Target Pair
