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Cytotoxic Triterpenes from Salacia crassifolia and Metabolite Profiling of Celastraceae Species

The new pentacyclic triterpene 11β-hydroxypristimerin (1), along with the known metabolites pristimerin (2), 6-oxopristimerol (3) and vitideasin (4), were isolated from a Salacia crassifolia root wood extract, following a bioassay-guided fractionation approach. Both the extract and the purified trit...

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Detalles Bibliográficos
Autores principales: Espindola, Laila S., Dusi, Renata G., Demarque, Daniel P., Braz-Filho, Raimundo, Yan, Pengcheng, Bokesch, Heidi R., Gustafson, Kirk R., Beutler, John A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6099938/
https://www.ncbi.nlm.nih.gov/pubmed/29925807
http://dx.doi.org/10.3390/molecules23061494
Descripción
Sumario:The new pentacyclic triterpene 11β-hydroxypristimerin (1), along with the known metabolites pristimerin (2), 6-oxopristimerol (3) and vitideasin (4), were isolated from a Salacia crassifolia root wood extract, following a bioassay-guided fractionation approach. Both the extract and the purified triterpenes displayed pronounced cytotoxic activity against human cancer cell lines. The NCI-60 cell line screen revealed that compound 2 was the most active, with a mean GI(50) of 0.17 μM, while compound 1 had a mean GI(50) of 8.7 μM. A COMPARE analysis of the screening results showed that pristimerin is likely to be the main compound responsible for the cytotoxic activity of the extract (mean GI(50) of 0.3 μg·mL(−1)). A targeted search for pristimerin and related derivatives using LC-MS/MS revealed the presence of pristimerin (2) and 6-oxopristimerol (3) in all Celastraceae species examined and in all plant parts tested, while vitideasin (4) was only detected in the genus Salacia.