Antibacterial and Cytotoxic Potential of Two Steroids from the Indonesian Soft Coral Sinularia polydactila

IF 1 Q4 PHARMACOLOGY & PHARMACY Jundishapur Journal of Natural Pharmaceutical Products Pub Date : 2021-09-18 DOI:10.5812/jjnpp.109432
M. Putra, F. Karim, Aji Nugroho
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Abstract

Background: Soft corals of the genus Sinularia are well recognized as a rich source of steroidal compounds. These constituents, mainly steroids, have been reported as possessing antitumor, antimicrobial, and antiviral activities. Objectives: This study was designed to isolate and elucidate antibacterial and cytotoxic compounds from the soft coral Sinularia polydactila. Methods: Structure elucidation of steroids was determined based on spectroscopic data through 1D and 2D NMR analyses and mass spectrometry, with the results compared to data in the literature. Antibacterial activity was determined using four human bacterial pathogens, namely B. subtilis (ATCC 6633), P. aeruginosa (ATCC 27853), S. aureus (ATCC 25923), and E. coli (ATCC 25922). Cytotoxic activity was evaluated using the human colon cancer cell HCT 116 and brine shrimp lethality assay (BSLA). Results: Two steroids (Compounds 1 - 2) were isolated from the Indonesian soft coral Sinularia polydactila. (22R,23R,24R)-22,23-methylene-24-methylcholest-6-en-5α,8α-epidioxy-3β-ol (1) and 5α,8α-Epidioxy-24(R)-methylcholesta-6,22-dien-3α-ol (2) showed moderate activity against colon carcinoma cancer HCT 116 at the concentrations of 24.8 and 27.3 μg/mL, respectively. Furthermore, compounds 1 and 2 showed cytotoxic activity using the brine shrimp lethality assay with the concentrations of 57.1 and 121.3 3 μg/mL, respectively. Compound 2 showed moderate activity against S. aureus and B. subtilis at the 250 μg/mL concentration. Conclusions: Two steroids isolated from soft coral Sinularia polydactila were found to possess moderate cytotoxic and antibacterial activities.
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印尼软珊瑚中两种类固醇的抗菌和细胞毒性
背景:Sinularia属的软珊瑚是公认的甾体化合物的丰富来源。据报道,这些成分主要是类固醇,具有抗肿瘤、抗菌和抗病毒活性。目的:本研究旨在从软珊瑚聚乳酸奇点中分离和阐明抗菌和细胞毒性化合物。方法:根据波谱数据,通过1D、2D NMR分析和质谱分析,确定甾体化合物的结构,并将结果与文献数据进行比较。使用四种人类细菌病原体,即枯草芽孢杆菌(ATCC 6633)、铜绿假单胞菌(ATCC 27853)、金黄色葡萄球菌(ATCC 25923)和大肠杆菌(ATCC25922)测定抗菌活性。使用人结肠癌癌症细胞HCT 116和盐水虾致死性测定(BSLA)来评估细胞毒性活性。结果:从印度尼西亚软珊瑚多节星藻中分离得到两种甾体化合物(化合物1-2)。(22R,23R,24R)-22,23-methylene-24-methycholest-6-en-5α,8α-表二氧-3β-醇(1)和5α,8-表二氧-4(R)-甲基cholesta-6,22-den-3α-醇(2)分别在24.8和27.3μg/mL的浓度下对结肠癌癌症HCT 116表现出中等活性。此外,使用浓度分别为57.1和121.33μg/mL的卤虾致死性测定,化合物1和2显示出细胞毒性活性。化合物2在250μg/mL浓度下对金黄色葡萄球菌和枯草芽孢杆菌显示中等活性。结论:从软珊瑚中分离得到的两种甾体化合物具有中等的细胞毒性和抗菌活性。
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1.40
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26
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