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A new phenylethanoid glycoside from Incarvillea compacta

, , , , , , , , , & show all
Pages 596-602 | Received 22 May 2015, Accepted 17 Sep 2015, Published online: 02 Dec 2015
 

Abstract

A new phenylethanoid glycoside, 3′′′-O-methylcampneoside I (1), was isolated from the 90% ethanolic extract of the roots of Incarvillea compacta, together with three known compounds, campneoside I (2), ilicifolioside A (3), and campneoside II (4). Their structures were determined spectroscopically and compared with previously reported spectral data. Compound 1 existed as epimers and displayed better 1,1-diphenyl-2-picrylhydrazyl (DPPH)-free radical scavenging activity using di-tert-butyl-4-methylphenol (BHT) as the positive control. In addition, pretreatment of human HepG2 cells with compound 1 significantly increased the viability on CCl4-induced cell death.

Disclosure statement

No potential conflict of interest was reported by the authors.

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