BDBM66857 5-(2-furanyl)-N-(3-hydroxyphenyl)-2-methyl-1,1-dioxo-1,2,6-thiadiazine-3-carboxamide::5-(2-furyl)-N-(3-hydroxyphenyl)-1,1-diketo-2-methyl-1,2,6-thiadiazine-3-carboxamide::5-(furan-2-yl)-N-(3-hydroxyphenyl)-2-methyl-1,1-bis(oxidanylidene)-1,2,6-thiadiazine-3-carboxamide::5-(furan-2-yl)-N-(3-hydroxyphenyl)-2-methyl-1,1-dioxo-1,2,6-thiadiazine-3-carboxamide::MLS001115570::SMR000626312::cid_16017207

SMILES N=C(N)NCCC[C@H](NC(=O)[C@H](CCCCN)NC(=O)[C@@H]1CCCN1C(=O)[C@@H]1CCCN1C(=O)CCl)C(=O)O

InChI Key InChIKey=BLMROVIDMVFTBT-UHFFFAOYSA-N

Data  1 EC50

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 1 hit for monomerid = 66857   

TargetN-terminal Xaa-Pro-Lys N-methyltransferase 1(Human)
Purdue Research Foundation

US Patent
LigandChemical structure of BindingDB Monomer ID 66857BDBM66857((2-chloroacetyl)-L-prolyl-L-prolyl-L-lysyl-L-argin...)
Affinity DataIC50: 1.60E+4nMAssay Description:Source (MLPCN Center Name): The Scripps Research Institute Molecular Screening Center (SRIMSC) Center Affiliation: The Scripps Research Institute (TS...More data for this Ligand-Target Pair
In Depth
Date in BDB:
4/6/2026
Entry Details
US Patent