null

SMILES Cl.[H][C@@]12CC[C@@H](C[C@]1([H])C[C@H](NC2)C(O)=O)Oc1cc(ccc1-c1nnn[nH]1)-c1ccccc1Cl

InChI Key InChIKey=XHNSHPIZOXRVRY-YDSLHZGRSA-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 = 50494366   

TargetGlutamate receptor ionotropic, kainate 1(Homo sapiens (Human))
Centro de Investigaci�n Lilly

Curated by ChEMBL
LigandPNGBDBM50494366(CHEMBL3088068)copy SMILEScopy InChI
Affinity DataKi:  1.00E+3nMAssay Description:Displacement of [3H]ATPA from human Gluk1 receptorMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2XS5ZBWPubMed
TargetGlutamate receptor 2(Homo sapiens (Human))
Centro de Investigaci�n Lilly

Curated by ChEMBL
LigandPNGBDBM50494366(CHEMBL3088068)copy SMILEScopy InChI
Affinity DataKi:  1.30E+4nMAssay Description:Displacement of [3H]AMPA from homomeric recombinant GluA2 receptor (unknown origin)More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2XS5ZBWPubMed