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Mar. Drugs 2013, 11(9), 3372-3380; doi:10.3390/md11093372
Published: 3 September 2013
Abstract: Two new 13-hydroxycembrane diterpenoids, arbolides A (1) and B (2), along with a known trihydroxysteroid, crassarosterol A (3), were isolated from the soft coral Sinularia arborea. The structures of new cembranes 1 and 2 were elucidated by spectroscopic methods. Steroid 3 was found to exhibit cytotoxicity toward K562 and MOLT-4 leukemia.
Previous studies on the chemical constituents of soft corals belonging to the genus Sinularia have led to the isolation of a number of interesting secondary metabolites and some of these were found to possess extensive bioactivities [1,2,3]. Continuation investigation on the chemical constituents of the marine invertebrates collected off the waters of Taiwan, two new cembrane-type diterpenoids, arbolides A (1) and B (2), and a known steroid, crassarosterol A (3) , were isolated from the soft coral Sinularia arborea (family Alcyonacea) (Figure 1). In this paper, we describe the isolation, structure determination and cytotoxicity of compounds 1–3.
2. Results and Discussion
Arbolide A (1) was isolated as a colorless oil that gave a pseudomolecular ion [M + Na]+ at m/z 359.2195 in the HRESIMS, indicating the molecular formula C20H32O4 (calcd for C20H32O4Na, 359.2198) (5° of unsaturation). The IR spectrum of 1 showed a broad band at 3345 cm−1, consistent with the presence of hydroxy group. The 13C NMR and DEPT spectra of 1 showed that this compound had 20 carbons (Table 1), including three methyls, six sp3 methylenes, two sp2 methylenes, four sp3 methines, an sp2 methine, an sp3 quaternary carbon and three sp2 quaternary carbons. The presence of a trisubstituted epoxide containing a methyl substituent was established from the NMR signals at δC 61.4 (CH), 61.1 (C) and δH 2.72 (1H, dd, J = 6.0, 6.0 Hz) and further confirmed by the proton signal of a methyl singlet at δH 1.27 (3H, s) (Table 1). A trisubstituted and two 1,1-disubstituted carbon-carbon double bonds were identified from the NMR signals at δC 138.4 (C), 125.3 (CH) and δH 5.48 (1H, br s); δC 147.3 (C), 113.2 (CH2) and δH 5.19 (1H, s), 5.15 (1H, s); δC 148.1 (C), 111.2 (CH2) and δH 4.75 (2H, br s), respectively. A hydroperoxy-bearing methine (δH 4.38, 1H, dd, J = 7.2, 4.8 Hz, δC 88.4, CH) [5,6,7] and a hydroxy-bearing methine (δH 3.92, 1H, dd, J = 6.0, 6.0 Hz, δC 76.4, CH) were identified from the characteristic NMR signal analysis. These data, combined with the five degrees of unsaturation implied by the molecular formula, suggested a bicyclic structure for 1.
|Table 1. 1H (400 MHz, CDCl3) and 13C (100 MHz, CDCl3) NMR data, 1H–1H COSY and HMBC correlations for cembrane 1.|
|Position||δH (J in Hz)||δC, Multiple||1H–1H COSY||HMBC|
|1||2.02 m||43.1, CH||H2-2, H2-14||C-2, -3, -13, -15, -17|
|2||1.89 m; 1.23 m||32.9, CH2||H-1, H-3||C-1, -3, -4, -14, -15|
|3||2.72 dd (6.0, 6.0)||61.4, CH||H2-2||C-2|
|5||1.96 m; 1.30 m||33.7, CH2||H2-6||C-3, -4, -6, -7, -18|
|6||1.66 m; 1.52 m||28.6, CH2||H2-5, H-7||C-4, -5, -7, -8|
|7||4.38 dd (7.2, 4.8)||88.4, CH||H2-6||C-5, -6, -19|
|9||2.24 m||31.3, CH2||H2-10, H2-19||C-8, -10, -11|
|10||2.41 m; 2.27 m||25.9, CH2||H2-9, H-11||C-9|
|11||5.48 br s||125.3, CH||H2-10, H3-20||n.o. a|
|13||3.92 dd (6.0, 6.0)||76.4, CH||H2-14||C-1, -12, -14, -20|
|14||1.80 dd (6.8, 6.0)||38.2, CH2||H-1, H-13||C-1, -2, -12, -13, -15|
|16||1.71 br s||18.8, CH3||H2-17||C-1, -15, -17|
|17||4.75 br s||111.2, CH2||H3-16||C-1, -15, -16|
|18||1.27 s||17.0, CH3||C-3, -4, -5|
|19||5.19 s; 5.15 s||113.2, CH2||H2-9||C-7, -8, -9|
|20||1.69 s||13.6, CH3||H-11||C-11, -12, -13|
|7-OOH||7.89 br s||n.o.|
a n.o. = not observed.
From the 1H–1H COSY spectrum of 1 (Table 1 and Figure 2), the separate spin systems of H-13/H2-14/H-1/H2-2/H-3, H2-5/H2-6/H-7 and H2-9/H2-10/H-11 were differentiated. These data, together with the key HMBC correlations between protons and quaternary carbons (Table 1 and Figure 2), such as H2-2, H2-5, H2-6, H3-18/C-4; H2-6, H2-9/C-8; H-13, H2-14/C-12; and H-1, H2-2, H2-14, H2-17/C-15, established the main carbon skeleton of 1. The vinyl methyls at C-12 and C-15 were confirmed by the HMBC correlations between H3-20/C-11, -12, -13 and H3-16/C-1, -15, -17; and further supported by the allylic couplings between H-11/H3-20 and H2-17/H3-16 in the 1H–1H COSY spectrum of 1. The exocyclic carbon-carbon double bonds at C-8 and C-15 were established by the HMBC correlations between H2-19/C-7, -8, -9 and H2-17/C-1, -15, -16; and further confirmed by the allylic couplings between H2-9/H2-19 and H2-17/H3-16 in the 1H–1H COSY spectrum of 1. The hydroperoxy-bearing methine unit at δC 88.4 was more shielded than that expected for a hydroxy-bearing methine [5,6], and was correlated to the methine proton appearing at δH 4.38 in the HMQC spectrum. Thus, the remaining hydroxy group should be positioned at C-13, as indicated by the key 1H–1H COSY correlations and characteristic NMR signals.
The relative configuration of 1 was elucidated mainly from a NOESY spectrum. In the NOESY experiment for 1 (Figure 3), H-1 correlated with H-13, but not with H-3 and H2-14, and H-3 showed correlations with H2-14, revealing the S*-, R*- and R*-configurations of the chiral carbons C-1, C-3 and C-13, respectively, by modeling analysis. H-3 did not exhibit correlation with H3-18, reflecting the trans stereochemistry of 3,4-epoxide. Additionally, correlations between H-11 and H-13, as well as the lack of correlation between H-11/H3-20, reflected the E geometry of the double bond at C-11/12. Furthermore, by comparison of the proton chemical shift and coupling pattern of H-7 in 1 (δH 4.38 dd, J = 7.2, 4.8 Hz) with those of known cembrane analogues, manaarenolides A (δH 4.52, t, J = 3.5 Hz) and B (δH 4.40 dd, J = 11.5, 3.5 Hz), which were found to possess 7α- and 7β-hydroperoxy group in their structures, respectively , the 7-hydroperoxy group in 1 was proven to be β-oriented and possessing an S*-configuration.
The HRESIMS spectrum of 2 (arbolide B) exhibited a pseudomolecular ion at m/z 327.2298 [M + Na]+, consistent with the molecular formula C20H32O2 and implying five degrees of unsaturation. The IR spectrum revealed the presence of hydroxy group (νmax3419 cm−1). The structure of cembrane 2 was deduced from its 13C NMR and DEPT spectra (Table 2), which showed that this compound has 20 carbons, including four methyls, seven methylenes (including an sp2 CH2), five methines (including two sp2 CH) and four quaternary carbons (including three sp2 quaternary carbons). From the 1H and 13C NMR spectra (Table 2), 2 was found to possess three olefinic groups (δH 5.05, 1H, ddq, J = 6.4, 6.4, 1.2 Hz; δC 123.2, CH; 135.1, C; δH 5.34, 1H, dd, J = 6.4, 6.4 Hz; δC 127.2, CH; 135.8, C; δH 4.71, 1H, dd, J = 2.0, 1.6 Hz; 4.64, 1H, dd, J = 1.6, 0.8 Hz; δC 147.6, C; 111.0, CH2). Signals at δC 63.3 (CH), 60.6 (C), 16.7 (CH3) and δH 2.74 (1H, dd, J = 10.0, 2.8 Hz), 1.23 (3H, s) revealed the presence of a methyl-containing trisubstituted epoxide. Detailed analysis of the 1H–1H COSY and HMBC correlations (Table 2 and Figure 4) further established the planar structure of 2 as a cembrane-type diterpenoid bearing a hydroxy group at C-13, two trisubstituted carbon-carbon double bonds at C-7/8 and C-11/12, a 1,1-disubstituted carbon-carbon double bond at C-15/17 and a methyl-containing epoxide at C-3/4.
|Table 2. 1H (400 MHz, CDCl3) and 13C (100 MHz, CDCl3) NMR data, 1H–1H COSY and HMBC correlations for cembrane 2.|
|Position||δH (J in Hz)||δC, Multiple||1H–1H COSY||HMBC|
|1||2.01 m||40.7, CH||H2-2, H2-14||C-3, -13, -15|
|2||1.77 m; 1.31 m||33.5, CH2||H-1, H-3||C-1, -3, -4, -14, -15|
|3||2.74 dd (10.0, 2.8)||63.3, CH||H2-2||C-2|
|5||2.06 m; 1.27 m||38.1, CH2||H2-6||C-3, -4, -6, -7|
|6||2.29 m; 2.10 m||24.0, CH2||H2-5, H-7||C-4, -5, -7, -8|
|7||5.05 ddq (6.4, 6.4, 1.2)||123.2, CH||H2-6, H3-19||C-6, -9, -19|
|9||2.20 m; 2.04 m||38.8, CH2||H2-10||C-7, -8, -10, -11, -19|
|10||2.16 m||24.1, CH2||H2-9, H-11||C-8, -9, -11, -12|
|11||5.34 dd (6.4, 6.4)||127.2, CH||H2-10||C-9, -10, -13, -20|
|13||3.87 br d (10.0)||75.3, CH||H2-14||C-11, -20|
|14||1.82 ddd (13.6, 10.8, 2.8) |
1.73 ddd (13.6, 10.0, 3.6)
|37.3, CH2||H-1, H-13||C-1, -2, -12, -15|
|16||1.67 br s||18.5, CH3||H2-17||C-1, -15, -17|
|17||4.71 dd (2.0, 1.6); 4.64 dd (1.6, 0.8)||111.0, CH2||H3-16||C-1, -15, -16|
|18||1.23 s||16.7, CH3||C-3, -4, -5|
|19||1.63 br s||16.2, CH3||H-7||C-7, -8, -9|
|20||1.67 s||13.0, CH3||C-11, -12, -13|
The relative structure of 2 was elucidated by analysis of NOESY correlations, as shown in Figure 5. In the NOESY experiment for 1, H-1 correlated with H-13, but not with H-3, and H-3 showed correlations with H2-14, but not with H3-18 revealing the S*-, R*-, R*- and R*-configurations of the chiral carbons C-1, C-3, C-4 and C-13, respectively, by modeling analysis. Correlations observed between H-7/H2-9 and H-11/H-13, as well as the lack of correlation between H-7/H3-19 and H-11/H3-20, reflected the E geometry of the double bonds at C-7/8 and C-11/12.
The steroid 3 was found to be identical with the known compound, crassarosterol A, which was first isolated from a Formosan soft coral Sinularia crassa, on the basis of the comparison of its physical and spectroscopic data with those reported previously .
Cytotoxicity of compounds 1–3 toward K562 (human erythromyeloblastoid leukemia), MOLT-4 (human acute lymphoblastic leukemia), HTC-116 (human acute promyelocytic leukemia), DLD-1 (human colorectal adenocarcinoma), T-47D (human breast ductal carcinoma), MDA-MB-231 (human breast adenocarcinoma) and MCF-7 (human breast adenocarcinoma) cells was studied, and the results are shown in Table 3. These data showed that crassarosterol A (3) exhibited significant cytotoxicity towards K562 and MOLT-4 leukemia.
|Table 3. Cytotoxic data of compounds 1–3.|
|Cell lines IC50 (μg/mL)|
a Doxorubicin was used as a positive control. NA = not active at 20 μg/mL for 72 h.
3. Experimental Section
3.1. General Experimental Procedures
Optical rotations were measured at a Jasco P-1010 digital polarimeter (Japan Spectroscopic Corporation, Tokyo, Japan). Infrared spectra were recorded on a Varian Diglab FTS 1000 FT-IR spectrometer (Varian Inc. Palo Alto, CA, USA); peaks are reported in cm−1. NMR spectra were recorded on a Varian Mercury Plus 400 NMR spectrometer (Varian Inc.) using the residual CHCl3 signal (δH 7.26 ppm) as the internal standard for 1H NMR and CDCl3 (δC 77.1 ppm) for 13C NMR. Coupling constants (J) are given in Hz. ESIMS and HRESIMS were recorded using a Bruker APEX II mass spectrometer (Bruker, Bremen, Germany). Column chromatography was performed on silica gel (230–400 mesh, Merck, Darmstadt, Germany). TLC was carried out on precoated Kieselgel 60 F254 (0.25 mm, Merck); spots were visualized by spraying with 10% H2SO4 solution followed by heating. The normal phase HPLC (NP-HPLC) was performed using a system comprised of a Hitachi L-7110 pump (Hitachi Ltd. Tokyo, Japan) and a Rheodyne 7725 injection port (Rheodyne LLC, Rohnert Park, CA, USA). Two normal phase columns (Supelco Ascentis® Si Cat #:581515-U, 25 cm × 21.2 mm, 5 μm; 581514-U, 25 cm × 10 mm, 5 μm, Sigma-Aldrich. Com. St. Louis, MO, USA) were used for NP-HPLC.
3.2. Animal Material
Specimens of the octocoral Sinularia arborea  were collected by hand using scuba equipment off the coast of southern Taiwan in October, 2012, and stored in a freezer (−20 °C) until extraction. A voucher specimen (NMMBA-TWSC-1200X) was deposited in the National Museum of Marine Biology and Aquarium, Taiwan.
3.3. Extraction and Isolation
Specimens of the soft coral Sinularia arborea (wet weight 1.6 kg, dry weight 576 g) were minced and extracted with ethyl acetate (EtOAc). The EtOAc extract left after removal of the solvent (12.5 g) was separated by silica gel and eluted using a mixture of n-hexane/EtOAc in a stepwise fashion from 100:1–pure EtOAc to yield 11 fractions A–K. Fraction G was separated by NP-HPLC, using a mixture of n-hexane and acetone (6:1) to yield 26 subfractions G1–G26. Fraction G13 was repurified by NP-HPLC, using a mixture of n-hexane and EtOAc (4:1) to yield 9 subfractions G13A–G13I. Fraction G13G was repurified by NP-HPLC, using a mixture of n-hexane and acetone (7:2, flow rate: 2.0 mL/min) to yield 2 (3.7 mg, tR = 8 m). Fraction G13I was repurified by NP-HPLC, using a mixture of dichloromethane and acetone (10:1, flow rate: 1.0 mL/min) to yield 1 (2.9 mg, tR = 332 m). Fraction H was purified by NP-HPLC, using a mixture of n-hexane and EtOAc (2:1) to obtain 14 subfractions H1–H14. Fraction H12 was repurified by NPLC, using a mixture of n-hexane and acetone (3:1, flow rate: 2.0 mL/min) to yield 3 (1.2 mg, tR = 149 m).
Arbolide A (1): colorless oil; +12 (c 0.15, CHCl3); IR (neat) νmax 3445 cm−1; 1H (400 MHz, CDCl3) and 13C (100 MHz, CDCl3) NMR data, see Table 1; ESIMS: m/z 359 [M + Na]+; HRESIMS: m/z 359.2195 (calcd for C20H32O4Na, 359.2198).
Arbolide B (2): colorless oil; −3 (c 0.19, CHCl3); IR (neat) νmax 3419 cm−1; 1H (400 MHz, CDCl3) and 13C (100 MHz, CDCl3) NMR data, see Table 2; ESIMS: m/z 327 [M + Na]+; HRESIMS: m/z 327.2298 (calcd for C20H32O2Na, 327.2300).
Crassarosterol A (3): white powder; −16 (c 0.06, CHCl3) (ref. , −45 (c 0.66, CHCl3)); IR (neat) νmax 3396 cm−1; ESIMS: m/z 453 [M + Na]+. The 1H and 13C NMR data of 3 are in full agreement with those reported previously .
3.4. Cytotoxicity Testing
Cytotoxicity of compounds 1–3 was assayed with a modification of the MTT [3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide] colorimetric method. Cytotoxicity assays were carried out according to previously described procedures [9,10].
In our continuing investigation on the chemical constituents of marine invertebrates collected off the waters of Taiwan, the soft coral Sinularia arborea has resulted in the isolation of two new cembrane-type diterpenoids, arbolides A (1) and B (2) and a known trihydroxysteroid crassarosterol A (3) . Steroid 3 was found to exhibit selective cytotoxicity toward the human leukemia K562 and MOLT-4 cells. To the best of our knowledge, this is the first time that the natural substances from Sinularia arborea have been reported.
This research was supported by grants from the National Dong Hwa University; the National Museum of Marine Biology and Aquarium; the Division of Marine Biotechnology, Asia-Pacific Ocean Research Center, National Sun Yat-sen University; and the National Science Council (Grant No. NSC 102-2325-B-291-001 and 101-2320-B-291-001-MY3), Taiwan, awarded to P.-J.S.
Conflicts of Interest
The authors declare no conflict of interest.
- Chen, W.-T.; Li, Y.; Guo, Y.-W. Terpenoids of Sinularia soft corals: Chemistry and bioactivity. Acta Pharm. Sin. B 2012, 2, 227–237.
- Yang, B.; Zhou, X.-F.; Lin, X.-P.; Liu, J.; Peng, Y.; Yang, X.-W.; Liu, Y. Cembrane diterpenes chemistry and biological properties. Curr. Org. Chem. 2012, 16, 1512–1539, doi:10.2174/138527212800672583.
- Rocha, J.; Peixe, L.; Gomes, N.C.M.; Calado, R. Cnidarians as a source of new marine bioactive compounds—an overview of the last decade and future steps for bioprospecting. Mar. Drugs 2011, 9, 1860–1886, doi:10.3390/md9101860.
- Chao, C.-H.; Chou, K.-J.; Huang, C.-Y.; Wen, Z.-H.; Hsu, C.-H.; Wu, Y.-C.; Dai, C.-F.; Sheu, J.-H. Steroids from the soft coral Sinularia crassa. Mar. Drugs 2012, 10, 439–450, doi:10.3390/md10020439.
- Su, J.-H.; Ahmed, A.F.; Sung, P.-J.; Chao, C.-H.; Kuo, Y.-H.; Sheu, J.-H. Manaarenolides A–I, diterpenoids from the soft coral Sinularia manaarensis. J. Nat. Prod. 2006, 69, 1134–1139, doi:10.1021/np050483q.
- Fattorusso, E.; Romano, A.; Taglialatela-Scafati, O.; Irace, C.; Maffettone, C.; Bavestrello, G.; Cerrano, C. Oxygenated cembranoids of the decaryiol type from the Indonesian soft coral Lobophytum sp. Tetrahedron 2009, 65, 2898–2904, doi:10.1016/j.tet.2009.02.008.
- Lin, W.-Y.; Lu, Y.; Su, J.-H.; Wen, Z.-H.; Dai, C.-F.; Kuo, Y.-H.; Sheu, J.-H. Bioactive cembranoids from the Dongsha atoll soft coral Sarcophyton crassocaule. Mar. Drugs 2011, 9, 994–1006, doi:10.3390/md9060994.
- Verseveldt, J. Octocorallia from North-Western Madagascar (Part II). Zool. Verh. 1971, 117, 1–73.
- Alley, M.C.; Scudiero, D.A.; Monks, A.; Hursey, M.L.; Czerwinski, M.J.; Fine, D.L.; Abbott, B.J.; Mayo, J.G.; Shoemaker, R.H.; Boyd, M.R. Feasibility of drug screening with panels of human tumor cell lines using a microculture tetrazolium assay. Cancer Res. 1988, 48, 589–601.
- Scudiero, D.A.; Shoemaker, R.H.; Paull, K.D.; Monks, A.; Tierney, S.; Nofziger, T.H.; Currens, M.J.; Seniff, D.; Boyd, M.R. Evaluation of a soluble tetrazolium/formazan assay for cell growth and drug sensitivity in culture using human and other tumor cell lines. Cancer Res. 1988, 48, 4827–4833.
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