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Figures & data

Figure 1. GC-MS chromatogram of n-hexane extract (F6) from A. cadamba (derivatization method). Peak 1. cycloeicosane (22.9 min), 2. E-15-heptadecenal (24.8 min), 3. myristic acid (25.4 min), 4. 1-eicosanol (28.3 min), 5. 1-tricosene (29.5 min), 6. palmitic acid (29.7 min), 7. octadecanoic acid (30.9 min), 8. nonadecanol (31.0 min), 9. 1-heneicosanol (31.5 min), 10. cyclotetracosane (33.7 min), 11. tetracosanol (34.4 min), 12. cyclooctacosane (36.8 min), 13. campasterol (46.8 min), 14. stigmasterol (47.5 min) 15. β-sitosterol (48.9 min), 16. stigmastanol (49.1 min), 17. lupeol (50.0 min), 18. lupeol acetate (50.4 min)

Figure 1. GC-MS chromatogram of n-hexane extract (F6) from A. cadamba (derivatization method). Peak 1. cycloeicosane (22.9 min), 2. E-15-heptadecenal (24.8 min), 3. myristic acid (25.4 min), 4. 1-eicosanol (28.3 min), 5. 1-tricosene (29.5 min), 6. palmitic acid (29.7 min), 7. octadecanoic acid (30.9 min), 8. nonadecanol (31.0 min), 9. 1-heneicosanol (31.5 min), 10. cyclotetracosane (33.7 min), 11. tetracosanol (34.4 min), 12. cyclooctacosane (36.8 min), 13. campasterol (46.8 min), 14. stigmasterol (47.5 min) 15. β-sitosterol (48.9 min), 16. stigmastanol (49.1 min), 17. lupeol (50.0 min), 18. lupeol acetate (50.4 min)

Figure 2. Lipophilic extractive composition (%) based on dried n-hexane extract from A. cadamba and A. macrophyllus

Figure 2. Lipophilic extractive composition (%) based on dried n-hexane extract from A. cadamba and A. macrophyllus

Table 3. Lipophilic components of n-hexane extracts from A. cadamba and A. macrophyllus.

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