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1.
Plants (Basel) ; 12(22)2023 Nov 11.
Artículo en Inglés | MEDLINE | ID: mdl-38005725

RESUMEN

To look in-depth into the phytochemical and pharmacological properties of Taiwan juniper, this study investigated the chemical profiles and anti-lymphangiogenic activity of Juniperus chinensis var. tsukusiensis. In this study, four new sesquiterpenes, 12-acetoxywiddrol (1), cedrol-13-al (2), α-corocalen-15-oic acid (3), 1,3,5-bisaoltrien-10-hydroperoxy-11-ol (4), one new diterpene, 1ß,2ß-epoxy-9α-hydroxy-8(14),11-totaradiene-3,13-dione (5), and thirty-three known terpenoids were successfully isolated from the heartwood of J. chinensis var. tsukusiensis. The structures of all isolates were determined through the analysis of physical data (including appearance, UV, IR, and optical rotation) and spectroscopic data (including 1D, 2D NMR, and HRESIMS). Thirty-four compounds were evaluated for their anti-lymphangiogenic effects in human lymphatic endothelial cells (LECs). Among them, totarolone (6) displayed the most potent anti-lymphangiogenic activity by suppressing cell growth (IC50 = 6 ± 1 µM) of LECs. Moreover, 3ß-hydroxytotarol (7), 7-oxototarol (8), and 1-oxo-3ß-hydroxytotarol (9) showed moderate growth-inhibitory effects on LECs with IC50 values of 29 ± 1, 28 ± 1, and 45 ± 2 µM, respectively. Totarolone (6) also induced a significant concentration-dependent inhibition of LEC tube formation (IC50 = 9.3 ± 2.5 µM) without cytotoxicity. The structure-activity relationship discussion of aromatic totarane-type diterpenes against lymphangiogenesis of LECs is also included in this study. Altogether, our findings unveiled the promising potential of J. chinensis var. tsukusiensis in developing therapeutics targeting tumor lymphangiogenesis.

2.
J Nat Prod ; 69(4): 665-7, 2006 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-16643048

RESUMEN

Calocedimers A, B, C, and D, together with four known compounds, platydiol, alpha-cadinol, ferrugiol, and 6,7-dehydroferrugiol, were isolated from the bark of Calocedrus macrolepis var. formosana. Calocedimers A, B, C, and D are the dimers of abietane-O-camphane, abietane-O-cadinane, abietane-O-abietane, and abietane-O-abietane, respectively. Their structures were elucidated from spectroscopic data.


Asunto(s)
Abietanos/aislamiento & purificación , Cupressaceae/química , Abietanos/química , Estructura Molecular , Resonancia Magnética Nuclear Biomolecular , Corteza de la Planta/química , Taiwán
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