Pinnisterols D–J, New 11-Acetoxy-9,11-secosterols with a 1,4-Quinone Moiety from Formosan Gorgonian Coral Pinnigorgia sp. (Gorgoniidae)

Abstract

Seven new marine 11-acetoxy-9,11-secosterols, pinnisterols D–J (1–7), with a 1,4-quinone moiety, were discovered from the gorgonian coral Pinnigorgia sp. In this study, the structures of secosterols 1–7 were revealed by spectroscopic analysis. Bioactivity study showed that secosterol 1 treatment inhibited cell viability in a hepatic stellate cell line, HSC-T6, with an IC₅₀ value of 3.93 μM; and secosterols 2, 5, and 7 reduced elastase enzyme release, and 3, 5, and 7 decreased the production of superoxide anions from human neutrophils.

1. Introduction

Since the isolation in 1972 of the first marine 9,11-secosteroid, 9-oxo-9,11-secogorgost-5-ene-3β, 11-diol 11-acetate, from the gorgonian coral Pseudopterogorgia americana [1], a series of compounds of this group has been prepared from various marine invertebrates, particularly sponges and octocorals, with complex structures and interesting bioactivities [2]. Our continued investigations of gorgonian coral Pinnigorgia sp. (phylum Cnidaria, class Anthozoa, subclass Octocorallia, order Alcyonacea, family Gorgoniidae) have yielded various interesting secondary metabolites [3,4,5,6,7,8], including 9,11-secosterols [3,4,5], some of which have been shown to possess bioactivity, such as anti-inflammatory and cytotoxic properties [3,4,5,6,7,8]. With the aim of discovering bioactive marine metabolites for new drug development in the future, we carried out an investigation of the chemical composition of the gorgonian coral Pinnigorgia sp. In this study, we performed compound preparation and structure determination, and investigated the cytotoxicity and anti-inflammatory activities of seven new 9,11-secosterols, pinnisterols D–J (1–7), following further study of Pinnigorgia sp. (Figure 1).

2. Results and Discussion

A new metabolite was isolated as a colorless oil, and was named pinnisterol D (1). The high-resolution electrospray ionization mass spectrum (HRESIMS) showed a signal at m/z 525.31853 (calcd. for C₃₀H₄₆O₆ + Na, 525.31921), and therefore the molecular formula of 1 was determined to be C₃₀H₄₆O₆ (8° of unsaturation). ¹³C and distortionless enhancement polarization transfer (DEPT) experimental data indicated that 1 had 30 carbons, including seven methyls, seven sp³ methylenes (including one oxymethylene), six sp³ methines (including one oxymethine), two sp³ quaternary carbons, one sp³ tertiary alcohol, three sp² methines, one sp² tertiary carbon, two ketonic carbonyls, and one ester carbonyl (

Table 1. Results of ¹H (400 MHz, CDCl₃) and ¹³C (100 MHz, CDCl₃) NMR experiments and ¹H–¹H COSY and HMBC correlations for secosterol 1.

Position	δH (J in Hz)	δC, Multiple	1H–1H COSY	HMBC
1	2.21 m; 1.78 m	25.9, CH2	H2-2	C-2, -10
2	2.00 m; 1.49 m	29.9, CH2	H2-1, H-3	n. o. a
3	4.03 m	66.7, CH	H2-2, H2-4	n. o.
4	2.17 m; 1.79 m	35.7, CH2	H-3	C-2, -3, -5, -6, -10
5		80.6, C
6		197.5, C
7	6.45 s	134.1, CH		C-5, -8, -9, -14
8		152.0, C
9		201.6, C
10		52.0, C
11	4.18 m	61.0, CH2	H2-12	C-12, -13, acetate carbonyl
12	1.68 m; 1.26 ddd (14.8, 9.2, 5.6)	37.1, CH2	H2-11	C-11, -13, -14, -17, -18
13		47.4, C
14	3.37 dd (10.8, 8.0)	43.9, CH	H2-15	C-7, -8, -9, -13, -15, -18
15	1.75 m; 1.66 m	27.1, CH2	H-14, H2-16	C-16
16	1.78 m; 1.57 m	25.6, CH2	H2-15, H-17	C-15
17	1.81 m	51.0, CH	H2-16, H-20	C-15, -16, -18, -21
18	0.73 s	18.0, CH3		C-12, -13, -14, -17
19	1.21 s	20.5, CH3		C-1, -5, -9, -10
20	2.24 m	38.3, CH	H-17, H3-21, H-22	C-16, -17, -22, -23
21	1.05 d (6.8)	21.8, CH3	H-20	C-17, -20, -22
22	5.23 dd (14.8, 6.8)	133.8, CH	H-20, H-23	C-20, -24
23	5.26 dd (14.8, 6.8)	133.5, CH	H-22, H-24	C-20, -24
24	1.86 m	43.0, CH	H-23, H-25, H3-28	C-22, -23, -25, -26, -27, -28
25	1.46 m	33.1, CH	H-24, H3-26, H3-27	C-23, -24, -26, -27, -28
26	0.84 d (7.2)	20.0, CH3	H-25	C-24, -25, -27
27	0.82 d (7.2)	19.7, CH3	H-25	C-24, -25, -26
28	0.91 d (6.8)	17.5, CH3	H-24	C-23, -24, -25
11-OAc		171.1, C
	2.02 s	21.1, CH3		Acetate carbonyl

^a n. o. = not observed.

). In addition, IR spectroscopy demonstrated that the compound contained hydroxy (ν_max 3446 cm⁻¹), ester (ν_max 1741 cm⁻¹), and α,β-unsaturated ketonic carbonyl (ν_max 1685 cm⁻¹) groups. The latter structural feature of 1 was further proven by the presence of signals at δ_C 197.5 (C-6), 134.1 (CH-7), 152.0 (C-8), and 201.6 (C-9) in the ¹³C NMR spectrum. Signals of carbons at δ_C 133.8 (CH-22) and 133.5 (CH-23) suggested the existence of a disubstituted olefin, and this was confirmed by two olefin proton signals at δ_H 5.26 (1H, dd, J = 14.8, 6.8 Hz, H-23) and 5.23 (1H, dd, J = 14.8, 6.8 Hz, H-22) (Table 1). The presence of Me-21, Me-28, Me-26, and Me-27 groups resulted in four doublets located at δ_H 1.05 (3H, J = 6.8 Hz), 0.91 (3H, J = 6.8 Hz), 0.84 (3H, J = 7.2 Hz), and 0.82 (3H, J = 7.2 Hz), respectively, and the existence of H₃-18 and H₃-19 resulted in two sharp singlets at δ_H 0.73 and δ_H 1.21, respectively. In the ¹H NMR spectrum, one acetyl methyl signal (δ_H 2.02, 3H, s) was observed. Based on the aforementioned findings, metabolite 1 was determined to be a tricyclic compound.

From the ¹H NMR spectrum and ¹H–¹H correlation spectroscopy (COSY) of 1 (Table 1), the following correlations were revealed: H₂-1/H₂-2/H-3/H₂-4, H₂-11/H₂-12, H-14/H₂-15/H₂-16/H-17/H-20/H-22/H-23/H-24/H-25/H₃-26, H-20/H₃-21, H-24/H₃-28, and H-25/H₃-27. Together with data of key heteronuclear multiple bond coherence (HMBC) correlations between H₂-4, H-7, H₃-19/C-5; H₂-4/C-6; H-7, H-14/C-8; H-7, H-14, H₃-19/C-9; H₂-1, H₂-4, H₃-19/C-10; and H₂-11, H₂-12, H-14, and H₃-18/C-13, all the information allowed determination of the main carbon skeleton of 1 (Table 1).

The correlations identified using nuclear Overhauser effect spectroscopy (NOESY) in addition to comparison of NMR data with those of known 9,11-secosterol 8, isolated from Korean marine sponge Ircinia sp. [9], and pinnisterol A (9) [4], enabled clarification of the configuration of 1 (Figure 1). The stereochemistries of stereogenic centers C-3, C-5, C-10, C-13, C-14, and C-17 in 1 were the same as those of 8. In addition, the main NOE correlations for 1 were interactions between H-3/H-2α (δ_H 2.00), H-2β (δ_H 1.49)/H₃-19, H-3/H-4α (δ_H 2.17), H-4β (δ_H 1.79)/H₃-19; thus, H-3 and the 5-hydroxy group in 1 should be positioned on the α-face (Figure 2).

There was a greater coupling constant between H-22 and H-23 (J = 14.8 Hz), which supported a trans relationship between H-22 and H-23. This implied that the configuration of C-24 should be R according to the ¹³C NMR chemical shift of C-28 (δ_C 17.5). A previous study showed that, for a known sterol, (22E,24R)-24-methylcholesta-5,22-dien-3β-ol, with an identical chain, and the 24S epimer, (22E,24S)-24-methylcholesta-5,22-dien-3β-ol, the ¹³C NMR value of C-28 resonates at δ_C 17.68 ppm in the 24R epimer, with a relative 0.4 ppm downfield chemical shift (Figure 3) [10].

Pinnisterol E (2) was present as a colorless oil. From HRESIMS analysis, the signal at m/z 527.33410 (calcd. for C₃₀H₄₈O₆ + Na, 527.33486) suggested the molecular formula of 2 to be C₃₀H₄₈O₆ (7° of unsaturation), and the IR spectrum demonstrated the existence of hydroxy (ν_max 3381 cm⁻¹), ester (ν_max 1740 cm⁻¹), and α,β-unsaturated ketonic carbonyl (ν_max 1686 cm⁻¹) groups. The whole series of spectroscopic data demonstrated that secosterols 2 and 1 had an identical core structure, the difference being limited to the absence in 2 of the carbon-carbon double bond between C-22/23. The complete assignments of ¹H and ¹³C NMR of 2 (

Table 2. ¹H NMR data for secosterols 2–4.

δH	2 a	3 b	4 b
1	2.21 m; 1.76 m	2.21 m; 1.74 m	2.20 m; 1.72 m
2	2.00 m; 1.47 m	2.00 m; 1.47 m	2.00 m; 1.49 m
3	4.04 m	4.04 m	4.04 m
4	2.15 ddd (14.4, 5.2, 2.0) c; 1.79 m	2.14 m; 1.77 m	2.13 m; 1.79 m
7	6.47 s	6.46 s	6.46 s
11	4.16 m	4.17 t (6.3)	4.18 m
12	1.73 m; 1.23 m	1.59 m; 1.30 m	1.69 m; 1.25 m
14	3.39 dd (10.8, 8.4)	3.37 t (9.8)	3.38 dd (11.2, 8.4)
15	1.76 m; 1.68 m	1.77 m; 1.69 m	1.76 m; 1.65 m
16	1.89 m; 1.53 m	1.75 m; 1.49 m	1.76 m; 1.55 m
17	1.76 m	1.97 m	1.77 m
18	0.74 s	0.73 s	0.73 s
19	1.22 s	1.21 s	1.22 s
20	1.42 m	1.46 m	2.23 m
21	0.99 d (6.8)	4.01 dd (10.5, 7.0); 3.96 dd (10.5, 7.0)	1.06 d (7.0)
22	1.44 m; 0.95 m	5.36 dd (15.4, 8.4)	5.24 dd (15.4, 8.4)
23	1.40 m; 0.96 m	5.22 dd (15.4, 8.4)	5.30 dd (15.4, 8.4)
24	1.20 m	1.90 m	2.19 m
25	1.61 m	1.45 m	1.71 m
26	0.79 d (6.8)	0.84 d (7.0)	0.85 d (7.0)
27	0.86 d (6.8)	0.82 d (7.0)	3.98 dd (10.5, 6.3); 3.85 dd (10.5, 6.3)
28	0.78 d (6.8)	0.93 d (7.0)	0.98 d (7.0)
11-OAc	2.02 s	2.02 s	2.03 s
21-OAc		2.04 s
27-OAc			2.07 s

^a Spectra recorded at 400 MHz in CDCl₃; ^b Spectra recorded at 700 MHz in CDCl₃; ^c J values (in Hz) in parentheses.

and

Table 3. ¹³C NMR data for secosterols 2–7.

δC	2 a	3 b	4 b	5 a	6 a	7 a
1	25.9, CH2	25.8, CH2	25.9, CH2	25.9, CH2	25.7, CH2	25.7, CH2
2	29.9, CH2	29.9, CH2	29.9, CH2	29.9, CH2	25.9, CH2	25.9, CH2
3	66.7, CH	66.7, CH	66.7, CH	66.7, CH	69.7, CH	69.8, CH
4	35.8, CH2	35.7, CH2	35.7, CH2	35.6, CH2	32.0, CH2	31.9, CH2
5	80.6, C	80.6, C	80.6, C	80.5, C	80.1, C	80.0, C
6	197.4, C	197.4, C	197.5, C	197.5, C	197.3, C	197.5, C
7	134.1, CH	134.1, CH	134.1, CH	134.2, CH	134.2, CH	134.2, CH
8	152.1, C	151.6, C	151.8, C	151.7, C	151.8, C	151.6, C
9	201.5, C	201.6, C	201.6, C	201.6, C	201.2, C	201.3, C
10	52.0, C	52.0, C	52.0, C	52.0, C	51.9, C	51.9, C
11	61.0, CH2	60.8, CH2	61.0, CH2	60.9, CH2	61.0, CH2	61.0, CH2
12	37.2, CH2	36.7, CH2	37.0, CH2	37.0, CH2	37.2, CH2	37.2, CH2
13	47.5, C	47.5, C	47.3, C	47.4, C	47.4, C	47.4, C
14	43.7, CH	43.5, CH	43.8, CH	43.7, CH	43.7, CH	43.8, CH
15	27.2, CH2	27.1, CH2	26.9, CH2	27.0, CH2	27.1, CH2	27.1, CH2
16	26.2, CH2	25.8, CH2	25.7, CH2	26.2, CH2	26.4, CH2	25.8, CH2
17	50.7, CH	46.3, CH	50.7, CH	51.4, CH	51.6, CH	50.9, CH
18	17.6, CH3	18.5, CH3	18.0, CH3	17.6, CH3	17.8, CH3	18.0, CH3
19	20.5, CH3	20.4, CH3	20.5, CH3	20.4, CH3	20.3, CH3	20.2, CH3
20	34.9, CH	42.2, CH	38.4, CH	33.2, CH	33.9, CH	38.2, CH
21	19.2, CH3	67.2, CH2	21.7, CH3	20.4, CH3	21.1, CH3	21.6, CH3
22	33.0, CH2	127.5, CH	135.4, CH	35.4, CH2	39.4, CH2	132.9, CH
23	21.4, CH2	138.1, CH	131.1, CH	76.7, CH	74.6, CH	134.5, CH
24	39.0, CH	43.4, CH	38.2, CH	42.7, CH	45.5, CH	75.0, C
25	31.5, CH	32.9, CH	37.4, CH	28.5, CH	27.7, CH	38.1, CH
26	17.6, CH3	20.0, CH3	13.1, CH3	21.6, CH3	21.7, CH3	17.5, CH3
27	20.5, CH3	19.7, CH3	67.9, CH2	18.6, CH3	17.6, CH3	17.1, CH3
28	15.4, CH3	17.5, CH3	18.3, CH3	11.0, CH3	10.5, CH3	25.2, CH3
3-OAc					170.8, C	170.9, C
					21.3, CH3	21.1, CH3
11-OAc	171.1, C	171.1, C	171.1, C	171.1, C	171.0, C	170.9, C
	21.1, CH3	21.1, CH3	21.1, CH3	21.1, CH3	21.1, CH3	21.1, CH3
21-OAc		171.1, C
		21.0, CH3
23-OAc				170.7, C
				21.4, CH3
27-OAc			171.3, C
			21.1, CH3

^a Spectra recorded at 100 MHz in CDCl₃; ^b Spectra recorded at 175 MHz in CDCl₃.

) were compared with the values of 1, and secosterol 2 was assigned as having structure 2, with the same configurations of the core rings A–C. In addition, both compounds had identical stereogenic centers at C-3, C-5, C-10, C-13, C-14, and C-17, and their ¹H and ¹³C NMR chemical shifts and proton coupling constants were in concurrence also. Based on the ¹³C NMR chemical shifts of C-25 (δ_C 31.5), C-26 (δ_C 17.6), and C-27 (δ_C 20.5), the configuration of the stereogenic center at C-24 was assigned as S. Previous study also showed that the ¹³C NMR values of C-25, C-26, and C-27 resonates at δ_C 31.54, 17.68, and 20.56 ppm in a 24S epimer of a known sterol, (24S)-24-methylcholest-5-en-3β-ol, with an identical side chain, and the ¹³C NMR values of C-25, C-26, and C-27 in a 24R epimer, (24R)-24-methylcholest-5-en-3β-ol, were observed at δ_C 32.49, 20.26, and 18.32 ppm, respectively (Figure 4) [10].

Pinnisterol F (3) was present as a colorless oil. From HRESIMS analysis, the signal at m/z 583.32406 (calcd. for C₃₂H₄₈O₈ + Na, 583.32469) suggested the molecular formula of 3 to be C₃₂H₄₈O₈ (9° of unsaturation). The NMR signals of 3 (Table 2 and Table 3) were similar to those of 1, except that the signals related to the C-21 methyl in 1 were substituted by signals for an acetoxymethylene group in 3. From the HMBC spectrum of 3, it was revealed that an ester carbonyl carbon at δ_C 171.1 correlated with a methyl signal at δ_H 2.04 and a pair of oxygenated methylene protons at δ_H 4.01 (1H, dd, J = 10.5, 7.0 Hz) and 3.96 (1H, dd, J = 10.5, 7.0 Hz), which revealed that an acetoxy group was at the position C-21 in the side chain of 3. Thus, pinnisterol F (3) was found to be the 21-acetoxy derivative of 1.

Pinnisterol G (4) had a molecular formula identical to that of 3, C₃₂H₄₈O₈, with a HRESIMS signal located at m/z 583.32432 (calcd. for C₃₂H₄₈O₈ + Na, 583.32469) with nine degrees of unsaturation, indicating that secosterols 3 and 4 were isomers. Comparison of the NMR data of 4 with those of 3 (Table 2 and Table 3) showed that both compounds possessed the same sterol nucleus and a similar side chain, but differed in terms of the location of one acetoxy group. From an HMBC experiment, it was revealed that one ester carbonyl carbon at δ_C 171.3 correlated with one methyl signal at δ_H 2.07 and a pair of oxymethylene protons signals at δ_H 3.98 (dd, J = 10.5, 6.3 Hz) and 3.85 (dd, J = 10.5, 6.3 Hz), which indicated that an acetoxy group was located at C-27 in the side chain. The configurations at C-24 and C-25 were therefore designated as S- and R-forms, respectively, on the basis of the ¹³C NMR chemical shifts of C-24 (δ_C 38.2), C-25 (δ_C 37.4), C-26 (δ_C 13.1), C-27 (δ_C 67.9), and C-28 (δ_C 18.3). It was reported that the ¹³C NMR values of C-24, C-25, C-26, C-27, and C-28 resonate at δ_C 38.2, 37.6, 13.0, 68.1, and 18.6 ppm in a 24S and a 25R epimer of a known sterol, echrebsteroid C, with the same side chain, and the ¹³C NMR values of C-24, C-25, C-26, C-27, and C-28 in a 24S and 25S epimer, echrebsteroid B, appeared at δ_C 38.8, 37.5, 14.1, 67.9, and 17.1 ppm (Figure 5) [11].

Pinnisterol H (5) was isolated as a colorless oil. Based on the HRESIMS signal located at m/z 585.33988 (calcd. for C₃₂H₅₀O₈ + Na, 585.34034), it was concluded that the molecular formula of 5 was C₃₂H₅₀O₈ (8° of unsaturation). The IR spectrum of 5 indicated the presence of hydroxy (ν_max 3448 cm⁻¹), ester (ν_max 1736 cm⁻¹) and α,β-unsaturated ketonic carbonyl (ν_max 1686 cm⁻¹) groups. The whole series of spectroscopic data showed that secosterol 5 and secosterol 1 shared the same core structure, with the exception of the addition of an acetoxy group to substitute the alkene at C-23 in 5. The complete assignments of the ¹³C and ¹H NMR of pinnisterol H (5) (Table 3 and

Table 4. ¹H NMR (400 MHz, CDCl₃) data for secosterols 5–7.

δH	5	6	7
1	2.22 m; 1.76 m	2.27 m; 1.78 m	2.28 m; 1.76 m
2	1.97 m; 1.48 m	1.98 m; 1.60 m	1.96 m; 1.61 m
3	4.02 m	5.05 m	5.05 m
4	2.12 m; 1.78 m	2.24 m; 1.81 m	2.24 m; 1.79 m
7	6.45 s	6.46 s	6.45 s
11	4.14 m	4.18 m	4.17 m
12	1.63 m; 1.23 m	1.70 m; 1.27 m	1.67 m; 1.26 m
14	3.36 dd (11.2, 8.4) a	3.39 dd (10.8, 8.0)	3.39 dd (10.4, 8.0)
15	1.76 m; 1.65 m	1.80 m; 1.69 m	1.76 m; 1.69 m
16	1.91 m; 1.52 m	1.93 m; 1.53 m	1.99 m; 1.53 m
17	1.69 m	1.81 m	1.81 m
18	0.73 s	0.74 s	0.73 s
19	1.20 s	1.22 s	1.21 s
20	1.54 m	1.63 m	2.28 m
21	1.02 d (6.8)	1.13 d (6.8)	1.08 d (6.8)
22	1.67 m; 1.24 m	1.72 m; 1.07 m	5.53 dd (15.6, 8.4)
23	5.01 m	3.59 m	5.48 (15.6)
24	1.47 m	1.32 m
25	1.57 m	1.84 m	1.67 m
26	0.93 d (6.8)	0.94 d (7.2)	0.89 d (6.8)
27	0.83 d (6.8)	0.84 d (7.2)	0.88 d (6.8)
28	0.81 d (6.8)	0.79 d (7.2)	1.21 s
3-OAc		2.04 s	2.04 s
11-OAc	2.02 s	2.02 s	2.02 s
23-OAc	2.03 s

^a J values (in Hz) in parentheses.

) were compared with the values of 1, and the HMBC correlations fully supported the positions of the functional groups of 5, indicating that it had a structure of the same configuration as secosterols 1–4 in the core rings A–C. The proton coupling constants and NMR chemical shift data also further supported this finding, though the configurations of C-23 and C-24 were not determined at this stage.

Pinnisterol I (6) was obtained as a colorless oil. The HRESIMS signal at m/z 585.33988 (calcd. for C₃₂H₅₀O₈ + Na, 585.34034) suggested the molecular formula of 6 to be C₃₂H₅₀O₈ (8° of unsaturation). The NMR signals of 6 (Table 3 and Table 4) were very similar to those of 5, with the exception that 5 had signals corresponding to 3-hydroxy and 23-acetoxy groups, which were substituted by signals for acetoxy and hydroxy groups, respectively, in 6. From a NOESY experiment, the correlations of data of 5 and 6 demonstrated that the configurations of the stereogenic centers in the core rings A–C were identical to those of 1. The configurations of stereogenic centers C-23 and C-24 of 6 were also not determined at this stage.

Pinnisterol J (7) was obtained as a colorless oil and had the molecular formula C₃₂H₄₈O₈, as determined by the HRESIMS signal at m/z 583.32433 (calcd. for C₃₂H₄₈O₈ + Na, 583.32469) (9° of unsaturation). According to the NMR spectroscopic data (Table 3 and Table 4), compound 7 showed the same nuclear structure as that of compound 6. In the ¹³C NMR data of 7, one additional disubstituted olefin was identified from signals of carbons at δ_C 132.9 (CH-22) and 134.5 (CH-23). The presence of a 24-hydroxy group was evidenced by HMBC correlations between H-22, H-23, H-25, H₃-26, H₃-27, and H₃-28/C-24 (δ_C 75.0), a methyl-containing oxygenated tertiary carbon. There was a greater coupling constant between H-22 and H-23 (J = 15.6 Hz), suggesting that a trans relationship existed between H-22 and H-23. The configuration of the C-24 stereogenic center was assigned as S on the basis of the ¹³C NMR chemical shifts of C-24 (δ_C 75.0), C-25 (δ_C 38.1), C-26 (δ_C 17.5), C-27 (δ_C 17.1), and C-28 (δ_C 25.2). It was reported that the ¹³C NMR values of C-24, C-25, C-26, C-27, and C-28 resonates at δ_C 75.1, 38.3, 17.7, 17.4, and 25.2 ppm in a 24S epimer of a known synthetic product, 24(S)-hydroxyvitamin D₂, with the same side chain (Figure 6) [12].

The hepatic stellate cell, a major cell type involved in liver fibrosis, is also responsible for liver damage by increasing proliferation and protein secretion associated with the formation of scar tissue. In cytotoxicity testing, secosterols 1–7 were examined in terms of their cytotoxic effects on HSC-T6, an immortalized rat hepatic stellate cell lines. At a concentration of 10 μM, secosterols 1, 3, and 5 significantly decreased the viability of HSC-T6 cells to 16.8 (IC₅₀ = 3.93 μM), 56.9 and 37.1%, respectively (Figure 7). These results implied that the functional groups in the side chain of secosterols 1–7 play important roles in determining the activity of the compounds.

In anti-inflammatory testing, secosterols 2, 5, and 7 displayed inhibitory effects on the release of elastase (IC₅₀ = 2.33, 2.59 and 3.89 μM, respectively), and secosterols 3, 5, and 7 showed inhibitory effects on human neutrophils in terms of the generation of superoxide anions (IC₅₀ = 5.52, 3.26, and 3.71 μM, respectively) (

Table 5. Inhibitory effects of secosterols 2–7 on elastase release and superoxide anion generation by human neutrophils in response to fMet-Leu-Phe/Cytochalastin B.

Compound	Elastase Release	Superoxide Anions
	IC50 (μM)	IC50 (μM)
2	2.33 ± 0.27	>10
3	>10	5.52 ± 1.06
4	>10	>10
5	2.59 ± 0.29	3.26 ± 0.33
6	>10	>10
7	3.89 ± 1.16	3.71 ± 0.51

).

3. Experimental Section

3.1. General Experimental Procedures

Optical rotations were measured with a digital polarimeter (P-1010; Japan Spectroscopic Corporation, Tokyo, Japan); and infrared spectra were recorded on a spectrometer (FT/IR-4100; Japan Spectroscopic Corporation); peaks are reported in cm⁻¹. NMR spectra were obtained on a 400 MHz NMR spectrometer (Mercury Plus; Varian, Palo Alto, CA, USA) and a 700 MHz NMR spectrometer (AVIIIHD700X; Bruker, Bremen, Germany), using the residual CHCl₃ signal (δ_H 7.26 ppm) and CDCl₃ (δ_C 77.1 ppm) as internal standards for ¹H NMR and ¹³C NMR, respectively. Coupling constant values (J) are given in Hz. ESIMS and HRESIMS were performed using mass spectrometry (Tesla solariX FTMS system, Bruker). TLC was carried out on Kieselgel 60 F₂₅₄ precoated plates (0.25 mm, Merck, Darmstadt, Germany), and spots were visualized by the standard method. Column chromatography was performed on silica gel at a size of 230–400 mesh (Merck). HPLC experiments were performed using the following systems: normal-phase HPLC (NP-HPLC) injection port, 7725 (Rheodyne, Rohnert Park, CA, USA); pump, L-7110 (Hitachi, Tokyo, Japan); and semi-preparative normal-phase column (Supelco Ascentis Si Cat #:581515-U, 25 cm × 21.2 mm, 5 μm, Sigma-Aldrich, St. Louis, MO, USA). Reverse-phase HPLC (RP-HPLC) injection port (7725; Rheodyne); pump, L-2130 (Hitachi); photodiode array detector (L-2455; Hitachi); and reverse-phase column (25 cm × 21.2 mm, Luna 5 μm C18(2) 100 Å, AXIA Packed; Phenomenex, Torrance, CA, USA).

3.2. Animal Material

Specimens of gorgonian coral Pinnigorgia sp. were collected in August 2012 by hand while scuba diving off the coast of Green Island located near the southeast of Taiwan. The samples were then stored in a freezer until extraction. A voucher specimen was deposited in the National Museum of Marine Biology & Aquarium, Taiwan (specimen No.: NMMBA-TW-GC-2012-130). Identification of the species of this organism was done by comparison as described in the previous publication [13].

3.3. Extraction and Separation

Extraction of compounds was performed at room temperature unless otherwise specified. Pinnigorgia sp. (wet weight 1.98 kg; dry weight 0.86 kg) was sliced, and the sliced bodies were then extracted with ethyl acetate (EtOAc). The EtOAc extract (84.9 g) was partitioned with n-hexane and methanol (MeOH). The MeOH layer (12.6 g) was separated on a Sephadex LH-20 column and elution was performed using a solvent mixture dichloromethane (DCM):MeOH (1:1); the separation yielded 7 subfractions A–G. Fraction F was separated by silica gel column chromatography and then eluted with n-hexane/acetone (stepwise, 50/50 %v/v to 100% acetone) to afford eight subfractions F1–F8. Fraction F2 was purified by silica gel column chromatography and then eluted with n-hexane/acetone (stepwise, 90/10 %v/v to 100% acetone) to yield 13 subfractions F2A–F2M. Fraction F2F was purified by NP-HPLC using a mixture of n-hexane/EtOAc (5:2) to afford 14 subfractions F2F1–F2F14. Fractions F2F5 and F2F6 were repurified by RP-HPLC using a mixture of MeOH/H₂O (90/10 %v/v at 5.0 mL/min flow rate) to yield 6 (1.8 mg) and 7 (4.8 mg), respectively. Fraction F2H was purified by NP-HPLC using a mixture of n-hexane/EtOAc (50/50 %v/v) to yield 14 subfractions F2H1–F2H14. Fractions F2H9 and F2H10 were repurified by RP-HPLC using a mixture of MeOH/H₂O (90/10 %v/v at 5.0 mL/min flow rate) to yield 1 (3.8 mg) and 2 (1.5 mg), respectively. Fraction F2I was repurified by NP-HPLC using a mixture of n-hexane/EtOAc (50/50 %v/v at 3.0 mL/min flow rate) to afford 15 subfractions F2I1–F2I15, including compound 5 (F2I9, 6.4 mg). Fraction F2I10 was purified by RP-HPLC using a mixture of MeOH/H₂O (85/15 %v/v at 5.0 mL/min, flow rate) to afford 3 (1.0 mg) and 4 (1.0 mg), respectively.

Pinnisterol D (1): colorless oil; [α]${}_{\mathrm{D}}^{25}$ +44 (c 1.3, CHCl₃); IR (neat) ν_max 3446, 1741, 1685 cm⁻¹; ¹H (400 MHz, CDCl₃) and ¹³C (100 MHz, CDCl₃) NMR data (see Table 1); ESIMS m/z 525 [M + Na]⁺; HRESIMS m/z 525.31853 (calcd. for C₃₀H₄₆O₆ + Na, 525.31921).

Pinnisterol E (2): colorless oil; [α]${}_{\mathrm{D}}^{25}$ −35 (c 0.5, CHCl₃); IR (neat) ν_max 3381, 1740, 1686 cm⁻¹; ¹H (400 MHz, CDCl₃) and ¹³C (100 MHz, CDCl₃) NMR data (see Table 2 and Table 3); ESIMS m/z 527 [M + Na]⁺; HRESIMS m/z 527.33410 (calcd. for C₃₀H₄₈O₆ + Na, 527.33486).

Pinnisterol F (3): colorless oil; [α]${}_{\mathrm{D}}^{27}$ −152 (c 0.3, CHCl₃); IR (neat) ν_max 3446, 1736, 1686 cm⁻¹; ¹H (700 MHz, CDCl₃) and ¹³C (175 MHz, CDCl₃) NMR data (see Table 2 and Table 3); ESIMS m/z 583 [M + Na]⁺; HRESIMS m/z 583.32406 (calcd. for C₃₂H₄₈O₈ + Na, 583.32469).

Pinnisterol G (4): colorless oil; [α]${}_{\mathrm{D}}^{27}$ −176 (c 0.3, CHCl₃); IR (neat) ν_max 3447, 1739, 1686 cm⁻¹; ¹H (700 MHz, CDCl₃) and ¹³C (175 MHz, CDCl₃) NMR data (see Table 2 and Table 3); ESIMS m/z 583 [M + Na]⁺; HRESIMS m/z 583.32432 (calcd. for C₃₂H₄₈O₈ + Na, 583.32469).

Pinnisterol H (5): colorless oil; [α]${}_{\mathrm{D}}^{25}$ −20 (c 0.3, CHCl₃); IR (neat) ν_max 3448, 1736, 1686 cm⁻¹; ¹H (400 MHz, CDCl₃) and ¹³C (100 MHz, CDCl₃) NMR data (see Table 3 and Table 4); ESIMS m/z 585 [M + Na]⁺; HRESIMS m/z 585.33988 (calcd. for C₃₂H₅₀O₈ + Na, 585.34034).

Pinnisterol I (6): colorless oil; [α]${}_{\mathrm{D}}^{25}$ −129 (c 0.5, CHCl₃); IR (neat) ν_max 3446, 1736, 1685 cm⁻¹; ¹H (400 MHz, CDCl₃) and ¹³C (100 MHz, CDCl₃) NMR data (see Table 3 and Table 4); ESIMS m/z 585 [M + Na]⁺; HRESIMS m/z 585.33988 (calcd. for C₃₂H₅₀O₈ + Na, 585.34034).

Pinnisterol J (7): colorless oil; [α]${}_{\mathrm{D}}^{25}$ −5 (c 0.2, CHCl₃); IR (neat) ν_max 3455, 1736, 1687 cm⁻¹; ¹H (400 MHz, CDCl₃) and ¹³C (100 MHz, CDCl₃) NMR data (see Table 3 and Table 4); ESIMS m/z 583 [M + Na]⁺; HRESIMS m/z 583.32433 (calcd. for C₃₂H₄₈O₈ + Na, 583.32469).

3.4. Anti-Hepatofibric Assay

The anti-hepatofibric effects of secosterols 1–7, at a concentration of 10 μM, were analyzed using a colorimetric assay (WST-1-based method). The steps of the assay were performed according to a previously-published method [14].

3.5. Generation of Superoxide Anions and Release of Elastase by Human Neutrophils

Human neutrophils were prepared by Ficoll centrifugation followed by dextran sedimentation. Measurements of superoxide anion generation and elastase release from neutrophils were performed based on published procedures [15,16]. Briefly, MeO-Suc-Ala-Ala-Pro-Valp-nitroanilide was used as the elastase substrate for the elastase release assay, and the method using superoxide dismutase-inhibitable reduction of ferricytochrome c was employed to measure superoxide anion production.

4. Conclusions

Our ongoing investigations of coral metabolites showed that gorgonian corals belonging to the genus Pinnigorgia are rich in 9,11-secosterols. In cytotoxicity tests, secosterol 1 showed significant cytotoxicity against HSC-T6 cells. In anti-inflammatory activity tests on human neutrophils, secosterols 2, 5, and 7 displayed inhibitory effects on elastase release, and 3, 5, and 7 showed inhibitory effects on the generation of superoxide anions. Our findings suggested that these new 9,11-secosterols could be developed as promising bioactive agents, and further biomedical study is necessary in order to identify their potential applications in the treatment of disease.