- freely available
Molecules 2014, 19(4), 4548-4559; doi:10.3390/molecules19044548
Published: 11 April 2014
Abstract: Four new withanolides named dmetelins A–D (compounds 1–4), along with the known compound 7α,27-dihydroxy-1-oxo-witha-2,5,24-trienolide (5) were isolated from the leaves of Datura metel L. (Solanaceae). Their structures were elucidated on the basis of detailed analysis of 1D and 2D NMR and mass spectrometry data. All the compounds were evaluated for their inhibitory effects on lipopolysaccharide (LPS)-induced nitric oxide (NO) production in RAW 264.7 cells. Compounds 1, 4 and 5 showed significant inhibitory activities, and compounds 2 and 3 showed moderate inhibitory activities with IC50 values of 17.8, 11.6, 14.9, 33.3 and 28.6 μM, respectively.
Withasteroids are a group of structurally diverse steroidal compounds with a C28 steroidal lactone skeleton, in which a characteristic feature is the presence of an α,β-unsaturated δ lactone ring in the side chain. They are presented primarily in the Solanaceae family, which includes Datura, Acnistus, Dunalia, Jaborosa, Physalis and Withania . The isolation and synthesis of withanolides have received considerable attention due to their significant biological activities, which include antitumor , cytotoxic [3,4], immunosuppressive , anti-inflammatory [5,6], and chemoprevention properties .
Flos daturae (baimantuoluo in Chinese), the dry flowers of Datura metel L. (Solanaceae), known as “Yangjinhua”, have been widely used in Traditional Chinese Medicine for the treatment of coughs, asthma, rheumatism, pain, and convulsions for centuries . It has also been reported that it displayed the most promising effects in treatment of psoriasis and were used in a clinical application at the First Affiliated Hospital of Heilongjiang University of Chinese Medicine (Heilongjiang, China) [9,10]. Withanolides have been studied for treating psoriasis as the main constituents of the effective part of flowers of D. metel [11,12]. Baimantuoluolines A–J, and baimantuoluosides A–H were also isolated and reported [8,13,14,15,16,17,18]. However, the dry flowers of D. metel have the disadvantages of long florescence and low yield in comparison to its leaves. At the same time, the leaves of this herb, which can be regenerated every year, were typically discarded. In order to expand the available resources, our group found that the leaves of D. metel have some similarities in chemical constituents with its flowers and significant advantages in terms of high and stable yield. As a result, four new withanolides were isolated and named dmetelins A–D (compounds 1–4), together with one known withanolide, 7α,27-dihydroxy-1-oxowitha-2,5,24-trienolide (5)  (Figure 1). The structures of compounds 1–5 were determined by the interpretation of spectroscopic analysis, including 1D and 2D NMR spectroscopy. All isolates were identified as major active constituents having inhibitory effects of NO production in LPS-activated macrophage cell line, RAW 264.7 murine macrophages. Herein, we report the isolation, structural elucidation, and NO inhibitory effects of these isolates.
2. Results and Discussion
Compound 1 was isolated as a white amorphous powder, and its molecular formula was determined to be C28H40O5 by HRESIMS (m/z 479.2779 [M+Na]+). The UV spectrum showed an absorption maximum at 224 nm, suggesting the presence of an α,β-unsaturated δ lactone, and carbonyl groups, respectively . The 1H-NMR spectrum of 1 (Table 1) displayed the characteristic signals of the common withanolide steroid. Three tertiary methyl groups at δ 0.78 (3H, s), 1.28 (3H, s), 2.10 (3H, s), and a secondary methyl group at 1.04 (3H, d, J = 6.6 Hz) were attributed to Me-18, Me-19, Me-28, and Me-21, respectively. The Me-27 signal was replaced by one set of oxygen-bearing methylene protons δ 4.37 (1H, d, J = 11.7 Hz) and 4.29 (1H, d, J = 11.7 Hz). An olefinic proton at δ 5.70 (1H, dd, J = 5.3, 1.2 Hz) showed 1H-1H COSY correlation peaks with H-7 δ 3.77 (1H, t, J = 3.8 Hz) (Figure 2), which was assigned to the vinylic protons H-6. The 13C-NMR spectrum of 1 (Table 2) revealed 28 carbons. It was composed of four methyl groups at δ 12.1 (C-18), 18.7 (C-19), 13.8 (C-21), and 20.2 (C-28). The presence of four olefin carbons at δ 146.6, 125.9, 157.9, and 126.4 were attributed to C-5, C-6, C-24, and C-25, respectively. The characteristic downfield at δ 215.9 and 168.6 were due to a carbonyl group C-1 and a lactone carbonyl group C-26. The signals at δ 65.1, 80.2, and 56.4 were assigned to the three oxygen-bearing carbons at C-7, C-22, and C-27. Assignments of all function groups of 1 were achieved by 1H-1HCOSY, HMBC and HSQC (Figure 2). Thus, the planar structure of 1 was determined as shown.
|Table 1. 1H-NMR data (400 MHz) of the aglycones of 1–4 (in CD3OD, δ in ppm).|
|1||3.88 br s|
|2||2.32 m, 2.67 m||1.85 m, 2.24 m||5.86 dd (10.0, 2.4)||5.84 dd (10.0, 2.5)|
|3||2.00 m, 1.62 m||4.11 t (7.4)||6.93 ddd (10.0, 4.8, 2.4)||6.91 ddd (10.0, 4.8, 2.5)|
|4||2.22 m, 2.63 m||5.48 br s||3.44 m||3.40 m|
|2.96 dd (21.5, 4.8)||2.93 dd (21.4, 4.8)|
|6||5.70 dd (5.3, 1.2)||5.98 dd (10.0, 2.3)||5.80 dd (5.8, 1.5)||5.48 br s|
|7||3.77 t (3.8)||5.63 br d (10.0)||3.80 t (5.5)||3.71 d (8.4)|
|8||1.43 m||2.07 m||1.46 m||1.42 m|
|9||1.99 m||1.54 m||2.00 m||1.68 m|
|11||1.50 m, 1.73 m||1.44 m, 1.66 m||1.59 m, 2.23 m||1.53 m, 2.24 m|
|12||1.29 m, 1.97 m||1.32 m, 2.03 m||1.34 m, 2.03 m||1.32 m, 2.04 m|
|14||1.54 m||1.24 m||1.32 m||1.24 m|
|15||1.78 m, 1.19 m||1.85 m, 1.37 m||1.84 m, 1.22 m||1.92 m, 1.53 m|
|16||1.79 m, 1.41 m||1.83 m, 1.43 m||1.83 m, 1.41 m||1.78 m, 1.37 m|
|17||1.24 m||1.30 m||1.28 m||1.22 m|
|18||0.78 s||0.82 s||0.79 s||0.80 s|
|19||1.28 s||1.00 s||1.24 s||1.28 s|
|20||1.95 m||1.98 m||1.98 m||1.94 m|
|21||1.04 d (6.6)||1.03 d (6.7)||1.05 d (6.6)||1.04 d (6.6)|
|22||4.47 dt (13.2, 3.4)||4.47 dt (13.3, 3.4)||4.50 dt (13.5, 3.6)||4.48 dt (13.2, 3.4)|
|23||2.56 dd (17.8, 13.7)||2.54 dd (18.0, 13.4)||2.58 dd (17.9, 13.6)||2.54 dd (18.0, 13.5)|
|2.18 dd (17.8, 3.4)||2.21 dd (18.0, 3.3)||2.22 dd (17.9, 3.0)||2.20 dd (18.0, 3.1)|
|27||4.29 d (11.7)||4.36 d (11.7)||4.47 d (11.2)||4.37 d (11.7)|
|4.37 d (11.7)||4.29 d (11.7)||4.62 d (11.2)||4.29 d (11.7)|
|28||2.10 s||2.10 s||2.14 s||2.10 s|
|Table 2. 13C-NMR (100 MHz) data of the aglycones of 1–4 (in CD3OD, δ in ppm).|
The configuration of compound 1 (Figure 3) was established by NOE correlations. Me-18/Me-21, H-20, H-16β, H-20/H-16β, and H-16/H-22 determined that C-20 of 1 had an S configuration. According to the literature [3,18], an α-oriented H-22 atom gives rise to H-22/H-23 values of 0.5–4.0 and 9.0–13.8 Hz, whereas the β-oriented form shows values of 2.5-7.0 and 2.0-5.0 Hz. Thus, the configuration of 1 at C-22 was determined as R due to the H-22 coupling constants (J = 3.4, 13.2 Hz). The orientation of hydroxyl group at C-7 was also deduced from the NOESY spectrum (Figure 3). The NOE correlations of Me-18/H-8β and H-8β/H-7β suggested the β-orientation of H-7 and α orientation of the 7-OH group. On the basis of the spectroscopic studies, the structure of 1 was fully established, and determined to be 7α,27-dihydroxy-(20S,22R)-1-oxo-witha-5,24-dienolide and given the trivial name dmetelin A.
Compound 2 was obtained as a white amorphous powder with the molecular formula C29H42O5, established by positive HRESIMS from the [M+Na]+ signal at m/z 493.2921. The NMR data of 2 exhibited a close resemblance to those of 1, and differences between them were observed only in their A/B rings. The NMR data of 1 showed a conjugated diene system composed of a disubstituted double bond (δ 5.98 and 130.1, δ 5.63 and 132.1), together with one trisubstituted double bond (δ 5.48, 143.3, and 123.4). The presence of an oxygenated methine at δ 72.5 (C-1) instead of the keto carbon in 1 implied that a hydroxyl group was attached to C-1. The HMBC correlations of δ 2.24 (H-2)/123.4, 2.07 (H-8)/130.1, and 1.54 (H-9)/132.1 suggested that the conjugated diene system was located at C-4, C-5, C-6, and C-7 (Figure 2). A three proton singlet at δ 3.38 (3H, s) was due to -OCH3 group, which was located at C-3 on the basis of δ 3.38/75.4 (C-3) observed in its HMBC spectrum (Figure 2). The orientation of the hydroxyl group at C-1 was assigned as α on the basis of the small coupling constants of H-1 δ 3.88 (1H, br s)/H-2. Furthermore, the NOESY correlation of Me-19/H-1β also supported the α orientation of 1-OH. In addition, NOEs between Me-19/H-2β and H-2α/H-3α suggested a β orientation of 3-OCH3. The configuration of C-20 and C-22 were in good agreement with that of 1. Consequently, compound 2 was identified as 1α,3β,27-trihydroxy-(20S,22R)-1-oxo-witha-4,6,24-trienolide and given the common name dmetelin B.
Compound 3 was isolated as a white amorphous powder. The HRESIMS spectrum showed peaks at 801.3694 [M+Na]+, corresponding to the molecular formula C40H58O15. The NMR spectra (Table 1 and Table 2) of 3 showed four methyl groups at δ 0.79 (3H, s, Me-18), 1.24 (3H, s, Me-19), 1.05 (3H, d, J = 6.6 Hz, Me-21), and 2.14 (3H, s, Me-28), two α, β-unsaturated olefinic protons at δ 5.86 (1H, dd, J = 10.0, 2.4 Hz, H-2) and 6.93 (1H, ddd, J = 10.0, 4.8, 2.4 Hz, H-3), along with one olefinic proton at δ 5.80 (1H, dd, J = 5.8, 1.5 Hz, H-6), which supported a withanolide possessing a 2, 5-dien-1-one system in rings A/B . Apart from the glycosidic signals, compound 3 displayed 28 carbons. The signals at δ 160.4, 123.6 and 168.6 were assigned to C-24, C-25 and C-26 of the α, β-unsaturation δ lactone ring respectively, in the six-member ring E. Two anomeric protons doublets at δ 4.34 (1H, d, J = 7.8 Hz, H-1′) and 4.41 (1H, d, J = 7.8 Hz, H-1″) were correlated to two anomeric carbons at δ 103.9 (C-1′) and 104.9 (C-1″), in its HSQC spectrum (Figure 2), which suggested that 3 contained a diglycosidic moiety. The attachment of one glucose unit to C-27 of the aglycone was confirmed by the HMBC correlations (Figure 2) observed from H-1′ to C-27. Other HMBC correlations to glucose linkages (Figure 2) were H-1″/C-6′ and H-6′/C-1″. The orientation of 7-OH could be deduced by Me-18/H-8β and H-8β/H-7β observed in the NOESY spectrum, which suggested that 7-OH has an α orientation. The configuration of C-20 and C-22 of 3 were established to be identical to those of 1 by their similar NOESY correlations, as depicted on the 3D structure (Figure 3). Hence, 3 was identified as 7α,27-dihydroxy-(20S,22R)-1-oxo-witha-2,5,24-trienolide-27-O-β-d-glucopyranosy-(6′→1″)-β-d-glucopyranoside and assigned the common name dmetelin C.
Compound 4 was obtained as a white amorphous powder. The molecular formula C28H38O5 was deduced from the HRESIMS with [M+H]+ at m/z 455.2715 (calcd. for C28H39O5, 455.2797). The NMR data of 4 (Table 1 and Table 2) were very similar to those of 7α,27-dihydroxy-1-oxowitha-2,5,24-trienolide , also isolated as compound 5 during this work. A comparison of the 13C-NMR data of these two compounds indicated that they have the same planar structure. The key differences were the signals for carbons around C-7, which suggested that these two compounds should have different orientations of the hydroxyl group at C-7. The orientation of 7-OH was deduced by the NOE observed for Me-18/H-12β, H-12α/H-9α, and H-9α/H-7α in the NOESY experiment (Figure 3), indicating the α-orientation of H-7 and β-orientation of the 7-OH group. The configuration of C-20 and C-22 were also akin to those of compound 1. Therefore, the structure of 4 was identified as 7β,27-dihydroxy-(20S,22R)-1-oxo-witha-2,5,24-trienolide and given the common name dmetelin D.
Since NO acts as an inflammatory mediator, inhibitors of NO production may exhibit therapeutic potential for the treatment of inflammation with overproduction of NO. Withanolides display great anti-inflammatory activity [22,23,24], so the compounds were evaluated for their effects on the inhibition of NO production in LPS-activated RAW264.7 cells . In our experiment, the assayed compounds were first dissolved in DMSO, and the final concentration 0.2% (v/v) in cell culture supernatants did not show any effect on the assay systems. The effect of compounds 1–5 on cell viability was evaluated by the MTT assay to ascertain the absence of cytotoxicity (over 90% cell survival) to macrophage cells at the concentration of 100 μM. The inhibitory effects of withanolides (Figure 4A) were evaluated by LPS-induced NO generation in RAW 264.7 cells. Compounds 1, 4 and 5 presented the significant anti-inflammatory activity, with IC50 values of 17.8, 11.6 and 14.9 μM, respectively. l-NMMA (IC50 = 13.1 μM) was used as positive control. Compounds 2 and 3 revealed moderate anti-inflammatory activity, with IC50 values of 33.3 and 28.6 μM (Figure 4B).
3. Experimental Section
Optical rotations were measured using a Perkin-Elmer 341 polarimeter. UV spectra were obtained on a Shimadzu UV-1601 instrument. IR spectra were recorded on a Shimadzu FTIR-8400S. NMR spectra were recorded in MeOH using TMS as an internal standard on Bruker DPX 400 instrument (400 MHz for 1H NMR and 100 MHz for 13C NMR). Chemical shifts (δ) were expressed in ppm with reference to the solvent signals. HRESIMS was recorded on IonSpec Ultima 7.0 FTICR; GC analysis was performed on Agilent 7890A-5975C gas chromatograph equipped with a DB-1701 column (60 m × 0.25 mm × 0.25 μm, film thickness); detection Triple-Axis Detector; Preparative HPLC (Waters, Delta 600-2487) was measured by Hypersil-ODS II (10 μm, 20 × 300 mm, Yilite, Da Lian, China); Column chromatography (CC) was carried out using silica gel of 200–300 mesh size (Qingdao Marine Chemical Ltd, Qingdao, China); All the solvents were of analytical grade and were purchased from TianJinFuYu Company Ltd. (Tianjin, China)
3.2. Plant Material
The leaves of D. metel were collected at Lingao County, Hainan Province, People’s Republic of China, in September 2012, and was identified by Prof. Zhenyue Wang (Department of Chinese Medicine Resources, Heilongjiang University of Chinese Medicine). A voucher specimen (2012184) has been deposited at the Herbarium of Heilongjiang University of Chinese Medicine, P. R. China.
3.3. Extraction and Isolation
The air-dried leaves of D. metel (16 kg) were extracted with 75% EtOH (100 L × 3.0 h × 3) at room temperature. The 75% EtOH extract was evaporated under vacuum (45 °C) to yield a residue (1.75 kg), which was suspended in water and then sequentially extracted with petroleum ether (PE) and EtOAc. The EtOAc portion of the extract (226 g) was chromatographed on silica gel with CH2Cl2/MeOH (30:1 → 0:1, v/v) to afford Fractions A–E. Fraction B (36.2 g) was rechromatographed on a silica gel column (CH2Cl2/MeOH 25:1 → 0:1, v/v) to give five subfractions (B1-B5). Compound 5 (22 mg) was obtained from fraction B2 after purification by CC using (CH2Cl2/MeOH 20:1 → 0:1, v/v), Subfraction B3 was further purified by ODS column, eluting with MeOH/H2O (1:9 → 1:0, v/v) to yield 4 (28 mg). Subfraction B4 was chromatographed over a ODS column (MeOH/H2O 2:8 → 1:0, v/v) and semi-preparative HPLC (66% MeOH/H2O, flow rate 3 mL/min) to give 1 (18 mg, tR = 39.1 min), and 2 (15 mg, tR = 45.3 min). Fraction E (11.6 g) was purified by CC and eluted with CH2Cl2/MeOH (10:1 → 0:1, v/v) to afford three subfractions (E1–E3), and Subfraction E3 was further purified by semi-preparative HPLC (40% MeOH/H2O, flow rate 3 mL/min) to yield 3 (15 mg, tR = 25.6 min).
Dmetelin A (1). + 28.0 (c = 0.10, MeOH); UV (MeOH) λmax (logε): 224 (4.37) nm; IR (KBr) vmax: 3401, 3169, 2933, 2688, 1701, 1689, 1262, 1068, 1023, 821 cm−1; 1H and 13C-NMR data, see Table 1 and Table 2; HRESIMS m/z: 479.2779 [M+Na]+ (calcd. for C28H40O5Na, 479.2773).
Dmetelin B (2). + 16.0 (c = 0.10, MeOH); UV (MeOH) λmax (logε): 225 (5.60) nm; IR (KBr) vmax: 3367, 2963, 2869, 1685, 1388, 1075 cm−1; 1H and 13C-NMR data, see Table 1 and Table 2; HRESIMS m/z 493.2921 [M+Na]+ (calcd. for C29H42O5Na, 493.2930).
Dmetelin C (3). + 44.0 (c = 0.10, MeOH); UV (MeOH) λmax (logε): 222 (5.28) nm; IR (KBr) vmax: 3400, 2937, 2360, 2349, 1716, 1695, 1681, 1219, 1126, 1028 cm−1; 1H and 13C-NMR data, see Table 1, Table 2, and Table 3; HRESIMS m/z 801.3694 [M+Na]+ (calcd. for C40H58O15Na, 801.3673).
Dmetelin D (4). + 20.0 (c = 0.10, MeOH); UV (MeOH) λmax (logε): 221 (6.52) nm; IR (KBr) vmax: 3402, 3367, 3129, 2963, 2915, 2869, 1685, 1075, 799 cm−1; 1H and 13C-NMR data, see Table 1 and Table 2; HRESIMS m/z 455.2715 [M+H]+ (calcd. for C28H39O5, 455.2797).
|Table 3. 1H- and 13C-NMR data (400/100 MHz) data of the glycosyl groups for 3 (in CD3OD, δ in ppm).|
|1′||4.34 d (7.8)||103.9||1″||4.41 d (7.8)||104.9|
|2′||3.18 t (8.9)||75.2||2″||3.36 t (9.2)||75.0|
|3′||3.41 m||77.9||3″||3.30 m||78.0|
|4′||3.28 m||71.7||4″||3.36 m||71.5|
|5′||3.43 m||77.2||5″||3.30 m||78.0|
|6′||3.78 dd (11.6, 5.8)||69.9||6″||3.68 dd (11.8, 5.0)||62.8|
|4.16 dd (11.6, 1.8)||3.86 dd (11.8, 2.0)|
3.4. Acid Hydrolysis of Compound 3 and GC Analysis
Compound 3 (2.0 mg) was refluxed with H2O (2 mL) and 2 N aqueous HCl (1 mL) at 80 °C on a water bath for 3 h. After that time, the reaction mixture was extracted with ethyl acetate (3 × 5 mL). The aqueous layer was neutralized with 2 M NaHCO3 and then evaporated to dryness. The residue of sugar was dissolved in 1 mL anhydrous pyridine and treated with l-cysteine methyl ester hydrochloride (1.5 mg) stirred at 60 °C for 1 h. HMDS-TMCS (150 μL hexamethyldisilazane-trimethylchlorosilane, 3:1) was added and the mixture was kept at 60 °C for another 30 min. The precipitate was centrifuged off, and the supernatant was concentrated under a N2 stream. The mixture was partitioned between n-hexane and H2O (0.1 mL each), and the hexane extracted (1 μL) was analyzed on an Agilent 7890A-5975C gas chromatograph equipped with a DB-1701 column (60 m × 0.25 mm × 0.25 μm, film thickness) under the following conditions: firstly temperature was maintained at 50 °C, secondly raising to 190 °C at the rate of 40 °C/min, thirdly raising the temperature to 200 °C at the rate of 0.5 °C/min, fourthly raising the temperature to 210 °C at the rate of 1 °C/min, finally, raising the temperature to 280 °C at the rate of 20 °C/min. The carrier gas was He (1.0 mL/min), injector temperature: 250 °C; and split ratio: 1/20. By comparison of the retention times of authentic samples of d-glucose, the absolute configurations of the sugar residues were gave to be d-glucose (tR = 17 min).
3.5. Cell Culture
Raw 264.7, a murine macrophage cell line was purchased from the Cell Bank of the Chinese Academic of Sciences, (Shanghai, China) and maintained in supplemented with 10% Fetal Bovine Serum (Hyclone, Logan City, UT, USA), penicillin (100 U/mL) and streptomycin (100 μg/mL) at 37 °C in a humidified incubator with 5% CO2.
3.6. Cell Viability Assay
Cell viability was assessed using the MTT assay as described previously [26,27]. In brief, RAW 264.7 cells were seeded into a 96-well plate at a density of 1.0 × 105 cells per well and incubated at 37 °C for 24 h. The cells were then treated with various concentrations of the samples. The maximum concentration of vehicle (dimethylsulfoxide, DMSO) in the culture media was 0.2% (v/v). After an additional 24 h incubation at 37 °C, 100 μL of MTT (0.5 mg/mL in PBS) was added to the wells, and the incubation continued for another 2 h. The medium was then discarded and 150 μL DMSO was added. The resulting color was assayed at 540 nm using a microplate reader (Molecular Devices, San Francisco, CA, USA).
3.7. The Determination of NO Production from RAW 264.7
To evaluate the effective of the tested materials on LPS-induced NO production, Raw 264.7 macrophages in 10% FBS-DMEM were plated at densities of 1.0 × 105 cell/wells in 96-well plates and grew overnight, after incubation, 20 μL serially diluted drugs (DMSO+serum-free DMEM as solvent) were applied to the cells for 4 h, and incubated in the medium with 20 μL LPS (lipopolysaccharide) of 1 μg/mL in the presence or absence of test samples for 24 h. Then, cells were dispensed into 96-well plates. One hundred μL of each supernatant was mixed with the same volume of Griess reagent  (1% sulfanilamide in 5% H3PO4 and 0.1% N-1-naphthyletylenediamide dihydrochloride) and incubated at room temperature, away from the light, for 10 min. The absorbance was measured at 540 nm using an ELISA reader (PerkinElmer, Waltham, MA, USA), and the concentration of nitrite was calculated by comparison with a sodium nitrite standard curve. For this assay, N-monomethyl-l-arginine (l-NMMA) was used as positive control. Three independent experiments were performed, with each one in triplicate.
3.8. Statistical Analysis
The IC50 values, the sample concentrations resulting in 50% inhibition of NO production, were determined by using nonlinear regression analysis (Sigma Plot 8.0; SPSS Inc. Chicago, IL, USA). The data are presented as mean ± S.D. of more than three independent experiments.
This study demonstrated that the leaves of D. metel were rich in withanolides, showing a similar structure as compounds found in its flowers. Moreover, five withanolides, including four new compounds 1–4, were isolated and identified, and these compounds were found to be responsible for the ability to inhibit NO production by activated macrophages. According to our results, further phytochemical and pharmacological studies of leaves D. metel are clearly worthwhile.
This work was financed by the Outstanding Young Scientists Program of Heilongjiang Province (No. JC201105).
Prof. Q.-H. W. and Prof. H.-X. K. were responsible for guarantor of integrity of entire study. Prof. B.-Y. Y. is responsible for study concepts. R. G. and L. T. performed research. G. R. and Y. L. analyzed data. C.-F. W., Z.-P. S. and Z.-B. W. are responsible for Statistical analysis. J. Z., Y.-G. X. and H. J. are responsible for manuscript preparation. Prof. B.-Y. Y. and R. G. wrote the paper. Prof. Q.-H. W. and H.-X. K. approved for manuscript final version.
Conflicts of Interest
The authors declare no conflict of interest.
- Zhang, H.P.; Samadi, A.K.; Gallagher, R.J.; Araya, J.J.; Tong, X.Q.; Day, V.W.; Cohen, M.S.; Kindscher, K.; Gollapudi, R.; Timmermann, B.N. Cytotoxic withanolide constituents of Physalis longifolia. J. Nat. Prod. 2011, 74, 2532–2544. [Google Scholar] [CrossRef]
- Jayaprakasam, B.; Zhang, Y.J.; Seeram, N.P.; Nair, M.G. Growth inhibition of human tumor cell lines by withanolides from Withania somnifera leaves. Life Sci. 2003, 74, 125–132. [Google Scholar] [CrossRef]
- Minguzzi, S.; Barata, L.S.; Shin, Y.G.; Jonas, P.F.; Chai, H.B.; Park, E.J.; Pezzuto, J.M.; Cordell, G.A. Cytotoxic withanolides from Acnistus arborescens. Phytochemistry 2002, 59, 635–641. [Google Scholar] [CrossRef]
- Habtemariam, S. Cytotoxicity and immunosuppressive activity of withanolides from Discopodium penninervium. Planta Med. 1997, 63, 15–17. [Google Scholar] [CrossRef]
- Jayaprakasam, B.; Nair, M.G. Cyclooxygenase-2 enzyme inhibitory withanolides from Withania somnifera leaves. Tetrahedron 2003, 59, 841–849. [Google Scholar] [CrossRef]
- Budhiraja, R.D.; Sudhir, S.; Garg, K.N. Antiinflammatory Activity of 3 β-Hydroxy-2,3-dihydro-withanolide F. Planta Med. 1984, 50, 134–136. [Google Scholar] [CrossRef]
- Su, B.N.; Park, E.J.; Nikolic, D.; Santarsiero, B.D.; Mesecar, A.D.; Vigo, J.S.; Graham, J.G.; Cabieses, F.; Breemen, R.B.; Fong, H.H.S.; et al. Activity-guided isolation of novel norwithanolides from Deprea subtriflora with potential cancer chemopreventive activity. J. Org. Chem. 2003, 68, 2350–2361. [Google Scholar]
- Kuang, H.X.; Yang, B.Y.; Xia, Y.G.; Wang, Q.H. Two new withanolide lactones from Flos Daturae. Molecules 2011, 16, 5833–5839. [Google Scholar] [CrossRef]
- Tang, L.; Wang, Q.H.; Yang, B.Y.; Xiao, H.B.; Sun, Y.P.; Kuang, H.X. Protective effects of active fraction and constituents from Flos Daturae on Chinese hamster ovary cells injuried by dimethyl sulfoxide. In Chin. Trad. Herbal Drug.; 2006; Volume 37, pp. 1826–1831.(In Chinese). [Google Scholar]
- Wang, Y.X. The report on Traditional Chinese medicine yangjinhua (Datura metel) is given priority to treat 242 patients with psoriasis. J. Trad. Chin. Med. 1985, 35, 32–33.(In Chinese). [Google Scholar]
- Wang, Q.H.; Xiao, H.B.; Yang, B.Y.; Yao, F.Y.; Kuang, H.X. Studies on pharmacological actions of the effective parts for psoriasis in Flos Daturae (I). Chin. J. Exp. Trad. Med. Formulae 2008, 14, 49–51.(In Chinese). [Google Scholar]
- Wang, Q.H.; Xiao, H.B.; Yang, B.Y.; Yao, F.Y.; Kuang, H.X. Studies on pharmacological actions of the active parts in Flos Daturae for psoriasis (II). Chin. J. Exp. Trad. Med. Formulae 2008, 14, 32–34.(In Chinese). [Google Scholar]
- Yang, B.Y.; Wang, Q.H.; Xia, Y.G.; Feng, W.S.; Kuang, H.X. Withanolide compounds from the flower of Datura metel L. Helv. Chim. Acta 2007, 90, 1522–1528. [Google Scholar] [CrossRef]
- Yang, B.Y.; Wang, Q.H.; Xia, Y.G.; Feng, W.S.; Kuang, H.X. Baiman-tuoluolines D–F, three new withanolides from the lower of Datura metel L. Helv. Chim. Acta 2008, 91, 964–971. [Google Scholar] [CrossRef]
- Yang, B.Y.; Xia, Y.G.; Wang, Y.Y.; Wang, Q.H.; Kuang, H.X. Two novel norwithasteroids with unusual Six- and seven-membered ether rings in side chain from flos Daturae. Evid. Based Complement. Alternat. Med. 2013. [Google Scholar] [CrossRef]
- Kuang, H.X.; Yang, B.Y.; Tang, L.; Xia, Y.G.; Dou, D.Q. Baimantuoluosides A-C, Three new withanolide glucosides from the flower of Datura metel L. Helv. Chim. Acta 2009, 92, 1315–1323. [Google Scholar] [CrossRef]
- Yang, B.Y.; Xia, Y.G.; Wang, Q.H.; Dou, D.Q.; Kuang, H.X. Baimantuoluosides D–G, four new withanolide glucosides from the lower of Datura metel L. Arch. Pharm. Res. 2010, 33, 1143–1148. [Google Scholar] [CrossRef]
- Yang, B.Y.; Xia, Y.G.; Liu, Y.; Li, L.; Jiang, H.; Yang, L.; Wang, Q.H.; Kuang, H.X. New antiproliferaive and immunosuppressive withanolides from the seeds of Datura metel. Phytochem. Lett. 2014, 8, 92–96. [Google Scholar] [CrossRef]
- Ma, L.; Xie, C.M.; Li, J.; Lou, F.C.; Hu, L.H. Daturametelins H, I, and J: Three new withanolide glycosides from Datura metel L. Chem. Biodivers. 2006, 3, 180–186. [Google Scholar] [CrossRef]
- Pavia, D.L.; Lampman, G.M.; Kriz, G.S. Introduction to Spectroscopy, 1st ed.; Saunders College Publishing Co.: Philadelphia, PA, USA, 1979; pp. 41–60. [Google Scholar]
- Rahman, A.U.; Shahwar, D.E.; Naz, A.; Choudhary, M.I. Withanolides from Withania coagulans. Phytochemistry 2003, 63, 387–390. [Google Scholar] [CrossRef]
- Chao, C.H.; Chou, K.J.; Wen, Z.H.; Wang, G.H.; Wu, Y.C.; Dai, C.F.; Sheu, J.H. Paraminabeolides A–F, cytotoxic and anti-inflammatory marine withanolides from the Soft Coral Paraminabea acronocephala. J. Nat. Prod. 2011, 74, 1132–1141. [Google Scholar] [CrossRef]
- Haq, I.U.; Youn, U.J.; Chai, X.; Park, E.J.; Kondratyuk, T.P.; Simmons, C.J.; Borris, R.P.; Mirza, B.; Pezzuto, J.M.; Chang, L.C. Biologically active withanolides from Withania coagulans. J. Nat. Prod. 2013, 76, 22–28. [Google Scholar] [CrossRef]
- Maldonado, E.; Amador, S.; Martínez, M.; Pérez-Castorena, A.L. Virginols A-C, three new withanolides from Physalis virginiana. Steroids 2010, 75, 346–349. [Google Scholar] [CrossRef]
- Lai, P.K.K.; Chan, J.Y.W; Wu, S.B.; Cheng, G.K.; Ho, G.K.W.; Lau, C.P.; Kennelly, E.J.; Leung, K.P. Anti-inflammatory activities of an active fraction isolated from the root of Astragalus memberanaceus in Raw 264.7 Macrophages. Phytother. Res. 2013. [Google Scholar] [CrossRef]
- Wu, S.B.; Su, J.J.; Sun, L.H.; Wang, W.X.; Zhao, Y.; Li, H.; Zhang, S.P.; Dai, G.H.; Wang, C.G.; Hu, J.F. Triterpenoids and steroids from the fruits of Melia toosendan and their cytotoxic effects on two human cancer cell lines. J. Nat. Prod. 2010, 73, 1898–1906. [Google Scholar] [CrossRef]
- Wu, S.B.; Fan, H.; Wen, Y.; Zhang, H.F.; Zhao, Y.; Hu, J.F. Antiproliferative and apoptotic activities of linear furocoumarins from Notopterygium incisum on cancer cell lines. Planta Med. 2010, 76, 82–85. [Google Scholar] [CrossRef]
- Green, L.C.; Wagner, D.A.; Glogowski, J.; Skipper, P.L.; Wishnok, J.S.; Tannenbaum, S.R. Analysis of nitrate, nitrite, and [15N]nitrate in biological fluids. Anal. Biochem. 1982, 126, 131–138. [Google Scholar] [CrossRef]
- Sample Availability: Samples of the compounds 1–5 are available from the authors.
© 2014 by the authors; licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/).