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Goniolanceolatins A–H, Cytotoxic Bis-styryllactones from Goniothalamus lanceolatus
- Source :
- Journal of Natural Products. 82:2430-2442
- Publication Year :
- 2019
- Publisher :
- American Chemical Society (ACS), 2019.
-
Abstract
- 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.
- Subjects :
- Pharmacology
chemistry.chemical_classification
010405 organic chemistry
Kinase
Goniothalamus lanceolatus
Organic Chemistry
Pharmaceutical Science
01 natural sciences
0104 chemical sciences
Analytical Chemistry
Amino acid
010404 medicinal & biomolecular chemistry
Complementary and alternative medicine
Biochemistry
chemistry
Docking (molecular)
Cell culture
Drug Discovery
Molecular Medicine
Cytotoxic T cell
Moiety
Cytotoxicity
Subjects
Details
- ISSN :
- 15206025 and 01633864
- Volume :
- 82
- Database :
- OpenAIRE
- Journal :
- Journal of Natural Products
- Accession number :
- edsair.doi...........412cb465302917a28566fd7806a45b6c
- Full Text :
- https://doi.org/10.1021/acs.jnatprod.8b01067