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Hoffmann, R. A wiki for the life sciences where authorship matters. Nature Genetics (2008)
 
Chemical Compound Review

AC1NSQPK     (E)-3-(4-methoxyphenyl)prop- 2-en-1-ol

Synonyms: SureCN1278751, NSC-26455, bmse010146, NSC26455, SBB087806, ...
 
 
 
 
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Disease relevance of p-Methoxycinnamyl alcohol

  • Various possibilities leading to deoxygenation of the latter were examined, including reduction of the side-chain double bond to form p-dihydrocoumaryl alcohol, followed by dehydration to afford chavicol, as well as formation of p-methoxycinnamyl alcohol, with further side-chain modification to afford methylchavicol [1].

References

  1. Chavicol formation in sweet basil (Ocimum basilicum): cleavage of an esterified C9 hydroxyl group with NAD(P)H-dependent reduction. Vassão, D.G., Gang, D.R., Koeduka, T., Jackson, B., Pichersky, E., Davin, L.B., Lewis, N.G. Org. Biomol. Chem. (2006) [Pubmed]
 
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