null

SMILES Cl.Clc1cc(cnc1Cl)C(=O)NCCCNc1c2CCCCc2nc2ccccc12

InChI Key InChIKey=VOEPOEYGZPYGGY-UHFFFAOYSA-N

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
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Similarity at least:  must be >=0.5
Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 3 hits for monomerid = 50292241   

TargetCholinesterase(Equus caballus (Horse))
Medical University of Lodz

Curated by ChEMBL
LigandPNGBDBM50292241(CHEMBL4159080)copy SMILEScopy InChI
Affinity DataIC50: 160nMAssay Description:Inhibition of equine serum BuChE using acetylthiocholine iodide as substrate after 8 mins by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WM1GZMPubMed
TargetHyaluronidase-1/Hyaluronidase-2(Bos taurus )
Medical University of Lodz

Curated by ChEMBL
LigandPNGBDBM50292241(CHEMBL4159080)copy SMILEScopy InChI
Affinity DataIC50: 4.66E+5nMAssay Description:Inhibition of bovine testes hyaluronidase using hyaluronic acid as substrate preincubated for 10 mins in dark followed by incubation with substrate f...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WM1GZMPubMed
TargetAcetylcholinesterase(Electrophorus electricus (Electric eel))
Medical University of Lodz

Curated by ChEMBL
LigandPNGBDBM50292241(CHEMBL4159080)copy SMILEScopy InChI
Affinity DataIC50: 1nMAssay Description:Inhibition of electric eel AChE using acetylthiocholine iodide as substrate after 10 mins by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WM1GZMPubMed