Reaction Details |
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Target | Hydroxyacylglutathione hydrolase, mitochondrial |
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Ligand | BDBM50039108 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_71297 (CHEMBL686102) |
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Ki | 3400±n/a nM |
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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] |
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More Info.: | Get all data from this article, Assay Method |
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Hydroxyacylglutathione hydrolase, mitochondrial |
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Name: | Hydroxyacylglutathione hydrolase, mitochondrial |
Synonyms: | GLO2 | GLO2_HUMAN | Glyoxalase II | HAGH | HAGH1 |
Type: | PROTEIN |
Mol. Mass.: | 33815.06 |
Organism: | Homo sapiens (Human) |
Description: | ChEMBL_71296 |
Residue: | 308 |
Sequence: | MVVGRGLLGRRSLAALGAACARRGLGPALLGVFCHTDLRKNLTVDEGTMKVEVLPALTDN
YMYLVIDDETKEAAIVDPVQPQKVVDAARKHGVKLTTVLTTHHHWDHAGGNEKLVKLESG
LKVYGGDDRIGALTHKITHLSTLQVGSLNVKCLATPCHTSGHICYFVSKPGGSEPPAVFT
GDTLFVAGCGKFYEGTADEMCKALLEVLGRLPPDTRVYCGHEYTINNLKFARHVEPGNAA
IREKLAWAKEKYSIGEPTVPSTLAEEFTYNPFMRVREKTVQQHAGETDPVTTMRAVRREK
DQFKMPRD
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BDBM50039108 |
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n/a |
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Name | BDBM50039108 |
Synonyms: | S-(N-Hydroxy-N-(4-chlorophenyl)carbamoyl)glutathione |
Type | Small organic molecule |
Emp. Form. | C17H20ClN4O8S |
Mol. Mass. | 475.881 |
SMILES | [NH3+]C(CCC(=O)NC(CSC(=O)N(O)c1ccc(Cl)cc1)C(=O)NCC([O-])=O)C([O-])=O |
Structure |
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