Isolation, Absolute Configuration and Cytotoxic Activities of Alkaloids from Hippeastrum goianum (Ravenna) Meerow (Amaryllidaceae)
Abstract
The phytochemical study of Hippeastrum goianum led to the identification of 13 compounds by means of gas chromatography-mass spectrometry (GC-MS) and nuclear magnetic resonance (NMR). Compounds 7-demethoxy-9-O-methylhostasine (1) and 7-deoxi-trans-dihydronarciclasine (2) had their absolute configurations determined by vibrational circular dichroism (VCD). This is the first time that compound 1 is described in the Amaryllidaceae family. The cytotoxicity of all isolated compounds was tested against colorectal carcinoma (HCT 116), breast carcinoma (MCF-7), and non-tumor human retinal pigment epithelium (RPE) cell lines. The half-maximum inhibitory concentration (IC50) of compound 2 against each cell line was equivalent to the positive control (doxorubicin), indicating a considerable cytotoxic activity.
Más información
Título según WOS: | ID WOS:000577634100019 Not found in local WOS DB |
Título de la Revista: | JOURNAL OF THE BRAZILIAN CHEMICAL SOCIETY |
Volumen: | 31 |
Número: | 10 |
Editorial: | SOC BRASILEIRA QUIMICA |
Fecha de publicación: | 2020 |
Página de inicio: | 2135 |
Página final: | 2145 |
DOI: |
10.21577/0103-5053.20200116 |
Notas: | ISI |