2010
DOI: 10.1016/j.phytochem.2010.07.013
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Triterpenoidal saponins of Pulsatilla koreana roots

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Cited by 40 publications
(40 citation statements)
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“…2) characterized by an a-L-arabinopyranose directly branched to the C-3 position were isolated from plants used in traditional Chinese medicine such as S. fagueti (Cioffi et al 2003), S. rotundifolia (Braca et al 2004), P. chinensis (Ye et al 2002) and P. koreana (Bang et al 2005a;Bang et al 2005b). As shown in Table 1, all of these saponins were evaluated in vitro for their cytotoxic activity against several cancer cell lines (A549, SKOV-3, SKMEL2, HCT15, K-562, HeLa and WEHI-164).…”
Section: Pharmacological Activity Of Natural Lupane-type Saponinsmentioning
confidence: 99%
“…2) characterized by an a-L-arabinopyranose directly branched to the C-3 position were isolated from plants used in traditional Chinese medicine such as S. fagueti (Cioffi et al 2003), S. rotundifolia (Braca et al 2004), P. chinensis (Ye et al 2002) and P. koreana (Bang et al 2005a;Bang et al 2005b). As shown in Table 1, all of these saponins were evaluated in vitro for their cytotoxic activity against several cancer cell lines (A549, SKOV-3, SKMEL2, HCT15, K-562, HeLa and WEHI-164).…”
Section: Pharmacological Activity Of Natural Lupane-type Saponinsmentioning
confidence: 99%
“…The major components of the methanol extract of Pulsatilla koreana are triterpenoid compounds, such as hederagenin, saponins, ursolic acid, monodesmoside (pulsatilla saponin A, B, D), and bisdesmoside (pulsatilla saponin F, H) (8). Those compounds are proposed to be responsible for the major biological functions of Pulsatilla koreana such as lowering blood glucose, cholesterol level and lowering blood pressure (9,10). However, no study has been done to elucidate the plausible mechanism of anti-inflammatory actions of Pulsatilla koreana.…”
Section: Introductionmentioning
confidence: 99%
“…3) In this paper, seven new saponins (1-4, 6-8) and a new lignan glucoside (14) were isolated from the extract of C. barbinervis, together with echinocystic acid 3-β-d-glucuronopyranoside (5), 4) hemsganoside B (9), 5,6) scheffleraside II (10), 5) rotundic acid (11), 7) barbinervic acid (12), 8) clethric acid (13), 9,10) 8-O-4′ neolignan 7-O-β-glucopyranoside (15), 11) rourinoside (16), 12) epicatechin (17), 13) pavetannin A (18), 14) 2-phenylethyl β-glucopyranoside (19), 15) 2-phenylethyl O-α-larabinofuranosyl-(1→ 6)-β-d-glucopyranoside (20), 16) 2-phenylethyl O-α-l-rhamnopyranosyl-(1→ 6)-β-d-glucopyranoside (21), 17) and methyl salicylate β-primeveroside (22) 18) (Figs. 1, 2).…”
mentioning
confidence: 99%
“…Fractions 2A (90.1%, 2.0 mg/mL), 2C (68.0%, 2.0 mg/mL), 2D (78.9%, 2.0 mg/mL), and 2E (71.7%, 2.0 mg/mL) separated from 1C (91.4%, 2.0 mg/mL) had high inhibitory activities. Nine constituents (14)(15)(16)(17)(18)(19)(20)(21)(22) were isolated from 2A, and 17 was active (IC 50 0.94 mm). Catechins are already known to have hyaluronidase inhibitory activity.…”
mentioning
confidence: 99%