Article
Asarone-derived Phenylpropanoids anda isoquinoline-derived alkaloids from the bark of Duguetia pycnastera (Annonaceae) and their cytotoxicities
Registro en:
SOUZA, César A. S. de et al. Asarone-derived Phenylpropanoids anda isoquinoline-derived alkaloids from the bark of Duguetia pycnastera (Annonaceae) and their cytotoxicities. Quimica Nova, v. 15, p. 1-7, 2020.
0100-4042
10.21577/0100-4042.20170617
Autor
Souza, César A. S. de
Nardellia, Victória B.
Paza, Weider H. P.
Pinheiro, Maria Lúcia B.
Rodrigues, Ana Carolina Borges da Cruz
Bomfim, Larissa Mendes
Soares, Milena Botelho Pereira
Bezerra, Daniel Pereira
Chaar, Jamal da S.
Koolen, Hector Henrique Ferreira
Silva, Felipe Moura Araujo da
Costa, Emmanoel Vilaça
Resumen
Analytical Center of the
Multidisciplinary Support Center at the UFAM (CA/CAM/UFAM)
for the NMR and MS analysis, and CNPq, CAPES, FINEP, FAPESB,
and UFAM for financial support and fellowship. The phytochemical investigation of the hexane and methanol extracts from the bark of Duguetia pycnastera Sandwith (Annonaceae)
afforded seven known compounds, two asarone-derived phenylpropanoids and five isoquinoline-derived alkaloids. The asarones,
γ-asarone (1-allyl-2,4,5-trimethoxybenzene) and 2,4,5-trimethoxy-styrene were isolated of the hexane extract while the aporphine
alkaloids, O-methylmoschatoline, lysicamine, nornuciferidine, and guatterine N-oxide, and the benzyltetrahydroisoquinoline
alkaloid, (S)-reticuline were isolated of the alkaloid fraction of the methanol extract. This is the first report of these compounds in D.
pycnastera. γ-Asarone is being reported for the first time in the Annonaceae. Nornuciferidine is described for the second time in the
Annonaceae while guatterine N-oxide is the third register. The structures of the isolated compounds were established by extensive
analyses using 1D and 2D NMR spectroscopy in combination with MS. The cytotoxic activity of the isolated compounds (except
for nornuciferidine) was evaluated against cancer and non-cancerous cell lines, in which lysicamine was the most active compound,
mainly against HL-60, HepG2, and K562 with IC50 values of 24.40, 28.86 and 38.75 μmol L-1, respectively.