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Acaricidal Activity of Bufadienolides Isolated from Drimia pancration against Tetranychus urticae, and Structural Elucidation of Arenobufagin-3-O-α-L-rhamnopyranoside.


ABSTRACT: Chemical characterization of the bulbs of Drimia pancration was conducted to isolate four steroidal saponins (1-4). Earlier, we focused on the structural elucidation of compounds 1-3. Herein, by means of 1H-NMR, 13C-NMR, Nuclear Overhauser Effects (NOE), and 2D-NMR spectra, the full stereochemical structure of 4 is reported, and all the 1H and 13C signals are assigned. Compounds 1-4 were tested for their acaricidal properties against the two-spotted spider mite Tetranychus urticae. Our results showed excellent activity of compound 1, with an LD50 (µg/cm2) of 0.29 and a LD90 (µg/cm2) of 0.96, whereas compounds 2, 3, and 4 showed moderate activity. Furthermore, the acaricidal and cytotoxic properties of the crude extract were also investigated. Of note, after 96 h of exposure, the acaricidal activity of compound 1 was higher than that of the positive control, hexythiazox. Indeed, for compound 1, LD50 and LD90 were 0.29 and 0.96 µg/cm2, respectively, while hexythiazox LD50(90) was 18.7 (132.5) µg/cm2. Additionally, D. pancration extract, after 72 h, induced a high cytotoxic effect in HaCaT and THP-1 cell lines, with an IC50 of 7.37 ± 0.5 µg/mL and 3.50 ± 0.15 µg/mL, respectively. Overall, D. pancration can be considered as a green source of novel acaricides effective against mites of agricultural importance, such as T. urticae, pending proper field validation and the assessment of non-target effects on other invertebrate species.

SUBMITTER: Badalamenti N 

PROVIDER: S-EPMC9268777 | biostudies-literature | 2022 Jun

REPOSITORIES: biostudies-literature

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Acaricidal Activity of Bufadienolides Isolated from <i>Drimia pancration</i> against <i>Tetranychus urticae,</i> and Structural Elucidation of Arenobufagin-3-<i>O-α</i>-L-rhamnopyranoside.

Badalamenti Natale N   Bruno Maurizio M   Pavela Roman R   Maggi Filippo F   Marinelli Oliviero O   Zeppa Laura L   Benelli Giovanni G   Canale Angelo A  

Plants (Basel, Switzerland) 20220621 13


Chemical characterization of the bulbs of <i>Drimia pancration</i> was conducted to isolate four steroidal saponins (<b>1</b>-<b>4</b>). Earlier, we focused on the structural elucidation of compounds <b>1</b>-<b>3</b>. Herein, by means of <sup>1</sup>H-NMR, <sup>13</sup>C-NMR, Nuclear Overhauser Effects (NOE), and 2D-NMR spectra, the full stereochemical structure of <b>4</b> is reported, and all the <sup>1</sup>H and <sup>13</sup>C signals are assigned. Compounds <b>1</b>-<b>4</b> were tested fo  ...[more]

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