Reaction Details |
| Report a problem with these data |
Target | Lactoylglutathione lyase |
---|
Ligand | BDBM50241121 |
---|
Substrate/Competitor | n/a |
---|
Meas. Tech. | ChEMBL_1367245 (CHEMBL3300061) |
---|
Ki | 80±n/a nM |
---|
Citation | Holewinski, RJ; Creighton, DJ Inhibition by active site directed covalent modification of human glyoxalase I. Bioorg Med Chem22:3301-8 (2014) [PubMed] Article |
---|
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
|
|
|
BDBM50241121 |
---|
n/a |
---|
Name | BDBM50241121 |
Synonyms: | (S)-5-((R)-3-(4-bromobenzylthio)-1-(carboxymethylamino)-1-oxopropan-2-ylamino)-2-amino-5-oxopentanoic acid | CHEMBL218644 | S-p-bromobenzyl glutatione | S-p-bromobenzylglutathione |
Type | Small organic molecule |
Emp. Form. | C17H22BrN3O6S |
Mol. Mass. | 476.342 |
SMILES | N[C@@H](CCC(=O)N[C@@H](CSCc1ccc(Br)cc1)C(=O)NCC(O)=O)C(O)=O |r| |
Structure |
|