New Sesquiterpenenoids from Ainsliaea yunnanensis

Wu, Xiang-Lei; Xiong, Xiao-Juan; Lu, Wen-Quan; Huang, Hao; Shen, Yun-Heng; Wu, Zhi-Jun; Chen, Wan-Sheng

doi:10.3390/molecules21081031

Open AccessArticle

New Sesquiterpenenoids from Ainsliaea yunnanensis

by

Xiang-Lei Wu

^1,2,†,

Xiao-Juan Xiong

^2,†,

Wen-Quan Lu

¹,

Hao Huang

²,

Yun-Heng Shen

³,

Zhi-Jun Wu

^1,* and

Wan-Sheng Chen

^1,*

¹

Department of Pharmacy, Changzheng Hospital, Second Military Medical University, 415 Fengyang Road, Shanghai 200003, China

²

College of Chemical and Biological Engineering, Yichun University, 576 Xuefu Road, Yichun 336000, China

³

College of Pharmacy, Second Military Medical University, 325 Guohe Road, Shanghai 200433, China

^*

Authors to whom correspondence should be addressed.

^†

These authors contributed equally to this paper.

Molecules 2016, 21(8), 1031; https://doi.org/10.3390/molecules21081031

Submission received: 22 June 2016 / Revised: 2 August 2016 / Accepted: 3 August 2016 / Published: 8 August 2016

(This article belongs to the Section Natural Products Chemistry)

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Abstract

:

Investigation of the ethanol extract of the whole plant of Ainsliaea yunnanensis led to the isolation of four new dimeric sesquiterpene lactones, ainsliadimer F–I (1–4), together with seven known dimeric sesquiterpene lactones (5–11) and ten sesquiterpenes (12–21). Their structures were elucidated by spectroscopic methods. The relative stereochemistry of ainsliadimer F was further confirmed by single crystal X-ray diffraction analysis. Compounds 1–21 were tested for the inhibition of nuclear factor kappa B (NF-κB) in the 293-NF-κB-luciferase reporter cell line induced by lipopolysaccharide (LPS), and Compounds 5, 18, 20 and 21 were further tested for the production of TNF-α, IL-1β, IL-6 and IL-10 in RAW 264.7 macrophages induced by LPS. Compounds 5, 18, 20 and 21 exhibited significant activity in anti-inflammatory activity assays.

Keywords:

Ainsliaea yunnanensis; Ainsliaea; sesquiterpenoid; anti-inflammatory activity

1. Introduction

The plants of Asteraceae are well known to contain biologically-active sesquiterpenoids [1,2,3,4]. Within this family, the genus Ainsliaea comprises 70 species, 48 of which are indigenous to China. Phytochemical studies have indicated that sesquiterpenoids are characteristic constituents of Ainsliaea species [5,6,7,8], and guaiane-type sesquiterpene, as one of the most important chemical types of sesquiterpenes, has attracted much interest due to the structural diversity and varied biological activities, such as anti-inflammatory [9] and antitumor [10,11]. A. yunnanensis, a plant of Ainsliaea, is mainly distributed in Yunnan province of China, which has been used in Chinese folk medicine to treat rheumatism, lumbago and gonitis [12]. Some chemical constituents of this plant have been reported previously [12,13].

As part of the consecutive study of Ainsliaea species, our investigation on A. yunnanensis led to the isolation of four new dimeric sesquiterpene lactones, ainsliadimer F (1), ainsliadimer G (2), ainsliadimer H (3) and ainsliadimer I (4), together with seven known dimeric sesquiterpene lactones, gochnatiolide A (5) [14], gochnatiolide B (6) [15], ainsliadimer A (7) [16], ainsliadimer B (8) [15], ainsliadimer C (9) [17], ainsliadimer D (10) [17] and ainsliadimer E (11) [18], and ten sesquiterpenes, curzerenone (12) [19], selin-11-en-4 alpha-ol (13) [20], zaluzanin C (14) [21], isolipidiol (15) [22], 11,13-dihydro-deacylcynaropicrin (16) [23], clovane-2 beta, 9 alpha-diol (17) [24], glucozaluzanin C (18) [25], ainsliatone A (19) [26], dihydroestafiatone (20) [27] and dihydroestafiatol (21) [27]. Their structures were elucidated by spectroscopic methods and by comparison with the literature. Their structures were show in Figure 1. These compounds were tested for anti-inflammatory activities, and Compounds 5, 18, 20 and 21 exhibited significant activities in anti-inflammatory activity assays.

2. Results and Discussion

2.1. Structure Elucidation of New Compounds

Compound 1 was obtained as colorless prisms, and its molecular formula was established to be C₃₀H₃₄O₇ by its HRESI (m/z 529.2206 [M + Na]⁺) and ¹³C-NMR spectra. The ¹³C-NMR spectrum exhibited 30 carbon resonances, classified into ten quaternary carbons, nine methines, including two oxygen-substituted carbons, nine methylenes and two methyls. The signals at δ_C 208.5, 222.3 were ascribed to two ketone groups. The characteristic signals at δ_C 12.6, 14.3 were ascribed to two methyls; the signals at δ_C 114.1, 121.6, 138.5 and 150.1 were ascribed to two exocyclic double bonds; the signals at δ_C 169.3, 178.6 were ascribed to two ester carbonyls; and the signals at δ_C 82.6, 83.9 were ascribed to two oxygen-bearing methines. In the ¹H-NMR spectrum, the signals at δ_H 1.27 (3H, d, J = 6.9 Hz) and δ_H 1.27 (3H, d, J = 7.1 Hz) implied the presence of two methyls; the signals at δ_H 4.72 (1H, brs), 5.09 (1H, brs), 5.58 (1H, d, J = 3.0 Hz) and 6.26 (1H, d, J = 3.4 Hz) implied the presence of two exocyclic double bonds; the signals at δ_H 4.16 (1H, t, J = 9.4 Hz) and 4.32 (1H, dd, J = 11.0, 9.6 Hz) implied the presence of two oxygen-bearing methines. The ¹H- and ¹³C-NMR spectra of Compound 1 indicated the presence of two guaianolide structure moieties. Comparison of the NMR data (Table 1) with those of the known compound gochnatiolide A (5) showed close resemblances [14], except that two exocyclic double bonds at C-4/C-15 and C-11/C-13 in gochnatiolide A were replaced by two methyls and two methines in Compound 1. This was confirmed by HMBC correlations of Me-15 (δ_H 1.27) with C-3 (δ_C 208.5), C-4 (δ_C 47.0), C-5 (δ_C 54.8) and Me-13 (δ_H 1.27) with C-7 (δ_C 54.9), C-11 (δ_C 41.9) and C-12 (δ_C 178.6). The relative configuration of Me-15 and Me-13 were deduced to be α-oriented based on the NOESY correlations of Me-15 with H-5α (δ_H 2.80) and Me-13 with H-7α (δ_H 1.84). The structure and relative configuration of 1 were further confirmed by the X-ray diffraction analysis (Figure 2). Compound 1 was named as ainsliadimer F.

Compound 2 was isolated as colorless prisms. The molecular formula of Compound 2 was determined as C₃₁H₃₄O₈ from the quasi-molecular ion peak [M + Na]⁺ at m/z 557.2148 in its positive HRESI. The ¹³C-NMR spectrum exhibited 31 carbon resonances, classified into eleven quaternary carbons, eight methines, including two oxygen-substituted carbons, eleven methylenes and one methoxyl group. The signals at δ_C 206.3, 222.5 were ascribed to two ketone groups. The signals at δ_C 170.1, 169.4 were ascribed to two ester carbonyls. The signals at δ_C 114.1, 119.2, 121.5, 138.6, 139.5 and 150.2 were ascribed to three exocyclic double bonds; the signals at δ_C 83.9, 82.6 were ascribed to two oxygen-substituted methines; the signal at δ_C 68.4 was linked to one oxygen atom; and the signal at δ_C 59.2 was ascribed to one methoxyl group. Analysis of NMR data (Table 1) revealed a dimeric sesquiterpene skeleton consisting of guaianolide moieties, and it was quite close to the known compound ainsliadimer D (10) [17], except for a methoxy group in Compound 2, replacing the hydroxyl group in ainsliadimer D. This was confirmed by the HMBC correlations of C-1°′(δ_C 59.2) with H-15 (δ_H 3.94, 3.74). The structure of 2 was established on the basis of 1D- and 2D-NMR spectra (¹H, ¹³C, DEPT, COSY, HSQC and HMBC). Accordingly, the structure of Compound 2 was named as ainsliadimer G. Compound 2 was a natural chemical constituent and not an isolation artifact, which was tested by HPLC (Figure S30) in a crude extract.

Compound 3 was obtained as a colorless powder and showed the [M + Na]⁺ ion peak at m/z 571.2310 in its HRESI, corresponding to a molecular formula of C₃₂H₃₆O₈. The ¹³C-NMR spectrum showed 32 carbon resonances, classified into eleven quaternary carbons, eight methines, including two oxygen-substituted carbons, twelve methylenes, including two oxygen-bearing carbons, and one methyl. Analysis of NMR data (Table 1) showed it to be quite close to Compound 2, except for an ethoxy group in Compound 3 replacing a methoxy group in Compound 2. This was confirmed by HMBC correlations of H-15 (δ_H 3.96, 3.76) with C-1″ (δ_C 66.8). Accordingly, the structure of Compound 3 was named as ainsliadimer H. Compound 3 was a natural chemical constituent, which was also tested by HPLC (Figure S31) in a crude extract.

Compound 4 was obtained as colorless prisms, and its molecular formula was established to be C₃₀H₃₂O₇ by its HRESI (m/z 527.2043 [M + Na]⁺) and ¹³C-NMR spectra. The ¹³C-NMR spectrum exhibited 30 carbon resonances, classified into eleven quaternary carbons, eight methines, including two oxygen-substituted carbons, ten methylenes and one methyl. The ¹H- and ¹³C-NMR spectra of 4 were quite close to those of ainsliadimer D (10) [17], except for one hydroxymethyl at the position C-4 in ainsliadimer D was replaced by one methyl in Compound 4. This was confirmed by HMBC correlations of Me-15 (δ_H 1.30) with C-3 (δ_C 208.4), C-4 (δ_C 47.0), C-5 (δ_C 55.1). The structure of 4 was established on the basis of 1D- and 2D-NMR spectra and was named ainsliadimer I.

In addition to four new dimeric sesquiterpene lactones (1–4), seventeen known sesquiterpenes, identified as gochnatiolide A (5), gochnatiolide B (6), ainsliadimer A (7), ainsliadimer B (8), ainsliadimer C (9), ainsliadimer D (10), ainsliadimer E (11), curzerenone (12), selin-11-en-4 alpha-ol (13), zaluzanin C (14), isolipidiol (15), 11,13-dihydro-deacylcynaropicrin (16), clovane-2 beta, 9 alpha-diol (17), glucozaluzanin C (18), ainsliatone A (19), dihydroestafiatone (20) and dihydroestafiatol (21). These compounds were identified by spectral analysis, and we found that their spectral data were consistent with the spectroscopic data reported in the corresponding literature.

2.2. Chemotaxonomic Significance

The present phytochemical investigation on this plant led to the isolation of twenty-one sesquiterpenoids from A. yunnanensis, including eighteen guaiane-type sesquiterpene lactones (1–11, 14–16 and 18–21), one bicyclic sesquiterpane (12), one eudesmane sesquiterpene (13) and one clovane sesquiterpene (17). The general chemotaxonomic pattern of A. yunnanensis is similar to other Ainsliaea species in terms of chemical classes; this is the first report of Compounds 5, 6, 7–10, 14–16, 18–19 from A. yunnanensis, and the first report of Compounds 1–4, 11–13, 17, 21–21 from the genus Ainsliaea.

The guaiane-type sesquiterpenes have wide-spread occurrence in the genus Ainsliaea species. Among them, Compounds 1–11 were dimeric guaiane-type sesquiterpene lactones; they were used as important chemotaxonomic markers in this genus [15,16,17]. They are generally biosynthesized from two monomeric sesquiterpene lactones through a six-membered cyclohexene of the 3,4-dihydro-2H-pyran ring via hetero Diels-Alder cycloaddition reactions, except ainsliadimer A (7), which represents the single dimeric sesquiterpene lactone with a five-membered cyclopentane ring [16]. On the other hand, Compound 11 has been reported to be present in the genera Gochnatia; we now report its presence for the first time in the Ainsliaea family, although the other dimeric guaiane-type sesquiterpene lactones were only isolated from Ainsliaea species. This is an interesting finding, as Gochnatia could be an alternative source of these compounds.

To conclude, the isolation of different sesquiterpene lactones is consistent with the chemical profile of the other Ainsliaea species. Of these, dimeric guaiane-type sesquiterpene lactones structurally characterized by a six-membered ring are systematically important and might serve as the common characteristic constituents of both Ainsliaea and Asteraceae families.

2.3. Evaluation of Biological Activity

Compounds 1–21 were assessed for inhibitory activity in a luciferase assay. Compared to the cell group, the luciferase activity of the LPS group was significantly enhanced, which indicated that the inflammatory cell model induced by LPS was constructed successfully. Then, we found that the luciferase activity of Compounds 5, 18, 20 and 21 was significantly decreased by comparing to the LPS group, which showed that they had significant inhibitory effect on NF-κB activity. The effects of Compounds 5, 18, 20 and 21 on the inflammatory response were investigated further. The anti-inflammatory effects were evaluated by investigating the inhibitory activity of the compounds on the production of TNF-α, IL-1β, IL-6 and IL-10 in RAW 264.7 macrophages induced by LPS. For all assays, ibuprofen was used as a positive control. Compared to the LPS group, these compounds were tested their inhibitory ratio of TNF-α, IL-1β, IL-6 and IL-10 release in LPS-stimulated RAW 264.7 macrophages in vitro at three different concentration (1 μg/mL, 10 μg/mL, 100 μg/mL). The concentration of TNF-α in the RAW 264.7 cells pretreated with Compounds 5, 18, 20 and 21 was reduced to 67.9%, 66.5%, 65.7% and 63.2% at 10 μg/mL and 33%, 15.5%, 16.9% and 37.7% at 100 μg/mL, respectively, while the inhibitory rates of the positive control ibuprofen were 73.8% and 23.0%. In the same way, the concentrations of IL-1β, IL-6 and IL-10 in the RAW 264.7 cells pretreated with Compounds 5, 18, 20 and 21 have a similar effect at the same concentration. The inhibition activity was dose-dependent (Figure 3, Figure 4, Figure 5, Figure 6 and Figure 7).

The results suggested that the basal skeleton of guaiane-type sesquiterpene lactone (18, 20, 21) might be crucial for the inhibitory activity on NF-κB production in RAW 264.7 cells. The functional groups such as hydroxyl groups linked at C-8 were found to decrease the inhibitory activity. The presence of the double bonds from the C-4 and C-11 contribution to the NF-κB decreased the activity according the results of zaluzanin C (14) and dihydroestafiatol (21), while the glucosyl group at C-3 slightly rose the inhibitory activity on NF-κB production. The significant inhibitory activity of gochnatiolide A (5) might be owed to the hydroxyl group linked at C-10 and the decrease of the methyl groups compared to other dimeric guaiane-type sesquiterpene lactones. The possible structure-activity relationships of these compounds should be further studied in the future, and it will be a significant topic.

3. Experimental Section

3.1. General Procedures

X-ray diffractions were measured on a Bruker SMART APEXII DUO (Bruker, Karlsruhe, Germany). Optical rotations were measured on a Perkin-Elmer 341 polarimeter (Perkin Elmer, Fremont, CA, USA). IR analyses were performed with a Nexus 470 FI-IR spectrometer (Thermo-Nicolet, Madison, WI, USA). UV spectra were recorded on Shimadzu UV/VIS-240 recording spectrophotometer (Shimadzu, Tokyo, Japan). 1D- and 2D-NMR spectra were obtained on a Bruker Avance 600 NMR spectrometer (Bruker, Karlsruhe, Germany). HR-ESIMS were acquired on an Agilent 6220 TOF LC-MS instrument (Agilent, Santa Clara, CA, USA). Column chromatography was performed by using silica gel (100–200 and 200–300 mesh; Yantai Jiangyou Silica Gel Development Co. Ltd., Yantai, China), Octadecylsilyl (50 μm; Wilmington, NC, USA), MCI Gel (75–150 μm; Mitsubishi Chemical Corporation, Tokyo, Japan); Sephadex LH-20 (40–70 μm; Pharmacia Company, Uppsala, Sweden). Semi-preparative HPLC isolation was achieved with an Agilent 1200 instrument (Agilent) equipped with a refractive index detector (RID), using a C₁₈ column (250 mm × 10 mm × 5 μm, YMC) and eluting with ACN–H₂O (30%–50%) and MeOH–H₂O (40%–60%) at 2.0 mL/min. Precoated silica gel GF₂₅₄ and HF₂₅₄ plates were used for TLC, and zones were visualized under UV light (254 nm and 365 nm) or by spray with 10% H₂SO₄–EtOH followed by heating.

3.2. Plant Material

The plant materials of A. yunnanensis were collected from Chuxiong, Yunnan province, during June 2013, and authenticated by Professor Ceming Tan (Jiujiang Forest Herbarium, Jiujiang, China). A voucher specimen (No. 20130629) was deposited at the Department of Pharmacognosy of the Second Military Medical University.

3.3. Extraction and Isolation

The air-dried A. yunnanensis (15 kg) was extracted three times with 80% ethanol (150 L) under reflux. After removal of the solvent by evaporation under vacuum, the residue was suspended in water (15 L) and then successively partitioned with petroleum, EtOAc and n-BuOH (3 × 15 L), respectively.

The EtOAc fraction (350 g) was chromatographed over a silica gel column (100–200 mesh, 120 × 1400 mm) and eluted with gradient CH₂Cl₂–MeOH (30:1 to 10:1) to obtain 5 fractions (A−E, respectively weighing 50 g, 63 g, 38 g, 16 g, 24 g). Fraction A was separated by silica gel column chromatography with CH₂Cl₂–MeOH (50:1 to 20:1) to obtain the fractions A1–A4 (17 g, 1 g, 7 g, 300 mg). Fraction A4 was separated on Sephadex LH-20 with CH₂Cl₂–MeOH (1:1) to yield Compound 12 (6 mg). Fraction B was separated on Sephadex LH-20 with CH₂Cl₂-MeOH (1:1) to obtain four subfractions (B1−B4); Fraction B2 (200 mg) was separated by silica gel column chromatography with CH₂Cl₂–MeOH (20:1 to 5:1) to obtain Compound 13 (19 mg) and the subfraction B2-1 (120 mg). The subfraction B2-1 was separated on Sephadex LH-20 with CH₂Cl₂–MeOH (1:1) to yield Compound 14 (75 mg). Fraction C (38 g) was separated on Sephadex LH-20 with CH₂Cl₂–MeOH (1:1) to obtain five subfractions (C1−C5); the fraction C4 (240 mg) was separated on the RP-18 column with MeOH–H₂O (1:1–9:1) to yield Compounds 20 (8 mg) and 21 (10 mg). Fraction D was separated on Sephadex LH-20 with CH₂Cl₂–MeOH (1:1) to obtain the subfractions D1−D5 (3 g, 1.8 g, 4.2 g, 600 mg, 900 mg). The fraction D2 (1.8 g) was separated by HPLC on a semi-preparative C₁₈ column with 48% ACN-H₂O as the mobile phase to obtain Compound 5 (750 mg) (2.0 mL/min, 205 nm, t_R = 90.0 min) and five fractions (Fr.D2-1–D2-5). Fr.D2-1 (27 mg) was separated by reversed-phase HPLC eluting with 35% ACN-H₂O to afford Compound 2 (13.0 mg) (2.0 mL/min, 205 nm, t_R = 49.0 min). Fr.D2-2 (253 mg) was separated by reversed-phase HPLC eluting with 38% ACN-H₂O to afford Compound 6 (70 mg) (2.0 mL/min, 205 nm, t_R = 46.0 min), Compound 4 (4.6 mg) (2.0 mL/min, 205 nm, t_R = 52.0 min) and Compound 9 (28 mg) (2.0 mL/min, 205 nm, t_R = 58.0 min). Fr.D2-3 (162 mg) was separated by reversed-phase HPLC eluting with 40% ACN to afford Compound 1 (27 mg) (2.0 mL/min, 205 nm, t_R = 43.0 min). Fr.D2-4 (108 mg) was also separated by reversed-phase HPLC eluting with 45% ACN-H₂O to afford Compound 3 (37 mg) (2.0 mL/min, 205 nm, t_R = 48.0 min). Fraction E (24 g) was subjected on the MCI gel column to MeOH–H₂O (1:1–9:1) as the eluting solvent to afford five subfractions E1−E5 (6 g, 800 mg, 500 mg, 1.4 g, 7.2 g). Fraction E3 (500 mg) was subjected by column chromatography Sephadex LH-20 to CH₂Cl₂–MeOH (1:1) as the eluting solvent to afford four subfractions (E3-1–E3-4). Fraction E3-1 (26 mg) was separated by HPLC on a semi-preparative C₁₈ column with 45% ACN-H₂O respectively as the mobile phase to yield Compound 11 (9 mg) (2.0 mL/min, 205 nm, t_R = 43.0 min). Fraction E3-3 (72 mg) was separated by HPLC on a semi-preparative C₁₈ column with 40% ACN-H₂O respectively as the mobile phase to yield Compound 7 (4.5 mg) (2.0 mL/min, 205 nm, t_R = 49.0 min); Fraction E3-E4 (35 mg) were separated by HPLC on a semi-preparative C₁₈ column with 38% ACN-H₂O respectively as the mobile phase to yield Compound 8 (12 mg) (2.0 mL/min, 205 nm, t_R = 46.0 min) and Compound 10 (14 mg) (2.0 mL/min, 205 nm, t_R = 47.0 min).

The n-BuOH fraction (400 g) was subjected to column chromatography on silica gel and gradient elution with CH₂Cl₂-MeOH (10:1 to 5:1) to obtain Fractions A–H (20 g, 19 g, 28 g, 33 g, 27 g, 15 g, 30 g, 68 g). The fraction D was separated on Sephadex LH-20 with CH₂Cl₂–MeOH (1:1) to obtain three subfractions D1–D3 (8 g, 1.2 g, 11 g); the fraction D2 (1.2 g) was separated on the ODS gel column chromatography with MeOH–H₂O (1:4 to 5:1) to obtain Compound 17 (12 mg) and Subfraction D2-1 (70 mg); then, the subfraction D2-1 was separated on Sephadex LH-20 with CH₂Cl₂-MeOH (1:1) to obtain Compound 15 (6 mg). Fraction F (15 g) was separated on Sephadex LH-20 with CH₂Cl₂-MeOH (1:1) to obtain four subfractions F1−F4 (2 g, 900 mg, 600 mg, 7 g). Fraction F2 (900 mg) was separated by MCI gel column chromatography with MeOH–H₂O (1:4 to 4:1) to obtain Compound 16 (5 mg). Fraction F3 (600 mg) was separated by ODS gel column chromatography with MeOH–H₂O (1:4–4:1) to obtain Compound 18 (200 mg) and the subfraction F3-1 (80 mg), then the fraction F3-1 was separated by HPLC on a semi-preparative C₁₈ column (250 mm × 10 mm, 2.0 mL/min.) with 30% ACN-H₂O as the mobile phase to afford the Compound 19 (16 mg).

3.4. Luciferase Assay

The NF-κB 293 cells were cultured in DMEM supplemented with 10% fetal bovine serum (FBS). The cells were pretreated with Compounds 1–21 at concentrations of 1, 10, 100 μg/mL for 4 h and then stimulated with 10 μg/mL lipopolysaccharide (LPS) for 24 h. The cells were rinsed twice with phosphate-buffered saline (PBS, pH 7.4) and lysed with passive lysis buffer (Promega, Madison, WI, USA). Then, the inhibitory effect on NF-κB was analyzed using the luciferase assay system (Promega) according to the manufacturer′s instructions [26].

3.5. Measurement of TNF-α, IL-1β, IL-6 and IL-10

The cells were cultured in serum-free medium for 8 h and then incubated in medium containing 1, 10, 100 μg/mL of Compounds 5, 18, 20 and 21 for 2 h. The cells were then treated with 10 μg/mL of LPS for 24 h. Ibuprofen (1, 10, 100 μg/mL) was used as a positive control. The supernatants of the cell culture were harvested and centrifuged at 3000× g at 4 °C for 2 min for the analysis of TNF-α, IL-1β, IL-6 and IL-10. Enzyme-linked immunosorbent assays for detecting the cytokines in the supernatants were carried out according to the instructions provided by the manufacturer. Finally, the standard provided with the kits was used to quantify each cytokine in the supernatants [27].

3.6. Characterization of Compounds

Ainsliadimer F (1): colorless, prisms; UV (MeOH) (log ε) λ_max 205 (1.84); [α

]_{D}^{20}

−60.4 (c 0.60, MeOH); IR (KBr) ν_max 3458, 3075, 2931, 2875, 2025, 1774, 1700, 1639, 1456, 1385, 1338, 1311, 1260, 1218, 1183, 1141, 1036, 999, 963, 936, 919, 874, 850, 813 cm⁻¹; ¹H- and ¹³C-NMR data; see Table 1; HRESIMS m/z: 529.2206 [M + Na]⁺ (calcd. for C₃₀H₃₄O₇, 506.2110).

Ainsliadimer G (2): white, amorphous powder; UV (MeOH) (log ε) λ_max 204 (1.42); [α

]_{D}^{20}

−92.6 (c 0.37, MeOH); IR (KBr) ν_max 3491, 3075, 2925, 2851, 2025, 1764, 1735, 1699, 1638, 1447, 1409, 1339, 1311, 1265, 1129, 1080, 1042, 1001, 968, 915, 874, 814, 735 cm⁻¹; ¹H- and ¹³C-NMR data; see Table 1; HRESIMS m/z: 557.2148 [M + Na]⁺ (calcd. for C₃₁H₃₄O₈, 534.2052).

Ainsliadimer H (3): white, amorphous powder; UV (MeOH) (log ε) λ_max 204 (1.40); [α

]_{D}^{20}

−157.0 (c 0.10, MeOH); IR (KBr) ν_max 3490, 3076, 2927, 2868, 2025, 1765, 1736, 1699, 1639, 1446, 1408, 1338, 1310, 1264, 1216, 1129, 1042, 1001, 972, 916, 814 cm⁻¹; ¹H- and ¹³C-NMR data; see Table 1; HRESIMS m/z: 571.2310 [M + Na]⁺, (calcd. for C₃₂H₃₆O₈, 548.2214).

Ainsliadimer I (4): white, amorphous powder; UV (MeOH) (log ε) λ_max 204 (1.35); [α

]_{D}^{20}

−88.5 (c 0.13, MeOH); IR (KBr) ν_max 3447, 2924, 2852, 2025, 1769, 1699, 1445, 1404, 1385, 1307, 1259, 1212, 1138, 1038, 998, 947, 813 cm⁻¹; ¹H- and ¹³C-NMR data; see Table 1; HRESIMS m/z 527.2043 [M + Na]⁺ (calcd. for C₃₀H₃₂O₇, 504.1947).

X-ray crystallographic study of ainsliadimer F (1): Crystal data: λ = 1.54178 Α, T = 193 (2) K, space group P21, 21, 21, a = 8.7146 (4), b = 15.2221 (6), c = 20.7579 (8). V = 2753.6 (2) A³, Z = 4, Dx = 1.309 g/cm³, crystal size: 0.65 × 0.19 × 0.17 mm³.

4. Conclusions

Four new dimeric sesquiterpene lactones, ainsliadimer F–I (1–4), together with seven known dimeric sesquiterpene lactones (5–11) and ten sesquiterpenes (12–21) have been obtained from A. yunnanensis. All of these compounds were reported to be isolated from A. yunnanensis for the first time. Compounds 5, 18, 20 and 21 showed significant activities in anti-inflammatory assays. Additionally, they exhibited good anti-inflammatory effects in a dose-dependent manner. The observed potential anti-inflammatory activity warrants further investigations.

Supplementary Materials

Supplementary materials can be accessed at: https://www.mdpi.com/1420-3049/21/8/1031/s1.

Acknowledgments

The work was financially supported by the National Natural Science Foundation of the People’s Republic of China (Grant Nos. 81274032, 81325024, 81470173) and the Scientific Foundation of Shanghai (Grant No. 15401972200). The authors thank Jun Wang for anti-inflammatory assays.

Author Contributions

Z.-J.W. and W.-S.C. designed the study. X.-L.W. and Z.-J.W. performed the experiment and wrote the manuscript. X.-L.W. and Y.-H.S. analyzed the data. W.-Q.L. and X.-J.X. collected A. yunnanensis. All authors read and approved the final manuscript.

Conflicts of Interest

The authors declare no conflict of interest.

References and Notes

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Sample Availability: Samples of the compounds 1–21 are available from the authors.

Figure 1. Structures of Compounds 1–21.

Figure 2. Single-crystal X-ray structure of Compound 1.

Figure 3. Inhibitory effects of Compounds 5, 18, 20 and 21 (1, 10, 100 μg/mL) on NF-κB in the luciferase activity assay. Data are expressed as the mean ± S.E.M. of three independent experiments. Cell: cultures were not exposed to lipopolysaccharide (LPS); LPS: cultures were subjected to LPS; LPS + Drug: compounds were added to the cultures during LPS; Positive control: LPS + Ibuprofen. ∗ p < 0.05 vs. LPS; ∗∗ p < 0.01 vs. LPS.

Figure 4. Inhibitory effects of Compounds 5, 18, 20 and 21 (1, 10, 100 μg/mL) on TNF-α production stimulated by LPS (10 μg/mL) in RAW 264.7 cells (mouse leukemic monocyte macrophage cell line). Data are expressed as the mean ± S.E.M. of three independent experiments. Cell: cultures were not exposed to lipopolysaccharide (LPS); LPS: cultures were subjected to LPS; LPS + Drug: compounds were added to the cultures during LPS; Positive control: LPS + Ibuprofen. ∗ p < 0.05 vs. LPS; ∗∗ p < 0.01 vs. LPS.

Figure 5. Inhibitory effects of Compounds 5, 18, 20 and 21 (1, 10, 100 μg/mL) on IL-1β production stimulated by LPS (10 μg/mL) in RAW 264.7 cells (mouse leukemic monocyte macrophage cell line). Data are expressed as the mean ± S.E.M. of three independent experiments. Cell: cultures were not exposed to lipopolysaccharide (LPS); LPS: cultures were subjected to LPS; LPS + Drug: compounds were added to the cultures during LPS; Positive control: LPS + Ibuprofen. ∗ p < 0.05 vs. LPS; ∗∗ p < 0.01 vs. LPS.

Figure 6. Inhibitory effects of Compounds 5, 18, 20 and 21 (1, 10, 100 μg/mL) on IL-6 production stimulated by LPS (10 μg/mL) in RAW 264.7 cells (mouse leukemic monocyte macrophage cell line). Data are expressed as the mean ± S.E.M. of three independent experiments. Cell: cultures were not exposed to lipopolysaccharide (LPS); LPS: cultures were subjected to LPS; LPS + Drug: compounds were added to the cultures during LPS; Positive control: LPS + Ibuprofen. ∗ p < 0.05 vs. LPS.

Figure 7. Inhibitory effects of Compounds 5, 18, 20 and 21 (1, 10, 100 μg/mL) on IL-10 production stimulated by LPS (10 μg/mL) in RAW 264.7 cells (mouse leukemic monocyte macrophage cell line). Data are expressed as the mean ± S.E.M. of three independent experiments. Cell: cultures were not exposed to lipopolysaccharide (LPS); LPS: cultures were subjected to LPS; LPS + Drug: compounds were added to the cultures during LPS; Positive control: LPS + Ibuprofen. ∗ p < 0.05 vs. LPS; ∗∗ p < 0.01 vs. LPS.

Table 1. ¹H- (600 MHz) and ¹³C- (150 MHz) NMR spectroscopic data of Compounds 1–4 ^a.

**Table 1.** ¹H- (600 MHz) and ¹³C- (150 MHz) NMR spectroscopic data of Compounds 1–4 ^a.
No.	1		2		3		4
No.	¹H	¹³C	¹H	¹³C	¹H	¹³C	¹H	¹³C
1	-	172.0, qC	-	173.2, qC	-	173.1, qC	-	171.6, qC
2	-	140.2, qC	-	140.6, qC	-	140.8, qC	-	140.4, qC
3	-	208.5, qC	-	206.3, qC	-	206.5, qC	-	208.4, qC
4	2.52 (dd, 7.2, 4.2)	47.0, CH	2.63, m	52.0, CH	2.62, m	51.8, CH	2.56 (dd, 7.1, 4.2)	47.0, CH
5	2.80 (dd, 11.1, 4.1)	54.8, CH	3.52 (dd, 12.3, 5.3)	48.3, CH	3.52 (dd, 11.3, 4.1)	48.5, CH	2.91 (dd, 11.2, 4.2)	55.1, CH
6	4.32 (dd, 11.0, 9.6)	82.6, CH	4.38 (dd, 11.2, 9.8)	82.6, CH	4.36 (dd, 11.3, 9.7)	82.6, CH	4.33 (dd, 11.1, 9.7)	82.6, CH
7	1.84, m	54.9, CH	2.87, m	51.6, CH	2.86, m	51.7, CH	2.75, m	51.6, CH
8	2.05, m 1.85, m	22.5, CH₂	2.16, m 2.08, m	21.0, CH₂	2.11, m 2.03, m	21.0, CH₂	2.10, m 2.02, m	21.0, CH₂
9	1.97, m 1.70, m	36.2, CH₂	2.00, m 1.73, m	36.2, CH₂	1.95, m 1.73, m	36.2, CH₂	1.71, m 1.68, m	36.1, CH₂
10	-	68.1, qC	-	68.4, qC	-	68.4, qC	-	68.3, qC
11	2.35, m	41.9, CH	-	139.5, qC	-	139.6, qC	-	139.4, qC
12	-	178.6, qC	-	170.1, qC	-	170.1, qC	-	170.0, qC
13	1.27 (d, 6.9)	12.6, CH₃	6.23 (d, 3.3) 5.56 (d, 3.0)	119.1, CH₂	6.21 (d, 3.3) 5.54 (d, 3.1)	119.1, CH₂	6.20 (d, 3.2) 5.52 (d, 3.1)	119.1, CH₂
14	1.86, m 1.69, m	36.3, CH₂	2.12, m 1.94, m	36.0, CH₂	2.09, m 1.93, m	36.0, CH₂	1.86, m 1.69, m	36.3, CH₂
15	1.27 (d, 7.1) -	14.3, CH₃	3.94 (dd, 9.5, 2.2) 3.74 (dt, 9.5, 3.2)	69.2, CH₂	3.96 (dd, 9.6, 2.3) 3.76 (dd, 9.7, 3.1)	67.2, CH₂	1.30 (d, 7.2) -	14.2, CH₃
1′	3.22, m	40.0, CH	3.22, m	40.0, CH	3.24 (t, 9.3)	40.0, CH	3.22 (t, 9.0)	40.0, CH
2′	3.22, m 2.63, m	44.7, CH₂	3.22, m 2.63, m	44.8, CH₂	2.68, m 2.62, m	44.8, CH₂	3.23, m 2.64, m	44.7, CH₂
3′	-	222.3, qC	-	222.5, qC	-	222.4, qC	-	222.1, qC
4′	-	50.9, qC	-	50.9, qC	-	50.9, qC	-	50.9, qC
5′	3.20 (d, 4.9)	49.6, CH	3.25 (t, 10.2)	49.6, CH	3.17 (t, 9.3)	49.7, CH	3.19 (t, 8.7)	49.5, CH
6′	4.16 (t, 9.4)	83.9, CH	4.19 (t, 9.2)	83.9, CH	4.18 (t, 9.8)	83.8, CH	4.17 (t, 9.2)	83.9, CH
7′	3.00, m	43.5, CH	3.05, m	43.4, CH	3.03, m	43.5, CH	3.01, m	43.5, CH
8′	2.31, m 1.47, m	31.9, CH₂	2.35, m 1.51, m	32.0, CH₂	2.33, m 1.51, m	32.0, CH₂	2.35, m 1.48, m	31.9, CH₂
9′	2.64, m 2.20, m	39.5, CH₂	2.65, m 2.24, m	39.5, CH₂	2.64, m 2.23, m	39.5, CH₂	2.65, m 2.22, m	39.5, CH₂
10′	-	150.1, qC	-	150.2, qC	-	150.2, qC	-	150.1, qC
11′	-	138.5, qC	-	138.6, qC	-	138.5, qC	-	138.4, qC
12′	-	169.3, qC	-	169.4, qC	-	169.2, qC	-	169.3, qC
13′	6.26 (d, 3.4) 5.58 (d, 3.0)	121.6, CH₂	6.29 (d, 3.4) 5.60 (d, 3.0)	121.5, CH₂	6.27 (d, 3.4) 5.59 (d, 3.0)	121.5, CH₂	6.27 (d, 3.4) 5.58 (d, 3.0)	121.7, CH₂
14′	5.09, brs 4.72, brs	114.1, CH₂	5.12, brs 4.75, brs	114.1, CH₂	5.11, brs 4.74, brs	114.1, CH₂	5.09, brs 4.72, brs	114.1, CH₂
15′	2.13, m 2.02, m	25.8, CH₂	2.12, m 2.07, m	25.9, CH₂	2.12, m 2.07, m	25.9, CH₂	2.11, m 1.97, m	25.8, CH₂
1″	-	-	3.29, s	59.2, OCH₃	3.42 (dd, 7.0, 3.5)	66.8, OCH₂	-	-
2″	-	-	-	-	1.06 (t, 7.0)	15.0, CH₃	-	-

^a 1–4 was measured in CDCl₃.

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Wu, X.-L.; Xiong, X.-J.; Lu, W.-Q.; Huang, H.; Shen, Y.-H.; Wu, Z.-J.; Chen, W.-S. New Sesquiterpenenoids from Ainsliaea yunnanensis. Molecules 2016, 21, 1031. https://doi.org/10.3390/molecules21081031

AMA Style

Wu X-L, Xiong X-J, Lu W-Q, Huang H, Shen Y-H, Wu Z-J, Chen W-S. New Sesquiterpenenoids from Ainsliaea yunnanensis. Molecules. 2016; 21(8):1031. https://doi.org/10.3390/molecules21081031

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Wu, Xiang-Lei, Xiao-Juan Xiong, Wen-Quan Lu, Hao Huang, Yun-Heng Shen, Zhi-Jun Wu, and Wan-Sheng Chen. 2016. "New Sesquiterpenenoids from Ainsliaea yunnanensis" Molecules 21, no. 8: 1031. https://doi.org/10.3390/molecules21081031

APA Style

Wu, X.-L., Xiong, X.-J., Lu, W.-Q., Huang, H., Shen, Y.-H., Wu, Z.-J., & Chen, W.-S. (2016). New Sesquiterpenenoids from Ainsliaea yunnanensis. Molecules, 21(8), 1031. https://doi.org/10.3390/molecules21081031

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New Sesquiterpenenoids from Ainsliaea yunnanensis

Abstract

1. Introduction

2. Results and Discussion

2.1. Structure Elucidation of New Compounds

2.2. Chemotaxonomic Significance

2.3. Evaluation of Biological Activity

3. Experimental Section

3.1. General Procedures

3.2. Plant Material

3.3. Extraction and Isolation

3.4. Luciferase Assay

3.5. Measurement of TNF-α, IL-1β, IL-6 and IL-10

3.6. Characterization of Compounds

4. Conclusions

Supplementary Materials

Acknowledgments

Author Contributions

Conflicts of Interest

References and Notes

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