BDBM50005504 CHEMBL13206::N-((5-Ethylsulfanylmethyl-furan-2-ylmethyl)-dimethyl-amine)l-N-[1-(((5-Ethylsulfanylmethyl-furan-2-ylmethyl)-dimethyl-amine)amino)-2-nitrovinyl]amine

SMILES CN(C)Cc1ccc(CSCCNCC(=NCCSCc2ccc(CN(C)C)o2)[N+]([O-])=O)o1

InChI Key InChIKey=JEBFKPNZVWPIMY-UHFFFAOYSA-N

Data  4 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 4 hits for monomerid = 50005504   

TargetMuscarinic acetylcholine receptor M1(Mus musculus)
University Of South Carolina

Curated by ChEMBL
LigandPNGBDBM50005504(CHEMBL13206 | N-((5-Ethylsulfanylmethyl-furan-2-yl...)
Affinity DataIC50:  900nMAssay Description:Compound was evaluated for the competitive inhibition of [3H]pirenzepine binding to muscarinic acetylcholine receptor M1 of mouse cerebral cortexMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCholinesterase(Homo sapiens (Human))
University Of South Carolina

Curated by ChEMBL
LigandPNGBDBM50005504(CHEMBL13206 | N-((5-Ethylsulfanylmethyl-furan-2-yl...)
Affinity DataIC50:  1.30E+3nMAssay Description:The compound was evaluated for the inhibition human of ButyrylcholinesteraseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
University Of South Carolina

Curated by ChEMBL
LigandPNGBDBM50005504(CHEMBL13206 | N-((5-Ethylsulfanylmethyl-furan-2-yl...)
Affinity DataIC50:  74nMAssay Description:The compound was evaluated for the inhibition of human AcetylcholinesteraseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMuscarinic acetylcholine receptor M2(Mus musculus)
University Of South Carolina

Curated by ChEMBL
LigandPNGBDBM50005504(CHEMBL13206 | N-((5-Ethylsulfanylmethyl-furan-2-yl...)
Affinity DataIC50:  500nMAssay Description:Compound was evaluated for the competitive inhibition of [3H]methylscopolamine binding to muscarinic acetylcholine receptor M2 of mouse cerebral cort...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed