Platycoside O, a New Triterpenoid Saponin from the Roots of Platycodon grandiflorum

A new unusual minor triterpenoid saponin, platycoside O (1), was isolated from the 75% EtOH extract obtained from the roots of Platycodon grandiflorum, together with four known saponins: platycoside M-3 (2), platycoside J (3), platycoside F (4) and platycoside B (5). The structure of 1 was determined as 3-O-β-D-glucopyranosyl-(1→6)-β-D-glucopyranosyl-2β,3β,16α,23-tetrahydroxyolean-12-en-24-methoxyl, 24-oxo-28-oic acid 28-O-β-D-xylopyranosyl-(1→4)-α-L-rhamnopyranosyl-(1→2)-α-L-arabinopyranoside on the basis of spectral analysis and chemical evidence.


Introduction
Platycodon grandiflorum (Campanulaceae) is a species of perennial flowering plant of the family Campanulaceae and the only member of the genus Platycodon. In traditional Oriental medicine, its root (Radix Platycodi) has been extensively used since ancient times as a traditional drug to treat coughs, colds, upper respiratory tract infections, sore throats, tonsillitis, and chest congestion [1]. In the northeastern of China and Korea, the root is also a popular ingredient in salads and traditional cuisine. Chemical investigation of P. radix revealed that triterpenoid saponins were the main chemical components [1], which exhibit a variety of pharmacological activities, such as anti-inflammatory [2,3], protective effects on the hepatotoxicity induced by chemicals [4,5], anti-antioxidant [6], anti-cancer [7,8] and adjuvant against hepatitis B antigen [9,10]. Till date, more than 40 triterpenoid saponins have been isolated from the roots of the plant [1,[11][12][13][14][15][16][17][18][19][20][21].
In our previous papers, we reported the isolation and structural elucidation of eleven new triterpenoid saponins, including several unusual A-ring lactone triterpenoid saponins, from the roots of P. grandiflorum A. DC [13][14][15][16]. Further investigation on the polar fractions of P. grandiflorum led to the isolation from the EtOH extract obtained from the roots of a new unusual minor triterpenoid saponin based on the sapogenin platycogenic acid A, named platycoside O, together with four known compounds. To the best of our knowledge, the triterpenoid saponins based on the sapogenin platycogenic acid A had been isolated only in the plant and reported in a few publications [19,22].

Results and Discussion
The 75% EtOH extract from the roots of Platycodon grandiflorum were partitioned with aqueous EtOAc. The aqueous layer was separated by a macroreticular resin column to give the 60% EtOH eluates that upon drying afforded the total saponins. The total saponins were chromatographed on silica gel, a reverse-phase column, and finally on HPLC to afford the compound 1 and four known compounds ( Figure 1). Platycoside O (1) was a white amorphous powder, and its molecular formula was assigned to be C 53 H 84 O 25 based on the high-resolution (HR)-FAB-MS spectrum. The spectral features and physicochemical properties revealed 1 to be a triterpenoid saponin. The IR spectrum exhibited absorptions at 3,421 cm −1 (OH), 1,738 cm −1 (ester carbonyl), 1,633 cm −1 (trisubstituted double bond), and 1,384 cm −1 (gem-dimethyl). Five tertiary methyl groups (δ 0.99, 1.14 × 2, 1.33, 1.55, 1.76) and one olefinic proton (δ 5.63, br s) were observed in the 1 H-NMR spectrum. The 13 C-NMR spectrum showed five sp 3 (Table 1), two carbonyl carbons at δ 170.5, and 175.9. The information on the 1 H-NMR spectrum coupled with the 13 C-NMR spectrum indicated that 1 has an 2β,3β,16α,23-trihydroxyolean-12-en-24,28-dioic acid skeleton [22]. The HMBC spectrum showed that correlation between H (δ H 3.69) of a methoxy group (δ H 3.69, δ C 52.1) and the carbon (δ C 170.5) at the C-24 carboxy group. A 2D NMR experiments such as COSY, DEPT, HMQC and HMBC and by the comparison with the data in the literature revealed that the aglycon was 2β,3β,16α,23-trihydroxyolean-12-en-24-methoxyl, 24-oxo-28-oic acid (24-methyl platycogenic acid A).

General
FAB-MS and HR-FAB-MS spectral were recorded on a JEOL JMS-SX 102A mass spectrometer. IR spectra were measured with a Bruker IFS-55 infrared spectrometer. 1 H-and 13 C-NMR spectra were recorded with a JEOL α 500/600 FT NMR spectrometer. Chemical shifts were reported in parts per million on the d scale with TMS as an internal standard. Silica gel (Qingdao Haiyang Chemical Co., Ltd. 200-300 mesh) and Lichroprep RP-18 (Merck) were used for silica gel column chromatography and MPLC. Preparative HPLC was performed using an octadecyl silica (ODS) column (Pegasil ODS, Senshu Pak, 250 mm × 10 mm i.d.) on a Hitachi liquid chromatography system with an RI detector. Gas liquid chromatography was carried out on a Shimadzu GC-7A under the following conditions: column, 3% ECNSS-M (2 m × 0.3 mm); column temperature, 190 °C; injection temperature, 210 °C; carrier gas, N 2 ; and flow rate, 25 mL/min. Spots were visualized by spraying with ethanol-10% H 2 SO 4 and heating (110 °C, 5 min).

Plant Material
The roots of P. grandiflorum were collected from Shenyang, Liaoning Province, China, in 2003 and were taxonomically identified by Professor Sun Qi-Shi of Shenyang Pharmaceutical University. A voucher specimen (No. 20030321) is deposited at the Herbarium of Shenyang Pharmaceutical University.

Extraction and Isolation
The air-dried roots of P. grandiflorum (10 kg) were pulverized and extracted with 75% EtOH (ethanol:water = 3:1, v/v) three times under reflux. The combined extract was evaporated in vacuo, suspended in water, and then partitioned with EtOAc. The aqueous layer was chromatographed over a macroporous resin D101 column and eluted with H 2 O, 60% EtOH, and 95% EtOH. The 60% EtOH elution was evaporated under a vacuum to obtain a residue (180 g). The residue (80 g) was fractioned

Characterization of Platycoside O (1)
Obtained as a white amorphous powder; IR

Acid Hydrolysis of 1
Compound 1 (2.0 mg) were heated 1M HCl (dioxane-H 2 O, 1:1, 1 mL) at 90 °C for 3 h in a water bath. Dioxane was removed, the solution was extracted with EtOAc (1 mL × 3), and the EtOAc was removed. The monosaccharide portions were analyzed by gas chromatography after conversion of the hydrolysates into corresponding alditol acetates. The arabinitol, glucitol, rhamnitol and xylitol acetates from compound 1 were detected in a ratio of 1:1:1:1 respectively using gas chromatography analysis. The absolute configurations of the sugars were determined according to the method reported by Hara and coworkers [14,15] using gas chromatography with the following conditions: column: 3% ECNSS-M (2 m × 0.3 mm); column temperature: 190 °C; injection temperature: 210 °C. The absolute configurations of the sugars were determined as D-xylose, L-arabinose, L-rhamnose and D-glucose by comparison of its retention times with those of authentic sample [14,15].

Conclusions
During the phytochemical survey of the roots extract of Platycodon grandiflorum, a new unusual minor triterpenoid saponin 1 was isolated and identified as platycoside O on the basis of spectral analysis and chemical evidence.