New Alkaloid and Sesquiterpenoid From the Leaves of <i>Cinnamomum bejolghota</i>

From the leave of Cinnamomum bejolghota (Buch.- Ham. ex Nees) Sweet, one new alkaloid, 3,6-dimethoxy-9H-pyrido[3,4-b]indole (1) and one new aromadendrane sesquiterpenoid, 4α,10α-dihydroxyaromadendrane-13-oic acid (2) along with seven known compounds, 4β,10α-dihydroxyaromadendrane (3), litseachromolaevane A (4), curcumin (5), pisumionoside (6), quercetin-3-O-α-L-rhamnopyranoside (7), rutin (8), and kaemperol 3-O-neohesperidoside (9) were isolated and structurally determined. Their chemical structures were elucidated through comprehensive spectroscopic analyses, including high-resolution electrospray ionization mass spectrometry, one- and two-dimensional nuclear magnetic resonance, and by comparison with the literature data. Compounds 1-9 were evaluated for their cytotoxic activities against four human cancer cell lines (KB, MCF-7, HepG-2, and SK-LU1), however, only compound 8 displayed weak inhibitory activity on HepG2, A549 cancer cell lines with 50% inhibitory concentration (IC<sub>50</sub>) values of 97.8 and 68.8 µM, respectively and moderate inhibitory activity on MCF7 cancer cell line with an IC<sub>50</sub> value of 49.7 µM.

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Publication Details

Journal
Chemistry & Biodiversity
Published
2025-09-23
DOI
https://doi.org/10.1002/cbdv.202502118
Primary Topic
Natural product bioactivities and synthesis
Type
article
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article

New Alkaloid and Sesquiterpenoid From the Leaves of Cinnamomum bejolghota

Bich Ngan Truong, Van Cuong Pham, Thi Phuong Le, Đoàn Thị Mai Hương et al.
Chemistry & Biodiversity
Natural product bioactivities and synthesis
article

New Alkaloid and Sesquiterpenoid From the Leaves of Cinnamomum bejolghota

Bich Ngan Truong, Van Cuong Pham, Thi Phuong Le, Đoàn Thị Mai Hương, Thùy Linh Nguyễn, Marc Litaudon
article en

Abstract

From the leave of Cinnamomum bejolghota (Buch.- Ham. ex Nees) Sweet, one new alkaloid, 3,6-dimethoxy-9H-pyrido[3,4-b]indole (1) and one new aromadendrane sesquiterpenoid, 4α,10α-dihydroxyaromadendrane-13-oic acid (2) along with seven known compounds, 4β,10α-dihydroxyaromadendrane (3), litseachromolaevane A (4), curcumin (5), pisumionoside (6), quercetin-3-O-α-L-rhamnopyranoside (7), rutin (8), and kaemperol 3-O-neohesperidoside (9) were isolated and structurally determined. Their chemical structures were elucidated through comprehensive spectroscopic analyses, including high-resolution electrospray ionization mass spectrometry, one- and two-dimensional nuclear magnetic resonance, and by comparison with the literature data. Compounds 1-9 were evaluated for their cytotoxic activities against four human cancer cell lines (KB, MCF-7, HepG-2, and SK-LU1), however, only compound 8 displayed weak inhibitory activity on HepG2, A549 cancer cell lines with 50% inhibitory concentration (IC<sub>50</sub>) values of 97.8 and 68.8 µM, respectively and moderate inhibitory activity on MCF7 cancer cell line with an IC<sub>50</sub> value of 49.7 µM.

Chemistry & BiodiversityVol. 22(12)
Centre National de la Recherche Scientifique (FR), Institut de Chimie des Substances Naturelles (FR), Institute of Mathematics (VN), Vietnam Academy of Science and Technology (VN), Hanoi University of Science and Technology (VN)
Openalex Percentile: Top 77%
Natural product bioactivities and synthesis
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