Unravelling the antifungal and antiprotozoal activities and LC-MS/MS quantification of steroidal saponins isolated from Panicum turgidum
Bioassay-guided investigation of extract resulted in the identification of seven steroidal saponins (Turgidosterones 1-7). They were evaluated for their antifungal, antileishmanial, and antitrypanosomal activities. Turgidosterone 6 was the most active antifungal against and (IC values of 2.84 and 1....
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Veröffentlicht in: | RSC advances 2022-01, Vol.12 (5), p.2980-2991 |
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Zusammenfassung: | Bioassay-guided investigation of
extract resulted in the identification of seven steroidal saponins (Turgidosterones 1-7). They were evaluated for their
antifungal, antileishmanial, and antitrypanosomal activities. Turgidosterone 6 was the most active antifungal against
and
(IC
values of 2.84 and 1.08 μg mL
, respectively). Turgidosterones 4-7 displayed antileishmanial activity against
promastigotes with IC
values ranging from 4.95 to 8.03 μg mL
and against
amastigote/THP with IC
values range of 4.50-9.29 μg mL
. Activity against
was also observed for Turgidosterones 4-7 with an IC
values range of 1.26-3.77 μg mL
. Turgidosterones 1-3 did not display any activity against the tested pathogens. The study of structure-activity relationships of the isolated saponins indicated that the antifungal, antileishmanial, and antitrypanosomal activities are markedly affected by the presence of spirostane-type saponins and the elongation of the sugar residue at C-3. To quantitatively determine the most abundant active ingredient in
extract, a single run, sensitive, and highly selective liquid chromatography-tandem mass spectrometry (LC-MS/MS) method has been applied under positive and negative modes. The obtained results showed that compound 5 was the most abundant (95.93 ± 1.10 mg per gram of dry
), followed by 6 (52.51 ± 1.05 mg gm
), 4 (32.71 ± 0.48 mg gm
), and 7 (13.19 ± 0.50 mg gm
). Docking of these saponins against the
oxidoreductases and
trypanothione reductase active sites revealed their potential to effectively bind with a number of key residues in both receptor targets. |
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ISSN: | 2046-2069 2046-2069 |
DOI: | 10.1039/d1ra08532h |