BDBM50535302 CHEMBL4568293

SMILES CCN(C)CCCCOc1ccc2c(c1)occ(-c1ccc(OCCN3CCCCC3)cc1)c2=O

InChI Key InChIKey=IKMDZEDNWBNJNC-UHFFFAOYSA-N

Data  3 IC50

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
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Similarity at least:  must be >=0.5
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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 3 hits for monomerid = 50535302   

TargetAcetylcholinesterase(Mouse)
Peking Union Medical College

Curated by ChEMBL
LigandPNGBDBM50535302(CHEMBL4568293)
Affinity DataIC50: 81nMAssay Description:Inhibition of mouse brain AChE using acetylthiocholine iodide as substrate measured after 30 mins by Ellman's methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
2/28/2021
Entry Details Article
PubMed
TargetHistamine H3 receptor(Human)
Peking Union Medical College

Curated by ChEMBL
LigandPNGBDBM50535302(CHEMBL4568293)
Affinity DataIC50: 270nMAssay Description:Inhibition of human H3R expressed in methylhistamine-induced human H3-bla U2OS cells incubated for 30 mins by beta-lactamase complementation technolo...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/28/2021
Entry Details Article
PubMed
TargetCholinesterase(Mouse)
Peking Union Medical College

Curated by ChEMBL
LigandPNGBDBM50535302(CHEMBL4568293)
Affinity DataIC50: 2.89E+3nMAssay Description:Inhibition of mouse plasma BuChE using S-butyrylacetylthiocholine iodide as substrate measured after 30 mins by Ellman's method relative to controlMore data for this Ligand-Target Pair
In Depth
Date in BDB:
2/28/2021
Entry Details Article
PubMed