null

SMILES N[C@@H](CCC(=O)N[C@@H](CSC(=O)N(O)c1ccc(Cl)cc1)C(=O)NCC(O)=O)C(O)=O

InChI Key InChIKey=AJDQQFLYKZABLT-RYUDHWBXSA-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 7 hits for monomerid = 50092824   

TargetLactoylglutathione lyase(Homo sapiens (Human))
University of Maryland

Curated by ChEMBL
LigandPNGBDBM50092824(CHEMBL131578 | S-(N-4chlorophenyl-N-hydroxycarbamo...)copy SMILEScopy InChI
Affinity DataKi:  46nMAssay Description:Competitive inhibition of GLO1 (unknown origin)More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q29025C5PubMed
TargetLactoylglutathione lyase(Homo sapiens (Human))
University of Maryland

Curated by ChEMBL
LigandPNGBDBM50092824(CHEMBL131578 | S-(N-4chlorophenyl-N-hydroxycarbamo...)copy SMILEScopy InChI
Affinity DataKi:  46nMAssay Description:Binding affinity for Glyoxalase IMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2BC3XS4PubMed
TargetLactoylglutathione lyase(Homo sapiens (Human))
University of Maryland

Curated by ChEMBL
LigandPNGBDBM50092824(CHEMBL131578 | S-(N-4chlorophenyl-N-hydroxycarbamo...)copy SMILEScopy InChI
Affinity DataKi:  46nMAssay Description:Inhibition of human erythrocyte Glyoxalase-1More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2Z60SG5PubMed
TargetLactoylglutathione lyase(Homo sapiens (Human))
University of Maryland

Curated by ChEMBL
LigandPNGBDBM50092824(CHEMBL131578 | S-(N-4chlorophenyl-N-hydroxycarbamo...)copy SMILEScopy InChI
Affinity DataKi:  46nMAssay Description:Inhibition of human glyoxalase 1More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26H4K7BPubMed
TargetHydroxyacylglutathione hydrolase, mitochondrial(Bos taurus)
Chengdu University

Curated by ChEMBL
LigandPNGBDBM50092824(CHEMBL131578 | S-(N-4chlorophenyl-N-hydroxycarbamo...)copy SMILEScopy InChI
Affinity DataKi:  1.70E+3nMAssay Description:Inhibition of bovine liver glyoxalase 2More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26H4K7BPubMed
TargetLactoylglutathione lyase(Homo sapiens (Human))
University of Maryland

Curated by ChEMBL
LigandPNGBDBM50092824(CHEMBL131578 | S-(N-4chlorophenyl-N-hydroxycarbamo...)copy SMILEScopy InChI
Affinity DataKi:  3.60E+3nMAssay Description:Binding affinity of the compound on yeast glyoxalase I (GlxI) was determinedMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2BC3XS4PubMed
TargetLactoylglutathione lyase(Homo sapiens (Human))
University of Maryland

Curated by ChEMBL
LigandPNGBDBM50092824(CHEMBL131578 | S-(N-4chlorophenyl-N-hydroxycarbamo...)copy SMILEScopy InChI
Affinity DataKi:  1.60E+4nMAssay Description:Binding affinity of the compound on Pseudomonas putida glyoxalase I (GlxI) was determinedMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2BC3XS4PubMed