BDBM50535300 CHEMBL4586884

SMILES O=c1c(coc2cc(OCCN3CCCC3)ccc12)-c1ccc(OCCN2CCCCC2)cc1

InChI Key InChIKey=LKWBRFHBJPNBMM-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 = 50535300   

TargetHistamine H3 receptor(Human)
Peking Union Medical College

Curated by ChEMBL
LigandPNGBDBM50535300(CHEMBL4586884)
Affinity DataIC50: 2.07E+3nMAssay 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
TargetAcetylcholinesterase(Mouse)
Peking Union Medical College

Curated by ChEMBL
LigandPNGBDBM50535300(CHEMBL4586884)
Affinity DataIC50: 710nMAssay 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
TargetCholinesterase(Mouse)
Peking Union Medical College

Curated by ChEMBL
LigandPNGBDBM50535300(CHEMBL4586884)
Affinity DataIC50: 4.55E+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