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A new thioglucoside, 2-methylpropylglucosinolate

From National Research Council Canada

DOIResolve DOI: https://doi.org/10.1016/S0031-9422(00)90177-8
AuthorSearch for: 1; Search for: 1
Affiliation
  1. National Research Council of Canada. Prairie Regional Laboratory
FormatText, Article
Abstract
Based on relative efficiencies of conversion of ¹⁴C from feeding labeled compounds to Conringia orientalis (L.) Andrz., the aglycone moiety of 2-hydroxy-2-methylpropylglucosinolate has been found to be formed from valine and the methyl carbon of acetate via leucine. Isobutyl isothiocyanate has been identified as the aglycone formed upon myrosinase hydrolysis of a new thioglucoside, 2-methylpropylglucosinolate, present in fresh plants of C. orientalis. It is suggested that 2-methylpropylglucosinolate may be an intermediate in the biosynthetic pathway between leucine and 2-hydroxy-2-methylpropylglucosinolate.
Publication date
PublisherElsevier
Pergamon Press
In
  • Phytochemistry 11, no. 6 (June 1972): 2085–2088.
LanguageEnglish
Peer reviewedYes
IdentifierS0031942200901778
NRCC-12267
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Record identifier94b2a5e6-a824-4513-931a-f7fd239b7eb5
Record created2023-10-10
Record modified2023-10-10
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