BDBM50091481 (S)-2-Amino-4-propylidene-pentanedioicacid::CHEMBL52295::LY-310683

SMILES CC\C=C(\C[C@H](N)C(O)=O)C(O)=O

InChI Key InChIKey=WKTPEUFZYFCNLY-LMXCLXGDSA-N

Data  2 KI  2 EC50

  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 4 hits for monomerid = 50091481   

TargetGlutamate receptor ionotropic, kainate 1(Homo sapiens (Human))
Eli Lilly

Curated by ChEMBL
LigandPNGBDBM50091481((S)-2-Amino-4-propylidene-pentanedioicacid | CHEMB...)
Affinity DataKi:  61nMAssay Description:Binding affinity of compound was determined against Ionotropic glutamate receptor ionotropic kainate 1 using cell membranes prepared from HEK293 cell...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGlutamate receptor ionotropic, kainate 2(Homo sapiens (Human))
Eli Lilly

Curated by ChEMBL
LigandPNGBDBM50091481((S)-2-Amino-4-propylidene-pentanedioicacid | CHEMB...)
Affinity DataKi:  1.80E+4nMAssay Description:Binding affinity of compound was determined against Ionotropic glutamate receptor ionotropic kainate 1 using cell membranes prepared from HEK293 cell...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGlutamate receptor ionotropic, kainate 1(Homo sapiens (Human))
Eli Lilly

Curated by ChEMBL
LigandPNGBDBM50091481((S)-2-Amino-4-propylidene-pentanedioicacid | CHEMB...)
Affinity DataEC50:  1.42E+4nMAssay Description:Compound was tested for agonistic activity at Glutamate receptor 5 using HEK293 cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGlutamate receptor ionotropic, kainate 2(Homo sapiens (Human))
Eli Lilly

Curated by ChEMBL
LigandPNGBDBM50091481((S)-2-Amino-4-propylidene-pentanedioicacid | CHEMB...)
Affinity DataEC50: >3.00E+5nMAssay Description:Compound was tested for agonistic activity at Glutamate receptor 6 using HEK293 cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed