null

SMILES Oc1ccccc1\C=C\c1ccc2ccccc2n1

InChI Key InChIKey=NXNDEWNGCMCWMA-ZRDIBKRKSA-N

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
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   Substructure
Similarity at least:  must be >=0.5
Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 3 hits for monomerid = 50001270   

TargetCysteinyl leukotriene receptor 1/2(Homo sapiens (Human))
Merck Frosst Centre for Therapeutic Research

Curated by ChEMBL
LigandPNGBDBM50001270(2-(2-(quinolin-2-yl)vinyl)phenol | 2-(2-Quinolin-2...)copy SMILEScopy InChI
Affinity DataIC50: 5.00E+4nMAssay Description:Inhibition of human carbonic anhydrase IIMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2TQ625NPubMed
TargetNeprilysin(Homo sapiens (Human))
Mount Sinai School of Medicine

Curated by ChEMBL
LigandPNGBDBM50001270(2-(2-(quinolin-2-yl)vinyl)phenol | 2-(2-Quinolin-2...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibition of Neprilysin (unknown origin)More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2319VN5PubMed
TargetEEF1AKMT4-ECE2 readthrough transcript protein(Homo sapiens (Human))
Mount Sinai School of Medicine

Curated by ChEMBL
LigandPNGBDBM50001270(2-(2-(quinolin-2-yl)vinyl)phenol | 2-(2-Quinolin-2...)copy SMILEScopy InChI
Affinity DataIC50: 6.42E+3nMAssay Description:Reduction of recombinant ECE2 (unknown origin) activity measured by McaBk2 fluorescent substrate hydrolysisMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2319VN5PubMed