BDBM50302538 (2R,3R)-methyl 5-(3-(4-guanidinobutylamino)-3-oxoprop-1-enyl)-2-(4-hydroxyphenyl)-2,3-dihydrobenzofuran-3-carboxylate::CHEMBL566264

SMILES [#6]-[#8]-[#6](=O)-[#6@H]-1-[#6@@H](-[#8]-c2ccc(-[#6]=[#6]-[#6](=O)-[#7]-[#6]-[#6]-[#6]-[#6]\[#7]=[#6](\[#7])-[#7])cc-12)-c1ccc(-[#8])cc1

InChI Key InChIKey=WYPBJTCSLQSQKK-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 = 50302538   

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

Curated by ChEMBL
LigandPNGBDBM50302538((2R,3R)-methyl 5-(3-(4-guanidinobutylamino)-3-oxop...)
Affinity DataIC50: 5.60E+5nMAssay 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
LigandPNGBDBM50302538((2R,3R)-methyl 5-(3-(4-guanidinobutylamino)-3-oxop...)
Affinity DataIC50: 9.72E+6nMAssay 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