Platyconic Acid A, a Genuine Triterpenoid Saponin from the Roots of Platycodon grandiflorum
by
Yeon Hee Choi
1,2, 
Dae Seok Yoo
1,
Chun Whan Choi
1,
Mi-Ran Cha
1,
Young Sup Kim
1,
Hyun Sun Lee
3,
Kang Ro Lee
2,* and
Shi Yong Ryu
1,* 1
Korea Research Institute of Chemical Technology, Taejeon 305-343, Korea
2
College of Pharmacy, Sungkyunkwan University, Suwon 440-746, Korea
3
Korea Research Institute of Bioscience & Biotechnology, Taejeon 305-333, Korea
*
Authors to whom correspondence should be addressed.
Molecules 2008, 13(11), 2871-2879; https://doi.org/10.3390/molecules13112871
Submission received: 14 October 2008
/
Revised: 29 October 2008
/
Accepted: 12 November 2008
/
Published: 18 November 2008
Abstract
:A genuine triterpenoid saponin, platyconic acid A (1) was isolated from the roots extract of Platycodon grandiflorum, together with five known saponins: deapioplatycoside E (2), platycoside E (3), platycodin D3 (4), platycodin D2 (5) and platycodin D (6). The structure of 1 was determined on the basis of spectral analysis and chemical evidence.
Introduction
The species Platycodon grandiflorum A. DC (Campanulaceae) is a perennial herb found throughout northeast Asia. The roots have been used as food and frequently employed as a folk remedy for bronchitis, asthma, pulmonary tuberculosis, hyperlipidemia, diabetes and inflammatory diseases. Many pharmacological activities of the species such as, cytotoxicity, inhibition of pancreatic lipase, inhibition of nitric oxide synthase and cyclooxygenase II, protection of oxidative hepatotoxicity and cognitive enhancing activity have been reported [1,2,3,4,5,6].
Triterpenoid saponins with unique chemical features on an oleanene backbone were known as the main chemical constituents of the species and more than 30 kinds of saponin components such as platycodin D have been reported so far [7,8,9,10,11,12,13].
In a previous paper, we reported the isolation of a novel triterpenoid saponin, deapioplatycoside E, from the species [1]. In continuation of our phytochemical investigation of the MeOH extract, we have now isolated a new genuine saponin which we have named platyconic acid A (1) and identified as platycogenic acid-A 3-O-[β-d-glucopyranoside]-28-O-[β-d-apiofuranosyl-(1 ![Molecules 13 02871 i001]()
3)-β-d-xylopyranosyl-(1 ![Molecules 13 02871 i001]()
4)-α-l-rhamnopyranosyl-(1 ![Molecules 13 02871 i001]()
2)-α-l-arabinopyranosyl] ester. It had been reported that two artifacts potentially derived from 1, a methylester 1a and a lactonized product, platyconate A lactone (1b), were isolated from the extract treated with excess amount of diazomethane [13]. From this result, the authors suggested the presence in the plant extract of the corresponding genuine saponin, 1, even though they had failed to isolate it. In this paper, we briefly describe an isolation of the genuine
![Molecules 13 02871 g001]()
saponin, platyconic acid A (1) from the roots and its structure elucidation on the basis of spectroscopic analyses and the comparison of 13C-NMR data with those of the related saponins 1a-e, which were obtained by chemical modification of 1 (Figure 1).
3)-β-d-xylopyranosyl-(1 4)-α-l-rhamnopyranosyl-(1 2)-α-l-arabinopyranosyl] ester. It had been reported that two artifacts potentially derived from 1, a methylester 1a and a lactonized product, platyconate A lactone (1b), were isolated from the extract treated with excess amount of diazomethane [13]. From this result, the authors suggested the presence in the plant extract of the corresponding genuine saponin, 1, even though they had failed to isolate it. In this paper, we briefly describe an isolation of the genuine
Figure 1.
Compounds 1-6 from the root extract of P. grandiflorum.
Results and Discussion
The molecular formula of 1 was established as C57H90O29 by MALDI-TOF/MS experiment (m/z) 1284 [M+2Na] and 13C-NMR data. The IR spectrum showed a hydroxyl group at 3402 cm-1 and an ester group at 1726 cm-1, respectively. The 1H-NMR and 13C-NMR spectral data of 1 indicated the presence of a sapogenin 2,3,16,23-tetrahydroxyolean-12-ene-24,28-dioic acid (platycogenic acid A) and oligosaccharide moieties. The 13C-NMR spectral data of 1 (Table 1) was superimposable with those of the reported platyconic acid A methyl ester (1a), the main difference being the methoxy signal (δ 51.3) in 1a, which was not present in 1. Instead, the carboxyl signal (δ 175.5) of 1a was found to be shifted downfield at δ 181.4 (Table 1). These spectral data strongly implied that 1 was an acid congener of 1a, a genuine saponin. All proton and carbon signals of 1 were assigned by the aid of two-dimensional NMR experiments such as COSY, DEPT, HMQC and HMBC and by the comparison with the data of 1a in the literature [13]. Besides, some chemical modifications of 1 were undertaken to confirm the proposed structure. Compound 1 was found to be easily converted to 1a by treatment with diazomethane, as mentioned on previous report [13]. On the other hand, the acid hydrolysis of 1 under different conditions afforded two kinds of prosapogenin, 1c, 1d, and an artificial sapogenin 1e (platycogenic acid-A lactone), all of which provided evidence supporting the proposed structure of 1 [8]. From these results obtained from the spectroscopic data and chemical evidence, the structure of 1
was determined unambiguously as a that of the genuine saponin, platyconic acid A (platycogenic acid-A 3-O-β-d-glucopyranoside]-28-O-[β-d-apiofuranosyl-(1 ![Molecules 13 02871 i001]()
3)-β-d-xylopyranosyl-(1 ![Molecules 13 02871 i001]()
4)-α-l-rhamno- pyranosyl-(1 ![Molecules 13 02871 i001]()
2)-α-l-arabinopyranoside. This is the first report on the isolation of compound 1 from natural sources.
| 1 | 1a | 1b | 1c | 1d | 1e | |
|---|---|---|---|---|---|---|
| C-1 | 46.7 | 45.8 | 41.6 | 41.7 | 41.4 | 42.0 |
| C-2 | 69.6 | 69.8 | 82.8 | 83.6 | 83.5 | 84.6 |
| C-3 | 83.3 | 84.4 | 89.8 | 89.5 | 89.5 | 81.8 |
| C-4 | 56.3 | 56.1 | 53.9 | 54.5 | 54.5 | 55.2 |
| C-5 | 49.6 | 50.1 | 52.5 | 52.3 | 52.2 | 52.1 |
| C-6 | 20.3 | 20.5 | 19.5 | 19.8 | 19.7 | 20.1 |
| C-7 | 33.7 | 33.7 | 33.6 | 33.9 | 33.8 | 34.0 |
| C-8 | 40.0 | 40.3 | 40.7 | 40.8 | 40.6 | 38.2 |
| C-9 | 47.2 | 47.6 | 48.5 | 48.5 | 48.5 | 49.1 |
| C-10 | 37.2 | 37.4 | 37.9 | 38.0 | 38.0 | 36.9 |
| C-11 | 24.4 | 24.4 | 24.7 | 25.0 | 25.0 | 25.2 |
| C-12 | 122.9 | 123.0 | 122.3 | 122.6 | 122.2 | 121.3 |
| C-13 | 144.2 | 144.4 | 145.0 | 145.6 | 146.2 | 147.3 |
| C-14 | 42.2 | 42.4 | 42.5 | 42.7 | 42.7 | 43.1 |
| C-15 | 36.2 | 36.1 | 36.0 | 36.5 | 36.9 | 36.7 |
| C-16 | 73.8 | 74.1 | 73.9 | 74.4 | 75.0 | 75.9 |
| C-17 | 49.5 | 50.1 | 50.0 | 50.2 | 49.3 | 50.8 |
| C-18 | 41.3 | 41.6 | 41.6 | 41.6 | 41.9 | 40.9 |
| C-19 | 47.1 | 47.2 | 47.2 | 47.6 | 47.7 | 48.1 |
| C-20 | 30.6 | 30.8 | 30.7 | 30.8 | 30.3 | 28.3 |
| C-21 | 35.9 | 36.1 | 36.0 | 36.4 | 36.8 | 34.2 |
| C-22 | 31.7 | 31.4 | 31.3 | 31.4 | 31.5 | 31.5 |
| C-23 | 63.5 | 64.5 | 57.5 | 57.6 | 57.5 | 58.3 |
| C-24 | 181.4 | 175.5 | 177.7 | 178.6 | 178.6 | 179.5 |
| C-25 | 16.1 | 15.8 | 17.4 | 17.8 | 17.7 | 18.3 |
| C-26 | 17.4 | 17.6 | 18.1 | 18.5 | 18.4 | 19.1 |
| C-27 | 27.0 | 27.2 | 27.4 | 27.7 | 27.7 | 26.9 |
| C-28 | 175.8 | 175.8 | 175.8 | 176.3 | 180.4 | 185.0 |
| C-29 | 33.3 | 33.1 | 33.0 | 33.7 | 33.3 | 31.7 |
| C-30 | 24.8 | 25.2 | 25.2 | 25.2 | 25.2 | 25.7 |
| 24-OCH3 | 51.3 | |||||
| 1 | 1a | 1b | 1c | 1d | ||
| glucose | ||||||
| C-1 | 106.0 | 106.3 | 105.1 | 105.7 | 105.7 | |
| C-2 | 74.8 | 75.3 | 75.0 | 75.6 | 75.7 | |
| C-3 | 78.2 | 78.5 | 78.2 | 79.0 | 79.2 | |
| C-4 | 71.8 | 72.0 | 71.8 | 71.5 | 71.8 | |
| C-5 | 78.2 | 78.1 | 78.2 | 78.8 | 78.8 | |
| C-6 | 61.8 | 63.0 | 62.9 | 63.0 | 63.0 | |
| arabinose | ||||||
| C-1 | 93.4 | 93.7 | 93.7 | 94.1 | ||
| C-2 | 75.5 | 75.7 | 75.7 | 75.8 | ||
| C-3 | 70.3 | 70.1 | 70.2 | 70.8 | ||
| C-4 | 66.2 | 65.8 | 65.9 | 66.8 | ||
| C-5 | 61.8 | 63.0 | 62.9 | 63.8 | ||
| rhamnose | ||||||
| C-1 | 101.2 | 101.1 | 101.1 | 101.7 | ||
| C-2 | 71.8 | 72.0 | 72.0 | 72.4 | ||
| C-3 | 72.3 | 72.4 | 72.4 | 73.2 | ||
| C-4 | 83.3 | 83.6 | 83.6 | 84.3 | ||
| C-5 | 68.4 | 68.7 | 68.6 | 69.1 | ||
| C-6 | 18.4 | 18.1 | 18.3 | 18.8 | ||
| xylose | ||||||
| C-1 | 106.2 | 106.5 | 106.5 | 107.4 | ||
| C-2 | 74.7 | 75.0 | 75.0 | 76.2 | ||
| C-3 | 85.2 | 85.5 | 85.6 | 79.2 | ||
| C-4 | 68.9 | 69.5 | 69.5 | 71.8 | ||
| C-5 | 66.5 | 66.8 | 66.8 | 67.9 | ||
| apiose | ||||||
| C-1 | 110.8 | 111.2 | 111.2 | |||
| C-2 | 77.8 | 77.9 | 77.9 | |||
| C-3 | 80.1 | 80.0 | 80.0 | |||
| C-4 | 74.3 | 75.0 | 75.0 | |||
| C-5 | 65.1 | 65.8 | 65.7 |
Data for 1a and 1b from ref. [13]
3)-β-d-xylopyranosyl-(1 4)-α-l-rhamno- pyranosyl-(1 2)-α-l-arabinopyranoside. This is the first report on the isolation of compound 1 from natural sources.Figure 2 shows the HPLC profile of the MeOH root extract.
Figure 2.
HPLC profile of saponin fraction from the MeOH root extract of P. grandiflorum.
Platyconic acid A (1), deapioplatycoside E (2), platycoside E (3), platycodin D3 (4), platycodin D2 (5) and platycodin D (6).
Conclusions
During the phytochemical survey of the roots extract of Platycodon grandiflorum, a new triterpenoid saponin 1 was isolated and identified on the basis of spectral analysis and chemical evidence as a genuine saponin, which we have named platyconic acid A.
Experimental
General
Optical rotations were determined using a Rudolph Autopol IV polarimeter. MS spectra were measured on a Voyager PE Biosystems USA MALDI-TOF/MS Spectrometer. 1H-NMR and 13C-NMR spectra was recorded on a Brucker AVANCE 800 NMR spectrometer using TMS as an internal standard. Preparative HPLC used a Futecs NS-3000i system equipped with an Optimapak column (50 x 250 mm, 10 μm, RSTech) and a ELSD (sofTA, USA).
Plant Material
The species, P. grandiflorum cultivated for three years at the mountainside of Kyungnam Province, Korea was harvested in September 2003. A voucher specimen (Herbarium No. JS-03024) has been preserved at the Herbarium of JangSaeng Doraji Co. LTD., Jinju, Korea.
Extraction and Isolation
Dried roots of P. grandiflorum (5 kg) were extracted three times with methanol at room temperature for 7 days. Concentration of the solvent gave a brown syrupy extract (1.4 kg) which was suspended in water and then partitioned successively with ethyl acetate (63 g) and n-butanol (130 g). The n-butanol layer was suspended in H2O (2 L) and poured onto a Diaion HP-20 column (Φ = 5.0 × 100 cm), which was stabilized with H2O. The column was washed with H2O (2 L) and then eluted with MeOH (5 L). The eluate was concentrated in a reduced pressure to give a crude saponin mixture (75 g).
Characterization of platyconic acid A (1)
Obtained as a white amorphous powder, ![Molecules 13 02871 i002]()
= - 8.89 (c 1, MeOH); IR νmax: 3402, 2927, 1726, 1076 and 1033 cm-1; MALDI-TOF/MS m/z: 1284 [M+2Na]; C57H90O29; 1H-NMR (pyridine-d5, 800 MHz): δ 0.98, 1.10, 1.52, 1.69, 1.75 (each 3H, H-25, 26, 27, 29, 30), 2.75 (1H, d, J = 13.3Hz, H-18), 5.61 (1H, brs, H-12); 13C-NMR (pyridine-d5, 200 MHz): see Table 1.
= - 8.89 (c 1, MeOH); IR νmax: 3402, 2927, 1726, 1076 and 1033 cm-1; MALDI-TOF/MS m/z: 1284 [M+2Na]; C57H90O29; 1H-NMR (pyridine-d5, 800 MHz): δ 0.98, 1.10, 1.52, 1.69, 1.75 (each 3H, H-25, 26, 27, 29, 30), 2.75 (1H, d, J = 13.3Hz, H-18), 5.61 (1H, brs, H-12); 13C-NMR (pyridine-d5, 200 MHz): see Table 1. Preparation of 1a by treatment of 1 with diazomethane
Compound 1 (200 mg) was dissolved in MeOH (10 mL), to which 10 equivalents of CH2N2 in ether was added and the resulting mixture was stirred overnight, then it was evaporated to dryness and purified by ODS gel column chromatography (MeOH-H2O) to afford 1a (140 mg) as an amorphous powder.
Preparation of 1c and 1d by partial hydrolysis of 1
Compound 1 (100 mg) was dissolved in 0.1 N HCl in MeOH (10 mL) and stirred at room temperature overnight. The solvent was removed under nitrogen to provide a colorless solid, which was purified by ODS to afford 1c (60 mg) as an amorphous powder. In a similar manner, 1 (100 mg) was dissolved in 1 N HCl in MeOH (10 mL) and refluxed on water bath for 1 hr. The reaction mixture was concentrated in vacuo to yield a colorless solid which was purified by ODS column chromatography to afford 1d (42 mg) as an amorphous powder.
Preparation of 1e by acid hydrolysis of 1
Compound 1 (100 mg) was dissolved in 4 N HCl in MeOH (10 mL) and refluxed on a water bath for 6 hr. The reaction mixture was concentrated in vacuo to yield a colorless solid which was purified by ODS column chromatography to afford 1e (21 mg) as an amorphous powder.
HPLC analysis of the roots extract of P. grandiflorum
A portion of the saponin fraction prepared from the roots extract of P. grandiflorum as described above in Extraction and Isolation (20 g) was purified by repeated preparative HPLC. The residue was dissolved in distilled water and passed through a solid-phase-extraction cartridge (RP-C18, CEREX No. 600-3506). The cartridge was washed with excess amount of distilled water and eluted with MeOH. The MeOH solution was injected onto an Optimapak column (4.6 x 250 mm, 5 µm, RSTech) maintained at 40°C on a Futecs NS-3000i system equipped with an ELSD detector (sofTA, USA). A mixture of 50 mM ammonium acetate solution (NH4Ac), acetonitrile and methanol was used as mobile phase as follows: eluent A = 85:10:5 NH4Ac-acetonitrile-methanol; eluent B = 55:40:5 NH4Ac-acetonitrile-methanol; flow rate: 0.8 mL/min; gradient: 0-5 min (0-15% B), 5-28 min (15-38% B), 28-33 min (38-40% B), 33-53 min (40-43% B), 53-63 min (43-60% B), 63-81 min (60-100% B). This allowed isolation of the six triterpenoid saponins 1-6, i.e., 660 mg of 1 (tR 42.8 min), 420 mg of 2 (tR 19.1 min), 1,450 mg of 3 (tR 20.3 min), 320 mg of 4 (tR 28.4 min), 56 mg of 5 (tR 49.5 min) and 980 mg of 6 (tR 51.4 min) (Figure 2). Compounds 2-6 were identified by direct comparison of their physical and spectral data (1H-NMR and 13C-NMR) with those in the literature [1,13,14,15].
Acknowledgments
This study was supported in part by a grant from Ministry of Science and Technology of Korea (MOST) and by Inter-Institutional Collaboration Research Program under Korea Research Council for Industrial Science & Technology (KOCI), Korea.
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- Sample Availability: Samples of the compounds 1-6 are available from the authors
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MDPI and ACS Style
Choi, Y.H.; Yoo, D.S.; Choi, C.W.; Cha, M.-R.; Kim, Y.S.; Lee, H.S.; Lee, K.R.; Ryu, S.Y. Platyconic Acid A, a Genuine Triterpenoid Saponin from the Roots of Platycodon grandiflorum. Molecules 2008, 13, 2871-2879. https://doi.org/10.3390/molecules13112871
AMA Style
Choi YH, Yoo DS, Choi CW, Cha M-R, Kim YS, Lee HS, Lee KR, Ryu SY. Platyconic Acid A, a Genuine Triterpenoid Saponin from the Roots of Platycodon grandiflorum. Molecules. 2008; 13(11):2871-2879. https://doi.org/10.3390/molecules13112871
Chicago/Turabian StyleChoi, Yeon Hee, Dae Seok Yoo, Chun Whan Choi, Mi-Ran Cha, Young Sup Kim, Hyun Sun Lee, Kang Ro Lee, and Shi Yong Ryu. 2008. "Platyconic Acid A, a Genuine Triterpenoid Saponin from the Roots of Platycodon grandiflorum" Molecules 13, no. 11: 2871-2879. https://doi.org/10.3390/molecules13112871
APA StyleChoi, Y. H., Yoo, D. S., Choi, C. W., Cha, M.-R., Kim, Y. S., Lee, H. S., Lee, K. R., & Ryu, S. Y. (2008). Platyconic Acid A, a Genuine Triterpenoid Saponin from the Roots of Platycodon grandiflorum. Molecules, 13(11), 2871-2879. https://doi.org/10.3390/molecules13112871
