BDBM50525811 CHEMBL4474244

SMILES [H][C@@]12[C@@H](CC(=O)[C@@]1(C)CC[C@]1([H])c3ccc(OCCCN4CCC[C@@H]4C)cc3CC[C@@]21[H])C(=O)N1CCCC1

InChI Key InChIKey=IBYVXJKTGRSNJL-UHFFFAOYSA-N

Data  2 KI  1 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 = 50525811   

TargetHistamine H3 receptor(Rat)
Chemical Works of Gedeon Richter

Curated by ChEMBL
LigandPNGBDBM50525811(CHEMBL4474244)
Affinity DataKi:  9nMAssay Description:Displacement of [3H]methyl- N-alpha methylhistamine dihydrochloride from Sprague-Dawley rat cerebral cortex H3 receptor measured after 30 mins by sci...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/25/2021
Entry Details Article
PubMed
TargetHistamine H3 receptor(Human)
Chemical Works of Gedeon Richter

Curated by ChEMBL
LigandPNGBDBM50525811(CHEMBL4474244)
Affinity DataKi:  30nMAssay Description:Displacement of [3H]methyl- N-alpha methylhistamine dihydrochloride from human recombinant H3 receptor expressed in CHOK1 cells measured after 30 min...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/25/2021
Entry Details Article
PubMed
TargetPotassium voltage-gated channel subfamily H member 2(Human)
Chemical Works of Gedeon Richter

Curated by ChEMBL
LigandPNGBDBM50525811(CHEMBL4474244)
Affinity DataIC50: 8.00E+4nMAssay Description:Inhibition of human ERGMore data for this Ligand-Target Pair
In Depth
Date in BDB:
2/25/2021
Entry Details Article
PubMed