- Reaction of acetaldehyde with 5-aminolevulinic acid via dihydropyrazine derivative.
Reaction of acetaldehyde with 5-aminolevulinic acid via dihydropyrazine derivative.
Chemical & pharmaceutical bulletin (2015-03-10)
Toshinori Suzuki, Naoki Yasuhara, Takashi Ueda, Michiyo Inukai, Mitsunobu Mio
PMID25748783
ABSTRACT
When a solution of 5-aminolevulinic acid (ALA) was incubated with acetaldehyde at neutral pH, a product was generated. This product was identified as 3-ethylpyrazine-2,5-dipropanoic acid (ETPY). ETPY was stable at neutral pH. It has been reported that ALA dimerizes at neutral pH generating 3,6-dihydropyrazine-2,5-dipropanoic acid (DHPY), and subsequently resulting in pyrazine-2,5-dipropanoic acid (PY) by autoxidation. In the present reaction, DHPY generated from ALA reacted with acetaldehyde, resulting in ETPY. Preadministration of ALA 3 min prior to acetaldehyde injection supressed the toxicity of acetaldehyde in male mice. These results suggest that ALA may be useful as a scavenger for acetaldehyde.
MATERIALS
Product Number
Brand
Product Description
Sigma-Aldrich
5-Aminolevulinic acid hydrochloride, BioReagent, suitable for cell culture, powder, ≥98%