BDBM50272629 CHEMBL4127877

SMILES Nc1c2CCCCc2nc2cc(ccc12)N1CCN(CCCC(=O)c2c[nH]c3ccc(cc23)C#N)CC1

InChI Key InChIKey=VSOMMGVYTLABPP-UHFFFAOYSA-N

Data  2 IC50  1 EC50

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
Find this compound or compounds like it in BindingDB:
   Substructure
Similarity at least:  must be >=0.5
Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 3 hits for monomerid = 50272629   

Target5-hydroxytryptamine receptor 1A(Human)
East China University of Science and Technology

Curated by ChEMBL
LigandPNGBDBM50272629(CHEMBL4127877)
Affinity DataEC50:  567nMAssay Description:Agonist activity at human 5-HT1A receptor expressed in HEK293 cells after 60 mins by Eu-cAMP solution based ultra LANCE assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
5/3/2020
Entry Details Article
PubMed
TargetAcetylcholinesterase(Rat)
East China University of Science and Technology

Curated by ChEMBL
LigandPNGBDBM50272629(CHEMBL4127877)
Affinity DataIC50: 1.98E+3nMAssay Description:Inhibition of rat cortex AChE using acetylthiocholine iodide as substrate after 20 mins by by Ellman's methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
5/3/2020
Entry Details Article
PubMed
TargetCarboxylic ester hydrolase(Rat)
East China University of Science and Technology

Curated by ChEMBL
LigandPNGBDBM50272629(CHEMBL4127877)
Affinity DataIC50: 370nMAssay Description:Inhibition of rat serum BChE using butyrylthiocholine iodide as substrate after 20 mins by by Ellman's methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
5/3/2020
Entry Details Article
PubMed