Bioactive compounds from transformed root cultures and aerial parts of Bethencourtia hermosae

A study of Bethencourtia hermosae, aerial parts and root cultures, afforded the undescribed sesquiterpenes ceratopicanol angelate, 8β-hydroxy-african-4(5)-en-3-one tiglate, 8β-hydroxy-african-4(5)-en-3-one 3′-angeloxy-2′-methylbutanoate, 1α,8β-dihydroxy-african-4(5)-en-3-one 8β-angelate, 6α,8β-dihyd...

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Veröffentlicht in:Phytochemistry (Oxford) 2014-12, Vol.108, p.220-228
Hauptverfasser: Fraga, Braulio M., Díaz, Carmen E., Amador, Leonardo J., Reina, Matías, Santana, Omar, González-Coloma, Azucena
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Sprache:eng
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Zusammenfassung:A study of Bethencourtia hermosae, aerial parts and root cultures, afforded the undescribed sesquiterpenes ceratopicanol angelate, 8β-hydroxy-african-4(5)-en-3-one tiglate, 8β-hydroxy-african-4(5)-en-3-one 3′-angeloxy-2′-methylbutanoate, 1α,8β-dihydroxy-african-4(5)-en-3-one 8β-angelate, 6α,8β-dihydroxy-african-4(5)-en-3-one8β-angelate (8), and the alkaloid hermosine. Their insect antifeedant and cytotoxic activities were also studied. [Display omitted] •Phytochemical study of Bethencourtia hermosae aerial parts.•Components of transformed root cultures of Bethencourtia hermosae.•Insect antifeedant and cytotoxic activities of africanane sesquiterpenes. A chemical study of Bethencourtia hermosae, aerial parts and in vitro root cultures, transformed by Agrobacterium rhizogenes, afforded the hitherto unreported sesquiterpenes ceratopicanol angelate (1), 8β-hydroxy-african-4(5)-en-3-one tiglate (4), 8β-hydroxy-african-4(5)-en-3-one 3′-angeloxy-2′-methylbutanoate (5), 1α,8β-dihydroxy-african-4(5)-en-3-one 8β-angelate (7) and 6α,8β-dihydroxy-african-4(5)-en-3-one 8β-angelate (8). In addition, 8β-hydroxy-african-4(5)-en-3-one (6) was isolated for the first time from a natural source, along with the rare sesquiterpenoid senecrassidiol (10) and two jacaranone derivatives 14 and 16. Known pyrrolizidine alkaloids, together with previously unreported hermosine (23), have also been isolated from this plant. The insect antifeedant activities of the extracts and compounds were studied together with their cytotoxic effects against insect (Sf9) and mammalian (CHO) cell lines.
ISSN:0031-9422
1873-3700
DOI:10.1016/j.phytochem.2014.09.010