BDBM50621817 CHEMBL5416421

SMILES CCN(CC)C(=O)c1ccc2n(CCC(C)C)c(Cc3ccc(OC(=O)N(C)c4ccccc4)cc3)nc2c1

InChI Key InChIKey=JIVUGVGICZGKIU-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 = 50621817   

TargetCholinesterase(Human)
Julius Maximilian University Wuerzburg

Curated by ChEMBL
LigandPNGBDBM50621817(CHEMBL5416421)
Affinity DataIC50: 1.01E+4nMAssay Description:Pseudo-irreversible inhibition of human BChE using butyrylthiocholine iodide as substrate incubated for 20 mins followed by substrate addition by Ell...More data for this Ligand-Target Pair
Ligand InfoSimilars
In Depth
Date in BDB:
12/16/2024
Entry Details
PubMed
TargetAcetylcholinesterase(Human)
Julius Maximilian University Wuerzburg

Curated by ChEMBL
LigandPNGBDBM50621817(CHEMBL5416421)
Affinity DataIC50: 3.46E+3nMAssay Description:Pseudo-irreversible inhibition of human AChE using acetylthiocholine iodide as substrate incubated for 20 mins followed by substrate addition by Ellm...More data for this Ligand-Target Pair
Ligand InfoSimilars
In Depth
Date in BDB:
12/16/2024
Entry Details
PubMed
TargetCannabinoid receptor 2(Human)
Julius Maximilian University Wuerzburg

Curated by ChEMBL
LigandPNGBDBM50621817(CHEMBL5416421)
Affinity DataIC50: 3.85E+3nMAssay Description:Displacement of [3H]CP55940 from human CB2 receptor expressed in HEK293 cell membrane incubated for 3 hrs by scintillation counter analysisMore data for this Ligand-Target Pair
Ligand InfoSimilars
In Depth
Date in BDB:
12/16/2024
Entry Details
PubMed