Reaction Details |
| Report a problem with these data |
Target | Lactoylglutathione lyase |
---|
Ligand | BDBM50039111 |
---|
Substrate/Competitor | n/a |
---|
Meas. Tech. | ChEMBL_71294 (CHEMBL684998) |
---|
Ki | 1200±n/a nM |
---|
Citation | Murthy, NS; Bakeris, T; Kavarana, MJ; Hamilton, DS; Lan, Y; Creighton, DJ S-(N-aryl-N-hydroxycarbamoyl)glutathione derivatives are tight-binding inhibitors of glyoxalase I and slow substrates for glyoxalase II. J Med Chem37:2161-6 (1994) [PubMed] |
---|
More Info.: | Get all data from this article, Assay Method |
---|
|
Lactoylglutathione lyase |
---|
Name: | Lactoylglutathione lyase |
Synonyms: | Aldoketomutase | GLO1 | Glx I | Glyoxalase 1 (GLO1) | Glyoxalase I | Ketone-aldehyde mutase | LGUL_HUMAN | Methylglyoxalase | S-D-lactoylglutathione methylglyoxal lyase |
Type: | Enzyme |
Mol. Mass.: | 20772.95 |
Organism: | Homo sapiens (Human) |
Description: | Q04760 |
Residue: | 184 |
Sequence: | MAEPQPPSGGLTDEAALSCCSDADPSTKDFLLQQTMLRVKDPKKSLDFYTRVLGMTLIQK
CDFPIMKFSLYFLAYEDKNDIPKEKDEKIAWALSRKATLELTHNWGTEDDETQSYHNGNS
DPRGFGHIGIAVPDVYSACKRFEELGVKFVKKPDDGKMKGLAFIQDPDGYWIEILNPNKM
ATLM
|
|
|
BDBM50039111 |
---|
n/a |
---|
Name | BDBM50039111 |
Synonyms: | S-(N-Hydroxy-N-(4-bromophenyl)carbamoyl)glutathione |
Type | Small organic molecule |
Emp. Form. | C17H20BrN4O8S |
Mol. Mass. | 520.332 |
SMILES | [NH3+]C(CCC(=O)NC(CSC(=O)N(O)c1ccc(Br)cc1)C(=O)NCC([O-])=O)C([O-])=O |
Structure |
|