A New Sesquiterpenoid Aminoquinone from an Indonesian Marine Sponge

被引:13
作者
Balansa, Walter [1 ,2 ]
Mettal, Ute [1 ,3 ]
Wuisan, Zerlina G. [1 ,3 ]
Plubrukarn, Anuchit [4 ]
Ijong, Frans G. [2 ,5 ]
Liu, Yang [1 ,3 ]
Schaeberle, Till F. [1 ,3 ,6 ]
机构
[1] Justus Liebig Univ Giessen, Inst Insect Biotechnol, D-35392 Giessen, Germany
[2] Nusa Utara Polytech, Dept Fisheries & Marine Sci, Tahuna 95812, North Sulawesi, Indonesia
[3] Fraunhofer Inst Mol Biol & Appl Ecol, Dept Bioresources, D-35394 Giessen, Germany
[4] Prince Songkla Univ, Fac Pharmaceut Sci, Dept Pharmacognosy & Pharmaceut Bot, Hat Yai 90110, Thailand
[5] Sam Ratulangi Univ, Fac Fisheries & Marine Sci, Manado 95115, Indonesia
[6] German Ctr Infect Res DZIF, Partner Site Giessen Marburg Langen, D-35392 Giessen, Germany
关键词
nakijiquinone; antibacterial activity; cytotoxicity; merosesquiterpenes; aminoquinone; QUINONES; ILLIMAQUINONE; SMENOSPONGINE; INHIBITION; VIRUS;
D O I
10.3390/md17030158
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Sponges are a well-known bioresource for bioactive compounds. In this study, antibacterial activity-guided fractionation of the extract from an Indonesian marine Dactylospongia elegans sponge led to the discovery of four merosesquiterpenoids, namely, a new sesquiterpenoid aminoquinone nakijiquinone V (1), along with illimaquinone (2), smenospongine (3), and dyctioceratine C (4). The structure of compound 1 was elucidated by 1D and 2D NMR as well as by LC-HRESIMS data analysis. Compounds 2-4 showed moderate to low antimicrobial activity against Bacillus megaterium DSM32 with a minimum inhibitory concentration (MIC) of 32 g/mL, 32 g/mL, and 64 g/mL, respectively. Furthermore, compounds 2 and 3 both inhibited Micrococcus luteus ATCC 4698 with a MIC of 32 g/mL. In conclusion, the isolated merosesquiterpenoids, which are known for their cytotoxic effects, showed antibacterial activity and prompt future structure activity relationship (SAR) studies concerning the various bioactivities observed for this group of natural products.
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页数:7
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