Secondary metabolites from the roots of Paronychia chionaea

Sibel Avunduk; Özgen Alankuş-Çalişkan; Tomofumi Miyamoto; Chiaki Tanaka; Marie Aleth Lacaille-Dubois

doi:10.1177/1934578x1100600212

Secondary metabolites from the roots of Paronychia chionaea

Sibel Avunduk, Özgen Alankuş-Çalişkan, Tomofumi Miyamoto, Chiaki Tanaka, Marie Aleth Lacaille-Dubois

Research output: Contribution to journal › Article › peer-review

4 Citations (Scopus)

Abstract

Two novel secondary metabolites, compounds (1-2) were isolated from the roots of Paronychia chionaea. On the basis of spectroscopic data including 1D and 2D NMR experiments (COSY, TOCSY, HSQC, and HMBC), and mass spectroscopy, their structures were established as 6-C-[α-L-arabinopyranosyl-(1→2)- β-D-glucopyranosyl]-7-O-[β-D-glucopyranosyl]-luteolin 3′-methyl ether (1), and 2-(methoxy)-2-(3,5-dimethoxy 4-hydroxyphenyl)-ethane-1,2-diol 1-O-β-D-glucopyranoside (2).

Original language	English
Pages (from-to)	205-208
Number of pages	4
Journal	Natural product communications
Volume	6
Issue number	2
DOIs	https://doi.org/10.1177/1934578x1100600212
Publication status	Published - Feb 2011

All Science Journal Classification (ASJC) codes

Pharmacology
Plant Science
Drug Discovery
Complementary and alternative medicine

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abstract = "Two novel secondary metabolites, compounds (1-2) were isolated from the roots of Paronychia chionaea. On the basis of spectroscopic data including 1D and 2D NMR experiments (COSY, TOCSY, HSQC, and HMBC), and mass spectroscopy, their structures were established as 6-C-[α-L-arabinopyranosyl-(1→2)- β-D-glucopyranosyl]-7-O-[β-D-glucopyranosyl]-luteolin 3′-methyl ether (1), and 2-(methoxy)-2-(3,5-dimethoxy 4-hydroxyphenyl)-ethane-1,2-diol 1-O-β-D-glucopyranoside (2).",

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AU - Avunduk, Sibel

AU - Alankuş-Çalişkan, Özgen

AU - Miyamoto, Tomofumi

AU - Tanaka, Chiaki

AU - Lacaille-Dubois, Marie Aleth

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Secondary metabolites from the roots of Paronychia chionaea

Abstract

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