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Salvia prionitis

An other example of Salvia quinone is salvicine, a structurally modified diterpenoid quinone derived from Salvia prionitis, which is cytotoxic against multidrug-resistant cancer cell lines of topoisomerase II inhibition by trapping the DNA-topoisomerase II complex (49). [Pg.201]

Chang J, Xu J, Li M, Zhao M, Ding J, Zhang JS. Novel cytotoxic seco-abietane rearranged diterpenoids from Salvia prionitis. [Pg.1195]

Source Salvia prionitis Hance Mol. formula C2QH24O2 Mol. wt. 296 Solvent CDClo... [Pg.630]

Constit. of Salvia prionitis. Cryst. Mp 61-62°. A 4,5-seco-5,10-friedoabietane. [Pg.246]

Diterpenoids are the most important compounds responsible of the biological activities found in numerous Salvia species. Antituberculous effects have been established for S. blepharochlyna [5], S. multicaulis also reported for it s antifungic effect [6] and S. prionitis which possess antiphlogistic and antibacterial properties [7,8] beside its antituberculous activity. [Pg.754]

See other pages where Salvia prionitis is mentioned: [Pg.289]    [Pg.648]    [Pg.133]    [Pg.377]    [Pg.289]    [Pg.648]    [Pg.133]    [Pg.377]    [Pg.270]   
See also in sourсe #XX -- [ Pg.779 ]

See also in sourсe #XX -- [ Pg.5 , Pg.31 , Pg.33 , Pg.36 ]

See also in sourсe #XX -- [ Pg.5 , Pg.31 , Pg.33 , Pg.36 ]



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