TY - JOUR
T1 - Secondary metabolites from the roots of Paronychia chionaea
AU - Avunduk, Sibel
AU - Alankuş-Çalişkan, Özgen
AU - Miyamoto, Tomofumi
AU - Tanaka, Chiaki
AU - Lacaille-Dubois, Marie Aleth
PY - 2011/2
Y1 - 2011/2
N2 - 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).
AB - 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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U2 - 10.1177/1934578x1100600212
DO - 10.1177/1934578x1100600212
M3 - Article
C2 - 21425675
AN - SCOPUS:79954536570
SN - 1934-578X
VL - 6
SP - 205
EP - 208
JO - Natural product communications
JF - Natural product communications
IS - 2
ER -