Goniolanceolatins A–H, Cytotoxic Bis-styryllactones from Goniothalamus lanceolatus
Eight new bis-styryllactones, goniolanceolatins A–H (1–8), possessing a rare α,β-unsaturated δ-lactone moiety with a (6S)-configuration, were isolated from the CH2Cl2 extract of the stembark and roots of Goniothalamus lanceolatus Miq., a plant endemic to Malaysia. Absolute structures were establishe...
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Veröffentlicht in: | Journal of natural products (Washington, D.C.) D.C.), 2019-09, Vol.82 (9), p.2430-2442 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | Eight new bis-styryllactones, goniolanceolatins A–H (1–8), possessing a rare α,β-unsaturated δ-lactone moiety with a (6S)-configuration, were isolated from the CH2Cl2 extract of the stembark and roots of Goniothalamus lanceolatus Miq., a plant endemic to Malaysia. Absolute structures were established through extensive 1D- and 2D-NMR data analysis, in combination with electronic dichroism (ECD) data. All of the isolates were evaluated for their cytotoxicity against human lung and colorectal cancer cell lines. Compounds 2 and 4 showed cytotoxicity, with IC50 values ranging from 2.3 to 4.2 μM, and were inactive toward human noncancerous lung and colorectal cells. Compounds 1, 3, 6, 7, and 8 showed moderate to weak cytotoxicity. Docking studies of compounds 2 and 4 showed that they bind with EGFR tyrosine kinase and cyclin-dependent kinase 2 through hydrogen bonding interactions with the important amino acids, including Lys721, Met769, Asn818, Arg157, Ile10, and Glu12. |
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ISSN: | 0163-3864 1520-6025 |
DOI: | 10.1021/acs.jnatprod.8b01067 |