null

SMILES Clc1ccc2c(-[#6]-[#6]-c3cccnc3\[#6]-2=[#6]-2\[#6]-[#6]-[#7](-[#6]-[#6]-2)-[#6](=O)-[#6]-[#6]-2-[#6]-[#6]-[#6]-[#6]-[#6]-2)c1

InChI Key InChIKey=YSJZQHPNURRVLN-UHFFFAOYSA-N

  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 = 50031121   

TargetHistamine H1 receptor(Homo sapiens (Human))
Max Planck Institute of Psychiatry

Curated by ChEMBL
LigandPNGBDBM50031121(CHEMBL3357045)copy SMILEScopy InChI
Affinity DataKi:  441nMAssay Description:Displacement of [3H]mepyramine from human histamine H1 receptor expressed in Sf9 cells by scintillation counting methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q22F7Q1HPubMed
TargetSodium-dependent neutral amino acid transporter B(0)AT2(Homo sapiens (Human))
Max Planck Institute of Psychiatry

Curated by ChEMBL
LigandPNGBDBM50031121(CHEMBL3357045)copy SMILEScopy InChI
Affinity DataIC50: 5.70E+3nMAssay Description:Inhibition of eGFP-tagged human B0AT2 expressed in HEK293 cells measured within 10 mins by [3H]proline uptake assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q22F7Q1HPubMed