| Literature DB >> 32901507 |
Loc Van Tran1,2, Ninh Pham Thi1,2, Luu Nguyen Thi1, Chien Van Tran1,2, Nhu Thi Quynh Vo3, Anh Ngoc Ho1, Viet Cong Do4, Van Sung Tran1,2, Thao Thi Phuong Tran1,2.
Abstract
Phytochemical investigation of the leaves of Lepisanthes rubiginosa led to the isolation of two new glycosides, lepisantheside A (1) and lepisantheside B (2), together with two known compounds acutoside A (3) and 3-O-[β-D-xylopyranosyl-(1→3)-β-D-glucopyranosyl-]-oleanolic acid (4). Their structures were elucidated by means of spectroscopic methods (HR-ESI-MS, 1D and 2D NMR), and by comparison with the reported data. The cytotoxicity of compounds 1-4 against four human cancer cell lines (KB, HepG2, SK-LU-1 and MCF7) was evaluated. Compound 4 exhibited significant activity with IC50 values of 9.57, 6.66, 6.97 and 18.32 µM, respectively, in comparison with the postive control ellipticine.Entities:
Keywords: Lepisanthes rubiginosa; Lepisantheside A; Lepisantheside B; cytotoxic activity; farnesyl glycoside; mangrove plant; oleanane glycoside
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Year: 2020 PMID: 32901507 DOI: 10.1080/14786419.2020.1817010
Source DB: PubMed Journal: Nat Prod Res ISSN: 1478-6419 Impact factor: 2.861