Anti-Inflammatory Cembrane-Type Diterpenoids and Prostaglandins from Soft Coral Lobophytum sarcophytoides.

Two new cembrane-type diterpenoids, lobophytins A (1) and B (3), and four new prostaglandins, (5E)-PGB2 (10), (5E)-13,14-dihydro-PGB2 (11), 13,14-dihydro-PGB2 (12) and 13,14-dihydro-PGB2-Me (13), together with ten known compounds were isolated from the soft coral Lobophytum sarcophytoides. The structures of these new secondary metabolites were identified by high resolution mass spectrometry (HR-ESIMS), nuclear magnetic resonance (NMR) and electron circular dichroism (ECD) analyses, as well as the modified Mosher's method. Compounds 6, 7, 9, 10, 12, 13, 15 and 16 showed potential anti-inflammatory activity by inhibiting the production of nitric oxide (NO) in RAW264.7 cells that were activated by lipopolysaccharide, with IC50 values ranging from 7.1 to 32.1 μM and were better than the positive control indomethacin, IC50 = 39.8 μM.

1. Introduction

Cembrane-type diterpenoids are a large and structurally varied group of natural products derived from both terrestrial and marine organisms [1,2]. Among them, highly functionalized cembranoid diterpenes, containing a five-membered lactone moiety, have been mainly isolated from marine soft corals, especially from the genera Lobophytum, Sarcophyton and Sinularia [3,4]. Some of them have many kinds of pharmacological activities, such as cytotoxic [2,5], anti-inflammatory [6,7], anti-protozoal [8], antifouling [9] and anti-HIV [10].

Prostaglandins are biologically active lipid compounds, being 20-carbon fatty acids derived enzymically from the essential fatty acids by cyclization and oxidation [11,12]. They are widely distributed in animals and human-beings, which regulate a wide range of physiological activities.

Recently, we searched for anti-inflammatory secondary metabolites from the South China Sea and the soft coral Lobophytum sarcophytoides was collected from Xisha Islands, China. EtOAc extract of soft coral L. sarcophytoides showed anti-inflammatory activity in vitro by inhibiting nitric oxide (NO) production in lipopolysaccharide activated in RAW264.7 cells. Subsequent chemical investigation led to the isolation of 16 secondary metabolites, including two new cembrane-type diterpenoids, lobophytins A (1) and B (3), and four new prostaglandins, (5E)-PGB2 (10), (5E)-13,14-dihydro-PGB2 (11), 13,14-dihydro-PGB2 (12) and 13,14-dihydro-PGB2-Me (13), as well as ten known compounds, sarcomililatin B (2), sarcomililatin A (4), (+)-isosarcophine (5), (1S,2E,4S,6E,8S,11R)-2,6,12(20)-cembratriene-4,8,11-triol (7), loliolide (8), apo-9′-fucoxanthinone (9), (13E)-PGB2 (14), PGB2 (15) and PGA2 (16) (Figure 1). Compounds 6, 7, 9, 10, 12, 13, 15 and 16 showed potential anti-inflammatory activity with IC50 values ranging from 7.1 to 32.1 μM. Herein, we report the isolation, structure determination and anti-inflammatory bioactivity of the secondary metabolites.

Figure 1

Chemical structures of 1–16.

2. Results and Discussion

Compound 1 was obtained as colorless oil and its molecular formula was established as C20H28O4 (seven degrees of unsaturation) according to the negative HR-ESIMS ion at m/z 331.1906 [M − H]− (calculated for C20 H27 O4, 331.1909) (Figure S1). The IR spectrum of 1 revealed the presence of hydroxy (3450 cm−1) group and an α, β-unsaturated γ-lactone moiety (1737 and 1675 cm−1) (Figure S2). The 1H NMR data (Table 1) showed resonances for two vinyl methyls [δH 1.79 (3H, s); 1.91 (3H, s)], a tertiary methyl [δH 1.21 (3H, s)], three olefinic protons [δH 4.99 (1H, dd, J = 10.0, 1.0 Hz); 4.92 (1H, d, J = 0.9 Hz); 5.19 (1H, t, J = 1.6 Hz)], three oxygenated methines [δH 5.64 (1H, dd, J = 10.0, 1.7 Hz); 3.83 (1H, dd, J = 10.7, 6.3 Hz); 2.69 (1H, dd, J = 10.3, 2.6 Hz)] (Figure S3). The 13C NMR data (Table 1) revealed the presence of 20 carbons belonging to three methyls, seven methylenes, four methines and six quaternary carbons. Detailed analysis of the 1H and 13C NMR data (Figure S4) suggested that 1 belongs to the cembrane-type diterpenoid class, which was quite similar to sarcomililatin A (2) [13].

Table 1

1H (400 MHz) and 13C (100 MHz) NMR data of compounds 1 and 3 (in MeOH-d4, J in Hz).

No.	1		3
	δC	δH, Mult.	δC	δH, Mult.
1	162.8, C		161.4, C
2	79.8, CH	5.64, dd (10.0, 1.7)	79.2, CH	5.42, d (10.2)
3	122.9, CH	4.99, dt (10.0, 1.0)	120.1, CH	4.90, d (10.2)
4	143.5, C		143.7, C
5	36.7, CH2	2.19, m2.56, ddd (13.1, 9.9, 3.3)	41.7, CH2	2.73, dd (13.8, 7.2)2.81, dd (13.8, 7.2)
6	32.9, CH2	1.40, m2.00, m	125.2, CH	5.83, dt (15.6, 7.2)
7	70.1, CH	3.83, dd (10.7, 6.3)	140.2, CH	5.68, d (15.6)
8	155.1, C		72.6, C
9	31.3, CH2	2.13, m2.37, (13.7, 7.9, 2.8)	39.6, CH2	1.81, m
10	31.7, CH2	1.41, m	24.1, CH2	1.64, m1.77, m
11	62.1, CH	2.69, dd (10.3, 2.6)	62.0, CH	2.76, m
12	61.1, C		60.1, C
13	35.0, CH2	1.56, m1.91, m	35.7, CH2	1.27, m1.9, m
14	22.4, CH2	2.27, m	23.7, CH2	2.20, m2.38, m
15	123.7, C		123.8, C
16	174.5, C		174.7, C
17	8.8, CH3	1.79, s	9.1, CH3	1.85, s
18	16.0, CH3	1.91, s	17.4, CH3	1.83, s
19	110.5, CH2	4.92, d (0.9)5.19, t (1.6)	28.5, CH3	1.41, s
20	17.9, CH3	1.21, s	16.7, CH3	1.29, s

The 1H-1H COSY spectrum (Figure S5) revealed the appearance of four isolated proton spin systems as depicted in Figure 2. The key heteronuclear multiple bond correlation (HMBC) correlations from H-17 to C-1, C-15 and C-16; H-18 to C-3, C-4 and C-5; H-19 to C-7, C-8 and C-9; H-20 to C-11, C-12 and C-13; H-2 to C-1, C-15 and C-16; and H-14 to C-1 and C-15 established the cembrane-type diterpenoid skeleton as shown in Figure 2. The epoxy ring was located at C-11 and C-12 on the base of the HMBC correlations from H-20 to C-11 and C-12, as well as the chemical shift values of C-11 (δC 62.1) and C-12 (δC 61.1). The position of the remaining hydroxy group was assigned at C-7 (δC 70.1) according to the HMBC correlations from H-19 to C-7 and the 1H-1H COSY correlation between H-6 and H-7. The relative configuration of 1 was deduced by analysis of the nuclear overhauser effect spectroscopy (NOESY) data (Figure 3). The observed NOE correlations H-18 with H-2 and H-7 indicated they are α-orientation. NOE correlations H-11 with H-7, but not with H-20 suggested that H-11 and H-20 are β and α-orientation, respectively. The absolute configuration of 1 was determined by comparing experimental and calculated ECD spectra. The predicted ECD spectrum of (2S, 7R, 11R, 12R)-1 was in good agreement with that of the experimental one (Figure 4). Finally, the gross structure of 1 was assigned as shown and was given the trivial name lobophytin A.

Figure 2

Key 1H-1H COSY (red line) and HMBC (blue arrow) correlations of compounds 1 and 3.

Figure 3

Key NOESY (red line) correlations of compounds 1 and 3.

Figure 4

Experimental and calculated ECD spectra of compounds 1, 3 and 4 (in MeOH).

Compound 3 was isolated as colorless oil. The molecular formula of 3 was determined as C20H28O4 on the base of the positive HR-ESIMS ion at m/z 333.2058 [M − H]+ (calculated for C20H29O4, 333.2060) (Figure S9). The IR spectrum of 3 revealed the presence of hydroxy (3450 cm−1) group and an α, β-unsaturated γ-lactone moiety (1737 and 1675 cm−1) (Figure S10). The 1H and 13C NMR data (Table 1) of 3 revealed its structure possessed great similarity to the known cembrane-type diterpenoid, sarcomililatin B (4) [13]. The main difference between them was that the hydroperoxy group in 4 was replaced by the hydroxyl group in 3. This replacement caused the chemical shift of C-8 to be shifted upfield ΔδC 11.4 ppm (δC 72.6 in 3; 84.0 in 4). The significant 1H-1H COSY (Figure S13) and HMBC correlations (Figure 2) allowed the complete assignment for the planar structure of 3. The relative configuration of 3 was deduced by analysis of the NOESY data (Figure 3). The observed NOE correlations H-2 with H-13a and H-3; H-5a with H-13a and H-3 indicated they are α-orientation. NOE correlations H-6 with H-18 and H-19; H-19 with H-11; H-20 with H-14a suggested that H-6, H-14a, H-11, H-18, H-19 and H-20 are β-orientation. Compound 3 and sarcomililatin B (4) [13] showed quite similar ECD spectra (Figure 4), with a positive Cotton effect at 223 nm (Δε = +27.2) and a negative Cotton effect at 248 nm (Δε = −2.9), indicating that they have the same absolute configurations as 2S, 8R, 11R and 12R. Therefore, the structure of 3 was elucidated as depicted, named as lobophytin B.

Compound 10 was isolated as colorless oil. It has the molecular formula C20H28O4 (six degrees of unsaturation), as deduced from the negative HR-ESIMS ion at m/z 333.2068 [M − H]− (calculated for C20H29O4, 333.2071) (Figure S17). The 1H and 13C NMR spectra (Figures S19 and S20) of compound 10 were similar to those of known prostaglandin, PGB2 (15), except for chemical shift variation of two olefinic (δC 131.8 and 128.3 in 10; 27.7 and 22.1 in 15) and two methylenes (δC 32.9 and 26.7 in 10; 27.7 and 22.1 in 15) carbons in 13C NMR spectrum (Table 2). This suggested that compound 10 was a geometric isomer of compound 15 with the replacement of 5E geometry of the double bond by 5Z (Figure 5) on the base of the 13C NMR chemical shifts of allylic methylene carbons (Z alkenes, δC < 28 ppm; E alkenes, δC > 30 ppm) of alkenes [14]. Detailed analysis of the 2D NMR spectroscopic data, the structure of 10 was established as (5E)-PGB2.

Table 2

1H (400 MHz) and 13C (100 MHz) NMR data of compounds 10–13.

No.	10 a		11 a		12 a		13 b
	δC, Type	δH, Mult (J in Hz)	δC, Type	δH, Mult (J in Hz)	δC, Type	δH, Mult (J in Hz)	δC, Type	δH, Mult (J in Hz)
1	177.6, C		178.0, C		174.1, C		177.8, C
2	34.7, CH2	2.19, t (6.9)	34.6, CH2	2.22, t (7.4)	33.8, CH2	2.33, t (7.5)	34.6, CH2	2.30, t (7.4)
3	26.0, CH2	1.59, m	25.9, CH2	1.61, m	25.6, CH2	1.66, m	26.1, CH2	1.66, m
4	32.9, CH2	1.97, m	32.9, CH2	1.99, m	27.2, CH2	2.20, q (7.2)	27.7, CH2	2.20, q (7.1)
5	131.8, CH	5.37, m	131.5, CH	5.39, m	129.8, CH	5.32, m	130.6, CH	5.34, m
6	128.3, CH	5.37, m	128.4, CH	5.39, m	128.2, CH	5.32, m	128.0, CH	5.30, m
7	26.7, CH2	2.95, m	26.8, CH2	2.89, m	21.9, CH2	2.92, m	22.1, CH2	2.94, d (6.6)
8	139.3, C		139.3, C		139.1, C		139.9, C
9	211.9, C		212.4, C		208.3, C		212.3, C
10	34.7, CH2	2.40, m	35.2, CH2	2.36, m	34.5, CH2	2.25, m	35.2, CH2	2.35, m
11	26.7, CH2	2.71, m	30.4, CH2	2.59, m	29.6, CH2	2.55, m	30.3, CH2	2.58, m
12	167.5, C		178.8, C		174.6, C		178.2, C
13	124.3, CH	6.86, d (15.7)	28.7, CH2	2.53, m	28.3, CH2	2.55, m	28.8, CH2	2.55, m
				2.61, m		2.62, m		2.61, m
14	143.7, CH	6.37, dd (15.7, 5.8)	35.9, CH2	1.58, m	36.0, CH2	1.59, m	35.9, CH2	1.59, m
				1.67, m		1.69, m		1.67, m
15	72.8, CH	4.23, q (5.8)	72.2, CH	3.53	71.2, CH	3.57	72.2, CH	3.53, m
16	38.1, CH2	1.54, m	38.4, CH2	1.45, m	38.4, CH2	1.45, m	38.4, CH2	1.45, m
17	26.2, CH2	1.32, m	26.5, CH2	1.32, m	26.2, CH2	1.34, m	26.5, CH2	1.32, m
		1.41, m		1.45, m		1.46, m		1.45, m
18	32.9, CH2	1.31, m	33.1, CH2	1.31, m	32.7, CH2	1.30, m	33.1, CH2	1.31, m
19	23.7, CH2	1.31, m	23.7, CH2	1.32, m	23.4, CH2	1.31, m	23.7, CH2	1.32, m
20	14.4, CH3	0.88, t (6.7)	14.3, CH3	0.90, t (6.9)	14.3, CH3	0.88 t (6.7)	14.4, CH3	0.90, t (6.7)
OCH3							51.5, CH3	3.62, s

a in MeOH-d4, b in acetone-d6.

Figure 5

Key 1H-1H COSY (red line) and HMBC (blue arrow) correlations of compounds 10–13.

Compound 11 was isolated as colorless oil and its molecular formula was established as C20H28O4 (five degrees of unsaturation) according to the negative HR-ESIMS ion at m/z 335.2231 [M − H]− (calculated for C20H31O4, 335.2227) (Figure S25). The 1H and 13C NMR spectra (Figures S27 and S28) of compound 11 were similar to those of prostaglandin, (5E)-PGB2 (10), except for the absence of two olefinic proton (δH 6.37 and 6.86; δC 124.3 and 143.7) and the presence of two additional methylenes (δH 2.53, 2.61; 1.58, 1.67). It means that compound 11 was an analogue of (5E)-PGB2 (10) with the replacement of two olefinic by two methylene group, which was supported by the 1H-1H COSY correlations of H-14 with H-13 and H-15 (Figure 5). Detailed analysis of the 2D NMR spectroscopic data (Figures S29–S31), the structure of 11 was established as shown in Figure 2 and named as (5E)-13,14-dihydro-PGB2.

Compound 12 was isolated as colorless oil. The molecular formula of 12 was established as C20H28O4 (five degrees of unsaturation) according to the negative HR-ESIMS ion at m/z 335.2231 [M − H]− (calculated for C20H31O4, 335.2227) (Figure S32). The 1H and 13C NMR spectra (Figures S34 and S35) of compound 12 were similar to those of (5E)-13,14-dihydro-PGB2 (11), except for chemical shift variation of two olefinic and two methylene carbons in 13C NMR spectrum (Table 2). This suggested that compound 12 was a geometric isomer of compound 11 with the replacement of 5Z geometry of the double bond by 5E according to the 13C NMR chemical shifts of allylic methylene carbons (Z alkenes, δC < 28 ppm; E alkenes, δC > 30 ppm) of alkenes. Therefore, the structure of 12 was established as 13,14-dihydro-PGB2.

Compound 13 was isolated as colorless oil. The molecular formula of 13 was assigned as C20H28O4 (five degrees of unsaturation) on the base of the negative HR-ESIMS ion at m/z 351.2535 [M − H]− (calculated for C21H35O4, 351.2535) (Figure S40). The 1H and 13C NMR spectra (Figures S42 and S43) of compound 13 were quite similar to those of 13,14-dihydro-PGB2 (12), except for the presence of an additional methyl group at δH 3.62 (δC 51.5) (Table 2). The difference revealed that compound 13 was a methylated analogue of compound 12, which was supported by the HMBC correlations from −OCH3 to C-1 (Figure 5). Finally, 2D NMR spectroscopic data (Figures S44–S46) further elucidated the structure of 13, as shown in Figure 5 and named as 13,14-dihydro-PGB2-Me.

All isolated prostaglandins 10–16 shared a secondary alcohol at C-15. Their absolute configurations at C-15 were assigned by the modified Mosher’s method and comparison of optical activity sign, in combination with biosynthetic considerations. Initially, the known compound with most amount, PGB2 (15) was used to determine absolute configuration by application of the modified Mosher’s method because the chemical shifts of H-13 and H-14 at the double bond near the secondary alcohol at C-15 would change obviously after the reaction with the Mosher’s reagent. The reaction of 15 with (R)- and (S)-MTPA chloride afforded the corresponding (S)-MTPA ester (15a) and (R)-MTPA ester (15b). The chemical shifts for H-14 and H-16 of 15a were δH 6.42 and 1.85, respectively, compared to δH 6.30 and 1.91 in 15b (Figures S49 and S51). The chemical shift values (Δδ = δS − δR) (Figure 6) suggested that the absolute configuration of C-15 is S. Similarly, the absolute configuration of (5E)-PGB2 (10) was clearly resolved by the modified Mosher’s method and was characterized as S. Then, we also tried to use the modified Mosher’s method to analyse the absolute configuration of (5E)-13,14-dihydro-PGB2 (11), 13,14-dihydro-PGB2 (12) and 13,14-dihydro-PGB2-Me (13), but the chemical shifts of H-14 and H-16 are overlapped and difficult to classify with the help of heteronuclear singular quantum correlation (HSQC) and 1H-1H COSY. Finally, optical rotations of all isolated prostaglandins 10–16 were measured and they have the same optical activity sign. Thus, the configuration at the hydroxy-bearing C-15 was deduced as S, as well as in combination with biosynthetic considerations.

Figure 6

∆δ = δS − δR values in ppm obtained from the MTPA esters of 10 and 15.

The known compound, sarcomililatin B (2) [13], sarcomililatin A (4) [13], (+)-isosarcophine (5) [15], (1S,2E,4S,6E,8S,11R)-2,6,12(20)-cembratriene-4,8,11-triol (7) [16], loliolide (8) [17], apo-9′-fucoxanthinone (9) [18], (13Z)-PGB2 (14) [19], PGB2 (15) [19,20] and PGA2 (16) [19] were identified by NMR, ESI-MS and optical rotation data analysis and comparison of spectroscopic data with literatures.

All isolated compounds (except for 14 with limited amount) were tested for their inhibition activity against LPS-activated NO production in RAW264.7 cells using the Griess assay. Two cembrane-type diterpenoids 6 and 7 displayed promising inhibitory effects on the production of NO with IC50 values 26.7 and 17.6 μM (the positive control indomethacin, IC50 = 39.8 μM). apo-9′-Fucoxanthinone (9) had good inhibition activity against LPS-activated NO production in RAW264.7 cells with 32.1 μM. Most of the isolated prostaglandins, 10, 12, 13, 15 and 16 showed potential anti-inflammatory activity with IC50 values 20.4, 24.8, 16.1, 15.9 and 7.1 μM, respectively. The other compounds were displayed weak or not anti-inflammatory. To evaluate the effects of all tested compounds on cell proliferation/viability, none of the compounds (up to 50 μM) showed any significant cytotoxicity with LPS treatment for 24 h using the thiazolyl blue tetrazolium bromide (MTT) method. The structure−activity relationships revealed that a methylene group at C-16 of five-member ring among cembrane-type diterpenoids was much more favorable than a carbonyl group for activity, as compound 5 was much more active than compounds 1−4. Among prostaglandins with 5E geometry, double bond at C-13 played an important role in their anti-inflammatory action because (5E)-PGB2 (10) was much more active than (5E)-13,14-dihydro-PGB2 (11). The side chain possessing a terminal carbonyl acid group made a more positive contribution to the anti-inflammatory activity than those with methoxycarbonyl group (12 vs. 13). The structure of PGA2 made a more positive contribution to the anti-inflammatory activity than those of PGB2 (16 vs. 15). In addition, the secondary metabolites (except for 14 with limited amount) were evaluated for their cytotoxicity using A549 (lung cancer), HepG2 (liver cancer) and MCF-7 (breast cancer) human cell lines and showed no cytotoxicity against all three cell lines at 50 μM.

3. Materials and Methods

3.1. General Experimental Procedures

Optical rotations were recorded on an MCP 200 (Anton Paar, Shanghai, China) polarimeter. UV data were measured on a Shimadzu UV-240 spectrophotometer (Shimadzu, Kyoto, Japan). IR spectra were detected on a Fourier transformation infra-red spectrometer coupled with infra-red microscope EQUINOX 55 (Bruker, Rheinstetten, Germany). 1D and 2D NMR spectra were performed on a Bruker Avance 400 MHz spectrometer with tetramethylsilane as internal standard. HR-ESIMS data were carried out on an LTQ-Orbitrap LC-MS spectrometer (Thermo Corporation, Waltham, MA, USA). ESIMS spectra were obtained on an ACQUITY QDA (Waters Corporation, Milford, MA, USA). HPLC was carried out on Essentia LC-16 with an SPD-16 Detector (Shimadzu, Shanghai, China). Column chromatography was performed on silica gel (200–300 mesh, Qingdao Marine Chemical Factory, China) and Sephadex LH-20 (GE Healthcare, Littile Chalfont, UK).

3.2. Biological Material

Lobophytum sarcophytoides SYSU-MS001 were collected along the coast of Xisha Islands (17°06′14.50″ N, 111°28′35.03″ E), South China Sea, in July 2018, at a depth of −25 m and were frozen immediately after collection. The soft coral has been preserved at the school of marine sciences, Sun Yat-Sen University.

3.3. Extraction, Isolation and Characterization

The soft coral (0.9 kg) was cut into small pieces and extracted three times with CH2Cl2/MeOH (1:1, 1 L) to afford the organic extract (10.3 g). The extract was subjected to silica gel column eluted with PE-EtOAc (from 80:20 to 0:100) to give seven fractions (A–F). Fr. B was separated by Sephadex LH-20 (CC, 3 × 50 cm) eluted with MeOH-CH2Cl2 (1:1) to give Fr.B.1-Fr.B.4. Fr.B.2 was further subjected to silica gel CC by elution by PE-EtOAc (75:25) to afford Fr.B.2.1-Fr.B.2.6 and Fr.B.2.3 was compound 5 (5 mg). Fr.B.2.4 was separated by the PR-HPLC (MeOH- H2O 75:25, flow rate 1.5 mL/min, Ultimate C18 column 10 × 250 nm, 5 μm) to give 4 (3 mg, tR = 15.5 min) and 2 (2 mg, tR = 17.0 min). Fr.B.3 was subjected to silica gel CC by elution by PE-EtOAc (75:25) to afford Fr.B.3.1- Fr.B.3.6, and Fr.B.3.5 was compound 6 (6 mg). Then Fr.B.3.5 was applied to the normal-phase HPLC (n-hexane/2-propanol 92:8, flow rate 1.5 mL/min, Ultimate SiO2 column 10 × 250 nm, 5 μm) to afford 9 (5 mg, tR = 19.0 min), 3 (2 mg, tR = 21.5 min). Fr. C was applied to a Sephadex LH-20 column with MeOH-CH2Cl2 (1:1) to Fr.C.2.1-Fr.C.2.5 and Fr.C.2 was fractionated on a silica gel column with PE-EtOAc (70:30) to give five fractions (Fr.C.2.1-Fr.C.2.5). Fr.C.2.3 was purified by the normal-phase HPLC (n-hexane/ 2-propanol 90:10, flow rate 1.5 mL/min, Ultimate SiO2 column 10 × 250 nm, 5 μm) to give 1 (3 mg, tR = 23 min) and 10 (8 mg, tR = 26 min). Fr.C.2.4 was separated by PR-HPLC (MeOH-H2O 75:25, flow rate 1.5 mL/min, ACE 5 C18-PFP column 250 × 10 mm, 5 μm) to give 8 (4 mg, tR = 17 min). Fr. D was subjected to a Sephadex LH-20 column with MeOH-CH2Cl2 (1:1) to Fr.D.4.1- Fr.D.4.4, then Fr.D.4.4 was purified by PR-HPLC (MeOH-H2O 75:25, flow rate 1.5 mL/min, ACE 5 C18-AR column 250 × 10 mm, 5 μm) to obtain 16 (10 mg, tR = 16.5 min), 15 (25 mg, tR = 24 min) and 11 (12 mg, tR = 18.5 min). Fr. E was subjected to a Sephadex LH-20 column with MeOH-CH2Cl2 (1:1) to Fr.E.1-Fr.E.4, then Fr.E.3 was fractionated on a silica gel column with PE-EtOAc (70:30) to give four fractions (Fr.E.3.1- Fr.E.3.4). Fr.E.3.3 was purified by PR-HPLC (MeOH-H2O 75:25, flow rate 1.5 mL/min, ACE 5 C18-AR column 250 × 10 mm, 5 μm) to obtain 12 (5 mg, tR = 17 min), 13 (7 mg, tR = 19 min) and 14 (1 mg, tR = 22 min). Fr.E.3.4 was also purified by PR-HPLC (MeOH-H2O 75:25, flow rate 1.5 mL/min, ACE 5 C18-AR column 250 × 10 mm, 5 μm) to give 7 (5 mg, tR = 15 min).

3.3.1. Lobophytin A (1)

Colorless oil; = 53.1 (MeOH, c 0.05); UV (MeOH) λmax (log ε) 212 (4.12) nm; CD (MeOH) λmax (Δε) 223 (+26.3), 248 (−2.5) nm; IR (neat) νmax 3450, 2921, 2854, 1737, 1675, 1446, 1093, 998, 904 cm−1; 1H NMR (400 MHz, MeOD) and 13C NMR (100 MHz, MeOD) data see Table 1; HR-ESIMS m/z 331.1906 [M − H]− (calculated for C20 H27 O4, 331.1909).

3.3.2. Lobophytin B (3)

Colorless oil; = 33.3 (MeOH, c 0.06); UV (MeOH) λmax (log ε) 209 (4.10), 280 (3.74) nm; CD (MeOH) λmax (Δε) 216 (+27.2), 250 (−2.9) nm; IR (neat) νmax 3422, 2922, 2853, 1733, 1671, 1438, 1364, 1243, 981 cm−1; 1H NMR (400 MHz, MeOD) and 13C NMR (100 MHz, MeOD) data see Table 1; HR-ESIMS m/z 333.2058 [M − H]+ (calculated for C20H29O4, 333.2060).

3.3.3. (5E)-PGB2 (10)

Colorless oil; 1.3 (c 0.21, MeOH); UV (MeOH) λmax (log ε) 280 (4.06); IR (neat) νmax 3357, 3191, 2920, 2852, 1694, 1624, 1415 cm−1; 1H NMR (400 MHz, MeOD) and 13C NMR (100 MHz, MeOD) data see Table 2; HR-ESIMS m/z 333.2068 [M − H]− (calculated for C20H29O4, 333.2071).

3.3.4. (5E)-13,14-dihydro-PGB2 (11)

Colorless oil; 0.4 (c 0.13, MeOH); UV (MeOH) λmax (log ε) 237 (4.07); IR (neat) vmax 3392, 2939, 2858, 1691, 1637, 1454, 1363, 1250, 1055 cm−1; 1H NMR (400 MHz, MeOD) and 13C NMR (100 MHz, MeOD) see Table 2; HR-ESIMS m/z 335.22312 [M − H]− (calculated for C20H31O4, 335.22278).

3.3.5. 13,14-dihydro-PGB2 (12)

Colorless oil; 0.3 (c 0.29, MeOH); UV (MeOH) λmax (log ε) 238 (4.11); IR (neat) vmax 3413, 2935, 2868, 1697, 1628, 1450, 1358, 1250, 1240, 1051 cm−1; 1H NMR (400 MHz, MeOD) and 13C NMR (100 MHz, MeOD) see Table 2; HR-ESIMS m/z 335.22312 [M − H]− (calculated for C20H31O4, 335.22278).

3.3.6. 13,14-dihydro-PGB2-Me (13)

Colorless oil; 0.9 (c 0.20, MeOH); UV (MeOH) λmax (log ε) 237 (4.09); IR (neat) νmax 3445, 2931, 2858, 1737, 1695, 1635, 1440, 1361, 1045 cm−1; 1H NMR (400 MHz, MeOD) and 13C NMR (100 MHz, MeOD) see Table 2; HR-ESIMS m/z 351.2535 [M − H]− (calculated for C21H35O4, 351.2535).

3.4. Preparation of (S)-MTPA Ester and (R)-MTPA Ester

3.4.1. (S)-MTPA Ester (15a) and (R)-MTPA Ester (15b)

A sample of 15 (1.0 mg, 4 μmol), (R)-MPTACl (5.0 μL, 25 μmol) and pyridine-d5 (0.5 mL) were used to react in an NMR tube at room temperature for 24 h, with the 1H NMR data of the (S)-MTPA ester derivative (15a) were obtained directly on the reaction mixture [21,22]. 1H NMR (selected signals, pyridine-d5, 400 MHz) δH: 7.21 (1H, d, H-13), 6.42 (1H, dd, H-14), 5.95 (1H, q, H-15), 1.85 (2H, m, H-16).

Similarly, the reaction mixture from another sample of 15 (1.0 mg, 4 μmol), (S)-MPTACl (5.0 μL, 26 μmol) and pyridine-d5 (0.5 mL) was processed as described above for 15a to afford 15b. 1H NMR (selected signals, pyridine-d5, 400 MHz) δH: 7.10 (1H, d, H-13), 6.30 (1H, dd, H-14), 5.94 (1H, q, H-15), 1.91 (2H, m, H-16).

3.4.2. (S)-MTPA Ester (10a) and (R)-MTPA Ester (10b)

Similar method was allowed to afford (S)-MTPA ester (10a) and (R)-MTPA Ester (10b). 1H NMR (selected signals, pyridine-d5, 400 MHz) 10a δH: 7.26 (1H, d, H-13), 6.46 (1H, dd, H-14), 5.95 (1H, q, H-15), 1.85 (2H, m, H-16). 10b δH: 7.11 (1H, d, H-13), 6.30 (1H, dd, H-14), 5.93 (1H, q, H-15), 1.91 (2H, m, H-16).

3.5. Calculation of ECD Spectra

Molecular Merck force field (MMFF) and density functional theory/time-dependent density functional theory (DFT/TD-DFT) calculations were performed on Spartan’14 (Wavefunction, Inc., Irvine, CA, USA) and the Gaussian 09 software (Gaussian, Wallingford, CT, USA), respectively [23]. Using DFT calculations at the B3LYP/6-31G (d) level was to generate and optimize conformers. Conformers with a Bolzmann distribution over 1% were chosen for ECD calculations in MeOH at the B3LYP/6311+G (2d, p) level. ECD spectra were generated by the software SpecDis 1.7.1 (University of Würzburg, Würzburg, Germany) and Origin Pro 8.5 (OriginLab, Ltd., Northampton, MA, USA) from dipole-length rotational strengths by applying Gaussian band shapes with sigma = 0.16 eV. All calculations were carried out on Tianhe-2 in the National Super Computer Center in Guangzhou.

3.6. Cytotoxic Assay

A549 (lung cancer), HepG2 (liver cancer) and MCF-7 (breast cancer) was used to evaluate the cytotoxicity of all tested compounds. The three human tumor cell lines human lung adenocarcinoma (A549), human hepatocellular carcinoma (HepG2), and the human breast adenocarcinoma cell line (MCF-7) were bought from the cell bank of the Chinese Academy of Sciences (Shanghai, China). The cytotoxic activities of the tested compounds were assayed according to the MTT method by using 96 well plates on the base of the previous reported procedures [24].

3.7. Anti-Inflammation Bioassays

The anti-inflammation activity of the isolated compounds was evaluated according to the reported procedures [25].

4. Conclusions

In summary, two new cembrane-type diterpenoids, lobophytins A (1) and B (3), and four new prostaglandins, (5E)-PGB2 (10), (5E)-13,14-dihydro-PGB2 (11), 13,14-dihydro-PGB2 (12) and 13,14-dihydro-PGB2-Me (13), together with ten known compounds were isolated from the soft coral Lobophytum sarcophytoides. The structures of new compounds were determined by analysis of HR-ESIMS, 1D and 2D NMR spectroscopic data and the absolute configurations were further determined by comparison of the experimental and calculated ECD spectra, as well as the modified Mosher’s method. Two cembrane-type diterpenoid displayed promising inhibitory effects on the production of NO with IC50 values 26.7 and 17.6 μM (the positive control indomethacin, IC50 = 39.8 μM). Most of the isolated prostaglandins, 10, 12, 13, 15 and 16 showed potential anti-inflammatory activity with IC50 values ranging from 7.1 to 24.8 μM.