BDBM66875 9-chloranyl-N-[3-(4-methylpiperazin-1-yl)propyl]-5,6,7,8-tetrahydroacridine-3-carboxamide::9-chloro-N-[3-(4-methyl-1-piperazinyl)propyl]-5,6,7,8-tetrahydroacridine-3-carboxamide::9-chloro-N-[3-(4-methylpiperazin-1-yl)propyl]-5,6,7,8-tetrahydroacridine-3-carboxamide::9-chloro-N-[3-(4-methylpiperazino)propyl]-5,6,7,8-tetrahydroacridine-3-carboxamide::MLS000924735::SMR000623663::cid_6619836

SMILES NCCCC[C@H](C(=O)NCc1nc2ccccc2[nH]1)[C@]1(C(N)=O)CCCN1C(=O)Cc1cccc2ccccc12

InChI Key InChIKey=DGWMMZMTYNKYLU-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 = 66875   

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

US Patent
LigandChemical structure of BindingDB Monomer ID 66875BDBM66875((S)-((S)-1-(((1H-benzo[d]imidazol-2-yl)methyl)amin...)
Affinity DataIC50: 1.30E+3nMAssay 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