Steroidal and Phenolic Glycosides from the Bulbs of Lilium pumilum DC and Their Potential Na⁺/K⁺ ATPase Inhibitory Activity

Abstract

A new steroidal saponin, named pumilum A (1), and a new phenolic glycoside, threo-1-(4′-hydroxy-2′-methoxyphenyl)-2-(2′′,4′′-dihydroxyphenyl)-1,3-propanediol-4′-O-β-D-glucopyranoside (7) were isolated from the methanolic extract of the bulbs of Lilium pumilum DC, along with five known steroidal saponins. Their chemical structures were elucidated on the basis of detailed spectroscopic analysis, including 1D and 2D NMR techniques and chemical methods. In addition, the inhibitory activity of all the isolates on Na⁺/K⁺ ATPase was evaluated.

1. Introduction

“Bǎi-hé”, a Chinese crude drug, is prepared from the bulbs of the Lilium species and is regularly used nowadays in China as a sedative, antitussive and anti-inflammatory agent [1,2,3,4]. Previously, phenolic glycosides, steroidal saponins and steroidal alkaloids have been isolated from the bulbs of the Lilium species [5,6,7,8,9,10,11,12]. However, to date, a survey of the literature showed that no chemical work has been done on Lilium pumilum DC.

Our studies indicated that the methanolic extract of the bulbs of Lilium pumilum DC showed significant Na⁺/K⁺ ATPase inhibition activity (IC₅₀ value: 0.5 × 10^{−5 M}). To further investigate the constituents and screen the bioactive constituents from its bulbs, a phytochemical study was performed that resulted in the isolation of new compounds 1 and 7, along with five known steroidal saponins. In the present article, we describe the structural elucidation of new compounds 1 and 7, together with the Na⁺/K⁺ ATPase inhibitory activity of all these compounds 1–7 (Figure 1).

Figure 1. Structures of compounds 1–7 isolated from the bulbs of Lilium pumilum DC.

Figure 1. Structures of compounds 1–7 isolated from the bulbs of Lilium pumilum DC.

2. Results and Discussion

The methanolic extract from the bulbs of Lilium pumilum DC was successively subjected to column chromatography over silica gel, ODS, Diaion HP-20 and semipreparative HPLC to afford six steroidal saponins and a new phenolic glycoside. All compounds were obtained from this plant for the first time.

Compound 1 had the molecular formula C₃₉H₆₂O₁₅, as deduced from the positive-ion HR-ESI-MS (m/z 793.6704 [M+Na]⁺) and ¹³C-NMR spectrum. The glycosidic nature of 1 was indicated by the strong absorption bands at 3435 cm⁻¹ and 1045 cm^{−1 in} the IR spectrum. The typical absorptions at 975, 915, 895, and 860 cm⁻¹ in the IR spectrum suggested that 1 was a spirostanol saponin [13,14]. The intensity of the absorptions (895 > 915) indicated that the absolute configuration of C-25 was R. The ¹H-NMR spectrum contained signals for two oxygenated methylene proton signals at δ 4.58 (2H, d, J = 7.8 Hz, H-26), 3.74 (1H, dd, J = 10.6, 5.5 Hz, H-27a) and 3.67 (1H, dd, J = 10.7, 7.2 Hz, H-27b), two anomeric proton signals at δ 6.13 (1H, br s, H-1″) and 5.11 (1H, d, J = 7.2 Hz, H-1′), as well as four methyl proton signals at δ 0.82 (3H, s), 0.91 (3H, s), 1.21 (3H, d, J = 7.0 Hz), and 1.81 (3H, d, J = 6.8 Hz). The signal at δ 1.81 was due to the methyl group of rhamnose (Table 1). The ¹³C-NMR and DEPT spectrum showed a quaternary carbon signal at δ 109.7, which is the characteristic C-22 of a spirostanol skeleton [15,16]. The presence of a carbonyl group in 1 was established from the IR (1707 cm⁻¹) and ¹³C-NMR spectra (δ 209.4). The existence of D-glucose and L-rhamnose were determined by hydrolysis of 1 with 1 M HCl and GC analysis. The J values of the anomeric proton signals indicated the β- and α-configuration at the anomeric centers of D-glucose and L-rhamnose, respectively. These findings showed that 1 was a (25R)-spirostanol diglycoside.

Table 1. ¹³C and ¹H-NMR data of 1 in pyridine-d₅ (400 MHz for H, 100 MHz for C).

NO.	C	H	NO.	C	H
1	36.8	1.56 (1H, m)	20	44.7	2.21 (1H, q, J = 7.2 Hz)
		1.08 (1H, m)	21	9.7	1.21 (3H, d, J = 6.8 Hz)
2	29.3	1.84 (1H, m)	22	109.7
		1.37 (1H, m)	23	31.5	1.92 (1H, m)
3	76.0	3.99 (1H, m)			1.45 (1H, m)
4	26.4	2.21 (1H, m)	24	24.1	2.17 (1H, m)
		1.75 (1H, m)			1.38 (1H, m)
5	56.4	2.26 (1H, m)	25	39.2	2.03 (1H, m)
6	209.4		26	64.0	4.58 (2H, d, J = 7.8 Hz)
7	46.9	2.54 (1H, m)	27	64.5	3.74 (1H, dd, J = 11, 5.5 Hz)
		2.42 (1H, m)			3.67 (1H, dd, J = 11, 7.2 Hz)
8	38.1	1.83 (1H, m)	Glc
9	53.7	1.37 (1H, m)	1′	99.2	5.11 (1H, d, J = 7.2 Hz)
10	40.8		2′	79.5	4.22 (1H, m)
11	21.2	1.34 (1H, m)	3′	78.4	4.30 (1H, m)
		1.57 (1H, m)	4′	72.1	4.15 (1H, m)
12	32.0	2.13 (1H, m)	5′	78.2	3.86 (1H, m)
		1.49 (1H, m)	6′	62.8	4.33 (1H, m)
13	45.8				4.49 (1H, m)
14	53.2	2.17 (1H, m)	Rha
15	32.0	2.17 (1H, m)	1″	102.4	6.13 (1H, br s)
		1.46 (1H, m)	2″	72.6	4.68 (1H, m)
16	89.8	4.42 (1H, m)	3″	72.9	4.37 (1H, m)
17	89.9		4″	74.2	4.39 (1H, m)
18	17.3	0.82 (3H, s)	5″	69.5	4.81 (1H, m)
19	13.2	0.91 (3H, s)	6″	18.7	1.81 (3H, d, J = 6.8 Hz)

Table 1. ¹³C and ¹H-NMR data of 1 in pyridine-d₅ (400 MHz for H, 100 MHz for C).

NO.	C	H	NO.	C	H
1	36.8	1.56 (1H, m)	20	44.7	2.21 (1H, q, J = 7.2 Hz)
		1.08 (1H, m)	21	9.7	1.21 (3H, d, J = 6.8 Hz)
2	29.3	1.84 (1H, m)	22	109.7
		1.37 (1H, m)	23	31.5	1.92 (1H, m)
3	76.0	3.99 (1H, m)			1.45 (1H, m)
4	26.4	2.21 (1H, m)	24	24.1	2.17 (1H, m)
		1.75 (1H, m)			1.38 (1H, m)
5	56.4	2.26 (1H, m)	25	39.2	2.03 (1H, m)
6	209.4		26	64.0	4.58 (2H, d, J = 7.8 Hz)
7	46.9	2.54 (1H, m)	27	64.5	3.74 (1H, dd, J = 11, 5.5 Hz)
		2.42 (1H, m)			3.67 (1H, dd, J = 11, 7.2 Hz)
8	38.1	1.83 (1H, m)	Glc
9	53.7	1.37 (1H, m)	1′	99.2	5.11 (1H, d, J = 7.2 Hz)
10	40.8		2′	79.5	4.22 (1H, m)
11	21.2	1.34 (1H, m)	3′	78.4	4.30 (1H, m)
		1.57 (1H, m)	4′	72.1	4.15 (1H, m)
12	32.0	2.13 (1H, m)	5′	78.2	3.86 (1H, m)
		1.49 (1H, m)	6′	62.8	4.33 (1H, m)
13	45.8				4.49 (1H, m)
14	53.2	2.17 (1H, m)	Rha
15	32.0	2.17 (1H, m)	1″	102.4	6.13 (1H, br s)
		1.46 (1H, m)	2″	72.6	4.68 (1H, m)
16	89.8	4.42 (1H, m)	3″	72.9	4.37 (1H, m)
17	89.9		4″	74.2	4.39 (1H, m)
18	17.3	0.82 (3H, s)	5″	69.5	4.81 (1H, m)
19	13.2	0.91 (3H, s)	6″	18.7	1.81 (3H, d, J = 6.8 Hz)

Comparison of the ¹H and ¹³C-NMR spectra of 1 with those of 2 indicated that 1 contained a same sugar chain as 2, the difference between these two saponins only appearing in the F-ring of their aglycons. The ¹H and ¹³C-NMR spectra of 1 clearly displayed that C-27, which was presented as a methyl in 2 [¹H-NMR: δ 0.71 (3H, d, J = 5.4 Hz); ¹³C-NMR: δ 17.3 (Me)], was modified to a hydroxymethyl in 1 [¹H-NMR: δ 3.74 (1H, dd, J = 11, 5.5 Hz) and 3.67 (1H, dd, J = 11, 7.2 Hz); ¹³C-NMR: δ 64.5 (-CH₂OH)]. The chemical shift values of C/H-27 and detailed 2D-NMR analysis of COSY, ROESY and HMBC correlations also implied that the aglycone moiety of 1 had one more hydroxyl group attached at C-27 (Figure 2 and Figure 3). On the basis of the above evidence, the structure of 1 was formulated as (25R)-3β,17α,27-triol-spirostan-6-one 3-O-α-L-rhamnopyranosyl-(1→2)-β-D-gluco- pyranoside, and it was named pumilum A.

Figure 2. Key HMBC and ¹H-¹H COSY correlations of 1 and 7.

Figure 2. Key HMBC and ¹H-¹H COSY correlations of 1 and 7.

Figure 3. Selected ROESY correlations of 1.

Figure 3. Selected ROESY correlations of 1.

Compound 7 had the molecular formula C₂₂H₂₈O₁₁, deduced from the negative-ion HR-ESI-MS (m/z 467.1936 [M−H]⁻) and ¹³C-NMR spectrum, which exhibited 16 carbon signals due to the aglycone, in addition to six carbon signals of a β-D-glucopyranosyl group. The ¹H and ¹³C-NMR spectra of 7 showed the presence of two aromatic ABX systems [δ (H) 7.55 (1H, d, J = 8.4 Hz, H-6′), 7.16 (1H, d, J = 8.0 Hz, H-6′′), 7.04 (1H, dd, J = 2.0, 8.4 Hz, H-5′), 7.08 (1H, d, J = 2.0 Hz, H-3′ ), 6.69 (1H, d, J = 2.0 Hz, H-3′′), and 6.51 (1H, dd, J = 2.0, 8.0 Hz, H-5′′); δ (C) 161.8 (C-4′′), 161.5 (C-2′′), 159.9 (C-4′), 157.3 (C-2′), 132.8 (C-6′), 125.6 (C-6′′), 119.9 (C-1′′), 114.8 (C-1′), 111.2 (C-5′), 106.7 (C-5′′), 105.8 (C-3′), and 97.4 (C-3′′)] (Table 2), suggesting the presence of two 1, 2, 4-trisubstituted phenyls in 7. The detailed 2D-NMR analysis of ¹H-¹H COSY, HMQC, and HMBC correlations also suggested that the aglycone moiety of 7 had two 1, 2, 4-trisubstituted phenyls (Figure 2). In the aliphatic region, the ¹H-NMR spectra of 7 were completely identical to those of 1, 2-bis(4-hydroxy-3-methoxyphenyl)-1,3-propandiol 4′-O-β-D-glucopyranoside [17], ABMX-type signals were clearly observed [including an oxygen-bearing methylene at δ 4.27 (2H, dd, J = 9.8, 5.0 Hz, H-3), an oxygen-bearing methine at δ 5.56 (1H, d, J = 7.4 Hz, H-1), and a methine at δ 3.50 (1H, td, J = 7.4, 5.0 Hz, H-2)]. In combination with the presence of three aliphatic carbon signals [δ 66.8 (C-3), 78.9 (C-1), and 44.9 (C-2)] in the ¹³C-NMR spectrum of 7 supported the presence of the aliphatic 1,3-propanediol chain. Additionally, the ¹H and ¹³C-NMR spectra of 7 displayed the presence of one glucopyranosyl unit [δ (H) 5.71 (1H, d, J = 7.6 Hz, H-1′′′), δ (C) 102.4 (C-1′′′)], as well as a methoxyl group [δ (H) 3.66 (3H, s), δ (C) 55.6]. The HMBC spectrum of 7 exhibited long-range correlations from H-1 (δ 5.56) to C-2 (δ 44.9), C-3 (δ 66.8), C-1′ (δ 114.8), C-2′ (δ 157.3), C-6′ (δ 132.8) and C-1′′ (δ 119.9); and from H-2 (δ 3.50) to C-1 (δ 78.9), C-3 (δ 66.8), C-1′ (δ 114.8), C-1′′ (δ 119.9), C-2′′ (δ 161.5), and C-6′′ (δ 125.6), respectively, indicated the locations of the two phenyls linked to the aliphatic chain, 1,3-propanediol. In addition, the HMBC spectra of 7 revealed the methoxyl group (δ 3.67) was coupled to aromatic carbon C-4′′ (δ 161.8), suggesting that the methoxyl groups was linked to C-4′′ in 7 (Figure 2). Thus, the aglycone of 7 was believed to be 1-(4′-hydroxy-2′-methoxyphenyl)-2-(2′′,4′′-dihydroxyphenyl)-1, 3-propanediol.

Table 2. ¹³C and ¹H-NMR data of 7 in pyridine-d₅ (500 MHz for H, 125 MHz for C).

NO.	C	H	NO.	C	H
1	78.9	5.56 (1H, d, J = 7.4 Hz)	3′′	97.4	6.69 (1H, d, J = 2.0 Hz)
2	44.9	3.50 (1H, td, J = 7.4, 5.0 Hz)	4′′	161.8
3	66.8	4.27 (2H, dd, J = 9.8, 5.0 Hz)	5′′	106.7	6.51 (1H, dd, J = 2.0, 8.0 Hz)
1′	114.8		6′′	125.6	7.16 (1H, d, J = 8.0 Hz)
2′	157.3		1′′′	102.4	5.71 (1H, d, J = 7.6 Hz)
3′	105.3	7.08 (1H, d, J = 2.0 Hz)	2′′′	74.9	4.27 a
4′	159.9		3′′′	79.0	4.11 (1H, m)
5′	111.2	7.04 (1H, dd, J = 2.0, 8.4 Hz)	4′′′	71.2	4.26 a
6′	132.8	7.55 (1H, d, J = 8.4 Hz)	5′′′	78.4	4.43 (1H, m)
1′′	119.9		6′′′	62.5	4.31 (1H, m)
2′′	161.5		2′-CH3O	55.6	3.67 (3H, s)

^a Overlapped signals.

Table 2. ¹³C and ¹H-NMR data of 7 in pyridine-d₅ (500 MHz for H, 125 MHz for C).

NO.	C	H	NO.	C	H
1	78.9	5.56 (1H, d, J = 7.4 Hz)	3′′	97.4	6.69 (1H, d, J = 2.0 Hz)
2	44.9	3.50 (1H, td, J = 7.4, 5.0 Hz)	4′′	161.8
3	66.8	4.27 (2H, dd, J = 9.8, 5.0 Hz)	5′′	106.7	6.51 (1H, dd, J = 2.0, 8.0 Hz)
1′	114.8		6′′	125.6	7.16 (1H, d, J = 8.0 Hz)
2′	157.3		1′′′	102.4	5.71 (1H, d, J = 7.6 Hz)
3′	105.3	7.08 (1H, d, J = 2.0 Hz)	2′′′	74.9	4.27 a
4′	159.9		3′′′	79.0	4.11 (1H, m)
5′	111.2	7.04 (1H, dd, J = 2.0, 8.4 Hz)	4′′′	71.2	4.26 a
6′	132.8	7.55 (1H, d, J = 8.4 Hz)	5′′′	78.4	4.43 (1H, m)
1′′	119.9		6′′′	62.5	4.31 (1H, m)
2′′	161.5		2′-CH3O	55.6	3.67 (3H, s)

^a Overlapped signals.

The J value (7.6 Hz) of the anomeric proton implied the β-configuration of the glucose moiety. The β-D-glucopyranosyl group was attached to the C-4′ position of the aglycone, which was supported by a long-range correlation between the anomeric proton signal (δ 5.71) of the β-D-glucopyranosyl group and the C-4′ signal (δ 159.9) in the HMBC spectrum of 7. The relative stereochemistry of C-1 and C-2 of 7 was determined to be threo by comparing the coupling constant H-1 and H-2 (J = 7.4 Hz) with those of the erythro and threo isomers [18,19]. Therefore, 7 was assigned as threo-1-(4′-hydroxy-2′-methoxyphenyl)-2-(2′′, 4′′-dihydroxyphenyl)-1, 3-propanediol-4′-O-β-D-glucopyranoside.

The structures of the other isolated components, namely (25R)-3β,17α-diol-5α-spirostan-6-one 3-O-α-L-rhamnopyranosyl-(1→2)-β-D-glucopyranoside (2), (25R)-3β-hydroxyl-5α-spirostan-6-one 3-O-α-L-rhamnopyranosyl-(1→2)-β-D-glucopyranoside (3), (25R)-3β-hydroxy-5α-spirostan-6-one 3-O-α-L arabinopyranosyl-(1→6)-β-D-glucopyranoside (4), dioscin (5), and (25R)-5α-spirostan-3β,17α-diol 3-O-β-D-xylopyranosyl-(1→4)-[α-L-arabinopyranosyl-(1→6)]-β-D-glucopyranoside (6) were determined by comparison to the ¹H and ¹³C-NMR spectral data in the literature [2,20,21,22,23].

The inhibitory activity of 1–7 on Na⁺/K⁺ ATPase was assayed. Ouabain was used as a positive control (IC₅₀ value: 0.1 × 10^{−5 M}). Saponins 3 and 4 were found to inhibit sensitive Na⁺/K⁺ ATPase with the IC₅₀ values of 7.3 × 10⁻⁵ and 9.1 × 10⁻⁶ M, respectively, while the others were inactive [IC₅₀ > 1.0 × 10⁻⁴ M]. Thus, this research suggested that the saponins from the methanolic extract may be primary Na⁺/K⁺ ATPase inhibitors. The weak Na⁺/K⁺ ATPase inhibitory activity of the initial extract (compounds 1–7) is thus presumably due to other as yet unidentified compounds. One possible reason for this is that compounds with highly Na⁺/K⁺ ATPase inhibitory activity are low in the BuOH-soluble fraction of the methanolic extract from the bulbs of Lilium pumilum DC. Another possible reason is compounds with increased activity may be found in other extraction fractions (ethyl acetate extract, chloroform extract and petroleum ether extract) of the methanolic extract from the bulbs of this medicine plant. Therefore, more chemical work needs to be done in the future.

3. Experimental

3.1. General

Specific rotation measurements were recorded on a Perkin-Elmer 242 MC polarimeter. UV spectra were recorded on a Hewlett-Packard HP-845 UV-VIS spectrophotometer. IR spectra were recorded on a Nicolet 470 spectrometer and MS on a Varian MAT-212 mass spectrometer and a Shimadzu GC-MS model QP2010 Plus spectrophotometer, respectively. NMR spectra were recorded on a Bruker AM-400 spectrameter (400 MHz for ¹H-NMR) or a Bruker DRX-500 (500 MHz for ¹H-NMR) spectrameter using standard Bruker pulse programs. Chemical shifts are given as δ values with reference to tetramethylsilane (TMS) as internal standard. Column chromatography separations were carried out on silica gel (200–300 mesh, Qingdao Haiyang Chemical Co. Ltd, Qingdao, China), ODS (50 mesh, AA12S50, YMC), Diaion HP-20 (Pharmacia, Peapack, NJ, USA) and Sephadex LH-20 (Pharmacia, Peapack, NJ, USA). Ouabain sensitive dog kidney Na⁺/K⁺ ATPase was obtained from Sigma (Shanghai, China). All other chemicals used were of biochemical reagent grade.

3.2. Plant Material

The bulbs of Lilium pumilum DC were collected in Lanzhou, Gansu Province of China in September 2010, and were identified by one of the authors (Chun-Yan Fu of Department of Pharmacy, Shaoyang Medical College Level Speciaity School, Shaoyang). A voucher specimen (NO. 20100908) has been deposited in the authors’ laboratory.

3.3. Extraction and Isolation

Fresh bulbs of Lilium pumilum DC (5 kg) were cut into pieces and extracted with methanol (3 × 8 L, 3h each) under reflux. The solvent was removed at reduced pressure to give a viscous residue (328 g). The entire crude extract was suspended in H₂O (3 L), and extracted with n-BuOH five times (3 L each) to give an n-BuOH extract (206 g). This extract was then fractionated by silica gel column chromatography (column: 90 cm × 9 cm) using a mobile phase composed of CHCl₃-MeOH (9:1–6:1–4:1–2:1–1:1, v/v), and finally with MeOH alone to afford six fractions [Fr.1 (98 mg), Fr.2 (11.2 g), Fr.3 (37.8 g), Fr.4 (11.1 g), Fr.5 (14.3 g), and Fr.6 (51.6 g)]. Fr.2 (11.2 g) was chromatographed on silica gel (column: 70cm × 4 cm) eluting with CHCl₃-MeOH-H₂O (40:10:1) and ODS silica gel with MeOH-H₂O (4:1) and MeCN-H₂O (1:1) to furnish 3 (14.5 mg), 4 (16.8 mg), 5 (16.3 mg), and 6 (20.7 mg). Fr.1 (98 mg) was passed through a Diaion HP-20 column with a gradient mixture of MeOH-H₂O and the MeOH eluate fraction was subjected to silica gel column eluting with CHCl₃-MeOH-H₂O (40:10:1; 30:10:1) and ODS silica gel with CH₃CN-H₂O (1:1–5:7–1:2) to give 2 (15.6 mg) and 7 (17.2 mg) as the pure compounds, and 1 with a few impurities. Final purification of 1 (19.4 mg) was accomplished by semipreparative HPLC. The method was an isocratic gradient of 70% methanol in H₂O over 15 min, and then followed by 95% methanol for 5 min (flow rate: 3 mL/min).

3.4. Characterization of Pumilum A (1)

Obtained as a white amorphous powder, : −88.7° (c 0.048, MeOH); UV λ_max (MeOH): 279 nm; IR v_max (KBr): 3435, 2945, 2880, 1707, 1455, 1375, 1245, 1205, 1155, 1080, 1045, 985, 975, 915, 895, 860, 805, 710 cm⁻¹. HR-ESI-MS m/z 793.6907 (C₃₉H₆₂O₁₅Na [M+Na]⁺, Cal. 793.6904). ¹H-NMR and ¹³C-NMR (pyridine d₅) data see Table 1.

3.5. Characterization of Threo-1-(4′-hydroxy-2′-methoxyphenyl)-2-(2′′,4′′-dihydroxy-phenyl)-1,3-propanediol-4′-O-β-D-glucopyranoside (7)

Obtained as an amorphous powder. : −76.3° (c 0.5, MeOH). UV (MeOH) λ_max: 282 nm. IR v_max (KBr): 3433, 3391, 1630, 1601, 1495, 1470, 1441, 1386, 1345, 1253, 1202, 1172, 1143, 1041, 955, 860, 826 cm⁻¹. HR-ESI-MS m/z 467.1936 ([M−H]⁻, Calcd. for C₂₂H₂₇O₁₁, 467.1903). ¹H-NMR and ¹³C-NMR (pyridine d₅) data see Table 2.

3.6. Acid Hydrolysis of Compound 1

A solution (2.5 mg) of 1 in 1 M HCl (1 mL) was heated at 100 °C for 2 h under an N₂ atmosphere. After cooling, the solution was removed by blowing with N₂. The residue was dissolved in a solution of 1-(trimethylsilyl) imidazole (0.5 mg) in pyridine (1.0 mL), and stirred at 60 °C for 5 min. After removal of the solvent with a stream of N₂, the residue was partitioned between H₂O and CH₂Cl₂ (1:1 v/v). The CH₂Cl₂ fraction was analyzed by GC using a L-Chirasil-Val column (0.32 mm × 25 m). The temperature of the injector and detector were 200 °C. A temperature gradient system was used for the oven, starting at 100 °C for 1 min and increasing up to 180 °C at a rate of 5 °C/min. The peaks of the hydrolysates of 1 were confirmed by comparison of retention times of authentic samples D-glucose, L-rhamnose treated with 1-(trimethylsilyl) imidazole [24].

3.7. Assay of Na⁺/K⁺ ATPase Activity

The Na⁺/K⁺ ATPase activity was assayed according to the reported method with some modification [25]. The reaction mixture composed of 50 mM Tris-HCl (pH 7.3, 37 °C), 3 mM ATP, 4 mM Mg²⁺, 130 mM Na⁺, 20 mM K⁺, and 0.02 units of Na⁺/K⁺ ATPase, with or without test compound dissolved in dimethyl sulfoxide (DMSO), was incubated for 20 min at 37 °C. The concentration of DMSO in the reaction mixture was held at 5%. The reaction was terminated by addition of 50% CCl₃COOH. The released inorganic phosphate was determined by the following method. To the test solution was added 0.5% sodium dodecyl sulfate, 0.1% 2,4-diaminophenol 2 M HCl in 1% Na₂SO₃ and 1% ammonium heptamolybdate in 1 M H₂SO₄. After 25 min, the absorbance at 660 nm was recorded.

4. Conclusions

Two new compounds, pumilum A (1) and threo-1-(4′-hydroxy-2′-methoxyphenyl)-2-(2′′,4′′-dihydroxyphenyl)-1,3-propanediol-4′-O-β-D-glucopyranoside (7) were isolated from the the bulbs of Lilium pumilum DC, along with five known steroidal saponins. Compounds 3 and 4 exhibited weak inhibitory activity on Na⁺/K⁺ ATPase with the IC₅₀ values of 7.3 × 10⁻⁵ and 9.1 × 10^{−6 M}, respectively.