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Structural elucidation and evaluation of multidrug-resistance modulatory capability of amarissinins A–C, diterpenes derived from Salvia amarissima
FRANCISCO ELIHU BAUTISTA REDONDA
MABEL CLARA FRAGOSO SERRANO
NAYTZE DALIA ORTIZ PASTRANA
Rubén A. Toscano
Alfredo Ortega
Acceso Abierto
Atribución-NoComercial-SinDerivadas
https://doi.org/10.1016/j.fitote.2016.08.007
Lamiaceae
Salvia amarissima
Clerodane diterpenes
Cytotoxic
MDR modulation
"Three new diterpenes (amarissinins A-C, 1–3) containing several oxygenated functionalities were isolated from the leaves and flowers of Salvia amarissima. The structures of these compounds were established through the analysis of their NMR spectroscopy and mass spectrometry data. The structures of compounds 1 and 2 were confirmed by single crystal X-ray diffraction. Compound 2was identified as a C-10 epimer of dugesin F (5). The cytotoxic activity of these compounds against five human cancer cell lines was determined. Additionally, the capability to modulate the multidrug resistance (MDR) in the MCF-7 cancer cell line resistant to vinblastine was tested."
Elsevier
2016
Artículo
Elihú Bautista, Mabel Fragoso-Serrano, Naytzé Ortiz-Pastrana, Rubén A. Toscano, Alfredo Ortega, Structural elucidation and evaluation of multidrug-resistance modulatory capability of amarissinins A–C, diterpenes derived from Salvia amarissima, Fitoterapia, Volume 114, 2016, Pages 1-6.
FARMACOLOGÍA
Versión aceptada
acceptedVersion - Versión aceptada
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