null

SMILES CCCCCCSCC(NC(=O)CCC(N)C(O)=O)C(=O)NCC(O)=O

InChI Key InChIKey=HXJDWCWJDCOHDG-UHFFFAOYSA-N

PDB links: 1 PDB ID matches this monomer.

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Similarity at least:  must be >=0.5
Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 4 hits for monomerid = 50043758   

TargetGlutathione S-transferase A1(Homo sapiens (Human))
Terrapin Technologies

Curated by ChEMBL
LigandPNGBDBM50043758(2-Amino-4-[1-(carboxymethyl-carbamoyl)-2-hexylsulf...)copy SMILEScopy InChI
Affinity DataKi:  840nMAssay Description:Inhibitory activity of the compound was measured on recombinant human Glutathione-S-transferase A1 enzymeMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q21V5D1VPubMed
TargetGlutathione S-transferase Mu 1(Homo sapiens (Human))
Terrapin Technologies

Curated by ChEMBL
LigandPNGBDBM50043758(2-Amino-4-[1-(carboxymethyl-carbamoyl)-2-hexylsulf...)copy SMILEScopy InChI
Affinity DataKi:  2.00E+3nMAssay Description:Inhibitory activity of the compound was measured on recombinant human Glutathione S-transferase Mu 1More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q21V5D1VPubMed
TargetGlutathione S-transferase P(Homo sapiens (Human))
Terrapin Technologies

Curated by ChEMBL
LigandPNGBDBM50043758(2-Amino-4-[1-(carboxymethyl-carbamoyl)-2-hexylsulf...)copy SMILEScopy InChI
Affinity DataKi:  1.00E+4nMAssay Description:Inhibitory activity of the compound was measured on recombinant human Glutathione S-transferase PMore data for this Ligand-Target Pair
TargetGlutathione S-transferase Mu 2(Homo sapiens (Human))
Terrapin Technologies

Curated by ChEMBL
LigandPNGBDBM50043758(2-Amino-4-[1-(carboxymethyl-carbamoyl)-2-hexylsulf...)copy SMILEScopy InChI
Affinity DataKi:  3.60E+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
BindingDB Entry DOI: 10.7270/Q21V5D1VPubMed