BDBM50582083 CHEMBL5084158

SMILES Clc1ccc2c(NCCCCCCCNC3CCc4[nH]c(=O)ccc4C3)c3CCCCc3nc2c1

InChI Key InChIKey=SPUPUJFQNOIJFY-UHFFFAOYSA-N

Data  3 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 3 hits for monomerid = 50582083   

TargetCarboxylic ester hydrolase(Rat)
The Hong Kong University of Science and Technology

Curated by ChEMBL
LigandPNGBDBM50582083(CHEMBL5084158)
Affinity DataIC50: 893nMAssay Description:Inhibition of rat serum BChE using butyrylthiocholine iodide as substrate by Ellman's methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
3/5/2023
Entry Details Article
PubMed
TargetAcetylcholinesterase(Rat)
The Hong Kong University of Science and Technology

Curated by ChEMBL
LigandPNGBDBM50582083(CHEMBL5084158)
Affinity DataIC50: 15nMAssay Description:Inhibition of rat cortex AChE using acetylthiocholine iodide as substrate by Ellman's methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
3/5/2023
Entry Details Article
PubMed
TargetPotassium voltage-gated channel subfamily H member 2(Human)
The Hong Kong University of Science and Technology

Curated by ChEMBL
LigandPNGBDBM50582083(CHEMBL5084158)
Affinity DataIC50: 6.36E+3nMAssay Description:Inhibition of hERG expressed in CHO-K1 cells assessed as reduction in thallium influx incubated for 30 minutes by FLIPRMore data for this Ligand-Target Pair
In Depth
Date in BDB:
3/5/2023
Entry Details Article
PubMed