Tropical Journal of Pharmaceutical Research

Original Research Article | OPEN ACCESS

Antibacterial and cytotoxic properties of isoprenoids from the red sea soft coral, Lobophytum sp

Khalid O Al-Footy¹, Walied M Alarif² , Muhammad S Zubair^1,3, Mohamed A Ghandourah², Magda M Aly⁴

¹Department of Chemistry, Faculty of Science; ²Department of Marine Chemistry, Faculty of Marine Sciences, King Abdulaziz University, PO Box 80207, Jeddah 21589, Saudi Arabia; ³Department of Pharmacy, Faculty of Science, Tadulako University, Kampus Bumi Tadulako Tondo, Palu 94118, Indonesia; ⁴Department of Biology, Faculty of Science, King Abdulaziz University, PO. Box 80203, Jeddah 21589, Saudi Arabia.

For correspondence:- Walied Alarif Email: welaref@kau.edu.sa Tel:+966560352034

Received: 31 March 2016 Accepted: 19 June 2016 Published: 31 July 2016

Citation: Al-Footy KO, Alarif WM, Zubair MS, Ghandourah MA, Aly MM. Antibacterial and cytotoxic properties of isoprenoids from the red sea soft coral, Lobophytum sp. Trop J Pharm Res 2016; 15(7):1431-1438 doi: 10.4314/tjpr.v15i7.11

© 2016 The authors.
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Abstract

Purpose: To evaluate the antibacterial and cytotoxic activities of the secondary metabolites of Lobophytum sp.

Methods: Maceration with methanol: chloroform (1:1) was applied to extract the coral material. Chromatographic and spectroscopic techniques were employed for fractionation, isolation and elucidation of pure compounds. Antibacterial activities were performed by well diffusion method against three Gram-positive and four Gram-negative bacteria. Brine shrimp lethality test was employed to predict toxicity, while antitumor activity were tested by 3-(4, 5-dimethylthiazol-2-yl)-2, 5-diphenyltetrazolium bromide (MTT) method against Ehrlich carcinoma cells.

Results: Four sesquiterpenes, one cembranoid type diterpenes and two steroids were isolated. 1 exhibited significant antibacterial activity against four tested bacteria (P. aeruginosa, S. aureus, S. epidermis, and S. pneumonia) with MIC value of 15 μg/mL. Moreover, 1 showed high diameter zone of inhibition ranging from 16 - 18 mm against test bacteria. Compounds 4 and 5 displayed moderate antibacterial activity against all test bacteria with inhibition zone diameter (IZD) ranging from 11 – 15 mm and MIC values of 30 μg/mL. 2, 3, 6 and 7 exhibited weak antibacterial activity (IZD, 7 - 11 mm; MIC ≥ 30 μg/mL). In addition, only diterpene compound (4) showed high toxicity against A. Salina and antitumor activity against Erhlich carcinoma cells with the LD₅₀ of 25 and 50 μg/mL, respectively.

Conclusion: This study reveals the strong antibacterial activity of sesquiterpene alismol (1) and the potential antibacterial and antitumor activity of cembranoid type diterpene, cembrene A (4).

Keywords: Soft coral, Lobophytum sp., Red Sea, Antibacterial, Cytotoxicity, Sesquiterpene Alismol, Cembranoid, Diterpene, Cembrene

Introduction

Marine soft corals of the subclass Alcyonaria (Octocorallia) have fascinated a great attention in the light of the structural diversity and broad range of biological activities of their metabolites, such as sesquiterpenoids, diterpenoids, tetraterpenoids and steroids [1]. In a continuing efforts at studying marine metabolites, collected from Red Sea Saudi Arabia, with biological activity, we have previously isolated several bioactive secondary metabolites from Sarcophyton trocheliophorum and S. glaucum [2-5] Recently, our interest in allcyonaria coral, led us to isolate several secondary metabolites from Lobophytum sp. Literature survey showed that metabolites of Lobophytum sp exhibited various biological activities, such as antitumor [6-13], antibacterial [14], anti-inflammatory activities [14-16] and antiviral [17]. Our investigation led to the isolation and characterization of four sesquiterpenes: alismol (1), nardol (2) aristol-9-ene (3), alismoxide (5), one cembranoid type diterpene, cembrene A (4), and two steroid type compounds, Chalinasterol (6) and Nephalsterol C (7). To the best of our knowledge, this is the first report of the presence of sesquiterpenes from soft coral Lobophytum sp. Antibacterial and antitumor activities of all metabolites were also evaluated. This paper describes isolation, NMR structural elucidation and biological activity of the following compounds.

Methods

Animal material

The soft coral, Lobophytum sp., was collected in May. 2014, off the Saudi Arabia Red Sea Coast at Jeddah and identified by Dr. Mohsen El-Sherbiny (Marine Biology Department, Faculty of Marine Sciences, King Abdulaziz University). Voucher sample (no. JAD 09063B) was deposited in the herbarium of the Marine Biology Department, Faculty of Marine Sciences, King Abdulaziz University, Jeddah, Saudi Arabia

General experimental procedures

Chromatographic material: Silica gel 60 for column chromatography (60–120 mesh LR), for thin-layer chromatography. TLC aluminum sheets 20 x 20 cm. Silica gel 60 F254 was used for preparative, Pre-coated TLC glass plates SIL G-25 UV254, 0.25 mm silica gel (E. Merck, Darmstadt, Germany). Nuclear Magnetic Resonance spectra were recorded for 1D- and 2D-NMR: Bruker AVANCE III WM at 600 MHz and ¹³C-NMR at 150 MHz spectrometer. Chemical shifts are given d (ppm) relative to TMS as internal standard. Electron impact mass spectra were determined at 70 eV using a Kratos GCMS-25 instrument. All chemicals were purchased from Sigma Chemical Company (St. Louis, MO. USA).

Bacterial isolates

Seven bacteria were obtained from King Fahd General Hospital, Jeddah, Saudi Arabia; they were Staphylococcus aureus, Staphylococcus epidermidis, and Streptococcus pneumonia (Gram-positive bacteria), Pseudomonas aeruginosa, Escherichia coli, Klebsiela pneumoniae, and Acinetobacter spp (Gram-negative bacteria), Brine shrimp Artemia salina, and Ehrlich carcinoma cells were from the culture collection of Microbiology Department, Faculty of Science, King Abdulaziz University, Jeddah, Saudi Arabia.

Extraction and isolation

Coral material was washed with water and dried in the shade at room temperature. The dried material (90 g) was exhaustively extracted by maceration method with equal volumes of CHCl₃/MeOH (2 x 6 l, 24 h for each batch) at room temperature.

The residue (20 g) was chromatographed on NP (Merck, 60G) column chromatography employing n-hexane/methylene chloride, followed by ethyl acetate/methanol mixtures with increasing polarity. Fractions of ~100 mL were collected. TLC was carried out by employing silica gel chromatoplates, appropriate solvent system, and 50 %-sulfuric acid in methanol as spraying reagent. Fractions containing a single compound were combined and further purified by preparative TLC of glass supported silica gel plates (20 x 20 cm) of 250 μm thickness.

The fraction 1 eluted with n-hexane - dichloromethane (9:1, 37.00 mg) was purified by preparative TLC using solvent system n-hexane: ethyl acetate (9:1) to give two bands. The first band with R_f = 0.96 (brown color with sulfuric acid–methanol) was taken to give compound 3 as crystalline (5.0 mg). The second band with R_f = 0.36 (black color with sulfuric acid–methanol) was taken to give compound 4 as colorless oil (4.8 mg). The fraction 2 eluted with n-hexane - dichloromethane (7:3, 35.00 mg) was purified by preparative TLC using the solvent system n-hexane:ethyl acetate (8:2) to give two bands. The first band with R_f = 0.48 (broad purple color after spraying with sulfuric acid–methanol) was taken to give crystalline of compound 1 (6.5 mg). The second band with R_f = 0.30 (purple color with sulfuric acid–methanol) was taken to give colorless oil of compound 2 (4.6 mg). The fraction 3 eluted with n-hexane - dichloromethane (5:5, 40.00 mg) was purified by preparative TLC using solvent system n-hexane: ethyl acetate (7:3) to give one band with R_f = 0.72 (brown color with sulfuric acid–methanol) was taken to give compound 6 as crystalline (5.0 mg). The fraction 4 eluted with dichloromethane:ethyl acetate (9:1, 42.00 mg) was purified by preparative TLC using the solvent system n-hexane : ethyl acetate (6:4) to give one band with R_f = 0.38 (broad purple color after spraying with sulfuric acid–methanol) was taken to give crystalline of compound 5 (8.0 mg). The fraction 5 eluted with dichloromethane:ethyl acetate (8:2, 41.00 mg) was purified by preparative TLC using the solvent system n-hexane:ethyl acetate (5:5) to give one band with R_f = 0.62 (brown color after spraying with sulfuric acid–methanol) was taken to give powder of compound 7 (4.2 mg).

Antibacterial activity assay

The growth inhibition of the isolated compounds against several pathogenic bacteria was carried out using agar well diffusion method as described by Holder and Boyce (1994) [18]. 0.1 mL of suspended bacterium in sterile medium (1.5 x 10⁸ CFU/mL) was spread on Mueller–Hinton agar. 50 μl of each sample (10 μg/mL) were poured to the wells (6-mm diameter). All plates were left for 1 h at 48 ^oC and then incubated for 24 h at 37 ^oC. Inhibition zone diameters formed around the well were measured and mean diameter of three replica was calculated. DMSO was used as a negative control and ampicillin as a positive control. Minimum inhibitory concentrations (MICs) were determined by modified method described by Chand et al [19] and Aly and Gumgumji [20]. 175 μL of an exponentially growing culture (x10⁶–10⁷ CFU/mL) was delivered into each well of microtiter plate along with 20 μL solution of each concentration of the isolated compounds. The appropriate solvent was used as control. After incubation for 40 min., 5 μL of a solution of Fluorescein diacetate (FDA) 0.2 % (w/v) in acetone was added into microtiter plate, then the incubation was continued for 90 min. The green color produced from the hydrolysis of FDA was measured at 490 nm (MR7000 automatic ELISA tray reader) along with the blanked wells and control wells containing microbial cultures.

Toxicity activity assay

The cytotoxicity of the isolated compounds can be measured by using brine shrimp lethality test [21]. Isolated compounds were dissolved in DMSO at varying concentrations and then incubated with the brine shrimp larvae in sea water. Brine shrimp larvae as positive control and DMSO as negative control were also incubated. The average number of larvae that survived in each vial was determined after 24 h. The mean of mortality percentage was plotted against the logarithm of concentrations. The concentration that killed fifty percent of the larvae (LC₅₀) was determined from the graph.

Antitumor activity assay

Ehrlich carcinoma cell lines was used to determine the antitumor activity of the isolated compounds. The cells were grown in Roswell Park Memorial Institute (RPMI) 1640 medium (Sigma, USA) with 10 % fetal calf serum (Gibco, USA) at 37 ^oC under a humidified atmosphere (95 % air and 5 % CO₂) for 48 h. Cells were treated with different concentration of the isolated compounds (200–1,000 μl/mL) for 24 h, centrifuged for 2 min at 1,500 g and counted under hemacytometer after removing the supernatant using trypan blue (Sigma, USA) in normal saline (1:1 v/v). The percentage of cell viability was assessed to determine the 50 % lethal dose by which 50 % of cells are killed (LD₅₀).

Statistical analysis

All experiments were performed in triplicate. Data are presented as mean ± standard deviation (SD). Unpaired student t-test was carried out to detect any significant differences between the results of control and the treated samples using GraphPad InStat (ISI Software). Differences were considered significant at p < 0.05.

Results

Compounds

Identification of secondary metabolites was analyzed based on MS and 1D/2D NMR data and comparison with the literature. The chemical structure of isolated compounds can be seen in the .

Alismol (1): Colorless oil; HRESIMS: m/z=220.3505 (Calc. for C₁₅H₂₄O, 220.1820); ¹H NMR (600 MHz, CDCl₃): δ_H 5.55 (1H, br s, H-6), 4.76 (1H, s, Ha-15), 4.70 (1H, s, Hb-15), 2.28 (1H, dd, J= 14.4, 7.4 Hz, H-5), 2.50 (dd, J= 21.6, 10.2 Hz, H₁-1), 2.06 (dd, J=38.4, 10.2 Hz, H₂-1), 2.30 (1H, d, J= 7.4 Hz, H-1), 2.24 (1H, m, H-11), 2.20 (1H, m, Ha-8), 2.10 (1H, m, Hb-8), 1.90 (1H, m, H-2), 1.74 (2H, m, H-3), 1.72 (1H, m, H-2’), 1.25 (3H, s, H-14), 1.01 (3H, d, J = 6.6 Hz, H-12), 0.98 (3H, d, J = 6.6 Hz, H-13); ¹³C NMR (200 MHz, CDCl₃): δ_C 153.93 (C-10), 149.78 (C-7), 121.30 (C-6), 106.51 (C-15), 80.69 (C-4), 55.01 (C-1), 47.27 (C-5), 40.25 (C-3), 37.44 (C-11), 37.08 (C-9), 30.00 (C-8), 24.76 (C-2), 24.09 (C-14), 21.48 (C-13), 21.30 (C-12).

Nardol (2): Colorless Oil; HRESIMS: m/z=222.3663 (Calc. for C₁₅H₂₆O, 222.1984); ¹H NMR (600 MHz, CDCl₃): δH 4.73 (1H, s, H-15’), 4.71 (1H, s, H-15), 2.89 (1H, d, H-1), 2.40 (1H, m, H-9), 2.30 (1H, m, H-7), 2.16 (1H, m, H-8), 2.14 (1H, m, H-9’), 1.94 (1H, m, H-6), 1,84 (1H, m, H-3), 1.72 (1H, m, H-6’), 1.71 (1H, m, H-5), 1.62 (1H, m, H-3’), 1.58 (1H, m, H-11), 1.52 (1H, m, H-8’), 1.44 (3H, s, H-14), 1.30 (2H, m, H-2), 1.01 (3H, d, J = 6.6 Hz, H-12), 0.96 (3H, d, J = 6.6 Hz, H-13); ¹³C NMR (200 MHz, CDCl₃): δC 151.63 (C-10), 107.28 (C-15), 80.31 (C-4), 62.18 (C-1), 57.57 (C-5), 47.91 (C-7), 41.50 (C-3), 34.58 (C-11), 34.06 (C-9), 29.15 (C-8), 26.27 (C-6), 24.95 (C-14), 22.71 (C-2), 18.72 (C-13), 17.74 (C-12).

Aristol-9-ene (3): Colorless oil; HRESIMS: m/z= 204.3511 (Calc. for C₁₅H₂₄, 204.1878); ¹H NMR (600 MHz, CDCl₃): δ_H 5.10 (1H, ddd, 2.4,2.4,4.2 Hz, H-9), 2.16 (1H, m, H-1), 1.98 (1H, m, H-1), 2.08 (1H, dd, 2.4, 4.2, Ha-8), 2,04 (1H, dd, 2.4, 4.2, Hb-8), 1.69 (1H, dd, 1.2, 2.4, H-4), 1.62 (H, m, Ha-3), 1.42 (1H, m, Ha-2), 1.36 (1H, m, Hb-3), 1.3 (1H, m, Hb-2), 1.18 (3H, s, H-13), 1.12 (3H, s, H-12), 1.05 (3H, s, H-15), 0.98 (3H, d, J=4.8 Hz, H-14), 0.75 (1H, dd, J= 6, 8.5 Hz, H-7), 0.60 (1H, d, J= 8.5 Hz, H-6);¹³C nmr (200 MHz, CDCl₃): δ_C 141.30 (C-10), 118.5 (C-9), 37.86 (C-4), 36.82 (C-5), 33.04 (C-1), 32.09 (C-6), 31.32 (C-2), 28.44 (C-7), 27.21 (C-3) 21.77 (C-8), 21.29 (C-13), 19.29 (C-14), 17.9 (C-11), 15.91 (C-12), 15.65 (C-15).

Cembrene A (4): Colorless oil, HRESIMS: m/z= 272.4681 (Calc.for C₂₀H₃₂, 272.2504); ¹H NMR (600 MHz, CDCl₃): δ_H 5.31 (1H, dd, J= 6.8, 15.3 Hz, H-7), 5.25 (1H, dt, J=1.7, 6.8, 8.5 Hz, H-3), 5.08 (1H, dt, J= 6.0, 12.0, H-11), 4.82 (2H, d, J=1.0, H-16), 2.26, (1H, m, Ha-6), 2.21 (1H, dddd, J=3.4, 4.25, 10.2, 13.6 Hz, H-1), 2.17 (1H, m, Ha-2), 2.15 (2H, m, H-10), 2.15 (1H, m, Ha-5), 2.13 (1H, m, Hb-6), 2.12 (1H, m, Ha-13), 2.09 (2H, m, H-9), 2.02 (1H, m, Hb-2), 1.96 (1H, m, Hb-5), 1.93 (1H, m, Hb-13), 1.79 (dq, J= 10.2; 13.6 Hz, Ha-14), 1.41 (m, Hb-14), 1.63 (3H, s, H-17), 1.60 (3H, s, H-18), 1.55 (3H, s, H-19), 1.54 (3H, s, H-20); ¹³C NMR (150 MHz, CDCl₃); δ_C 148.87 (C-15), 134.55 (C-8), 133.48 (C-4), 133.10 (C-12), 126.08 (C-11), 124.19 (C-7), 121.91 (C-3), 110.44 (C-16), 46.17 (C-1), 39.49 (C-9), 39.01 (C-5), 33.99 (C-13), 32.64 (C-2), 28.19 (C-14), 24.98 (C-6), 23.85 (C-10), 18.99 (C-17), 17.97 (C-18), 15.5 (C-19), 15.28 (C-20).

Alismoxide (5): Colorless oil, HRESIMS: m/z= 238.3657 (Calc. for C₁₅H₂₆O₂, 238.1930), ¹H NMR (600 MHz, CDCl₃): δ_H 5.50 (1H, dd, J = 2.0; 1.2 Hz, H-6), 2.24 (1H, sept, H-11), 2.22 (1H, m, Ha-8), 2.18 (1H, m, H-5), 1.95 (1H, dd, 10.4; 1.2 Hz, Hb-8), 1.89 (1H, m, H-1), 1.80 (1H, m, Ha-2), 1.80 (1H, m, Ha-9), 1.70 (1H, m, Ha-3), 1.68 (1H, m, Hb-2), 1.62 (1H, m, Hb-3), 1.47 (1H, m, Hb-9), 1.27 (3H, s, H-14), 1.21 (3H, s, H-15), 0.99 (3H, d, J = 6.8 Hz, H-12), 0.98 (3H, J=6.8 Hz, H-13); ¹³C NMR (150 MHz, CDCl₃): δ_C 149.69 (C-7), 121.33 (C-6), 80.25 (C-4), 75.25 (C-10), 50.77 (C-1), 50.38 (C-5), 42.67 (C-9), 40.52 (C-3), 37.33 (C-11), 25.12 (C-8), 21.44 (C-14), 21.55 (C-2), 22.61 (C-15), 21.20 (C-13), 21.42 (C-12).

Chalinasterol (6): Amorphous powder, HRESIMS: m/z= 398.6642 (Calc. for C₂₈H₄₆O, 398.3540), ¹H NMR (600 MHz, CDCl₃); δ_H 5.38 (1H, s, H-6), 4.71 (1H, s, Ha-28), 4.65 (1H, s, Hb-28), 3.6 (1H, m, H-3), 1.03 (3H, d, J = 6.8 Hz, H-27), 1.02 (3H, d, J=6.8 Hz, H-26’), 1.01 (3H, s, H-19), 0.98 (3H, d, J=6.8 Hz, H-26), 0.94 (3H, d, J= 6.8, H-21), 0.68 (3H, s, H-18). ¹³C NMR (150 MHz, CDCl₃): δ_C 156.98 (C-24), 140.79 (C-5), 121.73 (C-6), 105.91 (C-28), 71.83 (C-3), 56.77 (C-14), 55.99 (C-17), 50.13 (C-9), 42.37 (C-13), 42.31 (C-4), 39.79 (C-12), 37.48 (C-1), 36.51 (C-10), 35.7 (C-20), 34.69 (C-23), 33.81 (C-25), 38.58 (C-8), 32.0 (C-7), 31.68 (C-2), 30.98 (C-22), 28.23 (C-16), 24.3 (C-15), 22.01 (C-27), 21.88 (C-26), 21.10 (C-11), 19.42 (C-19), 18.72 (C-21), 11.88 (C-18).

Nephalsterol C (7): Amorphous powder, HRESIMS: m/z= 472.6997 (Calc. for C₃₀H₄₈O₄, 472.3550), ¹H NMR (600 MHz, CDCl₃): δH 5.58 (1H, t, J = 2 Hz, H-6), 4.90 (1H, dd, J = 2.5, 6 Hz, H-7), 4.71 (1H, d, J = 0.85 Hz, Ha-28), 4.65 (1H, d, J = 0.85 Hz, Hb-28), 3.80 (1H, d, J = 11.9 Hz, H-19), 3.65 (1H, d, J = 11.9 Hz, H-19’), 3.60 (1H, tt, J = 10.2 5.1 Hz, H-3), 2.38 (1H, dddd, J = 1.7, 2.5, 4.25, 5.95 Hz, H-4), 2.20 (1H, tt, 6.8, 12.75, H-4’), 2.02 (3H, s, OAc), 1.02 (3H, d, J = 5.1 Hz, H-26), 1.01 (3H, d, J = 5.1 Hz, H-27), 0.94 (3H, d, J = 5.9 Hz, H-21), 0.74 (3H, s, H-18). ¹³C NMR (150 MHz, CDCl3): δ_C 171.38 (MeCOO-), 156.81 (C-24), 140.02 (C-5), 126.78 (C-6), 106.02 (C-28), 75.11 (C-7), 70.92 (C-3), 62.9 (C-19), 56.33 (C-14), 55.27 (C-17), 48.53 (C-9), 42.6 (C-13), 41.63 (C-4), 41.45 (C-10), 39.74 (C-12), 35.65 (C-8), 37.84 (C-20), 34.65 (C-22), 33.78 (C-25), 33.20 (C-1), 31.80 (C-2), 30.95 (C-23), 28.39 (C-16), 24.98 (C-15), 21.73 (C-26), 21.86 (C-27), 21.7 (CH₃COO), 22.01 (C-11), 18.74 (C-21), 12.13 (C-18).

Antibacterial activity

Antibacterial activity assay were performed against several bacteria. The result of diameter of zone of inhibitons (mm) of isolated compounds were presented in . There were significant differences (p < 0.05) among antibacterial activities of all isolated compounds. Compound 1 has significant antibacterial activity (p < 0.05) against both gram-positive bacteria (S. aureus, S. S. epidermis and S. pneumonia) and gram-negative bacteria (P. aeruginosa) with the MIC value of 15 μg/mL (). Moreover, compound 1 showed the larger diameter of inhibition zone ranging from 16-18 mm against those four bacteria. The diameter of inhibition zone against S. epidermis was recorded to be largest (18 ± 2.0 mm). Meanwhile, compound 4 and 5 exhibited moderate antibacterial activity with the diameter of inhibiton zone ranging from 11 – 15 mm and MIC value of 30 μg/mL. Compound 2, 3, 6 and 7 showed weak antibacterial activity with diameter of inhibition zone ranging from 7 – 10 mm and MIC value ≥ 30 μg/mL.

Toxicity and antitumor activity

The result of toxicity and antitumor activity test can be seen in . All compounds did not show appreciable toxicity and antitumor properties against Artemia salina and Erhlich carcinoma cells, except for cembrene A (compound 4). It exhibited significant toxicity and antitumor activity (p < 0.05) with the LD₅₀ values of 25 and 50 μg/mL, respectively.

Discussion

Compound 1 was isolated as colorless oil. HRESIMS at m/z of 220.3505 and ¹³C NMR suggesting a molecular formula of C₁₅H₂₄O with 4 degrees of unsaturation. The obtained spestroscopic data (cf. exp.) was found to be identical with the structural data of alismol, a guaiane sesquiterpene isolated previously from the rhizome of Alisma plantago-aquatu L var orlentale Samuelsson (Altsmataceae) [22,23].

Compound 2 was isolated as colorless oil. A search of chemical database using science finder found that the spectroscopic data of 2 was in accordance with the chemical structure of nardol, isolated previously from the rhizome of Nardostachys jatamansi [24]. This is the first report of ¹³C-NMR from this compound.

Compound 3 was isolated as colorless oil. The resulted spectroscopic data (cf. exp.) gave conclusion that the compound similar to aristol-(9)-ene, previously isolated from a soft coral Lemnalia humesi [25].

Compound 4 was isolated as colorless oil. 4 was found to be Cembrene A, a cembranoid previously isolated from the paracloacal glands of the Chinese Alligator (Alligator sinensis) [26].

Compound 5 was isolated as colorless oil. The spectroscopic data of 5 (Cf. exp.) was found to be stereochemically similar with the structure of alismoxide, a guaianediol with stereostructure 1S*, 4S*, 5S*, 10R*-4, 10-guaianediol, isolated previously from the rhizome of Alisma plantago-aquatu and soft coral Sinularia sp. [22,27].

Compound 6 was isolated as amorphous powder. The obtained spectroscopic data (cf. exp.) of 6 was found to be stereochemically similar with the structure of chalinasterol, a steroid isolated previously from a soft coral of Sinularia gibberosa and Lytophyton arboretum [28,29].

Compound 7 was isolated as amorphous powder. A constructed structure based on the analysis of the spectral data (cf. exp.) was searched by science finder and found to be similar in structure with Nephalsterol C, a steroid isolated previously from a soft coral Lytophyton arboreum [29].

Biological activity assays confirmed that isoprenoids type compounds from Lobophytum sp. possessing antibacterial and antitumor activity. Compound 1 (alismol) has strong antibacterial activity against both gram positive (S. aureus, S. epidermis, and S. pneumonia) and negative bacteria (P. aeruginosa). Nevertheless, the antitumor activity was not detected. Compound 4 (cembrene A) showed moderate activity against all tested bacteria. Moreover, it also possesed high toxicity (25 μg/mL) against A. salina and appreciable antitumor activity (50 μg/mL) against Erhlich carcinoma cells.

Conclusion

Four sesquiterpenes, one cembranoid type diterpene and two steroids have been isolated and identified from the Red Sea soft coral Lobophyton sp. Compound 1 (alismol) has significant antibacterial activity against gram-positive (S. aureus, S. epidermis, and S. pneumonia) and gram-negative bacteria (P. aeruginosa). Compound 4 (cembrene A) also exhibited moderate antibacterial activity against all tested bacteria and appreciable antitumor properties against Erhlich carcinoma cells. Compounds 1 and 4 display potentials for treating pathogenic bacteria associated with many diseases and/or tumor and therefore, require further investigation

Declarations

Acknowledgement

The authors wish to thank Dr. Mohsen El-Sherbiny, Researcher, Marine Biology Department, Faculty of Marine Sciences, King Abdulaziz University, for collection and identification of the soft coral sample.

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