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A new inositol derivative from Prenanthes macrophylla

Author:
Zhang, Yong-Hong, Chen, Yong-Sheng, Lin, Xiao-Yan, Chen, Shi-Wu, Li, Peng, Zhong, Lin-Jing
Source:
Journal of Asian natural products research 2012 v.14 no.2 pp. 182-185
ISSN:
1477-2213
Subject:
carbon, electrospray ionization mass spectrometry, luteolin, myo-inositol, nuclear magnetic resonance spectroscopy, oleanolic acid, stable isotopes, ursolic acid
Abstract:
A new chiro-inositol ester, 4-hydroxyphenylacetyl-3-d-chiro-inositol ester (1), was isolated from the whole plants of Prenanthes macrophylla Franch., along with 10 known compounds, 4-hydroxyphenylacetic acid (2), trans-ethyl caffeate (3), cis-ethyl caffeate (4), protocatechualdehyde (5), luteolin (6), luteolin-7-O-β-d-glucoside (7), 15-hydroxy-2-oxo-guai-3-en-1α,5α,6β,7α,10α,11βH-12,6-olide (8), 15-glucopyranosyloxy-2-oxo-guaia-3,11(13)-dien-1α,5α,6β,7α,10αH-12,6-olide (9), ursolic acid (10), and oleanolic acid (11). Their structures were elucidated on the basis of spectroscopic analyses including HR-ESI-MS, ESI-MS, ¹H and ¹³C NMR, HSQC, HMBC, and ROESY, and chemical evidences.
Agid:
257139