| Literature DB >> 31434501 |
Yves Salomon Makong1, Ghislain Wabo Fotso2, Gervais Happi Mouthe2, Bruno Lenta3, Robert Rennert4, Norbert Sewald5, Norbert Arnold4, Jean Duplex Wansi1, Bonaventure Tchaleu Ngadjui2.
Abstract
The chemical investigation of the root barks leaves and stem barks of Brucea antidysenterica J. F. Mill. (Simaroubaceae) led to the isolation of a new pregnane glycoside, named Bruceadysentoside A or 3-O-β-L-arabinopyranosyl-pregn-5-en-20-one (1) together with seventeen known compounds. Their structures were established from spectral data, mainly HRESIMS, 1 D and 2 D NMR and by comparison with literature data. Compounds 1, 2, 5, 6, 8, 10, 12 and 13 were tested in vitro for their effects on the viability of two different human cancer cell lines, namely prostate PC-3 adenocarcinoma cells and colorectal HT-29 adenocarcinoma cells. No substantial activities were recorded for 2, 10, 12 and 13 (up to 10 μM concentration). 1, 5 and 8 did not show strong anti-proliferative effects up to 100 μM, however, 6 exhibited a stronger anti-proliferative effect with IC50 values of ∼ 100 μM against PC-3 and ∼ 200 μM against HT-29.Entities:
Keywords: Brucea antidysenterica; Bruceadysentoside A; Simaroubaceae; cytotoxic activities; hydnocarpin; pregnane glycoside
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Year: 2019 PMID: 31434501 DOI: 10.1080/14786419.2019.1655024
Source DB: PubMed Journal: Nat Prod Res ISSN: 1478-6419 Impact factor: 2.861