BDBM66893 MLS001105910::N-[1-(4-methoxyphenyl)-6,6-dimethyl-5,7-dihydro-4H-indazol-4-yl]-2-(4-methyl-1,2,5-oxadiazol-3-yl)acetamide::N-[1-(4-methoxyphenyl)-6,6-dimethyl-5,7-dihydro-4H-indazol-4-yl]-2-(4-methyl-1,2,5-oxadiazol-3-yl)ethanamide::N-[1-(4-methoxyphenyl)-6,6-dimethyl-5,7-dihydro-4H-indazol-4-yl]-2-(4-methylfurazan-3-yl)acetamide::SMR000653609::cid_24793838

SMILES NCCCC[C@H](NC(=O)[C@@H](CCCCN)[C@]1(C(N)=O)CCCN1C(=O)Cc1cccc2ccccc12)C(=O)NCCOCC(N)=O

InChI Key InChIKey=ZVNBDZKLVZEEBQ-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 = 66893   

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

US Patent
LigandChemical structure of BindingDB Monomer ID 66893BDBM66893((S)-((S)-6-amino-1-(((S)-6-amino-1-((2-(2-amino-2-...)
Affinity DataIC50: 86nMAssay 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