BDBM50043759 2-Amino-4-[2-benzylsulfanyl-1-(2-carboxy-ethylcarbamoyl)-ethylcarbamoyl]-butyric acid::CHEMBL58451

SMILES NC(CCC(=O)NC(CSCc1ccccc1)C(=O)NCCC(O)=O)C(O)=O

InChI Key InChIKey=QLVGMERIDWMEBM-UHFFFAOYSA-N

Data  4 KI

  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 = 50043759   

TargetGlutathione S-transferase Mu 1(Homo sapiens (Human))
Terrapin Technologies

Curated by ChEMBL
LigandPNGBDBM50043759(2-Amino-4-[2-benzylsulfanyl-1-(2-carboxy-ethylcarb...)
Affinity DataKi:  2.20E+4nMAssay Description:Inhibitory activity of the compound was measured on recombinant human Glutathione S-transferase Mu 1More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGlutathione S-transferase Mu 2(Homo sapiens (Human))
Terrapin Technologies

Curated by ChEMBL
LigandPNGBDBM50043759(2-Amino-4-[2-benzylsulfanyl-1-(2-carboxy-ethylcarb...)
Affinity DataKi:  2.60E+4nMAssay Description:Inhibitory activity of the compound was measured on recombinant human Glutathione S-transferase Mu 2More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGlutathione S-transferase A1(Homo sapiens (Human))
Terrapin Technologies

Curated by ChEMBL
LigandPNGBDBM50043759(2-Amino-4-[2-benzylsulfanyl-1-(2-carboxy-ethylcarb...)
Affinity DataKi:  3.60E+5nMAssay Description:Inhibitory activity of the compound was measured on recombinant human Glutathione-S-transferase A1 enzymeMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGlutathione S-transferase P(Homo sapiens (Human))
Terrapin Technologies

Curated by ChEMBL
LigandPNGBDBM50043759(2-Amino-4-[2-benzylsulfanyl-1-(2-carboxy-ethylcarb...)
Affinity DataKi:  7.10E+5nMAssay Description:Inhibitory activity of the compound was measured on recombinant human Glutathione S-transferase PMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed