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. 2023 Jul 17;14:1214881. doi: 10.3389/fphar.2023.1214881

TABLE 1.

Trivial name, side chain structure and dietary plant source of Glucosinolates and Isothiocyanates.

GLCs trivial name ITCs trivial name Side chain name and structure of R group Main dietary source
Aliphatic group
 Sinigrin (Glucobrassicin) Allyl ITC CH2 = CH-CH2 -2-Propenyl Cabbage, horseradish, wasabi, mustard Cartea and Velasco. (2008)
 Glucoerucin Erucin CH3-S-CH2-CH2-CH2-CH2-4-Methyl thiobutyl Turnip, kohlrabi, arugula, broccoli seeds Avato and Argentieri. (2015)
 Glucoraphanin Sulforaphane CH3-SO-CH2-CH2-CH2-CH2-4-Methylsulphinylbutyl Broccoli, cauliflower, kale, brussels sprout, cabbage Fahey et al. (2001)
 Glucoraphenin Sulforaphane CH3-SO-CH = CH-CH2-CH2 -4-Methylsulfinyl-3-butenyl Radish, brussels sprout Fahey et al. (2001); Avato and Argentieri. (2015)
 Glucoraphasatin Raphasatin CH3-S-CH = CH-CH2-CH2-4- methylsulfanyl 3-butenyl Japanese Daikon Jaafaru et al. (2019b)
 Glucoiberin Iberin CH3-SO-CH2-CH2-CH2 -3-Methylsulfinylpropyl Broccoli, cabbage Fahey et al. (2001); Cancer et al. (2004)
Aromatic group
 Glucotropaeolin Benzyl ITC C6H5-CH2 -Benzyl Wasabi and mustard Mithen et al. (2000); Verkerk et al. (2009)
 Gluconasturtiin Phenylethyl ITC C6H5-(CH2)2 -2-Phenylethyl Watercress, radish, turnips, broccoli, kale Cartea and Velasco. (2008)
 Glucomoringin Moringin C13H15O5 Drumstick tree Lopez-Rodriguez et al. (2020)
Indolyl ITC
 Indol-3-yl-methylglucosinolate Indole 3-carbinol C8H6N-CH2OH 1H-Indol-3-yl-methanol All vegetables Amarakoon et al. (2023)