Marine Drugs
ISSN 1660-3397 www.mdpi.com/journal/marinedrugs Article
Briarenolides F and G, New Briarane Diterpenoids from a
Briareum sp. Octocoral
Pei-Han Hong 1,2, Yin-Di Su 2,3, Jui-Hsin Su 1,2,3, Yung-Husan Chen 2, Tsong-Long Hwang 4, Ching-Feng Weng 1,5, Chia-Hung Lee 1,5, Zhi-Hong Wen 3, Jyh-Horng Sheu 3, Nai-Cheng Lin 2, Yueh-Hsiung Kuo 6,* and Ping-Jyun Sung 1,2,3,5,*
1 Graduate Institute of Marine Biotechnology, National Dong Hwa University, Pingtung 944, Taiwan;
E-Mails: [email protected] (P.-H.H.); [email protected] (J.-H.S.); [email protected] (C.-F.W.); [email protected] (C.-H.L.)
2 National Museum of Marine Biology and Aquarium, Pingtung 944, Taiwan;
E-Mails: [email protected] (Y.-D.S.); [email protected] (Y.-H.C.); [email protected] (N.-C.L.)
3 Department of Marine Biotechnology and Resources and Division of Marine Biotechnology,
Asia-Pacific Ocean Research Center, National Sun Yat-sen University, Kaohsiung 804, Taiwan; E-Mails: [email protected] (Z.-H.W.); [email protected] (J.-H.S.)
4 Graduate Institute of Natural Products, Chang Gung University, Taoyuan 333, Taiwan;
E-Mail: [email protected]
5 Department of Life Science and Institute of Biotechnology, National Dong Hwa University,
Hualien 974, Taiwan
6 Tsuzuki Institute for Traditional Medicine, China Medical University, Taichung 404, Taiwan
* Authors to whom correspondence should be addressed; E-Mails: [email protected] (Y.-H.K.); [email protected] (P.-J.S.); Tel.: +886-4-2207-1693 (Y.-H.K.); +886-8-882-5037 (P.-J.S.); Fax: +886-4-2207-1693 (Y.-H.K.); +886-8-882-5087 (P.-J.S.).
Received: 19 April 2012; in revised form: 15 May 2012 / Accepted: 22 May 2012 / Published: 23 May 2012
Abstract: Two new briarane diterpenoids, briarenolides, F (1) and G (2), were isolated from an octocoral identified as Briareum sp. The structures of briaranes 1 and 2 were established by spectroscopic methods and by comparison of the spectroscopic data with those of known briarane analogues. Briarenolide F was proven to be the first 6-hydroperoxybriarane derivative and this compound displayed a significant inhibitory effect on the generation of superoxide anion by human neutrophils.
Keywords: briarenolide; briarane; Briareum; superoxide anion
1. Introduction
Among the diterpenoids isolated from octocorals, the briarane-type metabolites (3,8-cyclized cembranes) are a major group of compounds [1–3]. The compounds of this type were suggested to be of marine origin and the octocorals belonging to the genus Briareum have been proven to be the most important source of briarane-type compounds [4–7]. In previous studies, a series of interesting terpenoid derivatives, including briarane [8–35], cembrane [36] and carotenoid [37], had been isolated from the octocorals belonging to the genus Briareum that were distributed in the waters off Taiwan, at the intersection point of the Kuroshio current and the South China Sea surface current. In a continuation of our search for new substances from the Formosan marine invertebrates, the chemical constituents of a specimen octocoral identified as Briareum sp. (Briareidae) were studied. A fraction of its organic extract (fraction H, see Experimental Section) displayed inhibitory effects on the generation of superoxide anion (inhibition rate 36.8%) and the release of elastase (inhibition rate 90.3%) at a concentration of 10 μg/mL. We further isolated two new briarane-type diterpenoids, briarenolides, F (1) and G (2) (Figure 1), from the octocoral Briareum sp. In this paper, we report the isolation, structure determination and bioactivity of briaranes 1 and 2.
Figure 1. The structures of briarenolides F (1) and G (2).
(1) (2) 2. Results and Discussion
Briarenolide F (1) was isolated as a white powder. The molecular formula of 1 was established as C28H40O12 (nine degrees of unsaturation) from a sodium adduct at m/z 591 in the ESIMS spectrum and
further supported by HRESIMS (C28H40O12Na, m/z 591.2420, alculated 591.2417). The IR spectrum of
1 showed bands at 3498, 1789 and 1743 cm−1, consistent with the presence of hydroxy, γ-lactone and ester carbonyl groups. The 13C NMR and DEPT spectra of 1 showed that this compound had
28 carbons (Table 1), including seven methyls, four sp3 methylenes, eight sp3 methines, three sp3 quaternary carbons, an sp2 methine and five sp2 quaternary carbons. From the 1Hand 13C NMR spectra
(Table 1), 1 was found to possess two acetoxy groups (δH 1.99, 2.01, each 3H × s; δC 170.6, 2 × qC;
t, J = 7.2 Hz; δC 13.7, CH3; 18.4, CH2; 36.3, CH2; 173.1, qC), a γ-lactone moiety (δC 171.0, qC-19) and
a trisubstituted olefin (δH 5.65, 1H, br d, J = 13.6 Hz, H-4; δC 130.3, CH-4; 128.8, qC-5). The presence
of a tetrasubstituted epoxide containing a methyl substituent was established from the signals of two quaternary oxygenated carbons at δC 68.8 (qC-8) and 58.4 (qC-17) and further confirmed by the proton
signal of a methyl singlet at δH 1.49 (3H, s, H3-18). Thus, from the above NMR data, five degrees of
unsaturation were accounted for and 1 was identified as a tetracyclic compound.
Table 1. 1H (400 MHz, CDCl3) and 13C (100 MHz, CDCl3) NMR data, 1H–1H COSY and
HMBC correlations for briarane 1.
C/H δ (J in Hz) δC, Mult. 1H–1H COSY HMBC (H→C) 1 44.9, qC 2 5.22 d (8.0) 75.4, CH H2-3 C-1, -4, -10, -15, acetate carbonyl 3α β 1.89 m 3.81 dd (17.2, 13.6) 33.3, CH2 H-2, H-3β, H-4 H-2, H-3α, H-4 N.O. C-4, -5 4 5.65 br d (13.6) 130.3, CH H2-3, H3-16 N.O. 5 128.8, qC 6 4.65 d (2.4) 84.9, CH H-7 C-4, -5, -7, -8, -16 7 5.33 d (2.4) 77.2, CH H-6 C-5, -6 8 68.8, qC 9 4.59 d (4.8) 75.1, CH OH-9 C-1, -8, -10, -11, -17 10 2.06 d (4.0) 39.4, CH H-11 C-1, -8, -9, -15, -20 11 2.28 m 40.2, CH H-10, H-12, H3-20 C-1, -10, -12 12 4.98 ddd (12.4, 5.2, 5.2) 70.7, CH H-11, H2-13 C-20, n-butyrate carbonyl 13 1.87–1.97 m 26.5, CH2 H-12, H-14 C-12 14 4.88 dd (3.2, 2.4) 74.9, CH H2-13 N.O. 15 1.37 s 15.9, CH3 C-1, -2, -10, -14 16 1.77 br s 25.4, CH3 H-4 C-4, -5, -6 17 58.4, qC 18 1.49 s 8.8, CH3 C-8, -17, -19 19 171.0, qC 20 1.22 d (7.2) 10.6, CH3 H-11 C-10, -11, -12 2-OAc 1.99 s 170.6, qC 21.3, CH3 Acetate carbonyl 6-OOH 8.71 br s N.O. 9-OH 2.95 d (4.8) H-9 N.O. 12-OC(O)Pr 2.27 t (7.2) 1.63 sext (7.2) 0.94 t (7.2) 173.1, qC 36.3, CH2 18.4, CH2 13.7, CH3 H2-3' H2-2', H3-4' H2-3' C-1', -3', -4' C-1', -2', -4' C-2', -3' 14-OAc 2.01 s 170.6, qC 21.3, CH3 Acetate carbonyl
N.O. = Not observed.
1H–1H couplings in the COSY spectrum of 1 enabled identification of the C-2/-3/-4, C-6/-7,
assembled with the assistance of an HMBC experiment. The HMBC correlations between protons and quaternary carbons of 1, such as H-2, H-9, H-10, H-11, H3-15/C-1; H-3β, H-6, H-7, H3-16/C-5; H-6,
H-9, H-10, H3-18/C-8; H-9, H3-18/C-17; and H3-18/C-19, permitted the elucidation of the carbon
skeleton (Table 1). The vinyl methyl at C-5 was confirmed by the allylic coupling between H-4/H3-16
in the 1H–1H COSY spectrum and by the HMBC correlations between H3-16/C-4, -5, -6 and H-6/C-16.
The ring junction C-15 methyl group was positioned at C-1 from the HMBC correlations between H3-15/C-1, -2, -10, -14; H-2/C-15; and H-10/C-15. In addition, the carbon signal at δC 173.1 (qC) was
correlated with the signal of the methylene protons at δH 2.27 in the HMBC spectrum and was
consequently assigned as the carbon atom of the n-butyrate carbonyl. Additionally, the n-butyrate positioned at C-12 was confirmed by the connectivity between H-12 (δH 4.98) and the carbonyl carbon
(δC 173.1, qC) of the n-butyrate. Furthermore, an acetate ester at C-2 was established by a correlation
between H-2 (δH 5.22) and the acetate carbonyl (δC 170.6, qC) observed in the HMBC spectrum of 1.
The presence of a hydroxy group at C-9 was deduced from the 1H–1H COSY correlation between a hydroxy proton (δH 2.95) and H-9 (δH 4.59). The presence of a hydroperoxy group in 1 was supported
by a hydroperoxy proton signal at δH 8.71 as a broad signlet [22,32,38]. Due to absence of HMBC
correlations for H-14 (δH 4.88) and the hydroperoxy proton (δH 8.71), the positions for the remaining
acetoxy and hydroperoxy groups could not be determined by this method. By comparison the 1H and
13C NMR data of C-14 oxymethine for 1 (δ
H 4.88; δC 74.9) with those of a known briarane analogue,
excavatolide F (3) (δH 4.94; δC 74.1) (Figure 2) [10], which possesses a similar cyclohexane moiety as
that of 1, the remaining acetoxy group in 1 was placed at C-14. Thus, the hydroperoxy group is positioned at C-6, an oxymethine at δC 84.9 (CH), by analysis of the 1H–1H COSY correlations and
characteristic NMR signal analysis.
Figure 2. The structures of briarenolide F (1) and excavatolide F (3).
(1) (3)
In all naturally-occurring briaranes, H-10 is trans to the C-15 methyl group, and these two groups are assigned as α- and β-oriented in most briarane derivatives [4–7]. The relative configuration of 1 was elucidated from the interactions observed in a NOESY experiment and was found to be compatible with that of 1 offered by computer modeling (Figure 3) [39] and that obtained from vicinal proton coupling constant analysis. In the NOESY experiment of 1, the correlations of H-10 with H-2, H-9, H-11 and H-12, but not with H3-15 and H3-20, indicated that these protons (H-2, H-9, H-10, H-11
C-20 methyls are β-substituents at C-1 and C-11, respectively. H-14 was found to exhibit an interaction with H3-15, but not with H-10, revealing the β-orientation of this proton. The configuration
at C-9 is worthy of comment. H-9 was found to exhibit correlations with H-10, H-11, H3-18 and H3-20.
From a consideration of molecular models, H-9 was found to be reasonably close to H-10, H-11, H3-18
and H3-20, while it was placed on the α face in 1. The C-16 vinyl methyl showed correlations with H-4
and H-6, demonstrating the Z configuration of Δ4,5 and the hydroperoxy group at C-6 was α-oriented. The cis relationship between H-6 and H-7 was established by a correlation between H-6 and H-7 and a small coupling constant (J = 2.4 Hz) between these two protons. Moreover, an acetyl methyl (δH 2.01)
exhibited correlations with H-12 and H-2, further supporting an acetoxy group was positioned on the α-position at C-14 in 1. Based on the above findings, the configurations of all chiral carbons of 1 were assigned as 1S*, 2S*, 6S*, 7S*, 8R*, 9S*, 10S*, 11R*, 12S*, 14S*, 17R*, and the structure of 1 was established unambiguously. To the best of our knowledge, briarane derivatives possessing a hydroperoxy group are rarely found [22,32,38] and briarenolide F (1) is the first briarane derivative possessing a 6-hydroperoxy group. A double bond positioned at C-4(5) in briarane-type metabolites is also rarely found [31,40–42].
Figure 3. The stereoview of 1 (generated from computer modeling) and the calculated distances (Å) between selected protons with key NOESY correlations.
1S* 2S* 6S* 7S* 8R* 9S* 10S* 11R* 12S* 14S* 17R* 15 16 18 20 : NOESY H/H (Å) H-2/H-10 H-4/H3-16 H-6/H-7 H-6/H3-16 H-9/H-10 H-9/H-11 H-9/H3-18 H-9/H3-20 H-10/H-11 H-10/H-12 H-14/H3-15 2.36 2.25 2.92 2.25 2.75 2.18 2.24 2.36 2.38 2.56 2.37
Briarenolide G (2) was isolated as a white powder whose HRESIMS showed a molecular ion at m/z 397.1989 implying that 2 had the molecular formula C22H30O5 (C22H30O5Na, calculated 397.1991).
The IR spectrum revealed absorptions for hydroxy (3397 cm−1) and ester carbonyl (1757 and 1734 cm−1) groups. The 1H NMR data (Table 2) showed resonances due to an acetyl methyl (δH 2.03, 3H, s), three
vinyl methyls (δH 1.78, 3H, br s, H3-16; 1.87, 3H, d, J = 1.6 Hz, H3-18; 1.63, 3H, d, J = 0.8 Hz, H3-20),
a quaternary methyl (δH 0.77, 3H, s, H3-15), two olefinic protons (δH 5.29, 1H, br s, H-6; 5.12, 1H, m,
H-12) and an oxymethine signal (δH 4.78, 1H, br s, H-14). The 13C NMR and DEPT spectra of 2
(Table 2) revealed the presence of a tetrasubstituted (δC 160.8, qC-8; 125.1, qC-17) and two
trisubstituted (δC 144.4, qC-5; 124.6, CH-6; 136.3, qC-11; 117.8, CH-12) carbon-carbon double bonds,
a hemiketal carbon (δC 106.7, qC-7), an acetate carbonyl (δC 170.9, qC), an α,β-unsaturated-γ-lactone
carbonyl (δC 171.1, qC-19), a tetrasubstituted carbon atom bearing a carbon substituent (δC 39.1, qC-1)
Table 2. 1H (400 MHz, CDCl3) and 13C (100 MHz, CDCl3) NMR data, 1H–1H COSY and
HMBC correlations for briarane 2.
C/H δΗ (J in Hz) δC, Mult. 1H–1H COSY HMBC (H→C) 1 39.1, qC 2α β 1.69 m 1.29 m 35.4, CH2 H-2β, H2-3 H-2α, H2-3 C-3, -14 C-1, -3, -10, -14 3 1.72 m 23.7, CH2 H2-2, H2-4 C-2 4α β 1.90 m 3.72 m 29.6, CH2 H2-3, H-4β H2-3, H-4α N.O. C-3, -16 5 144.4, qC 6 5.29 br s 124.6, CH H3-16 C-4, -7, -16 7 106.7, qC 8 160.8, qC 9α β 2.54 br d (15.2) 2.37 dd (15.2, 10.8) 25.3, CH2 H-9β, H-10 H-9α, H-10 C-8, -10, -11, -17 C-7, -8, -10, -11, -17 10 3.76 d (10.8) 35.9, CH H2-9 N.O. 11 136.3, qC 12 5.12 m 117.8, CH H2-13, H3-20 N.O. 13α β 2.06 m 2.33 m 29.3, CH2 H-12, H-13β H-12, H-13α C-11, -12, -14 C-11 14 4.78 br s 77.2, CH H2-13 C-12 15 0.77 s 21.9, CH3 C-1, -2, -10, -14 16 1.78 br s 23.9, CH3 H-6 C-4, -5, -6 17 125.1, qC 18 1.87 d (1.6) 9.1, CH3 C-8, -17, -19 19 171.7, qC 20 1.63 d (0.8) 21.9, CH3 H-12 C-10, -11, -12 7-OH 3.35 s C-6, -7, -8 14-OAc 2.03 s 170.9, qC 21.7, CH3 Acetate carbonyl
N.O. = Not observed.
From the 1H–1H COSY experiment of 2 (Table 2), it was possible to establish the separate spin systems that map out the proton sequences from H2-2/H2-3/H2-4 and H2-9/H-10. These data,
together with the HMBC correlations between H2-2/C-1, -3, -10; H2-3/C-2; H-4β/C-3; H-6/C-4, -7; and
H2-9/C-7, -8, -10, established the connectivity from C-1 to C-10 in the ten-membered ring (Table 2).
The vinyl methyl at C-5 was confirmed by the HMBC correlations between H3-16/C-4, -5, -6;
H-4β/C-16; and H-6/C-16, and further supported by the allylic coupling between H-6 and H3-16. The
methylcyclohexene ring, which is fused to the ten-membered ring at C-1 and C-10, was elucidated by the 1H–1H COSY correlations between H-12/H2-13/H-14 and H-12/H3-20 (by allylic coupling) and by
the HMBC correlations between H2-2/C-14, H2-9/C-11 and H3-20/C-10, -11, -12. The ring junction
C-15 methyl group was positioned at C-1 from the HMBC correlations between H3-15/C-1, -2, -10, -14.
In addition, the acetate ester at C-14 was established by a correlation between H-14 (δH 4.78) and the
acetate carbonyl observed in the HMBC spectrum of 2. The presence of a hydroxy group at C-7 was deduced from the HMBC correlations between the hydroxy proton (δH 3.35, 1H, s, OH-7) and C-6, C-7,
and C-8. The C-7 hydroxy group was concluded to be a part of hemiketal constellation on the basis of a characteristic carbon signal at δC 106.7 (a quaternary hemiketal carbon, qC-7). These data, together
with the HMBC correlations between H3-18/C-8, -17, -19, were used to establish the molecular
framework of 2.
NOESY measurements were carried out in order to deduce the relative stereochemical features of 2 (Figure 4). Thus, H3-15 gave a correlation with H-14, but not with H-10, indicating that H3-15 and
H-14 are located on the same face (assigned as the β-face) and that H-10 lies on the opposite side, α-face. The NOESY spectrum showed correlations between H-6/H3-16 and H-12/H3-20, revealing the
Z geometry of the C-5/6 and C-11/12 double bonds in 2. Due to the absence of NOESY correlations for the C-7 hydroxy group, the configuration at that chiral center could not be determined by this method. By comparison of the 13C NMR chemical shifts of C-6 (δC 124.6), C-7 (δC 106.7) and C-8
(δC 160.8) for 2 with those of an unnamed known 7β-hydroxybriarane analogue 4 (δC 124.8, C-6;
106.2, C-7, 160.1, C-8), which was obtained from a Caribbean octocoral Briareum polyanthes [43] (Figure 5), we deduced that the C-7 hydroxy group was β-oriented and the configuration of all the chiral carbons in 2 were assigned as 1R*, 7S*, 10S*, 14S*.
Figure 4. The stereoview of 2 (generated from computer modeling) and the calculated distances (Å) between selected protons with key NOESY correlations.
: NOESY 1R* 7S* 10S* 16 6 20 12 14S* 18 8 17 H/H (Å) H-6/H3-16 H-12/H3-20 H-14/H3-15 2.39 2.61 2.28
Figure 5. The structures of briarenolide G (2) and briarane (4).
The in vitro anti-inflammatory effects of briaranes 1 and 2 were tested. Briarenolide F (1) was found to display a significant inhibitory effect on the generation of superoxide anion by human neutrophils (Table 3).
Table 3. Inhibitory effects of briaranes 1 and 2 on the generation of superoxide anion and the release of elastase by human neutrophils in response to FMLP/CB.
Superoxide Anion Elastase Release
Compounds IC50 (µg/mL) Inh% a IC50 (µg/mL) Inh% a
1 3.82 ± 0.45 76.65 ± 4.21 >10.0 27.48 ± 6.60 2 >10.0 22.04 ± 3.43 >10.0 12.98 ± 4.68 DPI b 0.82 ± 0.31
Elastatinal b 31.82 ± 5.92
a Percentage of inhibition (Inh%) at a concentration of 10 µg/mL; b DPI (diphenylene indoniumn) and elastatinal were used as reference compounds.
3. Experimental Section
3.1. General Experimental Procedures
Optical rotations were measured on a Jasco P-1010 digital polarimeter. Infrared spectra were recorded on a Varian Diglab FTS 1000 FT-IR spectrometer; peaks are reported in cm−1. The NMR spectra were recorded on a Varian Mercury Plus 400 NMR spectrometer. Coupling constants (J) are given in Hz. 1H and 13C NMR assignments were supported by 1H–1H COSY, HMQC, HMBC and NOESY experiments. ESIMS and HRESIMS were recorded on a Bruker APEX II mass spectrometer. 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), and spots were visualized by
spraying with 10% H2SO4 solution followed by heating. HPLC was performed using a system
comprised of a Hitachi L-7100 pump and a Rheodyne injection port. A normal phase column (Hibar 250 × 10 mm, Merck, silica gel 60, 5 μm) was used for HPLC.
3.2. Animal Material
Specimens of the octocorals Briareum sp. were collected by hand using scuba equipment off the coast of southern Taiwan in July 2011 and stored in a freezer until extraction. A voucher specimen (NMMBA-TW-SC-2011-77) was deposited in the National Museum of Marine Biology and Aquarium. This organism was identified by comparison with previous descriptions [44–47].
3.3. Extraction and Isolation
Sliced bodies of Briareum sp. (wet weight 6.32 kg, dry weight 2.78 kg) were extracted with a mixture of methanol (MeOH) and dichloromethane (DCM) (1:1). The extract was partitioned between ethyl acetate (EtOAc) and H2O. The EtOAc layer was separated on silica gel and eluted using
n-hexane/EtOAc (stepwise, 100:1–pure EtOAc) to yield 18 fractions A–R. Fraction H was chromatographed on silica gel and eluted using n-hexane/acetone (stepwise, 40:1–pure acetone) to
afford 45 fractions H1–H45. Fraction H11 was separated by normal-phase HPLC (NP-HPLC) using a mixture of n-hexane and EtOAc (5:2) as the mobile phase to afford compound 2 (0.4 mg). Fraction H16 was further purified by normal-phase HPLC using a mixture of n-hexane and acetone as the mobile phase (7:2) to afford compound 1 (2.3 mg).
Briarenolide F (1): white powder; mp 141–142 °C; [α]25
D +32 (c 0.1, CHCl3); IR (neat) νmax 3498,
1789, 1743 cm–1; 1H (CDCl3, 400 MHz) and 13C (CDCl3, 100 MHz) NMR data, see Table 1; ESIMS:
m/z 591 [M + Na]+; HRESIMS: m/z 591.2420 (calcd for C28H40O12Na, 591.2417).
Briarenolide G (2): white powder; mp 78–80 °C; [α]25
D −97 (c 0.02, CHCl3); IR (neat) νmax 3397,
1757, 1734 cm–1; 1H (CDCl3, 400 MHz) and 13C (CDCl3, 100 MHz) NMR data, see Table 2; ESIMS:
m/z 397 [M + Na]+; HRESIMS: m/z 397.1989 (calcd for C22H30O5Na, 397.1991).
3.4. Molecular Mechanics Calculations
Implementation of the MM2 force field [39] in CHEM3D PRO software from CambridgeSoft Corporation (version 9.0, Cambridge, MA, USA; 2005) was used to calculate the molecular models. 3.5. Superoxide Anion Generation and Elastase Release by Human Neutrophils
Human neutrophils were obtained by means of dextran sedimentation and Ficoll centrifugation. Measurements of superoxide anion generation and elastase release were carried out according to previously described procedures [48,49]. Briefly, superoxide anion production was assayed by monitoring the superoxide dismutase-inhibitable reduction of ferricytochrome c. Elastase release experiments were performed using MeO-Suc-Ala-Ala-Pro-Valp-nitroanilide as the elastase substrate. 4. Conclusions
Briarane-type natural products (3,8-cyclized cembranoid) were found in various marine organisms, particularly with the octocorals belonging to the genus Briareum (family Briareidae) [4–7]. It is interesting to note that the briarane-type natural products are major constituents of the extracts of octocorals Briareum spp. distributed in the tropical and subtropical Indo-Pacific Ocean. In the past 35 years, over 500 briarane analogues have been obtained and the number is still increasing based on their structural complexity and interesting bioactivities. It is worth noting that only three hydroperoxybriarane analogues have been isolated to date [22,32,38] and that briarenolide F (1) is the first 6-hydroperoxybriarane. 7-Hydroxybriarane derivatives are also rarely found [43,50–52]; the new briarane, briarenolide G (2) was the first 7-hydroxybriarane derivative isolated from the octocorals collected off the waters of Taiwan. The study material Briareum sp. has begun to be transplanted in tanks for the extraction of natural products in order to establish a stable supply of bioactive material. Acknowledgments
This research was supported by grants from the National Museum of Marine Biology and Aquarium (Grant No. 100100101 and No. 100200311); the National Dong Hwa University: the Division of Marine Biotechnology, Asia-Pacific Ocean Research Center, National Sun Yat-sen University (Grant
No. 00C-0302-05); the Department of Health Clinical Trial and Research Center of Excellence (Grant No. DOH101-TD-C-111-004); the National Research Program for Biopharmaceuticals, National Science Council (Grant No. NSC 101-2325-B-291-001, 100-2325-B-291-001 and 98-2320-B-291-001-MY3), Taiwan, awarded to Y.-H.K. and P.-J.S.
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Samples Availability: Not available.
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