Weight | 72.063 g/mol |
---|---|
Formula | C3H4O2 |
Hydrogen Acceptors | 2 |
Hydrogen Donors | 0 |
Aromatic Rings | 0 |
Rotatable Bonds | 1 |
methylglyoxal (78-98-8)
Pyruvic Aldehyde · Pyruvaldehyde · Oxopropanal
Score:
#502 in Biochemistry
,
#1582 in Biology
,
#1857 in Chemistry
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- Formation of glyoxal, methylglyoxal and 3-deoxyglucosone in the glycation of proteins by glucose. (Biochemical Journal, 1999)
- Binding and modification of proteins by methylglyoxal under physiological conditions. A kinetic and mechanistic study with N alpha-acetylarginine, N alpha-acetylcysteine, and N alpha-acetyllysine, and bovine serum albumin. (Journal of Biological Chemistry, 1994)
- N-epsilon-(carboxyethyl)lysine, a Product of the Chemical Modification of Proteins by Methylglyoxal, Increases with Age in Human Lens Proteins (Biochemical Journal, 1997)
- Pharmacology of methylglyoxal: formation, modification of proteins and nucleic acids, and enzymatic detoxification-A role in pathogenesis and antiproliferative chemotherapy (General Pharmacology-the Vascular System, 1996)
- The formation of methylglyoxal from triose phosphates. Investigation using a specific assay for methylglyoxal. (FEBS Journal, 1993)
- Methylglyoxal in living organisms : Chemistry, biochemistry, toxicology and biological implications (Toxicology Letters, 1999)
-
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - Pyruvic Aldehyde
- Pyruvaldehyde
- Oxopropanal
- Acetylformaldehyde
-
SMILESCC(=O)C=O
-
InChIKeyAIJULSRZWUXGPQ-UHFFFAOYSA-N
- Pubchem - methylglyoxal
- Wikipedia - methylglyoxal
Methylglyoxal, also called pyruvaldehyde or 2-oxopropanal, is the organic compound with the formula CH3C(O)CHO. Gaseous methylglyoxal has two carbonyl groups, an aldehyde and a ketone but in the presence of water, it exists as hydrates and oligomers. It is a reduced derivative of pyruvic acid.
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