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
Hauptverfasser: Bihud, Nur V, Rasol, Nurulfazlina E, Imran, Syahrul, Awang, Khalijah, Ahmad, Fasihuddin B, Mai, Chun-Wai, Leong, Chee-Onn, Cordell, Geoffrey A, Ismail, Nor Hadiani
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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.
ISSN:0163-3864
1520-6025
DOI:10.1021/acs.jnatprod.8b01067