Two new 3,4-seco-ent-kaurenes, caracasine (1) and caracasine acid (2), were isolated from non-polar extracts of the flowers of Croton caracasana (Euphorbiaceae), together with six known terpenes, stigmasterol (4), stigmastenone (5), 2,6-dimethylocta-3,7-diene-2, 6-diol (6), spathulenol (7), caryophyllene oxide (8), and aromadendrene (9), and the flavonoid tribuloside (10). The chemical structures were determined by spectroscopic means and chemical correlations. All isolated compounds are being described for the first time for this species.
Four new crotofolane-type diterpenoids, crotocarasin (A-D) (1-4), together with the known crotofolin E, were isolated from a dichloromethane extract of the stems of Croton caracasanus Pittier. The structures of the new compounds were determined by spectroscopic methods, and the structure of 3 was further confirmed by single-crystal X-ray data analyses.
In the course of searching for bioactive compounds from Croton species from Venezuela, two seco-entkaurenes isolated from flowers of Croton caracasana were evaluated in vitro for their effect on cell viability by the standard MTT assay in nine human cancer cell lines of different origins and one primary culture. Both compounds induced cytotoxicity in the range of 2 to 25 µM for caracasine and 0.8 to 12 µM for caracasine acid. However, for the normal fibroblasts and the cell lines, HeLa, MCF-7, PC-3, LoVo, X-17, Jurkat E6.1 and Jurkat JCaM1.6, the IC 50 values of caracasine acid were lower than their counterparts. Interestingly, no differences in IC 50 were recorded for the leukemic cell lines U937 and K562. It can be concluded that the acid moiety in the structure enhances the cytotoxic effect of caracasine by a pathway which seems not to be activated in the leukemic cell lines tested.
From the stems of Croton micans Sw., five new 3,4-seco-ent-kaurene dimers: micansinoic acid (1), isomicansinoic acid (2), and the dimethyl (3), monomethyl (4) and monoethyl ester (5) of micansinoic acid were isolated. The structures of the new compounds were elucidated by spectroscopic data interpretation, mainly 1D and 2D NMR experiments and MS. These compounds are the first 3,4-seco-ent-kaurene dimers from a Croton species.
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