BDBM50622667 CHEMBL5411566
SMILES Oc1ccc2c(ccc(NC(=O)c3cc(C=O)n4CCCCc34)c2c1)C#N
InChI Key InChIKey=BXKKQOBMSRNNSV-UHFFFAOYSA-N
Data 3 IC50
Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB
Found 3 hits for monomerid = 50622667
Affinity DataIC50: 8.00E+3nMAssay Description:Inhibition of N-terminal 6His/SUMO-tagged SARS-CoV-2 NSP14 expressed in Escherichia coli Rosetta 2 (DE3) PlysS cells using 5'GpppACCCCCCCCC-Biotin 3'...More data for this Ligand-Target Pair
Ligand InfoSimilars
TargetHistone-lysine N-methyltransferase EHMT1(Human)
University of California San Francisco
Curated by ChEMBL
University of California San Francisco
Curated by ChEMBL
Affinity DataIC50: 1.40E+4nMAssay Description:Inhibition of human GLP using biotin-tagged Histone H3 and 3H-SAM as substrate incubated for 1 hrs by TopCount scintillation proximity assayMore data for this Ligand-Target Pair
Ligand InfoSimilars
TargetHistone-lysine N-methyltransferase EHMT2(Human)
University of California San Francisco
Curated by ChEMBL
University of California San Francisco
Curated by ChEMBL
Affinity DataIC50: 3.00E+4nMAssay Description:Inhibition of human G9a using biotin-tagged Histone H3 and 3H-SAM as substrate incubated for 1 hrs by TopCount scintillation proximity assayMore data for this Ligand-Target Pair
Ligand InfoSimilars
