Mohamed A. Tammam , Nikolaos Tsoureas , Dafni-Ioanna Diakaki , Carlos M. Duarte , Vassilios Roussis , Efstathia Ioannou
{"title":"Thuwalamides A-E:从沙特阿拉伯红海采集的海洋海绵 Lamellodysidea herbacea 中提取的多氯酰胺。","authors":"Mohamed A. Tammam , Nikolaos Tsoureas , Dafni-Ioanna Diakaki , Carlos M. Duarte , Vassilios Roussis , Efstathia Ioannou","doi":"10.1016/j.phytochem.2024.114315","DOIUrl":null,"url":null,"abstract":"<div><div>Thuwalamides A–E (<strong>1</strong>, <strong>3</strong>, <strong>5</strong>, <strong>6</strong> and <strong>8</strong>), previously undescribed polychlorinated amides, along with ten previously reported related compounds (<strong>2</strong>, <strong>4</strong>, <strong>7</strong> and <strong>9</strong>–<strong>15</strong>), were isolated from the organic extract of the marine sponge <em>Lamellodysidea herbacea</em> (Keller), collected off the village of Thuwal in the Red Sea at Saudi Arabia. The structures of the isolated compounds have been determined through extensive analysis of their NMR and MS data, while their absolute stereochemistry was unequivocally established via single crystal X-ray diffraction. Additionally, the absolute stereochemistry of the previously reported compounds <strong>2</strong> and <strong>4</strong>, whose configuration was not determined, has also been established using single-crystal X-ray crystallographic analysis. The antibacterial activity of compounds <strong>1</strong>–<strong>15</strong> was evaluated against <em>Escherichia coli</em> and <em>Staphylococcus aureus</em>. Among them, compound <strong>14</strong> displayed activity against <em>S. aureus</em> comparable to vancomycin that was used as a positive control with a MIC value of 4 μg/mL.</div></div>","PeriodicalId":20170,"journal":{"name":"Phytochemistry","volume":"230 ","pages":"Article 114315"},"PeriodicalIF":3.2000,"publicationDate":"2024-11-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Thuwalamides A–E: Polychlorinated amides from the marine sponge Lamellodysidea herbacea collected from the Saudi Arabian Red Sea\",\"authors\":\"Mohamed A. Tammam , Nikolaos Tsoureas , Dafni-Ioanna Diakaki , Carlos M. Duarte , Vassilios Roussis , Efstathia Ioannou\",\"doi\":\"10.1016/j.phytochem.2024.114315\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>Thuwalamides A–E (<strong>1</strong>, <strong>3</strong>, <strong>5</strong>, <strong>6</strong> and <strong>8</strong>), previously undescribed polychlorinated amides, along with ten previously reported related compounds (<strong>2</strong>, <strong>4</strong>, <strong>7</strong> and <strong>9</strong>–<strong>15</strong>), were isolated from the organic extract of the marine sponge <em>Lamellodysidea herbacea</em> (Keller), collected off the village of Thuwal in the Red Sea at Saudi Arabia. The structures of the isolated compounds have been determined through extensive analysis of their NMR and MS data, while their absolute stereochemistry was unequivocally established via single crystal X-ray diffraction. Additionally, the absolute stereochemistry of the previously reported compounds <strong>2</strong> and <strong>4</strong>, whose configuration was not determined, has also been established using single-crystal X-ray crystallographic analysis. The antibacterial activity of compounds <strong>1</strong>–<strong>15</strong> was evaluated against <em>Escherichia coli</em> and <em>Staphylococcus aureus</em>. Among them, compound <strong>14</strong> displayed activity against <em>S. aureus</em> comparable to vancomycin that was used as a positive control with a MIC value of 4 μg/mL.</div></div>\",\"PeriodicalId\":20170,\"journal\":{\"name\":\"Phytochemistry\",\"volume\":\"230 \",\"pages\":\"Article 114315\"},\"PeriodicalIF\":3.2000,\"publicationDate\":\"2024-11-06\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Phytochemistry\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0031942224003522\",\"RegionNum\":2,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"BIOCHEMISTRY & MOLECULAR BIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Phytochemistry","FirstCategoryId":"99","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0031942224003522","RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
引用次数: 0
摘要
从沙特阿拉伯红海 Thuwal 村附近采集的海洋海绵 Lamellodysidea herbacea(Keller)的有机萃取物中分离出了 Thuwalamides A-E(1、3、5、6 和 8),它们是之前未曾描述过的多氯酰胺,以及之前报道过的 10 种相关化合物(2、4、7 和 9-15)。通过对这些分离化合物的核磁共振和质谱数据进行广泛分析,确定了它们的结构,并通过单晶 X 射线衍射明确确定了它们的绝对立体化学结构。此外,先前报告的化合物 2 和 4 的构型尚未确定,其绝对立体化学结构也通过单晶 X 射线晶体分析得以确定。评估了化合物 1-15 对大肠杆菌和金黄色葡萄球菌的抗菌活性。其中,化合物 14 对金黄色葡萄球菌的活性与作为阳性对照的万古霉素相当,其 MIC 值为 4 μg/mL。
Thuwalamides A–E: Polychlorinated amides from the marine sponge Lamellodysidea herbacea collected from the Saudi Arabian Red Sea
Thuwalamides A–E (1, 3, 5, 6 and 8), previously undescribed polychlorinated amides, along with ten previously reported related compounds (2, 4, 7 and 9–15), were isolated from the organic extract of the marine sponge Lamellodysidea herbacea (Keller), collected off the village of Thuwal in the Red Sea at Saudi Arabia. The structures of the isolated compounds have been determined through extensive analysis of their NMR and MS data, while their absolute stereochemistry was unequivocally established via single crystal X-ray diffraction. Additionally, the absolute stereochemistry of the previously reported compounds 2 and 4, whose configuration was not determined, has also been established using single-crystal X-ray crystallographic analysis. The antibacterial activity of compounds 1–15 was evaluated against Escherichia coli and Staphylococcus aureus. Among them, compound 14 displayed activity against S. aureus comparable to vancomycin that was used as a positive control with a MIC value of 4 μg/mL.
期刊介绍:
Phytochemistry is a leading international journal publishing studies of plant chemistry, biochemistry, molecular biology and genetics, structure and bioactivities of phytochemicals, including ''-omics'' and bioinformatics/computational biology approaches. Phytochemistry is a primary source for papers dealing with phytochemicals, especially reports concerning their biosynthesis, regulation, and biological properties both in planta and as bioactive principles. Articles are published online as soon as possible as Articles-in-Press and in 12 volumes per year. Occasional topic-focussed special issues are published composed of papers from invited authors.