2020
DOI: 10.1080/14786419.2019.1709188
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Cytotoxic and larvicidal activities of Stemona alkaloids from the aerial parts and roots of Stemona curtisii Hook.f.

Abstract: A new Stemona alkaloid glycoside derivative, 6-hydroxy-5,6-seco-stemocurtisinoside (4), was isolated from the ethanolic extract of the aerial parts of Stemona curtisii Hook.f., together with stemocurtisine (1), (11Z)-1',2'-didehydrostemofoline (2) and 6-hydroxy-5,6-seco-stemocurtisine (3).Whereas, stemocurtisine (1), stemocurtisinol (5) and oxyprotostemonine (6) were isolated from the roots. Their structures were elucidated using 1D and 2D NMR spectroscopy as well as MS experiments. The extract and the pure is… Show more

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Cited by 7 publications
(5 citation statements)
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“…To date, more than 300 chemical components have been isolated from stemona, including the alkaloid monomers stemofoline and stemospironine with proven insecticidal effects (Chalom et al 2021 ). Both stemofoline and stemospironine are toxic to silkworm larvae, but employ different mechanisms (Sakata et al 1978 ).…”
Section: Discussionmentioning
confidence: 99%
“…To date, more than 300 chemical components have been isolated from stemona, including the alkaloid monomers stemofoline and stemospironine with proven insecticidal effects (Chalom et al 2021 ). Both stemofoline and stemospironine are toxic to silkworm larvae, but employ different mechanisms (Sakata et al 1978 ).…”
Section: Discussionmentioning
confidence: 99%
“…Thus indicating hydroxylation is specifically directed at C-6 by substrate orientation in the enzyme active site. Interestingly, in plants the pyrido[1,2a]azepine alkaloid stemocurtisine (4) gives rise to other natural products most likely via hydroxylation and ring opening reactions of the azepine ring at C-6 [21,22]. However, it was found to be inert to biotransformation by C. elegans.…”
Section: Discussionmentioning
confidence: 99%
“…Among them, oxyprotostemonine was the most active component. Chalom et al 112 examined larvicidal activities against the dengue vector, Aedes aegypti of the extract of aerial parts of Stemona curtisii and the pure isolated compounds including 6-hydroxy-5,6-secostemocurtisinoside, stemocurtisine, (11Z)-1 ′ ,2 ′ didehydrostemofoline, and 6-hydroxy-5,6-seco-stemocurtisine. (11Z )-1 ′ ,2 ′ didehydrostemofoline displayed the strongest larvicidal activity with a LC50 value of 2.44 mM.…”
Section: Other Bioactivitiesmentioning
confidence: 99%
“…Chalom et al 112 separated a new Stemona alkaloid glycoside derivative, 6-hydroxy-5,6-secostemocurtisinoside ( 264 ) from the ethanolic extract of the aerial parts of Stemona curtisii (Figure 10). Tuberostemoline F ( 265 ) was produced from the roots of Stemona tuberosa and its structure was elucidated by spectroscopic data, X-ray single-crystal diffraction, and modified Mosher method (Figure 10).…”
Section: Phytochemistrymentioning
confidence: 99%