BDBM50525644 CHEMBL4545912

SMILES C#CCNC1CCc2cc(OCCCN3CCCCC3)ccc12

InChI Key InChIKey=RXNWZWWEYCPZCV-UHFFFAOYSA-N

Data  6 KI  6 IC50

  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 12 hits for monomerid = 50525644   

TargetHistamine H3 receptor(Homo sapiens (Human))
Heinrich Heine University D£Sseldorf

Curated by ChEMBL
LigandPNGBDBM50525644(CHEMBL4545912)
Affinity DataKi:  2.60nMAssay Description:Displacement of [3H] N-alpha methylhistamine from human recombinant H3 receptor expressed in HEK293 cells incubated for 90 minMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetHistamine H3 receptor(Homo sapiens (Human))
Heinrich Heine University D£Sseldorf

Curated by ChEMBL
LigandPNGBDBM50525644(CHEMBL4545912)
Affinity DataKi: >10nMAssay Description:Displacement of [3H] N-alpha methylhistamine from human recombinant H3 receptor expressed in HEK293 cells incubated for 90 minMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetD(3) dopamine receptor(Homo sapiens (Human))
Heinrich Heine University D£Sseldorf

Curated by ChEMBL
LigandPNGBDBM50525644(CHEMBL4545912)
Affinity DataKi: >1.00E+4nMAssay Description:Displacement of [3H] spiperone from human D3 dopamine receptorMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetHistamine H1 receptor(Homo sapiens (Human))
Heinrich Heine University D£Sseldorf

Curated by ChEMBL
LigandPNGBDBM50525644(CHEMBL4545912)
Affinity DataKi: >1.00E+4nMAssay Description:Displacement of [3H] pyrilamine from human H1 histamine receptorMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetD(2) dopamine receptor(Homo sapiens (Human))
Heinrich Heine University D£Sseldorf

Curated by ChEMBL
LigandPNGBDBM50525644(CHEMBL4545912)
Affinity DataKi: >1.00E+4nMAssay Description:Displacement of [3H] spiperone from human D2 dopamine receptorMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetHistamine H4 receptor(Homo sapiens (Human))
Heinrich Heine University D£Sseldorf

Curated by ChEMBL
LigandPNGBDBM50525644(CHEMBL4545912)
Affinity DataKi: >1.00E+5nMAssay Description:Displacement of [3H] histamine from human H4 histamine receptorMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetAmine oxidase [flavin-containing] B(Homo sapiens (Human))
Heinrich Heine University D£Sseldorf

Curated by ChEMBL
LigandPNGBDBM50525644(CHEMBL4545912)
Affinity DataIC50:  256nMAssay Description:Inhibition of human recombinant MAO-B using kynuramine as substrate preincubated for 60 mins followed by substrate addition by discontinuous fluorime...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetAmine oxidase [flavin-containing] A(Homo sapiens (Human))
Heinrich Heine University D£Sseldorf

Curated by ChEMBL
LigandPNGBDBM50525644(CHEMBL4545912)
Affinity DataIC50: >1.00E+5nMAssay Description:Inhibition of human recombinant MAO-A using kynuramine as substrate preincubated for 30 mins followed by substrate addition by discontinuous fluorime...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetAmine oxidase [flavin-containing] B(Homo sapiens (Human))
Heinrich Heine University D£Sseldorf

Curated by ChEMBL
LigandPNGBDBM50525644(CHEMBL4545912)
Affinity DataIC50:  1.05E+3nMAssay Description:Inhibition of human recombinant MAO-B using kynuramine as substrate preincubated for 30 mins followed by substrate addition by discontinuous fluorime...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetAmine oxidase [flavin-containing] A(Homo sapiens (Human))
Heinrich Heine University D£Sseldorf

Curated by ChEMBL
LigandPNGBDBM50525644(CHEMBL4545912)
Affinity DataIC50: >1.00E+4nMAssay Description:Inhibition of human recombinant MAO-A using kynuramine as substrate preincubated for 60 mins followed by substrate addition by discontinuous fluorime...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetAmine oxidase [flavin-containing] A(Homo sapiens (Human))
Heinrich Heine University D£Sseldorf

Curated by ChEMBL
LigandPNGBDBM50525644(CHEMBL4545912)
Affinity DataIC50: >1.00E+5nMAssay Description:Inhibition of human recombinant MAO-A using kynuramine as substrate by discontinuous fluorimetric analysisMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetAmine oxidase [flavin-containing] B(Homo sapiens (Human))
Heinrich Heine University D£Sseldorf

Curated by ChEMBL
LigandPNGBDBM50525644(CHEMBL4545912)
Affinity DataIC50:  991nMAssay Description:Inhibition of human recombinant MAO-B using kynuramine as substrate by discontinuous fluorimetric analysisMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed