Antiproliferative activity of spinasterol isolated of (Benth, 1844).

Cancer is the major cause of death in the world, representing a significant public health problem. Plants have been shown as a great source of secondary metabolites with anticancer activity. The aim of this work was evaluated the antiproliferative activity of the methanolic extracts, chemical fractions and the compound spinasterol isolated of medicinal plant . The methanolic extracts of stem, leaf and stem/leaf was obtained by maceration. The methanolic extract of stem was purified by successive extractions with solvents as -hexane, ethyl acetate and ethanol. The -hexane fraction was separated by column chromatographic and monitored by thin layer chromatographic. The compound spinasterol was characterized by H NMR, C NMR and Mass Spectrometry. Methanolic extracts, chemical, chromatographic fractions and spinasterol was evaluated against RAW 264.7, M12.C3.F6, , LS-180, A549 and HeLa cancer cell lines by the standardized method MTT for determinate the antiproliferative activity. Methanolic extract of stem shown the better antiproliferative activity against the murine macrophage cancer cell line RAW 264.7. -Hexane chemical fraction shown antiproliferative activity against human alveolar cancer cell line A549 and RAW 264.7. Was isolated and characterized a compound by NMR H and C, revealing the presence of sterol spinasterol. Spinasterol shown have antiproliferative activity against cervical cancer cell line HeLa and RAW 264.7, that spinasterol can be a responsible compound of antiproliferative activity found in the methanolic extract of .