BDBM87060 Lignan, 4::MLS001138823::N-(4-methylcyclohexyl)-3-(4-methylpiperazin-1-yl)sulfonyl-benzamide::N-(4-methylcyclohexyl)-3-(4-methylpiperazin-1-yl)sulfonylbenzamide::N-(4-methylcyclohexyl)-3-(4-methylpiperazino)sulfonyl-benzamide::N-(4-methylcyclohexyl)-3-[(4-methyl-1-piperazinyl)sulfonyl]benzamide::SMR000715032::cid_24983123

SMILES CC1CCC(CC1)NC(=O)c1cccc(c1)S(=O)(=O)N1CCN(C)CC1

InChI Key InChIKey=TYRMMZAVHFLIQF-UHFFFAOYSA-N

Data  1 KI  1 IC50

  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 2 hits for monomerid = 87060   

TargetChymotrypsin-C(Homo sapiens (Human))
University of Karachi

LigandPNGBDBM87060(Lignan, 4 | MLS001138823 | N-(4-methylcyclohexyl)-...)
Affinity DataKi:  4.71E+4nM ΔG°:  -5.90kcal/molepH: 7.6 T: 2°CAssay Description:Chymotrypsin inhibitory activity of compunds was perfomred by the method of Cannel.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHigh affinity choline transporter 1(Homo sapiens (Human))
Johns Hopkins Ion Channel Center

Curated by PubChem BioAssay
LigandPNGBDBM87060(Lignan, 4 | MLS001138823 | N-(4-methylcyclohexyl)-...)
Affinity DataIC50:  4.68E+3nMAssay Description:Data Source (MLPCN Center Name): Johns Hopkins Ion Channel Center (JHICC) Center Affiliation: Johns Hopkins University, School of Medicine Screening ...More data for this Ligand-Target Pair
In DepthDetails PCBioAssay