Triterpenoid Saponins from Anemone rivularis var. Flore-Minore and Their Anti-Proliferative Activity on HSC-T6 Cells.

Five previously undescribed triterpenoid saponins (1-5), along with eight known ones (6-13), were isolated from the whole plants of Anemone rivularis var. flore-minore. Their structures were clarified by extensive spectroscopic data and chemical evidence. For the first time, the lupane-type saponins (3 and 12) were reported from the Anemone genus. The anti-proliferative activity of all isolated saponins was evaluated on hepatic stellate cells (HSC-T6). Saponins 12 and 13, which possess more monosaccharides than the others, displayed potent anti-proliferative activity, with IC50 values of 18.21 and 15.56 μM, respectively.

1. Introduction

The genus Anemone belongs to the family Ranunculaceae, which consists of about 150 species with a near global distribution. Triterpenoid saponins have been proved to be the main bioactive substances of this genus, which possess potentially useful bioactivities. These bioactivities include antitumor, antibacterial, insect deterrence, and anti-peroxidation, among others [1,2,3,4,5,6,7,8]. For a long time, several species of this genus, such as A. flaccida, A. raddeana, A. tomentosa, A. anhuiensis, A. altaica, have been used as Chinese traditional medicines. Anemone rivularis var. flore-minore is widely distributed in western China. The whole plants of A. rivularis var. flore-minore, named “Poniuqi”, have been used as a folk medicine in Shaanxi Province for the treatment of hepatitis, stranguria, edema, emissions, etc. [9]. As part of our continuing study to explore bioactive natural products from the genus Anemone [10,11,12,13,14,15,16,17], we continued the investigation of this plant. In our present study, five new triterpenoid saponins (1–5), together with eight known ones (6–13) (Figure 1) were isolated, among which lupane-type saponins (3 and 12) were first reported from the Anemone genus. Herein, we describe the isolation and structural identification of these saponins, as well as their anti-proliferative activity on HSC-T6 cells.

Figure 1

Structures of saponins 1–13.

2. Results and Discussion

Saponin 1 was obtained as a white amorphous powder and showed positive results in the Liebermann–Burchard and Molisch tests. Its molecular formula was established as C47H74O17 (m/z 933.4829 [M + Na]+, calcd. for C47H74O17Na+, 933.4825) by high resolution electrospray ionization mass spectrometry (HRESIMS). The 1H and 13C NMR spectra exhibited signals for six tertiary methyl groups at δH 0.86 (H3-29), 0.87 (H3-30), 0.89 (H3-25), 1.05 (H3-25), 1.19 (H3-27), and 1.34 (H3-24), one olefinic proton signal at δH 5.41 (1H, br s) with two typical olefinic carbon signals at δC 122.7 and 144.1, one carbonyl signal at δC 176.6, and one aldehyde proton signal at δH 9.65 (1H, s), with the corresponding aldehyde carbon signal at δC 206.5. These data indicated that 1 was an oleanane-type saponin with one of the aglycone methyl groups substituted by an aldehyde function. The aldehyde function located at C-23 was deduced from the highfield shifts (−6.7 ppm, −8.2 ppm, and −6.9 ppm) exhibited by C-3 (δC 81.9), C-5 (δC 47.8), and C-24 (δC 10.3), respectively, and the downfield shift (+15.9 ppm) exhibited by C-4 (δC 55.4) in comparison with the same carbon resonances in an oleanane skeleton bearing a Me-23 [15]. The α-configuration for the 23-CHO function was determined by the correlations of H-23 (δH 9.65) with H-3 (δH 4.04) and H-5 (δH 1.36) observed in the NOESY spectrum (Figure 2). The HMBC spectrum confirmed the 23-CHO function position by showing the correlations between H-23 (δH 9.65) and C-3 (δC 81.9), C-4 (δC 55.4) and C-24 (δC 10.3) (Figure 2). The assignments of the NMR signals of the aglycone moiety were derived from 1H-1H COSY, TOCSY, HSQC, HMBC, and NOESY spectra (Table 1). The aglycone of 1 was thus elucidated as gypsogenin [17,18,19]. The 13C-NMR shifts of C-3 at δC 81.9 and C-28 at δC 176.6 implied that sugar linkages were at both C-3 and C-28. The β-configuration for the 3-O-sugar moiety was deduced from the correlations of H-3 with H-23 and H-5 observed in the NOESY spectrum (Figure 2).

Figure 2

Key NOESY and HMBC correlations for compound 1.

Table 1

1H- (500 MHz) and 13C-NMR (125 MHz) data for the aglycone moieties of 1–5 in pyridine-d5.

C	1		2		3		4		5
	δC	δH	δC	δH	δC	δH	δC	δH	δC	δH
1	38.5	0.97, 1.55 m	38.6	1.00, 1.59 m	39.4	1.60, 0.89 m	38.8	0.93, 1.45 m	38.9	0.95, 1.46 m
2	25.7	1.84, 2.09 m	25.6	1.87, 2.10 m	26.8	2.18, 1.86 m	26.6	1.84, 2.06 m	26.7	1.87, 2.08 m
3	81.9	4.04 m	81.8	4.06 m	88.7	3.34 m	88.7	3.26 dd(3.7, 11.6)	88.8	3.28 dd(3.9, 11.6)
4	55.4	-	55.6	-	39.6	-	39.4	-	39.5	-
5	47.8	1.36 m	48.0	1.37 m	56.0	0.74 m	56.0	0.77 d (11.5)	56.1	0.79 d (11.6)
6	20.6	0.98, 1.39 m	20.7	0.99, 1.42 m	18.4	1.67, 1.45 m	18.4	1.25, 1.44 m	18.5	1.26, 1.46 m
7	32.6	1.17, 1.42 m	32.7	1.19, 1.42 m	34.5	1.30, 1.28 m	33.1	1.25, 1.40 m	33.2	1.25, 1.42 m
8	40.0	-	40.2	-	41.1	-	39.7	-	39.9	-
9	47.8	1.69 m	48.1	1.70 m	50.8	1.30 m	48.1	1.66 m	48.2	1.68 m
10	36.0	-	36.2	-	37.1	-	36.9	-	37.0	-
11	23.2	1.90, 1.99 m	23.4	1.91, 2.03 m	21.1	1.31, 1.13 m	23.7	1.86, 1.92 m	23.8	1.87, 1.94 m
12	122.7	5.41 br s	122.6	5.42 br s	26.0	1.84, 1.13 m	122.6	5.43 br s	122.8	5.44 br s
13	144.1	-	144.2	-	38.3	2.64 m	144.1	-	144.3	-
14	41.6	-	41.8	-	42.7	-	42.2	-	42.4	-
15	28.1	1.13, 2.04 m	28.3	1.15, 2.06 m	30.1	2.00, 1.18 m	28.5	1.15, 2.30 m	28.6	1.16, 2.32 m
16	23.2	1.77, 2.01 m	23.3	1.78, 2.05 m	32.4	2.63, 1.48 m	27.0	2.35, 3.08 m	27.1	2.37, 3.11 m
17	47.2	-	47.3	-	57.0	-	47.1	-	47.2	-
18	41.5	3.14 dd(3.3, 13.4)	41.7	3.15 dd(3.9, 13.5)	49.8	1.71 m	41.5	3.36 dd(3.3, 14.0)	41.7	3.38 dd(3.4, 13.9)
19	46.1	1.23, 1.74 m	46.2	1.24, 1.75 m	47.4	3.36 m	41.3	1.70, 1.21 m	41.5	1.73, 1.22 m
20	30.6	-	30.7	-	150.8	-	35.6	-	35.7	-
21	33.8	1.12, 1.34 m	34.0	1.13, 1.36 m	30.8	2.15, 1.40 m	73.2	3.66 br s	73.4	3.67 br s
22	32.3	1.71, 1.89 m	32.4	1.73, 1.91 m	37.1	2.19, 1.45 m	39.5	2.25, 2.27 m	39.6	2.26, 2.28 m
23	206.5	9.65 s	206.6	9.66 s	28.1	1.24 s	28.1	1.29 s	28.2	1.30 s
24	10.3	1.34 s	10.5	1.35 s	16.3	0.77 s	17.2	1.15 s	17.3	1.16 s
25	15.6	0.89 s	15.7	0.89 s	16.7	0.92 s	15.5	0.87 s	15.7	0.88 s
26	17.3	1.05 s	17.5	1.06 s	16.4	1.10 s	17.4	1.08 s	17.6	1.10 s
27	26.2	1.19 s	26.3	1.22 s	14.8	1.03 s	25.5	1.31 s	25.7	1.33 s
28	176.6	-	176.7	-	174.9	-	176.4	-	176.6	-
29	33.0	0.86 s	33.1	0.87 s	110.1	4.85, 4.70(br s)	28.3	1.13 s	28.5	1.14 s
30	23.7	0.87 s	23.8	0.88 s	19.4	1.70 s	24.8	0.99 s	25.1	1.01 s

The monosaccharides of 1 were determined as L-arabinose (Ara), L-rhamnose (Rha), and D-glucose (Glc), in a ratio of 1:1:1 by acidic hydrolysis followed by gas chromatography (GC) analysis [20]. The 1H-NMR spectrum of compound 1 exhibited three anomeric protons at δH = 6.32 (d, J = 8.2 Hz), 6.17 (s) and 5.03 (d, J = 7.3 Hz), and one methyl group of 6-deoxy-hexopyranosyl moiety at δH 1.62 (d, J = 6.2 Hz). The α anomeric configuration of the Ara unit was deduced from the 3JH-1/H-2 (7.3 Hz) value observed in the 4C1 form. The Glc unit was determined to have a β anomeric configuration on the basis of its 3JH-1/H-2 coupling constant (8.2 Hz). Although the anomeric proton of the Rha moiety was observed as a singlet in the 1H-NMR spectrum, the 13C-NMR shift of Rha C-5 at δC = 69.6 indicated the α anomeric configuration [21,22]. The complete assignments of proton signals belonging to sugars were based on 2D NMR of 1H-1H COSY, TOCSY, and NOESY, and the carbon signals were assigned by HSQC and further confirmed by the HMBC spectrum (Table 2). The above NMR data indicated that all the monosaccharides were in their pyranose forms. The sequence and binding sites of the oligosaccharide chains were deduced from the HMBC spectrum (Figure 2). A cross peak between C-3 of the aglycone and H-1 of Ara revealed that Ara was connected to C-3 of the aglycone. Similarly, the linkage of Glc at C-28 of the aglycone was indicated by the cross peak Glc H-1/C-28, and the linkage of Rha at C-2 of Ara was indicated by the cross peak Rha H-1/Ara C-2. This conclusion was also supported by the NOESY correlations (Figure 2). On the basis of the above analysis, the structure of 1 was elucidated as 3β-O-α-L-rhamnopyranosyl-(1→2)-α-L-arabinopyranosyl gypsogenin 28-O-β-D-glucopyranosyl ester.

Table 2

1H- (500 MHz) and 13C-NMR (125 MHz) data for the sugar moieties of 1–5 in pyridine-d5.

C	1		2		3		4		5
	δC	δH	δC	δH	δC	δH	δC	δH	δC	δH
3-O-sugar
Ara
1	104.6	5.03 d (7.3)	104.7	5.04 d (7.0)	107.5	4.76 d (7.0)	107.4	4.77 d (6.8)	104.5	5.03 d (7.3)
2	75.7	4.43 m	75.5	4.53 m	72.9	4.40 m	72.8	4.41 m	75.5	4.43 m
3	74.7	4.16 m	75.2	4.04 m	74.6	4.13 m	74.4	4.14 m	74.6	4.16 m
4	69.3	4.20 m	69.9	4.12 m	69.5	4.29 m	69.5	4.27 m	69.3	4.20 m
5	65.7	3.75, 4.42 m	66.3	3.56, 4.32 m	67.1	3.80, 4.28 m	67.0	3.81, 4.26 m	65.5	3.76, 4.42 m
Rha I
1	101.6	6.17 s	101.3	6.32 s					101.7	6.17 s
2	72.3	4.71 br s	71.9	4.89 brs					72.3	4.71 br s
3	72.5	4.59 m	82.8	4.75 m					72.4	4.59 m
4	74.1	4.28 m	72.9	4.45 m					74.0	4.27 m
5	69.6	4.61 m	69.6	4.62 m					69.8	4.61 m
6	18.5	1.62 d (6.2)	18.4	1.52 d (6.2)					18.6	1.62 d (6.2)
Xyl
1			107.5	5.35 d (7.7)
2			75.6	4.05 m
3			78.4	4.15 m
4			71.1	4.19 m
5			67.4	3.69, 4.30 m
28-O-sugar
Glc I
1	95.7	6.32 d (8.2)	95.6	6.23 d (8.1)	95.3	6.34 d (8.2)	95.5	6.24 d (8.2)	95.6	6.23 d (8.1)
2	74.1	4.19 m	73.8	4.08 m	74.0	4.08 m	73.7	4.07 m	73.8	4.10 m
3	79.2	4.02 m	78.7	4.15 m	78.7	4.20 m	78.6	4.16 m	78.7	4.17 m
4	71.1	4.34 m	70.8	4.28 m	70.9	4.29 m	70.8	4.27 m	70.7	4.30 m
5	78.9	4.26 m	78.0	4.08 m	78.0	4.08 m	77.9	4.06 m	78.0	4.09 m
6	62.3	4.40, 4.43 m	69.1	4.31, 4.63 m	69.4	4.30, 4.66 m	69.1	4.27, 4.64 m	69.0	4.30, 4.63 m
Glc II
1			104.9	4.97 d (7.7)	105.2	4.92 d (7.8)	104.8	4.97 d (7.8)	104.9	4.98 d (7.8)
2			75.3	3.92 m	75.3	3.92 m	75.2	3.91 m	75.3	3.92 m
3			76.5	4.12 m	76.4	4.11 m	76.4	4.12 m	76.5	4.14 m
4			78.1	4.40 m	78.2	4.39 m	78.1	4.37 m	78.2	4.39 m
5			77.1	3.62 m	77.2	3.63 m	77.0	3.64 m	77.1	3.64 m
6			61.2	4.07, 4.18 m	61.3	4.06, 4.18 m	61.2	4.04, 4.19 m	61.3	4.06, 4.20 m
Rha II
1			102.6	5.85 s	102.7	5.84 s	102.6	5.84 s	102.7	5.86 s
2			72.6	4.66 m	72.6	4.65 m	72.5	4.63 m	72.6	4.64 m
3			72.7	4.53 m	72.8	4.50 m	72.7	4.50 m	72.7	4.54 m
4			74.1	4.31 m	74.0	4.30 m	74.0	4.30 m	74.1	4.32 m
5			70.3	4.94 m	70.3	4.95 m	70.3	4.92 m	70.4	4.95 m
6			18.5	1.68 d (6.2)	18.5	1.69 m	18.5	1.67 d (6.2)	18.6	1.66 d (6.2)

Saponin 2 was also obtained as a white powder. A pseudomolecular ion at m/z 1065.5252 (calcd. for 1065.5246 [M + Na]+) was found in HRESIMS, establishing the molecular formula of C52H82O21. By comparing with the 1D NMR data of 1, the aglycone moiety of 2 was identical to 1 (Table 1), suggesting the same gypsogenin aglycone. The types of sugar units were determined as L-arabinose, D-xylose, L-rhamnose, and D-glucose in a 1:1:2:2 ratio by acid hydrolysis, followed by GC analysis. Six anomeric protons (δH 6.32 (s), 6.23 (d, J = 8.1 Hz), 5.85 (s), 5.35 (d, J = 7.7 Hz), 5.04 (d, J = 7.0 Hz), and 4.97 (d, J = 7.7 Hz)) and six anomeric carbons (δC 107.5, 104.9, 104.7, 102.6, 101.3, and 95.6) were observed in the NMR spectra of 2. The linkage sites and the sequence of sugar moieties were deduced from the HMBC and NOESY correlations of signals at δH 5.04 (H-1 of Ara) with δC 81.8 (C-3 of the aglycone), δH 6.32 (H-1 of Rha I) with δC 75.5 (C-2 of Ara), δH 5.35 (H-1 of Xyl ) with δC 82.8 (C-3 of Rha I), δH 6.23 (H-1 of Glc I) with δC 176.7 (C-28 of the aglycone), δH 4.97 (H-1 of Glc II) with δC 69.1 (C-6 of Glc I), and δH 5.85 (H-1 of Rha II) with δC 78.1 (C-4 of Glc II) (Figure S1 in Supplementary data). Thus, the structure of 2 was assigned as 3β-O-β-D-xylopyranosyl-(1→3)-α-L-rhamnopyranosyl-(1→2)-α-L-arabinopyranosyl gypsogenin 28-O-α-L-rhamnopyranosyl-(1→4)-β-D-glucopyranosyl-(1→6)-β-D-glucopyranosyl ester.

Saponin 3 was obtained as a white powder. HRESIMS of 3 showed a quasi-molecular ion at m/z 1081.8564 (calcd. for 1081.8559 [M + Na]+), establishing the molecular formula of C53H86O21. The 1D NMR data of 3 exhibited signals for six tertiary methyl groups at 0.77 (H3-24), 0.92 (H3-25), 1.03 (H3-27), 1.10 (H3-26), 1.24 (H3-23), and 1.70 (H3-30), an exomethylene group at δH 4.70 and 4.85 with two olefinic carbon signals at δC 110.1 and 150.8, and one carbonyl signal at δC 174.9, which were characteristic of the Δ20(29)-lupane-type aglycone. The full assignments of the aglycone NMR signals were derived from 2D NMR data (Table 1), suggesting that the aglycone of 3 was betulinic acid [23,24]. The sugar moieties of 3 were determined as L-arabinose, L-rhamnose, and D-glucose in a ratio of 1:1:2 by acid hydrolysis, followed by GC analysis. Meanwhile, the 1D NMR spectra of 3 exhibited four anomeric protons at δH 6.34 (d, J = 8.2 Hz), 5.84 (s), 4.92 (d, J = 7.8 Hz), and 4.76 (d, J = 7.0 Hz), and four anomeric carbons at δC 107.5, 105.2, 102.7, and 95.3. The sequence and binding sites of the sugar units to each other and to the aglycone were deduced from the HMBC and NOESY spectra (Figure S2 in Supplementary data). On the basis of these findings, the structure of 3 was thus elucidated as 3β-O-α-L-arabinopyranosyl betulinic acid 28-O-α-L-rhamnopyranosyl-(1→4)-β-D-glucopyranosyl-(1→6)-β-D-glucopyranosyl ester. The lupane-type saponin was reported from this genus for the first time.

Saponin 4 was obtained as a white amorphous powder. In the positive-ion mode HRESIMS, a pseudomolecular ion peak at m/z 1097.5515 [M + Na]+ (calcd. for C53H86O22Na+, 1097.5508) was observed, suggesting a molecular formula C53H86O22. Seven tertiary methyl groups at δH 0.87 (H3-25), 0.99 (H3-30), 1.08 (H3-26), 1.13 (H3-29), 1.15 (H3-24), 1.29 (H3-23), and 1.31 (H3-27), one olefinic proton at δH 5.43 (1H, br s) with two typical olefinic carbon signals (at δC 122.6 and 144.1), and one carbonyl signal at δC 176.5 were observed in the 1D NMR spectra of 4. This revealed 4 as an oleanane-type saponin. Due to the change of chemical shift of C-21 from δC 31.4 in oleanolic acid [25] to δC 73.2 (+41.8) and the other of carbons such as C-18 [δC 41.5 (−1.4)], C-19 [δC 41.3 (−5.0)], C-20 [δC 35.6 (+4.7)], C-22 [δC 39.5 (+6.3)], C-29 [δC 28.3 (−6.9)], and C-30 [δC 24.8 (+0.1)], C-21 must be an oxygen-bearing methylene carbon in the aglycone of 4, which was confirmed by the HMBC experiment (Figure S3 in Supplementary data). The NOESY correlations between H-21 (δH 3.66) and H3-30 (δH 0.99) indicated the α-orientation of 21-OH (Figure S3 in Supplementary data). The assignments of the NMR signals associated with the aglycone moiety were derived from 2D NMR spectra (Table 1). These data revealed that the aglycone of 4 was 21α-hydroxy-oleanolic acid, which was in a good agreement when comparing the literature data [26,27]. Further comparison of the 1D NMR data assignable to the sugar part between 4 and 3 led to the determination of the same monosaccharide units and glycosylation sequence observed for both at C-3 and C-28 (Table 2). The conclusion was confirmed by the HMBC and NOESY spectra data (Figure S3 in Supplementary data). Therefore, the structure of saponin 4 was elucidated as 3β-O-α-L-arabinopyranosyl 21α-hydroxy-oleanolic acid 28-O-α-L-rhamnopyranosyl-(1→4)-β-D-glucopyranosyl-(1→6)-β-D-glucopyranosyl ester.

Saponin 5 was obtained as a white amorphous powder. The molecular formula of 5 was established as C59H96O26 from the quasi-molecular ion at m/z 1243.6094 (calcd. for 1243.6088 [M + Na]+) in HRESIMS. The 1D NMR spectra data assignable to the aglycone moiety of 5 were identical to those of 4 (Table 1), suggesting the same 21α-hydroxy-oleanolic acid aglycone. The spectra data assignable to the sugar moieties of 5 were similar to those of 4, except for the presence of an additional α-L-rhamnopyranose moiety (Rha I). The downfield-shifted carbon signal of Ara C-2 (δC 75.5) in the 13C-NMR spectrum and the correlation between Rha I H-1 (δH 6.17) and Ara C-2 (δC 75.5) observed in the HMBC spectrum indicated that Rha I was attached to Ara C-2. The conclusion was supported by the NOESY spectrum (Figure S4 in Supplementary data). Thus, saponin 5 was elucidated as 3β-O-α-L-rhamnopyranosyl-(1→2)-α-L-arabinopyranosyl 21α-hydroxy-oleanolic acid 28-O-α-L-rhamnopyranosyl-(1→4)-β-D-glucopyranosyl-(1→6)-β-D-glucopyranosyl ester.

Additionally, the eight known saponins were identified as kalopanax saponin A (6) [28], pulsatilloside D (7) [29], 3β-O-{β-D-glucopyranosyl-(1→2)-α-L-arabinopyranosyl} oleanolic acid 28-O-β-D-glucopyranoside (8) [30], cauloside D (9) [31], cauloside F (10) [32], hederasaponin B (11) [33], 3β-O-{α-L-rhamnopyranosyl-(1→2)-[β-D-glucopyranosyl-(1→4)]-α-L-arabinopyranosyl} betulinic acid 28-O-α-L-rhamnopyranosyl-(1→4)-β-D-glucopyranosyl-(1→6)-β-D-glucopyranosyl ester (12) [34], and sieboldianoside A (13) [35]. This was accomplished by comparing their physicochemical and spectroscopic data with reported data [28,29,30,31,32,33,34,35].

For a long time, A. rivularis var. flore-minore was used as a folk medicine in Shaanxi Province for the treatment of hepatitis [9]. Inhibition of hepatic stellate cell (HSC) proliferation plays a key role in the pathogenesis of liver fibrosis caused by chronic hepatocellular damage [36]. HSC-T6, an immortalized rat hepatic stellate cell line, has generally been applied as a screening tool to evaluate the potential antifibrotic activity [37].

In this study, the anti-proliferative activity of isolated saponins on HSC-T6 cells was evaluated by 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide MTT colorimetric assay. Colchicine was used as a positive control. As shown in Table 3, saponins 12 and 13 displayed potent anti-proliferative activity with IC50 values of 18.21 and 15.56 μM, respectively. Saponins 3–5 and 8–11 showed moderate antiproliferative activity with IC50 values ranging from 22.85 to 52.65 μM. These results revealed that the number of monosaccharides in sugar chains (both at C-3 and C-28) increased the anti-proliferative activity (Figure 3). The gypsogenin aglycone saponins (1 and 2) and monodesmosidic ones (6 and 7) were inactive, which suggested that the aldehyde functional group at C-23 and the free carboxyl functional group at C-28 had negative effects on anti-proliferative activity (Figure 3). It is worth mentioning that the monodesmosidic saponins (the sugar chain attached at C-3 and a free carboxylic acid at C-28) were cytotoxic against tumor cells in previous studies [10,14,15,17]. These opposing effects may be due to their different mechanisms against different types of cells. Nevertheless, the anti-proliferative activity of these saponins was very sensitive to their precise functionalization, especially for the sugar moieties. Further research is needed to approach a significative structure–activity relationship.

Table 3

Anti-proliferation activity of saponins 1–13 on HSC-T6 cells (mean ± SD, n = 3).

Saponins a	IC50 (μM)	Saponins a	IC50 (μM)
3	28.62 ± 0.76	10	38.62 ± 1.58
4	22.85 ± 2.21	11	25.43 ± 2.86
5	25.74 ± 1.34	12	18.21 ± 0.92
8	52.65 ± 3.19	13	15.56 ± 1.58
9	43.65 ± 2.85	Colchicine b	9.35 ± 0.25

a Compounds 1, 2, 6, and 7 were inactive (IC50 >80 μM); b Colchicine was used as a positive control.

Figure 3

Brief structure–activity relationship analysis of the isolated saponins.

3. Experimental Section

3.1. General

Optical rotations were performed on a Perkin-Elmer 343 polarimeter (Perkin-Elmer Inc., Bridgeport, CT, USA). The ESIMS and HRESIMS were carried out on a Micromass Quattro mass spectrometer (Micromass Inc., Manchester, UK). NMR data were recorded on a Bruker AVANCE-500 spectrometer (Bruker Biospin AG, Fallanden, Switzerland). GC was tested on a Finnigan Voyager apparatus with an L-Chirasil-Val column (0.32 mm × 25 m; injector temperature: 230 °C; column temperature: 100–180 °C, rate 5 °C/min; column head pressure: 12 Pa; carrier gas: He, 2 mL/min) (Thermo Finnigan Inc, San Jose, CA, USA). Semi-preparative HPLC was performed on a Dionex P680 liquid chromatograph (Dionex Inc, Sunnyvale, CA, USA) equipped using a UV 170 UV/Vis detector at 206 nm. A YMC-Pack R&D ODS-A column (20 × 250 mm i.d., 5 μm, YMC Co., Ltd., Kyoto, Japan) was used. Materials for column chromatography (CC) were silica gel (10–40 μm, Qingdao Marine Chemical Inc., Qingdao, China), reversed phase silica gel ODS-A (50 μm, YMC Co., Ltd., Kyoto, Japan), and Sephadex LH-20 (40–70 μm, GE-Healthcare, Uppsala, Sweden). The Liebermann–Burchard reagent was prepared with acetic anhydride and sulfuric acid (Tianjin Fuyu Fine Chemical Co., Ltd., Tianjin, China), and the Molisch reagent was prepared with α-naphthol and sulfuric acid (Tianjin Fuyu Fine Chemical Co., Ltd., Tianjin, China).

3.2. Plant Material

The plant material was collected on Tsinling Mountains, Shaanxi Province, China, in October 2016. The plant was identified by Prof. Ji-Tao Wang at the Department of Pharmacognosy, School of Pharmacy, Shaanxi University of Chinese Medicine. A voucher specimen (No. 161018) was deposited in the Herbarium of Shaanxi University of Chinese Medicine.

3.3. Extraction and Isolation

The air-dried whole plants of A. rivularis var. flore-minore (5 kg) were powdered and extracted with 70% EtOH (3 × 8 L × 2 h) under reflux to give a crude extract (800 g), which was further suspended in water (8 L) and partitioned successively with petroleum ether (8 L × 2) and n-BuOH (8 L × 2). The n-BuOH extract (140 g) was divided into seven fractions (Fr. 1–Fr. 7) by using silica gel CC with a stepwise gradient of CHCl3–MeOH–H2O (10:1:0.04–6:4:0.7). Fr. 4 (16.5 g) was separated by silica gel CC with a CHCl3–MeOH–H2O gradient (10:1:0.1–7:3:0.4) to give six sub-fractions (Fr. 4.1–Fr. 4.6) and further purified by on a Sephadex LH-20 column in MeOH. Saponins 6 (37 mg, tR 17.4 min) and 7 (26 mg, tR 23.5 min) were obtained from Fr. 4.3 (2.2 g) by semi-preparative HPLC (MeOH–H2O (82:18), 7.2 mL/min). Fr. 4.4 (3.2 g) and Fr. 4.5 (2.5 g) were subjected to semi-preparative HPLC to give saponin 8 (18 mg, MeOH–H2O (61:39), 8 mL/min, tR 19.2 min from Fr. 4.4), saponin 1 (22 mg, MeOH–H2O (60:40), 8.0 mL/min, tR 20.5 min from Fr. 4.5) and saponin 9 (20 mg, MeOH–H2O (60:40), 8.0 mL/min, tR 24.5 min from Fr. 4.5). Fr. 5 (23 g) was separated by silica gel CC with a stepwise gradient of CHCl3–MeOH–H2O gradient (10:1:0.1–7:3:0.4) to yield eight sub-fractions (Fr. 5.1–Fr. 5.8). Fr. 5.2 (1.8 g) and Fr. 5.3 (2.4 g) were purified by gel CC over Sephadex LH-20 (MeOH), and further submitted to semi-preparative HPLC to give saponin 2 (24 mg, MeOH–H2O (72:28), 8 mL/min, tR 19.0 min) and 3 (18 mg, MeOH–H2O (76:24), 8 mL/min, tR 17.5 min), respectively. Saponins 10 (25 mg, tR 18.6 min) and 4 (16 mg, tR 26.9 min) were obtained from Fr. 5.4 by semi-preparative HPLC (MeOH–H2O (58:42), 7.5 mL/min). Fr. 5.5 (4.3 g) was subjected to ODS CC with a MeOH–H2O (1:10–3:1) gradient to afford Fr. 5.5.1–Fr. 5.5.4. Saponins 11 (35 mg, tR 23.5 min) and 5 (20 mg, tR 27.3 min) were obtained from Fr. 5.5.3 by semi-preparative HPLC (MeOH–H2O (58:42), 8 mL/min). Fr. 6 (16 g) was separated by silica gel CC with a stepwise gradient of CHCl3–MeOH–H2O (8:2:0.2–6:4:0.5) to yield Fr. 6.1–Fr. 6.5. Fr. 6.2 (4.5 g) was subjected to ODS CC with a stepwise MeOH–H2O (1:4–4:1) gradient to afford four Fr. 6.2.1–Fr. 6.2.4. Saponins 12 (18 mg, MeOH–H2O (70:30), 8 mL/min, tR 15.2 min) and 13 (26 mg, MeOH–H2O (68:32), 8 mL/min, tR 18.5 min) were obtained by semi-preparative HPLC from Fr. 6.2.2 and Fr. 6.2.3, respectively. The purity of all compounds was assessed by HPLC as more than 95%.

3.4. Compound Characterization Data

Compound 1: White amorphous powder; [α +21.5 (c 0.18, MeOH); for 1H- and 13C-NMR spectroscopic data, see Table 1 and Table 2; key HMBC and NOESY correlations, see Figure 2; HRESIMS (pos. ion mode) m/z 933.4829 [M + Na]+ (calcd. for C47H74NaO17, 933.4824); ESIMS (pos. ion mode) m/z 933 [M + Na]+.

Compound 2: White amorphous powder; [α −11.6 (c 0.15, MeOH); for 1H- and 13C-NMR spectroscopic data, see Table 1 and Table 2; key HMBC and NOESY correlations, see Figure S1 in Supplementary data; HRESIMS (pos. ion mode) m/z 1065.5252 [M + Na]+ (calcd. for C52H82NaO21, 1065.5246); ESIMS (pos. ion mode) m/z1065 [M + Na]+.

Compound 3: White amorphous powder; [α +17.2 (c 0.20, MeOH); for 1H- and 13C-NMR spectroscopic data, see Table 1 and Table 2; key HMBC and NOESY correlations, see Figure S2 in Supplementary data; HRESIMS (pos. ion mode) m/z 1081.8564 [M + Na]+ (calcd. for C53H86NaO21, 1081.8559); ESIMS (pos. ion mode) m/z1081 [M + Na]+.

Compound 4: White amorphous powder; [α +12.3 (c 0.14, MeOH); for 1H- and 13C-NMR spectroscopic data, see Table 1 and Table 2; key HMBC and NOESY correlations, see Figure S3 in Supplementary data; HRESIMS (pos. ion mode) m/z 1097.5515 [M + Na]+ (calcd. for C53H86NaO22, 1097.5508); ESIMS (pos. ion mode) m/z 1097 [M + Na]+.

Compound 5: White amorphous powder; [α −11.4 (c 0.15, MeOH); for 1H- and 13C-NMR spectroscopic data, see Table 1 and Table 2; key HMBC and NOESY correlations, see Figure S4 in Supplementary data; HRESIMS (pos. ion mode) m/z 1243.6094 [M + Na]+ (calcd. for C59H96NaO26, 1243.6088); ESIMS (pos. ion mode) m/z 1243 [M + Na]+.

3.5. Acid Hydrolysis and GC Analysis of the Sugar Moieties in

Saponins 1–5 (each 4 mg) were hydrolyzed with 2 mol/L CF3COOH (5 mL) at 100 °C for 3 h, respectively. The mixture of reactants was evaporated in vacuo, and the residue was partitioned between H2O and CHCl3 three times. The residue was dissolved in pyridine (4 mL) and 1-(trimethylsilyl)-imidazole (0.5 mL). The reaction mixture was stirred at 60 °C for 5 min and dried with a stream of N2. Then, the residue was partitioned between H2O and hexane, and the latter layer was subjected to GC analysis with an l-Chirasil-Val column. The configurations of the monosaccharide units were established by comparing retention times with those of the trimethylsilylated derivatives prepared in the same manner from the authentic standard monosaccharides [38]. Retention times for authentic samples were detected at 8.92 and 9.95 min (d-arabinose), 9.60 and 10.38 min (l-rhamnose), 10.91 and 12.15 min (d-xylose), and 14.82 min (d-glucose), respectively. l-arabinose, l-rhamnose, and d-glucose were measured in a ratio of 1:1:1 for 1, 1:1:2 for 3 and 4, and 1:2:2 for 5, while the sugar moieties of 2 were identified as l-arabinose, l-rhamnose d-xylose and d-glucose in the ratio of 1:1:1:1.

3.6. HSC-T6 Cell Culture and Cell Viability Assay

The anti-proliferative activity of saponins 1–13 was evaluated on hepatic stellate cell (HSC)-T6 cells (Chinese Academy of Science Committee Type Culture Collection Cell Bank, Shanghai, China). The HSC-T6 cells were found to be mycoplasma free by PCR. HSC-T6 cells were maintained in dulbecco’s modified Eagle’s medium (DMEM) (Sigma-Aldrich, St. Louis, MO, USA), which was supplemented with 10% heat-inactivated fetal bovine serum, 100 IU/mL penicillin (Sigma-Aldrich), and 100 μg/mL streptomycin (Sigma-Aldrich) at 37 °C in a humidified atmosphere of 95% air–5% CO2. Cell viability was evaluated by MTT colorimetric assay, with colchicine (Sigma-Aldrich) used as a positive control. The cells were seeded in 96-well plates at a density of 5 × 104 cells/mL and incubated for 24 h. Each saponin was dissolved in DMSO and diluted with distilled water to reach the desired concentrations. The cells were treated with these drugs (0.5, 1, 5, 10, 20, 40, and 80 μM) in triplex wells for 48 h at 37 °C in a humidified 5% CO2 atmosphere. An amount of 20 μL MTT (Sigma-Aldrich) reagent solved in PBS was added to each well (final concentration = 5 mg/mL), and further incubated for 4 h. After removing the supernatant, DMSO was added to solubilize the formazan crystals. The optical density of each well was measured with a Bio-Rad 680 microplate reader at 560 nm. Anti-proliferative activity was expressed as the concentration of compound producing 50% of cell inhibitory rate (IC50).

4. Conclusions

In this study, thirteen triterpenoid saponins, including five new ones, were isolated from A. rivularis var. flore-minore. All the structures were established on the basis of extensive spectroscopic studies along with MS analyses and acid hydrolysis. Five kinds of aglycones were identified, i.e., gypsogenin, betulinic acid, 21-hydroxy-oleanolic acid, hederagenin, and oleanolic acid. The lupane-type saponins (3 and 12) were reported from the Anemone genus for the first time. The anti-proliferative activity of all isolated saponins was evaluated on hepatic stellate cells (HSC-T6). The preliminary structure–activity relationship analyses revealed that the more monosaccharides the saponins possessed, the stronger the anti-proliferative activity exhibited. This work will not only enrich the diversity of triterpenoid saponins of this genus, but will also provide a reference for the discovery of potential lead compounds for liver disease drug development.