BDBM50604204 CHEMBL5188949

SMILES CCc1cc(=O)[nH]c(n1)-n1nc(C)cc1NC(=O)c1cccc(C)c1

InChI Key InChIKey=PIFYSUAUZBQCOJ-UHFFFAOYSA-N

Data  1 KI  3 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 4 hits for monomerid = 50604204   

Target5-hydroxytryptamine receptor 2B(Homo sapiens (Human))
Purdue University

Curated by ChEMBL
LigandPNGBDBM50604204(CHEMBL5188949)
Affinity DataKi:  900nMAssay Description:Binding affinity to 5-HT2B receptor (unknown origin) assessed as displacement of radioligand at 10 uM by radioligand binding assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails PubMed
Target5-hydroxytryptamine receptor 2B(Homo sapiens (Human))
Purdue University

Curated by ChEMBL
LigandPNGBDBM50604204(CHEMBL5188949)
Affinity DataIC50:  420nMAssay Description:Antagonist activity at 5-HT2B receptor (unknown origin) transfected in HEK293 cells assessed as beta-arrestin translocation by Tango assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails PubMed
TargetAdenylate cyclase type 1(Homo sapiens (Human))
Purdue University

Curated by ChEMBL
LigandPNGBDBM50604204(CHEMBL5188949)
Affinity DataIC50:  410nMAssay Description:Inhibition of Ca2+/ CAM stimulated human AC1 activity expressed in AC3 and AC6-knockout HEK293 cells assessed as A23187 stimulated cAMP accumulation ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails PubMed
TargetAdenylate cyclase type 8(Homo sapiens (Human))
Purdue University

Curated by ChEMBL
LigandPNGBDBM50604204(CHEMBL5188949)
Affinity DataIC50:  2.70E+3nMAssay Description:Inhibition of Ca2+/ CAM stimulated human AC8 activity expressed in AC3 and AC6-knockout HEK293 cells assessed as A23187 stimulated cAMP accumulation ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails PubMed