BDBM50422383 CHEMBL1203235

SMILES COc1cc2nc(nc(N)c2cc1OC)N(C)CCCCCCN(C)C(=O)c1ccc(CNCCCCCCNCCSSCCNCCCCCCNCc2ccc(cc2)C(=O)N(C)CCCCCCN(C)c2nc(N)c3cc(OC)c(OC)cc3n2)cc1

InChI Key InChIKey=KBSVQQQDGQQCLB-UHFFFAOYSA-N

Data  3 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 3 hits for monomerid = 50422383   

TargetAlpha-1D adrenergic receptor(Rattus norvegicus (Rat))
University Of Bologna

Curated by ChEMBL
LigandPNGBDBM50422383(CHEMBL1203235)
Affinity DataIC50:  3.20nMAssay Description:Antagonist affinity [non competitive (irreversible)] at alpha-1D-adrenoreceptors on isolated thoracic aorta from ratMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAlpha-1B adrenergic receptor(Rattus norvegicus (rat))
University Of Bologna

Curated by ChEMBL
LigandPNGBDBM50422383(CHEMBL1203235)
Affinity DataIC50:  2.14E+3nMAssay Description:Antagonist affinity [non competitive (irreversible)] at alpha-1B-adrenoreceptors on isolated spleen from ratMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAlpha-1A adrenergic receptor(Rattus norvegicus (Rat))
University Of Bologna

Curated by ChEMBL
LigandPNGBDBM50422383(CHEMBL1203235)
Affinity DataIC50:  4.68E+3nMAssay Description:Antagonist affinity [non competitive (irreversible)] at alpha-1A-adrenoreceptors on isolated prostatic Vas deferens from ratMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed