null

SMILES Cl.COc1ccc(\C=C\C2=NN(CCCCN)C(=O)N(Cc3ccc4ccccc4c3)c3ccccc23)cc1

InChI Key InChIKey=NKZTVWHDNWNDGG-XDJHFCHBSA-N

  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 2 hits for monomerid = 50269945   

TargetUrotensin-2 receptor(RAT)
Universit£ de Montr£al

Curated by ChEMBL
LigandPNGBDBM50269945(CHEMBL4092221)copy SMILEScopy InChI
Affinity DataEC50:  8.5nMAssay Description:Allosteric modulation of urotensin-2 receptor in Sprague-Dawley rat thoracic aorta assessed as change in URP-mediated aortic ring contraction by meas...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2V1279DPubMed
TargetUrotensin-2 receptor(RAT)
Universit£ de Montr£al

Curated by ChEMBL
LigandPNGBDBM50269945(CHEMBL4092221)copy SMILEScopy InChI
Affinity DataEC50:  3.60nMAssay Description:Allosteric modulation of urotensin-2 receptor in Sprague-Dawley rat thoracic aorta assessed as change in human urotensin-2-mediated aortic ring contr...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2V1279DPubMed