| Literature DB >> 25301666 |
Braulio M Fraga1, Carmen E Díaz2, Leonardo J Amador2, Matías Reina2, Omar Santana3, Azucena González-Coloma4.
Abstract
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.Entities:
Keywords: Africanane; Alkaloids; Bethencourtia hermosae; Ceratopicane; Cytotoxic effects; Insect antifeedants; Senecrassane; Sesquiterpenes; Transformed roots
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Year: 2014 PMID: 25301666 DOI: 10.1016/j.phytochem.2014.09.010
Source DB: PubMed Journal: Phytochemistry ISSN: 0031-9422 Impact factor: 4.072