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- Name help_outline (R)-S-lactoylglutathione Identifier CHEBI:57474 Charge -1 Formula C13H20N3O8S InChIKeyhelp_outline VDYDCVUWILIYQF-CSMHCCOUSA-M SMILEShelp_outline C[C@@H](O)C(=O)SC[C@H](NC(=O)CC[C@H]([NH3+])C([O-])=O)C(=O)NCC([O-])=O 2D coordinates Mol file for the small molecule Search links Involved in 2 reaction(s) Find molecules that contain or resemble this structure Find proteins in UniProtKB for this molecule
- Name help_outline glutathione Identifier CHEBI:57925 Charge -1 Formula C10H16N3O6S InChIKeyhelp_outline RWSXRVCMGQZWBV-WDSKDSINSA-M SMILEShelp_outline [NH3+][C@@H](CCC(=O)N[C@@H](CS)C(=O)NCC(=O)[O-])C(=O)[O-] 2D coordinates Mol file for the small molecule Search links Involved in 100 reaction(s) Find molecules that contain or resemble this structure Find proteins in UniProtKB for this molecule
- Name help_outline methylglyoxal Identifier CHEBI:17158 (Beilstein: 906750; CAS: 78-98-8) help_outline Charge 0 Formula C3H4O2 InChIKeyhelp_outline AIJULSRZWUXGPQ-UHFFFAOYSA-N SMILEShelp_outline [H]C(=O)C(C)=O 2D coordinates Mol file for the small molecule Search links Involved in 25 reaction(s) Find molecules that contain or resemble this structure Find proteins in UniProtKB for this molecule
Cross-references
| RHEA:19069 | RHEA:19070 | RHEA:19071 | RHEA:19072 | |
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| Reaction direction help_outline | undefined | left-to-right | right-to-left | bidirectional |
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Publications
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The stereochemical configuration of the lactoyl group of S-lactoylglutathionine formed by the action of glyoxalase I from porcine erythrocytes and yeast.
Ekwall K., Mannervik B.
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The mechanism of action of glyoxalase.
RACKER E.