BDBM50302536 (2S,3R)-N-(4-guanidinobutyl)-5-(3-(4-guanidinobutylamino)-3-oxoprop-1-enyl)-2-(4-hydroxyphenyl)-2,3-dihydrobenzofuran-3-carboxamide::CHEMBL568182

SMILES [#7]\[#6](-[#7])=[#7]\[#6]-[#6]-[#6]-[#6]-[#7]-[#6](=O)-[#6]=[#6]-c1ccc2-[#8]-[#6@@H](-[#6@H](-[#6](=O)-[#7]-[#6]-[#6]-[#6]-[#6]\[#7]=[#6](\[#7])-[#7])-c2c1)-c1ccc(-[#8])cc1

InChI Key InChIKey=CRSXQPHWASLXTK-UHFFFAOYSA-N

Data  2 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 2 hits for monomerid = 50302536   

TargetAlpha-1A adrenergic receptor(Rat)
University of Shizuoka and Global Coe Program

Curated by ChEMBL
LigandPNGBDBM50302536((2S,3R)-N-(4-guanidinobutyl)-5-(3-(4-guanidinobuty...)
Affinity DataIC50: 2.44E+6nMAssay Description:Displacement of [3H]prazosin from rat salivary gland alpha1A adrenoceptorMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/30/2010
Entry Details Article
PubMed
TargetAlpha-1A adrenergic receptor(Rat)
University of Shizuoka and Global Coe Program

Curated by ChEMBL
LigandPNGBDBM50302536((2S,3R)-N-(4-guanidinobutyl)-5-(3-(4-guanidinobuty...)
Affinity DataIC50: 1.77E+7nMAssay Description:Antagonist activity at rat alpha1A adrenoceptor assessed as inhibition of phenylephrine-induced contraction of caudal arteryMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/30/2010
Entry Details Article
PubMed