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2D NMR Studies of Bromotyrosine Alkaloid, Purpurealidin K from Marine Sponge Psammaplysilla purpurea

机译:2D NMR研究的溴诺酪氨酸生物碱,紫脂蛋白K的海绵psammaplysilla purpurea

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摘要

Marine sponges of the order Verongida and related organisms are the richest source of bioactive bromotyrosine alkaloids. Purpurealidin K (1) along with purealidin Q (2), aerophobin 2 (3) and aplysamine 2 (4) were isolated from methanol extract of marine sponge Psammaplysilla purpurea collected from Madapam, Tamil Nadu, India. The structure of natural product, purpurealidin K (1) was assigned by extensive 1 H, 13 C, DEPT, TOCSY, HSQC & HMBCNMR experiments and electrospray ionization-quadrupole time-of-flight (ESI-QTOF MS/MS) mass spectrometric measurements. For the first time, the complete set of spectroscopic data of compound (1) has been obtained. Moreover, compounds (2-4) were identified by using various spectroscopic data and their comparison with literature reports. These bromotyrosine derived metabolites were evaluated against multiple drug resistance bacterial cells and against clinical pathogens, wherein purpurealidin K (1) displayed moderate activities against Methicillin Resistant Staphylococcus aureus (MRSA), Escherichia coli, Pseudomonas aeruginosa.
机译:verongida阶的海洋海绵和相关生物是生物活性溴诺酮生物碱的最丰富来源。紫脂蛋白K(1)以及葡萄霉素Q(2),酸磷脂2(3)和丙酰胺2(4)从印度泰米尔纳德邦Madapam收集的海洋海绵psammaplysilla purpurea的甲醇提取物中分离出来。天然产物的结构,紫purealidin k(1)的结构由1小时,13 C,部,TOCSY,HSQC和HMBCNMR实验和电喷雾电离 - Quadrupole飞行时间(ESI-QTOF MS/MS)质谱测量值分配。 。首次获得了化合物(1)的完整光谱数据集。此外,通过使用各种光谱数据及其与文献报告进行比较来鉴定化合物(2-4)。评估了这些溴诺酮衍生的代谢产物针对多种耐药细菌细胞和临床病原体的评估,其中紫豆性素K(1)显示出对甲氧西林抗甲氧西林金黄色葡萄球菌(MRSA),Escherichia Coli,Pseudomonas erugoginosa的中度活性。

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