2. Results and Discussion
Sanggenon X (
Figure 1) was obtained as a yellowish-brown amorphous powder. Its IR spectrum showed absorption bands assigned to carbonyl (1685 cm
−1) and aromatic (1605, 1509 and 1459 cm
−1) groups. The molecular formula C
34H
26O
10 was determined by (+)-ESI HR-MS (electrospray ionization high resolution mass spectrometry) at
m/
z 595.1586 [M + H]
+ (calcd for C
34H
27O
10+, 595.1599). The
1H-NMR spectrum of
1 (
Table 1) showed three aromatic moieties as follows: (a) a trisubstituted benzoyl at
δH 7.44 (d,
J = 8.7 Hz, H-14″), 6.48 (d,
J = 8.7 Hz, H-13″), and 6.09 (s, H-11″); (b) a trisubstituted phenyl ring at
δH 6.51 (d,
J = 9.0 Hz, H-20″), 6.22 (d,
J = 9.0 Hz, H-19″), and 6.23 (s, H-17″); (c) a stilbene moiety at
δH 7.30 (d,
J = 8.4 Hz, H-6), 6.23 (d,
J = 8.4 Hz, H-5), 6.30 (s, H-3), 6.44 (s, H-6′), 6.16 (s, H-2′), 7.09 (d,
J = 16.2 Hz, H-α), and 6.74 (d,
J = 16.2 Hz, H-β). These fragments in the downfield region were similar to a known D–A adduct, kuwanon Y [
15,
16]. In addition, the spectrum showed five singlets assigned to active hydroxyl protons at
δH 9.55 (OH-2), 9.38 (OH-4), 9.29 (OH-18″), 8.85 (OH-3′), and 6.64 (OH-2″). In the upfield region, there were two methines at
δH 3.17 (s, H-3″) and 2.66 (s, H-5″); one methylene at
δH 2.51 (d,
J = 13.8 Hz, H-6″) and 1.77 (dd,
J = 13.8, 3.0 Hz, H-6″); and one methyl group at
δH 1.61 (s, H-7″). Combined with the seven aliphatic carbons
δC 109.1 (C-2″), 91.4 (C-4″), 74.4 (C-1″), 47.3 (C-3″), 36.6 (C-5″), 30.1 (C-6″), 22.1 (C-7″) in the
13C-NMR spectrum, the spectroscopic data established that the structure was a methylcyclohexane D-A skeleton, as shown in
Figure 1.
In the HMBC spectrum (
Figure 2), the cross-peaks from methyl protons H-7″ to C-1″/C-2″/C-6″; from methine H-3″ to C-2″; from methane H-5″ to C-1″/C-3″/C-4″; and from methylene H-6″ to C-1″/C-2″/C-4″ established that the D-A skeleton was 1″,2″,4″-trioxymethylcyclohexane. The proton H-3″ was correlated with C-3′/C-4′/C-5′ (
δC 154.2, 110.7, and 159.2) of stilbene, suggesting that the stilbene was attached to the C-3″ of the D-A skeleton at C-4′ position. The cross-peaks from H-3″/H-5″ to C-8″ (
δC 194.9) confirmed the linkage from benzoyl C-8″ to C-4″. The correlations from H-5″ to C-16″/C-20″ (
δC 154.6 and 133.3) showed that the phenyl group was connected at C-15″ to C-5″. The cross-peaks from an unusual active proton OH-2″ to C-2″ and C-3″, combined with the chemical shift of C-2″ (
δC 109.1), demonstrated that the C-2″ was a hemiketal carbon. Because four phenolic hydroxyl protons (O
H-2, 4, 3′, 18″) were correlated with their own adjacent carbons, there must be three oxygen-bridges connecting C-1″, C-2″, or C-4″ of cyclohexane to C-5′, C-10″, C-12″, or C-16″ of the aromatic moieties, given the molecular formula C
34H
26O
10.
Because all the oxygenated bridgeheads (C-1″, 2″, 4″) were quaternary carbons, the methylation of compound
1 with CH
3I/K
2CO
3 was carried out to confirm the linkages of three
O-bridges. Two products—
1a and
1b as shown in
Figure 3—were identified by the 1D and 2D-NMR spectra.
In 1a, the 13C-NMR spectrum showed two carbonyl carbons at δC 193.6 (C-2″) and 193.0 (C-8″), two olefinic carbons at δC 127.7 (C-3″) and 160.4 (C-4″), four aliphatic carbons at δC 75.9 (C-1″), 33.7(C-5″), 35.6 (C-6″), and 22.7 (C-7″), and the aromatic moieties. The 1H-NMR spectrum showed one methyl at δH 1.57 (s, H-7″), one methine at δH 3.84 (t, J = 3.0 Hz, H-5″), and one methylene at δH 2.65, 2.23 (each dd, J = 13.3, 3.0 Hz, H-6″). The HMBC showed correlations from H-5″ to C-1″/C-3″, from H-6″ to C-1″/C-2″/C-5″, and from H-7″ to C-1″/C-2″/C-6″, establishing that the D-A skeleton was 1″-oxymethylcyclohex-3″-en-2″-one. In addition, the cross-peaks from H-2′ (δH 6.42) to C-3′ (δC 157.7) and from H-6′ (δH 6.41) to C-5′ (δC 157.8) provided the assignments for C-3′ and C-5′ of the stilbene. The cross-peaks from H-11″ (δH 6.39)/H-14″ (δH 7.04) to C-10″ (δC 159.7) and from H-11″/H-13″ (δH 6.33)/H-14″ (δH 7.04) to C-12″ (δC 164.2) provided the assignments for C-10″ and C-12″ of the benzoyl group. The cross-peaks from H-17″ (δH 6.47)/H-20″ (δH 6.97) to C-16″ (δC 153.8)/C-18″ (δC 160.2) provided the assignments of the oxygenated carbons (C-16″ and C-18″) of trisubstituted benzene. All of the methoxylated carbons were assigned by the cross-peaks from methyl groups to their ipso carbons, and only C-1″ and C-16″ were not substituted by a methyl group. Therefore, one O-bridge was assigned between C-1″ and C-16″.
In
1b, the A-D skeleton was determined to be 1″,2″,4″-trioxymethylcyclohexene, which was deduced from one methyl at
δH 1.57 (s, H-7″), one methylene at
δH 2.28 (dd,
J = 13.5, 1.2 Hz, H-6″
a) and 1.87 (dd,
J = 13.5, 4.2 Hz, H-6″
e), and seven carbons at
δC 76.4 (C-1″), 148.0 (C-2″), 122.4 (C-3″), 99.4 (C-4″), 33.9 (C-5″), 31.3 (C-6″), and 23.2 (C-7″). This was further confirmed by the HMBC correlations from the H-6″ to C-1″/C-2″/C-4″/C-5″ and from H-7″ to C-1″/C-2″/C-6″. In addition, the cross-peaks from H-2′ (
δH 6.56) to C-3′ (
δC 155.7) and from H-6′ (
δH 6.36) to C-5′ (
δC 161.8) provided the assignments for C-3′ and C-5′ of the stilbene moiety. The cross-peaks from H-11″ (
δH 6.62)/H-14″ (
δH 7.24) to C-10″ (
δC 159.6)/C-12″ (
δC 163.6) were used to assign C-10″ and C-12″ of the benzoyl group. The cross-peaks from H-17″ (
δH 6.27)/H-20″ (
δH 7.12) to C-16″ (
δC 154.9)/C-18″ (
δC 160.0) provided the assignments for the oxygenated aromatic carbon C-16″ and C-18″. All methoxylated carbons were assigned by the cross-peaks from methyl groups to their
ipso carbons. Four carbons C-1″, C-4″, C-5′, and C-10″ were not substituted by a methyl group. Given the molecular formula C
41H
40O
10 as calculated by HRMS, there should be two
O-bridges in
1b between C-1″/C-10″ and C-4″/C-5′, or between C-1″/C-5′ and C-4″/C-10″. Finally, the
O-bridges were attributed at C-1″/C-10″ and C-4″/C-5′ due to the weak NOESY cross-peak between H-6″
a (
δH 2.28)/H-14″ (
δH 7.24). The structure of
1b could be further confirmed by the unreasonably twisted double bond C2″-C3″ that would be present if the
O-bridges were located on C-1″/C-5′ and C-4″/C-10″ (
1b* in
Figure 3).
Given the structures of 1a and 1b, the three O-bridges in 1 were suggested to be at C-1″/C-16″, C-2″/C-10″, and C-4″/C-5′, depending on the proposed reaction mechanism. In the methylation of 1, there were two reactive centers: the hemiketal at C-2″ and its adjacent benzyl proton H-3″. In pathway A, deprotonation at C-3″ under alkali conditions formed a ketone from the hemiketal. Subsequently, the two O-bridges at C-2″ and C-4″ were broken to form a 1,4-butenedione. In pathway B, the hydroxyl group at C-2″ hemiketal was first methylated before deprotonation at C-3″ under alkali conditions. A double bond was formed as the O-bridge at C-2″ migrated to C-1″ with an intramolecular 1,2-rearrangement, and the O-bridge between C-1″/C-16″ was broken. Meanwhile, a configuration inversion of the C-7″ methyl group was observed from 1 to 1b. This phenomenon was further confirmation of the intramolecular O-bridge migration from C-2″ to C-1″.
Because the two bridged rings on C1″/C5″ and C2″/C4″ were adjacent to each other, they must be on opposite sides of the hexane plane. Thus, the orientation of C-3″ yielded two sets of epimers—
cis-trans or
all-trans, in agreement with the biosynthesis pathway [
17] of the D-A adducts in the genus
Morus. Although the benzyl carbonyl of
1 was coplanar with the aromatic ring, its CD (Circular Dichroism) spectrum did not show the split Cotton effects typical of non-
O-bridged D-A adducts, such as mulberrofurans C and J [
16]. Two positive Cotton effect peaks at 349 nm and 308 nm were observed, in accordance with the calculated ECD (Electronic Circular Dichroism) spectrum (
Figure 4) of one 3″H-α epimer—i.e., (3″
R, 4″
S, 5″
R)—by using the TDDFT (Time-Dependent Density Functional Theory) method. Therefore, the absolute configuration of
1 was determined to be (1″
R, 2″
R, 3″
R, 4″
S, 5″
R).
The genus
Morus is a plant source with rich D-A adducts. More than 50 D-A adducts have been found in the previous studies [
18]. However, a natural product with a highly oxygenated D-A skeleton is rarely reported [
19]. A plausible biosynthetic pathway for
1 was postulated in
Figure 5, based on the KEGG pathway prediction. Kuwanon Y, a D-A adduct found in genus
Morus [
16], afforded
1 through three oxidization steps. First, the double bond of the D-A skeleton was oxidized to an epoxide by an oxidase [
20] or putative Cyt P450 monooxygenase [
19], then the epoxide was attacked by 16″-OH at C-1″, and 2″-OH was formed. Sequentially, the newly formed 2″-OH was oxidized to a carbonyl by an oxidoreductase [
21] and was attracted by 10″-OH to form a hemiketal [
22]. Finally, the α-position of the 8″-carbonyl was oxidized to form an electrophilic center and was trapped by 5′-OH [
23] to afford
1.
In in vitro bioassays, sanggenon X (1) showed significant antioxidant activity against Fe2+-Cys-induced lipid peroxidation in rat liver microsomes with 81.25% inhibition of malondialdehyde (MDA) release, similar to the positive control, curcumin, with an 81.75% inhibition ratio.
3. Experimental
3.1. General Experimental Procedures
Melting points were determined on an XT5B melting point apparatus (Beijing Keyi Electric Light Instrument Factory, Beijing, China) and were uncorrected. Optical rotations were measured with a P-2000 polarimeter (Jasco, Tokyo, Japan). ECD spectra were recorded at room temperature with a J-815 spectropolarimeter (Jasco, Tokyo, Japan). UV spectra were collected in MeOH on a V-650 spectrophotometer (Jasco, Tokyo, Japan). IR spectra were recorded on a Nicolet 5700 spectrometer (Thermo, Madison, WI, USA) by the FT-IR transmission electron microscopy method. 1H- and 13C-NMR spectra were acquired using an AVIIIHD 600 spectrometer (Bruker, Billerica, MA, USA). ESI HR-MS were recorded on a 1200 series LC/6520 quadrupole time of flight (QTOF) spectrometer (Agilent). Column chromatography (CC) purification was performed using silica gel (160–200 mesh), Sephadex LH-20 (GE, Boston, MA, USA), and C18 (50 μm, YMC, Kyoto, Japan). CC fractions were analyzed by thin-layer chromatography (TLC) using silica gel GF254.
3.2. Plant Material
The Cortex Mori Radicis were bought from Anguo herb market, Hebei, China, and were collected from Hunan Province, China, in 2012. These samples were identified by Professor Lin Ma, Institute of Materia Medica, Chinese Academy of Medical Science and Peking Union Medical College, China. A voucher specimen (ID-S-2604) was deposited in the Institute of Materia Medica, Chinese Academy of Medical Science and Peking Union Medical College, China.
3.3. Extraction and Isolation
The powdered Cortex Mori Radicis (50 kg) were soaked with 50% EtOH for 24 h and percolated with 300 L 50% EtOH. Then evaporation of the solvent under reduced pressure gave a liquid extract, which was suspended in H2O and partitioned with EtOAc. The EtOAc extract (ca. 1 kg) was applied to a silica gel (100–200 mesh, 2 kg) column, eluting with a gradient of increasing MeOH concentration (0–100%) in CHCl3, to yield 22 fractions A–V. Fraction M–O (50 g) was applied to a Sephadex LH-20 (3 L) column, using 90% MeOH as eluent, to give subfractions MO-1 to 13. Fraction MO-11 (8 g) was loaded on a silica gel (100–200 mesh, 160 g) column and eluted with a gradient of increasing MeOH concentration (0–100%) in CH2Cl2 to yield five subfractions. The second fraction (3.2 g) was chromatographed over Sephadex LH-20 (400 mL, eluted by MeOH), MPLC over C18 (eluted by MeOH:H2O 10–60%), and HPLC (YMC C18 20 × 250 mm, 5 μm, 65% MeOH in H2O, flow rate 5 mL/min) to give 1 (68 mg, tR = 39 min).
Sanggenon X (
1): Yellowish-brown amorphous powder; m.p. 199.0–200.3 °C (d);
= −8.76° (
c = 1.00, MeOH); UV (MeOH) λ
max (log
ε) 208.5 (4.73), 285 (4.40), 326 (4.51) nm; CD (MeOH) 232.5 (∆
ε −16.00), 308 (∆
ε +7.88), 349.5 (∆
ε +4.24) nm; IR υ
max 3392, 1685, 1605, 1509, 1459, 1279, 1217, 1165, 1125, 1064, 995, 973, 838, 767, 661, 636, 525 cm
−1;
1H-NMR (DMSO-
d6, 600 MHz) 9.55 (1H, s 2-OH), 9.38 (1H, s 4-OH), 8.85 (1H, s 3′-OH), 6.64 (1H, s 2″-OH), 9.29 (1H, s 18″-OH), other data see
Table 1;
13C-NMR (DMSO-
d6, 150 MHz) data, see
Table 1; (+)-ESIMS
m/
z 595 [M + H]
+, 617 [M + Na]
+; (+)HR-ESIMS
m/
z 595.1586 [M + H]
+ (calcd. for C
34H
27O
10+, 595.1599). (
Supplementary Materials Figure S1a–j, Table S1).
1a: (+)HR-ESIMS
m/
z 693.2708 [M + H]
+ (calcd for C
41H
41O
10+, 693.2694).
1H-NMR (DMSO-
d6, 600 MHz) 3.44 s (2-OMe), 3.77 (3H, s, 4-OMe), 3.37 (3H, s, 3′-OMe), 3.82 (3H, s, 5′-OMe), 3.71 3H, s, 10″-OMe), 3.71 (3H, s, 12″-OMe), 3.71 (3H, s, 18″-OMe), other data see
Table 1.
13C-NMR (DMSO-
d6, 150 MHz) 55.2 (2-OMe), 55.3 (4-OMe), 55.7 (3′-OMe), 55.6 (5′,10″,12″,18″-OMe), other data see
Table 1. (
Supplementary Materials Figure S2a–f, Table S1).
1b: (+)HR-ESIMS
m/
z 693.2708 [M + H]
+ (calcd. for C
41H
41O
10+, 693.2694).
1H-NMR (DMSO-
d6, 600 MHz) 3.77 (3H, s, 2-OMe), 3.73 (3H, s, 4-OMe), 3.76 (9H, s, 3′,12″,16″-OMe), 3.32 (3H, s, 2″-OMe), 3.60 (3H, s, 18″-OMe), other data see
Table 1.
13C-NMR (DMSO-
d6, 150 MHz) 56.0 (2-OMe), 55.8 (4-OMe), 56.1 (3′,16″-OMe), 60.7 (2″-OMe), 56.2 (12″-OMe), 55.5 (18″-OMe), other data see
Table 1. (
Supplementary Materials Figure S3a–h, Table S1).
3.4. Methylation of 1
Twenty milligrams of 1 was dissolved in dried acetone, 200 mg K2CO3 and 400 μL CH3I were added and then stirred for 24 h. Then, the solution was dried and purified by RP-HPLC (Grace Adsorbosphere XL C18 10 × 250 mm, 5 μm, 90% MeOH in H2O, flow rate 2 mL/min) to yield compounds 1a and 1b (1a: 3.5 mg, 11.7%, tR = 11.9 min; 1b: 3.4 mg, 11.3%, tR = 25.9 min).
3.5. Calculation of ECD
Calculated ECD was performed on the 3″H-α (1″R, 2″R, 3″R, 4″S, 5″R), 3″H-β (1″R, 2″R, 3″S, 4″S, 5″R), and their enantiomers of 1. Conformation search was done with the MMFF94 molecular mechanics force field via the MOE software package (MOE2009.10, Chemical Computing Group Inc., Montreal, QC, Canada). Calculated ECD was performed using the TDDFT method (Gaussian 09 B.01, Gaussian, Wallingford, CT, USA, 2009) at B3LYP/6-31+G(d,p)//B3LYP/6-311+G(d,p) level for the configurations within an energy window of 5 kcal/mol. The conductor-like polarizable continuum model was used with MeOH (ε = 32.613) in order to take the solvent effects into consideration. The Boltzmann distribution was calculated based on the relative free energy (ΔG) and the final ECD (σ = 0.25 eV, UV shift = 10 nm) was simulated by using SpecDis (V1.64, University of Wuerzburg, Germany, 2015).
3.6. Lipid Peroxidation Assay
Antioxidative activity was evaluated as the inhibitory activity of compounds against Fe2+-Cys-induced lipid peroxidation in rat liver microsomes by the formation of malondialdehyde-thiobarbituric acid (MDA-TBA) adduct. Microsomes were isolated from SD rat livers and suspended in 100 mM TMS buffer (pH 7.4). The microsomal suspension (1 mg protein/mL), different concentrations of compound or vehicle, and 0.2 mM cysteine in 0.1 M PBS (pH 7.4) were incubated at 37 °C for 15 min, 50 µM FeSO4 was added, and the reaction mixture was then incubated at 37 °C for 15 min again. An equal volume of 20% (w/v) TCA (Trichloroacetic Acid) and 0.6% (w/v) TBA were added and kept in a boiling water bath for 10 min. After the mixture was centrifuged at 3000× g for 10 min, the absorbance of supernatant was measured at 532 nm and the concentration of MDA was calculated as C = (OD − 0.006)/0.07 × 10 nmol/mL. Lipid peroxidation inhibitory activity was calculated as follows: [1 − (T − B)/(C − B)] × 100%, in which T, C, and B are MDA concentrations of the sample treated, the control without sample, and the zero time control, respectively. Curcumin (10−4 M) was used as the positive control.