http://www.cnr.it/ontology/cnr/individuo/prodotto/ID28132
Astersedifolioside A-C, three new oleane-type saponins with antiproliferative activity (Articolo in rivista)
- Type
- Label
- Astersedifolioside A-C, three new oleane-type saponins with antiproliferative activity (Articolo in rivista) (literal)
- Anno
- 2004-01-01T00:00:00+01:00 (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#doi
- 10.1016/j.bmc.2004.06.042 (literal)
- Alternative label
Corea G., Iorizzi M., Lanzotti V., Cammareri M., Conicella C., Laezza C., Bifulco M. (2004)
Astersedifolioside A-C, three new oleane-type saponins with antiproliferative activity
in Bioorganic & medicinal chemistry (Print)
(literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
- Corea G., Iorizzi M., Lanzotti V., Cammareri M., Conicella C., Laezza C., Bifulco M. (literal)
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- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#numeroVolume
- Rivista
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- ISI Web of Science (WOS) (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#affiliazioni
- 1. Univ Molise, Dipartimento Sci & Tecnol Agroalimentari Ambietal, I-86100 Campobasso, Italy
2. Univ Naples Federico 2, Dipartimento Chim Sostanze Nat, I-80131 Naples, Italy
3. CNR IGV, Ist Genet Vegetale, Sez Portici, I-80055 Portici, NA, Italy
4. Univ Naples Federico 2, CNR, Ist Endocrinol & Oncol Sperimentale, I-80131 Naples, Italy
5. Univ Salerno, Dipartimento Sci Farmaceut, I-84084 Fisciano, SA, Italy (literal)
- Titolo
- Astersedifolioside A-C, three new oleane-type saponins with antiproliferative activity (literal)
- Abstract
- A phytochemical analysis of Aster sedifolius has led to the isolation of three novel triterpenoid saponins, based on an
oleane-type skeleton and named astersedifolioside A (1), B (2) and C (3). On the basis of chemical, and 2D NMR and mass spectrometry
data, the structures of the new compounds were elucidated as 3-O-[a-L-rhamnopyranosyl (1!2)-b-D-glucopyranosyl] echinocystic
acid 28-[O-a-L-rhamnopyranosyl (1!2)-a-L-arabinopyranoside] (1), 3-O-[a-L-rhamnopyranosyl (1!2)-b-D-glucopyranosyl]
echinocystic acid 28-[O-b-D-xylopyranosyl (1!4)-O-a-L-rhamnopyranosyl (1!2)-a-L-arabinopyranoside] (2) and 3-O-[a-Lrhamnopyranosyl
(1!2)-b-D-glucopyranosyl (1!2)-b-D-glucopyranosyl] echinocystic acid 28-[O-b-D-xylopyranosyl (1!4)-O-a-
L-rhamnopyranosyl (1!2)-a-L-arabinopyranoside] (3). The isolated compounds showed antiproliferative effect in KiMol, a transformed
thyroid cell line. (literal)
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