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    New bioactive lupane triterpene coumaroyl esters isolated from Buxus cochinchinensis
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    Abstract:
    Five new lupane triterpene coumaroyl esters (1 – 5) were isolated from a CHCl3-soluble partition of a methanol extract of Buxus cochinchinensis Pierre ex Gagnep. (Buxaceae) collected in South Vietnam. Isolation work was monitored using human colon cancer cells (HT-29). The structures of the new compounds (1 – 5) were determined on the basis of spectroscopic data interpretation. In addition to the cytotoxicities against HT-29 cells and NF-κB (p65) inhibitory activities in an ELISA assay, all isolates were also evaluated for their in vitro antimalarial and antifungal activities.
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    Terpene
    Cancer cell lines
    From oleoresin of Aucoumea klaineana Pierre, five triterpenes are isolated; one pentacyclic triterpene: alpha-amyrin and four tetracyclic triterpenes: masticadienediol which seems to be new in this family, 3alpha-hydroxytirucalla-8,24-dien-21-oic acid, 3 alpha-hydroxytirucalla-7,24-dien-21-oic acid which have been already isolated in some Burseraceae and 3-oxotirucalla-7,24-dien-21-oic acid which seems to be a new triterpene.
    Terpene
    Burseraceae
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    The Zimbabwean medicinal plant Monadenium lugardae was evaluated as a potential source of new anticancer constituents. Four new tetracyclic triterpene (1-4) were isolated, accompanied by four previously known triterpenes (5-8). Against a panel of human tumor cell lines, lugardstatins 1 (1) and 2 (2) had good cancer cell growth inhibitory activity. All of the triterpene structures (1-8) were established by 1D and 2D NMR spectrometric and HR mass spectrometric analysis.
    Terpene
    Cancer cell lines
    Three new styrylpyrone analogues, digoniodiol (2), deoxygoniopypyrone A (3), and goniofupyrone A (4), along with ten known styryllactones, were isolated from the aerial parts of Goniothalamus amuyon. Among these compounds, 2 is the first example of a bis-styrylpyrone. Compound 4 represents a new skeleton for styryllactones. All structures were established on the basis of spectroscopic data. The stereochemistry of 2 and 4 was determined by X-ray crystallographic analysis. The absolute configuration of 3 and 4 was further confirmed by Mosher ester derivatives. All styryllactones were subjected to cytotoxicity assays. Among them, goniothalamin, goniothalamin epoxide, and 8-chlorogoniodiol showed significant cytotoxicity against the HepG2 cancer cell line with IC50 in the range of 0.19 - 0.64 μg/mL, and moderate activity toward Hep3B, MDA-MB-231, and MCF-7 cancer cell lines.
    Cancer cell lines
    Absolute Configuration
    Citations (41)
    The bark of the giant neem tree Melia dubia was found to contain 11 euphane-type triterpenes. Five new compounds, meliastatins 1-5 (1-5), proved to inhibit growth of the P388 lymphocytic leukemia cell line (ED(50) 1.7-5.6 microg/mL). Four of the others, the previously known methyl kulonate (8), kulinone (9), 16-hydroxybutyrospermol (10), and kulactone (11), were also found to inhibit (ED(50) 2.5-6.2 microg/mL) the P388 cancer cell line. In addition, two new euphane triterpenes were isolated and named dubione A (6) and dubione B (7). Structures for each of the 11 euphane triterpenes were established by spectral techniques that included HRMS and 2D NMR.
    Terpene
    Cancer cell lines
    Meliaceae
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    Triterpenes are multiringed natural products useful as drugs, agrochemicals, and even cosmetics. Researchers report that a single amino acid mutation in the enzymes that synthesize these compounds can produce novel products with four-ring triterpene core structures instead of the usual five-ring ones (Proc. Natl. Acad. Sci. USA 2016, DOI: 10.1073/pnas.1605509113). The modified enzymes could be engineered into microorganisms or plants to generate a variety of novel triterpenes that would be difficult or impossible to synthesize any other way. The researchers, led by Anne Osbourn of the John Innes Centre, notes that their findings reveal "hidden functional diversity within triterpene synthases." They hope to use the mutant enzymes in a "triterpene machine" that yields custom-built triterpenes. Plants make triterpenes by using triterpene synthase enzymes to cyclize a linear substrate, 2,3-oxidosqualene, into pentacyclic natural products, such as the analgesic and anti-inflammatory agent β-amyrin. Other enzymes then further modify these triterpenes to produce
    Terpene
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