TY - JOUR
T1 - Isolation and structure elucidation of Eumitrin A1 from lichen Usnea blepharea motyka and its cytotoxic activity
AU - Maulidiyah,
AU - Herry Cahyana, A.
AU - Suwarso, Wahyudi Priyono
AU - Nurdin, Muhammad
PY - 2015/1/1
Y1 - 2015/1/1
N2 - The purpose of this research was to isolate and elucidate structure of secondary metabolite compoundand to examine its cytotoxic activity of lichen Usnea blepharea Motyka obtained from Sulawesi – Indonesia. Powder of lichen was extracted using an acetone and continued separation by employing column chromatography (CC) with n-hexane and ethyl acetate solvents in a gradient elutionto produce a pure isolate. The structure was determined by UV-Vis, LC-MS, FTIR, 1H-NMR, 13C-NMR, 2D-NMR (HMBC, HMQC, COSY). The UV-Visspectrophotometer measurement was obtained maximumwavelength of 229 nm and 334 nm. The LC-MS data of this compound showed a molecular weight of680. The 1H-NMR, 13C-NMR with DEPT spectrums showedthat this compound has 34 carbon atoms consisting of 2 methyl groups, 2 methoxy groups, 1 methyl group, 6 metin groups, 3 methylene groups, and 20 C quartener atoms. The2D-NMR (HMBC, HMQC,COSY) spectrums of analysis could be inferred that this compound is a Eumitrin A1 with the formula structure C34H32O15. The Eum itrin A1 was examined its cytotoxic activityagainst Murine Leukemia P388 cells with IC504.5 μg/mL (very active).
AB - The purpose of this research was to isolate and elucidate structure of secondary metabolite compoundand to examine its cytotoxic activity of lichen Usnea blepharea Motyka obtained from Sulawesi – Indonesia. Powder of lichen was extracted using an acetone and continued separation by employing column chromatography (CC) with n-hexane and ethyl acetate solvents in a gradient elutionto produce a pure isolate. The structure was determined by UV-Vis, LC-MS, FTIR, 1H-NMR, 13C-NMR, 2D-NMR (HMBC, HMQC, COSY). The UV-Visspectrophotometer measurement was obtained maximumwavelength of 229 nm and 334 nm. The LC-MS data of this compound showed a molecular weight of680. The 1H-NMR, 13C-NMR with DEPT spectrums showedthat this compound has 34 carbon atoms consisting of 2 methyl groups, 2 methoxy groups, 1 methyl group, 6 metin groups, 3 methylene groups, and 20 C quartener atoms. The2D-NMR (HMBC, HMQC,COSY) spectrums of analysis could be inferred that this compound is a Eumitrin A1 with the formula structure C34H32O15. The Eum itrin A1 was examined its cytotoxic activityagainst Murine Leukemia P388 cells with IC504.5 μg/mL (very active).
KW - Cytotoxic
KW - Eumitrin A<inf>1</inf>
KW - Murine Leukemia P388 Cells
KW - Usnea blepharea Motyka
UR - http://www.scopus.com/inward/record.url?scp=84939157431&partnerID=8YFLogxK
M3 - Article
SN - 0974-4304
VL - 8
SP - 782
EP - 789
JO - International Journal of PharmTech Research
JF - International Journal of PharmTech Research
IS - 4
ER -