1996
DOI: 10.1021/np960013j
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A New Quassinoid from Castela texana

Abstract: A new quassinoid, 11-O-trans-p-coumaroyl amarolide (1) was isolated from Castela texana, and the structure was elucidated by spectroscopic analysis. Compound 1 is the first coumaroyl quassinoid derivative to have been isolated from nature. The known compounds amarolide (2), chaparrinone, chaparrin, glaucarubolone, holacanthone, and 15-O-beta-D-glucopyranosyl glaucarubol were also isolated. All isolated compounds were tested for their cytotoxicity and antiprotozoal activities.

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Cited by 41 publications
(28 citation statements)
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(16 reference statements)
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“…For initial (primary) evaluation, extracts and fractions are screened at a single concentration (100 µg/mL). Follow-up secondary assays are conducted at three concentrations (10, 3.3, and 1.1 µg/mL), using a culture-treated 96-well microplate (Dou et al, 1996). The level of toxicity of each sample is determined by measuring the effect on a fibroblast cell line from African green monkey kidney (VERO; non-transformed).…”
Section: Introductionmentioning
confidence: 99%
“…For initial (primary) evaluation, extracts and fractions are screened at a single concentration (100 µg/mL). Follow-up secondary assays are conducted at three concentrations (10, 3.3, and 1.1 µg/mL), using a culture-treated 96-well microplate (Dou et al, 1996). The level of toxicity of each sample is determined by measuring the effect on a fibroblast cell line from African green monkey kidney (VERO; non-transformed).…”
Section: Introductionmentioning
confidence: 99%
“…On the FBIT test, leaves also displayed interesting results (1.03 mg/ml), even more active than the bark extract (1.43 mg/ml). We did not find in the literature any activity reported for Castela coccinea, but another Castela species, Castela texana Rose from North-Eastern Mexico was evaluated, and antimalarial activity was reported for five quassinoids, with level of activity ranking from 0.01 to 0.92 g/ml (Dou et al, 1996). Of course, it is not the first time that antimalarial activity has been reported for Simaroubaceae species, as the very first biodiversity browsing for new antimalarial agents was initiated by Merck in South America in 1947, and already stressed out the pharmacological importance of Simaroubaceae together with Amaryllidaceae species.…”
Section: Castela Coccinea Griseb (Simaroubaceae)mentioning
confidence: 86%
“…A primary assay for initial extracts/ fractions used a single concentration (100 mg/mL). In a secondary assay active extracts/pure compounds were tested at three concentrations (10, 3.3 and 1.1 mg/mL), using a culture-treated 96-well microplate (Dou et al, 1996). The level of general toxicity of each sample was also determined by measuring their effect on a fibroblast cell line from African green monkey kidney (VERO; non-transformed).…”
Section: Methodsmentioning
confidence: 99%