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A new cyclolignan glycoside from the tubers of Pinellia ternata.

Authors :
Wu YY
Huang XX
Wu J
Zhou L
Li DQ
Liu QB
Li LZ
Yan XJ
Song SJ
Source :
Journal of Asian natural products research [J Asian Nat Prod Res] 2015; Vol. 17 (11), pp. 1097-103. Date of Electronic Publication: 2015 May 19.
Publication Year :
2015

Abstract

A new 2,7'-type cyclolignan glycoside, cyclolignanyingoside A (1), together with six known compounds (2-7) were isolated from the tubers of Pinellia ternata (Thunb.) Breit. The structure of 1 was elucidated on the basis of chemical and spectral analysis, including 1D, 2D NMR analyses, HR-ESI-MS, and CD spectrometry. The cytotoxic, antioxidant and tyrosinase-inhibiting activities of all the isolates were determined. However, all the isolates exhibited no activity on the selected cell lines (Hep-3B, Bcap-37, and MCF-7). In addition, compounds 1-3 and 7 exhibited strong 2,2'-azino-bis (3-ethylbenzothiazoline-6-sulphonic acid) free radical scavenging activity, and compounds 2 and 4 showed a moderate mushroom tyrsinase inhibitory activity.

Details

Language :
English
ISSN :
1477-2213
Volume :
17
Issue :
11
Database :
MEDLINE
Journal :
Journal of Asian natural products research
Publication Type :
Academic Journal
Accession number :
25989151
Full Text :
https://doi.org/10.1080/10286020.2015.1041931