Journal of Food Bioactives, ISSN 2637-8752 print, 2637-8779 online
Journal website www.isnff-jfb.com

Review

Volume 8, December 2019, pages 42-50


Chemistry, pharmacology and processing method of rhubarb (Rheum species): a review

Tables

Table 1. Anthraquinones and anthrone derivatives isolated from different species of rhubarb
 
No.CompoundsBotanical sourcesReferences
1aloe-emodinR. officinale; R. palmatum; R. qinjingense; R. spiciforme; R. tanguticum; R. undulatumXiuwei et al., 1998; Huiyan et al., 2003; Jin et al., 2006; Tan, 2006; Xu Qing et al., 2009; Gao and Liangliang, 2013
21-methyl-8-hydroxyl-9,10-anthraquinone-3-O-β-D-(6′-O-cinnamoyl) glucopyranosideR. glabrucauleCun et al., 2010
36-methyl-aloe-emodinR. emodiSingh et al.
46-methyl-rheinR. emodiSingh et al., 2005
5aloe-emodin-1-O-β-D-glucopyranosideR. undulatumMatsuda et al., 2001
6aloe-emodin-3-(hydroxymethyl)-O-β-D-glucopyranosideR. palmatum; R. glabrucauleWei et al., 2005; Xu Qing, 2009
7aloe-emodin-8-O-β-D-glucopyranosideR. qinjingense; R. tanguticumXiuwei et al., 1998; Jin, Ge et al., 2006
8chrysaronR. rhaponticumHesse, 1908
9chrysophanolR. palmatum; R. tanguticum; R. officinale; R. emodiSuresh Babu et al., 2004; Jin, Ge et al., 2006; Tan, 2006; Xu Qing et al., 2009; Wang et al., 2010; Gao and Liangliang, 2013
10chrysophanol-1-O-β-D-glucopyranosideR. palmatumXu Qing et al., 2009
11chrysophanol-8-Me etherR. glabrucauleWei et al., 2005
12chrysophanol-8-O-β-D-(6′-O-acetyl)-glucopyranosideR. emodiKrenn et al., 2004
13chrysophanol-8-O-β-D-(6′-O-galloyl)-glucopyranosideR. undulatumMatsuda et al., 2001
14chrysophanol-8-O-β-D-(6′-O-malonyl)-glucopyranosideR. qinjingenseXiuwei et al., 1998
15chrysophanol-8-O-β-D-glucopyranosideR. palmatum; R. tanguticum; R. officinale; R. emodi; R. glabrucauleSuresh Babu et al., 2004; Jin et al., 2006; Tan, 2006; Wang et al., 2010; Gao and Liangliang, 2013; Xu Qing et al., 2009
16citreoroseinR. glabrucauleWei et al., 2004
17emodinR. palmatum; R. tanguticum; R. emodi; R. qinjingense; R. undulatum; R. SpiciformeXiuwei et al., 1998; Huiyan et al., 2003; Suresh Babu et al., 2004; Jin et al., 2006; Xu Qing et al., 2009; Wang et al., 2010; Gao and Liangliang, 2013
18emodin-1-O-β-D-glucopyranosideR. undulatumKo, 2000
19emodin-6-O-β-D-glucopyranosideR. palmatumZhu et al., 2016
20emodin-8-O-β-D-glucopyranosideR. emodi; R. glabrucauleWei et al., 2005; Wang et al., 2010
21emodin-8-O-β-D-glucopyranosyl-6-O-sulfateR. emodiLiselotte et al., 2004
22emodin-gemtiobiosideR. nanumXiang et al., 2005
23physcionR. palmatum; R. tanguticum; R. officinale; R. emodi; R. qinjingenseXiuwei et al., 1998; Suresh Babu et al., 2004; Jin et al., 2006; Tan, 2006; Xu Qing et al., 2009; Wang et al., 2010; Gao and Liangliang, 2013
24physcion-1-O-β-D-glucopyranosideR. emodiSingh et al., 2016
25physcion-8-O-β-D-gentiobiosideR. officinaleHolzschuh et al., 1982
26physcion-8-O-β-D-glucopyranosideR. palmatum; R. emodi; R. qinjingense; R. undulatumXiuwei et al., 1998; Ko, 2000; Xu Qing et al., 2009; Wang et al., 2010
27revandchinone-3R. emodiSuresh Babu et al., 2004
28rheinR. palmatum; R. tanguticum; R. undulatum; R. SpiciformeXiuwei et al., 1998; Huiyan et al., 2003; Jin et al., 2006; Xu Qing et al., 2009; Gao and Liangliang, 2013
29rhein-8-O-β-D-[6′-O-(3″-methoxyl malonyl)] glucopyranosideR. palmatumCun et al., 2010
30rhein-8-O-β-D-glucopyranosideR. palmatumGao and Liangliang, 2013
3110-hydroxycascaroside CR. emodiKrenn et al., 2004
3210-hydroxycascaroside DR. emodiKrenn et al., 2004
3310R-chrysaloin1-O-β-D-glucopyranosideR. emodiKrenn et al., 2004
34cascaroside CR. emodiKrenn et al., 2004
35cascaroside DR. emodiKrenn et al., 2004
36cassialoinR. emodiKrenn et al., 2004
37palmidin AR. palmatumDequeker et al., 1964
38palmidin BR. palmatumDequeker et al., 1964
39palmidin CR. palmatumDequeker et al., 1964
40rendin AR. palmatumLEMLI et al., 1964
41rendin BR. palmatumLEMLI et al., 1964
42rendin CR. palmatumLEMLI et al., 1964
43revandchinone-1R. emodiSuresh Babu et al., 2004
44revandchinone-2R. emodiSuresh Babu et al., 2004
45revandchinone-4R. emodiYamagishi et al., 1987
46rheinoside AR. palmatumYamagishi et al., 1987
47rheinoside BR. palmatumYamagishi et al., 1987
48rheinoside CR. palmatumYamagishi et al., 1987
49rheinoside DR. palmatumYamagishi et al., 1987
50sennidin CR. palmatumZwaving, 1965
51sennoside AR. palmatumOshio et al., 1974
52sennoside BR. palmatumOshio et al., 1974
53sennoside CR. palmatumOshio et al., 1974
54sennoside DR. palmatumOshio et al., 1974
55sennoside ER. palmatumOshio et al., 1974
56sennoside FR. palmatumOshio et al., 1974

 

Table 2. Stilbene derivatives isolated from different species of rhubarb
 
No.CompoundsBotanical sourcesReferences
573,4′,5-trihydroxystlbene-4′-O-β-D-(6″-O-galloyl) glucopyranosideR. palmatum; R. tanguticum; R. officinaleNonaka et al., 1981; Komatsu et al., 2006
583,4′,5-trihydroxystlbene-4′-O-β-D-glucopyranosideR. palmatum; R. tanguticum; R. officinaleNonaka et al., 1981; Komatsu et al., 2006
59deoxyrhaponticinR. undulatumKo, 2000
60desoxyrhaponticinR. emodi; R. undulatumMatsuda et al., 2001; Suresh Babu et al., 2004
61desoxyrhapontigeninR. undulatumMatsuda et al., 2001
62gentin CR. nanumXiang et al., 2005
63isorhapontinR. undulatumMatsuda et al., 2001
64maximol AR. palaestinumShikishima et al., 2001
65maximol BR. palaestinumShikishima et al., 2001
66piceatannolR. undulatumKo et al., 1999
67piceatannol 3′-O-β-D-glucopyranosideR. hotaoense; R. undulatumLi et al., 1998; Matsuda et al., 2001
68piceatannol 4′-O-(6″-p-coumaroyl)β-D-glucopyranosideR. emodiWang et al., 2010
69piceatannol 4′-O-β-D-glucopyranosideR. nanumXiang et al., 2005
70piceatannol-3,4′-O-β-D-diglucopyranosideR. undulatumKo, 2000
71resveratrolR. undulatumMatsuda et al., 2001
72resveratrol 4′-O-β-D-(6″-O-galloyl)-glucopyranosideR. tanguticumGao and Liangliang, 2013
73resveratrol 4′-O-β-D-glucopyranosideR. tanguticumGao and Liangliang, 2013
74rhaponticinR. tanguticum; R. undulatum; R. palaestinumLi, Li et al., 1998; Ko et al., 1999; Matsuda et al., 2001; Matsuda et al., 2001; Jin et al., 2006; Aburjai, 2000
75rhapontigeninR. palmatum; R. tanguticum; R. emodi; R. undulatumLi, Li et al., 1998; Ko et al., 1999; Matsuda et al., 2001; Matsuda et al., 2001; Suresh Babu et al., 2004; Jin, Ge et al., 2006; Xu Qing et al., 2009
76rhaponticin 2″-O-gallateR. tanguticum; R. undulatumMatsuda et al., 2001; Jin et al., 2006

 

Table 3. Flavonoids and acylglucosides isolated from different species of rhubarb
 
No.CompoundsBotanical sourcesReferences
77(+)-catechinR. palmatum; R. tanguticumNonaka et al., 1981; Lu et al., 1998; Jin et al., 2006
78(−)epicatechin-3-O-gallateR. tanguticum; R. officinaleNonaka et al., 1981; Jin et al., 2006; Tan, 2006
79(−)epigallocatechin-3-O-gallateR. officinaleTan, 2006
80gallic acidR. palmatumNonaka et al., 1981; Xu Qing et al., 2009
81kaempferol-3-O-rhamnosideR. undulatumHam et al., 1994
82kaempferol-3-O-(2′,6′-di-O-rhamnopyranosyl)-β-D-galactopyra-nosideR. undulatumHam et al., 1994
83gallic acid 3-O-β-D-glucopyranosideR. palmatumKashiwada et al., 1986
84gallic acid 4-O-β-D-glucopyranosideR. palmatumKashiwada et al., 1986
851-O-galloyl-6-O-cinnamoyl-β-D-glucoseR. palmatumKashiwada et al., 1988
861,2-di-O-galloyl-6-O-cinnamoyl-β-D-glucoseR. palmatumKashiwada et al., 1988
871,2,6-tri-O-galloyglucoseRhei Radix et RhizomaNonaka et al., 1981
88glucopyranosyl-galloyl-glucoseR. palmatumWang et al., 2011
89coumaroyl-O-galloyl-glucoseR. palmatumWang et al., 2011
90lindleyinR. tanguticumGao and Liangliang, 2013
911′-O-galloylsucroseR. coreanumKashiwada et al., 1988
922-O-galloylsucroseR. coreanumKashiwada et al., 1988
936-O-galloylsucroseR. coreanumKashiwada et al., 1988
946′-O-galloylsucroseR. coreanumKashiwada et al., 1988