Tetramethylpyrazine
From Wikipedia, the free encyclopedia
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| Preferred IUPAC name
Tetramethylpyrazine | |
| Other names
Ligustrazine; Tetrapyrazine
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3D model (JSmol)
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| ChemSpider | |
| ECHA InfoCard | 100.013.084 Edit this at Wikidata |
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PubChem CID
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CompTox Dashboard (EPA)
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| Properties | |
| C8H12N2 | |
| Molar mass | 136.198 g·mol−1 |
| Melting point | 84–86 °C (183–187 °F; 357–359 K) |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Chemical compound
Tetramethylpyrazine, also known as ligustrazine, is a chemical compound found in nattō and in fermented cocoa beans.[1] In an observational study, tetramethylpyrazine was the dominant volatile organic compound in one sourdough starter.[2] When purified, tetramethylpyrazine is a colorless solid. It is classified as an alkylpyrazine. Its biosynthesis involves amination of acetoin, the latter derived from pyruvate.[3] It exhibits potential nootropic and antiinflammatory activities in rats.[4] [5]
References
[edit ]- ^ Hashim, Puziah; Selamat, Jinap; Syed Muhammad, Sharifah Kharidah; Ali, Asbi (1998). "Effect of mass and turning time on free amino acid, peptide-N, sugar and pyrazine concentration during cocoa fermentation". Journal of the Science of Food and Agriculture. 78 (4): 543–550. Bibcode:1998JSFA...78..543H. doi:10.1002/(SICI)1097-0010(199812)78:4<543::AID-JSFA152>3.0.CO;2-2.
- ^ Landis, Elizabeth A.; Oliverio, Angela M (January 26, 2021). "The diversity and function of sourdough starter microbiomes". eLife. 10: e61644. doi:10.7554/eLife.61644 . PMC 7837699 . PMID 33496265.
- ^ Kosuge, Takuo; Adachi, Tahei; Kamiya, Hiroko (1962). "Isolation of Tetramethylpyrazine from Culture of Bacillus natto, and Biosynthetic Pathways of Tetramethylpyrazine". Nature. 195 (4846): 1103. Bibcode:1962Natur.195.1103K. doi:10.1038/1951103a0. PMID 14458746.
- ^ Wu, W; Yu, X; Luo, XP; Yang, SH; Zheng, D (2013). "Tetramethylpyrazine protects against scopolamine-induced memory impairments in rats by reversing the cAMP/PKA/CREB pathway". Behavioural Brain Research. 253: 212–6. doi:10.1016/j.bbr.2013年07月05日2. PMID 23916742. S2CID 9100537.
- ^ Kao, TK; Chang, CY; Ou, YC; Chen, WY; Kuan, YH; Pan, HC; Liao, SL; Li, GZ; Chen, CJ (2013). "Tetramethylpyrazine reduces cellular inflammatory response following permanent focal cerebral ischemia in rats". Experimental Neurology. 247: 188–201. doi:10.1016/j.expneurol.2013年04月01日0. PMID 23644042. S2CID 20967364.
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