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Microwave-assisted Intramolecular Dehydrogenative Diels-Alder Reactions for the Synthesis of Functionalized Naphthalenes/Solvatochromic Dyes
Published on: April 1, 2013
Pyranonaphthoquinone derivative dimer and naphthalene derivatives from Ventilago denticulata (willd.) roots:
Kanokwan Photai1, Mongkol Nontakitticharoen1, Jiratthakan Prathumchat1
1Natural Products Research Unit, Department of Chemistry and Center of Excellence for Innovation in Chemistry, Faculty of Science, Khon Kaen University, Khon Kaen, Thailand.
Abstract:
Phytochemical investigation of the roots of Ventilago denticulata afforded three previously undescribed metabolites, a pyranonaphthoquinone derivative dimer, ventilanone W (1), and two naphthalene derivatives, ventilagodenins C (2) and D (3), together with sixteen known compounds (4-19). The structures were established by IR, one-dimensional (1H,13C, and DEPTQ-135) and two-dimensional (HSQC, COSY, NOESY, and HMBC) NMR, and high-resolution mass spectrometry. The structure of 1 was further confirmed by single-crystal X-ray diffraction. Selected isolates were assessed for in vitro cytotoxicity against HeLa, A549, and MCF-7 cell lines using the MTT assay. Compound 2 showed moderate cytotoxicity, with IC50 values of 28.54 ± 0.45, 25.56 ± 0.71, and 30.57 ± 0.54 µM, respectively, while 8 exhibited moderate activity, with IC50 values of 32.97 ± 0.44, 21.28 ± 0.13, and 12.17 ± 0.10 µM, respectively. These results enrich the phytochemical profile of V. denticulata and highlight 2 and 8 as bioactive constituents.

