BDBM50615422 CHEMBL5288750

SMILES [H][C@@]12CC[C@H](N3CCCC3)[C@@]1(C)CC[C@@]1([H])[C@@]2([H])CC=C2C[C@H](CC[C@]12C)OCCCN1CCCC1

InChI Key InChIKey=FBJPHKBMEPBIQC-UHFFFAOYSA-N

Data  2 KI

  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 2 hits for monomerid = 50615422   

TargetHistamine H3 receptor(Human)
Chemical Works of Gedeon Richter

Curated by ChEMBL
LigandPNGBDBM50615422(CHEMBL5288750)
Affinity DataKi:  4.30nMAssay Description:Displacement of N-alpha-[methyl-3H]-methylhistamine dihydrochloride from recombinant human histamine H3 receptor expressed in CHO-K1 cells assessed a...More data for this Ligand-Target Pair
In Depth
Date in BDB:
4/23/2024
Entry Details
PubMed
TargetHistamine H3 receptor(Rat)
Chemical Works of Gedeon Richter

Curated by ChEMBL
LigandPNGBDBM50615422(CHEMBL5288750)
Affinity DataKi:  10nMAssay Description:Displacement of N-alpha-[methyl-3H]-methylhistamine dihydrochloride from Sprague-Dawley rat brain membrane histamine H3 receptor assessed as inhibiti...More data for this Ligand-Target Pair
In Depth
Date in BDB:
4/23/2024
Entry Details
PubMed