Skimmia anquetilia, N. P. Taylor & Airy Shaw, N. P. Taylor & Airy Shaw
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https://doi.org/ 10.1016/j.phytochem.2015.02.014 |
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https://doi.org/10.5281/zenodo.10519237 |
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https://treatment.plazi.org/id/03A0E701-A37F-FFBF-FF97-0665FA5440CE |
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Felipe |
scientific name |
Skimmia anquetilia |
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3.1. S. anquetilia View in CoL
S. anquetilia is an aromatic erect or creeping shrub, native to the Himalayan region and often cultivated for decorative purposes ( Kumar et al., 2012). An ethanolic extract of leaves from S. anquetilia yielded six coumarins, 7,8-dihdroxy-6-[3 0 -β- D- glucopyranosyloxy-2 0 (Ę)-hydroxy-3 0 -methylbutyl]-coumarin glucoside 34, 6- (2,3-dihydroxy-3-methylbutyl)-7-methoxycoumarin 30, skimmine 22, osthol 38, esculetin 23, and scopoletin 24. Moreover, the coumarin 6-methoxy-7-(2 0 -hydroxy-3 0 -methylbutyl)-coumarin 33 was isolated (Sharma et al., 2008).
Prakash et al. (2011) showed that essential oils separately obtained by hydro-distillation from seeds and fruits and analysed by GC–MS contained up to 70 compounds. Fatty acids and their esters were found to be common components for both in similar percentages. On the other hand α- cadinol, α- terpineol, selinene, neo-isolongifolene, linalool, cis -Z-α- bisabolene oxide, aromadendrene, and (―)-selinene were the main points of differences between the two essential oils. The essential oil obtained from flowers and leaves and analysed by the same methodology as above indicated the presence of β- phellandrene (1.8% in leaves and 18.4% in flowers), geijerene (2.0%, 15.0%), germacrene B (11.6%, 2.0%), linalyl acetate (7.3%, 11.2%), linalool (9.5%, 9.4%), αterpineol (5.6%, 4.4%), and pregeijerene (0.2%, 5.6%) as the most abundant mono- and sesquiterpenes (Gondwal et al., 2012).
No known copyright restrictions apply. See Agosti, D., Egloff, W., 2009. Taxonomic information exchange and copyright: the Plazi approach. BMC Research Notes 2009, 2:53 for further explanation.
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