Table 4.

The aromatic glycosides and its structure of Atractylodis Rhizoma.

Chemical compounds	Nos.	Compounds name	Structure	Origin and Ref.
Aromatic glycosides	190	4-hydroxy-3-methoxyphenol-β-D-glucopyranoside		A. lancea (Kitajima et al., 2003b)
	191	seguinoside B,4-hydroxyphenyl 1-O-β-D - apiopyranosyl-(1 → 6)-β-D-glucopyranoside]
	192	syringin [4-[(1E)-3-Hydroxyprop-1-en-1-yl]-2,6-dimethoxyphenyl-β-D-glucopyranoside]
	193	4-hydroxy-3-methoxyphenol-β-D-apiopyranosyl-(1 → 6)-D-glucopyranoside
	194	4-hydroxy-3-methoxyphenyl-β-xylopyranosyl-(1 → 6)-β-glucopyranoside
	195	icariside F2 [benzyl β-D-apiopyranosyl-(1 → 6)-β-D-glucopyranoside]
	196	icariside D1 [phenethyl β-D-apiopyranosyl-(1 → 6)-β-D-glucopyranoside]
	197	phenethyl α-L-rhamnopyranosyl-(1 → 6)-β-D-glucopyranoside
	198	scopoletin-D-xylopyranosyl-(1 → 6)-D-glucopyranoside
	199	p-hydroxybenzoic acid-4-O-β-D-glucopyranosyl-(1 → 3)-α-L-rhamnopyranoside		A. lancea (Xu et al., 2016b)
	200	vanillic acid-4-O-β-D-glucopyranosyl-(1 → 3)-α-L-rhamnopyranoside
	201	1,3-di-O-caffeoylquinic acid		A. lancea (Feng et al., 2018)
	202	chlorogenic acid (1S,3R,4R,5R)-3-[3-(3,4-dihydroxyphenyl)prop-2-enoyloxy]-1,4,5-trihydroxycyclohexanecarboxylic acid
	203	5-O-feruloylquinic acid (1R,3R,4S,5R)-1,3,4-trihydroxy-5-[(2E)-3-(4-hydroxy-3-methoxyphenyl)-prop-2-enoyl]-oxycyclohexane-1-carboxylic acid