Chemical investigation of Santolina insularis afforded eleven germacrane sesquiterpenes (1-11), four of which (2, 3, 10, and 11) are new. The stereostructures of these compounds have been established by a combination of spectroscopic techniques (mainly NMR), chemical transformations and application of the modified Mosher method. Compounds 8 and 10 showed a potent and selective cytotoxic activity against the human colon carcinoma cell line.

Cytotoxic germacrane sesquiterpenes from the aerial parts of Santolina insularis / Appendino, G.; Aviello, G.; Ballero, M.; Borrelli, Francesca; Fattorusso, Ernesto; Petrucci, F.; Santelia, F. U.; TAGLIALATELA SCAFATI, Orazio. - In: JOURNAL OF NATURAL PRODUCTS. - ISSN 0163-3864. - STAMPA. - 68:(2005), pp. 853-857. [10.1021/np050120q]

Cytotoxic germacrane sesquiterpenes from the aerial parts of Santolina insularis

G. AVIELLO;BORRELLI, FRANCESCA;FATTORUSSO, ERNESTO;TAGLIALATELA SCAFATI, ORAZIO
2005

Abstract

Chemical investigation of Santolina insularis afforded eleven germacrane sesquiterpenes (1-11), four of which (2, 3, 10, and 11) are new. The stereostructures of these compounds have been established by a combination of spectroscopic techniques (mainly NMR), chemical transformations and application of the modified Mosher method. Compounds 8 and 10 showed a potent and selective cytotoxic activity against the human colon carcinoma cell line.
2005
Cytotoxic germacrane sesquiterpenes from the aerial parts of Santolina insularis / Appendino, G.; Aviello, G.; Ballero, M.; Borrelli, Francesca; Fattorusso, Ernesto; Petrucci, F.; Santelia, F. U.; TAGLIALATELA SCAFATI, Orazio. - In: JOURNAL OF NATURAL PRODUCTS. - ISSN 0163-3864. - STAMPA. - 68:(2005), pp. 853-857. [10.1021/np050120q]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11588/200722
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