BDBM50259250 CHEMBL4062122

SMILES CC1CCCN(Cc2ccc(COc3ccc(cc3)C(C)=O)cc2)C1

InChI Key InChIKey=VIJXBNYOIBJHGJ-UHFFFAOYSA-N

Data  3 KI

  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 = 50259250   

TargetHistamine H3 receptor(Human)
Bioprojet-Biotech

Curated by ChEMBL
LigandPNGBDBM50259250(CHEMBL4062122)
Affinity DataKi:  22nMAssay Description:Antagonist activity at H3 receptor (unknown origin)More data for this Ligand-Target Pair
In Depth
Date in BDB:
12/30/2019
Entry Details Article
PubMed
TargetHistamine H4 receptor(Human)
Bioprojet-Biotech

Curated by ChEMBL
LigandPNGBDBM50259250(CHEMBL4062122)
Affinity DataKi:  1.64E+4nMAssay Description:Antagonist activity at H4 receptor (unknown origin)More data for this Ligand-Target Pair
In Depth
Date in BDB:
12/30/2019
Entry Details Article
PubMed
TargetHistamine H4 receptor(Human)
Bioprojet-Biotech

Curated by ChEMBL
LigandPNGBDBM50259250(CHEMBL4062122)
Affinity DataKi:  1.64E+4nMAssay Description:Antagonist activity at human H4 receptor expressed in CHO cells co-expressing Galphai2 assessed as inhibition of imetit-induced GTPgamma[35S] binding...More data for this Ligand-Target Pair
In Depth
Date in BDB:
12/30/2019
Entry Details Article
PubMed