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. 2020 Feb;29:102118. doi: 10.1016/j.jasrep.2019.102118

Table 1.

List of identified compounds labelled on chromatograms in Fig. 6, Fig. 7, Fig. 8. Samples marked * were analysed and identified as TMS derivatives. CH = Cherry Hinton lump; R = Ringlemere pot.

Type Compound TMS Sample
Pentacyclic triterpenoids Lup-2,20(29)-diene * CH
Lupa-2,20(29)-dien-28-ol * CH; R
Lupenone CH; R
Lupeol * CH
betulone CH; R
Betulin * CH; R
Triterpenoid esters Lup-2,20(29)-dien-28-yl palmitate CH; R
Betulin myristate * CH
Lup-2,20(29)-dien-28-yl stearate CH; R?
Betulin palmitate * CH
Betulin stearate * CH
Acyl lipids Dodecanoic acid (lauric acid); C12:0 * R
Tetradecanoic acid (myristic acid); C14:0 * R
Pentadecanoic acid (pentadecylic acid); C15:0 * R
(9Z)-hexadec-9-enoic acid (palmitoleic acid); C16:1 * CH; R
Hexadecanoic acid (palmitic acid); C16:0 * CH; R
Heptadecanoic acid (margaric acid); C17:0 * R
(9Z)-Octadec-9-enoic acid (oleic acid); C18:1 * CH; R
Octadecanoic acid (stearic acid); C18:0 * CH; R
Eicosanoic acid (arachidic acid); C20:0 * R
Docosanoic acid (behenic acid); C22:0 * R
Sterols Cholesterol * R