Literature DB >> 25748783

Reaction of acetaldehyde with 5-aminolevulinic acid via dihydropyrazine derivative.

Toshinori Suzuki1, Naoki Yasuhara, Takashi Ueda, Michiyo Inukai, Mitsunobu Mio.   

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.

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Year:  2015        PMID: 25748783     DOI: 10.1248/cpb.c14-00694

Source DB:  PubMed          Journal:  Chem Pharm Bull (Tokyo)        ISSN: 0009-2363            Impact factor:   1.645


  1 in total

1.  New Carboxamides and a New Polyketide from the Sponge-Derived Fungus Arthrinium sp. SCSIO 41421.

Authors:  Jianglian She; Yi Chen; Yuxiu Ye; Xiuping Lin; Bin Yang; Jiao Xiao; Yonghong Liu; Xuefeng Zhou
Journal:  Mar Drugs       Date:  2022-07-25       Impact factor: 6.085

  1 in total

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