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more general categories information about this item 04. Bioactive Capabilities of Specific Chemicals 04. Bioactive Capabilities of Specific Chemicals Oxidoreductases [EC:1] (1697) Acting on the CH-OH group of donors [EC:1.1] (576) With NAD or NADP as acceptor [EC:1.1.1] (507) Methylglyoxal reductase (NADH-dependent) [EC:1.1.1.78] (5) methylglyoxal [CHEBI:17158] (1) Methylglyoxal reductase (NADPH-dependent) [EC:1.1.1.283] (5) methylglyoxal [CHEBI:17158] (1) Acting on single donors with incorporation of molecular oxygen (oxygenases) [EC:1.13] (176) With incorporation of two atoms of oxygen [EC:1.13.11] (139) Acetylacetone-cleaving enzyme [EC:1.13.11.50] (5) methylglyoxal [CHEBI:17158] (1) Transferases [EC:2] (1441) Transferring aldehyde or ketonic groups [EC:2.2] (35) Transketolases and Transaldolases [EC:2.2.1] (35) 6-deoxy-5-ketofructose 1-phosphate synthase [EC:2.2.1.11] (6) methylglyoxal [CHEBI:17158] (1) Lyases [EC:4] (743) Carbon-oxygen lyases [EC:4.2] (393) Hydro-Lyases [EC:4.2.1] (219) D-lactate dehydratase [EC:4.2.1.130] (4) methylglyoxal [CHEBI:17158] (1) Acting on Phosphates [EC:4.2.3] (175) Methylglyoxal synthase [EC:4.2.3.3] (2) methylglyoxal [CHEBI:17158] (1) Carbon-sulfur lyases [EC:4.4] (49) (only sub-subclass identified to date) [EC:4.4.1] (49) Lactoylglutathione lyase [EC:4.4.1.5] (3) methylglyoxal [CHEBI:17158] (1) 08. Chemical Category 08. Chemical Category main group molecular entity [CHEBI:33579] (25650) p-block molecular entity [CHEBI:33675] (25343) chalcogen molecular entity [CHEBI:33304] (15225) oxygen molecular entity [CHEBI:25806] (14414) organooxygen compound [CHEBI:36963] (11352) carbonyl compound [CHEBI:36586] (5928) aldehyde [CHEBI:17478] (258) ketoaldehyde [CHEBI:6124] (4) 2-oxo aldehyde [CHEBI:27659] (3) methylglyoxal [CHEBI:17158] (1) propanals [CHEBI:26282] (8) methylglyoxal [CHEBI:17158] (1) organochalcogen compound [CHEBI:36962] (11874) organooxygen compound [CHEBI:36963] (11352) carbonyl compound [CHEBI:36586] (5928) aldehyde [CHEBI:17478] (258) ketoaldehyde [CHEBI:6124] (4) 2-oxo aldehyde [CHEBI:27659] (3) methylglyoxal [CHEBI:17158] (1) propanals [CHEBI:26282] (8) methylglyoxal [CHEBI:17158] (1) carbon group molecular entity [CHEBI:33582] (23847) organic molecular entity [CHEBI:50860] (23769) heteroorganic entity [CHEBI:33285] (15197) organochalcogen compound [CHEBI:36962] (11874) organooxygen compound [CHEBI:36963] (11352) carbonyl compound [CHEBI:36586] (5928) aldehyde [CHEBI:17478] (258) ketoaldehyde [CHEBI:6124] (4) 2-oxo aldehyde [CHEBI:27659] (3) methylglyoxal [CHEBI:17158] (1) propanals [CHEBI:26282] (8) methylglyoxal [CHEBI:17158] (1) organic molecule [CHEBI:72695] (11399) organic oxo compound [CHEBI:36587] (5932) carbonyl compound [CHEBI:36586] (5928) aldehyde [CHEBI:17478] (258) ketoaldehyde [CHEBI:6124] (4) 2-oxo aldehyde [CHEBI:27659] (3) methylglyoxal [CHEBI:17158] (1) propanals [CHEBI:26282] (8) methylglyoxal [CHEBI:17158] (1) polyatomic entity [CHEBI:36357] (18777) molecule [CHEBI:25367] (11520) organic molecule [CHEBI:72695] (11399) organic oxo compound [CHEBI:36587] (5932) carbonyl compound [CHEBI:36586] (5928) aldehyde [CHEBI:17478] (258) ketoaldehyde [CHEBI:6124] (4) 2-oxo aldehyde [CHEBI:27659] (3) methylglyoxal [CHEBI:17158] (1) propanals [CHEBI:26282] (8) methylglyoxal [CHEBI:17158] (1) ChEBI Compound Accession Identifier: [CHEBI:17158] ChEBI Compound Description: A 2-oxoaldehyde derived from propanal. ChEBI Compound Identification Number: 17158 ChEBI InChI Value: InChI=1S/C3H4O2/c1-3(5)2-4/h2H,1H3 ChEBI InChIKey Value: AIJULSRZWUXGPQ-UHFFFAOYSA-N ChEBI Compound Name: methylglyoxal ChEBI SMILES Value: [H]C(=O)C(C)=O ChEBI Substance ID: 8145726 ChEBI URL: ChEBI:17158 ChemSpider ID: NS Ontomatica Chemical Accession Key (OnChAKey): AIJULSRZWUXGPQ_UHFFFAOYSA_N_000_000000 PubChem Compound ID: 880
